GlyCosmos Portal

Table Filtering

Gene ID

Gene Name

Gene Symbol

Organism

Taxonomy ID

Disease Ontology

Disease Ontology ID

Gene Ontology

Gene Ontology ID

Display
results per page.

Clear

Submissions

GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **126 - 150** of **1582** in total

« First

‹ Prev

1

2

3

4

5

6

7

8

9

10

…

Next ›

Last »
Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
81849	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5	ST6GALNAC5 Aliases: MGC3184 ST6GalNAcV	Homo sapiens (human)	arteriosclerotic cardiovascular disease atherosclerosis breast cancer cancer central nervous system cancer central nervous system lymphoma cervical adenocarcinoma cervical cancer cervix carcinoma cervix disease cervix uteri carcinoma in situ coronary artery disease embryoma gliosarcoma high grade glioma lymphoma mixed glioma nutmeg liver obsolete ymphosarcoma rheumatoid arthritis
27090	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4	ST6GALNAC4 Aliases: SIAT3C ST6GALNACIV	Homo sapiens (human)	Guillain-Barre syndrome Miller Fisher syndrome cancer thyroid gland follicular carcinoma
256435	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	ST6GALNAC3 Aliases: ST6GALNAC III	Homo sapiens (human)	diabetes mellitus gestational diabetes idiopathic scoliosis prostate cancer prostate carcinoma type 2 diabetes mellitus
10610	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	ST6GALNAC2 Aliases: ST6GalNAII STHM	Homo sapiens (human)	IgA glomerulonephritis breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma depressive disorder embryoma large intestine cancer major depressive disorder melancholic depression melanoma obsolete melancholia skin melanoma thyroid gland follicular carcinoma
55808	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 1	ST6GALNAC1 Aliases: ST6GalNAcI	Homo sapiens (human)	acute myocardial infarction bladder carcinoma breast cancer cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary thrombosis embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma inflammatory bowel disease 1 inflammatory bowel disease large intestine cancer myocardial infarction ovarian cancer ovarian carcinoma schizophrenia silent myocardial infarction stomach cancer stomach carcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer
84620	ST6 beta-galactoside alpha-2,6-sialyltransferase 2	ST6GAL2 Aliases: KIAA1877 St6GalII	Homo sapiens (human)	breast cancer esophageal cancer esophageal carcinoma thyroid gland follicular carcinoma
6480	ST6 beta-galactoside alpha-2,6-sialyltransferase 1	ST6GAL1 Aliases: CDw75 ST6Gal I	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Graves' disease IgA glomerulonephritis Kawasaki disease Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia adenocarcinoma adenoma adult hepatocellular carcinoma alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis allergic asthma allergic contact dermatitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bladder carcinoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma childhood hepatocellular carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease cribriform carcinoma diabetes mellitus diabetic ketoacidosis embryoma esophageal cancer esophageal carcinoma gallbladder disease giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatitis hepatocellular carcinoma high grade glioma hyperthyroidism influenza intrinsic asthma large intestine cancer liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma microphthalmia mixed glioma obesity obsolete Matthew-Wood syndrome ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma parapsoriasis primary immunodeficiency disease prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole rheumatoid arthritis sarcomatoid carcinoma scleroderma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma systemic scleroderma thyrotoxicosis tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer
10402	ST3 beta-galactoside alpha-2,3-sialyltransferase 6	ST3GAL6 Aliases: ST3GALVI	Homo sapiens (human)	cancer carcinoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer multiple myeloma sarcomatoid carcinoma stomach cancer
8869	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	ST3GAL5 Aliases: SIATGM3S ST3GalV ganglioside GM3 synthase lactosylceramide alpha-2,3-sialyltransferase	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 MASA syndrome Mast syndrome Niemann-Pick disease type C1 Niemann-Pick disease Rett syndrome SPOAN syndrome Troyer syndrome Unverricht-Lundborg syndrome agnosia arthritis arthropathy blepharospasm blindness cerebral palsy congenital nystagmus developmental and epileptic encephalopathy 36 dissociated nystagmus dystonia early myoclonic encephalopathy endocrine exophthalmos focal hand dystonia hemiplegia hepatocellular carcinoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer locked-in syndrome microcephaly optic atrophy paroxysmal nonkinesigenic dyskinesia 1 paroxysmal nonkinesigenic dyskinesia 2 pathologic nystagmus quadriplegia salt and pepper syndrome sensorineural hearing loss spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spontaneous ocular nystagmus status epilepticus stereotypic movement disorder syndromic X-linked intellectual disability 94 thromboangiitis obliterans trichohepatoenteric syndrome 1 trichohepatoenteric syndrome visual epilepsy
6484	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	ST3GAL4 Aliases: FLJ11867 SAT3 ST3Gal IV STZ	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction adenoid cystic carcinoma alopecia amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant intellectual developmental disorder 4 autosomal dominant intellectual developmental disorder autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy brain stem infarction campomelic dysplasia cancer carcinoma cardiomyopathy cataract cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma collecting duct carcinoma colon carcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis craniometaphyseal dysplasia dementia depressive disorder diabetes mellitus diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism distal myopathy dysthymic disorder embryoma encephalitis encephalomyelitis endomyocardial fibrosis essential hypertension facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial hyperlipidemia frontotemporal dementia gallbladder disease gestational diabetes granuloma annulare hepatocellular carcinoma hyperglycemia hyperinsulinism hypertension hypertrophic cardiomyopathy hypoglycemia large intestine cancer limb-girdle muscular dystrophy liver cancer liver disease major depressive disorder melancholic depression melanoma mucopolysaccharidosis IV mucopolysaccharidosis IVA muscular dystrophy myelitis myocardial infarction neuropathy neurotic disorder nonpapillary renal cell carcinoma obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete melancholia obsolete type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy osteoporosis pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peripheral nervous system disease polyneuropathy renal carcinoma renal cell carcinoma renal osteodystrophy retinal disease retinitis retrograde amnesia salivary gland adenoid cystic carcinoma salivary gland cancer sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma squamous cell carcinoma steatotic liver disease thrombophilia tongue squamous cell carcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus
6487	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	ST3GAL3 Aliases: N-acetyllactosaminide alpha-2,3-sialyltransferase ST3Gal III	Homo sapiens (human)	Unverricht-Lundborg syndrome West syndrome agnosia amyotrophic lateral sclerosis attention deficit hyperactivity disorder autosomal recessive intellectual developmental disorder 12 autosomal recessive intellectual developmental disorder bipolar disorder blepharospasm brain cancer breast cancer breast carcinoma cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma choreatic disease congenital disorder of glycosylation depressive disorder developmental and epileptic encephalopathy 15 developmental coordination disorder diabetes mellitus dysthymic disorder dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy embryoma epilepsy focal epilepsy focal hand dystonia hepatocellular carcinoma influenza intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia pancreatic adenocarcinoma partial motor epilepsy progressive muscular atrophy prostate cancer prostate carcinoma pterygium schizophrenia stereotypic movement disorder stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 type 2 diabetes mellitus visual epilepsy
6483	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	ST3GAL2 Aliases: ST3GALII ST3GalA.2	Homo sapiens (human)	Parkinson's disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma late onset Parkinson's disease mucopolysaccharidosis IV mucopolysaccharidosis IVA nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
6482	ST3 beta-galactoside alpha-2,3-sialyltransferase 1	ST3GAL1 Aliases: CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase SIATFL ST3Gal I ST3GalA.1 ST3O	Homo sapiens (human)	Graves' disease bipolar disorder bladder carcinoma breast cancer breast carcinoma cancer cervical squamous cell carcinoma chronic myeloid leukemia embryoma hyperthyroidism mucopolysaccharidosis IV mucopolysaccharidosis IVA ovarian cancer ovarian carcinoma ovary serous adenocarcinoma prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder scleroderma skin squamous cell carcinoma systemic scleroderma thyrotoxicosis urinary bladder cancer
5552	serglycin	SRGN Aliases: PPG serglycin proteoglycan	Homo sapiens (human)	MHC class II deficiency Sertoli cell-only syndrome Y-linked spermatogenic failure 1 acute myeloid leukemia acute promyelocytic leukemia adenosine deaminase deficiency adult respiratory distress syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis carcinoma central nervous system cancer childhood type dermatomyositis cleft palate colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary aneurysm coronary artery disease coronary stenosis degenerative disc disease dental caries dentin caries dermatomyositis diabetes mellitus diabetic cataract diabetic retinopathy diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health embryoma enterocele esophagus squamous cell carcinoma essential hypertension giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance gynecomastia hepatitis B hepatocellular carcinoma high grade glioma hypertension infant gynecomastia isolated cleft palate large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus male infertility malignant pleural mesothelioma mixed glioma multiple myeloma nasopharynx carcinoma newborn respiratory distress syndrome nutmeg liver oligospermia oral candidiasis osteoarthritis prediabetes syndrome psychotic disorder sarcomatoid carcinoma severe combined immunodeficiency type 2 diabetes mellitus
79644	steroid 5 alpha-reductase 3	SRD5A3 Aliases: 3-oxo-5-alpha-steroid 4-dehydrogenase (NADP(+)) FLJ13352 SRD5A2L SRD5A2L1 polyprenol reductase	Homo sapiens (human)	Creutzfeldt-Jakob disease Hailey-Hailey disease Kahrizi syndrome Marfan syndrome Rothmund-Thomson syndrome acquired hyperkeratosis agnosia angioma serpiginosum antithrombin III deficiency autistic disorder autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bilateral optic nerve hypoplasia blindness capillary hemangioma cataract cavernous hemangioma cerebellar ataxia cerebellar disease coloboma congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congenital hypothyroidism congenital nystagmus craniosynostosis cutis laxa dermatitis developmental coordination disorder dissociated nystagmus epilepsy eye disease fundus dystrophy glaucoma hypertrichosis hypothyroidism ichthyosis inguinal hernia intellectual disability isolated cleft palate isolated growth hormone deficiency learning disability mal de Meleda microcytic anemia microphthalmia myxedema nonepidermolytic palmoplantar keratoderma obsolete infantile epileptic encephalopathy optic atrophy palmoplantar keratosis pathologic nystagmus pituitary hypoplasia prostate cancer prostate carcinoma protein C deficiency protein S deficiency recurrent corneal erosion restrictive dermopathy situs inversus spontaneous ocular nystagmus syndromic X-linked intellectual disability 94 thrombophilia tuberous sclerosis visual epilepsy
6716	steroid 5 alpha-reductase 2	SRD5A2 Aliases: 3-oxo-5-alpha-steroid 4-dehydrogenase 2	Homo sapiens (human)	Sertoli cell-only syndrome Turner syndrome Y-linked spermatogenic failure 1 abdominal obesity-metabolic syndrome 1 adenosarcoma alcohol dependence alcohol use disorder alopecia androgen insensitivity syndrome androgenic alopecia azoospermia breast cancer breast carcinoma cancer childhood acute lymphocytic leukemia cryptorchidism diabetes mellitus diabetic ketoacidosis disorder of sexual development embryoma endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis of uterus endometriosis gallbladder disease gonadal dysgenesis hepatitis C hepatocellular carcinoma hermaphroditism hyperprolactinemia hypogonadotropic hypogonadism 23 with or without anosmia hypospadias liver cancer liver carcinoma liver disease nephroblastoma nodular prostate oligospermia ovarian cancer ovarian carcinoma pancreatitis peripheral artery disease phimosis polycystic ovary syndrome post-traumatic stress disorder prostate cancer prostate carcinoma prostate disease prostatic adenoma pseudohermaphroditism schizophrenia type 2 diabetes mellitus urinary tract obstruction uterine corpus cancer
6715	steroid 5 alpha-reductase 1	SRD5A1 Aliases: 3-oxo-5-alpha-steroid 4-dehydrogenase 1	Homo sapiens (human)	abdominal aortic aneurysm alcohol dependence alcohol use disorder alopecia androgenic alopecia anxiety disorder bipolar disorder breast cancer breast carcinoma cancer central nervous system cancer congenital hypothyroidism depressive disorder diabetes mellitus dysthymic disorder embryoma endometriosis of ovary endometriosis of uterus endometriosis generalized anxiety disorder gliosarcoma high grade glioma hyperprolactinemia hypospadias hypothyroidism intermittent claudication major depressive disorder melancholic depression mixed glioma myxedema neurotic disorder nodular prostate obesity obsolete melancholia panic disorder peripheral artery disease peripheral vascular disease phobic disorder polycystic ovary syndrome primary cutaneous amyloidosis prostate cancer prostate carcinoma prostatic adenoma prostatic hypertrophy type 2 diabetes mellitus
6713	squalene epoxidase	SQLE Aliases: squalene monooxygenase	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebral degeneration colorectal cancer colorectal carcinoma embryoma esophagus squamous cell carcinoma hepatocellular carcinoma large intestine cancer liver cancer long QT syndrome lung benign neoplasm lung cancer lung carcinoma lung squamous cell carcinoma microphthalmia neuroendocrine carcinoma neuroendocrine tumor obsolete Matthew-Wood syndrome prostate cancer prostate carcinoma sick sinus syndrome steatotic liver disease tinea corporis
165679	serine palmitoyltransferase small subunit B	SPTSSB Aliases: ADMP androgen down regulated in mouse prostate small subunit of serine palmitoyltransferase B ssSPTb	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease
171546	serine palmitoyltransferase small subunit A	SPTSSA Aliases: small subunit of serine palmitoyltransferase A ssSPTa	Homo sapiens (human)	hereditary spastic paraplegia 90A hereditary spastic paraplegia 90B
55304	serine palmitoyltransferase long chain base subunit 3	SPTLC3 Aliases: FLJ11112 LCB2B hLCB2b	Homo sapiens (human)	autosomal dominant cerebellar ataxia bacterial sepsis head and neck squamous cell carcinoma hereditary sensory and autonomic neuropathy type 1 neurodegenerative disease neuropathy peripheral nervous system disease polyneuropathy sensory peripheral neuropathy spinocerebellar ataxia type 7
9517	serine palmitoyltransferase long chain base subunit 2	SPTLC2 Aliases: KIAA0526 LCB2 LCB2A hLCB2a	Homo sapiens (human)	Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease acute myocardial infarction agenesis of the corpus callosum with peripheral neuropathy anhidrosis cancer coronary thrombosis diarrhea hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory and autonomic neuropathy type 1C hereditary sensory and autonomic neuropathy type 2 hereditary sensory neuropathy hypohidrosis liver cancer motor peripheral neuropathy myocardial infarction neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum osteomyelitis parapsoriasis peripheral nervous system disease psoriasis pustulosis of palm and sole sensory peripheral neuropathy silent myocardial infarction teratocarcinoma
10558	serine palmitoyltransferase long chain base subunit 1	SPTLC1 Aliases: HSAN1 LCB1 SPTI hLCB1	Homo sapiens (human)	Alzheimer's disease Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Riley-Day syndrome acquired hyperkeratosis agenesis of the corpus callosum with peripheral neuropathy alternating hemiplegia of childhood autonomic neuropathy bipolar disorder brain cancer breast cancer cancer central nervous system cancer central nervous system disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma dementia diabetes mellitus disease of mental health embryoma frontotemporal dementia gliosarcoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory and autonomic neuropathy type 2 hereditary sensory and autonomic neuropathy type 5 hereditary sensory neuropathy type 4 hereditary sensory neuropathy high grade glioma juvenile amyotrophic lateral sclerosis type 27 keratosis mixed glioma motor peripheral neuropathy nervous system disease neurodegenerative disease neuropathy nonpapillary renal cell carcinoma obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum papillary renal cell carcinoma peripheral nervous system disease polyneuropathy psychotic disorder renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder sensorineural hearing loss sensory peripheral neuropathy skin disease type 2 diabetes mellitus
56848	sphingosine kinase 2	SPHK2	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Kaposi's sarcoma Pick's disease Reye syndrome actinic keratosis acute lymphoblastic leukemia acute pancreatitis adrenoleukodystrophy adult acute lymphocytic leukemia adult lymphoma alcoholic hepatitis alcoholic liver cirrhosis amnestic disorder anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bile duct adenocarcinoma bile duct carcinoma bone disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease cartilage disease central nervous system cancer central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease chikungunya childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood lymphoma childhood osteosarcoma cholangiocarcinoma chondrosarcoma chronic fatigue syndrome chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma connective tissue disease coronary artery disease cystic fibrosis dengue disease dengue hemorrhagic fever diabetes mellitus diabetic ketoacidosis embryoma encephalitis encephalomyelitis essential hypertension fibrillary astrocytoma gallbladder disease gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma heart disease hematologic cancer hepatocellular carcinoma high grade glioma hypertension idiopathic interstitial pneumonia immune system disease influenza intrahepatic cholangiocarcinoma juvenile pilocytic astrocytoma large intestine cancer liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lupus erythematosus lymphoblastic lymphoma lymphoma lymphopenia malignant astrocytoma malignant pleural mesothelioma metabolic dysfunction-associated steatohepatitis middle cerebral artery infarction mixed glioma multiple myeloma multiple sclerosis myelitis neuroblastoma neurodegenerative disease obesity obsolete asthenopia obsolete ymphosarcoma osteoarthritis osteoglophonic dysplasia osteosarcoma pancreatic cancer pancreatic carcinoma pancreatitis papillary adenocarcinoma papillary renal cell carcinoma parapsoriasis pilocytic astrocytoma pneumonia postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma protoplasmic astrocytoma psoriasis pulmonary fibrosis pustulosis of palm and sole retinal disease retinitis retrograde amnesia rheumatoid arthritis sarcomatoid carcinoma seborrheic keratosis skin disease skin squamous cell carcinoma steatotic liver disease subependymal giant cell astrocytoma synovitis systemic lupus erythematosus tenosynovitis thrombocytopenia thyroid gland papillary carcinoma type 2 diabetes mellitus ureteral obstruction vascular disease viral infectious disease yellow fever
8877	sphingosine kinase 1	SPHK1 Aliases: SPHK	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Clouston syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Pick's disease Reye syndrome Sjogren's syndrome acute myeloid leukemia adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma adrenoleukodystrophy anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome bacterial sepsis benign mesothelioma bile duct adenocarcinoma bile duct carcinoma biliary tract cancer bladder carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardia cancer cardiomyopathy central nervous system cancer cerebral degeneration cervical cancer cervix carcinoma cholangiocarcinoma chromophobe renal cell carcinoma chronic fatigue syndrome chronic obstructive pulmonary disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease dengue disease diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma distal arthrogryposis embryoma encephalitis encephalomyelitis endocrine exophthalmos esophagus squamous cell carcinoma essential hypertension follicular adenoma gallbladder cancer gallbladder carcinoma gastroenteritis generalized anxiety disorder giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatitis B hepatitis hepatocellular carcinoma high grade glioma hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma keratoconjunctivitis sicca kidney cancer kidney disease kwashiorkor large intestine cancer liver cancer liver carcinoma liver cirrhosis lung cancer lung carcinoma lung non-small cell carcinoma lymphopenia malaria malignant mesothelioma malignant pleural mesothelioma marasmus microcystic adenoma mixed glioma multiple myeloma multiple sclerosis myelitis myelodysplastic syndrome nasopharynx carcinoma nephritis nonpapillary renal cell carcinoma nutrition disease obesity obsolete ymphosarcoma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma parapsoriasis primary pulmonary hypertension prostate cancer prostate carcinoma protein-energy malnutrition psoriasis pustulosis of palm and sole renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma type 2 diabetes mellitus ulcerative colitis ureteral obstruction urinary bladder cancer viral infectious disease yellow fever

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements