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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 **351 - 375** of **1582** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
3556	interleukin 1 receptor accessory protein	IL1RAP Aliases: C3orf13 IL-1RAcP IL1R3	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 Kawasaki disease Pick's disease Reye syndrome X-linked adrenal hypoplasia congenita acute monocytic leukemia acute myeloid leukemia arteriosclerotic cardiovascular disease atherosclerosis autism spectrum disorder autistic disorder bacterial infectious disease cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma chronic myeloid leukemia chronic obstructive pulmonary disease ciliary body disease colitis coronary artery disease endometriosis of uterus endometriosis gallbladder disease gastroenteritis head and neck squamous cell carcinoma hepatocellular carcinoma ileitis ileocolitis intellectual disability iris disease learning disability liver cancer liver disease obesity pancreatic adenocarcinoma panuveitis parapsoriasis premenstrual tension psoriasis pustulosis of palm and sole rheumatoid arthritis scleroderma skin disease systemic lupus erythematosus systemic scleroderma uveitis
3572	interleukin 6 cytokine family signal transducer	IL6ST	Homo sapiens (human)	Alzheimer's disease arteriosclerosis brain ischemia hepatocellular carcinoma hyper IgE recurrent infection syndrome 4 hyperandrogenism hypertension primary immunodeficiency disease rheumatoid arthritis status epilepticus stomach cancer visual epilepsy
3607	forkhead box K2	FOXK2	Homo sapiens (human)
3612	inositol monophosphatase 1	IMPA1 Aliases: myo-inositol monophosphatase 1	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 Duchenne muscular dystrophy Lewy body dementia Pick's disease Reye syndrome alcohol dependence alcohol use disorder antisocial personality disorder aplastic anemia autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 intellectual developmental disorder 59 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 avoidant personality disorder bipolar disorder brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral atherosclerosis cerebral degeneration cerebral infarction cerebrovascular disease chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cone-rod dystrophy congenital muscular dystrophy conjunctivitis cryptosporidiosis cystitis delusional disorder dermatophytosis diabetes mellitus distal myopathy embryoma epilepsy essential hypertension facioscapulohumeral muscular dystrophy focal epilepsy fundus albipunctatus fungal infectious disease gallbladder disease gliosarcoma glycogen storage disease IV glycogen storage disease VI glycogen storage disease VII heart disease high grade glioma hypertension intellectual disability intracranial arteriosclerosis large intestine cancer learning disability limb-girdle muscular dystrophy liver disease lung benign neoplasm lung cancer lung carcinoma mixed glioma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 narcissistic personality disorder 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 oculopharyngeal muscular dystrophy ovarian cancer ovarian carcinoma paranoid schizophrenia partial motor epilepsy primary pulmonary hypertension retinitis pigmentosa rippling muscle disease 2 sickle cell anemia syndromic X-linked intellectual disability 94 systemic primary carnitine deficiency disease trigonitis type 2 diabetes mellitus visual epilepsy
3613	inositol monophosphatase 2	IMPA2 Aliases: myo-inositol monophosphatase 2	Homo sapiens (human)	bipolar disorder borderline personality disorder cancer cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma depressive disorder dysthymic disorder embryoma endometriosis of ovary endometriosis of uterus endometriosis intermittent explosive disorder major depressive disorder melancholic depression mood disorder neurotic disorder nonpapillary renal cell carcinoma obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia
3628	inositol polyphosphate-1-phosphatase	INPP1	Homo sapiens (human)	bipolar disorder cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer obsolete major affective disorder 2
3630	insulin	INS	Homo sapiens (human)	Alzheimer's disease cholangiocarcinoma diabetes mellitus diabetic retinopathy disease of metabolism gestational diabetes hyperinsulinism hypertension hyperuricemia insulinoma maturity-onset diabetes of the young type 10 maturity-onset diabetes of the young neonatal diabetes osteoarthritis pancreatic cancer pancreatic ductal carcinoma permanent neonatal diabetes mellitus prostate cancer steatotic liver disease type 1 diabetes mellitus 2 type 1 diabetes mellitus type 2 diabetes mellitus
3631	inositol polyphosphate-4-phosphatase type I A	INPP4A Aliases: Type I inositol 3,4-bisphosphate 4-phosphatase	Homo sapiens (human)	Marfan syndrome Unverricht-Lundborg syndrome allergic asthma asthma autosomal dominant dyskeratosis congenita 1 bladder carcinoma cancer early myoclonic encephalopathy embryoma intrinsic asthma lung cancer lung non-small cell carcinoma pancreatic cancer pancreatic carcinoma situs inversus tuberous sclerosis urinary bladder cancer
3632	inositol polyphosphate-5-phosphatase A	INPP5A Aliases: 43 kDa inositol polyphosphate 5-phophatase 5PTASE CTCL tumor antigen HD-CL-02 InsP3 5-phosphatase inositol polyphosphate 5-phophatase, 40kDa type I inositol-1,4,5-trisphosphate 5-phosphatase	Homo sapiens (human)	actinic keratosis ascending cholangitis cancer cholangitis inverted follicular keratosis keratoacanthoma melanoacanthoma oculocerebrorenal syndrome primary sclerosing cholangitis schizophrenia sclerosing cholangitis seborrheic keratosis skin benign neoplasm skin cancer skin disease skin squamous cell carcinoma squamous cell carcinoma suppurative cholangitis tongue squamous cell carcinoma
3633	inositol polyphosphate-5-phosphatase B	INPP5B Aliases: type II inositol 1,4,5-trisphosphate 5-phosphatase	Homo sapiens (human)	Dent disease Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome amyotrophic lateral sclerosis autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 congenital hypothyroidism congenital muscular dystrophy distal myopathy facioscapulohumeral muscular dystrophy giant cell glioblastoma glaucoma glioblastoma hypothyroidism limb-girdle muscular dystrophy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myxedema 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 oculopharyngeal muscular dystrophy progressive muscular atrophy rippling muscle disease 2
3635	inositol polyphosphate-5-phosphatase D	INPP5D Aliases: SH2 domain-containing inositol 5'-phosphatase 1 SHIP SHIP1 hp51CN	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 Burkitt lymphoma Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Down syndrome Marfan syndrome Paget's disease of bone Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia adult lymphoma allergic disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease childhood leukemia childhood lymphoma chronic interstitial cystitis chronic myeloid leukemia chronic obstructive pulmonary disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease cystic fibrosis dementia dermatitis diabetic ketoacidosis diffuse large B-cell lymphoma embryoma essential thrombocythemia gastroenteritis glomerulonephritis gout hematologic cancer hepatocellular carcinoma idiopathic interstitial pneumonia ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease interstitial cystitis interstitial keratitis juvenile myelomonocytic leukemia kidney disease large intestine cancer leukemia liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoblastic lymphoma lymphoma melanoma microphthalmia multiple myeloma myelodysplastic syndrome myeloproliferative neoplasm nephritis nephrosis obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oculocerebrorenal syndrome oral candidiasis osteoarthritis periodontitis postinflammatory pulmonary fibrosis primary cutaneous amyloidosis pulmonary fibrosis pyoureter rheumatoid arthritis situs inversus skin melanoma steatotic liver disease stuttering systemic lupus erythematosus tuberous sclerosis 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 ulcerative colitis viral infectious disease visceral leishmaniasis
3636	inositol polyphosphate phosphatase like 1	INPPL1 Aliases: 51C protein SH2 domain-containing inositol 5'-phosphatase 2 SHIP2 phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2	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 Laron syndrome Pick's disease Reye syndrome Richter's syndrome Turner syndrome abdominal obesity-metabolic syndrome 1 achondroplasia alternating hemiplegia of childhood amnestic disorder atrial fibrillation autonomic neuropathy bone disease breast cancer breast carcinoma cancer cartilage disease central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease chronic lymphocytic leukemia chronic myeloid leukemia cleft palate colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure connective tissue disease cryptorchidism depressive disorder diabetes mellitus diabetic ketoacidosis disease of metabolism dysthymic disorder elephantiasis embryoma essential hypertension giant cell glioblastoma glioblastoma glucose intolerance gonadal dysgenesis gonorrhea hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hypertension insulinoma isolated cleft palate isolated growth hormone deficiency large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer liver cancer lung cancer lung non-small cell carcinoma lymphedema major depressive disorder melancholic depression multiple myeloma nervous system disease neurodegenerative disease neurotic disorder obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 osteoporosis-pseudoglioma syndrome papillary adenocarcinoma papillary renal cell carcinoma polyhydramnios prediabetes syndrome retrograde amnesia schneckenbecken dysplasia scoliosis stomach cancer stomach carcinoma thyroid gland papillary 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
3651	pancreatic and duodenal homeobox 1	PDX1	Homo sapiens (human)	acute necrotizing pancreatitis cerebral infarction diabetes mellitus diabetic retinopathy hyperglycemia maturity-onset diabetes of the young type 4 maturity-onset diabetes of the young obesity pancreatic agenesis placental insufficiency type 1 diabetes mellitus type 2 diabetes mellitus
3703	STT3 oligosaccharyltransferase complex catalytic subunit A	STT3A Aliases: MGC9042 STT3-A TMC dolichyl-diphosphooligosaccharide protein glycotransferase	Homo sapiens (human)	IgA glomerulonephritis anthrax disease attention deficit hyperactivity disorder bipolar disorder cervical adenocarcinoma cervical cancer cervix carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital disorder of glycosylation Iw congenital disorder of glycosylation type I congenital disorder of glycosylation depressive disorder epidermodysplasia verruciformis focal epilepsy herpes simplex large intestine cancer major depressive disorder melancholic depression microcephaly mucoepidermoid carcinoma obsolete melancholia partial motor epilepsy schizophrenia skin benign neoplasm skin cancer skin squamous cell carcinoma sleeping sickness thyroid gland follicular carcinoma trypanosomiasis visual epilepsy
3705	inositol-tetrakisphosphate 1-kinase	ITPK1	Homo sapiens (human)	acute myeloid leukemia acute myocardial infarction arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation cancer cerebral infarction cerebrovascular disease chronic obstructive pulmonary disease congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis idiopathic scoliosis myelomeningocele myocardial infarction silent myocardial infarction spina bifida tethered spinal cord syndrome type 2 diabetes mellitus
3706	inositol-trisphosphate 3-kinase A	ITPKA Aliases: IP3-3KA IP3KA	Homo sapiens (human)	allergic asthma asthma bronchus cancer bronchus carcinoma cancer central nervous system cancer embryoma gliosarcoma high grade glioma intrinsic asthma lung cancer lung carcinoma mixed glioma
3707	inositol-trisphosphate 3-kinase B	ITPKB Aliases: IP3-3KB IP3KB	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 Pick's disease Reye syndrome allergic disease bronchus cancer bronchus carcinoma cancer cerebral degeneration dental caries dentin caries embryoma lung benign neoplasm lung cancer lung carcinoma obsolete ymphosarcoma sick sinus syndrome
3767	potassium inwardly rectifying channel subfamily J member 11	KCNJ11	Homo sapiens (human)	Parkinsonism diabetes mellitus familial hyperinsulinemic hypoglycemia 2 hyperinsulinism hypertension maturity-onset diabetes of the young type 13 permanent neonatal diabetes mellitus prediabetes syndrome sciatic neuropathy status epilepticus type 2 diabetes mellitus visual epilepsy
3784	potassium voltage-gated channel subfamily Q member 1	KCNQ1	Homo sapiens (human)	Jervell-Lange Nielsen syndrome atrial fibrillation familial atrial fibrillation hypertension long QT syndrome 1 long QT syndrome seminoma short QT syndrome type 2 diabetes mellitus
3795	ketohexokinase	KHK Aliases: fructokinase	Homo sapiens (human)	cancer cardiovascular system disease central nervous system cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma disease of metabolism embryoma essential fructosuria gliosarcoma heart disease hepatocellular carcinoma hereditary fructose intolerance syndrome high grade glioma hyperuricemia hypoglycemia kidney disease liver cancer lung cancer lung non-small cell carcinoma mixed glioma nonpapillary renal cell carcinoma obesity papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma steatotic liver disease
3820	killer cell lectin like receptor B1	KLRB1 Aliases: CD161 CLEC5B NKR-P1 NKR-P1A hNKR-P1A natural killer cell surface protein P1A	Homo sapiens (human)	Goodpasture syndrome Takayasu's arteritis acquired immunodeficiency syndrome acute promyelocytic leukemia aggressive NK-cell leukemia allergic asthma arthritis arthropathy asthma autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bone disease bronchus cancer bronchus carcinoma cancer cartilage disease cataract connective tissue disease eclampsia embryoma familial multiple nevi flammei granulomatosis with polyangiitis hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma hidradenitis suppurativa hidradenitis human immunodeficiency virus infectious disease immune system disease influenza intermittent claudication intrinsic asthma liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 melanoma mitral valve stenosis multiple myeloma multiple sclerosis myocarditis osteoarthritis peeling skin syndrome periodontitis placental insufficiency pneumonia polyarteritis nodosa pompholyx prostate cancer prostate carcinoma psoriatic arthritis rheumatoid arthritis scleroderma skin melanoma spondyloarthropathy spondylosis systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma tuberculosis urinary bladder cancer viral infectious disease
3821	killer cell lectin like receptor C1	KLRC1 Aliases: CD159a NKG2-1/B activating NK receptor NKG2-A NKG2-B	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 Barrett's esophagus Behcet's disease Graves' disease Japanese encephalitis Kawasaki disease Marfan syndrome Pick's disease Reye syndrome acquired immunodeficiency syndrome adult lymphoma allergic rhinitis autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome bacterial sepsis cancer central nervous system lymphoma cerebral degeneration childhood lymphoma choriocarcinoma chromophobe renal cell carcinoma chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma dengue disease embryoma endometriosis of uterus endometriosis enthesopathy fibromyalgia hematologic cancer hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma human immunodeficiency virus infectious disease hyperthyroidism immune system disease large intestine cancer leukemia liver cancer liver carcinoma lymphoma melanoma multiple myeloma multiple sclerosis nonpapillary renal cell carcinoma obsolete ymphosarcoma papillary renal cell carcinoma parapsoriasis placenta cancer psoriasis pustulosis of palm and sole renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma situs inversus skin melanoma systemic lupus erythematosus thyrotoxicosis tongue cancer tropical spastic paraparesis tuberous sclerosis vasomotor rhinitis viral infectious disease vitiligo yellow fever
3823	killer cell lectin like receptor C3	KLRC3 Aliases: NKG2-E	Homo sapiens (human)	diabetic ketoacidosis endometrial cancer endometrial carcinoma giant cell glioblastoma glioblastoma obsolete type 1 diabetes mellitus 9 sickle cell anemia 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 uterine corpus cancer
3824	killer cell lectin like receptor D1	KLRD1	Homo sapiens (human)	Behcet's disease Evans' syndrome Peutz-Jeghers syndrome acquired immunodeficiency syndrome acute myeloid leukemia acute promyelocytic leukemia adult lymphoma allergic asthma asthma autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura bacterial infectious disease cancer central nervous system lymphoma cervix uteri carcinoma in situ chikungunya childhood lymphoma chronic NK-cell lymphocytosis common wart dengue hemorrhagic fever diabetic ketoacidosis embryoma enthesopathy fibromyalgia hepatitis B hepatitis C hepatocellular carcinoma human immunodeficiency virus infectious disease idiopathic scoliosis immune system disease infectious mononucleosis influenza intrinsic asthma liver cancer lung cancer lung non-small cell carcinoma lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 multiple sclerosis obsolete malignant histiocytosis obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma primary immunodeficiency disease rheumatoid arthritis systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus tropical spastic paraparesis 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 von Hippel-Lindau disease
3897	L1 cell adhesion molecule	L1CAM Aliases: CAML1 CD171 NCAM-L1 neural cell adhesion molecule L1	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 Charcot-Marie-Tooth disease type 5 Henoch-Schoenlein purpura Hirschsprung's disease Kallmann syndrome Laron syndrome MASA syndrome Mast syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Rett syndrome Reye syndrome SPOAN syndrome Sheehan syndrome Troyer syndrome X-linked dominant hypophosphatemic rickets achondroplasia acne acute chest syndrome adenomatoid tumor adrenal gland cancer adrenoleukodystrophy alternating hemiplegia of childhood anxiety disorder aphasia atrophic gastritis autism spectrum disorder autistic disorder autonomic neuropathy benign ependymoma benign intermediate mesothelioma benign mesothelioma bile duct adenocarcinoma bile duct carcinoma bipolar disorder bone osteosarcoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma celiac disease cellular ependymoma central nervous system cancer central nervous system disease cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma childhood ependymoma cholangiocarcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma clubfoot collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communicating hydrocephalus congenital hypothyroidism congenital nystagmus craniosynostosis depressive disorder diabetes mellitus differentiated thyroid gland carcinoma dissociated nystagmus duodenum cancer embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma epilepsy esophagus squamous cell carcinoma familial retinoblastoma fibromyalgia gastrointestinal stromal tumor giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance heart cancer 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 high grade glioma holoprosencephaly 1 holoprosencephaly hydrocephalus hypersensitivity vasculitis hypertropia hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism hypothalamic disease hypothyroidism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease intellectual disability intracranial hypertension intrahepatic cholangiocarcinoma isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency kidney cancer large intestine cancer learning disability liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma major depressive disorder malignant mesothelioma malignant pleural mesothelioma mechanical strabismus melanoma microcephaly microinvasive gastric cancer microphthalmia mixed glioma mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis myxedema myxopapillary ependymoma nephrogenic diabetes insipidus nervous system disease neuroblastoma neurotic disorder nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete intestinal pseudo-obstruction obstructive hydrocephalus ophthalmoplegia osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatic ductal carcinoma panhypopituitarism papillary adenocarcinoma papillary ependymoma papillary renal cell carcinoma paralytic ileus paraplegia parathyroid gland disease pathologic nystagmus pheochromocytoma phobic disorder prediabetes syndrome primary biliary cholangitis prostate cancer prostate carcinoma pseudotumor cerebri renal carcinoma renal cell carcinoma restless legs syndrome retinoblastoma rickets sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia seminoma senile degeneration of brain skin melanoma small intestine cancer spontaneous ocular nystagmus squamous cell carcinoma stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability 94 systemic lupus erythematosus tanycytic ependymoma testicular cancer testis seminoma thymus gland disease thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma trilateral retinoblastoma type 2 diabetes mellitus uterine cancer uterine carcinosarcoma uterine corpus cancer

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