GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **251 - 275** of **18496** in total

« First

‹ Prev

…

7

8

9

10

11

12

13

14

15

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
O95573	Fatty acid CoA ligase Acsl3	ACSL3 ACS3 FACL3 LACS3	Homo sapiens (human)	1	allergic asthma asthma bronchus cancer bronchus carcinoma cancer central nervous system cancer craniosynostosis embryoma familial hyperlipidemia gliosarcoma hepatitis C hepatocellular carcinoma high grade glioma intrinsic asthma liver cancer lung benign neoplasm lung cancer lung carcinoma melanoma mixed glioma ovarian cancer ovarian carcinoma prostate cancer prostate carcinoma sarcoma skin melanoma syndactyly
P61803	Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit DAD1	DAD1	Homo sapiens (human)	1	Barrett's esophagus allergic asthma asthma cancer embryoma intrinsic asthma lung small cell carcinoma neuroendocrine carcinoma neuroendocrine tumor
Q96KN3	Homeobox protein PKNOX2	PKNOX2 PREP2	Homo sapiens (human)	1
P78413	Iroquois-class homeodomain protein IRX-4	IRX4 IRXA3	Homo sapiens (human)	1
Q969S3	Cytoplasmic 60S subunit biogenesis factor ZNF622	ZNF622 ZPR9	Homo sapiens (human)	1
Q96MN5	Transcription elongation factor A N-terminal and central domain-containing protein 2	TCEANC2 C1orf83	Homo sapiens (human)	1
Q9Y2L6	FERM domain-containing protein 4B	FRMD4B GRSP1 KIAA1013	Homo sapiens (human)	1
Q92551	Inositol hexakisphosphate kinase 1	IP6K1 IHPK1 KIAA0263	Homo sapiens (human)	1
Q9P2W1	Homologous-pairing protein 2 homolog	PSMC3IP HOP2 TBPIP	Homo sapiens (human)	1
Q3B820	Protein FAM161A	FAM161A	Homo sapiens (human)	1
Q9NUQ9	CYFIP-related Rac1 interactor B	CYRIB CYRI FAM49B	Homo sapiens (human)	1
O95295	SNARE-associated protein Snapin	SNAPIN BLOC1S7 SNAP25BP SNAPAP	Homo sapiens (human)	1
Q9GZT9	Egl nine homolog 1	EGLN1 C1orf12	Homo sapiens (human)	1
P78382	CMP-sialic acid transporter	SLC35A1	Homo sapiens (human)	1	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 Behcet's disease Marfan syndrome Papillon-Lefevre disease Pick's disease Reye syndrome acute myocardial infarction agranulocytosis amyotrophic lateral sclerosis anhidrosis anterior horn cell disease aortic valve insufficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis brain disease brain stem infarction cancer cardiovascular system disease cellulitis central nervous system cancer cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cone-rod dystrophy 2 cone-rod dystrophy congenital disorder of glycosylation Iq congenital disorder of glycosylation type II congenital disorder of glycosylation type IIf congenital disorder of glycosylation congenital nystagmus congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis diabetic macular edema dissociated nystagmus embryoma epilepsy episodic kinesigenic dyskinesia 1 essential hypertension gliosarcoma glucose intolerance heart disease hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypohidrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intellectual disability lateral sclerosis learning disability lingual-facial-buccal dyskinesia liver cancer microcephaly mixed glioma motor neuron disease myocardial infarction myotonic dystrophy type 2 neutropenia obesity obsolete type 1 diabetes mellitus 9 osteoarthritis pathologic nystagmus placental insufficiency pneumonia prediabetes syndrome progressive bulbar palsy progressive muscular atrophy proteinuria severe congenital neutropenia silent myocardial infarction situs inversus spontaneous ocular nystagmus substance abuse substance-related disorder thrombocytopenia 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 type 2 diabetes mellitus ulcerative colitis viral infectious disease visual epilepsy
Q16637	Survival motor neuron protein	SMN1 SMN2 SMN SMNC SMNT	Homo sapiens (human)	1
Q15651	High mobility group nucleosome-binding domain-containing protein 3	HMGN3 TRIP7	Homo sapiens (human)	1
O95600	Krueppel-like factor 8	KLF8 BKLF3 ZNF741	Homo sapiens (human)	1
Q8N999	RNA ligase 1	RLIG1 C12orf29	Homo sapiens (human)	1
Q00325	Solute carrier family 25 member 3	SLC25A3 PHC	Homo sapiens (human)	1
P49757	Protein numb homolog	NUMB C14orf41	Homo sapiens (human)	1
Q9UBM7	7-dehydrocholesterol reductase	DHCR7 D7SR	Homo sapiens (human)	1	3-methylglutaconic aciduria Behcet's disease Dandy-Walker syndrome Hailey-Hailey disease Laron syndrome Marfan syndrome Meckel syndrome Potter's syndrome Rapp-Hodgkin syndrome Rothmund-Thomson syndrome Smith-Lemli-Opitz syndrome X-linked ichthyosis achondroplasia ankyloblepharon-ectodermal defects-cleft lip/palate syndrome arteriosclerotic cardiovascular disease atherosclerosis atrioventricular septal defect autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal dominant polycystic kidney disease 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 bilateral renal aplasia cardiovascular system disease choanal atresia coloboma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc coronary artery disease cutis laxa dermatitis diabetes mellitus diabetic ketoacidosis fissured tongue glaucoma glycoproteinosis heart disease hepatitis C hepatocellular carcinoma hydrocephalus hypohidrotic ectodermal dysplasia hypospadias immune system disease intellectual disability interstitial nephritis large intestine cancer learning disability leukocyte adhesion deficiency 2 leukocyte adhesion deficiency lingual-facial-buccal dyskinesia liver cancer liver cirrhosis mal de Meleda microcephaly movement disease multiple sclerosis nutmeg liver obsolete type 1 diabetes mellitus 9 oligohydramnios osteomalacia periventricular nodular heterotopia photosensitive epilepsy photosensitivity disease placental insufficiency polycystic ovary syndrome polydactyly polyhydramnios pyelitis pyelonephritis restrictive dermopathy rheumatoid arthritis rickets scoliosis sensorineural hearing loss situs inversus syndromic X-linked intellectual disability type 10 tongue disease 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 type 2 diabetes mellitus ventricular septal defect
Q86Y22	Collagen alpha-1(XXIII) chain	COL23A1	Homo sapiens (human)	1
Q10567	AP-1 complex subunit beta-1	AP1B1 ADTB1 BAM22 CLAPB2	Homo sapiens (human)	1
Q658T7	Putative protein FAM90A2P	FAM90A2P	Homo sapiens (human)	1
Q96AP4	Zinc finger-containing ubiquitin peptidase 1	ZUP1 C6orf113 ZUFSP	Homo sapiens (human)	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements