GlyCosmos Portal

Displaying entries **1601 - 1625** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q8NGL9	Olfactory receptor 4C16	OR4C16	1	0
P05000	Interferon omega-1	IFNW1	1	4
R9RH39	MHC class I antigen (Fragment)	HLA-C	1	0
Q86X10	Ral GTPase-activating protein subunit beta	RALGAPB KIAA1219	4	3
E9PQY3	Lysosomal acid phosphatase	ACP2	2	0
Q9MYC8	MHC class I antigen (Fragment)	HLA-B	1	0
Q9H3H5	UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase	DPAGT1 DPAGT2	2	2	Bell's palsy Ebola hemorrhagic fever Lambert-Eaton myasthenic syndrome acute intermittent porphyria agnosia alternating exotropia breast cancer cancer cataract clubfoot colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ij congenital disorder of glycosylation type I congenital disorder of glycosylation congenital myasthenic syndrome 13 congenital myasthenic syndrome congenital nystagmus congenital ptosis cutaneous leishmaniasis developmental and epileptic encephalopathy 36 developmental coordination disorder dissociated nystagmus epilepsy essential hypertension exotropia facial nerve disease facial paralysis familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome glycoproteinosis hepatocellular carcinoma hypertension intellectual disability isolated elevated serum creatine phosphokinase levels large intestine cancer learning disability leishmaniasis liver cancer microcephaly monocular exotropia mucolipidosis II alpha/beta myopathy pathologic nystagmus pseudosarcomatous fibromatosis ptosis scoliosis spontaneous ocular nystagmus squamous cell carcinoma stomach cancer stomach carcinoma stuttering syndromic X-linked intellectual disability 94 tongue squamous cell carcinoma tuberculosis visceral leishmaniasis visual epilepsy
Q9NYK1	Toll-like receptor 7	TLR7	14	3
O94925	Glutaminase kidney isoform, mitochondrial	GLS GLS1 KIAA0838	1	7
Q4FZB7	Histone-lysine N-methyltransferase KMT5B	KMT5B SUV420H1	2	5
Q8NH04	Olfactory receptor 2T27	OR2T27	1	0
Q6PF06	tRNA methyltransferase 10 homolog B	TRMT10B RG9MTD3	1	1
Q6PI48	Aspartate--tRNA ligase, mitochondrial	DARS2	0	1
Q8IX03	Protein KIBRA	WWC1 KIAA0869 KIBRA	1	1
Q6UXX9	R-spondin-2	RSPO2	1	1
P10323	Acrosin	ACR ACRS	2	1
A0A6B7FWV6	MHC class I antigen	HLA-B	1	0
P0DP72	V-set and immunoglobulin domain-containing protein 10-like 2	VSIG10L2	3	0
A0A060VCX9	MHC class I antigen (Fragment)	HLA-C	1	0
A0A7I2V3T9	Pro-cathepsin H	CTSH	2	0
Q16821	Protein phosphatase 1 regulatory subunit 3A	PPP1R3A PP1G	1	1	Alzheimer's disease adult lymphoma atrial fibrillation atypical chronic myeloid leukemia, BCR-ABL1 negative breast cancer cancer carcinoma central nervous system lymphoma childhood lymphoma chronic monocytic leukemia colorectal cancer colorectal carcinoma communication disorder congestive heart failure diabetes mellitus diabetic ketoacidosis embryoma glucose intolerance hematologic cancer language disorder large intestine cancer laryngeal squamous cell carcinoma lymphoid leukemia lymphoma myeloid leukemia obsolete ymphosarcoma prediabetes syndrome prostate cancer prostate carcinoma sarcomatoid carcinoma type 2 diabetes mellitus
A0A678ZW60	MHC class I antigen	HLA-B	1	0
A0A7I2V3M3	Cathepsin F	CTSF	2	0
B2ZCX3	MHC class I antigen (Fragment)	HLA-B	1	0
Q8N271	Prominin-2	PROM2 PROML2	5	17

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