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 **18426 - 18450** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q8N5M4	Tetratricopeptide repeat protein 9C	TTC9C	Homo sapiens (human)	1
P78346	Ribonuclease P protein subunit p30	RPP30 RNASEP2	Homo sapiens (human)	1
Q9UNZ2	NSFL1 cofactor p47	NSFL1C UBXN2C	Homo sapiens (human)	1
P57772	Selenocysteine-specific elongation factor	EEFSEC SELB	Homo sapiens (human)	1
P13533	Myosin-6	MYH6 MYHCA	Homo sapiens (human)	1
Q96A26	Protein FAM162A	FAM162A C3orf28 E2IG5	Homo sapiens (human)	1
O95198	Kelch-like protein 2	KLHL2	Homo sapiens (human)	1
P50479	PDZ and LIM domain protein 4	PDLIM4 RIL	Homo sapiens (human)	1
Q86UQ8	Transcription factor NF-E4	NFE4	Homo sapiens (human)	1
P50607	Tubby protein homolog	TUB	Homo sapiens (human)	1
Q9NRR6	Phosphatidylinositol polyphosphate 5-phosphatase type IV	INPP5E	Homo sapiens (human)	1	Bannayan-Riley-Ruvalcaba syndrome Bardet-Biedl syndrome 10 Bardet-Biedl syndrome 11 Bardet-Biedl syndrome 12 Bardet-Biedl syndrome 13 Bardet-Biedl syndrome 14 Bardet-Biedl syndrome 15 Bardet-Biedl syndrome 16 Bardet-Biedl syndrome 17 Bardet-Biedl syndrome 18 Bardet-Biedl syndrome 19 Bardet-Biedl syndrome 1 Bardet-Biedl syndrome 2 Bardet-Biedl syndrome 3 Bardet-Biedl syndrome 4 Bardet-Biedl syndrome 5 Bardet-Biedl syndrome 6 Bardet-Biedl syndrome 7 Bardet-Biedl syndrome 8 Bardet-Biedl syndrome 9 Bardet-Biedl syndrome Cogan syndrome Hirschsprung's disease Joubert syndrome 1 Joubert syndrome Kartagener syndrome Klippel-Feil syndrome Laurence-Moon syndrome Meckel syndrome 1 Meckel syndrome adult medulloblastoma autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease blindness cancer cataract central sleep apnea childhood medulloblastoma cleft palate clubfoot coloboma of optic nerve coloboma communicating hydrocephalus congenital nystagmus congenital ptosis cystic kidney disease dextrocardia diffuse interstitial keratitis dissociated nystagmus embryoma epilepsy episodic kinesigenic dyskinesia 1 fundus dystrophy glomerulonephritis hepatocellular carcinoma hydrocephalus hypertropia inguinal hernia intellectual disability interstitial lung disease isolated cleft palate kidney disease kidney failure learning disability leukoplakia of penis liver cancer liver cirrhosis mechanical strabismus medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma nephritis nephrosis non-congenital cyst of kidney obesity obstructive hydrocephalus oculocerebrorenal syndrome ophthalmoplegia patent ductus arteriosus pathologic nystagmus polycystic kidney disease 4 polydactyly portal hypertension primary ciliary dyskinesia 1 primary ciliary dyskinesia ptosis pyoureter scoliosis senile degeneration of brain skin melanoma spondylolisthesis spontaneous ocular nystagmus strabismus viral infectious disease visual epilepsy visual pathway disease
Q4W5G0	Tigger transposable element-derived protein 2	TIGD2	Homo sapiens (human)	1
P21281	V-type proton ATPase subunit B, brain isoform	ATP6V1B2 ATP6B2 VPP3	Homo sapiens (human)	1
P14060	3 beta-hydroxysteroid dehydrogenase/Delta 5-->4-isomerase type 1	HSD3B1 3BH HSDB3A	Homo sapiens (human)	1	Bartter disease Conn's syndrome Waterhouse-Friderichsen syndrome acne adenocarcinoma adenoma adrenal gland hyperfunction alopecia aortic valve insufficiency bladder carcinoma breast cancer breast carcinoma cancer carcinoma choriocarcinoma congenital adrenal hyperplasia congenital hypothyroidism diabetes mellitus diabetic ketoacidosis disorder of sexual development endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis essential hypertension follicular adenoma hermaphroditism hyperprolactinemia hypertension hypogonadism hypothyroidism kwashiorkor lesion of sciatic nerve marasmus microcystic adenoma myxedema nutrition disease obsolete Cushing's syndrome papillary adenoma placenta cancer polycystic ovary syndrome pre-eclampsia primary cutaneous amyloidosis primary hyperaldosteronism prostate cancer prostate carcinoma protein-energy malnutrition pseudohermaphroditism sarcomatoid carcinoma sciatic neuropathy stomach cancer stomach carcinoma trophoblastic neoplasm type 2 diabetes mellitus urinary bladder cancer uterine corpus cancer
P11182	Lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex, mitochondrial	DBT BCATE2 BCKDHE2	Homo sapiens (human)	1	acute pancreatitis autoimmune hepatitis borderline personality disorder brain edema breast cancer breast carcinoma cancer carcinoma cardiovascular system disease central nervous system cancer dilated cardiomyopathy 1A dilated cardiomyopathy dystonia eating disorder embryoma epilepsy focal hand dystonia generalized dystonia giant cell glioblastoma glioblastoma gliosarcoma heart disease high grade glioma hypoglycemia intellectual disability intermittent explosive disorder lactic acidosis learning disability maple syrup urine disease melanoma mixed glioma pancreatitis post-traumatic stress disorder primary biliary cholangitis skin melanoma substance abuse substance-related disorder syndromic X-linked intellectual disability 94 visual epilepsy
P13861	cAMP-dependent protein kinase type II-alpha regulatory subunit	PRKAR2A PKR2 PRKAR2	Homo sapiens (human)	1
Q99584	Protein S100-A13	S100A13	Homo sapiens (human)	1
P30419	Glycylpeptide N-tetradecanoyltransferase 1	NMT1 NMT	Homo sapiens (human)	1
O00308	NEDD4-like E3 ubiquitin-protein ligase WWP2	WWP2	Homo sapiens (human)	1
Q5JY77	G-protein coupled receptor-associated sorting protein 1	GPRASP1 GASP KIAA0443	Homo sapiens (human)	1
P34949	Mannose-6-phosphate isomerase	MPI PMI1	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 Pick's disease Reye syndrome Zollinger-Ellison syndrome acute myeloid leukemia acute myocardial infarction antithrombin III deficiency anxiety disorder arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant cerebellar ataxia autosomal recessive hypercholesterolemia autosomal recessive polycystic kidney disease blindness blood coagulation disease campomelic dysplasia cancer cardiovascular system disease celiac disease central nervous system cancer cerebral degeneration chronic kidney disease congenital disorder of glycosylation Ia congenital disorder of glycosylation Ib congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congestive heart failure coronary artery disease coronary thrombosis craniometaphyseal dysplasia cryptococcosis cystic fibrosis developmental and epileptic encephalopathy 36 diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy dry eye syndrome egg allergy elephantiasis embryoma epilepsy essential hypertension familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 gallbladder disease generalized anxiety disorder gliosarcoma heart disease hepatitis B high grade glioma hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia laryngeal disease liver cirrhosis liver disease lymphedema marasmus mixed glioma myocardial infarction neurotic disorder nutmeg liver obsolete inherited blood coagulation disease phobic disorder placental insufficiency polycystic kidney disease 4 post-traumatic stress disorder postpartum depression protein C deficiency protein S deficiency protein-losing enteropathy schizophrenia silent myocardial infarction spinocerebellar ataxia type 6 steatotic liver disease thrombocytopenia thrombophilia tracheal disease tropical sprue type 2 diabetes mellitus visual epilepsy xerophthalmia
P0C5J1	Putative protein N-methyltransferase FAM86B2	FAM86B2	Homo sapiens (human)	1
Q6ZS17	Rho family-interacting cell polarization regulator 1	RIPOR1 FAM65A KIAA1930	Homo sapiens (human)	1
P13647	Keratin, type II cytoskeletal 5	KRT5	Homo sapiens (human)	1
O95707	Ribonuclease P protein subunit p29	POP4 RPP29	Homo sapiens (human)	1

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