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 **15826 - 15850** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q8IZD6	Solute carrier family 22 member 15	SLC22A15 FLIPT1	Homo sapiens (human)	4	0
Q16557	Pregnancy-specific beta-1-glycoprotein 3	PSG3	Homo sapiens (human)	4	0
Q5TB30	DEP domain-containing protein 1A	DEPDC1 DEPDC1A	Homo sapiens (human)	4	1
Q7Z304	MAM domain-containing protein 2	MAMDC2	Homo sapiens (human)	4	2
O43242	26S proteasome non-ATPase regulatory subunit 3	PSMD3	Homo sapiens (human)	4	2
P49796	Regulator of G-protein signaling 3	RGS3	Homo sapiens (human)	4	1
Q14571	Inositol 1,4,5-trisphosphate receptor type 2	ITPR2	Homo sapiens (human)	4	9
Q15058	Kinesin-like protein KIF14	KIF14 KIAA0042	Homo sapiens (human)	4	1
Q8N130	Sodium-dependent phosphate transport protein 2C	SLC34A3 NPT2C NPTIIC	Homo sapiens (human)	4	0
Q96NU0	Contactin-associated protein-like 3B	CNTNAP3B CASPR3B	Homo sapiens (human)	4	4
Q8TEQ8	GPI ethanolamine phosphate transferase 3	PIGO	Homo sapiens (human)	4	2	Cogan syndrome Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome absence epilepsy blepharospasm capillary disease childhood absence epilepsy cleft palate colorectal cancer colorectal carcinoma craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia imperforate anus intellectual disability isolated cleft palate large intestine cancer learning disability monocular esotropia nonepidermolytic palmoplantar keratoderma oligohydramnios palmoplantar keratosis scoliosis sensorineural hearing loss situs inversus syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis visual epilepsy
P55291	Cadherin-15	CDH15 CDH14 CDH3	Homo sapiens (human)	4	0
P0DQD5	Neuropeptide Y receptor type 4-2	NPY4R2	Homo sapiens (human)	4	0
P78316	Nucleolar protein 14	NOP14 C4orf9 NOL14	Homo sapiens (human)	4	1
Q96GX1	Tectonic-2	TCTN2 C12orf38 TECT2	Homo sapiens (human)	4	0
P30260	Cell division cycle protein 27 homolog	CDC27 ANAPC3 D0S1430E D17S978E	Homo sapiens (human)	4	3
P54762	Ephrin type-B receptor 1	EPHB1 ELK EPHT2 HEK6 NET	Homo sapiens (human)	4	1
O14791	Apolipoprotein L1	APOL1 APOL	Homo sapiens (human)	4	3
Q9BYT9	Anoctamin-3	ANO3 C11orf25 TMEM16C	Homo sapiens (human)	4	0
Q96EG1	Arylsulfatase G	ARSG KIAA1001	Homo sapiens (human)	4	0	Usher syndrome type 2 Usher syndrome type 3 Usher syndrome type 3A Usher syndrome anxiety disorder astigmatism blepharospasm blindness cancer cataract cerebellar ataxia cerebellar disease congenital stationary night blindness 1A congenital stationary night blindness depressive disorder dysthymic disorder dystonia embryoma focal dystonia focal hand dystonia generalized anxiety disorder generalized dystonia lysosomal storage disease major depressive disorder melancholic depression metachromatic leukodystrophy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis neurotic disorder night blindness obsolete melancholia peripheral retinal degeneration prostate cancer prostate carcinoma retinitis pigmentosa-deafness syndrome schizophrenia scotoma sensorineural hearing loss
Q7Z410	Transmembrane protease serine 9	TMPRSS9	Homo sapiens (human)	4	0
Q9UNA3	Alpha-1,4-N-acetylglucosaminyltransferase	A4GNT	Homo sapiens (human)	4	0	adenocarcinoma adenoma cancer cribriform carcinoma embryoma gastric adenocarcinoma gastritis granular cell carcinoma pancreatic cancer pancreatic carcinoma peptic ulcer disease stomach cancer stomach carcinoma tubular adenocarcinoma
Q5JTW2	Centrosomal protein of 78 kDa	CEP78 C9orf81	Homo sapiens (human)	4	1
Q96DZ1	Endoplasmic reticulum lectin 1	ERLEC1 C2orf30 XTP3TPB	Homo sapiens (human)	4	4	anorexia nervosa bronchus cancer bronchus carcinoma cancer cholestasis lung benign neoplasm lung cancer lung carcinoma spinal cord disease syringomyelia
O75030	Microphthalmia-associated transcription factor	MITF BHLHE32	Homo sapiens (human)	4	1

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