GlyCosmos Portal

Displaying entries **3601 - 3625** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
Q9H813	Proton-activated chloride channel	PACC1 C1orf75 TMEM206	3	3
O15034	RIMS-binding protein 2	RIMBP2 KIAA0318 RBP2	3	1
P28336	Neuromedin-B receptor	NMBR	3	0
G3XAK1	Macrophage stimulating 1	MST1	3	0
V9HWD8	Epididymis secretory sperm binding protein Li 163pA	HEL-S-163pA	3	0
P03372	Estrogen receptor	ESR1 ESR NR3A1	3	1
A0A2C9F2P4	Palmitoyl-protein thioesterase 1	PPT1	3	0
P41271	Neuroblastoma suppressor of tumorigenicity 1	NBL1 DAN DAND1	3	14
P46095	G-protein coupled receptor 6	GPR6	3	0
Q8TDG2	Actin-related protein T1	ACTRT1 ARPT1	3	1
Q9Y5E1	Protocadherin beta-9	PCDHB9 PCDH3H	3	1
H3BMA1	Mesothelin (Fragment)	MSLN	3	0
Q9HAW9	UDP-glucuronosyltransferase 1A8	UGT1A8 GNT1 UGT1	3	2	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia beta thalassemia bilirubin metabolic disorder bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardiac arrest cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colorectal cancer colorectal carcinoma cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma female reproductive organ cancer galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease hemoglobin H disease hepatitis D hereditary spherocytosis influenza kernicterus due to isoimmunization kernicterus large intestine cancer leiomyoma leukopenia liver disease myofibroma neonatal jaundice neutropenia nodular prostate obesity prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia severe congenital neutropenia sickle cell anemia steatotic liver disease stomach cancer stomach carcinoma thalassemia type 2 diabetes mellitus urinary bladder cancer uterine fibroid visual epilepsy xeroderma pigmentosum group D
Q0D2K0	Magnesium transporter NIPA4	NIPAL4 ICHN NIPA4	3	0
P32927	Cytokine receptor common subunit beta	CSF2RB IL3RB IL5RB	3	0
A0A023SER7	MHC class I polypeptide-related protein A (Fragment)	MICA	3	0
Q8IZT6	Abnormal spindle-like microcephaly-associated protein	ASPM MCPH5	3	1
Q7Z3S7	Voltage-dependent calcium channel subunit alpha-2/delta-4	CACNA2D4	3	1	achromatopsia acquired color blindness acquired immunodeficiency syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness blue color blindness borderline personality disorder color blindness cone dystrophy cone-rod dystrophy 2 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness disease of mental health dissociated nystagmus eye disease human immunodeficiency virus infectious disease hypertropia intermittent explosive disorder mechanical strabismus night blindness obsolete asthenopia ophthalmoplegia pathologic nystagmus psychotic disorder red color blindness red-green color blindness spontaneous ocular nystagmus strabismus
Q92538	Golgi-specific brefeldin A-resistance guanine nucleotide exchange factor 1	GBF1 KIAA0248	3	1
Q9UPS8	Ankyrin repeat domain-containing protein 26	ANKRD26 KIAA1074	3	1
A0A0G2JPR0	Complement C4-A	C4A	3	0
Q8TCN5	Zinc finger protein 507	ZNF507 KIAA1084	3	2
P13747	HLA class I histocompatibility antigen, alpha chain E	HLA-E HLA-6.2 HLAE	3	8
Q8IVF7	Formin-like protein 3	FMNL3 FHOD3 FRL2 KIAA2014 WBP3	3	1
O60293	Zinc finger C3H1 domain-containing protein	ZFC3H1 CCDC131 KIAA0546 PSRC2	3	1

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