GlyCosmos Portal

Displaying entries **15701 - 15725** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q8TE58	A disintegrin and metalloproteinase with thrombospondin motifs 15	ADAMTS15	4	2
Q96T37	RNA-binding protein 15	RBM15 OTT OTT1	4	2
O15511	Actin-related protein 2/3 complex subunit 5	ARPC5 ARC16	4	1
O60487	Myelin protein zero-like protein 2	MPZL2 EVA EVA1	4	34
Q8IYD8	Fanconi anemia group M protein	FANCM KIAA1596	4	3
Q13509	Tubulin beta-3 chain	TUBB3 TUBB4	4	2
Q9NSI5	Immunoglobulin superfamily member 5	IGSF5 JAM4	4	1
P31937	3-hydroxyisobutyrate dehydrogenase, mitochondrial	HIBADH	4	2
Q9NQ40	Solute carrier family 52, riboflavin transporter, member 3	SLC52A3 C20orf54 RFT2 RFVT3	4	2
O15232	Matrilin-3	MATN3	4	2
Q9NX62	Golgi-resident adenosine 3',5'-bisphosphate 3'-phosphatase	BPNT2 IMPA3 IMPAD1	4	16
Q6UW63	Protein O-glucosyltransferase 2	POGLUT2 EP58 KDELC1	4	5	bipolar disorder
Q8IYK4	Procollagen galactosyltransferase 2	COLGALT2 C1orf17 GLT25D2 KIAA0584	4	6	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 bone osteosarcoma breast cancer cerebral degeneration hepatitis A hepatitis lung benign neoplasm osteoarthritis osteosarcoma
P32241	Vasoactive intestinal polypeptide receptor 1	VIPR1	4	0
Q8NFZ4	Neuroligin-2	NLGN2 KIAA1366	4	2
O95259	Potassium voltage-gated channel subfamily H member 1	KCNH1 EAG EAG1	4	1
Q01973	Inactive tyrosine-protein kinase transmembrane receptor ROR1	ROR1 NTRKR1	4	5
Q658N2	Sialate:O-sulfotransferase 1	WSCD1 KIAA0523	4	3
Q7RTP6	[F-actin]-monooxygenase MICAL3	MICAL3 KIAA0819 KIAA1364	4	1
O75635	Serpin B7	SERPINB7	4	1
Q5T4B2	Inactive glycosyltransferase 25 family member 3	CERCAM CEECAM1 GLT25D3 KIAA1502	4	0
Q9BSA4	Protein tweety homolog 2	TTYH2 C17orf29	4	0
Q9UMN6	Histone-lysine N-methyltransferase 2B	KMT2B HRX2 KIAA0304 MLL2 MLL4 TRX2 WBP7	4	1
P22310	UDP-glucuronosyltransferase 1A4	UGT1A4 GNT1 UGT1	4	2	Crigler-Najjar syndrome Fleck corneal dystrophy 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 breast cancer breast carcinoma cancer carcinoma cardiac arrest celiac disease cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colorectal cancer colorectal carcinoma cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy female reproductive organ cancer galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease hematologic cancer hemoglobin H disease hepatitis D hereditary spherocytosis influenza kernicterus due to isoimmunization kernicterus large intestine cancer leukopenia liver disease neonatal jaundice neutropenia nodular prostate obesity prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia steatotic liver disease stomach cancer stomach carcinoma thalassemia type 2 diabetes mellitus visual epilepsy xeroderma pigmentosum group D
Q86TE4	Leucine zipper protein 2	LUZP2	4	3

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