GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **119751 - 119775** of **126547** in total

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UniProt ID ▲	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9UBC5	Unconventional myosin-Ia	MYO1A MYHL	Homo sapiens (human)	1	1
Q9UBD0	Heat shock transcription factor, X-linked	HSFX1 HSFX2 LW-1	Homo sapiens (human)	1	1
Q9UBD6	Ammonium transporter Rh type C	RHCG C15orf6 CDRC2 PDRC2 RHGK	Homo sapiens (human)	1	0
Q9UBD9	Cardiotrophin-like cytokine factor 1	CLCF1 BSF3 CLC NNT1	Homo sapiens (human)	1	0
Q9UBE0	SUMO-activating enzyme subunit 1	SAE1 AOS1 SUA1 UBLE1A	Homo sapiens (human)	0	1
Q9UBF2	Coatomer subunit gamma-2	COPG2	Homo sapiens (human)	0	1
Q9UBF6	RING-box protein 2	RNF7 RBX2 ROC2 SAG	Homo sapiens (human)	1	1
Q9UBF8	Phosphatidylinositol 4-kinase beta	PI4KB PIK4CB	Homo sapiens (human)	0	1	EAST syndrome hepatitis C severe acute respiratory syndrome
Q9UBF9	Myotilin	MYOT TTID	Homo sapiens (human)	0	1
Q9UBG0	C-type mannose receptor 2	MRC2 CLEC13E ENDO180 KIAA0709 UPARAP	Homo sapiens (human)	16	50
Q9UBG7	Recombining binding protein suppressor of hairless-like protein	RBPJL RBPL RBPSUHL	Homo sapiens (human)	0	1
Q9UBI1	COMM domain-containing protein 3	COMMD3 BUP C10orf8	Homo sapiens (human)	0	1
Q9UBI9	Headcase protein homolog	HECA HDC	Homo sapiens (human)	2	1
Q9UBJ2	ATP-binding cassette sub-family D member 2	ABCD2 ALD1 ALDL1 ALDR ALDRP	Homo sapiens (human)	2	0
Q9UBK2	Peroxisome proliferator-activated receptor gamma coactivator 1-alpha	PPARGC1A LEM6 PGC1 PGC1A PPARGC1	Homo sapiens (human)	1	2
Q9UBK8	Methionine synthase reductase	MTRR	Homo sapiens (human)	1	2
Q9UBL0	cAMP-regulated phosphoprotein 21	ARPP21 TARPP	Homo sapiens (human)	0	1
Q9UBL3	Set1/Ash2 histone methyltransferase complex subunit ASH2	ASH2L ASH2L1	Homo sapiens (human)	1	2
Q9UBL9	P2X purinoceptor 2	P2RX2 P2X2	Homo sapiens (human)	3	1
Q9UBM4	Opticin	OPTC OPT	Homo sapiens (human)	1	0
Q9UBM7	7-dehydrocholesterol reductase	DHCR7 D7SR	Homo sapiens (human)	0	1	3-methylglutaconic aciduria Behcet's disease Dandy-Walker syndrome Hailey-Hailey disease Laron syndrome Marfan syndrome Meckel syndrome Potter's syndrome Rapp-Hodgkin syndrome Rothmund-Thomson syndrome Smith-Lemli-Opitz syndrome X-linked ichthyosis achondroplasia ankyloblepharon-ectodermal defects-cleft lip/palate syndrome arteriosclerotic cardiovascular disease atherosclerosis atrioventricular septal defect autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal dominant polycystic kidney disease autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bilateral optic nerve hypoplasia bilateral renal aplasia cardiovascular system disease choanal atresia coloboma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc coronary artery disease cutis laxa dermatitis diabetes mellitus diabetic ketoacidosis fissured tongue glaucoma glycoproteinosis heart disease hepatitis C hepatocellular carcinoma hydrocephalus hypohidrotic ectodermal dysplasia hypospadias immune system disease intellectual disability interstitial nephritis large intestine cancer learning disability leukocyte adhesion deficiency 2 leukocyte adhesion deficiency lingual-facial-buccal dyskinesia liver cancer liver cirrhosis mal de Meleda microcephaly movement disease multiple sclerosis nutmeg liver obsolete type 1 diabetes mellitus 9 oligohydramnios osteomalacia periventricular nodular heterotopia photosensitive epilepsy photosensitivity disease placental insufficiency polycystic ovary syndrome polydactyly polyhydramnios pyelitis pyelonephritis restrictive dermopathy rheumatoid arthritis rickets scoliosis sensorineural hearing loss situs inversus syndromic X-linked intellectual disability type 10 tongue disease tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ventricular septal defect
Q9UBM8	Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase C	MGAT4C	Homo sapiens (human)	2	0	diabetes mellitus nicotine dependence prostate cancer prostate carcinoma type 2 diabetes mellitus
Q9UBN1	Voltage-dependent calcium channel gamma-4 subunit	CACNG4	Homo sapiens (human)	2	0
Q9UBN4	Short transient receptor potential channel 4	TRPC4	Homo sapiens (human)	1	1
Q9UBN6	Tumor necrosis factor receptor superfamily member 10D	TNFRSF10D DCR2 TRAILR4 TRUNDD	Homo sapiens (human)	3	1

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