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 **16876 - 16900** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
P38936	Cyclin-dependent kinase inhibitor 1	CDKN1A CAP20 CDKN1 CIP1 MDA6 PIC1 SDI1 WAF1	Homo sapiens (human)	1
H3BTG2	Testis-expressed protein 46	TEX46 C1orf234	Homo sapiens (human)	1
Q7Z3U7	Protein MON2 homolog	MON2 KIAA1040 SF21	Homo sapiens (human)	1
Q6P6C2	RNA demethylase ALKBH5	ALKBH5 ABH5 OFOXD1	Homo sapiens (human)	1
P62942	Peptidyl-prolyl cis-trans isomerase FKBP1A	FKBP1A FKBP1 FKBP12	Homo sapiens (human)	1
P61962	DDB1- and CUL4-associated factor 7	DCAF7 HAN11 WDR68	Homo sapiens (human)	1
P05976	Myosin light chain 1/3, skeletal muscle isoform	MYL1	Homo sapiens (human)	1
P49407	Beta-arrestin-1	ARRB1 ARR1	Homo sapiens (human)	1
B5ME19	Eukaryotic translation initiation factor 3 subunit C-like protein	EIF3CL	Homo sapiens (human)	1
A8MQ27	E3 ubiquitin-protein ligase NEURL1B	NEURL1B NEURL3	Homo sapiens (human)	1
Q9GZP9	Derlin-2	DERL2 DER2 FLANA	Homo sapiens (human)	1
Q9UBZ9	DNA repair protein REV1	REV1 REV1L	Homo sapiens (human)	1
Q9UPW0	Forkhead box protein J3	FOXJ3 KIAA1041	Homo sapiens (human)	1
Q53EZ4	Centrosomal protein of 55 kDa	CEP55 C10orf3 URCC6	Homo sapiens (human)	1
P28065	Proteasome subunit beta type-9	PSMB9 LMP2 PSMB6i RING12	Homo sapiens (human)	1
Q9H3K6	BolA-like protein 2	BOLA2 BOLA2B BOLA2A	Homo sapiens (human)	1
Q9NWS0	PIH1 domain-containing protein 1	PIH1D1 NOP17	Homo sapiens (human)	1
Q9H2B2	Synaptotagmin-4	SYT4 KIAA1342	Homo sapiens (human)	0
P13489	Ribonuclease inhibitor	RNH1 PRI RNH	Homo sapiens (human)	1
Q9NTJ4	Alpha-mannosidase 2C1	MAN2C1 MANA MANA1	Homo sapiens (human)	1	alpha-mannosidosis breast cancer breast carcinoma carcinoma esophageal cancer esophageal carcinoma intellectual disability learning disability post-traumatic stress disorder prostate cancer prostate carcinoma sarcomatoid carcinoma
Q8IWU9	Tryptophan 5-hydroxylase 2	TPH2 NTPH	Homo sapiens (human)	1
Q15669	Rho-related GTP-binding protein RhoH	RHOH ARHH TTF	Homo sapiens (human)	1
O60762	Dolichol-phosphate mannosyltransferase subunit 1	DPM1	Homo sapiens (human)	1	Duchenne muscular dystrophy antithrombin III deficiency autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy capillary disease cavernous hemangioma chorioangioma congenital disorder of glycosylation Ie congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital muscular dystrophy distal myopathy facioscapulohumeral muscular dystrophy glomus tumor hemangioma hereditary hemorrhagic telangiectasia histiocytoid hemangioma intramuscular hemangioma isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lymphangioma microcephaly muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 nonsyndromic congenital nail disorder 9 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy patent ductus arteriosus protein C deficiency protein S deficiency rippling muscle disease 2 telangiectasis thrombophilia
Q9H2V7	Protein spinster homolog 1	SPNS1 SPIN1	Homo sapiens (human)	1
A6NKD2	Testis-specific Y-encoded protein 2	TSPY2 TSPYQ1	Homo sapiens (human)	1

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