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 **113426 - 113450** 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
Q9Z0Z7	Krueppel-like factor 5	Klf5 Bteb2 Iklf	Mus musculus (house mouse)	1	1
P13489	Ribonuclease inhibitor	RNH1 PRI RNH	Homo sapiens (human)	0	1
A0A087WS46	Eukaryotic translation elongation factor 1 beta 2	Eef1b2	Mus musculus (house mouse)	0	1
Q86SU0	Immunoglobulin-like domain-containing receptor 1	ILDR1	Homo sapiens (human)	2	1
Q64152	Transcription factor BTF3	Btf3	Mus musculus (house mouse)	1	1
V5DCV2	Acyl-CoA dehydrogenase	TCDM_06407	Trypanosoma cruzi Dm28c	0	1
Q5XIF6	Tubulin alpha-4A chain	Tuba4a Tuba4	Rattus norvegicus (Norway rat)	0	1
Q91XE8	Transmembrane protein 205	Tmem205	Mus musculus (house mouse)	0	1
Q9WV48	SH3 and multiple ankyrin repeat domains protein 1	Shank1	Rattus norvegicus (Norway rat)	0	1
Q9NTJ4	Alpha-mannosidase 2C1	MAN2C1 MANA MANA1	Homo sapiens (human)	0	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)	0	1
A0A1P8BBU0	MEI2-like protein 1	ML1 AML1 MEI2-like protein 1	Arabidopsis thaliana (thale cress)	0	1
B6KR20	Guanylate binding protein, putative	BN1205_106310	Toxoplasma gondii VEG	0	1
O43312	Protein MTSS 1	MTSS1 KIAA0429 MIM	Homo sapiens (human)	6	1
A2AT02	NSFL1 cofactor p47	Nsfl1c	Mus musculus (house mouse)	0	1
K2NLQ2	60S ribosomal protein L7, putative	MOQ_001105	Trypanosoma cruzi marinkellei	0	1
Q15669	Rho-related GTP-binding protein RhoH	RHOH ARHH TTF	Homo sapiens (human)	0	1
O60762	Dolichol-phosphate mannosyltransferase subunit 1	DPM1	Homo sapiens (human)	0	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
Q3T1I4	Protein PRRC1	Prrc1	Rattus norvegicus (Norway rat)	0	1
Q9NYL9	Tropomodulin-3	TMOD3	Homo sapiens (human)	1	1
Q9H2V7	Protein spinster homolog 1	SPNS1 SPIN1	Homo sapiens (human)	0	1
P36070	RNA polymerase I-specific transcription initiation factor RRN3	RRN3	Saccharomyces cerevisiae S288C	1	1
Q15386	Ubiquitin-protein ligase E3C	UBE3C KIAA0010 KIAA10	Homo sapiens (human)	1	1
Q8NGJ3	Olfactory receptor 52E1	OR52E1 OR52E1P	Homo sapiens (human)	2	1
Q8CHR6	Dihydropyrimidine dehydrogenase [NADP(+)]	Dpyd	Mus musculus (house mouse)	0	1

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