GlyCosmos Portal

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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 **16976 - 17000** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▲	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q86UB9	Transmembrane protein 135	TMEM135	Homo sapiens (human)	1	1
Q9NPI0	Transmembrane protein 138	TMEM138	Homo sapiens (human)	1	0
Q9NV12	Transmembrane protein 140	TMEM140	Homo sapiens (human)	1	0
Q8NBT3	Transmembrane protein 145	TMEM145	Homo sapiens (human)	2	2
Q9P0S9	Transmembrane protein 14C	TMEM14C C6orf53	Homo sapiens (human)	0	1
Q6UXP3	Transmembrane protein 14EP	TMEM14EP TMEM14E	Homo sapiens (human)	0	1
Q86TG1	Transmembrane protein 150A	TMEM150A TMEM150	Homo sapiens (human)	2	0
A6NC51	Modulator of macroautophagy TMEM150B	TMEM150B TMEM224	Homo sapiens (human)	1	0
Q8N4L1	Transmembrane protein 151A	TMEM151A TMEM151	Homo sapiens (human)	2	1
Q6P9G4	Transmembrane protein 154	TMEM154	Homo sapiens (human)	3	1
Q8N614	Transmembrane protein 156	TMEM156	Homo sapiens (human)	3	2
Q8WZ71	Transmembrane protein 158	TMEM158 HBBP RIS1	Homo sapiens (human)	1	0
Q9NX00	Transmembrane protein 160	TMEM160	Homo sapiens (human)	0	1
Q9NX61	Transmembrane protein 161A	TMEM161A	Homo sapiens (human)	2	1
Q8NDZ6	Transmembrane protein 161B	TMEM161B	Homo sapiens (human)	3	0
Q9HC07	Putative divalent cation/proton antiporter TMEM165	TMEM165 TPARL	Homo sapiens (human)	4	3	Camurati-Engelmann disease Laron syndrome Marfan syndrome X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 achondroplasia acoustic neuroma amelogenesis imperfecta hypomaturation type 2A2 amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta hypomaturation type 2A4 amelogenesis imperfecta hypomaturation type 2A5 amelogenesis imperfecta type 1A amelogenesis imperfecta type 1B amelogenesis imperfecta type 1C amelogenesis imperfecta type 1E amelogenesis imperfecta type 1F amelogenesis imperfecta type 1G amelogenesis imperfecta type 1H amelogenesis imperfecta type 2A1 amelogenesis imperfecta type 3A amelogenesis imperfecta type 4 amelogenesis imperfecta cancer cellular schwannoma chondrodysplasia punctata congenital disorder of glycosylation type II congenital disorder of glycosylation type IIk congenital disorder of glycosylation dentin dysplasia dentinogenesis imperfecta embryoma hepatocellular carcinoma isolated elevated serum creatine phosphokinase levels liver cancer melanotic neurilemmoma meningioma neurilemmoma neurofibromatosis osteoporosis pituitary adenoma plexiform schwannoma scoliosis situs inversus tuberous sclerosis vestibular schwannomatosis
Q8TBQ9	Protein kish-A	TMEM167A TMEM167	Homo sapiens (human)	1	1
Q9H0V1	Transmembrane protein 168	TMEM168	Homo sapiens (human)	3	0
Q86X19	Transmembrane protein 17	TMEM17	Homo sapiens (human)	3	3
Q8WVE7	Transmembrane protein 170A	TMEM170A TMEM170	Homo sapiens (human)	2	0
Q5T4T1	Transmembrane protein 170B	TMEM170B	Homo sapiens (human)	1	0
Q8WVE6	Transmembrane protein 171	TMEM171	Homo sapiens (human)	1	1
Q96HP8	Transmembrane protein 176A	TMEM176A HCA112	Homo sapiens (human)	1	2
Q8NBL3	Transmembrane protein 178A	TMEM178A TMEM178	Homo sapiens (human)	1	0
H3BS89	Transmembrane protein 178B	TMEM178B	Homo sapiens (human)	2	0

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