GlyCosmos Portal

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Displaying entries **12901 - 12925** 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
Q96EY4	Translation machinery-associated protein 16	TMA16 C4orf43	Homo sapiens (human)	0	1
Q96EY1	DnaJ homolog subfamily A member 3, mitochondrial	DNAJA3 HCA57 TID1	Homo sapiens (human)	0	1
Q96EX1	Small integral membrane protein 12	SMIM12 C1orf212	Homo sapiens (human)	0	1
Q96EV8	Dysbindin	DTNBP1 BLOC1S8	Homo sapiens (human)	2	1
Q96EV2	RNA-binding protein 33	RBM33 PRR8	Homo sapiens (human)	8	2
Q96ET8	Golgi apparatus membrane protein TVP23 homolog C	TVP23C FAM18B2	Homo sapiens (human)	1	1
Q96ES7	SAGA-associated factor 29	SGF29 CCDC101	Homo sapiens (human)	1	1
Q96ER9	Mitochondrial potassium channel	CCDC51 MITOK	Homo sapiens (human)	0	1
Q96ER3	Protein SAAL1	SAAL1	Homo sapiens (human)	0	1
Q96EQ0	Small glutamine-rich tetratricopeptide repeat-containing protein beta	SGTB SGT2	Homo sapiens (human)	5	1
Q96EP9	Sodium/bile acid cotransporter 4	SLC10A4	Homo sapiens (human)	5	0
Q96EP5	DAZ-associated protein 1	DAZAP1	Homo sapiens (human)	0	1
Q96EN8	Molybdenum cofactor sulfurase	MOCOS	Homo sapiens (human)	0	1
Q96EM0	Trans-3-hydroxy-L-proline dehydratase	L3HYPDH C14orf149	Homo sapiens (human)	0	1
Q96EL2	Small ribosomal subunit protein uS3m	MRPS24	Homo sapiens (human)	0	1
Q96EK6	Glucosamine 6-phosphate N-acetyltransferase	GNPNAT1 GNA1	Homo sapiens (human)	0	1	diabetes mellitus diabetic ketoacidosis type 2 diabetes mellitus
Q96EK5	KIF-binding protein	KIFBP KBP KIAA1279 KIF1BP	Homo sapiens (human)	0	1
Q96EK4	THAP domain-containing protein 11	THAP11	Homo sapiens (human)	1	1
Q96EK2	PHD finger protein 21B	PHF21B KIAA1661	Homo sapiens (human)	0	1
Q96EI5	Transcription elongation factor A protein-like 4	TCEAL4	Homo sapiens (human)	0	1
Q96EH5	Ribosomal protein eL39-like 2	RPL39L RPL39L1	Homo sapiens (human)	2	1
Q96EG3	Zinc finger protein 837	ZNF837	Homo sapiens (human)	1	1
Q96EG1	Arylsulfatase G	ARSG KIAA1001	Homo sapiens (human)	4	0	Usher syndrome type 2 Usher syndrome type 3 Usher syndrome type 3A Usher syndrome anxiety disorder astigmatism blepharospasm blindness cancer cataract cerebellar ataxia cerebellar disease congenital stationary night blindness 1A congenital stationary night blindness depressive disorder dysthymic disorder dystonia embryoma focal dystonia focal hand dystonia generalized anxiety disorder generalized dystonia lysosomal storage disease major depressive disorder melancholic depression metachromatic leukodystrophy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis neurotic disorder night blindness obsolete melancholia peripheral retinal degeneration prostate cancer prostate carcinoma retinitis pigmentosa-deafness syndrome schizophrenia scotoma sensorineural hearing loss
Q96EF0	Myotubularin-related protein 8	MTMR8	Homo sapiens (human)	1	1	breast cancer
Q96EE4	Coiled-coil domain-containing protein 126	CCDC126	Homo sapiens (human)	2	1

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