GlyCosmos Portal

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Displaying entries **12601 - 12625** 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
Q96NL6	Sodium channel and clathrin linker 1	SCLT1 SAP1	Homo sapiens (human)	0	1
Q96NJ6	Zinc finger protein 3 homolog	ZFP3 ZNF752	Homo sapiens (human)	1	1
Q96NJ3	Zinc finger protein 285	ZNF285 ZNF285A	Homo sapiens (human)	1	1
Q96NI6	Leucine-rich repeat and fibronectin type-III domain-containing protein 5	LRFN5 C14orf146 SALM5	Homo sapiens (human)	6	0
Q96NH3	Protein broad-minded	TBC1D32 BROMI C6orf170 C6orf171	Homo sapiens (human)	1	1
Q96NG8	Zinc finger protein 582	ZNF582	Homo sapiens (human)	0	1
Q96NG3	Outer dynein arm-docking complex subunit 4	ODAD4 TTC25	Homo sapiens (human)	0	1
Q96ND8	Zinc finger protein 583	ZNF583	Homo sapiens (human)	0	1
Q96NB3	Zinc finger protein 830	ZNF830 CCDC16	Homo sapiens (human)	1	1
Q96N87	Inactive sodium-dependent neutral amino acid transporter B(0)AT3	SLC6A18 B0AT3 XTRP2	Homo sapiens (human)	4	0
Q96N77	Zinc finger protein 641	ZNF641	Homo sapiens (human)	0	1
Q96N76	Urocanate hydratase	UROC1	Homo sapiens (human)	2	1
Q96N67	Dedicator of cytokinesis protein 7	DOCK7 KIAA1771	Homo sapiens (human)	1	1
Q96N66	Lysophospholipid acyltransferase 7	MBOAT7 BB1 LENG4 OACT7	Homo sapiens (human)	1	1	abdominal obesity-metabolic syndrome 1 adrenoleukodystrophy agnosia alcoholic hepatitis alcoholic liver cirrhosis attention deficit hyperactivity disorder autism spectrum disorder autistic disorder cardiovascular system disease cerebral degeneration choreatic disease chronic kidney disease communicating hydrocephalus depressive disorder developmental coordination disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder dystonia epilepsy focal epilepsy gallbladder disease heart disease hepatitis B hepatitis C hepatitis hepatocellular carcinoma hydrocephalus intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer liver cirrhosis liver disease major depressive disorder melancholic depression microcephaly neurotic disorder obesity obsolete infantile epileptic encephalopathy obsolete melancholia obstructive hydrocephalus partial motor epilepsy senile degeneration of brain steatotic liver disease stereotypic movement disorder stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 type 2 diabetes mellitus visual epilepsy
Q96N64	PWWP domain-containing protein 2A	PWWP2A KIAA1935 MST101	Homo sapiens (human)	1	1
Q96N58	Zinc finger protein 578	ZNF578	Homo sapiens (human)	0	1
Q96N53	Putative uncharacterized protein encoded by LINC00167	PRDM10-DT C11orf37 LINC00167 NCRNA00167	Homo sapiens (human)	0	1
Q96N46	Tetratricopeptide repeat protein 14	TTC14 KIAA1980	Homo sapiens (human)	7	3
Q96N21	AP-4 complex accessory subunit Tepsin	TEPSIN C17orf56 ENTHD2	Homo sapiens (human)	0	1
Q96N19	Integral membrane protein GPR137	GPR137 C11orf4 GPR137A TM7SF1L1	Homo sapiens (human)	2	0
Q96N06	Spermatogenesis-associated protein 33	SPATA33 C16orf55	Homo sapiens (human)	3	2
Q96MZ4	Protein FAM218A	FAM218A C4orf39	Homo sapiens (human)	0	1
Q96MY7	Protein FAM161B	FAM161B C14orf44	Homo sapiens (human)	1	1
Q96MY1	Nucleolar protein 4-like	NOL4L C20orf112 C20orf113	Homo sapiens (human)	5	1
Q96MX3	Zinc finger protein 48	ZNF48 ZNF553	Homo sapiens (human)	0	1

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