GlyCosmos Portal

Displaying entries **1726 - 1750** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of GlyTouCan IDs	Disease Ontology
O43169	Cytochrome b5 type B	CYB5B CYB5M OMB5	1
Q13445	Transmembrane emp24 domain-containing protein 1	TMED1 IL1RL1L IL1RL1LG	1	acquired immunodeficiency syndrome breast cancer human immunodeficiency virus infectious disease
Q9HCC0	Methylcrotonoyl-CoA carboxylase beta chain, mitochondrial	MCCC2 MCCB	1
Q7L0X2	Glutamate-rich protein 6	ERICH6 C3orf44 FAM194A	1
Q9UKN8	General transcription factor 3C polypeptide 4	GTF3C4	1
Q5TB80	Centrosomal protein of 162 kDa	CEP162 C6orf84 KIAA1009 QN1	1
Q9HCI5	Melanoma-associated antigen E1	MAGEE1 HCA1 KIAA1587	1
Q969M7	NEDD8-conjugating enzyme UBE2F	UBE2F NCE2	1
A6NGY5	Olfactory receptor 51F1	OR51F1 OR51F1P	1
Q8TD16	Protein bicaudal D homolog 2	BICD2 KIAA0699	1
P36639	Oxidized purine nucleoside triphosphate hydrolase	NUDT1 MTH1	1
Q9BV86	N-terminal Xaa-Pro-Lys N-methyltransferase 1	NTMT1 C9orf32 METTL11A NRMT NRMT1	1
Q96LM1	Putative uncharacterized protein encoded by LINC00615	LINC00615 C12orf37	1
Q8N9L1	Zinc finger protein ZIC 4	ZIC4	1
Q99618	Cell division cycle-associated protein 3	CDCA3 C8 GRCC8 TOME1	1
Q03112	Histone-lysine N-methyltransferase MECOM	MECOM EVI1 MDS1 PRDM3	1
Q6UXN9	WD repeat-containing protein 82	WDR82 SWD2 TMEM113 WDR82A	1
P84157	Matrix-remodeling-associated protein 7	MXRA7	1
Q9NW81	Distal membrane-arm assembly complex protein 2	DMAC2 ATP5SL	1
Q15583	Homeobox protein TGIF1	TGIF1 TGIF	1
Q9UBV8	Peflin	PEF1 ABP32	1
Q9BR11	Zinc finger SWIM domain-containing protein 1	ZSWIM1 C20orf162	1
Q15119	[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 2, mitochondrial	PDK2 PDHK2	1
Q5JVG2	Zinc finger protein 484	ZNF484	1
Q15738	Sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating	NSDHL H105E3	1	Bloch-Sulzberger syndrome Joubert syndrome Miller-Dieker lissencephaly syndrome Potter's syndrome Sjogren-Larsson syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 acquired hyperkeratosis autosomal dominant chondrodysplasia punctata autosomal recessive congenital ichthyosis bilateral renal aplasia chondrodysplasia punctata cleft lip complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cutaneous fibrous histiocytoma epidermal nevus epilepsy granuloma annulare head and neck squamous cell carcinoma heart septal defect hidradenoma hydranencephaly hydronephrosis hypertropia hypomelanosis of Ito intellectual disability learning disability lissencephaly mechanical strabismus microcephaly obsolete congenital ichthyosiform erythroderma omphalocele ophthalmoplegia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly skin papilloma skin tag strabismus syndromic X-linked intellectual disability Najm type syringoma umbilical hernia ventricular septal defect verruciform xanthoma of skin visual epilepsy

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