GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **8901 - 8925** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
197257	lactate dehydrogenase D	LDHD	aniridia chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma intellectual disability learning disability microcephaly nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
197258	fucose kinase	FCSK FLJ39408 L-fucose kinase	congenital disorder of glycosylation congenital nystagmus dissociated nystagmus epilepsy esophagitis gastroesophageal reflux disease hypertropia intellectual disability learning disability mechanical strabismus ophthalmoplegia optic atrophy pathologic nystagmus peptic esophagitis spontaneous ocular nystagmus strabismus visual epilepsy
197259	mixed lineage kinase domain like pseudokinase	MLKL
197322	acyl-CoA synthetase family member 3	ACSF3 malonyl-CoA synthetase	B-cell lymphoma adult lymphoma amnestic disorder brain disease central nervous system lymphoma childhood lymphoma combined malonic and methylmalonic acidemia diarrhea disease of metabolism dystonia hypoglycemia inherited metabolic disorder lymphoma methylmalonic acidemia microcephaly migraine obsolete ymphosarcoma retrograde amnesia
199223	tetratricopeptide repeat domain 21A	TTC21A
199675	mast cell expressed membrane protein 1	MCEMP1
199699	DAN domain BMP antagonist family member 5	DAND5
199720	gametogenetin	GGN
199731	cell adhesion molecule 4	CADM4
199857	ALG14 UDP-N-acetylglucosaminyltransferase subunit	ALG14 MGC19780	Bell's palsy agnosia clubfoot congenital myasthenic syndrome 15 congenital myasthenic syndrome congenital ptosis developmental coordination disorder facial nerve disease facial paralysis familial periodic paralysis idiopathic scoliosis intellectual disability isolated elevated serum creatine phosphokinase levels learning disability myopathy ptosis scoliosis syndromic X-linked intellectual disability 94
199953	transmembrane protein 201	TMEM201
200008	CUB domain containing protein 2	CDCP2
200010	solute carrier family 5 member 9	SLC5A9
200014	coiled-coil and C2 domain containing 1B	CC2D1B
200081	taxilin alpha	TXLNA
200150	phospholipase D family member 5	PLD5
200162	sperm associated antigen 17	SPAG17
200185	keratinocyte associated protein 2	KRTCAP2 KCP2
200186	CREB regulated transcription coactivator 2	CRTC2	type 2 diabetes mellitus
200205	iron-sulfur cluster assembly factor IBA57	IBA57
200312	ring finger protein 215	RNF215
200350	forkhead box D4 like 1	FOXD4L1
200373	cilia and flagella associated protein 221	CFAP221
200403	von Willebrand factor A domain containing 3B	VWA3B
200407	cellular repressor of E1A stimulated genes 2	CREG2

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