GlyCosmos Portal

Displaying entries **8501 - 8525** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
135250	retinoic acid early transcript 1E	RAET1E
135295	serine and arginine rich splicing factor 12	SRSF12
135644	tripartite motif containing 40	TRIM40
135656	mucin like 3	MUCL3
135924	olfactory receptor family 9 subfamily A member 2	OR9A2
135935	NOBOX oogenesis homeobox	NOBOX
135941	olfactory receptor family 2 subfamily A member 14	OR2A14
135946	olfactory receptor family 6 subfamily B member 1	OR6B1
135948	olfactory receptor family 2 subfamily F member 2	OR2F2
136227	collagen type XXVI alpha 1 chain	COL26A1
136541	serine protease 58	PRSS58
136853	scavenger receptor cysteine rich family member with 4 domains	SSC4D
137209	zinc finger protein 572	ZNF572
137492	VPS37A subunit of ESCRT-I	VPS37A
137695	transmembrane protein 68	TMEM68
137797	LY6/PLAUR domain containing 2	LYPD2 RGTR430 UNQ430
137868	sarcoglycan zeta	SGCZ
137902	peroxidasin like	PXDNL
137964	glycerol-3-phosphate acyltransferase 4	GPAT4 DKFZp586M1819 LPAAT-zeta TSARG7 lysophosphatidic acid acyltransferase, zeta	diabetes mellitus type 2 diabetes mellitus
137970	unc-5 netrin receptor D	UNC5D
137994	leucine zipper and EF-hand containing transmembrane protein 2	LETM2
138050	heparan-alpha-glucosaminide N-acetyltransferase	HGSNAT FLJ32731 HGNAT	Zollinger-Ellison syndrome agnosia amnestic disorder blindness bulimia nervosa cataract cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal disease developmental coordination disorder diabetes mellitus diarrhea dissociated nystagmus echolalia enterocele epilepsy fundus albipunctatus fundus dystrophy glaucoma hyperinsulinism hypertrichosis hypertrophic cardiomyopathy 1 hypogonadism intellectual disability keratoconus learning disability mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis night blindness obesity obsolete asthenopia ophthalmoplegia optic atrophy pathologic nystagmus peripheral retinal degeneration retinitis pigmentosa 73 retinitis pigmentosa retrograde amnesia scoliosis sensorineural hearing loss spontaneous ocular nystagmus stereotypic movement disorder type 2 diabetes mellitus visual epilepsy
138199	carnosine N-methyltransferase 1	CARNMT1
138255	cilia and flagella associated protein 95	CFAP95
138307	lipocalin 8	LCN8

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