GlyCosmos Portal

Displaying entries **7326 - 7350** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
79731	asparaginyl-tRNA synthetase 2, mitochondrial	NARS2
79733	E2F transcription factor 8	E2F8
79736	transcription elongation factor, mitochondrial	TEFM
79741	coiled-coil domain containing 7	CCDC7
79742	divergent protein kinase domain 2B	DIPK2B
79745	CAP-Gly domain containing linker protein family member 4	CLIP4
79748	lectin, mannose binding 1 like	LMAN1L ERGIC-53L ERGL
79750	zinc finger protein 385D	ZNF385D
79755	zinc finger protein 750	ZNF750
79767	engulfment and cell motility 3	ELMO3
79770	thioredoxin domain containing 15	TXNDC15
79776	zinc finger homeobox 4	ZFHX4
79778	MICAL like 2	MICALL2
79781	IQ motif containing with AAA domain 1	IQCA1
79784	myosin heavy chain 14	MYH14
79789	calmin	CLMN
79791	F-box protein 31	FBXO31
79792	gasdermin D	GSDMD
79794	SREBF pathway regulator in golgi 1	SPRING1
79796	ALG9 alpha-1,2-mannosyltransferase	ALG9 dol-P-Man dependent alpha-1,2-mannosyltransferase dolichyl-P-Man:Man(6)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase dolichyl-P-Man:Man(8)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase	Gilles de la Tourette syndrome Marfan syndrome Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome autosomal dominant polycystic kidney disease cardiovascular system disease congenital disorder of glycosylation Il congenital disorder of glycosylation type I congenital disorder of glycosylation congenital heart disease congestive heart failure craniosynostosis cystic kidney disease cystinuria enophthalmos epilepsy esotropia galactokinase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease heart disease heart septal defect hemopericardium intellectual disability learning disability microcephaly monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia neuroendocrine carcinoma neuroendocrine tumor obsolete exophthalmos orbital disease osteochondrodysplasia pericardial effusion polycystic kidney disease 1 polycystic liver disease psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder situs inversus tuberous sclerosis visual epilepsy
79799	UDP glucuronosyltransferase family 2 member A3	UGT2A3 FLJ21934
79802	HHIP like 2	HHIPL2
79805	vasohibin 2	VASH2
79811	SAFB like transcription modulator	SLTM
79812	multimerin 2	MMRN2

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