Genes | GeDiPNet - Gene Disease Pathway & Associations

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All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

1781 to 1790 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1781	123803	NTAN1	N-terminal asparagine amidase	PNAA, PNAD	Kidney disease, Kidney failure
1782	123811	CEP20	Centrosomal protein 20	C16orf63, FOPNL, FOR20, PHSECRG2	Multiple myeloma
1783	123872	DNAAF1	Dynein axonemal assembly factor 1	CILD13, DAU1, LRRC50, ODA7, swt	Asthenozoospermia, Asthma, Bronchiectasis, Bronchitis, Ciliary dyskinesia, Ciliopathies, Asplenia, Congenital pectus excavatum, Corneal dystrophy, Hearing loss, Hydrocephalus, Hypertension, Lung diseases, Nasal polyposis, Otitis media View all (4 more)
1784	123879	DCUN1D3	Defective in cullin neddylation 1 domain containing 3	44M2.4, DCNL3, SCCRO3	Malignant neoplasm
1785	124	ADH1A	Alcohol dehydrogenase 1A (class I), alpha polypeptide	ADH1	Non-alcoholic fatty liver disease
1786	1240	CMKLR1	Chemerin chemokine-like receptor 1	CHEMERINR, ChemR23, DEZ, ERV1, RVER1	Granulosa cell tumor, Lung carcinoma, Mental depression
1787	124045	SPATA33	Spermatogenesis associated 33	C16orf55	Carcinoma, Melanoma, Melanosis
1788	124093	CCDC78	Coiled-coil domain containing 78	C16orf25, CNM4, JFP10, hsCCDC78	Centronuclear myopathy, Centronuclear myopathy, x-linked, Congenital myopathy with fiber type disproportion, Congenital myopathy with internal nuclei and atypical cores, Congenital structural myopathy, Impaired cognition, Myopathy, Tubular aggregate myopathy
1789	1241	LTB4R	Leukotriene B4 receptor	BLT1, BLTR, CMKRL1, GPR16, LTB4R1, LTBR1, P2RY7, P2Y7
1790	124152	IQCK	IQ motif containing K	-	Alzheimer disease, Senile dementia

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