Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "D"

561 to 570 of 594 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
561	100288687	DUX4	Double homeobox 4	DUX4L	Facioscapulohumeral muscular dystrophy
562	503835	DUXA	Double homeobox A	-	Dupuytren contracture
563	1855	DVL1	Dishevelled segment polarity protein 1	DRS2, DVL, DVL1L1, DVL1P1	Robinow syndrome, Breast cancer, Cancer, Colorectal cancer, Desbuquois syndrome, Digeorge syndrome, Estrogen-receptor negative breast cancer, Lung cancer, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Squamous cell carcinoma
564	1856	DVL2	Dishevelled segment polarity protein 2	-	Alzheimer disease, Hearing loss, Pelvic organ prolapse, Very long chain acyl-coa dehydrogenase deficiency
565	1857	DVL3	Dishevelled segment polarity protein 3	DRS3	Robinow syndrome, Clinodactyly, Desbuquois syndrome, Hypertension, Major depressive disorder
566	1797	DXO	Decapping exoribonuclease	DOM3L, DOM3Z, NG6, RAI1	Cervical cancer
567	84332	DYDC2	DPY30 domain containing 2	-	Gout, Sarcoidosis
568	54808	DYM	Dymeclin	DMC, SMC	Alzheimer disease, Congenital cartilage disorder, Connective tissue disease, Dental caries, Desbuquois syndrome, Dyggve-melchior-clausen syndrome, Osteoarthritis, Osteochondrodysplasias, Schizophrenia, Smith-mccort dysplasia
569	284254	DYNAP	Dynactin associated protein	C18orf26	Asthma, Oligodendroglioma, Uveal melanoma
570	1778	DYNC1H1	Dynein cytoplasmic 1 heavy chain 1	CDCBM13, CMT2O, DHC1, DHC1a, DNCH1, DNCL, DNECL, DYHC, Dnchc1, HL-3, SMALED1, p22	Amyotrophic lateral sclerosis, Arthrogryposis multiplex congenita, Autism, Cerebellar ataxia, Charcot-marie-tooth disease, Childhood-onset spinal muscular atrophy, Distal hereditary motor neuropathy, Nonsyndromic intellectual disability, Cerebellar atrophy, Congenital neurologic anomalies, Congenital pes cavus, Cortical dysplasia with other brain malformations, Dejerine-sottas disease, Distal spinal muscular atrophy, Spinal muscular atrophy View all (23 more)

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