Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "D"

141 to 150 of 466 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
141	1747	DLX3	Distal-less homeobox 3	AI4, TDO	Amelogenesis imperfecta, Dentin dysplasia, Dentinogenesis imperfecta, Desbuquois syndrome, Peripheral pulmonary artery stenosis, Tricho-dento-osseous syndrome
142	1748	DLX4	Distal-less homeobox 4	BP1, DLX7, DLX8, DLX9, OFC15	Orofacial cleft
143	1749	DLX5	Distal-less homeobox 5	SHFM1, SHFM1D	Alzheimer disease, Bone disease, Craniofacial abnormalities, Desbuquois syndrome, Ectrodactyly, Gastroesophageal reflux disease, Klippel-trenaunay syndrome, Osteoarthritis, Rubinstein-taybi syndrome, Split hand-foot malformation, Vacterl association
144	1750	DLX6	Distal-less homeobox 6	-	Attention deficit hyperactivity disorder, Autism, Craniofacial abnormalities, Desbuquois syndrome, Ectrodactyly, Split hand-foot malformation, Substance abuse
145	1755	DMBT1	Deleted in malignant brain tumors 1	GP340, SAG, SALSA, muclin	Obstructive pulmonary disease, Colonic neoplasm, Myocardial infarction
146	1756	DMD	Dystrophin	BMD, CMD3B, DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272, MRX85	Alzheimer disease, Arrhythmogenic right ventricular cardiomyopathy, Ataxia, Atrial septal defect, Autism, Bipolar disorder, Blepharoptosis, Breast cancer, Calcinosis, Cardiomegaly, Cardiomyopathy, Delirium, dementia, and cognitive disorders, Dilated cardiomyopathy, Duchenne muscular dystrophy, Restrictive cardiomyopathy View all (26 more)
147	1758	DMP1	Dentin matrix acidic phosphoprotein 1	ARHP, ARHR, DMP-1	Hypophosphatemic rickets, Desbuquois syndrome
148	1759	DNM1	Dynamin 1	DEE31, DEE31A, DEE31B, DNM, EIEE31	Asthma, Attention deficit hyperactivity disorder, Cerebellar ataxia, Developmental and epileptic encephalopathy, Developmental disability, Epilepsy, Global developmental delay, Insomnia, Lennox-gastaut syndrome, Neurodevelopmental disorders, Retinopathy of prematurity, Schizophrenia, West syndrome
149	1760	DMPK	DM1 protein kinase	DM, DM1, DM1PK, DMK, MDPK, MT-PK	Bethlem myopathy, Myotonic dystrophy, Noonan syndrome, Catecholaminergic polymorphic ventricular tachycardia
150	1761	DMRT1	Doublesex and mab-3 related transcription factor 1	CT154, DMT1	46, xx disorder of sex development, 46,xy complete gonadal dysgenesis, Color vision deficiency, Dementia, Major depressive disorder, Male infertility, Male infertility single gene azoospermia, Obesity, Selective iga deficiency disease, Testicular azoospermia, Testicular carcinoma, Uterine fibroid

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