Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "D"
321 to 330 of 594 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

321
DNA methyltransferase 1 associated protein 1
DNMAP1, DNMTAP1, EAF2, MEAF2, SWC4
Intellectual developmental disorder

322
Deleted in malignant brain tumors 1
GP340, SAG, SALSA, muclin
Obstructive pulmonary disease, Colonic neoplasms, Myocardial infarction

323
Diencephalon/mesencephalon homeobox 1
Atx, MBX, OTX3, PAXB
Central nervous system cancer, Neurodevelopmental disorder, Glioblastoma, Glioma, Global developmental delay, Hearing impairment, Hyperopia, Non-specific syndromic intellectual disability, Strabismus

324
DNA meiotic recombinase 1
DMC1H, LIM15, dJ199H16.1
Azoospermia, Cholecystolithiasis, Cryptospermia, Gallstones, Spermatogenic failure, Testicular azoospermia

325
Dystrophin
BMD, CMD3B, DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272, MRX85
Alzheimer disease, Arrhythmogenic right ventricular cardiomyopathy, Ataxia, Atrial septal defect, Autism, Becker muscular dystrophy, Benign congenital myopathy, Bipolar disorder, Blepharoptosis, Breast cancer, Calcinosis, Cardiomegaly, Cardiomyopathy, Dilated cardiomyopathy, Clinodactyly
View all (29 more)

326
Dimethylglycine dehydrogenase
DMGDHD, ME2GLYDH
Obstructive pulmonary disease, Dimethylglycine dehydrogenase deficiency, Gastric ulcer, Metabolic syndrome, Diabetes mellitus type 2

327
Dentin matrix acidic phosphoprotein 1
ARHP, ARHR, DMP-1
Hypophosphatemic rickets, Desbuquois syndrome

328
DM1 protein kinase
DM, DM1, DM1PK, DMK, MDPK, MT-PK
Bethlem myopathy, Myotonic dystrophy, Congenital-onset steinert myotonic dystrophy, Noonan syndrome, Catecholaminergic polymorphic ventricular tachycardia

329
Doublesex and mab-3 related transcription factor 1
CT154, DMT1
46,xx ovotesticular disorder of sex development, 46,xy disorder of sex developmen, Color vision deficiency, Dementia, Major depressive disorder, Male infertility, Male infertility single gene azoospermia, Obesity, Selective iga deficiency disease, Swyer syndrome, Testicular azoospermia, Testicular carcinoma, Testicular germ cell tumor, Testicular neoplasms, Uterine fibroid

330
Doublesex and mab-3 related transcription factor 2
DSXL-2
Obstructive pulmonary disease, Jarcho-levin syndrome, Language development disorders, Spermatocele, Spondylocostal dysostosis, Diabetes mellitus type 2, Uterine fibroid