Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3621 to 3630 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3621
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

3622
DNA meiotic recombinase 1
DMC1H, LIM15, dJ199H16.1
Azoospermia, Cholecystolithiasis, Cryptospermia, Gallstones, Spermatogenic failure, Testicular azoospermia

3623
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)

3624
Dimethylglycine dehydrogenase
DMGDHD, ME2GLYDH
Obstructive pulmonary disease, Dimethylglycine dehydrogenase deficiency, Gastric ulcer, Metabolic syndrome, Diabetes mellitus type 2

3625
Dentin matrix acidic phosphoprotein 1
ARHP, ARHR, DMP-1
Hypophosphatemic rickets, Desbuquois syndrome

3626
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

3627
Doublesex and mab-3 related transcription factor 1
CT154, DMT1
46, xx disorder of sex development, 46, xy disorder of sex development, 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

3628
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

3629
Doublesex and mab-3 related transcription factor 3
DMRTA3
Premature ovarian failure, Uterine fibroid

3630
DMRT like family A1
DMO, DMRT4
Eczema, Lymphocytic leukemia, Crohn disease, Dental caries, Endometrial cancer, Endometrial neoplasms, Lymphoid leukemia, Post-traumatic stress disorder, Scoliosis, Diabetes mellitus type 2