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"
331 to 340 of 594 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

331
Doublesex and mab-3 related transcription factor 3
DMRTA3
Premature ovarian failure, Uterine fibroid

332
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

333
DMRT like family A2
-
Male infertility single gene azoospermia

334
DMRT like family B with proline rich C-terminal 1
-
Scoliosis

335
Cyclin D binding myb like transcription factor 1
DMP1, DMTF, MRUL, hDMP1
Autism, Bipolar disorder, Major depressive disorder, Schizophrenia

336
DM1 locus, WD repeat containing
D19S593E, DMR-N9, DMRN9, gene59
Obstructive pulmonary disease, Respiratory system disease

337
Dmx like 1
-
Alzheimer disease, Coronary artery disease, Glioma, Myocardial infarction

338
Dmx like 2
DEE81, DFNA71, EIEE81, PEPNS, RC3
Anorexia nervosa, Asthma, Attention deficit hyperactivity disorder, Autism, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Developmental and epileptic encephalopathy, Hearing loss, Insomnia, Major depressive disorder, Metabolic syndrome, Pituitary stalk interruption syndrome, Primary aldosteronism, Diabetes mellitus type 2

339
DNA replication helicase/nuclease 2
DNA2L, RTS4, hDNA2
Congenital myopathy, Desbuquois syndrome, Dna2-related mitochondrial dna deletion syndrome, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Mitochondrial myopathy, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Rothmund-thomson syndrome, Seckel syndrome, Sheehan syndrome

340
Dynein axonemal assembly factor 1
CILD13, DAU1, LRRC50, ODA7, swt
Autism, Ciliary dyskinesia, Congenital nasopharyngeal atresia, Situs ambiguus