Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3611 to 3620 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3611
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

3612
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

3613
Doublesex and mab-3 related transcription factor 3
DMRTA3
Premature ovarian failure, Uterine fibroid

3614
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

3615
DMRT like family A2
-
Male infertility single gene azoospermia

3616
DMRT like family B with proline rich C-terminal 1
-
Scoliosis

3617
Cyclin D binding myb like transcription factor 1
DMP1, DMTF, MRUL, hDMP1
Autism, Bipolar disorder, Major depressive disorder, Schizophrenia

3618
DM1 locus, WD repeat containing
D19S593E, DMR-N9, DMRN9, gene59
Obstructive pulmonary disease, Respiratory system disease

3619
Dmx like 1
-
Alzheimer disease, Coronary artery disease, Glioma, Myocardial infarction

3620
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