Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3631 to 3640 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3631
DMRT like family A2
-
Male infertility single gene azoospermia

3632
DMRT like family B with proline rich C-terminal 1
-
Scoliosis

3633
Cyclin D binding myb like transcription factor 1
DMP1, DMTF, MRUL, hDMP1
Autism, Bipolar disorder, Major depressive disorder, Schizophrenia

3634
DM1 locus, WD repeat containing
D19S593E, DMR-N9, DMRN9, gene59
Obstructive pulmonary disease, Respiratory system disease

3635
Dmx like 1
-
Alzheimer disease, Coronary artery disease, Glioma, Myocardial infarction

3636
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

3637
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

3638
Dynein axonemal assembly factor 1
CILD13, DAU1, LRRC50, ODA7, swt
Autism, Ciliary dyskinesia, Congenital nasopharyngeal atresia, Situs ambiguus

3639
Dynein axonemal assembly factor 10
WDR92
Lung cancer, Osteoarthritis, Squamous cell carcinoma

3640
Dynein axonemal assembly factor 11
CILD19, LRRC6, LRTP, TSLRP, tilB
Ciliary dyskinesia, Congenital nasopharyngeal atresia, Sarcoidosis, Scoliosis, Situs ambiguus