Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
3601 to 3610 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3601
Distal membrane arm assembly component 1
C9orf123, TMEM261
Attention deficit hyperactivity disorder, Cannabis abuse, Conduct disorder, Connective tissue disease, Conotruncal cardiac defect, Corneal astigmatism, Dementia, Dental caries, Insomnia, Osteonecrosis, Prostate cancer, Sarcopenia, Diabetes mellitus type 2

3602
Distal membrane arm assembly component 2
ATP5SL
Androgenetic alopecia, Heart failure

3603
DNA methyltransferase 1 associated protein 1
DNMAP1, DNMTAP1, EAF2, MEAF2, SWC4
Intellectual developmental disorder

3604
Deleted in malignant brain tumors 1
GP340, SAG, SALSA, muclin
Obstructive pulmonary disease, Colonic neoplasms, Myocardial infarction

3605
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

3606
DNA meiotic recombinase 1
DMC1H, LIM15, dJ199H16.1
Azoospermia, Cholecystolithiasis, Cryptospermia, Gallstones, Spermatogenic failure, Testicular azoospermia

3607
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)

3608
Dimethylglycine dehydrogenase
DMGDHD, ME2GLYDH
Obstructive pulmonary disease, Dimethylglycine dehydrogenase deficiency, Gastric ulcer, Metabolic syndrome, Diabetes mellitus type 2

3609
Dentin matrix acidic phosphoprotein 1
ARHP, ARHR, DMP-1
Hypophosphatemic rickets, Desbuquois syndrome

3610
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