Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3541 to 3550 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3541
DExH-box helicase 58
D11LGP2, D11lgp2e, LGP2, RLR-3
Alzheimer disease, Coronary artery disease

3542
DEAH-box helicase 8
DDX8, Dhr2, HRH1, PRP22, PRPF22
Alzheimer disease, Congenital anomalies of the kidney and urinary tract, Dupuytren contracture, Metabolic syndrome, Mitral valve prolapse, Diabetes mellitus type 2

3543
DExH-box helicase 9
DDX9, LKP, MRD75, NDH2, NDHII, RHA
Charcot-marie-tooth disease, Intellectual developmental disorder

3544
Diablo IAP-binding mitochondrial protein
DFNA64, SMAC
Isolated sensorineural deafness, Nonsyndromic hearing loss, Brain ischemia, Deafness, Hearing impairment, Huntington disease, Hypertension, Osteoarthritis, Prostatic neoplasms

3545
Diaphanous related formin 1
DFNA1, DIA1, DRF1, LFHL1, SCBMS, hDIA1, mDia1
Asthma, Auditory neuropathy, Nonsyndromic hearing loss, Neonatal convulsions, Deafness, Vascular dementia, Sensorineural hearing loss thrombocytopenia syndrome, Epilepsy, Global developmental delay, Hearing impairment, Hereditary hearing loss, Metabolic syndrome, Moyamoya disease, Pendred syndrome, Seizures
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3546
Diaphanous related formin 2
DIA, DIA2, DRF2, POF, POF2, POF2A
Diverticular disease, Premature ovarian failure, Schizophrenia

3547
Diaphanous related formin 3
AN, AUNA1, DIA2, DRF3, NSDAN, diap3, mDia2
Angioedema, Auditory neuropathy, Isolated sensorineural deafness, Nonsyndromic hearing loss, Biliary atresia, Kidney disease, Dementia, Diabetic neuropathy, Hearing impairment, Insomnia, Metabolic syndrome, Willis-ekbom disease, Hypertension, Diabetes mellitus type 2

3548
Dicer 1, ribonuclease III
DCR1, Dicer, Dicer1e, GLOW, HERNA, K12H4.8-LIKE, MNG1, RMSE2, aviD
Dicer1 syndrome, Dicer1 tumor-predisposition syndrome, Dicer1-related tumor predisposition, Embryonal nuclear cataract, Endometriosis, Global developmental delay, Liver neoplasms, Granulosa cell tumor of ovary, Sertoli-leydig cell tumor of ovary, Neurodevelopmental disorder, Rhabdomyosarcoma, Schizophrenia, Vertebral anomalies with endocrine and t-cell dysfunction, Wilms tumor

3549
Death inducer-obliterator 1
BYE1, C20orf158, DATF-1, DATF1, DIDO2, DIDO3, DIO-1, DIO1, dJ885L7.8
Esophageal squamous cell carcinoma, Metabolic syndrome, Obesity, Diabetes mellitus type 2

3550
Iodothyronine deiodinase 1
5DI, THMA2, TXDI1
Hyperthyroxinemia, Multiple myeloma, Thyroid disease, Thyroid hormone metabolism disorder