Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3551 to 3560 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3551
DEAH-box helicase 35
C20orf15, DDX35, KAIA0875
Basal cell carcinoma, Breast cancer, Kidney disease, Color vision deficiency, Colorectal cancer, Crohn disease, Keratinocyte carcinoma, Scoliosis

3552
DEAH-box helicase 36
DDX36, G4R1, MLEL1, RHAU
Colorectal cancer, Metabolic syndrome, Myocardial infarction, Retinopathy, Diabetes mellitus type 2

3553
DEAH-box helicase 37
DDX37, Dhr1, NEDBAVC, SRXY11
46, xy complete gonadal dysgenesis, Congenital adrenal insufficiency with 46,xy sex reversal due to cyp11a1 deficiency, 46, xy sex reversal, Choreoathetosis, Coloboma, Renal agenesis, Dental enamel hypoplasia, Gonadal dysgenesis, Intellectual developmental disorder, Male infertility single gene azoospermia, Male infertility spermatogenesis disorder, Cortical development malformation, Neurodevelopmental disorder, Polymicrogyria, Swyer syndrome
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3554
DEAH-box helicase 38
DDX38, PRP16, PRPF16, RP84
Retinitis pigmentosa, Coronary artery disease, Hyperlipidemia, Gout

3555
DEAH-box helicase 40
ARG147, DDX40, PAD
Retinitis pigmentosa

3556
DExH-box helicase 57
DDX57
Obesity

3557
DExH-box helicase 58
D11LGP2, D11lgp2e, LGP2, RLR-3
Alzheimer disease, Coronary artery disease

3558
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

3559
DExH-box helicase 9
DDX9, LKP, MRD75, NDH2, NDHII, RHA
Charcot-marie-tooth disease, Intellectual developmental disorder

3560
Diablo IAP-binding mitochondrial protein
DFNA64, SMAC
Isolated sensorineural deafness, Nonsyndromic hearing loss, Brain ischemia, Deafness, Hearing impairment, Huntington disease, Hypertension, Osteoarthritis, Prostatic neoplasms