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
3531 to 3540 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

3531
DEAH-box helicase 16
DBP2, DDX16, NMOAS, PRO2014, PRP8, PRPF2, Prp2
Intellectual developmental disorder, Periventricular heterotopia

3532
DExH-box helicase 30
DDX30, NEDMIAL, RETCOR
Autism, Global developmental delay, Hearing impairment, Intellectual developmental disorder, Neurodevelopmental disorder, Prostatic neoplasms, Strabismus

3533
DEAH-box helicase 32 (putative)
DDX32, DHLP1
Retinitis pigmentosa

3534
DExH-box helicase 34
DDX34, HRH1
Intellectual developmental disorder, Neurodevelopmental disorder, Polycystic kidney disease, Polydactyly

3535
DEAH-box helicase 35
C20orf15, DDX35, KAIA0875
Basal cell carcinoma, Breast cancer, Kidney disease, Color vision deficiency, Colorectal cancer, Crohn disease, Keratinocyte carcinoma, Scoliosis

3536
DEAH-box helicase 36
DDX36, G4R1, MLEL1, RHAU
Colorectal cancer, Metabolic syndrome, Myocardial infarction, Retinopathy, Diabetes mellitus type 2

3537
DEAH-box helicase 37
DDX37, Dhr1, NEDBAVC, SRXY11
46,xy gonadal dysgenesis, 46,xy partial gonadal dysgenesis, 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
View all (1 more)

3538
DEAH-box helicase 38
DDX38, PRP16, PRPF16, RP84
Retinitis pigmentosa, Coronary artery disease, Hyperlipidemia, Gout

3539
DEAH-box helicase 40
ARG147, DDX40, PAD
Retinitis pigmentosa

3540
DExH-box helicase 57
DDX57
Obesity