Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "D"
121 to 130 of 596 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

121
DEAD-box helicase 18
Has1, MrDb
Alzheimer disease, Central nervous system cancer, Glioblastoma, Glioma, Insomnia, Obesity, Oligodendroglioma, Diabetes mellitus type 2

122
DEAD-box helicase 19B
DBP5, DDX19, RNAh
Gout

123
DEAD-box helicase 20
DP103, GEMIN3
Amyotrophic lateral sclerosis, Venous thromboembolism

124
DExD-box helicase 21
GUA, GURDB, II/Gu, RH, RH II/Gu, RH-II/GU, RH-II/GuA, gu-alpha
Insomnia, Major depressive disorder

125
DEAD-box helicase 23
PRPF28, SNRNP100, U5-100K, U5-100KD, prp28
Cardiovascular disease, Intellectual developmental disorder, Neurodevelopmental disorder, Perisylvian syndrome

126
DEAD-box helicase 25
GRTH
Alzheimer disease, Azoospermia, Bipolar disorder, Male infertility single gene azoospermia, Squamous cell carcinoma

127
DEAD-box helicase 27
DRS1, Drs1p, HSPC259, PP3241, RHLP, dJ686N3.1
Alzheimer disease, Attention deficit hyperactivity disorder, Autism

128
DEAD-box helicase 31
PPP1R25
Color vision deficiency, Coronary artery disease, Venous thromboembolism

129
DExD-box helicase 39B
BAT1, D6S81E, UAP56
Eczema, Diabetes mellitus type 1, Insomnia, Myositis, Neurodevelopmental disorder, Stevens-johnson syndrome, Toxic epidermal necrolysis

130
DEAD-box helicase 3 X-linked
CAP-Rf, DBX, DDX14, DDX3, HLP2, MRX102, MRXSSB
Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Corpus callosum agenesis with facial anomalies and robin sequence, Epilepsy, Global developmental delay, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Medulloblastoma, Mesothelioma, Neurodevelopmental disorder, Osteoarthritis, Partington syndrome, Toriello-carey syndrome, X-linked intellectual disability