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
3421 to 3430 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

3421
DExD-box helicase 52
HUSSY19, ROK1
Bipolar disorder, Esophageal disease, Major depressive disorder, Schizophrenia, Diabetes mellitus type 2

3422
DEAD-box helicase 53
CAGE, CT26
Male infertility single gene azoospermia, Nephrotic syndrome

3423
DEAD-box helicase 54
DP97
Congenital hypoplasia of kidney, Intellectual developmental disorder, Liver neoplasms, Pancreatic cancer, Polycystic ovary syndrome

3424
DEAD-box helicase 56
DDX21, DDX26, NOH61
Cardiovascular disease, Hyperlipidemia, Metabolic syndrome, Schizophrenia, Scoliosis, Diabetes mellitus type 2

3425
DEAD-box helicase 59
OFD5, ZNHIT5
Hypothyroidism, Myocardial infarction, Orofaciodigital syndrome

3426
DEAD-box helicase 6
HLR2, IDDILF, P54, RCK, Rck/p54
Alzheimer disease, Rheumatoid arthritis, Asthma, Biliary cirrhosis, Celiac disease, Diffuse cutaneous systemic sclerosis, Endometriosis, Immune system disease, Intellectual developmental disorder speech dysmorphic, Lymphoma, Non-specific syndromic intellectual disability, Biliary cholangitis, Systemic lupus erythematosus, Systemic sclerosis

3427
DExD/H-box helicase 60
-
Color vision deficiency

3428
DExD/H-box 60 like
-
Liver cirrhosis, Nonalcoholic fatty liver disease, Obesity, Psoriasis, Scoliosis

3429
DEAF1 transcription factor
MRD24, NEDHELS, NUDR, SPN, VSVS, ZMYND5
Alzheimer disease, Autism, Nonsyndromic intellectual disability, Biliary cirrhosis, Neurodevelopmental disorder, Major depressive disorder, Developmental disability, Intellectual developmental disorder, Intellectual developmental disorder seizures extrapyramidal, Non-specific syndromic intellectual disability, Biliary cholangitis, Scoliosis, Systemic lupus erythematosus, Depression, Vulto-van silfhout-de vries syndrome

3430
2,4-dienoyl-CoA reductase 1
DECR, NADPH, SDR18C1
2,4-dienoyl-coa reductase deficiency, Insomnia, Liver disease