Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14831 to 14840 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14831
Wnt family member 9B
WNT14B, WNT15
Anti-neutrophil antibody associated vasculitis, Kidney disease, Renal agenesis, Congenital hypoplasia of kidney, Coronary artery disease, Cystic kidney disease, Hypertension, Congenital heart septal defect, Multiple sclerosis, Open angle glaucoma, Orofacial cleft, Prostate cancer

14832
WD repeat containing antisense to TP53
DKCB3, TCAB1, WDR79
Body weight, Dyskeratosis congenita, Li-fraumeni syndrome, Telomere syndrome, Uterine fibroid

14833
WRN RecQ like helicase
RECQ3, RECQL2, RECQL3
Attention deficit hyperactivity disorder, Autism, Cardiovascular disease, Cataract, Ischemic heart disease, Coronary artery disease, Diabetes mellitus type 2, Diffuse cutaneous systemic sclerosis, Dna repair-deficiency disorders, Myocardial infarction, Myocardial ischemia, Osteosarcoma, Scoliosis, Senile cataract, Werner syndrome

14834
WRN helicase interacting protein 1
CFAP93, FAP93, WHIP, bA420G6.2
Astrocytoma, Major depressive disorder

14835
WD repeat and SOCS box containing 2
SBA2
Rhinosinusitis, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Diabetes mellitus type 2

14836
WSC domain containing 1
-
Bipolar disorder, Corneal neovascularization, Essential tremor, Hypotension, Irritable bowel syndrome, Keratitis, Liver neoplasms, Lung cancer, Migraine, Non-small cell lung carcinoma, Ovarian cancer, Hypertension

14837
WSC domain containing 2
-
Attention deficit hyperactivity disorder, Bipolar disorder, Color vision deficiency, Diabetes mellitus, Lung cancer, Metabolic syndrome, Osteoarthritis, Parkinson disease, Pelvic organ prolapse, Periprosthetic osteolysis, Prostate cancer, Schizophrenia, Squamous cell carcinoma, Substance abuse, Diabetes mellitus type 2

14838
WT1 transcription factor
AWT1, GUD, NPHS4, WAGR, WIT-2, WT-1, WT33
11p partial monosomy syndrome, Alzheimer disease, Ambiguous genitalia, Aniridia, Breast neoplasms, Cholelithiasis, Kidney disease, Colonic neoplasms, Color vision deficiency, Congenital aniridia, Coronary artery disease, Denys drash syndrome, Desmoplastic small round cell tumor, Drash syndrome, Endometriosis
View all (28 more)

14839
WT1 associated protein
Mum2
Esophageal disease, Esophageal ulcer, Prostate cancer

14840
WW and C2 domain containing 1
HBEBP3, HBEBP36, KIBRA, MEMRYQTL, PPP1R168
Alzheimer disease, Major depressive disorder, Diabetic neuropathy, Ovarian epithelial cancer, Mesothelioma, Metabolic syndrome, Non-organic psychosis, Ovarian cancer, Psychotic disorders, Diabetes mellitus type 2