Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "W"
71 to 80 of 96 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

71
Wnt family member 7A
SANTOS, Wnt-7a
Amyotrophic lateral sclerosis, Atrial fibrillation, Bladder exstrophy and epispadias complex, Obstructive pulmonary disease, Color vision deficiency, Desbuquois syndrome, Female infertility, Irritable bowel syndrome, Motor neuron disease, Ocular sarcoidosis, Ovarian neoplasm, Sanjad-sakati syndrome, Urogenital neoplasm

72
Wnt family member 7B
-
Alzheimer disease, Androgenetic alopecia, Anophthalmia, Anophthalmia/microphthalmia-esophageal atresia syndrome, Astrocytoma, Breast cancer, Colorectal cancer, Eye disease, Tourette syndrome, Laryngeal carcinoma, Major depressive disorder, Male reproductive system disease, Laryngeal cancer, Diabetes mellitus, type 2

73
Wnt family member 8A
WNT8D
Alzheimer disease, Atrial fibrillation, Atrial flutter, Hypospadias, Diabetes mellitus, type 2

74
Wnt family member 8B
-
Hirschsprung disease

75
Wnt family member 10B
SHFM6, STHAG8, WNT-12
Breast neoplasm, Desbuquois syndrome, Ectrodactyly, Obesity, Prostatic neoplasm, Split hand-foot malformation, Tooth agenesis

76
Wnt family member 11
HWNT11
Bladder exstrophy and epispadias complex, Bone fragility with contractures, arterial rupture, and deafness, Hypospadias, Osteoarthritis, Osteoporosis-pseudoglioma syndrome, Respiratory system disease, Diabetes mellitus, type 2

77
Wnt family member 2B
WNT13
Cardiovascular disease, Cerebrovascular disorder, Heart failure, Hypertension, Hypothyroidism, Major depressive disorder, Pancreatic cancer, Primary aldosteronism, Scoliosis, Stroke

78
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, Myocardial infarction, Myocardial ischemia, Osteosarcoma, Scoliosis, Senile cataract, Severe acute respiratory syndrome, Werner syndrome

79
WT1 transcription factor
AWT1, GUD, NPHS4, WAGR, WIT-2, WT-1, WT33
11p partial monosomy syndrome, Alzheimer disease, Ambiguous genitalia, Aniridia, Breast neoplasm, Cholelithiasis, Kidney disease, Colonic neoplasm, Color vision deficiency, Congenital aniridia, Coronary artery disease, Denys drash syndrome, Drash syndrome, Endometriosis, Idiopathic steroid-resistant nephrotic syndrome
View all (27 more)

80
WD repeat domain 77
HKMT1069, MEP-50, MEP50, Nbla10071, p44, p44/Mep50
Ovarian neoplasm