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
Showing genes starting with "W"
101 to 110 of 123 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

101
Wnt family member 4
SERKAL, WNT-4
Attention deficit hyperactivity disorder, Autism, Breast cancer, Epithelial ovarian carcinoma, Carpal tunnel syndrome, Colorectal cancer, Dwarfism, Endometriosis, Female infertility, Kidney disease, Ovarian epithelial cancer, Mayer-rokitansky-kuster-hauser syndrome, Obesity, Ovarian cancer, Pelvic organ prolapse
View all (5 more)

102
Wnt family member 5A
hWNT5A
Robinow syndrome, Desbuquois syndrome, Female infertility, Idiopathic pulmonary fibrosis, Lung neoplasms, Scoliosis, Uterine neoplasms, Vesicoureteral reflux

103
Wnt family member 5B
-
Adenoid cystic carcinoma, Diaphragm disease, Gout, Leiomyoma, Salivary gland neoplasms

104
Wnt family member 6
-
Androgenetic alopecia, Desbuquois syndrome, Diabetes mellitus type 2

105
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 neoplasms, Synovitis, acne, pustulosis, hyperostosis, and osteitis, Urogenital neoplasms

106
Wnt family member 7B
-
Alzheimer disease, Androgenetic alopecia, Anophthalmia, Anophthalmia/microphthalmia-esophageal atresia syndrome, Astrocytoma, Breast cancer, Colorectal cancer, Contracture, Dupuytren contracture, Eye disease, Tourette syndrome, Laryngeal carcinoma, Major depressive disorder, Male reproductive system disease, Laryngeal neoplasms
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107
Wnt family member 8A
WNT8D
Alzheimer disease, Atrial fibrillation, Atrial flutter, Hypospadias, Diabetes mellitus type 2

108
Wnt family member 8B
-
Hirschsprung disease

109
Wnt family member 9A
WNT14
Moyamoya disease, Parkinson disease

110
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