Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14741 to 14750 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14741
WIZ zinc finger
ZNF803
Bladder exstrophy and epispadias complex, Coronary artery disease

14742
Wnt ligand secretion mediator
C1orf139, EVI, GPR177, MRP, ZKS, mig-14
Osteoarthritis, Osteoporosis, Preeclampsia, Zaki syndrome

14743
WNK lysine deficient protein kinase 1
HSAN2, HSN2, KDP, PPP1R167, PRKWNK1, PSK, p65
Eczema, Central serous retinopathy, Charcot-marie-tooth disease, Colorectal cancer, Hereditary motor and sensory neuropathies, Hereditary sensory and autonomic neuropathy, Hypertension, Kidney disease, Lung cancer, Metabolic syndrome, Peripheral neuropathy, Pseudohypoparathyroidism, Psoriasis, Sensory neuropathy, Squamous cell carcinoma
View all (3 more)

14744
WNK lysine deficient protein kinase 2
NY-CO-43, P/OKcl.13, PRKWNK2, SDCCAG43
Alzheimer disease, Bipolar disorder, Coronary artery disease, Essential tremor, Gout

14745
WNK lysine deficient protein kinase 3
MRXS2, PRKWNK3, PRS
Alzheimer disease, Autism, Congenital retrognathism, Neurodevelopmental disorder, Prostate cancer, Schizophrenia, Sleep apnea

14746
WNK lysine deficient protein kinase 4
PHA2B, PRKWNK4
Hypertension, Pseudohypoparathyroidism

14747
Wnt family member 1
BMND16, INT1, OI15
Attention deficit hyperactivity disorder, Autism, Bone disease, Bone fragility with contractures, arterial rupture, and deafness, Breast neoplasms, Connective tissue disease, Desbuquois syndrome, Osteoporosis, Keratoconus, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome

14748
Wnt family member 10A
ECTD16, OODD, SSPS, STHAG4
Androgenetic alopecia, Hypohidrotic ectodermal dysplasia, Bladder exstrophy and epispadias complex, Dental caries, Tooth agenesis, Ectodermal dysplasia, Schopf-schulz-passarge syndrome

14749
Wnt family member 10B
SHFM6, STHAG8, WNT-12
Breast neoplasms, Desbuquois syndrome, Tooth agenesis, Ectrodactyly, Obesity, Prostatic neoplasms, Split hand-foot malformation

14750
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