Details for Gene WNT10A

GENE NAME WNT10A
CHROMOSOME 2
ENSEMBL ID None
ENTREZ ID ENSG00000135925
UNIPROT ACCESSION NUMBER Q9GZT5
GO MOLECULAR FUNCTION ['receptor ligand activity', 'cytokine activity', 'frizzled binding']
ESSENTIAL IN MOUSE None
PATHWAYS hsa04150; hsa04310; hsa04390; hsa04550; hsa04916; hsa04934; hsa05010; hsa05022; hsa05165; hsa05200; hsa05205; hsa05217; hsa05224; hsa05225; hsa05226; hsa04150; hsa04310; hsa04390; hsa04550; hsa04916; hsa04934; hsa05010; hsa05022; hsa05165; hsa05200; hsa05205; hsa05217; hsa05224; hsa05225; hsa05226; R-HSA-162582; R-HSA-195721; R-HSA-3238698; R-HSA-372790; R-HSA-373080; R-HSA-500792
16 combinations linked to WNT10A OLI938; OLI162; OLI163; OLI1243; OLI1245; OLI1734; OLI1737; OLI164; OLI936; OLI1735; OLI1244; OLI576; OLI160; OLI159; OLI161; OLI937
8 variants linked to WNT10A WNT10A:c.511C>T, p.Arg171Cys; WNT10A:c.637G>A, p.Gly213Ser; WNT10A:c.682T>A, p.Phe228Ile; WNT10A:c.338G>A, p.Arg113His; WNT10A:c.499G>C, p.Glu167Gln; WNT10A:c.337C>T, p.Arg113Cys; WNT10A:c.682T>A, p.Phe228Ile; WNT10A:c.637G>A, p.Gly213Ser
2 diseases linked to WNT10A Hypodontia; Amelogenesis imperfecta
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