ORF » Species Summary » Homo sapiens » Reactome » APC truncation mutants have impaired AXIN binding

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Homo sapiens (human) APC truncation mutants have impaired AXIN binding (provided by Reactome)

Browse by Letter Index, Genomic Locus

14 gene

The longest variant of each gene is displayed. Click the see gene variants link to see all gene variants.


Gene Symbol Full Name
PPP2CB protein phosphatase 2 catalytic subunit beta
PPP2R5C protein phosphatase 2 regulatory subunit B'gamma
PPP2R5B protein phosphatase 2 regulatory subunit B'beta
APC APC, WNT signaling pathway regulator
PPP2CA protein phosphatase 2 catalytic subunit alpha
PPP2R5A protein phosphatase 2 regulatory subunit B'alpha
PPP2R1B protein phosphatase 2 scaffold subunit Abeta
GSK3B glycogen synthase kinase 3 beta
PPP2R1A protein phosphatase 2 scaffold subunit Aalpha
AMER1 APC membrane recruitment protein 1
PPP2R5E protein phosphatase 2 regulatory subunit B'epsilon
CSNK1A1 casein kinase 1 alpha 1
PPP2R5D protein phosphatase 2 regulatory subunit B'delta
AXIN1 axin 1
ORF
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