|Human Homolog||WNT9A, wingless-type MMTV integration site family, member 9A|
|NCBI Gene ID||7483|
|Human Chr (Location)||1q42; chr1:227921464-227947975 (-) GRCh38|
Homozygous inactivation of this gene results in neonatal lethality, altered chondrocyte maturation, cranial defects, and skeletal abnormalities including shortened appendicular long bones, partial joint fusions of carpal and tarsal elements, and chondroid metaplasia in synovial and fibrous joints.
|Process||anatomical structure development, canonical Wnt signaling pathway, ...|
|Component||extracellular region, extracellular space, ...|
|Function||frizzled binding, protein binding, ...|
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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