|Human Homolog||WNT2, wingless-type MMTV integration site family member 2|
|NCBI Gene ID||7472|
|Human Synonyms||INT1L1, IRP|
|Human Chr (Location)||7q31.2; chr7:117276631-117323289 (-) GRCh38|
Homozygous mutants exhibit impaired placental vascularization, runting and 50% perinatal mortality resulting from difficulties in breathing and nursing. Survivors of the perinatal period tend to recover, and adults are healthy and fertile.
|Process||atrial cardiac muscle tissue morphogenesis, canonical Wnt signaling pathway, ...|
|Component||cytoplasm, extracellular matrix, ...|
|Function||cytokine activity, frizzled binding, ...|
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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