1. Gene
  2. Wnt7a - Wnt family member 7A Gene

Wnt7a - Wnt family member 7A Gene

Rattus norvegicus
Gene ID: 114850 | Gene type: protein coding

About Wnt7a

Summary

Enables Frizzled binding activity. Involved in several processes, including canonical Wnt signaling pathway; positive regulation of JNK cascade; and response to estradiol. Predicted to be located in cell surface and extracellular matrix. Predicted to be active in Schaffer collateral - CA1 synapse; extracellular space; and glutamatergic synapse. Human ortholog(s) of this gene implicated in Fuhrmann syndrome and Schinzel type phocomelia. Orthologous to human WNT7A (Wnt family member 7A). [provided by Alliance of Genome Resources, Apr 2022]

Wnt7a Products(1)

mRNA Protein Name
NM_001100473.1 NP_001093943.1 protein Wnt-7a precursor
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables frizzled binding IPI
IPI: Inferred from physical interaction
18567805 RGD
enables protein binding IPI
IPI: Inferred from physical interaction
18567805 RGD
Biological Process GO Annotation Evidence Reference Source
involved in canonical Wnt signaling pathway IMP
IMP: Inferred from mutant phenotype
18567805 RGD
involved in positive regulation of JNK cascade IMP
IMP: Inferred from mutant phenotype
18567805 RGD
involved in positive regulation of cell population proliferation IMP
IMP: Inferred from mutant phenotype
18567805 RGD
involved in response to estradiol IEP
IEP: Inferred from expression pattern
16551644 RGD
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

protein Wnt-7a

wingless-related MMTV integration site 7A

wingless-type MMTV integration site 7A

wingless-type MMTV integration site family, member 7A

Orthologs Information

Species Symbol Source ID
Homo sapiens Wnt7a NCBI NCBI:7476