Gene

wnt7ab

ID
ZDB-GENE-100922-44
Name
wingless-type MMTV integration site family, member 7Ab
Symbol
wnt7ab Nomenclature History
Previous Names
None
Type
protein_coding_gene
Location
Unmapped
Description
Predicted to enable signaling receptor binding activity. Predicted to act upstream of or within Wnt signaling pathway. Predicted to be located in extracellular region. Is expressed in hindbrain and hindbrain neural keel.
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
2 figures from Beretta et al., 2011
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With wnt7ab Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Fuhrmann syndrome Alliance Fuhrmann syndrome 228930
Schinzel type phocomelia Alliance Ulna and fibula, absence of, with severe limb deficiency 276820
Associated With wnt7ab Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Conserved_site IPR018161 Wnt protein, conserved site
Family IPR005817 Wnt
Family IPR013300 Wnt-7 protein
Homologous_superfamily IPR043158 Wnt, C-terminal domain
Domain Details Per Protein
Protein Length Wnt Wnt-7 protein Wnt, C-terminal domain Wnt protein, conserved site
UniProtKB:E7FBM9
UniProtKB:A0A2R8QA19 283
Transcripts
Genome Browsers
No data available
No data available
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations