Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:protein
gptkb:gene |
| gptkbp:associatedWith |
gptkb:Al-Awadi/Raas-Rothschild/Schinzel_phocomelia_syndrome
gptkb:Fuhrmann_syndrome |
| gptkbp:encodedBy |
gptkb:WNT7A_gene
|
| gptkbp:Entrez_Gene_ID |
7477
|
| gptkbp:expressedIn |
brain
developing limb |
| gptkbp:function |
regulation of cell fate and patterning
|
| gptkbp:HGNC_ID |
12784
|
| https://www.w3.org/2000/01/rdf-schema#label |
Wnt7A
|
| gptkbp:involvedIn |
embryonic development
cell signaling limb development central nervous system development |
| gptkbp:locatedOnChromosome |
gptkb:chromosome_3
|
| gptkbp:memberOf |
gptkb:Wnt_family
|
| gptkbp:mutationAssociatedWith |
limb malformations
|
| gptkbp:orthologInMouse |
gptkb:Wnt7a
|
| gptkbp:proteinFamily |
gptkb:Wnt_proteins
|
| gptkbp:UniProtID |
O00755
|
| gptkbp:bfsParent |
gptkb:Wnt_family
|
| gptkbp:bfsLayer |
8
|