Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:alias |
gptkb:WNT7A_HUMAN
|
| gptkbp:associatedWith |
gptkb:Al-Awadi/Raas-Rothschild/Schinzel_phocomelia_syndrome
gptkb:Fuhrmann_syndrome |
| gptkbp:encodes |
gptkb:Wnt-7a_protein
|
| gptkbp:Entrez_Gene_ID |
7477
|
| gptkbp:expressedIn |
developing limb
|
| gptkbp:function |
dorsal-ventral patterning
regulation of limb development |
| gptkbp:HGNC_ID |
12784
|
| https://www.w3.org/2000/01/rdf-schema#label |
WNT7A
|
| gptkbp:involvedIn |
gptkb:Wnt_signaling_pathway
|
| gptkbp:locatedOnChromosome |
gptkb:chromosome_3
3p25 |
| gptkbp:memberOf |
gptkb:WNT_gene_family
|
| gptkbp:mutationAssociatedWith |
limb malformations
|
| gptkbp:OMIM |
613005
|
| gptkbp:orthologInMouse |
gptkb:Wnt7a
|
| gptkbp:proteinFamily |
gptkb:Wnt_family
|
| gptkbp:symbol |
gptkb:WNT7A
|
| gptkbp:UniProtID |
O00755
|
| gptkbp:bfsParent |
gptkb:WNT
|
| gptkbp:bfsLayer |
6
|