Wingless-type MMTV integration site family, member 7A
GPTKB entity
Statements (22)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:protein
|
| gptkbp:alternativeName |
gptkb:Protein_Wnt-7a
Wnt-7a |
| gptkbp:associatedWith |
limb development
female reproductive tract development |
| gptkbp:encodedBy |
gptkb:WNT7A_gene
|
| gptkbp:Entrez_Gene_ID |
7476
|
| gptkbp:expressedIn |
embryonic tissues
|
| gptkbp:family |
gptkb:Wnt_family
|
| gptkbp:function |
signaling protein
|
| gptkbp:gene |
gptkb:WNT7A
|
| gptkbp:HGNC_ID |
12784
|
| gptkbp:involves |
gptkb:Wnt_signaling_pathway
|
| gptkbp:locatedOnChromosome |
gptkb:chromosome_3p25
|
| gptkbp:mutationAssociatedWith |
gptkb:Al-Awadi/Raas-Rothschild/Schinzel_phocomelia_syndrome
gptkb:Fuhrmann_syndrome |
| gptkbp:OMIM |
613005
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:UniProtID |
O00755
|
| gptkbp:bfsParent |
gptkb:WNT7A_HUMAN
|
| gptkbp:bfsLayer |
8
|
| https://www.w3.org/2000/01/rdf-schema#label |
Wingless-type MMTV integration site family, member 7A
|