Statements (25)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:protein
gptkb:gene |
| gptkbp:alternativeName |
BRWD2
PPP1R112 |
| gptkbp:associatedWith |
gptkb:Kallmann_syndrome
congenital hypogonadotropic hypogonadism |
| gptkbp:biologicalProcess |
protein binding
|
| gptkbp:domain |
WD repeat domain
|
| gptkbp:encodes |
WD repeat-containing protein 11
|
| gptkbp:Entrez_Gene_ID |
55741
|
| gptkbp:expressedIn |
gptkb:pituitary_gland
gptkb:testis brain |
| gptkbp:foundIn |
gptkb:Homo_sapiens
|
| gptkbp:hasProteinID |
Q9BZH6
|
| https://www.w3.org/2000/01/rdf-schema#label |
WDR11
|
| gptkbp:involvedIn |
neural development
olfactory bulb development |
| gptkbp:locatedOnChromosome |
gptkb:chromosome_10
|
| gptkbp:mutationAssociatedWith |
Kallmann syndrome 8
|
| gptkbp:numberOfExons |
30
|
| gptkbp:OMIM |
614858
|
| gptkbp:UniProtID |
Q9BZH6
|
| gptkbp:bfsParent |
gptkb:chromosome_10
|
| gptkbp:bfsLayer |
6
|