Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:alias |
gptkb:MAGE-L2
gptkb:MAGE-like_2 |
| gptkbp:associatedWith |
gptkb:Prader-Willi_syndrome
gptkb:Schaaf-Yang_syndrome |
| gptkbp:Entrez_Gene_ID |
4118
ENSG00000137070 |
| gptkbp:expressedIn |
brain
|
| gptkbp:function |
neurodevelopment
regulation of circadian rhythm |
| gptkbp:HGNC_ID |
HGNC:6811
|
| https://www.w3.org/2000/01/rdf-schema#label |
MAGEL2
|
| gptkbp:imprint |
yes
|
| gptkbp:inheritance |
paternally expressed
|
| gptkbp:locatedOnChromosome |
gptkb:chromosome_15
|
| gptkbp:mutationAssociatedWith |
neurodevelopmental disorders
|
| gptkbp:OMIM |
605994
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:orthologIn |
gptkb:mouse_Magel2
|
| gptkbp:product |
gptkb:MAGE-like_protein_2
|
| gptkbp:proteinFamily |
gptkb:MAGE_family
|
| gptkbp:bfsParent |
gptkb:15q11-q13
|
| gptkbp:bfsLayer |
7
|