Sequence Detail

ID/Version

Q9QZ04 F8WIA8 (UniProt | EBI)

Last sequence update: 2015-09-16
Last annotation update: 2024-01-24

Sequence description from provider

RecName: Full=MAGE-like protein 2;AltName: Full=Protein nS7;

Provider

SWISS-PROT

Sequence

Polypeptide 1284 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Magel2	MAGE family member L2	28	128	3	11

Sequence references in MGI

J:58785 Boccaccio I, et al., The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region. Hum Mol Genet. 1999 Dec;8(13):2497-505
J:63703 Lee S, et al., Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype. Hum Mol Genet. 2000 Jul 22;9(12):1813-9
J:129971 Bischof JM, et al., Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome. Hum Mol Genet. 2007 Nov 15;16(22):2713-9
J:215866 Devos J, et al., Magel2, a Prader-Willi syndrome candidate gene, modulates the activities of circadian rhythm proteins in cultured cells. J Circadian Rhythms. 2011;9(1):12