HGNC:6882

GPTKB entity

Statements (21)
Predicate Object
gptkbp:instanceOf gptkb:gene
gptkbp:alias LAMA-2
MDC1A
Merosin
gptkbp:approvedBy laminin subunit alpha 2
gptkbp:approvedSymbol gptkb:LAMA2
gptkbp:associatedWith congenital muscular dystrophy type 1A
merosin-deficient congenital muscular dystrophy
gptkbp:Entrez_Gene_ID ENSG00000042980
3908
https://www.w3.org/2000/01/rdf-schema#label HGNC:6882
gptkbp:locatedOnChromosome 6
gptkbp:locusType gene with protein product
6q22.33
gptkbp:OMIM 156225
gptkbp:organism gptkb:Homo_sapiens
gptkbp:proteinFamily laminins
gptkbp:RefSeq NM_000426
gptkbp:UniProtID Q13751
gptkbp:bfsParent gptkb:MAPKAPK2
gptkbp:bfsLayer 7