MSH6

URI: https://gptkb.org/entity/MSH6
GPTKB entity
Statements (23)
Predicate Object
gptkbp:instanceOf gptkb:gene
gptkbp:alternativeName gptkb:GTBP
gptkb:hMSH6
p160
gptkbp:associatedWith gptkb:Lynch_syndrome
gptkb:hereditary_nonpolyposis_colorectal_cancer
gptkbp:encodes gptkb:DNA_mismatch_repair_protein_Msh6
gptkbp:Entrez_Gene_ID 2956
gptkbp:expressedIn gptkb:human
gptkbp:fullName gptkb:MutS_homolog_6
gptkbp:function DNA mismatch repair
gptkbp:HGNC_ID 7329
https://www.w3.org/2000/01/rdf-schema#label MSH6
gptkbp:interactsWith gptkb:MSH2
gptkbp:locatedOnChromosome chromosome 2
2p16.3
gptkbp:mutationAssociatedWith increased cancer risk
gptkbp:OMIM 600678
gptkbp:orthologInMouse gptkb:Msh6
gptkbp:proteinFamily gptkb:MutS_family
gptkbp:UniProtID P52701
gptkbp:bfsParent gptkb:Lynch_syndrome
gptkbp:bfsLayer 5