Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:alsoKnownAs |
gptkb:MSH2
|
| gptkbp:associatedWith |
gptkb:Lynch_syndrome
gptkb:hereditary_nonpolyposis_colorectal_cancer |
| gptkbp:discoveredIn |
1993
|
| gptkbp:encodes |
gptkb:DNA_mismatch_repair_protein_Msh2
|
| gptkbp:Entrez_Gene_ID |
4436
|
| gptkbp:expressedIn |
various tissues
|
| gptkbp:foundIn |
gptkb:Homo_sapiens
|
| gptkbp:function |
DNA mismatch repair
|
| gptkbp:HGNC_ID |
7325
|
| https://www.w3.org/2000/01/rdf-schema#label |
mutS homolog 2
|
| gptkbp:interactsWith |
gptkb:MSH6
gptkb:MSH3 |
| gptkbp:locatedOnChromosome |
chromosome 2
2p21 |
| gptkbp:mutationAssociatedWith |
increased cancer risk
microsatellite instability |
| gptkbp:OMIM |
609309
|
| gptkbp:orthologIn |
bacterial mutS gene
|
| gptkbp:UniProtID |
P43246
|
| gptkbp:bfsParent |
gptkb:MSH2
|
| gptkbp:bfsLayer |
6
|