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MSH5

mutS homolog 5

HCNC Approved Symbol
MSH5 (HGNC:7328)
Genomic Coordinates
6:31,740,005 - 31,762,676 (6p21.33)
Synonyms
G7
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the MSH5 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results
MSH5 - Gene browser | 3billion