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MYOT

myotilin

HCNC Approved Symbol
MYOT (HGNC:12399)
Genomic Coordinates
5:137,867,860 - 137,887,851 (5q31.2)
Synonyms
TTID, LGMD1A, LGMD1
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

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

Frequently observed phenotypes

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

No Results
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