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MIAT

myocardial infarction associated transcript

HCNC Approved Symbol
MIAT (HGNC:33425)
Genomic Coordinates
22:26,646,429 - 26,676,478 (22q12.1)
Synonyms
FLJ25967, Rncr2, gomafu, NCRNA00066, LINC00066, lncRNA-MIAT, C22orf35
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
{Myocardial infarction, susceptibility to}
608446-

Diagnosed Cases

0Patient

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

Frequently observed phenotypes

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

No Results