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FXR1

FMR1 autosomal homolog 1

HCNC Approved Symbol
FXR1 (HGNC:4023)
Genomic Coordinates
3:180,912,670 - 180,982,753 (3q26.33)
Synonyms
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Congenital myopathy 9A with respiratory insufficiency and bone fractures
618822AR
Congenital myopathy 9B, proximal, with minicore lesions
618823AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the FXR1 gene.

Frequently observed phenotypes

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

No Results