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MYRF

myelin regulatory factor

HCNC Approved Symbol
MYRF (HGNC:1181)
Genomic Coordinates
11:61,752,636 - 61,788,518 (11q12.2)
Synonyms
Ndt80, pqn-47, MRF, C11orf9
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

4Patients

In total, 4 patients were diagnosed with a variant in the MYRF gene.

Frequently observed phenotypes

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

Hypospadias
 2 (50.0%)
Ambiguous genitalia
 1 (25.0%)
Bilateral cryptorchidism
 1 (25.0%)
Micropenis
 1 (25.0%)
Penoscrotal hypospadias
 1 (25.0%)
MYRF - Gene browser | 3billion