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MFSD13A

major facilitator superfamily domain containing 13A

HCNC Approved Symbol
MFSD13A (HGNC:26196)
Genomic Coordinates
10:102,461,395 - 102,477,045 (10q24.32)
Synonyms
FLJ22529, bA18I14.8, C10orf77, TMEM180
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there are 6 patients* with variant(s) predicted to be damaging.*3 of the patients have been diagnosed with a variant in another gene.

MFSD13A - Gene browser | 3billion