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SLC7A6OS

solute carrier family 7 member 6 opposite strand

HCNC Approved Symbol
SLC7A6OS (HGNC:25807)
Genomic Coordinates
16:68,298,034 - 68,310,946 (16q22.1)
Synonyms
FLJ13291, Iwr1
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Epilepsy, progressive myoclonic, 12
619191AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SLC7A6OS gene.

Frequently observed phenotypes

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

No Results