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SLC22A4

solute carrier family 22 member 4

HCNC Approved Symbol
SLC22A4 (HGNC:10968)
Genomic Coordinates
5:132,294,394 - 132,344,190 (5q31.1)
Synonyms
OCTN1, MGC34546, DFNB60
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SLC22A4 gene.

Frequently observed phenotypes

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

No Results
SLC22A4 - Gene browser | 3billion