SLC22A18 - Gene browser

SLC22A18

solute carrier family 22 member 18

HCNC Approved Symbol: SLC22A18 (HGNC:10964)
Genomic Coordinates: 11:2,899,691 - 2,925,246 (11p15.4)
Synonyms: BWR1A, TSSC5, ITM, ORCTL2, BWSCR1A, IMPT1, SLC22A1L
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

0Patient

There are no patients diagnosed with a variant in the SLC22A18 gene.

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

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