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SLC16A12

solute carrier family 16 member 12

HCNC Approved Symbol
SLC16A12 (HGNC:23094)
Genomic Coordinates
10:89,430,299 - 89,556,704 (10q23.31)
Synonyms
MCT12, CRT2
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 SLC16A12 gene.

Frequently observed phenotypes

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

No Results
SLC16A12 - Gene browser | 3billion