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SLC5A7

solute carrier family 5 member 7

HCNC Approved Symbol
SLC5A7 (HGNC:14025)
Genomic Coordinates
2:107,986,524 - 108,013,994 (2q12.3)
Synonyms
hCHT, CHT1, ChT
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SLC5A7 gene.

Frequently observed phenotypes

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

No Results
SLC5A7 - Gene browser | 3billion