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SLC6A19

solute carrier family 6 member 19

HCNC Approved Symbol
SLC6A19 (HGNC:27960)
Genomic Coordinates
5:1,201,595 - 1,225,111 (5p15.33)
Synonyms
B0AT1
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the SLC6A19 gene.

Frequently observed phenotypes

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

Celiac disease
 1 (100.0%)
SLC6A19 - Gene browser | 3billion