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SLC46A1

solute carrier family 46 member 1

HCNC Approved Symbol
SLC46A1 (HGNC:30521)
Genomic Coordinates
17:28,394,642 - 28,406,592 (17q11.2)
Synonyms
HCP1, MGC9564, PCFT, HsPCFT, hPCFT
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 SLC46A1 gene.

Frequently observed phenotypes

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

Failure to thrive
 1 (100.0%)
Fever
 1 (100.0%)
Frequent infections
 1 (100.0%)
Hepatomegaly
 1 (100.0%)
Hypotonia
 1 (100.0%)
SLC46A1 - Gene browser | 3billion