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SLC39A7

solute carrier family 39 member 7

HCNC Approved Symbol
SLC39A7 (HGNC:4927)
Genomic Coordinates
6:33,200,867 - 33,204,437 (6p21.32)
Synonyms
H2-KE4, D6S2244E, KE4, RING5, ZIP7, HKE4
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

3Patients

In total, 3 patients were diagnosed with a variant in the SLC39A7 gene.

Frequently observed phenotypes

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

Atopic dermatitis
 3 (100.0%)
SLC39A7 - Gene browser | 3billion