SLC39A8 - Gene browser | 3billion

SLC39A8

SLC39A8

solute carrier family 39 member 8

HCNC Approved Symbol: SLC39A8 (HGNC:20862)
Genomic Coordinates: 4:102,251,041 - 102,345,482 (4q24)
Synonyms: BIGM103, ZIP8, ZIP-8
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 SLC39A8 gene.

Frequently observed phenotypes(Top 5 only)

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

01
Patient count

Abnormality of the skeletal system: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Dwarfism, disproportionate: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Lethal skeletal dysplasia: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

SLC39A8 - Gene browser | 3billion