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SPRTN

SprT-like N-terminal domain

HCNC Approved Symbol
SPRTN (HGNC:25356)
Genomic Coordinates
1:231,338,293 - 231,355,023 (1q42.2)
Synonyms
DKFZP547N043, Spartan, DVC1, C1orf124
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

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

Frequently observed phenotypes

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

No Results
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