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SNF8

SNF8 subunit of ESCRT-II

HCNC Approved Symbol
SNF8 (HGNC:17028)
Genomic Coordinates
17:48,929,316 - 48,944,842 (17q21.32)
Synonyms
EAP30, VPS22, Dot3
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SNF8 gene.

Frequently observed phenotypes

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

No Results
SNF8 - Gene browser | 3billion