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KCTD17

potassium channel tetramerization domain containing 17

HCNC Approved Symbol
KCTD17 (HGNC:25705)
Genomic Coordinates
22:37,051,742 - 37,063,390 (22q12.3)
Synonyms
FLJ12242
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 KCTD17 gene.

Frequently observed phenotypes

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

No Results
KCTD17 - Gene browser | 3billion