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KCTD1

potassium channel tetramerization domain containing 1

HCNC Approved Symbol
KCTD1 (HGNC:18249)
Genomic Coordinates
18:26,454,910 - 26,657,473 (18q11.2)
Synonyms
C18orf5
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 KCTD1 gene.

Frequently observed phenotypes

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

Multicystic dysplastic kidney
 1 (100.0%)
KCTD1 - Gene browser | 3billion