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CLXN

calaxin

HCNC Approved Symbol
CLXN (HGNC:25678)
Genomic Coordinates
8:48,710,789 - 48,735,311 (8q11.21)
Synonyms
FLJ11767, ODAD5, EFCAB1
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 CLXN gene.

Frequently observed phenotypes

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

No Results
CLXN - Gene browser | 3billion