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CEP57L1

centrosomal protein 57 like 1

HCNC Approved Symbol
CEP57L1 (HGNC:21561)
Genomic Coordinates
: - (6q21)
Synonyms
bA487F23.2, MGC21731, C6orf182
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there are 2 patients* with variant(s) predicted to be damaging.*2 of the patients have been diagnosed with a variant in another gene.

CEP57L1 - Gene browser | 3billion