21:7,000,001 - 10,900,000 (21p11.2 not on reference assembly)
Synonyms
CT2.3
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.
Diagnosed Cases
There are no diagnosed cases at this time. There are no patients* with variants predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.
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