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CC2D1A

coiled-coil and C2 domain containing 1A

HCNC Approved Symbol
CC2D1A (HGNC:30237)
Genomic Coordinates
19:13,906,201 - 13,930,879 (19p13.12)
Synonyms
FLJ20241, MRT3, Freud-1, Lgd2, TAPE, Aki-1
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Intellectual developmental disorder, autosomal recessive 3
608443AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the CC2D1A gene.

Frequently observed phenotypes

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

No Results