CITED2

This page contains an overview of the genetic variation in the CITED2 gene, including its role in inherited cardiac disease. For more details, click on the links below, or for a specific variant, enter the HGVS variant here:

CITED2 gene and transcript details

Gene Name
Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2

Gene Links
Ensembl: ENSG00000164442 - Locus Reference Genomic:

Genomic Location
Chromosome 6 : 139,694,269 - 139,695,081 (reverse strand)
View in: Ensembl - UCSC Genome Browser


Canonical Seqs Transcript (810 bases)Protein (270 aa)
ENST00000367651 ENSP00000356623
NM_006079.3
Q99967

Summary of CITED2 in Cardiomyopathies


CITED2 variants in ExAC

Details of the protein-altering CITED2 variants (missense, loss of function truncating, inframe indels and splice site regions) found in the ExAC database are shown below. To view lists of specific variants with links to detailed population frequency data, click on the variant numbers - for all or a particular variant class.

Total VariantsCombined frequency of rare variants
All Variants1350.00181
Truncating0nan
Missense1180.00165
Inframe130.00011
Splice Site40.00005

Rare variants are defined as having a mean allelic frequency of less than 0.0001.