The CNTNAP2 gene homepage

General information
Gene symbol CNTNAP2
Gene name contactin associated protein-like 2
Chromosome 7
Chromosomal band q35
Imprinted Unknown
Genomic reference NG_007092.2
Transcript reference NM_014141.5
Exon/intron information NM_014141.5 exon/intron table
Associated with diseases AUTS15, ID, PTHSL1
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 181
Unique public DNA variants reported 135
Individuals with public variants 97
Hidden variants 27
Date created September 13, 2012
Date last updated February 26, 2024
Version CNTNAP2:240226

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_014141.5.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 13830
Entrez Gene 26047
PubMed articles CNTNAP2
OMIM - Gene 604569
OMIM - Diseases AUTS15 (autism, susceptibility to, type 15 (AUTS-15))
PTHSL1 (Pitt-Hopkins like syndrome 1)
HGMD CNTNAP2
GeneCards CNTNAP2
GeneTests CNTNAP2
Orphanet CNTNAP2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001231 7 contactin associated protein-like 2 NM_014141.5 NP_054860.1 181


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