Overview

Variant ID 2922
Entrez Gene ID 129684
Gene CNTNAP5 (GeneCards)
Location hg19 2:127387461-127387461
hg38 2:126629884-126629884
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000002.11:g.127387461 G>A (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 243199373

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.2368
CADD Raw score (version 1.3) 0.034671 (Deleterious)
FATHMM raw prediction score 0.0933 (Tolerated)
Deleterious probability by DeFine 0.0834 (Neutral)
Entrez Gene ID 129684 (NCBI Gene)
Official Gene Symbol CNTNAP5 (GeneCards)
Number of variants in CNTNAP5 in this database 33 (view all the variants)
Full name contactin associated protein like 5
Band 2q14.3
Other IDs Vega: OTTHUMG00000153356
OMIM: 610519
HGNC: HGNC:18748
Ensembl: ENSG00000155052
Other names caspr5
Summary This gene product belongs to the neurexin family, members of which function in the vertebrate nervous system as cell adhesion molecules and receptors. This protein, like other neurexin proteins, contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, and thrombospondin N-terminal-like domains. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217584.03 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;