Overview

Variant ID 6010
Entrez Gene ID 118429
Gene ANTXR2 (GeneCards)
Location hg19 4:81070206-81070206
hg38 4:80149052-80149052
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000004.11:g.81070206 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 191154276

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.1216
CADD Raw score (version 1.3) -0.084664 (Deleterious)
FATHMM raw prediction score 0.0938 (Tolerated)
Deleterious probability by DeFine 0.1957 (Neutral)
Entrez Gene ID 118429 (NCBI Gene)
Official Gene Symbol ANTXR2 (GeneCards)
Number of variants in ANTXR2 in this database 5 (view all the variants)
Full name ANTXR cell adhesion molecule 2
Band 4q21.21
Other IDs Vega: OTTHUMG00000151982
OMIM: 608041
HGNC: HGNC:21732
Ensembl: ENSG00000163297
Other names HFS, ISH, JHF, CMG2, CMG-2
Summary This gene encodes a receptor for anthrax toxin. The protein binds to collagen IV and laminin, suggesting that it may be involved in extracellular matrix adhesion. Mutations in this gene cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

Individual #1

Individual ID 29217584.01 (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;