Overview

Variant ID 26397
Entrez Gene ID 4885
Gene NPTX2 (GeneCards)
Location hg19 7:98268485-98268485
hg38 7:98639173-98639173
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000007.13:g.98268485 G>T (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 159138663

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.00003231
EIGEN score -0.1938
CADD Raw score (version 1.3) -0.208647 (Deleterious)
FATHMM raw prediction score 0.10861 (Tolerated)
Deleterious probability by DeFine 0.3724 (Neutral)
Entrez Gene ID 4885 (NCBI Gene)
Official Gene Symbol NPTX2 (GeneCards)
Number of variants in NPTX2 in this database 6 (view all the variants)
Full name neuronal pentraxin 2
Band 7q22.1
Other IDs Vega: OTTHUMG00000154369
OMIM: 600750
HGNC: HGNC:7953
Ensembl: ENSG00000106236
Other names NP2, NARP, NP-II
Summary This gene encodes a member of the family of neuronal petraxins, synaptic proteins that are related to C-reactive protein. This protein is involved in excitatory synapse formation. It also plays a role in clustering of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)-type glutamate receptors at established synapses, resulting in non-apoptotic cell death of dopaminergic nerve cells. Up-regulation of this gene in Parkinson disease (PD) tissues suggests that the protein may be involved in the pathology of PD. [provided by RefSeq, Feb 2009]

Individual #1

Individual ID 29217587.02 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID