Variant ID | 15084 |
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Entrez Gene ID | 24145 |
Gene | PANX1 (GeneCards) |
Location | hg19 11:93922147-93922147
hg38 11:94188981-94188981 |
Disease | Asymptomatic |
Method | HiSeq 2000 |
Mutation(HGVS format) | NC_000011.9:g.93922147 G>A (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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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 | 135006516 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 0.9679 |
CADD Raw score (version 1.3) | 1.275484 (Deleterious) |
FATHMM raw prediction score | 0.93438 (Tolerated) |
Deleterious probability by DeFine | 0.7406 (Deleterious) |
Entrez Gene ID | 24145 (NCBI Gene) |
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Official Gene Symbol | PANX1 (GeneCards) |
Number of variants in PANX1 in this database | 6 (view all the variants) |
Full name | pannexin 1 |
Band | 11q21 |
Other IDs | Vega: OTTHUMG00000167757 OMIM: 608420 HGNC: HGNC:8599 Ensembl: ENSG00000110218 |
Other names | PX1, MRS1, UNQ2529 |
Summary | The protein encoded by this gene belongs to the innexin family. Innexin family members are the structural components of gap junctions. This protein and pannexin 2 are abundantly expressed in central nerve system (CNS) and are coexpressed in various neuronal populations. Studies in Xenopus oocytes suggest that this protein alone and in combination with pannexin 2 may form cell type-specific gap junctions with distinct properties. [provided by RefSeq, Jul 2008] |
Individual ID | 29217584.04 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217584 |
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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; |