| Variant ID | 10395 |
|---|---|
| Entrez Gene ID | 1365 |
| Gene | CLDN3 (GeneCards) |
| Location | hg19 7:73213743-73213743
hg38 7:73799413-73799413 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000007.13:g.73213743 G>A (Genome Assembly: GRCh37) |
| 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 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.1187 |
| CADD Raw score (version 1.3) | 0.512123 (Deleterious) |
| FATHMM raw prediction score | 0.19932 (Tolerated) |
| Deleterious probability by DeFine | 0.1205 (Neutral) |
| Entrez Gene ID | 1365 (NCBI Gene) |
|---|---|
| Official Gene Symbol | CLDN3 (GeneCards) |
| Number of variants in CLDN3 in this database | 1 (view all the variants) |
| Full name | claudin 3 |
| Band | 7q11.23 |
| Other IDs | Vega: OTTHUMG00000023424 OMIM: 602910 HGNC: HGNC:2045 Ensembl: ENSG00000165215 |
| Other names | RVP1, HRVP1, C7orf1, CPE-R2, CPETR2 |
| Summary | Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this intronless gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. It is also a low-affinity receptor for Clostridium perfringens enterotoxin, and shares aa sequence similarity with a putative apoptosis-related protein found in rat. [provided by RefSeq, Jul 2008] |
| Individual ID | 29217584.03 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |
| 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; |