Variant ID | 22966 |
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Entrez Gene ID | 1501 |
Gene | CTNND2 (GeneCards) |
Location | hg19 5:11583293-11583293
hg38 5:11583181-11583181 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000005.9:g.11583293 T>C (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 | 180915260 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.1326 |
CADD Raw score (version 1.3) | 0.788639 (Deleterious) |
FATHMM raw prediction score | 0.09442 (Tolerated) |
Deleterious probability by DeFine | 0.3871 (Neutral) |
Entrez Gene ID | 1501 (NCBI Gene) |
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Official Gene Symbol | CTNND2 (GeneCards) |
Number of variants in CTNND2 in this database | 24 (view all the variants) |
Full name | catenin delta 2 |
Band | 5p15.2 |
Other IDs | Vega: OTTHUMG00000090511 OMIM: 604275 HGNC: HGNC:2516 Ensembl: ENSG00000169862 |
Other names | GT24, NPRAP |
Summary | This gene encodes an adhesive junction associated protein of the armadillo/beta-catenin superfamily and is implicated in brain and eye development and cancer formation. The protein encoded by this gene promotes the disruption of E-cadherin based adherens junction to favor cell spreading upon stimulation by hepatocyte growth factor. This gene is overexpressed in prostate adenocarcinomas and is associated with decreased expression of tumor suppressor E-cadherin in this tissue. This gene resides in a region of the short arm of chromosome 5 that is deleted in Cri du Chat syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2013] |
Individual ID | 29217587.01 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217587 |
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Title | Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis. |
Journal | Science |
Publication date | 2018.02 |
Disease | Asymptomatic |
Number of cases | cases of unknown sex: 3; |