Variant ID | 10415 |
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Entrez Gene ID | 23242 |
Gene | COBL (GeneCards) |
Location | hg19 7:51892914-51892914
hg38 7:51825218-51825218 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000007.13:g.51892914 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 | 159138663 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.4607 |
CADD Raw score (version 1.3) | -0.301271 (Deleterious) |
FATHMM raw prediction score | 0.07237 (Tolerated) |
Deleterious probability by DeFine | 0.3085 (Neutral) |
Entrez Gene ID | 23242 (NCBI Gene) |
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Official Gene Symbol | COBL (GeneCards) |
Number of variants in COBL in this database | 33 (view all the variants) |
Full name | cordon-bleu WH2 repeat protein |
Band | 7p12.1 |
Other IDs | Vega: OTTHUMG00000155999 OMIM: 610317 HGNC: HGNC:22199 Ensembl: ENSG00000106078 |
Other names | None |
Summary | This gene encodes a protein that contains WH2 domains (WASP, Wiskott-Aldrich syndrome protein, homology domain-2) that interact with actin. The encoded actin regulator protein is required for growth and assembly of brush border microvilli that play a role in maintaining intestinal homeostasis. A similar protein in mouse functions in midbrain neural tube closure. A pseudogene of this gene is located on chromosome X. [provided by RefSeq, Oct 2016] |
Individual ID | 29217584.03 (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; |