Variant ID | 24052 |
---|---|
Entrez Gene ID | 140733 |
Gene | MACROD2 (GeneCards) |
Location | hg19 20:14280914-14280914
hg38 20:14300268-14300268 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000020.10:g.14280914 T>C (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 | 63025520 |
MAF in gnomAD genome (version 2.0.1) | 0 |
---|---|
EIGEN score | -0.4814 |
CADD Raw score (version 1.3) | -0.413634 (Deleterious) |
FATHMM raw prediction score | 0.0794 (Tolerated) |
Deleterious probability by DeFine | 0.3088 (Neutral) |
Entrez Gene ID | 140733 (NCBI Gene) |
---|---|
Official Gene Symbol | MACROD2 (GeneCards) |
Number of variants in MACROD2 in this database | 41 (view all the variants) |
Full name | MACRO domain containing 2 |
Band | 20p12.1 |
Other IDs | Vega: OTTHUMG00000031919 OMIM: 611567 HGNC: HGNC:16126 Ensembl: ENSG00000172264 |
Other names | C2orf133, C20orf133 |
Summary | The protein encoded by this gene is a deacetylase involved in removing ADP-ribose from mono-ADP-ribosylated proteins. The encoded protein has been shown to translocate from the nucleus to the cytoplasm upon DNA damage. [provided by RefSeq, May 2017] |
Individual ID | 29217587.01 (view all the variants in this individual) |
---|---|
Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217587 |
---|---|
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; |