Variant ID | 8197 |
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Entrez Gene ID | 375449 |
Gene | MAST4 (GeneCards) |
Location | hg19 5:66199748-66199748
hg38 5:66903920-66903920 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000005.9:g.66199748 C>G (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 | -0.3967 |
CADD Raw score (version 1.3) | -0.251303 (Deleterious) |
FATHMM raw prediction score | 0.11796 (Tolerated) |
Deleterious probability by DeFine | 0.4559 (Neutral) |
Entrez Gene ID | 375449 (NCBI Gene) |
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Official Gene Symbol | MAST4 (GeneCards) |
Number of variants in MAST4 in this database | 7 (view all the variants) |
Full name | microtubule associated serine/threonine kinase family member 4 |
Band | 5q12.3 |
Other IDs | Vega: OTTHUMG00000152471 OMIM: 618002 HGNC: HGNC:19037 Ensembl: ENSG00000069020 |
Other names | None |
Summary | This gene encodes a member of the microtubule-associated serine/threonine protein kinases. The proteins in this family contain a domain that gives the kinase the ability to determine its own scaffold to control the effects of their kinase activities. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014] |
Individual ID | 29217584.12 (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; |