Variant ID | 5377 |
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Entrez Gene ID | 4134 |
Gene | MAP4 (GeneCards) |
Location | hg19 3:47985562-47985562
hg38 3:47944072-47944072 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000003.11:g.47985562 G>A (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 | 198022430 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.2185 |
CADD Raw score (version 1.3) | 0.306323 (Deleterious) |
FATHMM raw prediction score | 0.07767 (Tolerated) |
Deleterious probability by DeFine | 0.1345 (Neutral) |
Entrez Gene ID | 4134 (NCBI Gene) |
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Official Gene Symbol | MAP4 (GeneCards) |
Number of variants in MAP4 in this database | 5 (view all the variants) |
Full name | microtubule associated protein 4 |
Band | 3p21.31 |
Other IDs | Vega: OTTHUMG00000156828 OMIM: 157132 HGNC: HGNC:6862 Ensembl: ENSG00000047849 |
Other names | None |
Summary | The protein encoded by this gene is a major non-neuronal microtubule-associated protein. This protein contains a domain similar to the microtubule-binding domains of neuronal microtubule-associated protein (MAP2) and microtubule-associated protein tau (MAPT/TAU). This protein promotes microtubule assembly, and has been shown to counteract destabilization of interphase microtubule catastrophe promotion. Cyclin B was found to interact with this protein, which targets cell division cycle 2 (CDC2) kinase to microtubules. The phosphorylation of this protein affects microtubule properties and cell cycle progression. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008] |
Individual ID | 29217584.13 (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; |