Variant ID | 913 |
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Entrez Gene ID | 89796 |
Gene | NAV1 (GeneCards) |
Location | hg19 1:201777908-201777908
hg38 1:201808780-201808780 |
Disease | Human Skin Fibroblasts (view all the variants in this disease) |
Method | HiSeq 2500 |
Mutation(HGVS format) | NC_000001.10:g.201777908 G>A (Genome Assembly: hg19) |
Exon or Intron | Exon |
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Position in protein | 1372 |
Amino acid changes in protein | G > G |
Position in cDNA | NA |
Changes in cDNA | NA > NA |
mRNA accession | NA |
mRNA length | NA |
Reference length | 249250621 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 1.6534 |
CADD Raw score (version 1.3) | 1.112044 (Deleterious) |
FATHMM raw prediction score | 0.97842 (Tolerated) |
Deleterious probability by DeFine | 0.9017 (Deleterious) |
Entrez Gene ID | 89796 (NCBI Gene) |
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Official Gene Symbol | NAV1 (GeneCards) |
Number of variants in NAV1 in this database | 3 (view all the variants) |
Full name | neuron navigator 1 |
Band | 1q32.1 |
Other IDs | Vega: OTTHUMG00000035766 OMIM: 611628 HGNC: HGNC:15989 Ensembl: ENSG00000134369 |
Other names | POMFIL3, UNC53H1, STEERIN1 |
Summary | This gene belongs to the neuron navigator family and is expressed predominantly in the nervous system. The encoded protein contains coiled-coil domains and a conserved AAA domain characteristic for ATPases associated with a variety of cellular activities. This gene is similar to unc-53, a Caenorhabditis elegans gene involved in axon guidance. The exact function of this gene is not known, but it is thought to play a role in in neuronal development and regeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009] |
Individual ID | 27788131.02 (view all the variants in this individual) |
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Pubmed ID | 27788131 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Human Skin Fibroblasts (view all the variants in this disease) |
OMIM ID | 120353 |
Pubmed ID | 27788131 |
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Title | The Impact of Environmental and Endogenous Damage on Somatic Mutation Load in Human Skin Fibroblasts. |
Journal | PLoS Genetics |
Publication date | 2016.10 |
Disease | Human Skin Fibroblasts |
Population | Caucasian |
Number of cases | Male cases: 2; |