Variant ID | 27276 |
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Entrez Gene ID | 26011 |
Gene | TENM4 (GeneCards) |
Location | hg19 11:79491338-79491338
hg38 11:79780294-79780294 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000011.9:g.79491338 C>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 | 135006516 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 0.4768 |
CADD Raw score (version 1.3) | 1.568923 (Deleterious) |
FATHMM raw prediction score | 0.2126 (Tolerated) |
Deleterious probability by DeFine | 0.6315 (Deleterious) |
Entrez Gene ID | 26011 (NCBI Gene) |
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Official Gene Symbol | TENM4 (GeneCards) |
Number of variants in TENM4 in this database | 23 (view all the variants) |
Full name | teneurin transmembrane protein 4 |
Band | 11q14.1 |
Other IDs | Vega: OTTHUMG00000166770 OMIM: 610084 HGNC: HGNC:29945 Ensembl: ENSG00000149256 |
Other names | Doc4, ETM5, ODZ4, TNM4, ten-4, Ten-M4 |
Summary | The protein encoded by this gene plays a role in establishing proper neuronal connectivity during development. Defects in this gene have been associated with hereditary essential tremor-5. [provided by RefSeq, Oct 2016] |
Individual ID | 29217587.02 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |