Variant ID | 28794 |
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Entrez Gene ID | 10178 |
Gene | TENM1 (GeneCards) |
Location | hg19 X:124209141-124209141
hg38 X:125075292-125075292 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000023.10:g.124209141 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 | 155270560 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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CADD Raw score (version 1.3) | 0.164617 (Deleterious) |
FATHMM raw prediction score | 0.14142 (Tolerated) |
Deleterious probability by DeFine | 0.6429 (Deleterious) |
Entrez Gene ID | 10178 (NCBI Gene) |
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Official Gene Symbol | TENM1 (GeneCards) |
Number of variants in TENM1 in this database | 5 (view all the variants) |
Full name | teneurin transmembrane protein 1 |
Band | Xq25 |
Other IDs | Vega: OTTHUMG00000022721 OMIM: 300588 HGNC: HGNC:8117 Ensembl: ENSG00000009694 |
Other names | TNM, ODZ1, ODZ3, TNM1, TEN-M1 |
Summary | The protein encoded by this gene belongs to the tenascin family and teneurin subfamily. It is expressed in the neurons and may function as a cellular signal transducer. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009] |
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 |