TERF1 telomeric repeat binding factor 1
Gene ID: 7013, updated on 28-Oct-2024Gene type: protein coding
Also known as: TRF; PIN2; TRF1; TRBF1; t-TRF1; hTRF1-AS
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- Go to complete Gene record for TERF1
- Go to Variation Viewer for TERF1 variants
Summary
This gene encodes a telomere specific protein which is a component of the telomere nucleoprotein complex. This protein is present at telomeres throughout the cell cycle and functions as an inhibitor of telomerase, acting in cis to limit the elongation of individual chromosome ends. The protein structure contains a C-terminal Myb motif, a dimerization domain near its N-terminus and an acidic N-terminus. Multiple transcripts of this gene are alternatively spliced products. [provided by RefSeq, Aug 2022]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. GeneReviews: Not available |
Genomic context
- Location:
- 8q21.11
- Sequence:
- Chromosome: 8; NC_000008.11 (73008864..73048123)
- Total number of exons:
- 14
Variation
Resource | Links for this gene |
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ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for TERF1 variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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