HELB DNA helicase B
Gene ID: 92797, updated on 17-Sep-2024Gene type: protein coding
Also known as: DHB; hDHB
- See all available tests in GTR for this gene
- Go to complete Gene record for HELB
- Go to Variation Viewer for HELB variants
Summary
This gene encodes a DNA-dependent ATPase which catalyzes the unwinding of DNA necessary for DNA replication, repair, recombination, and transcription. This gene is thought to function specifically during the S phase entry of the cell cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Genomic context
- Location:
- 12q14.3; 12q
- Sequence:
- Chromosome: 12; NC_000012.12 (66302493..66343643)
- Total number of exons:
- 14
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for HELB 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
- Variation ViewerRelated Variants
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