ESF1 ESF1 nucleolar pre-rRNA processing protein homolog
Gene ID: 51575, updated on 3-Nov-2024Gene type: protein coding
Also known as: ABTAP; C20orf6; HDCMC28P; bA526K24.1
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- Go to complete Gene record for ESF1
- Go to Variation Viewer for ESF1 variants
Summary
Enables RNA binding activity. Predicted to be involved in rRNA processing. Located in extracellular space. [provided by Alliance of Genome Resources, Nov 2024]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. GeneReviews: Not available |
Genomic context
- Location:
- 20p12.1
- Sequence:
- Chromosome: 20; NC_000020.11 (13714325..13784919, complement)
- Total number of exons:
- 14
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for ESF1 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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