L3MBTL4 L3MBTL histone methyl-lysine binding protein 4
Gene ID: 91133, updated on 2-Nov-2024Gene type: protein coding
Also known as: HsT1031
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- Go to complete Gene record for L3MBTL4
- Go to Variation Viewer for L3MBTL4 variants
Summary
Predicted to enable chromatin binding activity and histone binding activity. Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Nov 2024]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
A genome-wide association study of sleep habits and insomnia. GeneReviews: Not available | |
Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. GeneReviews: Not available |
Genomic context
- Location:
- 18p11.31
- Sequence:
- Chromosome: 18; NC_000018.10 (5954717..6415259, complement)
- Total number of exons:
- 32
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for L3MBTL4 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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