SLTM SAFB like transcription modulator
Gene ID: 79811, updated on 6-Oct-2024Gene type: protein coding
Also known as: Met
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- Go to complete Gene record for SLTM
- Go to Variation Viewer for SLTM variants
Summary
Enables RNA binding activity. Predicted to be involved in regulation of mRNA processing and regulation of transcription by RNA polymerase II. Located in nuclear body. [provided by Alliance of Genome Resources, Apr 2022]
Associated conditions
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Description | Tests |
---|---|
Variants in several genomic regions associated with asperger disorder. GeneReviews: Not available |
Genomic context
- Location:
- 15q22.1
- Sequence:
- Chromosome: 15; NC_000015.10 (58879050..58933679, complement)
- Total number of exons:
- 23
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for SLTM variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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