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MIRAGE
SIN3 transcription regulator family member A
Summary
- Gene Symbol
-
- SIN3A
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Acetylation
- Biological rhythms
- Coiled coil
- Disease variant
- Dwarfism
- Intellectual disability
- Isopeptide bond
- Nucleus
- Phosphoprotein
- Reference proteome
- Repeat
- Repressor
- Transcription regulation
- Ubl conjugation
- Proteins
| UniProt | Protein Name |
|---|---|
| Q96ST3 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| negative regulation of transcription by RNA polymerase II | ||
| negative regulation of transcription by RNA polymerase II | ||
| negative regulation of transcription by RNA polymerase II | ||
| in utero embryonic development | ||
| activation of innate immune response |
GO Hierarchy
- rhythmic process
biological process
metabolic process [inference]
cellular process [inference]
response to stimulus [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of metabolic process [inference]
regulation of biosynthetic process [inference]
negative regulation of metabolic process [inference]
regulation of cellular metabolic process [inference]
regulation of nitrogen compound metabolic process [inference]
regulation of macromolecule metabolic process [inference]
regulation of signaling [inference]
positive regulation of biological process [inference]
negative regulation of biological process [inference]
regulation of response to stimulus [inference]
regulation of developmental process [inference]
regulation of cellular process [inference]
regulation of cell communication [inference]
regulation of cellular metabolic process [inference]
positive regulation of cellular process [inference]
negative regulation of cellular process [inference]
regulation of cell cycle [inference]
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| DNA binding | ||
| chromatin binding | ||
| transcription corepressor activity | ||
| transcription corepressor activity | ||
| RNA binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- paired amphipathic helix protein
- Functional Category
-
- E: Amino acid transport and metabolism
- K: Transcription
- T: Signal transduction mechanisms
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060395 | chromosome 15q24 deletion syndrome |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 20466 | Xenbase:XB-GENE-480875 | MOUSE61594 | |
| 23309 | SGD:S000005364 | ||
| 25942 | Xenbase:XB-GENE-480875 | ||
| 36382 | Xenbase:XB-GENE-480875 | ||
| 363067 | RATNO42186 | ||
| 453759 | PANTR10850 | ||
| 518504 | BOVIN16623 | ||
| 563090 | DANRE27685 | ||
| 705719 | MACMU41485 | ||
| 854158 | Xenbase:XB-GENE-480875 |
