C1D (C1D nuclear receptor corepressor)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 10438 |
| Gene name | C1D nuclear receptor corepressor |
| Gene symbol | C1D |
| Synonyms (NCBI Gene) |
LRP1Rrp47SUN-CoRSUNCORhC1D
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| Chromosome | 2 |
| Chromosome location | 2p14 |
| Summary | The protein encoded by this gene is a DNA binding and apoptosis-inducing protein and is localized in the nucleus. It is also a Rac3-interacting protein which acts as a corepressor for the thyroid hormone receptor. This protein is thought to regulate TRAX/ |
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miRNA
miRNA information provided by mirtarbase database.
215
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q13901 | ||||||||||
| Protein name | Nuclear nucleic acid-binding protein C1D (hC1D) | ||||||||||
| Protein function | Plays a role in the recruitment of the RNA exosome complex to pre-rRNA to mediate the 3'-5' end processing of the 5.8S rRNA; this function may include MPHOSPH6. Can activate PRKDC not only in the presence of linear DNA but also in the presence o | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Ubiquitous. Expressed at very high levels in the hippocampus, medulla oblongata, mammary gland, thyroid and salivary gland. Expressed at high levels in the fetal; lung, liver and kidney. Expressed at low levels in skeletal muscle, appe | ||||||||||
| Sequence |
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| Sequence length | 141 | ||||||||||
| Interactions | View interactions | ||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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