C1D - C1D nuclear receptor corepressor Gene
Also Known as LRP1; hC1D; Rrp47; SUNCOR; SUN-CoR
Species: Homo sapiens
About C1D
This gene has 7 transcripts (splice variants) and 225 orthologues. Ubiquitous expression in bone marrow (RPKM 17.9), adrenal (RPKM 15.5) and 25 other tissues.
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/Translin complex formation. Alternate splicing results in multiple transcript variants that encode the same protein. Multiple pseudogenes of this gene are found on chromosome 10.[provided by RefSeq, Jun 2010]
C1D Products (4)
| mRNA | Protein | Name |
|---|---|---|
| NM_001190263.2 | NP_001177192.1 | nuclear nucleic acid-binding protein C1D |
| NM_001190265.2 | NP_001177194.1 | nuclear nucleic acid-binding protein C1D |
| NM_006333.4 | NP_006324.1 | nuclear nucleic acid-binding protein C1D |
| NM_173177.3 | NP_775269.1 | nuclear nucleic acid-binding protein C1D |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables RNA binding |
IDA
IDA: Inferred from direct assay
|
17412707 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
17412707 | GOA |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in maturation of 5.8S rRNA |
IMP
IMP: Inferred from mutant phenotype
|
17412707 | GOA |
C1D Protein Structure
Sas10_Utp3: Sas10/Utp3/C1D family (18 - 96)
- 0
- 100
- 141 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
nuclear nucleic acid-binding protein C1D |
|
C1D Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
C1D | Q13901 | ZGPAT | Homo sapiens | Q8N5A5-2 | 32296183 | |
|
Intra
|
C1D | Q13901 | GSC2 | Homo sapiens | O15499 | 32296183 | |
|
Intra
|
C1D | Q13901 | GSC2 | Homo sapiens | O15499 | 32296183 | |
|
Intra
|
C1D | Q13901 | SH3GLB1 | Homo sapiens | Q9Y371 | 32296183 | |
|
Intra
|
C1D | Q13901 | EXOSC10 | Homo sapiens | Q01780 | 33961781 | |
|
Intra
|
C1D | Q13901 | EXOSC10 | Homo sapiens | Q01780 | 17412707 | |
|
Intra
|
C1D | Q13901 | EXOSC10 | Homo sapiens | Q01780 | 17412707 | |
|
Intra
|
C1D | Q13901 | HIP1 | Homo sapiens | O00291 | 32814053 | |
|
Intra
|
C1D | Q13901 | HIP1 | Homo sapiens | O00291 | 32814053 | |
|
Intra
|
C1D | Q13901 | HIP1 | Homo sapiens | O00291 | 32814053 | |
|
Intra
|
C1D | Q13901 | WFS1 | Homo sapiens | O76024 | 32814053 | |
|
Intra
|
C1D | Q13901 | WFS1 | Homo sapiens | O76024 | 32814053 | |
|
Intra
|
C1D | Q13901 | WFS1 | Homo sapiens | O76024 | 32814053 |
Recombinant C1D Proteins
| Cat. No. | Product Name | Accession | Purity |
|---|---|---|---|
| HY-P74377 | C1D Protein, Human (His) | Q13901 (M1-S141) | ≥ 95%, as determined by reducing SDS-PAGE. |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Inflammatory Bowel Disease 12 |
|
|
| Pontocerebellar Hypoplasia |
|
|
| Primary Ciliary Dyskinesia |
|
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Canis familiaris | C1D | VGNC | VGNC:38573 |
| Felis catus | C1D | VGNC | VGNC:80037 |
| Mus musculus | C1D | MGD | MGI:1927354 |
| Bos taurus | C1D | VGNC | VGNC:26614 |
| Rattus norvegicus | C1D | RGD | RGD:1560600 |
| Others | C1D | NCBI |