CEP20 - centrosomal protein 20 Gene
Also Known as FOPNL; FOR20; C16orf63; PHSECRG2
Species: Homo sapiens
About CEP20
This gene has 9 transcripts (splice variants), 1 gene allele and 196 orthologues. Ubiquitous expression in thyroid (RPKM 17.8), esophagus (RPKM 13.1) and 25 other tissues.
Summary
Enables identical protein binding activity. Involved in cilium assembly. Located in centriolar satellite and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]
CEP20 Products (6)
| mRNA | Protein | Name |
|---|---|---|
| NM_001304497.2 | NP_001291426.1 | centrosomal protein 20 isoform 2 |
| NM_001304498.2 | NP_001291427.1 | centrosomal protein 20 isoform 3 |
| NM_001304499.2 | NP_001291428.1 | centrosomal protein 20 isoform 4 |
| NM_001304500.2 | NP_001291429.1 | centrosomal protein 20 isoform 5 |
| NM_001304502.2 | NP_001291431.1 | centrosomal protein 20 isoform 6 |
| NM_144600.4 | NP_653201.1 | centrosomal protein 20 isoform 1 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables identical protein binding |
IPI
IPI: Inferred from physical interaction
|
20551181 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
32296183 | GOA |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in cilium assembly |
IMP
IMP: Inferred from mutant phenotype
|
15616553 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in centriolar satellite |
IDA
IDA: Inferred from direct assay
|
15616553 | GOA |
| located in centrosome |
IDA
IDA: Inferred from direct assay
|
21399614 | GOA |
CEP20 Protein Structure
FOP_dimer: FOP N terminal dimerisation domain (50 - 113)
- 0
- 100
- 174 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
centrosomal protein 20 |
|
CEP20 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
CEP20 | Q96NB1 | OFD1 | Homo sapiens | O75665 | 33961781 | |
|
Intra
|
CEP20 | Q96NB1 | CEP20 | Homo sapiens | Q96NB1 | 31837246 | |
|
Intra
|
CEP20 | Q96NB1 | PCM1 | Homo sapiens | Q15154 | 20551181 | |
|
Intra
|
CEP20 | Q96NB1 | CEP20 | Homo sapiens | Q96NB1 | 20551181 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Orofaciodigital Syndrome I |
|
|
| Orofaciodigital Syndrome |
|
|
| Lissencephaly |
|
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Canis familiaris | CEP20 | VGNC | VGNC:40939 |
| Macaca mulatta | CEP20 | VGNC | VGNC:99500 |
| Bos taurus | CEP20 | VGNC | VGNC:29072 |
| Rattus norvegicus | CEP20 | RGD | RGD:1305823 |
| Mus musculus | CEP20 | MGD | MGI:1913336 |
| Felis catus | CEP20 | VGNC | VGNC:80574 |
| Others | CEP20 | NCBI |