CHMP2A - charged multivesicular body protein 2A Gene
Also Known as BC2; BC-2; VPS2; CHMP2; VPS2A
Species: Homo sapiens
About CHMP2A
This gene has 11 transcripts (splice variants), 199 orthologues and 4 paralogues. Ubiquitous expression in colon (RPKM 34.2), kidney (RPKM 32.8) and 25 other tissues.
Summary
CHMP2A belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface Receptor Proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008]
CHMP2A Products (2)
| mRNA | Protein | Name |
|---|---|---|
| NM_014453.4 | NP_055268.1 | charged multivesicular body protein 2a |
| NM_198426.3 | NP_940818.1 | charged multivesicular body protein 2a |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables phosphatidylcholine binding |
IMP
IMP: Inferred from mutant phenotype
|
18687924 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
14505570 | GOA |
| enables protein domain specific binding |
IPI
IPI: Inferred from physical interaction
|
17928862 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| part of ESCRT III complex |
IDA
IDA: Inferred from direct assay
|
18687924 | GOA |
| located in amphisome membrane |
IDA
IDA: Inferred from direct assay
|
17984323 | GOA |
| located in autophagosome membrane |
IDA
IDA: Inferred from direct assay
|
17984323 | GOA |
| located in chromatin |
IDA
IDA: Inferred from direct assay
|
28242692 | GOA |
| located in kinetochore |
IDA
IDA: Inferred from direct assay
|
26040712 | GOA |
| located in kinetochore microtubule |
IDA
IDA: Inferred from direct assay
|
26040712 | GOA |
| located in lysosomal membrane |
IDA
IDA: Inferred from direct assay
|
17984323 | GOA |
| part of membrane coat |
IMP
IMP: Inferred from mutant phenotype
|
24878737 | GOA |
| located in midbody |
IDA
IDA: Inferred from direct assay
|
26040712 | GOA |
| located in multivesicular body membrane |
IDA
IDA: Inferred from direct assay
|
16554368 | GOA |
| located in nuclear envelope |
IDA
IDA: Inferred from direct assay
|
26040712 | GOA |
| part of nuclear pore |
IDA
IDA: Inferred from direct assay
|
26040713 | GOA |
| located in plasma membrane |
IDA
IDA: Inferred from direct assay
|
24878737 | GOA |
CHMP2A Protein Structure
Snf7: Snf7 (17 - 185)
- 0
- 100
- 200
- 222 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
charged multivesicular body protein 2a |
|
CHMP2A Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
CHMP2A | O43633 | VPS4A | Homo sapiens | Q9UN37 | 16730941 | |
|
Intra
|
CHMP2A | O43633 | CHMP3 | Homo sapiens | Q9Y3E7 | 16730941 | |
|
Intra
|
CHMP2A | O43633 | CHMP3 | Homo sapiens | Q9Y3E7 | 23051622 | |
|
Intra
|
CHMP2A | O43633 | MITD1 | Homo sapiens | Q8WV92 | 16730941 | |
|
Intra
|
CHMP2A | O43633 | MITD1 | Homo sapiens | Q8WV92 | 16730941 | |
|
Intra
|
CHMP2A | O43633 | MITD1 | Homo sapiens | Q8WV92 | 32296183 | |
|
Intra
|
CHMP2A | O43633 | MITD1 | Homo sapiens | Q8WV92 | 32296183 | |
|
Intra
|
CHMP2A | O43633 | MITD1 | Homo sapiens | Q8WV92 | 16730941 | |
|
Intra
|
CHMP2A | O43633 | MITD1 | Homo sapiens | Q8WV92 | 32296183 | |
|
Intra
|
CHMP2A | O43633 | STAMBP | Homo sapiens | O95630 | 16730941 | |
|
Intra
|
CHMP2A | O43633 | HTT | Homo sapiens | P42858 | 32814053 | |
|
Intra
|
CHMP2A | O43633 | HTT | Homo sapiens | P42858 | 32814053 | |
|
Intra
|
CHMP2A | O43633 | HTT | Homo sapiens | P42858 | 32814053 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Breast Adenocarcinoma |
|
|
| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7 |
|
|
| Hypertrichosis Universalis Congenita, Ambras Type |
|
|