| GENE NAME | CHMP2B |
| CHROMOSOME | 3 |
| ENSEMBL ID | ENSG00000083937 |
| ENTREZ ID | 25978 |
| UNIPROT ACCESSION NUMBER | Q9UQN3 |
| GO MOLECULAR FUNCTION | protein binding |
| ESSENTIAL IN MOUSE | None |
| PATHWAYS | R-HSA-1643685; hsa04144; hsa04144; R-HSA-68882; R-HSA-9679506; R-HSA-69278; hsa04217; hsa04217; R-HSA-9678108; R-HSA-2555396; R-HSA-9610379; R-HSA-9668328; R-HSA-5653656; R-HSA-2995410; R-HSA-9679504; R-HSA-9694516; R-HSA-162599; hsa05022; R-HSA-162587; hsa05022; R-HSA-162588; R-HSA-9609646; hsa05014; hsa05014; R-HSA-9612973; R-HSA-9615710; R-HSA-9694676; R-HSA-1632852; R-HSA-1640170; R-HSA-199991; R-HSA-917729; R-HSA-5663205; R-HSA-162906; R-HSA-68886 |
| 1 combination linked to CHMP2B | OLI441 |
| 1 variant linked to CHMP2B | CHMP2B:c.412G>A, p.Ala138Thr |
| 1 disease linked to CHMP2B | Amyotrophic lateral sclerosis |