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Details of BCL7B gene in Homo sapiens
IDs | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Link outs | Gene Name | Alias | Uniprot ID | SwissProt ID | NCBI gene ID | ENSEMBL ID | Description | Source | |
|
| BCL7B | --- | Q9BQE9 | BCL7B_HUMAN | 9275 | ENSG00000263151 ENSG00000106635 | B-cell CLL/lymphoma 7 protein family member B | SPROT | |
Disease | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Disease | OMIM id | ||||||||
| Note=BCL7B is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region. Haploinsufficiency of BCL7B may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in the disease. | --- | ||||||||
Orthologs in other species | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| M. musculus | D. melonogaster | C. elegans | S. purpuratus | ||||||
| Bcl7b | BCL7-like | C28H8.1 | --- | ||||||
| Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
Complex ID | Corum | BioGrid | IRefWeb | Novelty |
|---|---|---|---|---|---|---|---|---|---|
| BCL7B | ARID1A | 1 | BCL7B | ARID1A | cpx6 | no | no | no | Novel |
| SMARCD1 | BCL7B | 1 | SMARCD1 | BCL7B | cpx6 | no | no | no | Novel |
| SMARCB1 | BCL7B | 1 | SMARCB1 | BCL7B | cpx6 | no | no | no | Novel |
| SMARCA2 | BCL7B | 1 | SMARCA2 | BCL7B | cpx6 | no | no | no | Novel |
| ARID1B | BCL7B | 1 | ARID1B | BCL7B | cpx6 | no | no | no | Novel |
| SMARCD3 | BCL7B | 1 | SMARCD3 | BCL7B | cpx6 | no | no | no | Novel |
| BCL7B | SMARCA4 | 1 | BCL7B | SMARCA4 | cpx6 | no | no | no | Novel |
| BCL7B | SMARCD2 | 1 | BCL7B | SMARCD2 | cpx6 | no | no | no | Novel |
| Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
|---|---|---|---|---|