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Metazoan complexes |
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Details of ABCB7 gene in Homo sapiens
IDs | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Link outs | Gene Name | Alias | Uniprot ID | SwissProt ID | NCBI gene ID | ENSEMBL ID | Description | Source | |
|
| ABCB7 | ABC7 | O75027 | ABCB7_HUMAN | 22 | ENSG00000131269 | ATP-binding cassette sub-family B member 7, mitochondrial | SPROT | |
Disease | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Disease | OMIM id | ||||||||
| Anemia, sideroblastic, spinocerebellar ataxia (ASAT) [MIM:301310]: A X-linked recessive disorder characterized by an infantile to early childhood onset of non-progressive cerebellar ataxia and mild anemia, with hypochromia and microcytosis. Note=The disease is caused by mutations affecting the gene represented in this entry. | 301310 | ||||||||
Orthologs in other species | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| M. musculus | D. melonogaster | C. elegans | S. purpuratus | ||||||
| Abcb7 | FBgn0035244 | abtm-1 | Sp-Abcb7 | ||||||
| Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
Complex ID | Corum | BioGrid | IRefWeb | Novelty |
|---|---|---|---|---|---|---|---|---|---|
| Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
|---|---|---|---|---|
| FKBP8 | ABCB7 | 0.074112343 | FKBP8 | ABCB7 |
| CKB | ABCB7 | 0.079858382 | CKB | ABCB7 |
| CSDA | ABCB7 | 0.084896535 | CSDA | ABCB7 |
| ACAT1 | ABCB7 | 0.092434368 | ACAT1 | ABCB7 |
| RAB2A | ABCB7 | 0.078749779 | RAB2A | ABCB7 |
| ABCB7 | EPRS | 0.07167932 | ABCB7 | EPRS |
| CKM | ABCB7 | 0.081318933 | CKM | ABCB7 |
| MAT2A | ABCB7 | 0.071859386 | MAT2A | ABCB7 |
| ABCB7 | RPN1 | 0.072881804 | ABCB7 | RPN1 |