Metazoan complexes |
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Emili & Marcotte labs |
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Details of B9D1 gene in Homo sapiens
IDs | |||||||||
---|---|---|---|---|---|---|---|---|---|
Link outs | Gene Name | Alias | Uniprot ID | SwissProt ID | NCBI gene ID | ENSEMBL ID | Description | Source | |
| B9D1 | MKSR1 | Q9UPM9 | B9D1_HUMAN | 27077 | ENSG00000108641 | B9 domain-containing protein 1 | SPROT |
Disease | |||||||||
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Disease | OMIM id | ||||||||
Meckel syndrome 9 (MKS9) [MIM:614209]: A disorder characterized by a combination of renal cysts and variably associated features including developmental anomalies of the central nervous system (typically encephalocele), hepatic ductal dysplasia and cysts, and polydactyly. Note=The disease is caused by mutations affecting the gene represented in this entry. | 614209 |
Orthologs in other species | |||||||||
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M. musculus | D. melonogaster | C. elegans | S. purpuratus | ||||||
B9d1 | FBgn0038342 | K03E6.4 | SPU_005186 |
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 |
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