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Details of SMARCE1 gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| SMARCE1 | BAF57 | Q969G3 | SMCE1_HUMAN | 6605
| ENSG00000073584
| SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 | SPROT |
Disease |
|---|
| Disease |
OMIM id |
| Note=Defects in SMARCE1 may be a cause of Coffin-Siris syndrome, a highly variable disease characterized by mental retardation associated with a broad spectrum of different clinical features. |
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Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
|
