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Details of SEPT9 gene in Homo sapiens
IDs |
Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
| SEPT9 | KIAA0991 | MSF | Q9UHD8 | SEPT9_HUMAN | B3KPM0 | B4DTL9 | Q96QF3 |
Disease |
Disease |
OMIM id |
Note=A chromosomal aberration involving SEPT9/MSF is found in therapy-related acute myeloid leukemia (t-AML). Translocation t(1117)(q23q25) with MLL. |
--- |
Hereditary neuralgic amyotrophy (HNA) [MIM:162100]: Autosomal dominant form of recurrent focal neuropathy characterized clinically by acute |
604061 |
Orthologs in other species |
M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
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