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Details of ZMYM2 gene in Homo sapiens
IDs |
Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
| ZMYM2 | FIM,RAMP,ZNF198 | Q9UBW7 | ZMYM2_HUMAN | 7750 | ENSG00000121741 | Zinc finger MYM-type protein 2 | SPROT |
Disease |
Disease |
OMIM id |
Note=A chromosomal aberration involving ZMYM2 may be a cause of stem cell leukemia lymphoma syndrome (SCLL). Translocation t(813)(p11q12) with FGFR1. SCLL usually presents as lymphoblastic lymphoma in association with a myeloproliferative disorder, often accompanied by pronounced peripheral eosinophilia and/or prominent eosinophilic infiltrates in the affected bone marrow. |
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Orthologs in other species |
M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
Zmym2 | woc | --- | |