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Details of NUP98 gene in Homo sapiens
IDs |
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| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| NUP98 | ADAR2 | P52948 | NUP98_HUMAN | 4928
| ENSG00000110713
| Nuclear pore complex protein Nup98-Nup96
Nuclear pore complex protein Nup98
Nuclear pore complex protein Nup96 | SPROT |
Disease |
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| Disease |
OMIM id |
| Note=A chromosomal aberration involving NUP98 is found in a form of acute myeloid leukemia. Translocation t(711)(p15p15) with HOXA9. Translocation t(1117)(p15p13) with PHF23. |
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Note=A chromosomal aberration involving NUP98 is found in childhood acute myeloid leukemia. Translocation t(511)(q35p15.5) with NSD1. Translocation t(811)(p11.2p15) with WHSC1L1. |
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Note=A chromosomal aberration involving NUP98 is found in a form of therapy-related myelodysplastic syndrome. Translocation t(1120)(p15q11) with TOP1. |
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Note=A chromosomal aberration involving NUP98 is found in a form of T-cell acute lymphoblastic leukemia (T-ALL). Translocation t(311)(q12.2p15.4) with LNP1. |
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Note=A chromosomal aberration involving NUP98 is associated with pediatric acute myeloid leukemia (AML) with intermediate characteristics between M2-M3 French-American-British (FAB) subtypes. Translocation t(911)(p22p15) with PSIP1/LEDGF. The chimeric transcript is an in-frame fusion of NUP98 exon 8 to PSIP1/LEDGF exon 4. |
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Orthologs in other species |
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| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
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