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Details of FIP1L1 gene in Homo sapiens
IDs |
Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
| FIP1L1 | FIP1,RHE | Q6UN15 | FIP1_HUMAN | 81608 | ENSG00000145216 | Pre-mRNA 3'-end-processing factor FIP1 | SPROT |
Disease |
Disease |
OMIM id |
Note=A chromosomal aberration involving FIP1L1 is found in some cases of hypereosinophilic syndrome. Interstitial chromosomal deletion del(4)(q12q12) causes the fusion of FIP1L1 and PDGFRA (FIP1L1-PDGFRA). |
607685 |
Orthologs in other species |
M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
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