FBXL7 (F-box and leucine rich repeat protein 7)

2007-04-01  

Identity

HGNC
LOCATION
5p15.1
LOCUSID
ALIAS
FBL6,FBL7
FUSION GENES

Other Information

Locus ID:

NCBI: 23194
MIM: 605656
HGNC: 13604
Ensembl: ENSG00000183580

Variants:

dbSNP: 23194
ClinVar: 23194
TCGA: ENSG00000183580
COSMIC: FBXL7

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000183580ENST00000329673J3KNM9
ENSG00000183580ENST00000504595Q9UJT9
ENSG00000183580ENST00000510662Q9UJT9

Expression (GTEx)

0
10
20
30
40
50
60

Pathways

PathwaySourceExternal ID
Immune SystemREACTOMER-HSA-168256
Adaptive Immune SystemREACTOMER-HSA-1280218
Class I MHC mediated antigen processing & presentationREACTOMER-HSA-983169
Antigen processing: Ubiquitination & Proteasome degradationREACTOMER-HSA-983168
Cell CycleREACTOMER-HSA-1640170
Cell Cycle, MitoticREACTOMER-HSA-69278
Mitotic G2-G2/M phasesREACTOMER-HSA-453274
G2/M TransitionREACTOMER-HSA-69275
FBXL7 down-regulates AURKA during mitotic entry and in early mitosisREACTOMER-HSA-8854050

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
358871492022FBXL7 Body Hypomethylation Is Frequent in Tumors from the Digestive and Respiratory Tracts and Is Associated with Risk-Factor Exposure.0
358871492022FBXL7 Body Hypomethylation Is Frequent in Tumors from the Digestive and Respiratory Tracts and Is Associated with Risk-Factor Exposure.0
3442782620217-Ethoxyrosmanol alleviates hyperglycemia-induced vascular endothelial dysfunction by regulating FBXL7 expression.1
3442782620217-Ethoxyrosmanol alleviates hyperglycemia-induced vascular endothelial dysfunction by regulating FBXL7 expression.1
316332972020Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome.8
321506712020miR-152-5p suppresses glioma progression and tumorigenesis and potentiates temozolomide sensitivity by targeting FBXL7.8
328395492020Epigenetic silencing of the ubiquitin ligase subunit FBXL7 impairs c-SRC degradation and promotes epithelial-to-mesenchymal transition and metastasis.20
316332972020Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome.8
321506712020miR-152-5p suppresses glioma progression and tumorigenesis and potentiates temozolomide sensitivity by targeting FBXL7.8
328395492020Epigenetic silencing of the ubiquitin ligase subunit FBXL7 impairs c-SRC degradation and promotes epithelial-to-mesenchymal transition and metastasis.20
256547632015F-box protein Fbxl18 mediates polyubiquitylation and proteasomal degradation of the pro-apoptotic SCF subunit Fbxl7.22
257783982015The Proapoptotic F-box Protein Fbxl7 Regulates Mitochondrial Function by Mediating the Ubiquitylation and Proteasomal Degradation of Survivin.40
256547632015F-box protein Fbxl18 mediates polyubiquitylation and proteasomal degradation of the pro-apoptotic SCF subunit Fbxl7.22
257783982015The Proapoptotic F-box Protein Fbxl7 Regulates Mitochondrial Function by Mediating the Ubiquitylation and Proteasomal Degradation of Survivin.40
223069982012Novel E3 ligase component FBXL7 ubiquitinates and degrades Aurora A, causing mitotic arrest.35

Citation

Dessen P

FBXL7 (F-box and leucine rich repeat protein 7)

Atlas Genet Cytogenet Oncol Haematol. 2007-04-01

Online version: http://atlasgeneticsoncology.org/gene/47427