1. Gene
  2. FBXL5 - F-box and leucine rich repeat protein 5 Gene

FBXL5 - F-box and leucine rich repeat protein 5 Gene

Homo sapiens

Also known as FBL4; FBL5; FLR1

Gene ID: 26234 | Gene type: protein coding

About FBXL5

Cytogenetic location: 4p15.32 Genomic coordinates (GRCh38): 4:15,604,381-15,681,569 (from NCBI)

This gene has 13 transcripts (splice variants), 238 orthologues and 15 paralogues. Ubiquitous expression in kidney (RPKM 49.5), fat (RPKM 39.0) and 25 other tissues.

Summary

This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein Ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class and, in addition to an F-box, contains several tandem leucine-rich repeats. Alternatively spliced transcript variants have been described for this locus. [provided by RefSeq, Aug 2010]

FBXL5 Products(3)

mRNA Protein Name
NM_001193534.2 NP_001180463.1 F-box/LRR-repeat protein 5 isoform 3
NM_001193535.2 NP_001180464.1 F-box/LRR-repeat protein 5 isoform 4
NM_012161.4 NP_036293.1 F-box/LRR-repeat protein 5 isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables iron ion binding IDA
IDA: Inferred from direct assay
19762596 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
17532294 GOA
Biological Process GO Annotation Evidence Reference Source
involved in SCF-dependent proteasomal ubiquitin-dependent protein catabolic process IDA
IDA: Inferred from direct assay
17532294 GOA
involved in intracellular iron ion homeostasis IEP
IEP: Inferred from expression pattern
19762597 GOA
involved in intracellular iron ion homeostasis IMP
IMP: Inferred from mutant phenotype
19762596 GOA
involved in protein ubiquitination IDA
IDA: Inferred from direct assay
17532294 GOA
Cellular Component GO Annotation Evidence Reference Source
part of SCF ubiquitin ligase complex IDA
IDA: Inferred from direct assay
19762596 GOA
located in perinuclear region of cytoplasm IDA
IDA: Inferred from direct assay
17532294 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

FBXL5 Protein Structure

Hemerythrin

Hemerythrin: Hemerythrin HHE cation binding domain (8 - 138)

F-box-like

F-box-like: F-box-like (205 - 249)

LRR_6

LRR_6: Leucine Rich repeat (355 - 371)

LRR_6

LRR_6: Leucine Rich repeat (382 - 401)

LRR_6

LRR_6: Leucine Rich repeat (625 - 647)

  • 0
  • 200
  • 400
  • 600
  • 691 a.a.
Protein Preferred Names Protein Names

F-box/LRR-repeat protein 5

F-box protein FBL4/FBL5

Related Diseases

Diseases Alias
Spastic Paraplegia 38, Autosomal Dominant

SPG38

Hereditary Spastic Paraplegia 38

Autosomal Dominant Spastic Paraplegia Type 38

Autosomal Dominant Spastic Paraplegia 38

Alzheimer Disease 3

AD3

Alzheimer Disease, Type 3

Alzheimer Disease, Type 3, With Spastic Paraparesis And Apraxia

Alzheimer Disease, Type 3, With Spastic Paraparesis And Unusual Plaques

Alzheimer'S Disease 3

Alzheimer Disease, Familial, 3, With Spastic Paraparesis And Apraxia

Alzheimer Disease 3, Early-Onset

Alzheimer Disease, Familial, 3

Alzheimer Disease, Protection Against, Due To Apoe3-Christchurch

Alzheimer Disease 3, Early Onset

Alzheimer Disease Familial 3

Early-Onset Familial Alzheimer Disease 3

Familial Alzheimer Disease 3

Familial Alzheimer Disease 3 With Spastic Paraparesis And Apraxia

Familial Alzheimer Disease 3 With Spastic Paraparesis And Unusual Plaques

Alzheimer Disease, Familial, 3, With Spastic Paraparesis And Unusual Plaques

Alzheimer Disease, Familial, Type 3

Deficiency Anemia

Anemia

Deficiency Anemias

Anaemia

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta FBXL5 VGNC VGNC:81408
Felis catus FBXL5 VGNC VGNC:78493
Rattus norvegicus FBXL5 RGD RGD:1306887
Mus musculus FBXL5 MGD MGI:2152883
Canis familiaris FBXL5 VGNC VGNC:40761
Bos taurus FBXL5 VGNC VGNC:28891