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

FBXL5 Protein Structure

Hemerythrin

F-box-like

LRR_6

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

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS04793	FBXL5 Human Pre-designed siRNA Set A		/	Unkown

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

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