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GeneQ18041228· pop 7· linked from 5 articles

Also known as CAL, FBLP-1, FBLP1, filamin binding LIM protein 1

Filamin-binding LIM protein 1 is a protein that in humans is encoded by the FBLIM1 gene.

Gene data

FBLIM1
Name
filamin binding LIM protein 1
Type
protein-coding
Position
15,756,604–15,786,594 (+)
Aliases
CAL, FBLP-1, FBLP1
RefSeq RNA
NM_001024215.1, NM_001024216.3, NM_001350151.2, NM_017556.4, XM_005245900.2
RefSeq protein
NP_001019386.1, NP_001019387.1, NP_001337080.1, NP_060026.2, XP_005245957.1

This gene encodes a protein with an N-terminal filamin-binding domain, a central proline-rich domain, and, multiple C-terminal LIM domains. This protein localizes at cell junctions and may link cell adhesion structures to the actin cytoskeleton. This protein may be involved in the assembly and stabilization of actin-filaments and likely plays a role in modulating cell adhesion, cell morphology and cell motility. This protein also localizes to the nucleus and may affect cardiomyocyte differentiation after binding with the CSX/NKX2-5 transcription factor. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008].

via MyGene.info

Wikidata facts

Image
Protein FBLIM1 PDB 2K9U.png
Show 5 more facts
HomoloGene ID
56774
genomic end
16113089
genomic start
16083102
cytogenetic location
1p36.21
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Filamin-binding LIM protein 1 is a protein that in humans is encoded by the FBLIM1 gene.

This gene encodes a protein with an N-terminal filamin-binding domain, a central proline-rich domain, and, multiple C-terminal LIM domains. This protein localizes at cell junctions and may link cell adhesion structures to the actin cytoskeleton. This protein may be involved in the assembly and stabilization of actin-filaments and likely plays a role in modulating cell adhesion, cell morphology and cell motility. This protein also localizes to the nucleus and may affect cardiomyocyte differentiation after binding with the CSX/NKX2-5 transcription factor. Alternative splicing results in multiple transcript variants encoding different isoforms.

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