FBLIM1
Filamin-binding LIM protein 1
Also known as: CAL, FBLI1_HUMAN, FBLP-1, migfilin
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8WUP2
- Gene
- FBLIM1
- Ensembl
- ENSG00000162458
- Chromosome
- 1
- Canonical length
- 373 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoli fibrillar center,Cell Junctions,Focal adhesion sites
OverviewNCBI 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. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
373 residues, UniProt reviewed canonical sequence.
>Q8WUP2|FBLIM1
1 MASKPEKRVA SSVFITLAPP RRDVAVAEEV RQAVCEARRG RPWEAPAPMK TPEAGLAGRP
61 SPWTTPGRAA ATVPAAPMQL FNGGCPPPPP VLDGEDVLPD LDLLPPPPPP PPVLLPSEEE
121 APAPMGASLI ADLEQLHLSP PPPPPQAPAE GPSVQPGPLR PMEEELPPPP AEPVEKGAST
181 DICAFCHKTV SPRELAVEAM KRQYHAQCFT CRTCRRQLAG QSFYQKDGRP LCEPCYQDTL
241 ERCGKCGEVV RDHIIRALGQ AFHPSCFTCV TCARCIGDES FALGSQNEVY CLDDFYRKFA
301 PVCSICENPI IPRDGKDAFK IECMGRNFHE NCYRCEDCRI LLSVEPTDQG CYPLNNHLFC
361 KPCHVKRSAA GCCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FBLIM1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.5
- Highest tissue expression
- 444 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 444 nTPM
- small intestine: 81 nTPM
- duodenum: 77 nTPM
- colon: 71 nTPM
- endometrium: 69 nTPM
- gallbladder: 65 nTPM
Single-cell type
- enterocytes: 268 nCPM
- colonocytes: 241 nCPM
- peritubular myoid cells: 235 nCPM
- foveolar cells: 228 nCPM
- extravillous trophoblasts: 197 nCPM
- ocular epithelial cells: 181 nCPM
Immune cell
- basophil: 1.5 nTPM
- neutrophil: 0.7 nTPM
- naive B-cell: 0.4 nTPM
- NK-cell: 0.4 nTPM
- plasmacytoid DC: 0.4 nTPM
- classical monocyte: 0.3 nTPM
Brain region
- choroid plexus: 11 nTPM
- cerebral cortex: 9.4 nTPM
- thalamus: 8.7 nTPM
- basal ganglia: 7.4 nTPM
- midbrain: 7.1 nTPM
- cerebellum: 7 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.25
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.53
- DepMap mean gene effect
- -0.38
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FBLIM1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads FBLIM1 as an antibody target. Whether an autoantibody or antibody against FBLIM1 could matter depends on whether native FBLIM1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FBLIM1 is annotated at the cell surface, where native FBLIM1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label FBLIM1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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