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FLNA
HPA
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  • FLNA
PROTEIN SUMMARY GENE INFORMATION RNA DATA ANTIBODY DATA
GENERAL INFORMATIONi

General description of the gene and the encoded protein(s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas project.

Gene namei

Official gene symbol, which is typically a short form of the gene name, according to HGNC.

FLNA
Synonyms ABP-280, FLN, FLN1, OPD1, OPD2
Gene descriptioni

Full gene name according to HGNC.

Filamin A
Protein classi

Assigned HPA protein class(es) for the encoded protein(s).

Disease related genes
Human disease related genes
Plasma proteins
Potential drug targets
Transporters
Predicted locationi

All transcripts of all genes have been analyzed regarding the location(s) of corresponding protein based on prediction methods for signal peptides and transmembrane regions.

  • Genes with at least one transcript predicted to encode a secreted protein, according to prediction methods or to UniProt location data, have been further annotated and classified with the aim to determine if the corresponding protein(s) are secreted or actually retained in intracellular locations or membrane-attached.

  • Remaining genes, with no transcript predicted to encode a secreted protein, will be assigned the prediction-based location(s).

The annotated location overrules the predicted location, so that a gene encoding a predicted secreted protein that has been annotated as intracellular will have intracellular as the final location.

Intracellular
Protein evidence Evidence at protein level (all genes)
GENE INFORMATIONi

Gene information from Ensembl and Entrez, as well as links to available gene identifiers are displayed here. Information was retrieved from Ensembl if not indicated otherwise.

Chromosome X
Cytoband q28
Chromosome location (bp) 154348524 - 154374634
Number of transcriptsi

Number of protein-coding transcripts from the gene as defined by Ensembl.

7
Ensembl ENSG00000196924 (version 109)
Entrez gene 2316
HGNC HGNC:3754
UniProt P21333 (UniProt - Evidence at protein level)
neXtProt NX_P21333
GeneCards FLNA
Antibodypedia FLNA antibodies


PROTEIN FUNCTION
Protein function (UniProt)i

Useful information about the protein provided by UniProt.

Promotes orthogonal branching of actin filaments and links actin filaments to membrane glycoproteins. Anchors various transmembrane proteins to the actin cytoskeleton and serves as a scaffold for a wide range of cytoplasmic signaling proteins. Interaction with FLNB may allow neuroblast migration from the ventricular zone into the cortical plate. Tethers cell surface-localized furin, modulates its rate of internalization and directs its intracellular trafficking (By similarity). Involved in ciliogenesis. Plays a role in cell-cell contacts and adherens junctions during the development of blood vessels, heart and brain organs. Plays a role in platelets morphology through interaction with SYK that regulates ITAM- and ITAM-like-containing receptor signaling, resulting in by platelet cytoskeleton organization maintenance (By similarity). During the axon guidance process, required for growth cone collapse induced by SEMA3A-mediated stimulation of neurons 1.... show less
Molecular function (UniProt)i

Keywords assigned by UniProt to proteins due to their particular molecular function.

Actin-binding
Biological process (UniProt)i

Keywords assigned by UniProt to proteins because they are involved in a particular biological process.

Cilium biogenesis/degradation
Gene summary (Entrez)i

Useful information about the gene from Entrez

The protein encoded by this gene is an actin-binding protein that crosslinks actin filaments and links actin filaments to membrane glycoproteins. The encoded protein is involved in remodeling the cytoskeleton to effect changes in cell shape and migration. This protein interacts with integrins, transmembrane receptor complexes, and second messengers. Defects in this gene are a cause of several syndromes, including periventricular nodular heterotopias (PVNH1, PVNH4), otopalatodigital syndromes (OPD1, OPD2), frontometaphyseal dysplasia (FMD), Melnick-Needles syndrome (MNS), and X-linked congenital idiopathic intestinal pseudoobstruction (CIIPX). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2009]... show less
PROTEIN INFORMATIONi

The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database.

The Splice variant identifier links to the Ensembl website protein summary for the selected splice variant. The data in the Swissprot and TrEMBL columns links to corresponding pages in the UniProt database.

The protein classes assigned to this protein are shown if expanding the data in the protein class column. Parent protein classes are in bold font and subclasses are listed under the parent class.

The length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide and number of predicted transmembrane region(s) according to in-house majority decision methods based on sets of predictors are also reported.
Splice variant SwissProt TrEMBL Protein class Gene ontology Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
FLNA-201
ENSP00000353467
ENST00000360319
P21333
[Direct mapping] Filamin-A
Show all
Transporters
   Accessory Factors Involved in Transport
   Phobius predicted membrane proteins
   SPOCTOPUS predicted membrane proteins
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Plasma proteins
Disease related genes
Potential drug targets
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the circulatory system
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
   Digestive system diseases
   Gastrointestinal diseases
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001664 [G protein-coupled receptor binding]
GO:0003723 [RNA binding]
GO:0003779 [actin binding]
GO:0005515 [protein binding]
GO:0005576 [extracellular region]
GO:0005634 [nucleus]
GO:0005730 [nucleolus]
GO:0005737 [cytoplasm]
GO:0005829 [cytosol]
GO:0005856 [cytoskeleton]
GO:0005886 [plasma membrane]
GO:0005911 [cell-cell junction]
GO:0005925 [focal adhesion]
GO:0005938 [cell cortex]
GO:0007010 [cytoskeleton organization]
GO:0007195 [adenylate cyclase-inhibiting dopamine receptor signaling pathway]
GO:0007597 [blood coagulation, intrinsic pathway]
GO:0010572 [positive regulation of platelet activation]
GO:0015459 [potassium channel regulator activity]
GO:0015629 [actin cytoskeleton]
GO:0016020 [membrane]
GO:0016479 [negative regulation of transcription by RNA polymerase I]
GO:0019900 [kinase binding]
GO:0030018 [Z disc]
GO:0030030 [cell projection organization]
GO:0030036 [actin cytoskeleton organization]
GO:0030334 [regulation of cell migration]
GO:0030426 [growth cone]
GO:0031267 [small GTPase binding]
GO:0031523 [Myb complex]
GO:0031532 [actin cytoskeleton reorganization]
GO:0034394 [protein localization to cell surface]
GO:0034988 [Fc-gamma receptor I complex binding]
GO:0035855 [megakaryocyte development]
GO:0042177 [negative regulation of protein catabolic process]
GO:0042307 [positive regulation of protein import into nucleus]
GO:0042803 [protein homodimerization activity]
GO:0042995 [cell projection]
GO:0043066 [negative regulation of apoptotic process]
GO:0043113 [receptor clustering]
GO:0043123 [positive regulation of I-kappaB kinase/NF-kappaB signaling]
GO:0043204 [perikaryon]
GO:0043232 [intracellular non-membrane-bounded organelle]
GO:0043433 [negative regulation of DNA-binding transcription factor activity]
GO:0044319 [wound healing, spreading of cells]
GO:0044325 [transmembrane transporter binding]
GO:0045184 [establishment of protein localization]
GO:0045296 [cadherin binding]
GO:0050821 [protein stabilization]
GO:0051015 [actin filament binding]
GO:0051020 [GTPase binding]
GO:0051209 [release of sequestered calcium ion into cytosol]
GO:0051220 [cytoplasmic sequestering of protein]
GO:0051764 [actin crosslink formation]
GO:0060271 [cilium assembly]
GO:0070062 [extracellular exosome]
GO:0070527 [platelet aggregation]
GO:0071526 [semaphorin-plexin signaling pathway]
GO:0072659 [protein localization to plasma membrane]
GO:0090042 [tubulin deacetylation]
GO:0090307 [mitotic spindle assembly]
GO:0140297 [DNA-binding transcription factor binding]
GO:1900026 [positive regulation of substrate adhesion-dependent cell spreading]
GO:1901381 [positive regulation of potassium ion transmembrane transport]
GO:1905000 [regulation of membrane repolarization during atrial cardiac muscle cell action potential]
GO:1905031 [regulation of membrane repolarization during cardiac muscle cell action potential]
GO:1990779 [glycoprotein Ib-IX-V complex]
GO:2001046 [positive regulation of integrin-mediated signaling pathway]
Show all
2639 aa
280 kDa
No 0
FLNA-202
ENSP00000358866
ENST00000369850
P21333
[Direct mapping] Filamin-A
Show all
Transporters
   Accessory Factors Involved in Transport
   Phobius predicted membrane proteins
   SPOCTOPUS predicted membrane proteins
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Plasma proteins
Disease related genes
Potential drug targets
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the circulatory system
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
   Digestive system diseases
   Gastrointestinal diseases
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001525 [angiogenesis]
GO:0001664 [G protein-coupled receptor binding]
GO:0001837 [epithelial to mesenchymal transition]
GO:0001974 [blood vessel remodeling]
GO:0003007 [heart morphogenesis]
GO:0003723 [RNA binding]
GO:0003779 [actin binding]
GO:0005080 [protein kinase C binding]
GO:0005515 [protein binding]
GO:0005576 [extracellular region]
GO:0005634 [nucleus]
GO:0005730 [nucleolus]
GO:0005737 [cytoplasm]
GO:0005802 [trans-Golgi network]
GO:0005829 [cytosol]
GO:0005856 [cytoskeleton]
GO:0005886 [plasma membrane]
GO:0005903 [brush border]
GO:0005911 [cell-cell junction]
GO:0005925 [focal adhesion]
GO:0005938 [cell cortex]
GO:0007010 [cytoskeleton organization]
GO:0007195 [adenylate cyclase-inhibiting dopamine receptor signaling pathway]
GO:0007597 [blood coagulation, intrinsic pathway]
GO:0010572 [positive regulation of platelet activation]
GO:0010977 [negative regulation of neuron projection development]
GO:0015459 [potassium channel regulator activity]
GO:0015629 [actin cytoskeleton]
GO:0016020 [membrane]
GO:0016479 [negative regulation of transcription by RNA polymerase I]
GO:0019900 [kinase binding]
GO:0030018 [Z disc]
GO:0030030 [cell projection organization]
GO:0030036 [actin cytoskeleton organization]
GO:0030334 [regulation of cell migration]
GO:0030426 [growth cone]
GO:0031267 [small GTPase binding]
GO:0031523 [Myb complex]
GO:0031532 [actin cytoskeleton reorganization]
GO:0032231 [regulation of actin filament bundle assembly]
GO:0032432 [actin filament bundle]
GO:0034394 [protein localization to cell surface]
GO:0034988 [Fc-gamma receptor I complex binding]
GO:0035855 [megakaryocyte development]
GO:0042177 [negative regulation of protein catabolic process]
GO:0042307 [positive regulation of protein import into nucleus]
GO:0042803 [protein homodimerization activity]
GO:0042995 [cell projection]
GO:0043066 [negative regulation of apoptotic process]
GO:0043113 [receptor clustering]
GO:0043123 [positive regulation of I-kappaB kinase/NF-kappaB signaling]
GO:0043204 [perikaryon]
GO:0043232 [intracellular non-membrane-bounded organelle]
GO:0043433 [negative regulation of DNA-binding transcription factor activity]
GO:0044295 [axonal growth cone]
GO:0044319 [wound healing, spreading of cells]
GO:0044325 [transmembrane transporter binding]
GO:0045022 [early endosome to late endosome transport]
GO:0045184 [establishment of protein localization]
GO:0045216 [cell-cell junction organization]
GO:0045296 [cadherin binding]
GO:0048680 [positive regulation of axon regeneration]
GO:0050808 [synapse organization]
GO:0050821 [protein stabilization]
GO:0051015 [actin filament binding]
GO:0051020 [GTPase binding]
GO:0051209 [release of sequestered calcium ion into cytosol]
GO:0051220 [cytoplasmic sequestering of protein]
GO:0051764 [actin crosslink formation]
GO:0060271 [cilium assembly]
GO:0070062 [extracellular exosome]
GO:0070527 [platelet aggregation]
GO:0071526 [semaphorin-plexin signaling pathway]
GO:0072659 [protein localization to plasma membrane]
GO:0090042 [tubulin deacetylation]
GO:0090307 [mitotic spindle assembly]
GO:0140297 [DNA-binding transcription factor binding]
GO:1900026 [positive regulation of substrate adhesion-dependent cell spreading]
GO:1901381 [positive regulation of potassium ion transmembrane transport]
GO:1905000 [regulation of membrane repolarization during atrial cardiac muscle cell action potential]
GO:1905031 [regulation of membrane repolarization during cardiac muscle cell action potential]
GO:1990779 [glycoprotein Ib-IX-V complex]
GO:2001046 [positive regulation of integrin-mediated signaling pathway]
Show all
2647 aa
280.7 kDa
No 0
FLNA-203
ENSP00000358872
ENST00000369856
Q60FE5
[Direct mapping] Filamin-A
Show all
   SPOCTOPUS predicted membrane proteins
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the circulatory system
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
   Digestive system diseases
   Gastrointestinal diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0003779 [actin binding]
GO:0005515 [protein binding]
GO:0005829 [cytosol]
GO:0005856 [cytoskeleton]
GO:0005886 [plasma membrane]
GO:0007010 [cytoskeleton organization]
GO:0015629 [actin cytoskeleton]
GO:0030036 [actin cytoskeleton organization]
GO:0043232 [intracellular non-membrane-bounded organelle]
GO:0051015 [actin filament binding]
Show all
2620 aa
278.2 kDa
No 0
FLNA-206
ENSP00000416926
ENST00000422373
A0A7P0NMY4
[Direct mapping] Filamin-A
Show all
   Phobius predicted membrane proteins
   SPOCTOPUS predicted membrane proteins
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the circulatory system
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
   Digestive system diseases
   Gastrointestinal diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0003779 [actin binding]
GO:0005515 [protein binding]
GO:0005856 [cytoskeleton]
GO:0007010 [cytoskeleton organization]
GO:0030036 [actin cytoskeleton organization]
GO:0043232 [intracellular non-membrane-bounded organelle]
GO:0051015 [actin filament binding]
Show all
1574 aa
167.9 kDa
No 0
FLNA-207
ENSP00000398215
ENST00000438732
H0Y5F3
[Direct mapping] Filamin-A
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the circulatory system
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
   Digestive system diseases
   Gastrointestinal diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005515 [protein binding]
GO:0005829 [cytosol]
GO:0005856 [cytoskeleton]
GO:0005886 [plasma membrane]
GO:0015629 [actin cytoskeleton]
GO:0030036 [actin cytoskeleton organization]
GO:0051015 [actin filament binding]
Show all
232 aa
25 kDa
No 0
FLNA-208
ENSP00000397824
ENST00000444578
H0Y5C6
[Direct mapping] Filamin-A
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the circulatory system
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
   Digestive system diseases
   Gastrointestinal diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005515 [protein binding]
GO:0005856 [cytoskeleton]
GO:0030036 [actin cytoskeleton organization]
GO:0051015 [actin filament binding]
Show all
281 aa
29.9 kDa
No 0
FLNA-219
ENSP00000501210
ENST00000673639
A0A669KBC6
[Direct mapping] Filamin-A
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the circulatory system
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
   Digestive system diseases
   Gastrointestinal diseases
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005515 [protein binding]
GO:0005856 [cytoskeleton]
GO:0030036 [actin cytoskeleton organization]
GO:0051015 [actin filament binding]
Show all
96 aa
10.1 kDa
No 0

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