FLNB

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Filamin B, beta (FLNB), also known as Filamin B, beta (truncated actin binding protein 278 homolog), is a cytoplasmic protein which in humans is encoded by the FLNB gene.

PDBOrtholog search: PDBe RCSB
AliasesFLNB, ABP-278, ABP-280, AOI, FH1, FLN-B, FLN1L, LRS1, SCT, TABP, TAP, filamin B
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FLNB
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesFLNB, ABP-278, ABP-280, AOI, FH1, FLN-B, FLN1L, LRS1, SCT, TABP, TAP, filamin B
External IDsOMIM: 603381; MGI: 2446089; HomoloGene: 37480; GeneCards: FLNB; OMA:FLNB - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001164317
NM_001164318
NM_001164319
NM_001457

NM_001081427
NM_134080

RefSeq (protein)

NP_001157789
NP_001157790
NP_001157791
NP_001448

NP_001074896
NP_598841

Location (UCSC)Chr 3: 58.01 – 58.17 MbChr 14: 14.52 – 14.65 Mb
PubMed search[3][4]
Wikidata
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FLNB regulates intracellular communication and signalling by cross-linking the protein actin to allow direct communication between the cell membrane and cytoskeletal network, to control and guide proper skeletal development.[5]

Mutations in the FLNB gene are involved in several lethal bone dysplasias, including boomerang dysplasia and atelosteogenesis type I.[6][7][8]

Interactions

FLNB has been shown to interact with GP1BA,[9] Filamin,[10] FBLIM1,[11] PSEN1,[12] CD29[13] and PSEN2.[12]

See also

References

Further reading

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