FLNB

FLNB
FLNB
Protein FLNB PDB 2di8.png
사용 가능한 구조
PDBOrtholog 검색: PDBe RCSB
식별자
에일리어스FLNB, ABP-278, ABP-280, AOI, FH1, FLN-B, FLN1L, LRS1, SCT, TABP, TAP, 필라민B
외부 IDOMIM: 603381 MGI: 2446089 HomoloGene: 37480 Genecards: FLNB
맞춤법
종.인간마우스
엔트레즈
앙상블
유니프로트
RefSeq(mRNA)

NM_001164317
NM_001164318
NM_001164319
NM_001457

NM_001081427
NM_134080

RefSeq(단백질)

NP_00115789
NP_00115790
NP_00115791
NP_001448

NP_001074896
NP_598841

장소(UCSC)Chr 3: 58.01 ~58.17 MbChr 14: 14.52 ~14.65 Mb
PubMed 검색[3][4]
위키데이터
인간 보기/편집마우스 표시/편집

필라민 B, 베타(FLNB) 또는 필라민 B, 베타(절단 액틴 결합 단백질 278 호몰로그)는 사람에게 FLNB 유전자에 의해 암호화되는 세포질 단백질이다.

FLNB는 세포막세포골격 네트워크 간의 직접적인 통신을 가능하게 하는 단백질 액틴을 가교함으로써 세포 내 통신과 신호 전달을 조절하여 적절한 골격 발달을 [5]제어하고 유도한다.

FLNB 유전자의 돌연변이는 부메랑 이형성증아텔로스테오제네이션 타입 [6][7][8]I을 포함한 몇 가지 치명적인 뼈 이형성에 관여한다.

상호 작용

FLNB는 GP1BA,[9] Filamin,[10] FBLIM1,[11] PSEN1,[12] CD29[13]PSEN2[12]상호작용하는 으로 나타났습니다.

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레퍼런스

  1. ^ a b c GRCh38: 앙상블 릴리즈 89: ENSG00000136068 - 앙상블, 2017년 5월
  2. ^ a b c GRCm38: 앙상블 릴리즈 89: ENSMUSG000025278 - 앙상블, 2017년 5월
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Lu J, Lian G, Lenkinski R, De Grand A, Vaid RR, Bryce T, Stasenko M, Boskey A, Walsh C, Sheen V (2007). "Filamin B mutations cause chondrocyte defects in skeletal development". Hum Mol Genet. 16 (14): 1661–1675. doi:10.1093/hmg/ddm114. PMID 17510210.
  6. ^ Bicknell LS, Morgan T, Bonife L, Wessels MW, Bialer MG, Willems PJ, Cohen DH, Krakow D, Robertson SP (2005). "Mutations in FLNB cause boomerang dysplasia". Am J Med Genet. 42 (7): e43. doi:10.1136/jmg.2004.029967. PMC 1736093. PMID 15994868.
  7. ^ Greally MT; Jewett T; Smith WL Jr.; Penick GD; Williamson RA (1993). "Lethal bone dysplasia in a fetus with manifestations of Atelosteogenesis type I and Boomerang dysplasia". Am J Med Genet. 47 (4): 1086–1091. doi:10.1002/ajmg.1320470731. PMID 8291529.
  8. ^ Nishimura G, Horiuchi T, Kim OH, Sasamoto Y (1997). "Atypical skeletal changes in otopalatodigital syndrome type II: phenotypic overlap among otopalatodigital syndrome type II, boomerang dysplasia, atelosteogenesis type I and type III, and lethal male phenotype of Melnick-Needles syndrome". Am J Med Genet. 73 (2): 132–138. doi:10.1002/(SICI)1096-8628(19971212)73:2<132::AID-AJMG6>3.0.CO;2-W. PMID 9409862.
  9. ^ Takafuta, T; Wu G; Murphy G F; Shapiro S S (Jul 1998). "Human beta-filamin is a new protein that interacts with the cytoplasmic tail of glycoprotein Ibalpha". J. Biol. Chem. UNITED STATES. 273 (28): 17531–8. doi:10.1074/jbc.273.28.17531. ISSN 0021-9258. PMID 9651345.
  10. ^ Sheen, Volney L; Feng Yuanyi; Graham Donna; Takafuta Toshiro; Shapiro Sandor S; Walsh Christopher A (Nov 2002). "Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact". Hum. Mol. Genet. England. 11 (23): 2845–54. doi:10.1093/hmg/11.23.2845. ISSN 0964-6906. PMID 12393796.
  11. ^ Takafuta, Toshiro; Saeki Mari; Fujimoto Tetsuro-Takahiro; Fujimura Kingo; Shapiro Sandor S (Apr 2003). "A new member of the LIM protein family binds to filamin B and localizes at stress fibers". J. Biol. Chem. United States. 278 (14): 12175–81. doi:10.1074/jbc.M209339200. ISSN 0021-9258. PMID 12496242.
  12. ^ a b Zhang, W; Han S W; McKeel D W; Goate A; Wu J Y (Feb 1998). "Interaction of presenilins with the filamin family of actin-binding proteins". J. Neurosci. UNITED STATES. 18 (3): 914–22. doi:10.1523/JNEUROSCI.18-03-00914.1998. ISSN 0270-6474. PMC 2042137. PMID 9437013.
  13. ^ van der Flier, Arjan; Kuikman Ingrid; Kramer Duco; Geerts Dirk; Kreft Maaike; Takafuta Toshiro; Shapiro Sandor S; Sonnenberg Arnoud (Jan 2002). "Different splice variants of filamin-B affect myogenesis, subcellular distribution, and determine binding to integrin [beta] subunits". J. Cell Biol. United States. 156 (2): 361–76. doi:10.1083/jcb.200103037. ISSN 0021-9525. PMC 2199218. PMID 11807098.

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