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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
人类
FLNA - Filamin A
Alias:
FLN
FMD
MNS
OPD
ABPX
CSBS
CVD1
FGS2
FLN1
NHBP
OPD1
OPD2
XLVD
XMVD
FLN-A
ABP-280
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码的蛋白质是一种与肌动蛋白结合的蛋白质,它可以交叉连接肌动蛋白丝并将肌动蛋白丝与膜糖蛋白连接起来。编码的蛋白质参与重塑细胞骨架,以影响细胞形状和迁移的变化。这个蛋白质与整联蛋白、跨膜受体复合物和第二信使相互作用。这个基因的缺陷是几种综合征的原因,包括周围室结节性异位(PVNH1,PVNH4),耳廓软骨发育不全综合征(OPD1,OPD2),长骨发育异常(FMD),Melnick-Needles综合征(MNS)和X连锁先天性特发性肠伪阻塞(CIIPX)。已发现这个基因有两个编码不同异型的转录变异体。[RefSeq,2009年3月提供]
Related ID:
NCBI:2316
ENSEMBL:ENSG00000196924
HGNC:3754
UNIPROT:P21333
OMIM:300017
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
2316
2
48
26104 bp
280.74
2764
22
6
82
FLNA Genetics information (-)
GRCh38
Sequence Homology
Related Diseases and Mutations
#
Disease
Anatomical Category
Score
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No data available
Transcripts & Proteins
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Transcript
Length(nt)
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CDS(bp)
Protein
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* This data comes from NCBI.
Gene Expression
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Cell-specific RNA expression
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Type
Name
MGI
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Mutations
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CAS Number
Status
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Link
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References Literature
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