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]

Basic Information

NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
2
48
26104 bp
280.74
2764
22
6
82

FLNA Genetics information (-)

GRCh38

Sequence Homology

Related Diseases and Mutations

#
Disease
Anatomical Category
Score
Mutations
No data available

Transcripts & Proteins

Table View
Tile View
#
Transcript
Length(nt)
Exon Count
CDS(bp)
Protein
Length(aa)
No data available
* This data comes from NCBI.

Gene Expression

Tissue-specific RNA expression

Organ
Abundance
Alphabetical

Cell-specific RNA expression

Organ
Abundance
Alphabetical

Interactions

Acting
Regulation
Detail
Mechanism
Target
Residues
Reference
Score
No data available

Related Mouse Models

Type
Name
MGI
Strain of Origin
Publications
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
Link
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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Mutation Direct
Sequence
Comparison
Al agent
Tutorials
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