人类

ACTA1 - Actin Alpha 1, Skeletal Muscle

Alias:
ACTA
ASMA
CFTD
MPFD
NEM1
NEM2
NEM3
SHPM
CFTD1
CFTDM
CMYP2A
CMYP2B
CMYP2C
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码的产物属于肌动蛋白家族蛋白质,这些蛋白质是高度保守的,在细胞运动性、结构和完整性中发挥作用。已识别出α、β和γ肌动蛋白异构体,其中α肌动蛋白是收缩装置的主要组成部分,而β和γ肌动蛋白涉及细胞运动性的调节。这个肌动蛋白是在骨骼肌中发现的α肌动蛋白。这个基因的突变导致各种肌病,包括Nemaline肌病、先天性肌病伴薄肌丝过多、先天性肌病伴核心和先天性肌病伴纤维型异常,这些疾病导致肌肉纤维缺陷,表现为肌无力。[RefSeq,2019年9月提供]

Basic Information

NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
1
7
2850 bp
42.05
462
19
4
29

ACTA1 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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