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中文人类
SEPTIN9 - Septin 9
Alias:
MSF
MSF1
NAPB
SEPT9
SINT1
PNUTL4
SeptD1
AF17q25
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这个基因是septin家族的一员，参与胞质分裂和细胞周期控制。这个基因是卵巢肿瘤抑制基因的候选基因。这个基因的突变导致遗传性神经病性肌萎缩，也称为具有臂倾向的神经炎。涉及17号染色体上的这个基因和11号染色体上的MLL基因的染色体易位导致急性髓单核细胞白血病。已经描述了多种可变剪接转录变异体，编码不同的异构体。[由RefSeq，2009年3月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
SEPTIN9 Genetics information (+)
GRCh38
Sequence Homology
Related Diseases and Mutations
#
Disease
Anatomical Category
Score
Mutations
Transcripts & Proteins
Table View
Tile View
#
Transcript
Length(nt)
Exon Count
CDS(bp)
Protein
Length(aa)
* 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
Related Mouse Models
Type
Name
MGI
Strain of Origin
Publications
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Link
References Literature
Title
PMID
Journal
Year
IF
