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中文人类
KALRN - Kalirin RhoGEF Kinase
Alias:
DUO
CHD5
DUET
TRAD
CHDS5
HAPIP
ARHGEF24
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亨廷顿病（HD）是一种以纹状体神经元丧失为特征的神经退行性疾病，由HD蛋白huntingtin中的多聚谷氨酰胺轨道扩张引起。该基因编码一种与huntingtin相关蛋白1相互作用的蛋白质，huntingtin相关蛋白1是可能在囊泡转运中起作用的huntingtin结合蛋白。[由RefSeq，2016年4月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
KALRN 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
