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中文人类
DCDC2 - Doublecortin Domain Containing 2
Alias:
NSC
RU2
RU2S
DCDC2A
DFNB66
NPHP19
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这个基因编码一个包含双皮质蛋白结构域的家族成员。双皮质蛋白结构域已被证明可以结合微管蛋白并增强微管聚合。这个家族成员被认为在神经元迁移中发挥作用，可能会影响初级纤毛的信号传导。这个基因的突变与阅读障碍（RD）2型，也被称为发育性阅读困难有关。这个基因的替代剪接转录变异体已被发现，它们编码相同的蛋白质。[由RefSeq，2013年1月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
DCDC2 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
