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中文人类
DLL3 - Delta Like Canonical Notch Ligand 3
Alias:
SCDO1
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这个基因编码一个属于delta蛋白配体家族的成员。这个家族作为Notch配体发挥作用，其特征是具有DSL结构域、EGF重复序列和跨膜结构域。这个基因的突变导致常染色体隐性遗传性脊柱软骨发育不良1型。已经在这个基因中鉴定出两种编码不同异质体的转录变异体。[由RefSeq，2008年7月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
DLL3 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
