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中文人类
NLGN3 - Neuroligin 3
Alias:
HNL3
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这个基因编码一个神经元细胞表面蛋白质家族的成员。这个家族的成员可以作为β-神经素的特异剪接位点配体，可能参与中枢神经系统突触的形成和重塑。这个基因的突变可能与自闭症和阿斯伯格综合症有关。已经发现了这个基因的多个转录变异体，它们编码不同的异构体。[由RefSeq，2009年10月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
NLGN3 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
