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中文大鼠
Plp1 - proteolipid protein 1
Alias:
Plp
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髓鞘的结构性成分。参与几个过程，包括AMPA选择性谷氨酸受体信号通路；神经系统发育；以及钙离子跨膜运输的积极调节。位于髓鞘中。是整合素alphav-beta3复合物的一部分。用于研究脱髓鞘疾病和视觉癫痫。这个基因的人类同源物与Pelizaeus-Merzbacher疾病和遗传性痉挛性截瘫2有关。与人类PLP1（蛋白脂质蛋白1）正交。[由基因组资源联盟，2022年4月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Related Mouse Models
Reference
Plp1 Genetics information (+)
mRatBN7.2
Sequence Homology
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
References Literature
Title
PMID
Journal
Year
IF
