Mus musculus Gene: Plp1
Summary
InnateDB Gene IDBG-173392.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Plp1
Gene Name proteolipid protein (myelin) 1
Synonyms DM20; jimpy; jp; msd; Plp; rsh
Species Mus musculus
Ensembl Gene ENSMUSG00000031425
Encoded Proteins
proteolipid protein (myelin) 1
proteolipid protein (myelin) 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000123560:
This gene encodes a transmembrane proteolipid protein that is the predominant myelin protein present in the central nervous system. It may play a role in the compaction, stabilization, and maintenance of myelin sheaths, as well as in oligodendrocyte development and axonal survival. Mutations in this gene cause X-linked Pelizaeus-Merzbacher disease and spastic paraplegia type 2. Alternatively spliced transcript variants encoding distinct isoforms or having different 5' UTRs, have been identified for this gene. [provided by RefSeq, Jul 2008]
This gene encodes a transmembrane proteolipid protein that is the predominant myelin protein present in the central nervous system. It may play a role in the compaction, stabilization, and maintenance of myelin sheaths, as well as in oligodendrocyte development and axonal survival. Mutations in this gene cause X-linked Pelizaeus-Merzbacher disease and spastic paraplegia type 2. Alternatively spliced transcript variants encoding distinct isoforms or having different 5\' UTRs, have been identified for this gene. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome X:136822671-136839733
Strand Forward strand
Band F1
Transcripts
ENSMUST00000033800 ENSMUSP00000033800
ENSMUST00000113085 ENSMUSP00000108708
ENSMUST00000125644
ENSMUST00000144880
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 9 experimentally validated interaction(s) in this database.
They are also associated with 4 interaction(s) predicted by orthology.
Experimentally validated
Total 9 [view]
Protein-Protein 9 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 4 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005198 structural molecule activity
GO:0005515 protein binding
GO:0019911 structural constituent of myelin sheath
Biological Process
GO:0006954 inflammatory response
GO:0007229 integrin-mediated signaling pathway
GO:0008366 axon ensheathment
GO:0010001 glial cell differentiation
GO:0010628 positive regulation of gene expression
GO:0014002 astrocyte development
GO:0021762 substantia nigra development
GO:0022010 central nervous system myelination
GO:0042552 myelination
GO:0042759 long-chain fatty acid biosynthetic process
GO:0048469 cell maturation
GO:0061564 axon development
Cellular Component
GO:0005886 plasma membrane
GO:0016021 integral component of membrane
GO:0043209 myelin sheath
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt P60202
TrEMBL Q3UYM8
UniProt Splice Variant
Entrez Gene 18823
UniGene Mm.385414 Mm.44535 Mm.445407 Mm.474602 Mm.474648
RefSeq NM_011123 NM_001290561 XM_006528513
OMIM
CCDS CCDS30424 CCDS72436
HPRD
IMGT
MGI ID MGI:97623
MGI Symbol Plp1
EMBL AK134554 AK160872 BC027010 M14674 M15442 M16472 M37329 M37330 M37331 M37332 M37333 M37334 M37335 X06375 X07215 X07216 X07217 X07218 X07219 X07220 X07221
GenPept AAA39950 AAA39951 AAA39952 AAA39953 AAA39954 AAA39955 AAH27010 BAE22184 BAE36061 CAA30184 CAB40821
RNA Seq Atlas 18823