Mus musculus Gene: Plp1 | |||||||||||||||||||||||||
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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
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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] |
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Gene Information | |||||||||||||||||||||||||
Type | Protein coding | ||||||||||||||||||||||||
Genomic Location | Chromosome X:136822671-136839733 | ||||||||||||||||||||||||
Strand | Forward strand | ||||||||||||||||||||||||
Band | F1 | ||||||||||||||||||||||||
Transcripts |
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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.
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Gene Ontology | |||||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||||||||
Species
Homo sapiens
Bos taurus
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Gene ID
Gene Order
Not yet available
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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 | ||||||||||||||||||||||||