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WormBase Tree Display for Gene: HGNC:9117

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Name Class

HGNC:9117IdentityNameCGC_namePmp2Inferred_automaticallyAGR_import
Other_nameRGD:1316684
CMT1G
FABP8
M-FABP
MP2
p2
myelin P2 protein
Public_namePmp2
DB_infoDatabaseHGNCid9117
AGRcURIHGNC:9117
EnsEMBLENSEMBL_geneIDENSG00000147588
UniProtUniProt_ACP02689
OMIMgene170715
DOidDOID:0111560
SpeciesHomo sapiens
StatusLive
Gene_infoBiotypeSO:0001217
OrthologWBGene00002258Caenorhabditis elegansFrom_analysisHieranoid
Inparanoid
OMA
OrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
WBGene00002260Caenorhabditis elegansFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OMA
OrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
WBGene00002257Caenorhabditis elegansFrom_analysisHieranoid
Inparanoid
OMA
OrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
WBGene00002259Caenorhabditis elegansFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OMA
OrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
Structured_descriptionAutomated_descriptionThe protein encoded by this gene localizes to myelin sheaths of the peripheral nervous system. The encoded protein can bind both the membrane layers of the sheaths and monomeric lipids, and is thought to provide stability to the sheath. A defect in this gene was shown to be a cause of dominant demyelinating CMT neuropathy. [provided by RefSeq, Jan 2017]Inferred_automaticallyAGR_import