WormBase Tree Display for Gene: HGNC:9117
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HGNC:9117 | Identity | Name | CGC_name | Pmp2 | Inferred_automatically | AGR_import |
---|---|---|---|---|---|---|
Other_name | RGD:1316684 | |||||
CMT1G | ||||||
FABP8 | ||||||
M-FABP | ||||||
MP2 | ||||||
p2 | ||||||
myelin P2 protein | ||||||
Public_name | Pmp2 | |||||
DB_info | Database | HGNC | id | 9117 | ||
AGR | cURI | HGNC:9117 | ||||
EnsEMBL | ENSEMBL_geneID | ENSG00000147588 | ||||
UniProt | UniProt_AC | P02689 | ||||
OMIM | gene | 170715 | ||||
DO | id | DOID:0111560 | ||||
Species | Homo sapiens | |||||
Status | Live | |||||
Gene_info | Biotype | SO:0001217 | ||||
Ortholog | WBGene00002258 | Caenorhabditis elegans | From_analysis | Hieranoid | ||
Inparanoid | ||||||
OMA | ||||||
OrthoFinder | ||||||
OrthoInspector | ||||||
Panther | ||||||
PhylomeDB | ||||||
SonicParanoid | ||||||
WBGene00002260 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | |||
Hieranoid | ||||||
Inparanoid | ||||||
OMA | ||||||
OrthoFinder | ||||||
OrthoInspector | ||||||
Panther | ||||||
PhylomeDB | ||||||
SonicParanoid | ||||||
WBGene00002257 | Caenorhabditis elegans | From_analysis | Hieranoid | |||
Inparanoid | ||||||
OMA | ||||||
OrthoFinder | ||||||
OrthoInspector | ||||||
Panther | ||||||
PhylomeDB | ||||||
SonicParanoid | ||||||
WBGene00002259 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | |||
Hieranoid | ||||||
Inparanoid | ||||||
OMA | ||||||
OrthoFinder | ||||||
OrthoInspector | ||||||
Panther | ||||||
PhylomeDB | ||||||
SonicParanoid | ||||||
Structured_description | Automated_description | The 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_automatically | AGR_import |