Statements (26)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:alternativeName |
P0
myelin protein zero |
| gptkbp:associatedWith |
gptkb:Charcot-Marie-Tooth_disease
gptkb:Dejerine–Sottas_disease hereditary neuropathy |
| gptkbp:encodes |
myelin protein zero
|
| gptkbp:Entrez_Gene_ID |
4350
|
| gptkbp:expressedIn |
Schwann cell
|
| gptkbp:foundIn |
gptkb:Homo_sapiens
|
| gptkbp:function |
formation and maintenance of myelin sheath in peripheral nervous system
|
| gptkbp:geneType |
protein-coding
|
| gptkbp:HGNC_ID |
HGNC:7459
|
| https://www.w3.org/2000/01/rdf-schema#label |
MPZ gene
|
| gptkbp:locatedOnChromosome |
chromosome 1
1q23.3 |
| gptkbp:mutationAssociatedWith |
peripheral neuropathy
|
| gptkbp:OMIM |
159440
|
| gptkbp:orthologInMouse |
Mpz
|
| gptkbp:product |
gptkb:P0_protein
|
| gptkbp:UniProtID |
P25189
|
| gptkbp:bfsParent |
gptkb:Charcot-Marie-Tooth_disease_type_1
gptkb:Dejerine–Sottas_disease gptkb:Myelin_P0_protein gptkb:Myelin_Protein_Zero |
| gptkbp:bfsLayer |
8
|