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PRX (gene)

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Periaxin is a protein that in humans is encoded by the PRX gene.[5][6][7]

AliasesPRX, CMT4F, periaxin
External IDsOMIM: 605725; MGI: 108176; GeneCards: PRX
PDBOrtholog search: PDBe RCSB
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PRX
Identifiers
AliasesPRX, CMT4F, periaxin
External IDsOMIM: 605725; MGI: 108176; GeneCards: PRX
Available structures
PDBOrtholog search: PDBe RCSB
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_020956
NM_181882

NM_019412
NM_198048

RefSeq (protein)

NP_066007
NP_870998

NP_062285
NP_932165

Location (UCSC)Chr 19: 40.39 – 40.41 MbChr 7: 27.2 – 27.22 Mb
PubMed search[3][4]
Wikidata
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The PRX gene encodes L- and S-periaxin, proteins of myelinating Schwann cells, and is mutated in Dejerine–Sottas syndrome (MIM 145900) and Charcot–Marie–Tooth disease type 4F (MIM 145900).[supplied by OMIM][7]

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