Homo sapiens Gene: PRND
Summary
InnateDB Gene IDBG-50108.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PRND
Gene Name prion protein 2 (dublet)
Synonyms dJ1068H6.4; DOPPEL; DPL; PrPLP
Species Homo sapiens
Ensembl Gene ENSG00000171864
Encoded Proteins
prion protein 2 (dublet)
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene is found on chromosome 20, approximately 20 kbp downstream of the gene encoding cellular prion protein, to which it is biochemically and structurally similar. The protein encoded by this gene is a membrane glycosylphosphatidylinositol-anchored glycoprotein that is found predominantly in testis. Mutations in this gene may lead to neurological disorders. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 20:4721910-4728460
Strand Forward strand
Band p13
Transcripts
ENST00000305817 ENSP00000306900
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0051260 protein homooligomerization
Cellular Component
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0031225 anchored component of membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q9UKY0
TrEMBL
UniProt Splice Variant
Entrez Gene 23627
UniGene Hs.406696
RefSeq NM_012409
HUGO HGNC:15748
OMIM 604263
CCDS CCDS13081
HPRD
IMGT
EMBL AF106918 AF187843 AF187844 AL133396 AY358985 BC043644 EU009729
GenPept AAF02424 AAG43448 AAG43449 AAH43644 AAQ89344 ABU40603 CAB75502
RNA Seq Atlas 23627