Gene Gene information from NCBI Gene database.
Entrez ID 23627
Gene name Prion like protein doppel
Gene symbol PRND
Synonyms (NCBI Gene)
DOPPELDPLPrPLPdJ1068H6.4
Chromosome 20
Chromosome location 20p13
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 g
miRNA miRNA information provided by mirtarbase database.
308
miRTarBase ID miRNA Experiments Reference
MIRT037276 hsa-miR-877-5p CLASH 23622248
MIRT1264829 hsa-miR-1253 CLIP-seq
MIRT1264830 hsa-miR-1254 CLIP-seq
MIRT1264831 hsa-miR-1275 CLIP-seq
MIRT1264832 hsa-miR-1293 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0005507 Function Copper ion binding IBA
GO:0005507 Function Copper ion binding IDA 20411530
GO:0005507 Function Copper ion binding IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005576 Component Extracellular region TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604263 15748 ENSG00000171864
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UKY0
Protein name Prion-like protein doppel (PrPLP) (Prion protein 2)
Protein function Required for normal acrosome reaction and for normal male fertility (By similarity). Can bind Cu(2+) (PubMed:15218028, PubMed:20411530).
PDB 1LG4
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF11466 Doppel 1 30 Prion-like protein Doppel Domain
PF00377 Prion 63 176 Prion/Doppel alpha-helical domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in testis, in Sertoli cells, ejaculated spermatozoa and in seminal fluid (at protein level). {ECO:0000269|PubMed:12200435}.
Sequence
Sequence length 176
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Post-translational modification: synthesis of GPI-anchored proteins
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
CREUTZFELDT JACOB DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Alzheimer Disease Associate 22453181
★☆☆☆☆
Found in Text Mining only
Anxiety Associate 22453181
★☆☆☆☆
Found in Text Mining only
Astrocytoma Associate 15274317, 16309242, 17201176, 18607068, 18936526, 20981146
★☆☆☆☆
Found in Text Mining only
Brain Neoplasms Associate 18936526
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Associate 22147650
★☆☆☆☆
Found in Text Mining only
Delusional Parasitosis Associate 22453181
★☆☆☆☆
Found in Text Mining only
Drug Related Side Effects and Adverse Reactions Stimulate 19129949
★☆☆☆☆
Found in Text Mining only
Glioblastoma Associate 15274317
★☆☆☆☆
Found in Text Mining only
Glioma Associate 18607068, 20981146
★☆☆☆☆
Found in Text Mining only
Leukemia T Cell Associate 15755294
★☆☆☆☆
Found in Text Mining only