Gene Gene information from NCBI Gene database.
Entrez ID 5201
Gene name Prefoldin subunit 1
Gene symbol PFDN1
Synonyms (NCBI Gene)
PDFPFD1
Chromosome 5
Chromosome location 5q31.3
Summary This gene encodes a member of the prefoldin beta subunit family. The encoded protein is one of six subunits of prefoldin, a molecular chaperone complex that binds and stabilizes newly synthesized polypeptides, thereby allowing them to fold correctly. The
miRNA miRNA information provided by mirtarbase database.
199
miRTarBase ID miRNA Experiments Reference
MIRT023289 hsa-miR-122-5p Microarray 17612493
MIRT023736 hsa-miR-1-3p Proteomics 18668040
MIRT1226113 hsa-miR-3202 CLIP-seq
MIRT1226114 hsa-miR-361-3p CLIP-seq
MIRT1226115 hsa-miR-4476 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0001540 Function Amyloid-beta binding IDA 23614719
GO:0005515 Function Protein binding IPI 16169070, 16876117, 21900206, 28514442, 32296183, 33961781
GO:0005737 Component Cytoplasm IBA
GO:0006457 Process Protein folding IBA
GO:0006457 Process Protein folding IDA 30955883
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604897 8866 ENSG00000113068
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O60925
Protein name Prefoldin subunit 1
Protein function Binds specifically to cytosolic chaperonin (c-CPN) and transfers target proteins to it. Binds to nascent polypeptide chain and promotes folding in an environment in which there are many competing pathways for nonnative proteins.
PDB 6NR8 , 6NR9 , 6NRB , 6NRC , 6NRD , 7WU7
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01920 Prefoldin_2 14 119 Prefoldin subunit Coiled-coil
Sequence
Sequence length 122
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATRIAL FIBRILLATION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTISM SPECTRUM DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinoma Hepatocellular Associate 35217267
★☆☆☆☆
Found in Text Mining only
Nasopharyngeal Carcinoma Associate 21052085
★☆☆☆☆
Found in Text Mining only
Stomach Neoplasms Associate 31957800
★☆☆☆☆
Found in Text Mining only