Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10213
Gene name Gene Name - the full gene name approved by the HGNC.
Proteasome 26S subunit, non-ATPase 14
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PSMD14
Synonyms (NCBI Gene) Gene synonyms aliases
PAD1, POH1, RPN11
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q24.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a component of the 26S proteasome. The 26S proteasome is a large multiprotein complex that catalyzes the degradation of ubiquitinated intracellular proteins. The encoded protein is a component of the 19S regulatory cap complex of the 26S
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT046307 hsa-miR-23b-3p CLASH 23622248
MIRT1270460 hsa-miR-1322 CLIP-seq
MIRT1270461 hsa-miR-186 CLIP-seq
MIRT1270462 hsa-miR-2276 CLIP-seq
MIRT1270463 hsa-miR-2355-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000165 Process MAPK cascade TAS
GO:0000209 Process Protein polyubiquitination TAS
GO:0000502 Component Proteasome complex IDA 17323924
GO:0000502 Component Proteasome complex TAS 19214193
GO:0000724 Process Double-strand break repair via homologous recombination IMP 22909820
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607173 16889 ENSG00000115233
Protein
UniProt ID O00487
Protein name 26S proteasome non-ATPase regulatory subunit 14 (EC 3.4.19.-) (26S proteasome regulatory subunit RPN11) (26S proteasome-associated PAD1 homolog 1)
Protein function Component of the 26S proteasome, a multiprotein complex involved in the ATP-dependent degradation of ubiquitinated proteins. This complex plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins, which
PDB 5GJQ , 5GJR , 5L4K , 5LN3 , 5M32 , 5T0C , 5T0G , 5T0H , 5T0I , 5T0J , 5VFP , 5VFQ , 5VFR , 5VFS , 5VFT , 5VFU , 5VGZ , 5VHF , 5VHH , 5VHI , 5VHS , 6MSB , 6MSD , 6MSE , 6MSG , 6MSH , 6MSJ , 6MSK , 6WJD , 6WJN , 7QXN , 7QXP , 7QXU , 7QXW , 7QXX , 7QY7 , 7QYA , 7QYB , 7W37 , 7W38 , 7W39 , 7W3A , 7W3B , 7W3C , 7W3F , 7W3G , 7W3H , 7W3I , 7W3J , 7W3K , 7W3M
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01398 JAB 26 139 JAB1/Mov34/MPN/PAD-1 ubiquitin protease Family
PF13012 MitMem_reg 173 307 Maintenance of mitochondrial structure and function Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed. Highest levels in heart and skeletal muscle. {ECO:0000269|PubMed:9374539}.
Sequence
Sequence length 310
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Neuroticism Neuroticism GWAS
Mental Depression Mental Depression GWAS
Crohn Disease Crohn Disease GWAS
Glioblastoma Glioblastoma CRISPR screening of E3 ubiquitin ligases reveals Ring Finger Protein 185 as a novel tumor suppressor in glioblastoma repressed by promoter hypermethylation and miR-587 GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Inhibit 27050411
Alzheimer Disease Associate 29848990
Breast Neoplasms Stimulate 34839279
Breast Neoplasms Associate 38017133
Carcinogenesis Associate 28653889, 31685442
Carcinoma Hepatocellular Associate 34745496
Colorectal Neoplasms Associate 31685442
Disease Associate 24625750
DNA Repair Deficiency Disorders Associate 34975746
Inflammation Associate 24005050, 34383385