Gene Gene information from NCBI Gene database.
Entrez ID 54913
Gene name Ribonuclease P/MRP subunit p25
Gene symbol RPP25
Synonyms (NCBI Gene)
-
Chromosome 15
Chromosome location 15q24.2
miRNA miRNA information provided by mirtarbase database.
175
miRTarBase ID miRNA Experiments Reference
MIRT700032 hsa-miR-218-5p HITS-CLIP 23313552
MIRT700031 hsa-miR-338-3p HITS-CLIP 23313552
MIRT700030 hsa-miR-4519 HITS-CLIP 23313552
MIRT700029 hsa-miR-3681-5p HITS-CLIP 23313552
MIRT700028 hsa-miR-6849-5p HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
20
GO ID Ontology Definition Evidence Reference
GO:0000172 Component Ribonuclease MRP complex IBA
GO:0000172 Component Ribonuclease MRP complex IDA 16723659
GO:0001682 Process TRNA 5'-leader removal IBA
GO:0001682 Process TRNA 5'-leader removal IDA 16723659, 30454648
GO:0003676 Function Nucleic acid binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619235 30361 ENSG00000178718
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BUL9
Protein name Ribonuclease P protein subunit p25 (RNase P protein subunit p25)
Protein function Component of ribonuclease P, a ribonucleoprotein complex that generates mature tRNA molecules by cleaving their 5'-ends (PubMed:12003489, PubMed:16723659, PubMed:30454648). Also a component of the MRP ribonuclease complex, which cleaves pre-rRNA
PDB 6AHR , 6AHU , 6CWX , 6LT7
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01918 Alba 36 101 Alba Family
Sequence
MENFRKVRSEEAPAGCGAEGGGPGSGPFADLAPGAVHMRVKEGSKIRNLMAFATASMAQP
ATRAIVFSGCGRATTKTVTCAEILKRRLAGLHQVTRLRYRS
VREVWQSLPPGPTQGQTPG
EPAASLSVLKNVPGLAILLSKDALDPRQPGYQPPNPHPGPSSPPAAPASKRSLGEPAAGE
GSAKRSQPEPGVADEDQTA
Sequence length 199
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Ribosome biogenesis in eukaryotes   tRNA processing in the nucleus
Major pathway of rRNA processing in the nucleolus and cytosol
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
MAJOR DEPRESSIVE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MYOCARDIAL INFARCTION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Autism Spectrum Disorders Autism Spectrum Disorder BEFREE 20632321
★☆☆☆☆
Found in Text Mining only
Autistic Disorder Autism BEFREE 20632321
★☆☆☆☆
Found in Text Mining only
Cartilage-hair hypoplasia Cartilage-Hair Hypoplasia BEFREE 18164267
★☆☆☆☆
Found in Text Mining only
Glioblastoma Multiforme Glioblastoma BEFREE 31763067
★☆☆☆☆
Found in Text Mining only
Pervasive Development Disorder Autism spectrum disorder BEFREE 20632321
★☆☆☆☆
Found in Text Mining only