Gene Gene information from NCBI Gene database.
Entrez ID 79622
Gene name Small nuclear ribonucleoprotein U11/U12 subunit 25
Gene symbol SNRNP25
Synonyms (NCBI Gene)
C16orf33
Chromosome 16
Chromosome location 16p13.3
Summary Two types of spliceosomes catalyze splicing of pre-mRNAs. The major U2-type spliceosome is found in all eukaryotes and removes U2-type introns, which represent more than 99% of pre-mRNA introns. The minor U12-type spliceosome is found in some eukaryotes a
miRNA miRNA information provided by mirtarbase database.
182
miRTarBase ID miRNA Experiments Reference
MIRT713312 hsa-miR-665 HITS-CLIP 19536157
MIRT713311 hsa-miR-4677-3p HITS-CLIP 19536157
MIRT713310 hsa-miR-3670 HITS-CLIP 19536157
MIRT713309 hsa-miR-4252 HITS-CLIP 19536157
MIRT713308 hsa-miR-6882-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
14
GO ID Ontology Definition Evidence Reference
GO:0000398 Process MRNA splicing, via spliceosome IEA
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005634 Component Nucleus IDA 18559850
GO:0005634 Component Nucleus IEA
GO:0005654 Component Nucleoplasm IDA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BV90
Protein name U11/U12 small nuclear ribonucleoprotein 25 kDa protein (U11/U12 snRNP 25 kDa protein) (U11/U12-25K) (Minus-99 protein)
PDB 8R7N , 8Y6O , 9GBW , 9GBZ , 9GCM
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF18036 Ubiquitin_4 41 129 Ubiquitin-like domain Domain
Sequence
Sequence length 132
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    mRNA Splicing - Minor Pathway
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
METABOLIC SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PANCREATIC CARCINOMA 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
Neoplasms Neoplasms BEFREE 25300797
★☆☆☆☆
Found in Text Mining only
Osteosarcoma Osteosarcoma BEFREE 25300797, 26738504
★☆☆☆☆
Found in Text Mining only
Osteosarcoma Osteosarcoma Pubtator 25300797, 25418192 Associate
★☆☆☆☆
Found in Text Mining only