Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84844
Gene name Gene Name - the full gene name approved by the HGNC.
PHD finger protein 5A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PHF5A
Synonyms (NCBI Gene) Gene synonyms aliases
INI, Rds3, SAP14b, SF3B7, SF3b14b, bK223H9.2
Chromosome Chromosome number
22
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q13.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a subunit of the splicing factor 3b protein complex. Splicing factor 3b, together with splicing factor 3a and a 12S RNA unit, forms the U2 small nuclear ribonucleoproteins complex (U2 snRNP). The splicing factor 3b/3a complex binds pre-m
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT052678 hsa-miR-1260b CLASH 23622248
MIRT532634 hsa-miR-6838-3p PAR-CLIP 22012620
MIRT532633 hsa-miR-6734-3p PAR-CLIP 22012620
MIRT532632 hsa-miR-20b-3p PAR-CLIP 22012620
MIRT532631 hsa-miR-4297 PAR-CLIP 22012620
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000398 Process MRNA splicing, via spliceosome IBA 21873635
GO:0000398 Process MRNA splicing, via spliceosome IDA 12234937, 29360106
GO:0000398 Process MRNA splicing, via spliceosome TAS
GO:0003677 Function DNA binding IEA
GO:0003723 Function RNA binding HDA 22658674, 22681889
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
617846 18000 ENSG00000100410
Protein
UniProt ID Q7RTV0
Protein name PHD finger-like domain-containing protein 5A (PHD finger-like domain protein 5A) (Splicing factor 3B-associated 14 kDa protein) (SF3b14b)
Protein function Component of the 17S U2 SnRNP complex of the spliceosome, a large ribonucleoprotein complex that removes introns from transcribed pre-mRNAs (PubMed:12234937, PubMed:27720643, PubMed:28541300, PubMed:32494006, PubMed:34822310). The 17S U2 SnRNP c
PDB 5IFE , 5O9Z , 5SYB , 5Z56 , 5Z57 , 5Z58 , 5ZYA , 6AH0 , 6AHD , 6EN4 , 6FF4 , 6FF7 , 6QX9 , 6Y50 , 6Y5Q , 7ABG , 7ABH , 7ABI , 7B0I , 7B91 , 7B92 , 7B9C , 7DVQ , 7EVN , 7EVO , 7OMF , 7ONB , 7OPI , 7Q3L , 7Q4O , 7Q4P , 7QTT , 7VPX , 8CH6 , 8H6E , 8H6J , 8H6K , 8H6L , 8HK1 , 8I0P , 8I0R , 8I0S , 8I0T , 8I0U , 8I0V , 8QO9 , 8QXD , 8QZS , 8R08 , 8R09 , 8R0A
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03660 PHF5 1 104 PHF5-like protein Family
Sequence
Sequence length 110
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Spliceosome   mRNA Splicing - Major Pathway
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Asthma Asthma 30929738 ClinVar, GWAS
Neurodevelopmental Disorders complex neurodevelopmental disorder GenCC
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 30932358
Breast Neoplasms Associate 30932358
Carcinogenesis Associate 37845358
Carcinoma Hepatocellular Associate 30766880
Carcinoma Non Small Cell Lung Stimulate 30932358
Congenital Microtia Associate 33811463
Glioblastoma Associate 30932358
HIV Infections Inhibit 36851760
Kidney Neoplasms Associate 25638191
Neoplasms Associate 26109171, 30766880, 37434235, 37845358