Gene Gene information from NCBI Gene database.
Entrez ID 57109
Gene name REX4 homolog, 3'-5' exonuclease
Gene symbol REXO4
Synonyms (NCBI Gene)
REX4XPMC2XPMC2H
Chromosome 9
Chromosome location 9q34.2
miRNA miRNA information provided by mirtarbase database.
111
miRTarBase ID miRNA Experiments Reference
MIRT028599 hsa-miR-30a-5p Proteomics 18668040
MIRT041926 hsa-miR-484 CLASH 23622248
MIRT040143 hsa-miR-615-3p CLASH 23622248
MIRT1301451 hsa-miR-1286 CLIP-seq
MIRT1301452 hsa-miR-1343 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
26
GO ID Ontology Definition Evidence Reference
GO:0003676 Function Nucleic acid binding IEA
GO:0003690 Function Double-stranded DNA binding IDA 21602889
GO:0003697 Function Single-stranded DNA binding IDA 21602889
GO:0003723 Function RNA binding HDA 22658674, 22681889
GO:0004518 Function Nuclease activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602930 12820 ENSG00000148300
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9GZR2
Protein name RNA exonuclease 4 (EC 3.1.-.-) (Exonuclease XPMC2) (Prevents mitotic catastrophe 2 protein homolog) (hPMC2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00929 RNase_T 244 394 Exonuclease Family
Sequence
MGKAKVPASKRAPSSPVAKPGPVKTLTRKKNKKKKRFWKSKAREVSKKPASGPGAVVRPP
KAPEDFSQNWKALQEWLLKQKSQAPEKPLVISQMGSKKKPKIIQQNKKETSPQVKGEEMP
AGKDQEASRGSVPSGSKMDRRAPVPRTKASGTEHNKKGTKERTNGDIVPERGDIEHKKRK
AKEAAPAPPTEEDIWFDDVDPADIEAAIGPEAAKIARKQLGQSEGSVSLSLVKEQAFGGL
TRALALDCEMVGVGPKGEESMAARVSIVNQYGKCVYDKYVKPTEPVTDYRTAVSGIRPEN
LKQGEELEVVQKEVAEMLKGRILVGHALHNDLKVLFLDHPKKKIRDTQKYKPFKSQVKSG
RPSLRLLSEKILGLQVQQAEHCSIQDAQAAMRLY
VMVKKEWESMARDRRPLLTAPDHCSD
DA
Sequence length 422
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Recurrent spontaneous abortion Uncertain significance rs1839299409 RCV001250900