Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
246243
Gene name Gene Name - the full gene name approved by the HGNC.
Ribonuclease H1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RNASEH1
Synonyms (NCBI Gene) Gene synonyms aliases
H1RNA, PEOB2, RNH1
Disease Acronyms (UniProt) Disease acronyms from UniProt database
PEOB2
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p25.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes an endonuclease that specifically degrades the RNA of RNA-DNA hybrids and plays a key role in DNA replication and repair. Alternate in-frame start codon initiation results in the production of alternate isoforms that are directed to the
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs373442996 G>A Pathogenic Stop gained, non coding transcript variant, coding sequence variant
rs766294940 C>T Pathogenic Coding sequence variant, missense variant, non coding transcript variant
rs1057517675 G>A Pathogenic Missense variant, coding sequence variant, non coding transcript variant
rs1229409884 ->C Likely-pathogenic 5 prime UTR variant, frameshift variant, non coding transcript variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT029640 hsa-miR-26b-5p Microarray 19088304
MIRT045143 hsa-miR-186-5p CLASH 23622248
MIRT043509 hsa-miR-331-3p CLASH 23622248
MIRT042080 hsa-miR-484 CLASH 23622248
MIRT534639 hsa-miR-5590-3p PAR-CLIP 21572407
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000287 Function Magnesium ion binding IEA
GO:0003676 Function Nucleic acid binding TAS 9799596
GO:0003723 Function RNA binding TAS 9799596
GO:0004523 Function RNA-DNA hybrid ribonuclease activity IBA 21873635
GO:0004523 Function RNA-DNA hybrid ribonuclease activity IDA 21700224
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604123 18466 ENSG00000171865
Protein
UniProt ID O60930
Protein name Ribonuclease H1 (RNase H1) (EC 3.1.26.4) (Ribonuclease H type II)
Protein function Endonuclease that specifically degrades the RNA of RNA-DNA hybrids (PubMed:10497183). Plays a role in RNA polymerase II (RNAp II) transcription termination by degrading R-loop RNA-DNA hybrid formation at G-rich pause sites located downstream of
PDB 2QK9 , 2QKB , 2QKK , 3BSU , 6VRD , 8SWB , 8SWC
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01693 Cauli_VI 27 70 Caulimovirus viroplasmin Family
PF00075 RNase_H 138 282 RNase H Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous.
Sequence
Sequence length 286
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  DNA replication  
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Cardiomyopathy Cardiomyopathies rs267607003, rs267607002, rs267607004, rs63750743, rs121908333, rs121908334, rs104894655, rs121434420, rs121434421, rs193922674, rs111517471, rs121908987, rs193922384, rs121909374, rs121909377
View all (900 more)
External ophthalmoplegia External Ophthalmoplegia rs1569484022
Migraine Migraine Disorders rs794727411
Progressive external ophthalmoplegia with mitochondrial dna deletions PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2 rs111033572, rs111033573, rs111033574, rs111033575, rs111033576, rs111033577, rs28937887, rs111033579, rs80356543, rs267606682, rs104894632, rs121918310, rs104893631, rs137854431, rs113994099
View all (39 more)
26094573
Unknown
Disease term Disease name Evidence References Source
Progressive external ophthalmoplegia Chronic progressive external ophthalmoplegia ClinVar
Ptosis Blepharoptosis, Ptosis ClinVar
Leigh Syndrome Leigh syndrome GenCC
External Ophthalmoplegia With Mitochondrial Myopathy adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy GenCC
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Non Small Cell Lung Associate 35166053
Chromosome Aberrations Inhibit 28575672
Immunodeficiency syndrome variable Associate 28117327
Infertility Male Associate 37378420
Leukemia Myeloid Acute Associate 37773887
Mitochondrial Encephalomyopathies Associate 26094573
Muscle Weakness Associate 26094573
Neoplasms Associate 30591567, 35166053
Ophthalmoplegia Chronic Progressive External Associate 26094573
Sensory ataxic neuropathy dysarthria and ophthalmoparesis Associate 33396418