Entity Details

Primary name RNASET2
Entity type gene
Source Source Link

Details

PrimaryID8635
RefseqGeneNG_016280
SymbolRNASET2
Nameribonuclease T2
Chromosome6
Location6q27
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-10-30
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsRNT2_HUMAN

GO terms

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GOName
GO:0003723 RNA binding
GO:0004521 endoribonuclease activity
GO:0004540 ribonuclease activity
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005758 mitochondrial intermembrane space
GO:0005764 lysosome
GO:0005788 endoplasmic reticulum lumen
GO:0006401 RNA catabolic process
GO:0016829 lyase activity
GO:0033897 ribonuclease T2 activity
GO:0035578 azurophil granule lumen
GO:0043202 lysosomal lumen
GO:0043312 neutrophil degranulation
GO:0045087 innate immune response
GO:0070062 extracellular exosome

Diseases

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Disease IDSourceNameDescription
612951 OMIMLeukoencephalopathy, cystic, without megalencephaly (LCWM)An infantile-onset syndrome of cerebral leukoencephalopathy. Affected newborns develop microcephaly and neurologic abnormalities including psychomotor impairment, seizures and sensorineural hearing impairment. The brain shows multifocal white matter lesions, anterior temporal lobe subcortical cysts, pericystic abnormal myelination, ventriculomegaly and intracranial calcifications. The disease is caused by variants affecting the gene represented in this entry.