full name
NOP2/Sun RNA methyltransferase family member 2

synonyms
MISU, MRT5, SAKI, TRM4, NSUN2, ENSG00000037474

HGNC
HGNC:25994

Entrez Gene
Gene:54888

ENSEMBL
ENSG00000037474

location
chr: 5
start: 6599352
stop: 6633473
strand: -

OMIM
OMIM:610916: NSUN2 (Autosomal recessive inheritance)
OMIM:611091: Mental retardation, autosomal recessive 5

transcripts
NM_001193455.1
NR_037947.1
NM_017755.5

pathways
Aurora B signaling [NCBI:138080] [Pathway Interaction Database:aurora_b_pathway] [PUBMED:14960279] [PUBMED:15249581] [PUBMED:17129783] [PUBMED:15263015] [PUBMED:15854913] [PUBMED:14605209] [PUBMED:12689593] [PUBMED:15499654] [PUBMED:17483322] [PUBMED:15316025] [PUBMED:11350965] [PUBMED:11516652] [PUBMED:11976319] [PUBMED:16222246] [PUBMED:12925766] [PUBMED:15260989] [PUBMED:16764853] [PUBMED:15796717] [PUBMED:16916643] [PUBMED:14667408] [PUBMED:17389228] [PUBMED:16687578] [PUBMED:14722118] [PUBMED:12082625] [PUBMED:17356064] [PUBMED:16222244] [PUBMED:11756469] [PUBMED:17457057] [PUBMED:15350530] [PUBMED:17322402] [PUBMED:11856369] [PUBMED:17199039] [PUBMED:17129782] [PUBMED:12419797] [PUBMED:16046481] [PUBMED:15064709] [PUBMED:12458200] [PUBMED:15064354] [PUBMED:14674694] [PUBMED:16179162] [PUBMED:17543862] [PUBMED:17215513] [PUBMED:12686604] [PUBMED:16537398]
Gene Expression [NCBI:1269649] [REACTOME:R-HSA-74160]
tRNA modification in the nucleus and cytosol [NCBI:1309090] [REACTOME:R-HSA-6782315] [PUBMED:24581449] [PUBMED:24898039] [PUBMED:23139145] [PUBMED:25692999] [PUBMED:24490730] [PUBMED:25780173] [PUBMED:25304425] [PUBMED:24315934]
tRNA processing [NCBI:1309088] [REACTOME:R-HSA-72306] [PUBMED:24315934] [PUBMED:24917879] [PUBMED:7759547] [PUBMED:24898039] [PUBMED:26016801] [PUBMED:24490730] [PUBMED:20810645] [PUBMED:21910628]