CTU2 (formerly known as C16orf84) is a human gene located on chromosome 16.[5] The mRNA encodes the longer isoform. The gene encodes a cytoplasmic protein that plays a probable role in tRNA modification.[6]

CTU2
Identifiers
AliasesCTU2, C16orf84, NCS2, UPF0432, cytosolic thiouridylase subunit 2, MFRG
External IDsOMIM: 617057; MGI: 1914215; HomoloGene: 79815; GeneCards: CTU2; OMA:CTU2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001012759
NM_001012762
NM_001318507
NM_001318513

NM_153775

RefSeq (protein)

NP_001012777
NP_001012780
NP_001305436
NP_001305442

NP_722470

Location (UCSC)Chr 16: 88.71 – 88.72 MbChr 8: 123.2 – 123.21 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000174177Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000049482Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: C16orf84". 24 December 2015.
  6. ^ "NCBI protein: cytoplasmic tRNA 2-thiolation protein 2 isoform 1".
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Further reading

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