RNU7-1 (RNA, U7 small nuclear 1)

2017-09-01  

Identity

HGNC
RNU7-1
LOCATION
12p13.31
LOCUSID
100147744
ALIAS
RNU7,U7.1

Other Information

Locus ID:

NCBI: 100147744
MIM: 617876
HGNC: 34033
Ensembl: ENSG00000238923

Variants:

dbSNP: 100147744
ClinVar: 100147744
TCGA: ENSG00000238923
COSMIC: RNU7-1

RNA/Proteins

References

Pubmed IDYearTitleCitations
353204312022Mutations in RNU7-1 Weaken Secondary RNA Structure, Induce MCP-1 and CXCL10 in CSF, and Result in Aicardi-Goutières Syndrome with Severe End-Organ Involvement.6
353204312022Mutations in RNU7-1 Weaken Secondary RNA Structure, Induce MCP-1 and CXCL10 in CSF, and Result in Aicardi-Goutières Syndrome with Severe End-Organ Involvement.6
332302972020cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing.72
332302972020cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing.72

Citation

Dessen P

RNU7-1 (RNA, U7 small nuclear 1)

Atlas Genet Cytogenet Oncol Haematol. 2017-09-01

Online version: http://atlasgeneticsoncology.org/gene/79579/rnu7-1-(rna-u7-small-nuclear-1)