Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
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 ID | Year | Title | Citations |
|---|---|---|---|
| 35320431 | 2022 | Mutations 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 |
| 35320431 | 2022 | Mutations 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 |
| 33230297 | 2020 | cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing. | 72 |
| 33230297 | 2020 | cGAS-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)
