1. Catalog
  2. Nodes
  3. g(HGNC:MIR196A1)

g(HGNC:MIR196A1)

Orthologies: 0 | Equivalencies: 0 | Classes: 0 | Children: 0 | Explore

Entity

Name
MIR196A1
Namespace
hgnc
Namespace Version
20190224
Namespace URL
https://raw.githubusercontent.com/pharmacome/terminology/efc856fb009a39e4d284269a6801f79ed3d3cf56/external/hgnc-names.belns

Appears in Networks 1

New insights into the role of microRNAs and long noncoding RNAs in most common neurodegenerative diseases v1.0.0

In-Edges 2

path(MESH:"Huntington Disease") association g(HGNC:MIR196A1) View Subject | View Object

A case in point is miR‐196a that affects HD PubMed:30663117

Appears in Networks:
Annotations
MeSH
Huntington Disease

path(MESH:"Huntington Disease") increases g(HGNC:MIR196A1) View Subject | View Object

Currently, miR‐10b‐5p, miR‐196a‐5p, miR‐196b‐ 5p, miR‐615‐3p, and miR‐1247‐5p increase in HD, and studies have shown that miR‐196a‐5p, miR‐196b‐5p, and miR‐615‐3p have been almost zero in the control group PubMed:30663117

Appears in Networks:
Annotations
MeSH
Huntington Disease

Out-Edges 1

g(HGNC:MIR196A1) association path(MESH:"Huntington Disease") View Subject | View Object

A case in point is miR‐196a that affects HD PubMed:30663117

Appears in Networks:
Annotations
MeSH
Huntington Disease

About

BEL Commons is developed and maintained in an academic capacity by Charles Tapley Hoyt and Daniel Domingo-Fernández at the Fraunhofer SCAI Department of Bioinformatics with support from the IMI project, AETIONOMY. It is built on top of PyBEL, an open source project. Please feel free to contact us here to give us feedback or report any issues. Also, see our Publishing Notes and Data Protection information.

If you find BEL Commons useful in your work, please consider citing: Hoyt, C. T., Domingo-Fernández, D., & Hofmann-Apitius, M. (2018). BEL Commons: an environment for exploration and analysis of networks encoded in Biological Expression Language. Database, 2018(3), 1–11.