C8ORF37-AS1 Gene

Name C8orf37 antisense RNA 1
Summary
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n Although the precise biological role of C8orf37‐AS1 remains to be fully defined, recent work in diverse settings has begun to illuminate its potential functions as a regulatory long noncoding RNA. In one study addressing siRNA target specificity in a familial form of multiple synostosis syndrome type 4, a previously unknown noncoding transcript—now identified as C8orf37‐AS1—was found to overlap a critical gene set, suggesting that mis‐regulation of this lncRNA may perturb developmental gene networks."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " In addition, large‐scale profiling of long noncoding RNAs under different socio‐environmental and aging conditions has revealed that transcripts such as C8orf37‐AS1 can be sensitive to both age and environmental stresses, implying a role in maintaining cellular homeostasis over the lifespan."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": " Furthermore, studies investigating genomic instability and complex genetic traits in disease contexts (for example, retrotransposition in esophageal carcinomas and immune biomarker associations in psychiatric disorders) reinforce the notion that noncoding RNAs play unexpected and multifaceted roles in human pathology."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": " Collectively, these findings support a model in which C8orf37‐AS1 acts as a regulatory molecule—perhaps operating in cis to influence neighboring gene expression—and may contribute, directly or indirectly, to developmental and age‐related pathologies. Further investigation is needed to clarify its molecular partners and downstream pathways.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Zhiming Fang, Zhongming Zhao, Valsamma Eapen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "siRNA Mediate RNA Interference Concordant with Early On-Target Transient Transcriptional Interference."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Genes (Basel) (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3390/genes12081290"}], "href": "https://doi.org/10.3390/genes12081290"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34440463"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34440463"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Nicole Noren Hooten, Michele K Evans "}, {"type": "b", "children": [{"type": "t", "text": "Age and poverty status alter the coding and noncoding transcriptome."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Aging (Albany NY) (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.18632/aging.101823"}], "href": "https://doi.org/10.18632/aging.101823"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30779705"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30779705"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Tara T Doucet-O'Hare, Reema Sharma, Nemanja Rodić, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Somatically Acquired LINE-1 Insertions in Normal Esophagus Undergo Clonal Expansion in Esophageal Squamous Cell Carcinoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Mutat (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/humu.23027"}], "href": "https://doi.org/10.1002/humu.23027"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27319353"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27319353"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Ruyue Zhang, Jie Song, Anniella Isgren, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Genome-wide study of immune biomarkers in cerebrospinal fluid and serum from patients with bipolar disorder and controls."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Transl Psychiatry (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41398-020-0737-6"}], "href": "https://doi.org/10.1038/s41398-020-0737-6"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32066700"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32066700"}]}]}]}
Synonyms C8orf37-AS1
NCBI Gene ID 100616530
API
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Predicted Functions View C8ORF37-AS1's ARCHS4 Predicted Functions.
Co-expressed Genes View C8ORF37-AS1's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View C8ORF37-AS1's ARCHS4 Predicted Functions.

Functional Associations

C8ORF37-AS1 has 145 functional associations with biological entities spanning 1 categories (cell line, cell type or tissue) extracted from 2 datasets.

Click the + buttons to view associations for C8ORF37-AS1 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CCLE Cell Line Gene CNV Profiles cell lines with high or low copy number of C8ORF37-AS1 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset.
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles cell lines with high or low copy number of C8ORF37-AS1 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset.