MIR137HG Gene

Name MIR137 host gene
Description Predicted to be involved in miRNA-mediated post-transcriptional gene silencing. Predicted to be part of RISC complex. [provided by Alliance of Genome Resources, Mar 2025]
Summary
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nMIR137HG, the host gene for microRNA‐137, has emerged as an important contributor to neurodevelopmental and neuropsychiatric processes. Variants such as rs1625579 have been implicated in schizophrenia, where they modulate brain structural phenotypes. For instance, one study reported that schizophrenia patients homozygous for the risk allele showed decreased gray matter concentration in occipital, parietal, and temporal lobes when combined with a higher genetic risk score from miR‐137–regulated genes, suggesting that alterations in miR‐137 biogenesis might underlie gray matter loss."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " In a related investigation, carriers of the MIR137HG risk allele in schizophrenia exhibited attenuated reduction in mid‐posterior corpus callosum volume, implying that MIR137HG influences brain morphology through mechanisms distinct from those typically producing callosal atrophy."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": " Complementary functional imaging studies in healthy adults have demonstrated that risk allele homozygotes show less deactivation of the posterior cingulate cortex, reduced connectivity with anterior cingulate and medial prefrontal regions, and decreased white matter integrity of the posterior cingulum during working memory tasks, thereby linking MIR137HG variation to alterations in neural network connectivity."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": " Furthermore, altered peripheral expression levels of MIR137HG have been observed in schizophrenia, with modest diagnostic discrimination between patients and controls, supporting its potential role as a biomarker."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond neuropsychiatric contexts, MIR137HG has been explored in several non‐psychiatric disorders. In periodontitis, although several long noncoding RNAs were analyzed, MIR137HG expression did not differ significantly between patients and healthy individuals."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": " In gastric cancer, preliminary work is underway to elucidate the function and underlying mechanisms of MIR137HG, although its precise role remains to be determined."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": " Genetic studies have also associated MIR137HG polymorphisms with musculoskeletal complications, as variants in this gene were linked to increased risk of alcohol-induced osteonecrosis of the femoral head."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "7"}]}, {"type": "t", "text": " Moreover, other investigations have identified a specific MIR137HG single-nucleotide polymorphism (rs7554283) that appears to confer a protective effect against high-altitude pulmonary edema in the Chinese population."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "8"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "C Wright, C N Gupta, J Chen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Polymorphisms in MIR137HG and microRNA-137-regulated genes influence gray matter structure in schizophrenia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Transl Psychiatry (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/tp.2015.211"}], "href": "https://doi.org/10.1038/tp.2015.211"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26836412"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26836412"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Veena S Patel, Sinead Kelly, Carrie Wright, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MIR137HG risk variant rs1625579 genotype is related to corpus callosum volume in schizophrenia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Neurosci Lett (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.neulet.2015.06.039"}], "href": "https://doi.org/10.1016/j.neulet.2015.06.039"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26123324"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26123324"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Zhifang Zhang, Tongjun Yan, Yanyan Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Polymorphism in schizophrenia risk gene "}, {"type": "a", "children": [{"type": "t", "text": "i"}], "href": "i"}, {"type": "t", "text": "MIR137"}, {"type": "a", "children": [{"type": "t", "text": "/i"}], "href": "/i"}, {"type": "t", "text": " is associated with the posterior cingulate Cortex's activation and functional and structural connectivity in healthy controls."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Neuroimage Clin (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.nicl.2018.03.039"}], "href": "https://doi.org/10.1016/j.nicl.2018.03.039"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30035013"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30035013"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Elham Badrlou, Soudeh Ghafouri-Fard, Mir Davood Omrani, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Expression of BDNF-Associated lncRNAs in Treatment-Resistant Schizophrenia Patients."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Mol Neurosci (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s12031-020-01772-9"}], "href": "https://doi.org/10.1007/s12031-020-01772-9"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33403596"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33403596"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Arezou Sayad, Soudeh Ghafouri-Fard, Bahareh Shams, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Blood and tissue levels of lncRNAs in periodontitis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Physiol (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/jcp.29764"}], "href": "https://doi.org/10.1002/jcp.29764"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32372456"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32372456"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Yantao Du, Yichen Chen, Tao Wu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "miR-2682-3p antagonizes its host lncRNA-MIR137HG by interacting with the same target FUS to regulate the progression of gastric cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "BMC Cancer (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/s12885-022-09740-9"}], "href": "https://doi.org/10.1186/s12885-022-09740-9"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35733138"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35733138"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Yongchang Guo, Yuju Cao, Xiaoyan Feng, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The effects of MIR137HG genetic polymorphisms on the susceptibility of alcohol-induced osteonecrosis of the femoral head in a Chinese male population."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Gene (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.gene.2021.145902"}], "href": "https://doi.org/10.1016/j.gene.2021.145902"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34403773"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34403773"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Shilin Xu, Xuemei Li, Xuguang Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Impact of "}, {"type": "a", "children": [{"type": "t", "text": "i"}], "href": "i"}, {"type": "t", "text": "MIR137HG"}, {"type": "a", "children": [{"type": "t", "text": "/i"}], "href": "/i"}, {"type": "t", "text": " rs7554283 on susceptibility to high-altitude pulmonary edema in the Chinese population."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Per Med (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/17410541.2024.2406738"}], "href": "https://doi.org/10.1080/17410541.2024.2406738"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "39439230"}], "href": "https://pubmed.ncbi.nlm.nih.gov/39439230"}]}]}]}
NCBI Gene ID 400765
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Download Associations
Predicted Functions View MIR137HG's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR137HG's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR137HG's ARCHS4 Predicted Functions.

Functional Associations

MIR137HG has 515 functional associations with biological entities spanning 4 categories (disease, phenotype or trait, chemical, cell line, cell type or tissue, gene, protein or microRNA) extracted from 20 datasets.

Click the + buttons to view associations for MIR137HG from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles tissues with high or low expression of MIR137HG gene relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray tissue samples with high or low expression of MIR137HG gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq tissue samples with high or low expression of MIR137HG gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles tissues with high or low expression of MIR137HG gene relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
CCLE Cell Line Gene CNV Profiles cell lines with high or low copy number of MIR137HG gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset.
COSMIC Cell Line Gene CNV Profiles cell lines with high or low copy number of MIR137HG gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
GEO Signatures of Differentially Expressed Genes for Diseases disease perturbations changing expression of MIR137HG gene from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
GEO Signatures of Differentially Expressed Genes for Gene Perturbations gene perturbations changing expression of MIR137HG gene from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
GEO Signatures of Differentially Expressed Genes for Kinase Perturbations kinase perturbations changing expression of MIR137HG gene from the GEO Signatures of Differentially Expressed Genes for Kinase Perturbations dataset.
GEO Signatures of Differentially Expressed Genes for Small Molecules small molecule perturbations changing expression of MIR137HG gene from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
GEO Signatures of Differentially Expressed Genes for Transcription Factor Perturbations transcription factor perturbations changing expression of MIR137HG gene from the GEO Signatures of Differentially Expressed Genes for Transcription Factor Perturbations dataset.
GTEx Tissue Gene Expression Profiles tissues with high or low expression of MIR137HG gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.
GWAS Catalog SNP-Phenotype Associations phenotypes associated with MIR137HG gene in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
GWASdb SNP-Disease Associations diseases associated with MIR137HG gene in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
GWASdb SNP-Phenotype Associations phenotypes associated with MIR137HG gene in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
HuBMAP Azimuth Cell Type Annotations cell types associated with MIR137HG gene from the HuBMAP Azimuth Cell Type Annotations dataset.
HuGE Navigator Gene-Phenotype Associations phenotypes associated with MIR137HG gene by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles cell lines with high or low copy number of MIR137HG gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset.
MotifMap Predicted Transcription Factor Targets transcription factors regulating expression of MIR137HG gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset.
Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles cell types and tissues with high or low DNA methylation of MIR137HG gene relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset.