MIAT - myocardial infarction associated transcript Gene
Also Known as RNCR2; GOMAFU; C22orf35; LINC00066; NCRNA00066; lncRNA-MIAT
Species: Homo sapiens
About MIAT
This gene has 30 transcripts (splice variants) and is associated with 1 phenotype. Biased expression in brain (RPKM 36.1), adrenal (RPKM 14.9) and 11 other tissues.
Summary
This gene encodes a spliced long non-coding RNA that may constitute a component of the nuclear matrix. Altered expression of this locus has been reported to be associated with a susceptibility to myocardial infarction. It has also been proposed that pathways involving this transcript may contribute to the pathophysiology of schizophrenia. A similar gene in mouse has been associated with retinal cell fate determination. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Dec 2014]
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Myocardial Infarction |
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| Substance Abuse |
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| Microvascular Complications Of Diabetes 5 |
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| Heroin Dependence |
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| Visual Epilepsy |
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| Stroke, Ischemic |
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| Schizophrenia |
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| Alzheimer Disease, Familial, 1 |
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| Leukemia, Chronic Lymphocytic |
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| Lung Cancer Susceptibility 3 |
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| Glioblastoma |
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| Dilated Cardiomyopathy |
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| Nervous System Disease |
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| Prostate Cancer |
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| Ovarian Cancer |
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| Gastric Cancer |
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| Lung Cancer |
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| Breast Cancer |
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| Paranoid Schizophrenia |
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| Macular Degeneration, Age-Related, 13 |
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| Retinitis Pigmentosa |
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Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Mus musculus | MIAT | MGD | MGI:2444886 |
| Rattus norvegicus | MIAT | RGD | RGD:7567380 |