2. Gene
  3. Miat - myocardial infarction associated transcript (non-protein coding) Gene

Miat - myocardial infarction associated transcript (non-protein coding) Gene

  • Gene
  • Ortholog
Mus musculus

Also known as Rncr2; gomafu; 3632434I06; A230057G18Rik

Gene ID: 330166 | Gene type: ncRNA

About Miat

Summary

This gene encodes a spliced long non-coding RNA that may constitute a component of the nuclear matrix. This transcript has been associated with retinal cell fate determination. Altered expression of a similar gene in human has been associated with a susceptibility to myocardial infarction, and is involved in pathways that may contribute to the pathophysiology of schizophrenia. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Dec 2014]

Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
25145264 MGI
Biological Process GO Annotation Evidence Reference Source
acts upstream of or within amacrine cell differentiation IMP
IMP: Inferred from mutant phenotype
20459797 MGI
acts upstream of or within radial glial cell differentiation IMP
IMP: Inferred from mutant phenotype
20459797 MGI
acts upstream of or within retinal rod cell development IMP
IMP: Inferred from mutant phenotype
16877424 MGI
acts upstream of or within stem cell population maintenance IMP
IMP: Inferred from mutant phenotype
20026622 MGI
Cellular Component GO Annotation Evidence Reference Source
located in nuclear body IDA
IDA: Inferred from direct assay
25145264 MGI
located in nucleus IDA
IDA: Inferred from direct assay
20459797 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

Orthologs Information

Species Symbol Source ID
Homo sapiens Miat NCBI NCBI:440823