Evidence Details for MIAT

Basic Information
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| Gene Symbol: | MIAT ( C22orf35,FLJ25887,FLJ25967,FLJ38367,FLJ45323,GOMAFU,NCRNA00066,RNCR2 ) |
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| Gene Full Name: | myocardial infarction associated transcript (non-protein coding) |
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| Band: | 22q12.1 |
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| Quick Links | Entrez ID:440823; OMIM: 611082; Uniprot ID:; ENSEMBL ID: ; HGNC ID: 33425 |
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| Relate to Another Database: |
SFARIGene;
denovo-db |

Evidence summary
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Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default. 
Syndromic Autism Gene
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Genome-Wide Association Studies(By Ethnic Group)
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Family Based Association Studies: 0
| Reference |
Stage |
Platform |
#Families |
Affecteds |
Result |
#Subjects (% Women) |
ADI-R |
ADOS |
Diagnosis |
Age (range) |
IQ (range) |
| No Evidence. |
Case Control Based Association Studies: 0
| Reference |
Stage |
Platform |
ASD Cases |
Normal Controls |
Result |
#Subjects (% Women) |
ADI-R |
ADOS |
Diagnosis |
Age (range) |
IQ |
#Subjects (% Women) |
Age (range) |
| No Evidence. |

CNV Studies
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| Reference |
Source |
Method |
ADI-R |
ADOS |
Diagnosis |
Family |
Individual |
| Total |
Simplex |
Multiplex |
Control |
Affected |
Control |
Total |
| No matched CNVs ! |

Linkage Studies
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