Evidence Details for ANKRD20A5

Basic Information
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Gene Symbol: | ANKRD20A5 ( MGC26718 ) |
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Gene Full Name: | ankyrin repeat domain 20 family, member A5 |
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Band: | 18p11.21 |
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Quick Links | Entrez ID:440482; OMIM: NA; Uniprot ID:; ENSEMBL ID: ; HGNC ID: |
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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 |
Gai, 2011 |
AGRE |
SNP microarray | - | - | autism |
- |
- |
- |
- |
1224 |
3801 |
5025 |

Linkage Studies
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Reference |
Source |
Method |
ADI-R |
ADOS |
Diagnosis |
Family |
Individual |
Total |
Simplex |
Multiplex |
Control |
Affected |
Control |
Total |
No Matched Linkage Regions ! |

Low Scale Association Studies (by Ethnic Group)
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Family Based Association Studies: 0
Reference |
Source |
Platform |
#Families |
Affecteds |
Result |
#Subjects (% Women) |
ADI-R |
ADOS |
Diagnosis |
Age (range) |
IQ (range) |
No Evidence. |
Case Control Based Association Studies: 0
Reference |
Source |
Platfrom |
ASD Cases |
Normal Controls |
Result |
ADI-R |
ADOS |
Diagnosis |
Age (range) |
IQ |
#Subjects (% Women) |
Age (range) |
No Evidence. |

Large Scale Expression Studies
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Microarray Studies: 1
Reference |
Source |
Tissue |
#Subjects (% Women) |
ADI-R |
ADOS |
Endo- pheno |
Diagnosis |
Normal Controls (% Women) |
Fold Change |
Up/ Down |
P/Q value |
Voineagu, 2011_1 |
Unknown |
16 frontal cortex(BA9) and 13 temporal cortex(BA41 |
16 (25.00%) |  |  | - | autism |
16 (6.25%) |
0.852133 |
Down |
10.35 | |
- Platform: Illumina Ref8 v3 microarrays
- ProbeSet: ILMN_1690304
- RefSeq_ID/ EST: -
- GEO_ID: GSE28521
- Statistic Method: SAM package and unless otherwise specified the significance threshold was FDR,0.05 and fold changes.1.3.
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Proteomics Studies:0
Reference |
Source |
Tissue |
Platform |
#Subjects (% Women) |
ADI-R |
ADOS |
Diagnosis |
Normal Controls(% Women) |
No Evidence. |

NGS
de novo Mutation Studies
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Reference |
Case Number |
Family Number |
de novo Number |
Title |
No matched NGS de novo Mutation Studies! |

NGS Mosaic SNV Studies
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Reference |
Case Number |
Family Number |
Mosaic Number |
Title |
No matched NGS Mosaic SNVs! |

NGS Other Studies
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Reference |
Source |
Platform |
ADI-R |
ADOS |
Diagnosis |
Family |
Affected |
Validation Method |
Total |
Simplex |
Multiplex |
No matched NGS Other Studies! |

Low Scale Gene Studies
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Abbreviations: AD, autistic disorder; ASD: autism spectrum disorder.
Reference |
Organism |
Tissue |
ADI-R |
ADOS |
Diagnosis |
Evidence Level |
Result |
No Evidence. |
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