Detail Information of AutCNV0000379
1. Sample AND Method Top
Users can click the chromosome coordinates of "Region" label to view information in UCSC Genome Browser.
Ancestry | ADI-R | ADOS | Diagnosis | Family | Individual | Reference | |||||
---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | |||||
Not Mentioned | autism | - | - | - | - | 105 | 267 | 372 | Zwaag, 2009 | ||
Population: | - | ||||||||||
Platform: | Illumina Humanhap300 Beadchip | ||||||||||
Method: | SNP microarray | ||||||||||
Marker: | DMRTC2 | ||||||||||
Band: | 19q13.2 | ||||||||||
Evidences: | CNVs Only Present In Patients; Significant Enriched CNVs; | ||||||||||
Region: | Chr19: 38708160-43108160 (Deduced by Band) | ||||||||||
Gain/Loss: |
2. Related Syndromic Genes Top
Abbreviations: AD, autosomal dominant; AR, autosomal recessive; ASD, autism spectrum disorder; ID, intellectual disability; XL, X linked.
Gene ID | Gene Symbol | Inheritance | Evidence Level |
---|---|---|---|
No data! |
3. Related Non-syndromic Genes Top
Gene ID | Gene Symbol | Evidence Score | Total Score | |||||
---|---|---|---|---|---|---|---|---|
Low-Scale Association | GWAS | Low-Scale Single Gene | Expression | CNV | Linkage | |||
AutG478 | ATP1A3 | 0 | 0 | 0 | 1 | 1 | 0 | 23 |
AutG29950 | SERTAD1 | 0 | 0 | 0 | 3 | 1 | 0 | 5 |
AutG7538 | ZFP36 | 0 | 0 | 0 | 3 | 1 | 0 | 5 |
AutG8190 | MIA | 0 | 0 | 0 | 2 | 1 | 0 | 4 |
AutG27335 | EIF3K | 0 | 0 | 0 | 1 | 1 | 0 | 3 |
AutG56891 | LGALS14 | 0 | 0 | 0 | 1 | 1 | 0 | 3 |
AutG57731 | SPTBN4 | 0 | 0 | 0 | 1 | 1 | 0 | 3 |
AutG284339 | TMEM145 | 0 | 0 | 0 | 1 | 1 | 0 | 3 |
AutG8857 | FCGBP | 0 | 0 | 0 | 1 | 1 | 0 | 3 |
AutG645 | BLVRB | 0 | 0 | 0 | 1 | 1 | 0 | 3 |
AutG9253 | NUMBL | 0 | 0 | 0 | 1 | 1 | 0 | 3 |
AutG9138 | ARHGEF1 | 0 | 0 | 0 | 1 | 1 | 0 | 3 |