Detail Information of AutCNV0000363


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: | NANOGP1 | ||||||||||
Band: | 12p13.31 | ||||||||||
Evidences: | CNVs Only Present In Patients; Significant Enriched CNVs; | ||||||||||
Region: | Chr12: 5429739-10108733 (Deduced by Band) | ||||||||||
Gain/Loss: |


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! |


Gene ID | Gene Symbol | Evidence Score | Total Score | |||||
---|---|---|---|---|---|---|---|---|
Low-Scale Association | GWAS | Low-Scale Single Gene | Expression | CNV | Linkage | |||
AutG4908 | NTF3 | 1 | 0 | 2 | 0 | 1 | 0 | 24 |
AutG283316 | CD163L1 | 0 | 0 | 0 | 1 | 1 | 0 | 21 |
AutG79923 | NANOG | 0 | 1 | 0 | 0 | 1 | 0 | 6 |
AutG9976 | CLEC2B | 0 | 0 | 0 | 3 | 1 | 0 | 5 |
AutG6843 | VAMP1 | 0 | 0 | 0 | 2 | 1 | 0 | 4 |
AutG928 | CD9 | 0 | 0 | 0 | 1 | 1 | 0 | 3 |
AutG55080 | TAPBPL | 0 | 0 | 0 | 1 | 1 | 0 | 3 |
AutG2026 | ENO2 | 0 | 0 | 0 | 1 | 1 | 0 | 3 |
AutG969 | CD69 | 0 | 0 | 0 | 1 | 1 | 0 | 3 |
AutG7132 | TNFRSF1A | 0 | 0 | 0 | 1 | 1 | 0 | 3 |
AutG2 | A2M | 0 | 0 | 0 | 1 | 1 | 0 | 3 |
AutG51348 | KLRF1 | 0 | 0 | 0 | 1 | 1 | 0 | 3 |