Detail Information of AutCNV0004967


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 | |||||
- | - | - | autistic | 1 | - | - | - | 2 | - | 2 | Okumura A, 2014 |
Complication: | Y | ||||||||||
Population: | - | ||||||||||
Platform: | SurePrint G3 Human CGH?+?SNP?Microarray?Kit with 180k?Oligo?arrays | ||||||||||
Method: | aCGH | ||||||||||
Marker: | - | ||||||||||
Band: | 3p14 | ||||||||||
Evidences: | CNVs Only Present In Patients; Denovo CNVs; | ||||||||||
Region: | Chr3: 60472496-67385119 | ||||||||||
Gain/Loss: | 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 | |||
AutG166336 | PRICKLE2 | 0 | 0 | 1 | 0 | 1 | 0 | 12 |
AutG55079 | FEZF2 | 0 | 2 | 0 | 1 | 1 | 0 | 11 |