Detail Information of AutLD0000119


Ancestry | ADI-R | ADOS | Diagnosis | Family | Individual | Reference | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Caucasion | ![]() | ![]() | ASD | 133 | - | 133 | - | 280 | - | - | Spence, 2006 | |
Endophenotype: | proband phrase and word speech delay | |||||||||||
Country: | USA | |||||||||||
Marker Number: | 335 | |||||||||||
Platform: | - | |||||||||||
Method: | microsatellite-based genomic screen | |||||||||||
Software Algorithm: | Genehunter | |||||||||||
Band: | 19q13.33-13.41 | |||||||||||
Marker: | - | |||||||||||
Region: | Chr19: 53800000 - 59100000 |


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 | |||
AutG79784 | MYH14 | 0 | 0 | 0 | 1 | 1 | 1 | 13 |
AutG4909 | NTF4 | 1 | 0 | 0 | 0 | 1 | 1 | 6 |
AutG5582 | PRKCG | 0 | 0 | 0 | 1 | 1 | 1 | 5 |
AutG3972 | LHB | 0 | 0 | 0 | 2 | 1 | 1 | 4 |
AutG4818 | NKG7 | 0 | 0 | 0 | 2 | 1 | 1 | 4 |
AutG54922 | RASIP1 | 0 | 0 | 0 | 1 | 1 | 1 | 3 |
AutG5518 | PPP2R1A | 0 | 0 | 0 | 1 | 1 | 1 | 3 |
AutG170958 | ZNF525 | 0 | 0 | 0 | 1 | 1 | 1 | 3 |
AutG2512 | FTL | 0 | 0 | 0 | 1 | 1 | 1 | 3 |
AutG90338 | ZNF160 | 0 | 0 | 0 | 1 | 1 | 1 | 3 |
AutG91663 | MYADM | 0 | 0 | 0 | 1 | 1 | 1 | 3 |