Detail Information of AutCNV0000262

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
Ancestry	ADI-R	ADOS	Diagnosis	Total	Simplex	Multiplex	Control	Affected	Control	Total	Reference
Not Mentioned			autism	-	-	-	-	1	-	1	Pescucci, 2003
Complication:	Rett-like feature
Population:	-
Platform:	-
Method:	STS mapping
Marker:	-
Band:	2q33.3-35
Evidences:	CNVs Only Present In Patients;
Region:	Chr2: 207140599-217211052
Gain/Loss:	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
Gene ID	Gene Symbol	Low-Scale Association	GWAS	Low-Scale Single Gene	Expression	CNV	Linkage	Total Score
AutG2335	FN1	0	0	0	1	0	0	21
AutG4133	MAP2	0	0	1	0	1	0	12
AutG2066	ERBB4	0	2	0	0	0	0	8
AutG8609	KLF7	0	0	0	1	1	0	3
AutG10314	LANCL1	0	0	0	1	1	0	3
AutG5746	PTH2R	0	0	0	1	0	0	1

Simple Query:

Paper Collected: 6/30/2018

Last Update: 8/26/2018