Annotation Detail for QRICH2

View Evidences	View Variants	View Annotations

Basic Information Top

Gene Symbol:	QRICH2 ( DKFZp434P0316 )
Gene Full Name:	glutamine rich 2
Band:	17q25.1
Quick Links	Entrez ID:84074; OMIM: NA; Uniprot ID:QRIC2_HUMAN; ENSEMBL ID: ENSG00000129646; HGNC ID: 25326
Relate to Another Database:	SFARIGene; denovo-db

Pathways, Diseases and Drugs

TF binding site

Post Translation Modification

Validated transcription factor binding site by ChIP-Chip and ChIP-Seq

RefSeq ID: NM_032134
Location:chr17 71781726-71815355
strand:-

Upstream the gene:1 results
Downstream the gene:2 results
Inside the gene:19 results

Transcrip Factors	Experimental Cell	Database	TF Binding Start	TF Binding End	TF Binding Length	The Distance to Gene
hScc1	Bcell	GSE12603	71814959	71815827	868	38

Transcrip Factors	Experimental Cell	Database	TF Binding Start	TF Binding End	TF Binding Length	The Distance to Gene
CTCF	G2	GSE9613	71781260	71781495	235	349
TFAP2C	MCF7	GSE21234	71780824	71781611	787	509

Transcrip Factors	Experimental Cell	Database	TF Binding Start	TF Binding End	TF Binding Length	The Distance to Gene
CTCF	CD4	GSE12889	71787246	71787564	318	0
CTCF	CD4	GSE12889	71806975	71807114	139	0
CTCF	CD4	SISSRdata	71787246	71787564	318	0
CTCF	CD4	SISSRdata	71806975	71807114	139	0
CTCF	G2	GSE9613	71783874	71785144	1270	0
CTCF	G2	GSE9613	71786961	71787546	585	0
CTCF	G2	GSE9613	71806592	71807103	511	0
CTCF	G2	GSE9613	71810876	71811233	357	0
GABP	Hela	GSE8489	71800051	71800837	786	0
Rb	Growing	GSE19898	71787224	71787420	196	0
TFAP2C	MCF7	GSE21234	71784338	71785121	783	0
hScc1	Bcell	GSE12603	71786461	71787720	1259	0
hScc1	Bcell	GSE12603	71806626	71807103	477	0
hScc1	Bcell	GSE12603	71810876	71811233	357	0
hScc1	CdLS	GSE12603	71786567	71787578	1011	0
hScc1	CdLS	GSE12603	71806626	71807103	477	0
hScc1	CdLS	GSE12603	71810876	71811233	357	0
hScc1	G2	GSE9613	71806592	71807103	511	0
hScc1	G2	GSE9613	71810876	71811233	357	0

Validated miRNA targets

Cis-Nats regulation

Simple Query:

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

Studies: 1,036
Genes: 1,379
CNVs/SVs: 5,420
SNVs/Indels: 11,669
de novo Mutations: 5,669
Mosaics: 789
Linkage Regions: 172

Paper Collected: 6/30/2018

Last Update: 8/26/2018

Copyright © 2017, Center for Bioinformatics , Peking University | All Rights Reserved