Annotation Detail for CUL9

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Basic Information Top

Gene Symbol:	CUL9 ( DKFZp686G1042,DKFZp686P2024,H7AP1,PARC,RP3-330M21.2 )
Gene Full Name:	cullin 9
Band:	6p21.1
Quick Links	Entrez ID:23113; OMIM: 607489; Uniprot ID:CUL9_HUMAN; ENSEMBL ID: ENSG00000112659; HGNC ID: 15982
Relate to Another Database:	SFARIGene; denovo-db

Pathways, Diseases and Drugs

TF binding site

Post Translation Modification

PTM Sites from Uniprot:1 results
Experimental PTM Sites from dbPTM:0 results
Predicted PTM Sites by profile HMM from dbPTM:0 results

Location(AA)	Modification
947	Phosphoserine.

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

RefSeq ID: NM_015089
Location:chr6 43257899-43300301
strand:+

Upstream the gene:6 results
Downstream the gene:0 results
Inside the gene:13 results

Transcrip Factors	Experimental Cell	Database	TF Binding Start	TF Binding End	TF Binding Length	The Distance to Gene
CTCF	G2	GSE9613	43257543	43257806	263	225
ETS1	Jurkat	GSE17954	43257290	43258351	1061	79
H3ac	HepG2	E	43256381	43259352	2971	33
Myc	hES	GSE17917	43257778	43258008	230	7
P300	T0-glioblastoma	GSE21026	43257493	43258200	707	53
hScc1	Bcell	GSE12603	43257543	43257918	375	169

Transcrip Factors	Experimental Cell	Database	TF Binding Start	TF Binding End	TF Binding Length	The Distance to Gene
CBP	T30-glioblastoma	GSE21026	43300035	43300439	404	0
CTCF	G2	GSE9613	43276373	43276587	214	0
CTCF	G2	GSE9613	43279426	43279720	294	0
CTCF	G2	GSE9613	43296297	43296994	697	0
CTCF	G2	GSE9613	43298379	43298628	249	0
CTCF	G2	GSE9613	43298934	43299394	460	0
H3K4me3	colorectal	cancer	43258490	43258965	475	0
NFkBII	GM10847	GSE19485	43299540	43300732	1192	0
NFkBII	GM12878	GSE19485	43299414	43300854	1440	0
NFkBII	GM18505	GSE19485	43299642	43300745	1103	0
PHF8	293T	GSE20725	43257452	43258416	964	0
PHF8	HeLa	GSE20725	43257371	43258427	1056	0
TAF	k562	GSE8489	43258426	43259244	818	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

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