Annotation Detail for AIDA

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Basic Information Top

Gene Symbol:	AIDA ( C1orf80,FLJ12806,FLJ32421,RP11-378J18.7 )
Gene Full Name:	axin interactor, dorsalization associated
Band:	1q41
Quick Links	Entrez ID:64853; OMIM: 612375; Uniprot ID:AIDA_HUMAN; ENSEMBL ID: ENSG00000186063; HGNC ID: 25761
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
144	Phosphoserine.

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

RefSeq ID: NM_022831
Location:chr1 220908450-220952438
strand:-

Upstream the gene:0 results
Downstream the gene:2 results
Inside the gene:11 results

Transcrip Factors	Experimental Cell	Database	TF Binding Start	TF Binding End	TF Binding Length	The Distance to Gene
CTCF	CD4	GSE12889	220894789	220895056	267	13528
CTCF	CD4	SISSRdata	220894789	220895056	267	13528

Transcrip Factors	Experimental Cell	Database	TF Binding Start	TF Binding End	TF Binding Length	The Distance to Gene
CTCF	G2	GSE9613	220940035	220940223	188	0
CTCF	G2	GSE9613	220951751	220952361	610	0
H3K4me3	colorectal	cancer	220951368	220951996	628	0
H3ac	HepG2	E	220951404	220952149	745	0
Myc	hES	GSE17917	220951945	220952262	317	0
Rb	shRbQuiescent	GSE19898	220951404	220951775	371	0
Rb	shRbSenescence	GSE19898	220951443	220951776	333	0
TFAP2C	MCF7	GSE21234	220951193	220951791	598	0
hScc1	Bcell	GSE12603	220951336	220951563	227	0
hScc1	Bcell	GSE12603	220951965	220952583	618	0
p130	shRbSenescent	GSE19898	220951851	220952135	284	0

Validated miRNA targets

Cis-Nats regulation

Cluster ID	Plue Type	Plus Gene Name	Plus Chromosome	Plus Start	Plus End	Overlap Length	Minus Type	Minus Gene Name	Minus Chromosome	Minus Star	Minus End	Type
2381	mRNA	C1orf58	chr1	219274300	219294502	174	HTC	C1orf80	chr1	219229751	219274474	Sense/Antisense (SA) pairs

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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