Annotation Detail for DYX1C1

View Evidences	View Variants	View Annotations

Basic Information Top

Gene Symbol:	DYX1C1 ( DYX1,DYXC1,EKN1,FLJ37882,MGC70618,RD )
Gene Full Name:	dyslexia susceptibility 1 candidate 1
Band:	15q21.3
Quick Links	Entrez ID:161582; OMIM: 608706; Uniprot ID:DYXC1_HUMAN; ENSEMBL ID: ENSG00000128845; HGNC ID:
Relate to Another Database:	SFARIGene; denovo-db

Pathways, Diseases and Drugs

TF binding site

Post Translation Modification

PTM Sites from Uniprot:0 results
Experimental PTM Sites from dbPTM:0 results
Predicted PTM Sites by profile HMM from dbPTM:6 results

No data

Location(AA)	Modification	Resource
62	Phosphoserine(CK1)	HMM predict
68	N-linked	HMM predict
156	Phosphothreonine(PKA)	HMM predict
241	N-linked	HMM predict
374	Phosphothreonine(PKA)	HMM predict
389	Phosphotyrosine(EGFR)	HMM predict

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

RefSeq ID: NM_001033560
Location:chr15 53497246-53587723
strand:-

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

Transcrip Factors	Experimental Cell	Database	TF Binding Start	TF Binding End	TF Binding Length	The Distance to Gene
Oct1	H2O2-Hela	GSE14283	53499061	53499128	67	0
Oct1	Hela	GSE14283	53499064	53499128	64	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
8849	mRNA	FLJ27352	chr15	53488037	53498200	949	mRNA	DYX1C1	chr15	53497251	53577838	Non-exonic Bidirectional (NOB) 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

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