AutismKB 2.0

Annotation Detail for HYLS1


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Basic Information Top
Gene Symbol:HYLS1 ( FLJ32915,HLS )
Gene Full Name: hydrolethalus syndrome 1
Band: 11q24.2
Quick LinksEntrez ID:219844; OMIM: 610693; Uniprot ID:HYLS1_HUMAN; ENSEMBL ID: ENSG00000198331; HGNC ID: 26558
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
No data
No data
Location(AA) Modification Resource
83Phosphoserine(IKK)HMM predict
116Phosphoserine(CK1)HMM predict
120Phosphoserine(CK1)HMM predict
120Phosphoserine(IKK)HMM predict
160Phosphotyrosine(Syk)HMM predict
194Phosphoserine(IKK)HMM predict
293ProlineHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_145014
  • Location:chr11 125258718-125275748
  • strand:+
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 125249716 125250028 312 8847
CTCF CD4SISSRdata 125249716 125250028 312 8847
Myc K562GSE19551 125249706 125249885 179 8923
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
FOXA1 DLD1GSE12801 125267120 125267896 776 0
Fos K562GSE19551 125262460 125262996 536 0
PHF8 HeLaGSE20725 125262592 125263462 870 0
PHF8 Hs68minusFBSGSE20725 125262634 125263432 798 0
PHF8 Hs68plusFBSGSE20725 125262526 125263420 894 0
hScc1 BcellGSE12603 125262057 125262522 465 0
hScc1 CdLSGSE12603 125262057 125262634 577 0
Validated miRNA targets Top
Micro RNA Name Stem Loop Name The chromosome that miRNA located Publication
hsa-miR-155 hsa-mir-155 21 16041695
hsa-miR-155* hsa-mir-155 21 16041695
No data
Cis-Nats regulation Top
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
5391 mRNA HYLS1 chr11 125258718 125275749 7159 mRNA PUS3 chr11 125268590 125278315 Non-exonic Bidirectional (NOB) pairs

Simple Query:


  (e.g. CHD8)

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