AutismKB 2.0

Annotation Detail for F11


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Basic Information Top
Gene Symbol:F11 ( FXI,MGC141891 )
Gene Full Name: coagulation factor XI
Band: 4q35.2
Quick LinksEntrez ID:2160; OMIM: 264900; Uniprot ID:FA11_HUMAN; ENSEMBL ID: ENSG00000088926; HGNC ID: 3529
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
17Phosphoserine.
22Phosphothreonine.
90N-linked (GlcNAc...).
126N-linked (GlcNAc...).
353N-linked (GlcNAc...).
450N-linked (GlcNAc...).
491N-linked (GlcNAc...).
Location(AA) Modifications Resource
90N-linked (GlcNAc...).Swiss-Prot 53.0
126N-linked (GlcNAc...).Swiss-Prot 53.0
353N-linked (GlcNAc...).Swiss-Prot 53.0
450N-linked (GlcNAc...).Swiss-Prot 53.0
491N-linked (GlcNAc...).Swiss-Prot 53.0
Location(AA) Modification Resource
40Phosphothreonine(MAPK)HMM predict
45Phosphotyrosine(Jak)HMM predict
71O-linkedHMM predict
90N-linkedHMM predict
115Phosphotyrosine(INSR)HMM predict
115Phosphotyrosine(EGFR)HMM predict
115Phosphotyrosine(Jak)HMM predict
126N-linkedHMM predict
174Phosphothreonine(MAPK)HMM predict
353N-linkedHMM predict
355Phosphoserine(CDC2)HMM predict
394Phosphoserine(CAMK2)HMM predict
411Phosphothreonine(PKC)HMM predict
450N-linkedHMM predict
472Phosphotyrosine(Jak)HMM predict
491N-linkedHMM predict
495Phosphoserine(ATM)HMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_000128
  • Location:chr4 187424111-187447828
  • strand:+
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 187456297 187456576 279 8608
hScc1 BcellGSE12603 187455188 187455763 575 7647
hScc1 CdLSGSE12603 187455111 187455666 555 7560
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
H3ac HepG2E 187424210 187425518 1308 0
Validated miRNA targets Top
Cis-Nats regulation Top

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


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