AutismKB 2.0

Annotation Detail for AFM


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Basic Information Top
Gene Symbol:AFM ( ALB2,ALBA,ALF,MGC125338,MGC125339 )
Gene Full Name: afamin
Band: 4q13.3
Quick LinksEntrez ID:173; OMIM: 104145; Uniprot ID:AFAM_HUMAN; ENSEMBL ID: ENSG00000079557; HGNC ID: 316
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
33N-linked (GlcNAc...).
109N-linked (GlcNAc...) (complex).
383N-linked (GlcNAc...) (complex).
402N-linked (GlcNAc...) (complex).
488N-linked (GlcNAc...).
Location(AA) Modifications Resource
33N-linked (GlcNAc...).Swiss-Prot 53.0
109N-linked (GlcNAc...) (Potential).Swiss-Prot 53.0
402N-linked (GlcNAc...).Swiss-Prot 53.0
488N-linked (GlcNAc...).Swiss-Prot 53.0
Location(AA) Modification Resource
33N-linkedHMM predict
45Phosphotyrosine(INSR)HMM predict
109N-linkedHMM predict
157Phosphoserine(CK1)HMM predict
191Phosphoserine(IKK)HMM predict
212Phosphotyrosine(Jak)HMM predict
219Phosphotyrosine(EGFR)HMM predict
264Phosphoserine(CK1)HMM predict
294Phosphoserine(IKK)HMM predict
334Phosphothreonine(CK2)HMM predict
402N-linkedHMM predict
488N-linkedHMM predict
492N-linkedHMM predict
519Phosphotyrosine(Jak)HMM predict
519Phosphotyrosine(Syk)HMM predict
562Phosphothreonine(CK2)HMM predict
582LysineHMM predict
586ProlineHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_001133
  • Location:chr4 74566325-74588580
  • strand:+
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
Oct1 HelaGSE14283 74590706 74590737 31 2141
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
Oct1 H2O2-HelaGSE14283 74575876 74575909 33 0
Oct1 H2O2-HelaGSE14283 74584666 74584693 27 0
Oct1 HelaGSE14283 74575876 74575910 34 0
Oct1 HelaGSE14283 74584666 74584694 28 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