AutismKB 2.0

Annotation Detail for PEX7


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Basic Information Top
Gene Symbol:PEX7 ( PTS2R,RCDP1,RD )
Gene Full Name: peroxisomal biogenesis factor 7
Band: 6q23.3
Quick LinksEntrez ID:5191; OMIM: 601757; Uniprot ID:PEX7_HUMAN; ENSEMBL ID: ENSG00000112357; HGNC ID: 8860
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
No data
No data
Location(AA) Modification Resource
14Phosphothreonine(MAPK)HMM predict
20Phosphotyrosine(Syk)HMM predict
116Phosphoserine(CK1)HMM predict
161O-linkedHMM predict
175Phosphoserine(IKK)HMM predict
251Phosphoserine(CDC2)HMM predict
271N-linkedHMM predict
277Phosphoserine(IKK)HMM predict
311IsoleucineHMM predict
320ThreonineHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_000288
  • Location:chr6 137185415-137276751
  • strand:+
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
P300 T0-glioblastomaGSE21026 137184969 137185823 854 20
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 137208958 137209159 201 0
CTCF CD4SISSRdata 137208958 137209159 201 0
CTCF G2GSE9613 137185234 137186077 843 0
Fos K562GSE19551 137184965 137185925 960 0
FoxA1 MCF7MACSdata 137252708 137252976 268 0
P300 T30-glioblastomaGSE21026 137184939 137185920 981 0
PAX3-FKHR Rh4GSE19063 137251742 137252737 995 0
PHF8 HeLaGSE20725 137184873 137186379 1506 0
PHF8 Hs68minusFBSGSE20725 137184951 137186076 1125 0
hScc1 BcellGSE12603 137185314 137186077 763 0
hScc1 CdLSGSE12603 137208866 137209122 256 0
Validated miRNA targets Top
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
23222 mRNA PEX7 chr6 137185415 137276752 847 HTC chr6 137263065 137263912 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