AutismKB 2.0

Annotation Detail for PRRX1


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Basic Information Top
Gene Symbol:PRRX1 ( PHOX1,PMX1,PRX1 )
Gene Full Name: paired related homeobox 1
Band: 1q24.2
Quick LinksEntrez ID:5396; OMIM: 167420; Uniprot ID:PRRX1_HUMAN; ENSEMBL ID: ENSG00000116132; HGNC ID: 9142
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
197Phosphoserine (Potential).
235OAR.
Location(AA) Modifications Resource
197Phosphoserine (Potential).Swiss-Prot 53.0
Location(AA) Modification Resource
21Phosphoserine(CAMK2)HMM predict
33N-linkedHMM predict
76Phosphothreonine(CDK)HMM predict
76Phosphothreonine(MAPK)HMM predict
97N-linkedHMM predict
99Phosphothreonine(PKA)HMM predict
102N-linkedHMM predict
132N-linkedHMM predict
197O-linkedHMM predict
197Phosphoserine(CDC2)HMM predict
197Phosphoserine(CDK)HMM predict
204O-linkedHMM predict
211N-linkedHMM predict
212N-linkedHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_006902
  • Location:chr1 168899936-168975163
  • strand:+
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
H3K27me3 colorectalcancer 168896569 168897157 588 3074
H3K27me3 colorectalcancer 168897529 168899522 1993 1411
hScc1 BcellGSE12603 168897127 168897413 286 2667
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CBP T30-glioblastomaGSE21026 168943756 168944238 482 0
CTCF G2GSE9613 168900071 168900278 207 0
Oct1 HelaGSE14283 168974992 168975035 43 0
P300 T30-glioblastomaGSE21026 168943502 168944523 1021 0
hScc1 BcellGSE12603 168907132 168907425 293 0
hScc1 BcellGSE12603 168925212 168925483 271 0
hScc1 CdLSGSE12603 168906913 168907530 617 0
hScc1 CdLSGSE12603 168925112 168925823 711 0
p63 keratinocytesGSE17611 168932435 168933140 705 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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