AutismKB 2.0

Annotation Detail for CSRNP2


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Basic Information Top
Gene Symbol:CSRNP2 ( C12orf2,C12orf22,FAM130A1,FLJ25576,TAIP-12 )
Gene Full Name: cysteine-serine-rich nuclear protein 2
Band: 12q13.12
Quick LinksEntrez ID:81566; OMIM: NA; Uniprot ID:CSRN2_HUMAN; ENSEMBL ID: ENSG00000110925; HGNC ID: 16006
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_030809
  • Location:chr12 49741256-49763599
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
ETS1 JurkatGSE17954 49763200 49764085 885 43
FOXA1 MCF7GSE15244 49765705 49766467 762 2487
KLF4 hESGSE17917 49763424 49763825 401 25
P300 T0-glioblastomaGSE21026 49763193 49764139 946 67
RARA MCF7GSE15244 49765666 49766467 801 2467
Rb SenescentGSE19898 49763621 49763995 374 209
p130 QuiescentGSE19898 49763526 49763884 358 106
p130 SenescentGSE19898 49763597 49764029 432 214
p130 shRbSenescentGSE19898 49763564 49764004 440 185
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 49763118 49763914 796 0
GATA3 MCF7GSE15244 49756125 49756666 541 0
GATA3 MCF7GSE15244 49757018 49758570 1552 0
H3K4me2 HCT116GSE10453 49761969 49763156 1187 0
H3K4me3 colorectalcancer 49762217 49762967 750 0
H3ac HepG2E 49761906 49763082 1176 0
NRSF pAbJurkat 49762866 49763329 463 0
P300 T30-glioblastomaGSE21026 49762420 49764230 1810 0
RARA MCF7GSE15244 49762313 49762722 409 0
Rb SenescentGSE19898 49762704 49763011 307 0
Rb shRbQuiescentGSE19898 49762758 49763016 258 0
TAF HelaGSE8489 49761939 49762901 962 0
USF1 HepG2E 49750041 49750530 489 0
hScc1 BcellGSE12603 49762930 49763463 533 0
hScc1 G2GSE9613 49762535 49764056 1521 0
p130 QuiescentGSE19898 49762963 49763251 288 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