AutismKB 2.0

Annotation Detail for SNRPN


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Basic Information Top
Gene Symbol:SNRPN ( DKFZp686C0927,DKFZp686M12165,DKFZp761I1912,DKFZp762N022,FLJ33569,FLJ36996,FLJ39265,HCERN3,MGC29886,PWCR,RT-LI,SM-D,SMN,SNRNP-N,SNURF-SNRPN )
Gene Full Name: small nuclear ribonucleoprotein polypeptide N
Band: 15q11.2
Quick LinksEntrez ID:6638; OMIM: 182279; Uniprot ID:RSMN_HUMAN; ENSEMBL ID: ENSG00000128739; HGNC ID: 11164
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
8N6-acetyllysine.
Location(AA) Modifications Resource
Location(AA) Modification Resource
108MethylarginineHMM predict
112MethylarginineHMM predict
138Phosphoserine(ATM)HMM predict
158O-linkedHMM predict
160O-linkedHMM predict
160O-linkedHMM predict
172MethylarginineHMM predict
174Phosphothreonine(CDK)HMM predict
181MethylarginineHMM predict
183Phosphothreonine(MAPK)HMM predict
211Phosphothreonine(CDC2)HMM predict
236ArginineHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_022805
  • Location:chr15 22652790-22774821
  • strand:+
No data
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CBP T0-glioblastomaGSE21026 22723442 22724081 639 0
ER E2-MCF7GSE14664 22678979 22679012 33 0
ER Fulvestrant-MCF7GSE14664 22689676 22689714 38 0
H3ac HepG2E 22674111 22674479 368 0
H3ac HepG2E 22707072 22707320 248 0
Nanog hESGSE18292 22747374 22747815 441 0
Oct1 H2O2-HelaGSE14283 22707021 22707058 37 0
Oct1 H2O2-HelaGSE14283 22728467 22728497 30 0
Oct1 HelaGSE14283 22658932 22658974 42 0
Oct1 HelaGSE14283 22728467 22728520 53 0
Oct4 hESGSE17917 22652698 22652976 278 0
P300 T0-glioblastomaGSE21026 22723554 22723872 318 0
TAF HelaGSE8489 22691680 22692475 795 0
TAF HelaGSE8489 22707072 22707376 304 0
USF1 HepG2E 22674111 22674613 502 0
USF2 HepG2E 22674111 22674479 368 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