AutismKB 2.0

Annotation Detail for PARVG


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Basic Information Top
Gene Symbol:PARVG ( - )
Gene Full Name: parvin, gamma
Band: 22q13.31
Quick LinksEntrez ID:64098; OMIM: 608122; Uniprot ID:PARVG_HUMAN; ENSEMBL ID: ENSG00000138964; HGNC ID: 14654
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
No data
No data
Location(AA) Modification Resource
25Phosphoserine(CK1)HMM predict
32Phosphotyrosine(Syk)HMM predict
55N-linkedHMM predict
107Phosphothreonine(PKA)HMM predict
155Phosphoserine(CK1)HMM predict
262Phosphotyrosine(Syk)HMM predict
262Phosphotyrosine(Jak)HMM predict
267Phosphoserine(CDC2)HMM predict
267Phosphoserine(IKK)HMM predict
274N-linkedHMM predict
293Phosphoserine(CDC2)HMM predict
305Phosphothreonine(PKC)HMM predict
319LysineHMM predict
326ProlineHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_022141
  • Location:chr22 42908189-42933866
  • strand:+
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
hScc1 BcellGSE12603 42945317 42945491 174 11538
p63 keratinocytesGSE17611 42951005 42951706 701 17489
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 42914753 42914972 219 0
CTCF G2GSE9613 42932768 42933209 441 0
P300 T0-glioblastomaGSE21026 42920617 42921271 654 0
P300 T30-glioblastomaGSE21026 42929443 42930238 795 0
TFAP2C MCF7GSE21234 42931948 42932257 309 0
hScc1 BcellGSE12603 42928021 42928825 804 0
hScc1 BcellGSE12603 42933209 42933762 553 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
17577 mRNA PARVG chr22 42901757 42927435 156 mRNA chr22 42903811 42908520Sense/Antisense (SA) 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


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