AutismKB 2.0

Annotation Detail for CORO7


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Basic Information Top
Gene Symbol:CORO7 ( 0610011B16Rik,CRN7,FLJ22021,FLJ44188,POD1 )
Gene Full Name: coronin 7
Band: 16p13.3
Quick LinksEntrez ID:79585; OMIM: 611668; Uniprot ID:CORO7_HUMAN; ENSEMBL ID: ENSG00000103426; HGNC ID: 26161
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
21Phosphoserine.
472N6-acetyllysine.
915Phosphoserine.
Location(AA) Modifications Resource
Location(AA) Modification Resource
21Phosphoserine(PKG)HMM predict
86Phosphoserine(ATM)HMM predict
148Phosphothreonine(PKC)HMM predict
204Phosphoserine(PKG)HMM predict
298O-linkedHMM predict
298Phosphoserine(MAPK)HMM predict
298Phosphoserine(CDC2)HMM predict
430Phosphoserine(CDC2)HMM predict
430O-linkedHMM predict
430Phosphoserine(IKK)HMM predict
433O-linkedHMM predict
434O-linkedHMM predict
434O-linkedHMM predict
436O-linkedHMM predict
436O-linkedHMM predict
437Phosphoserine(CDC2)HMM predict
437Phosphoserine(IKK)HMM predict
439O-linkedHMM predict
440Phosphothreonine(MAPK)HMM predict
440Phosphothreonine(CDK)HMM predict
440O-linkedHMM predict
442Phosphoserine(IKK)HMM predict
443O-linkedHMM predict
447Phosphoserine(IKK)HMM predict
450Phosphoserine(CK1)HMM predict
452O-linkedHMM predict
494N-linkedHMM predict
518O-linkedHMM predict
646Phosphoserine(IKK)HMM predict
680O-linkedHMM predict
683MethylarginineHMM predict
772Phosphoserine(IKK)HMM predict
775Phosphoserine(CDK)HMM predict
775Phosphoserine(CDC2)HMM predict
806Phosphoserine(PKG)HMM predict
866Phosphoserine(ATM)HMM predict
879Phosphoserine(PKG)HMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_024535
  • Location:chr16 4344545-4406571
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
Rb GrowingGSE19898 4406724 4406913 189 247
Rb QuiescentGSE19898 4406565 4406791 226 107
Rb SenescentGSE19898 4406569 4406954 385 190
Rb shRbSenescenceGSE19898 4406529 4406799 270 93
USF1 HepG2E 4408696 4409172 476 2363
p130 QuiescentGSE19898 4406636 4406912 276 203
p130 SenescentGSE19898 4406586 4407024 438 234
p130 shRbSenescentGSE19898 4406467 4407098 631 211
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 4349134 4349416 282 0
CTCF CD4SISSRdata 4349134 4349416 282 0
CTCF G2GSE9613 4344923 4345189 266 0
CTCF G2GSE9613 4349203 4349643 440 0
CTCF G2GSE9613 4350967 4351419 452 0
CTCF G2GSE9613 4356850 4357070 220 0
CTCF G2GSE9613 4358835 4359529 694 0
CTCF G2GSE9613 4376453 4376886 433 0
CTCF G2GSE9613 4384481 4384952 471 0
CTCF G2GSE9613 4391246 4391874 628 0
CTCF G2GSE9613 4392551 4395332 2781 0
CTCF G2GSE9613 4399020 4399433 413 0
CTCF G2GSE9613 4405833 4406025 192 0
ER Breast-CancerGSE22609 4358906 4359627 721 0
ER E2-MCF7GSE14664 4351717 4351756 39 0
ER E2-MCF7GSE14664 4356394 4356484 90 0
ER E2-MCF7GSE14664 4381377 4381425 48 0
ER Fulvestrant-MCF7GSE14664 4351718 4351761 43 0
ER Fulvestrant-MCF7GSE14664 4356061 4356114 53 0
ER MCF7GSE19013 4358782 4359849 1067 0
ER MCF7GSE19013 4361027 4362005 978 0
Oct1 H2O2-HelaGSE14283 4403986 4404028 42 0
Oct1 HelaGSE14283 4351675 4351754 79 0
Oct1 HelaGSE14283 4355994 4356029 35 0
Oct1 HelaGSE14283 4356065 4356100 35 0
Oct1 HelaGSE14283 4391606 4391637 31 0
Oct1 HelaGSE14283 4403955 4404032 77 0
P300 T0-glioblastomaGSE21026 4400388 4401453 1065 0
P300 T30-glioblastomaGSE21026 4400413 4401370 957 0
TFAP2C MCF7GSE21234 4358752 4359588 836 0
TFAP2C MCF7GSE21234 4378211 4378707 496 0
TFAP2C MCF7GSE21234 4400674 4401193 519 0
hScc1 BcellGSE12603 4356850 4357034 184 0
hScc1 BcellGSE12603 4394631 4394973 342 0
hScc1 BcellGSE12603 4405166 4406340 1174 0
p130 QuiescentGSE19898 4383340 4383603 263 0
p130 SenescentGSE19898 4382737 4383353 616 0
p130 shRbQuiescentGSE19898 4360384 4360969 585 0
p130 shRbQuiescentGSE19898 4382339 4383041 702 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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