AutismKB 2.0

Annotation Detail for CRY1


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:CRY1 ( PHLL1 )
Gene Full Name: cryptochrome 1 (photolyase-like)
Band: 12q23.3
Quick LinksEntrez ID:1407; OMIM: 601933; Uniprot ID:CRY1_HUMAN; ENSEMBL ID: ENSG00000008405; HGNC ID: 2384
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
247Phosphoserine; by MAPK (By similarity).
432Phosphotyrosine.
Location(AA) Modifications Resource
247Phosphoserine (by MAPK) (By similarity).Swiss-Prot 53.0
Location(AA) Modification Resource
30Phosphothreonine(PKC)HMM predict
92N-linkedHMM predict
190Phosphotyrosine(INSR)HMM predict
247Phosphoserine(CDK)HMM predict
247Phosphoserine(MAPK)HMM predict
247Phosphoserine(CDC2)HMM predict
259S-palmitoylHMM predict
262S-palmitoylHMM predict
279N-linkedHMM predict
281Phosphoserine(PKA)HMM predict
422Phosphothreonine(PKA)HMM predict
488Phosphotyrosine(EGFR)HMM predict
529Phosphoserine(IKK)HMM predict
531Phosphoserine(ATM)HMM predict
544Phosphoserine(ATM)HMM predict
568Phosphoserine(PKC)HMM predict
568PhosphoserineHMM predict
568Phosphoserine(ATM)HMM predict
568SerineHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_004075
  • Location:chr12 105909271-106011454
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 106022735 106023052 317 11439
CTCF CD4SISSRdata 106022735 106023052 317 11439
CTCF G2GSE9613 106022404 106023115 711 11305
ER E2-MCF7GSE14664 106022973 106023006 33 11535
ER Fulvestrant-MCF7GSE14664 106022973 106023008 35 11536
GATA3 MCF7GSE15244 106022497 106023362 865 11475
H3ac HepG2E 106011913 106012673 760 839
Oct1 HelaGSE14283 106022974 106023012 38 11539
PHF8 293TGSE20725 106010807 106012197 1390 48
RARA MCF7GSE15244 106022440 106023188 748 11360
STAT1 HeLaGSE12782 106027444 106028951 1507 16743
STAT1 HeLaGSE12783 106027478 106028951 1473 16760
hScc1 BcellGSE12603 106022368 106023003 635 11231
hScc1 CdLSGSE12603 106022440 106023115 675 11323
hScc1 G2GSE9613 106022473 106023039 566 11302
p130 SenescentGSE19898 106010938 106012268 1330 149
p130 shRbQuiescentGSE19898 106010685 106012316 1631 46
p130 shRbSenescentGSE19898 106011145 106011924 779 80
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 105932076 105932272 196 0
CTCF CD4GSE12889 105997172 105997345 173 0
CTCF CD4SISSRdata 105932076 105932272 196 0
CTCF CD4SISSRdata 105997172 105997345 173 0
CTCF G2GSE9613 106009699 106011913 2214 0
ER E2-MCF7GSE14664 105925806 105925870 64 0
ER E2-MCF7GSE14664 106005590 106005658 68 0
ER Fulvestrant-MCF7GSE14664 105925816 105925864 48 0
ER Fulvestrant-MCF7GSE14664 106005586 106005658 72 0
FOXA1 MCF7GSE15244 105975073 105975441 368 0
FOXA1 MCF7GSE15244 106010124 106010819 695 0
H3K4me2 HCT116GSE10453 106010229 106010780 551 0
H3K4me3 colorectalcancer 106010160 106011459 1299 0
H3ac HepG2E 106010195 106010847 652 0
Oct1 H2O2-HelaGSE14283 105991102 105991131 29 0
Oct1 HelaGSE14283 106006707 106006772 65 0
P300 T30-glioblastomaGSE21026 105945415 105945861 446 0
PHF8 HeLaGSE20725 106010704 106012190 1486 0
PHF8 Hs68plusFBSGSE20725 106010235 106012506 2271 0
RARA MCF7GSE15244 105975073 105975441 368 0
RARA MCF7GSE15244 106009945 106010702 757 0
RARG MCF7GSE15244 106010124 106010780 656 0
RNAII Tamoxifen-MCF7GSE14664 105925797 105925876 79 0
RNAII Tamoxifen-MCF7GSE14664 105998697 105998791 94 0
RNAII Tamoxifen-MCF7GSE14664 106001523 106001615 92 0
TAF HelaGSE8489 106010051 106010948 897 0
TFAP2C MCF7GSE21234 105931872 105932298 426 0
USF1 HepG2E 106009236 106012673 3437 0
USF2 HepG2E 106010265 106010819 554 0
hScc1 CdLSGSE12603 106009798 106010375 577 0
p63 keratinocytesGSE17611 105917200 105917971 771 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


Copyright © 2017, Center for Bioinformatics , Peking University | All Rights Reserved