AutismKB 2.0

Annotation Detail for CRYGS


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:CRYGS ( CRYG8 )
Gene Full Name: crystallin, gamma S
Band: 3q27.3
Quick LinksEntrez ID:1427; OMIM: 123730; Uniprot ID:CRBS_HUMAN; ENSEMBL ID: ENSG00000213139; HGNC ID: 2417
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
2N-acetylserine.
7N6-methylated lysine.
Location(AA) Modifications Resource
2N-acetylserine.Swiss-Prot 53.0
7N6-methylated lysine.Swiss-Prot 53.0
Location(AA) Modification Resource
39Phosphoserine(PKG)HMM predict
82Phosphoserine(PKB)HMM predict
109Phosphotyrosine(EGFR)HMM predict
117Phosphoserine(CK1)HMM predict
157Phosphotyrosine(INSR)HMM predict
167Phosphoserine(CDC2)HMM predict
167Phosphoserine(CDK)HMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_017541
  • Location:chr3 187738926-187744860
  • strand:-
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 187719648 187720222 574 18992
CTCF G2GSE9613 187723691 187724062 371 15050
CTCF G2GSE9613 187726828 187727003 175 12011
CTCF G2GSE9613 187729152 187729490 338 9606
CTCF G2GSE9613 187729889 187730384 495 8790
hScc1 BcellGSE12603 187719648 187719893 245 19156
hScc1 BcellGSE12603 187721964 187722435 471 16727
hScc1 CdLSGSE12603 187719613 187719965 352 19138
p130 QuiescentGSE19898 187721661 187721778 117 17207
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 187740931 187741311 380 0
CTCF CD4SISSRdata 187740931 187741311 380 0
CTCF G2GSE9613 187740796 187741596 800 0
hScc1 BcellGSE12603 187740683 187741486 803 0
hScc1 CdLSGSE12603 187740648 187741596 948 0
hScc1 G2GSE9613 187740721 187741596 875 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