AutismKB 2.0

Annotation Detail for CRYM


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Basic Information Top
Gene Symbol:CRYM ( DFNA40,THBP )
Gene Full Name: crystallin, mu
Band: 16p12.2
Quick LinksEntrez ID:1428; OMIM: 123740; Uniprot ID:CRYM_HUMAN; ENSEMBL ID: ENSG00000103316; HGNC ID: 2418
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_001014444
  • Location:chr16 21177343-21221917
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
Oct1 HelaGSE14283 21228878 21228913 35 6978
Oct1 HelaGSE14283 21236100 21236134 34 14200
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 21196912 21197456 544 0
CTCF G2GSE9613 21202398 21202769 371 0
CTCF G2GSE9613 21219574 21219886 312 0
CTCF G2GSE9613 21220196 21220858 662 0
FOXA1 MCF7GSE15244 21219574 21220513 939 0
Oct1 H2O2-HelaGSE14283 21202654 21202723 69 0
Oct1 H2O2-HelaGSE14283 21216236 21216264 28 0
Oct1 HelaGSE14283 21202649 21202724 75 0
Oct1 HelaGSE14283 21213558 21213608 50 0
RARA MCF7GSE15244 21219574 21220048 474 0
Rb SenescentGSE19898 21219471 21219881 410 0
TAF HelaGSE8489 21211990 21212305 315 0
TAF HelaGSE8489 21219574 21220161 587 0
hScc1 BcellGSE12603 21196912 21197567 655 0
hScc1 BcellGSE12603 21202653 21203080 427 0
hScc1 BcellGSE12603 21219574 21219886 312 0
hScc1 BcellGSE12603 21220260 21220858 598 0
hScc1 CdLSGSE12603 21196912 21197736 824 0
hScc1 CdLSGSE12603 21219105 21220680 1575 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
9712 mRNA FLJ41766 chr16 21219670 21236770 2248 mRNA CRYM chr16 21177343 21221918 Non-exonic Bidirectional (NOB) 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