AutismKB 2.0

Annotation Detail for RASGEF1B


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Basic Information Top
Gene Symbol:RASGEF1B ( FLJ31695,GPIG4,MGC46251 )
Gene Full Name: RasGEF domain family, member 1B
Band: 4q21.21
Quick LinksEntrez ID:153020; OMIM: NA; Uniprot ID:RGF1B_HUMAN; ENSEMBL ID: ENSG00000138670; HGNC ID: 24881
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
77Phosphotyrosine.
Location(AA) Modifications Resource
No data
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_152545
  • Location:chr4 82567242-82612084
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
Nanog ESGSE20650 82626702 82627177 475 14855
Oct1 HelaGSE14283 82630956 82630993 37 18890
TFAP2C MCF7GSE21234 82612168 82612757 589 378
TFAP2C MCF7GSE21234 82614032 82614469 437 2166
hScc1 CdLSGSE12603 82611833 82612916 1083 290
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
Fos K562GSE19551 82561466 82562190 724 5415
RARA MCF7GSE15244 82553496 82553710 214 13640
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 82607564 82607961 397 0
CTCF CD4SISSRdata 82607564 82607961 397 0
CTCF G2GSE9613 82567437 82567674 237 0
CTCF G2GSE9613 82600444 82600643 199 0
CTCF G2GSE9613 82607519 82607881 362 0
CTCF G2GSE9613 82611316 82612368 1052 0
Fos K562GSE19551 82588126 82588445 319 0
Fos K562GSE19551 82594545 82595500 955 0
H3K4me3 colorectalcancer 82609971 82611652 1681 0
Nanog hESGSE18292 82607729 82607999 270 0
hScc1 BcellGSE12603 82607632 82607954 322 0
hScc1 BcellGSE12603 82611043 82612701 1658 0
hScc1 CdLSGSE12603 82607411 82608028 617 0
hScc1 G2GSE9613 82607519 82607992 473 0
p63 keratinocytesGSE17611 82576131 82576943 812 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