RASGEF1B (RasGEF domain family member 1B)

2006-10-01  

Identity

HGNC
LOCATION
4q21.21
LOCUSID
ALIAS
GPIG4
FUSION GENES

Other Information

Locus ID:

NCBI: 153020
MIM: 614532
HGNC: 24881
Ensembl: ENSG00000138670

Variants:

dbSNP: 153020
ClinVar: 153020
TCGA: ENSG00000138670
COSMIC: RASGEF1B

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000138670ENST00000264400Q0VAM2
ENSG00000138670ENST00000335927Q0VAM2
ENSG00000138670ENST00000436139Q8N437
ENSG00000138670ENST00000504863D6RE71
ENSG00000138670ENST00000509081Q0VAM2
ENSG00000138670ENST00000512716A0A0G2JLL4
ENSG00000138670ENST00000514050A0A1B0GW78
ENSG00000138670ENST00000613784Q8N437
ENSG00000138670ENST00000638048A0A1B0GVA7

Expression (GTEx)

0
5
10
15

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
273625602016Inducible RasGEF1B circular RNA is a positive regulator of ICAM-1 in the TLR4/LPS pathway.40
196457192009RasGEF1A and RasGEF1B are guanine nucleotide exchange factors that discriminate between Rap GTP-binding proteins and mediate Rap2-specific nucleotide exchange.9
2230379520118.6Mb interstitial deletion of chromosome 4q13.3q21.23 in a boy with cognitive impairment, short stature, hearing loss, skeletal abnormalities and facial dysmorphism.5
310446212019Genome-wide association study of white-coat effect in hypertensive patients.0

Citation

Dessen P

RASGEF1B (RasGEF domain family member 1B)

Atlas Genet Cytogenet Oncol Haematol. 2006-10-01

Online version: http://atlasgeneticsoncology.org/gene/43451/rasgef1b