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RASGRP1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

RASGRP1

RAS guanyl-releasing protein 1 is a protein that in humans is encoded by the RASGRP1 gene.[5][6][7]

Quick Facts Available structures, PDB ...
RASGRP1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesRASGRP1, CALDAG-GEFI, CALDAG-GEFII, RASGRP, hRasGRP1, RAS guanyl releasing protein 1, IMD64
External IDsOMIM: 603962; MGI: 1314635; HomoloGene: 4195; GeneCards: RASGRP1; OMA:RASGRP1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001128602
NM_001306086
NM_005739

NM_011246

RefSeq (protein)

NP_001122074
NP_001293015
NP_005730

NP_035376

Location (UCSC)Chr 15: 38.49 – 38.57 MbChr 2: 117.11 – 117.17 Mb
PubMed search[3][4]
Wikidata
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Function

RAS guanyl nucleotide-releasing protein (RASGRP) is a member of a family of genes characterized by the presence of a Ras superfamily guanine nucleotide exchange factor (GEF) domain. It functions as a diacylglycerol (DAG)-regulated nucleotide exchange factor specifically activating Ras through the exchange of bound GDP for GTP. It activates the Erk/MAP kinase cascade and regulates T-cells and B-cells development, homeostasis and differentiation.[7]

Gene

Alternatively spliced transcript variants encoding different isoforms have been identified. The corresponding rat gene rbc7, which lacks a 5-prime exon, represents a 5-prime and 3-prime truncated version of a larger normal rat transcript that encodes a predicted 90-kD protein. This shorter transcript has not been found in humans.[7]

Clinical significance

In November 2016 a 12-year-old patient was hospitalized for repetitive infections. Scientists have assumed that a genetic problem might be the reason. More specifically, the genetic cause is a defect of the RASGRP1 gene which makes it inactive. .

RASGRP1 plays a role in the functions of natural killer cell dyneins. Since dyneins are motor proteins, their function is to circulate the elements inside the cells. Dr. Orange's laboratory studies have established a functional link between the defects of natural killer cells and dyneins, which in combination with Other observations led doctors to try the drug lenalidommide to treat the patient. The drug was able to reverse certain effects of the mutation RASGRP1.

References

Further reading

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