Incidental Mutation 'P0021:Rasgrp3'
ID 7654
Institutional Source Beutler Lab
Gene Symbol Rasgrp3
Ensembl Gene ENSMUSG00000071042
Gene Name RAS, guanyl releasing protein 3
Synonyms LOC240168
MMRRC Submission 038274-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # P0021 (G1)
Quality Score
Status Validated
Chromosome 17
Chromosomal Location 75742891-75836049 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 75807708 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Leucine at position 255 (R255L)
Ref Sequence ENSEMBL: ENSMUSP00000129393 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095204] [ENSMUST00000164192]
AlphaFold Q6NZH9
Predicted Effect probably damaging
Transcript: ENSMUST00000095204
AA Change: R255L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000092828
Gene: ENSMUSG00000071042
AA Change: R255L

DomainStartEndE-ValueType
RasGEFN 2 125 6.77e-12 SMART
RasGEF 148 384 4.57e-104 SMART
EFh 424 452 1.07e-1 SMART
EFh 453 481 4.04e0 SMART
C1 495 544 5.47e-17 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000164192
AA Change: R255L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000129393
Gene: ENSMUSG00000071042
AA Change: R255L

DomainStartEndE-ValueType
RasGEFN 2 125 6.77e-12 SMART
RasGEF 148 384 4.57e-104 SMART
EFh 424 452 1.07e-1 SMART
EFh 453 481 4.04e0 SMART
C1 495 544 5.47e-17 SMART
Meta Mutation Damage Score 0.9444 question?
Coding Region Coverage
  • 1x: 73.1%
  • 3x: 63.5%
  • 10x: 31.6%
  • 20x: 17.3%
Validation Efficiency 79% (146/184)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Members of the RAS (see HRAS; MIM 190020) subfamily of GTPases function in signal transduction as GTP/GDP-regulated switches that cycle between inactive GDP- and active GTP-bound states. Guanine nucleotide exchange factors (GEFs), such as RASGRP3, serve as RAS activators by promoting acquisition of GTP to maintain the active GTP-bound state and are the key link between cell surface receptors and RAS activation (Rebhun et al., 2000 [PubMed 10934204]).[supplied by OMIM, Mar 2008]
PHENOTYPE: Homozygous mutant mice are viable and fertile with no obvious abnormalities in the kidneys or vasculature. [provided by MGI curators]
Allele List at MGI

All alleles(4) : Targeted(3) Gene trapped(1)

Other mutations in this stock
Total: 7 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Fas A G 19: 34,284,610 (GRCm39) E39G probably damaging Het
Fig4 A G 10: 41,127,821 (GRCm39) S548P probably damaging Het
Msh4 T A 3: 153,594,455 (GRCm39) E115D probably damaging Het
Ptpn13 A G 5: 103,676,686 (GRCm39) E683G probably benign Het
Rnf168 C T 16: 32,117,705 (GRCm39) T422I probably damaging Het
Smarcd1 T C 15: 99,610,242 (GRCm39) probably benign Het
Stxbp1 T C 2: 32,713,550 (GRCm39) K29E probably damaging Het
Other mutations in Rasgrp3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02270:Rasgrp3 APN 17 75,823,368 (GRCm39) missense probably benign 0.00
IGL02529:Rasgrp3 APN 17 75,832,097 (GRCm39) missense possibly damaging 0.84
IGL02672:Rasgrp3 APN 17 75,803,412 (GRCm39) missense probably benign 0.00
IGL02935:Rasgrp3 APN 17 75,804,065 (GRCm39) missense probably benign 0.00
Aster UTSW 17 75,816,822 (GRCm39) splice site probably null
aston UTSW 17 75,807,753 (GRCm39) critical splice donor site probably null
centre UTSW 17 75,807,729 (GRCm39) missense possibly damaging 0.50
PIT4243001:Rasgrp3 UTSW 17 75,807,134 (GRCm39) missense probably damaging 1.00
R0090:Rasgrp3 UTSW 17 75,805,456 (GRCm39) missense probably damaging 1.00
R0907:Rasgrp3 UTSW 17 75,816,822 (GRCm39) splice site probably null
R1182:Rasgrp3 UTSW 17 75,810,185 (GRCm39) missense probably benign 0.01
R1412:Rasgrp3 UTSW 17 75,816,822 (GRCm39) splice site probably null
R1572:Rasgrp3 UTSW 17 75,807,729 (GRCm39) missense possibly damaging 0.50
R1664:Rasgrp3 UTSW 17 75,831,172 (GRCm39) missense probably damaging 1.00
R2094:Rasgrp3 UTSW 17 75,810,136 (GRCm39) missense probably damaging 1.00
R2111:Rasgrp3 UTSW 17 75,807,753 (GRCm39) critical splice donor site probably null
R3026:Rasgrp3 UTSW 17 75,831,916 (GRCm39) missense possibly damaging 0.52
R4052:Rasgrp3 UTSW 17 75,803,963 (GRCm39) missense probably damaging 1.00
R4348:Rasgrp3 UTSW 17 75,818,975 (GRCm39) missense probably benign 0.00
R4509:Rasgrp3 UTSW 17 75,807,668 (GRCm39) missense probably damaging 1.00
R4642:Rasgrp3 UTSW 17 75,805,443 (GRCm39) missense possibly damaging 0.64
R4791:Rasgrp3 UTSW 17 75,807,168 (GRCm39) missense probably benign 0.37
R4901:Rasgrp3 UTSW 17 75,821,111 (GRCm39) nonsense probably null
R4927:Rasgrp3 UTSW 17 75,823,350 (GRCm39) missense probably benign 0.00
R5410:Rasgrp3 UTSW 17 75,804,042 (GRCm39) missense probably benign 0.01
R5444:Rasgrp3 UTSW 17 75,810,370 (GRCm39) missense probably damaging 0.99
R5483:Rasgrp3 UTSW 17 75,832,013 (GRCm39) missense probably damaging 1.00
R5518:Rasgrp3 UTSW 17 75,823,354 (GRCm39) missense probably benign 0.36
R5755:Rasgrp3 UTSW 17 75,831,940 (GRCm39) missense probably benign 0.44
R5845:Rasgrp3 UTSW 17 75,810,142 (GRCm39) missense possibly damaging 0.61
R6310:Rasgrp3 UTSW 17 75,801,204 (GRCm39) missense probably damaging 1.00
R6604:Rasgrp3 UTSW 17 75,810,110 (GRCm39) missense probably benign 0.10
R6826:Rasgrp3 UTSW 17 75,810,241 (GRCm39) missense probably damaging 1.00
R7409:Rasgrp3 UTSW 17 75,823,411 (GRCm39) missense possibly damaging 0.48
R7507:Rasgrp3 UTSW 17 75,804,055 (GRCm39) missense probably damaging 1.00
R7536:Rasgrp3 UTSW 17 75,821,128 (GRCm39) missense probably damaging 1.00
R7538:Rasgrp3 UTSW 17 75,803,411 (GRCm39) missense probably benign
R8089:Rasgrp3 UTSW 17 75,804,056 (GRCm39) missense possibly damaging 0.54
R8677:Rasgrp3 UTSW 17 75,819,055 (GRCm39) missense probably benign 0.00
R9483:Rasgrp3 UTSW 17 75,807,717 (GRCm39) missense probably benign 0.22
R9521:Rasgrp3 UTSW 17 75,821,158 (GRCm39) missense probably null 1.00
R9557:Rasgrp3 UTSW 17 75,807,139 (GRCm39) missense probably damaging 0.98
R9727:Rasgrp3 UTSW 17 75,810,239 (GRCm39) missense probably damaging 1.00
R9757:Rasgrp3 UTSW 17 75,807,719 (GRCm39) missense probably damaging 1.00
X0011:Rasgrp3 UTSW 17 75,832,161 (GRCm39) nonsense probably null
Z1177:Rasgrp3 UTSW 17 75,819,090 (GRCm39) missense probably benign 0.03
Protein Function and Prediction

RASGRP3 is a guanine nucleotide exchange factor that is proposed to function as a angiogenic factor (1).  RasGRP3 is heavily phosphorylated after activation of the B cell receptor (BCR) (2) and links the BCR to Ras (3). Also RasGRP3 has been shown to mediate phorbol ester-induced exocytosis (4).

Expression/Localization

RT-PCR ELISA detected highest expression in heart, brain, lung, and kidney, and intermediate expression in liver, skeletal muscle, pancreas, spleen testis, and ovary (5). RasGRP3 is expressed in embryonic blood vessels, down-regulated in mature adult vessels, and reexpressed in newly formed vessels during pregnancy and tumorigenesis (1).  Ras GRP3 is selectively expressed in B cells (2).

Background

Rasgrp3tm1Jstn/tm1Jstn; MGI:3625862

involves: 129P3/J * C57BL/6J

In this model, homozygous animals have decreased B cell numbers, abnormal humoral immune responses, and decreased IgG levels (6).

Rasgrp3Gt(Pt1-ATG)1Vb/Gt(Pt1-ATG)1Vb; MGI:3525522 (gene trap)

involves: CD-1

Homozygous mutant mice are viable and fertile with no obvious abnormalities in the kidneys or vasculature (1).

References
Posted On 2012-10-29
Science Writer Anne Murray