Incidental Mutation 'R7459:Rgs3'
ID 578302
Institutional Source Beutler Lab
Gene Symbol Rgs3
Ensembl Gene ENSMUSG00000059810
Gene Name regulator of G-protein signaling 3
Synonyms 4930506N09Rik, C2PA-RGS3, C2pa, PDZ-RGS3, RGS3S
MMRRC Submission 045533-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.081) question?
Stock # R7459 (G1)
Quality Score 225.009
Status Not validated
Chromosome 4
Chromosomal Location 62478079-62621256 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 62543391 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 242 (E242G)
Ref Sequence ENSEMBL: ENSMUSP00000065447 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000065870] [ENSMUST00000084521] [ENSMUST00000098031] [ENSMUST00000107424]
AlphaFold Q9DC04
Predicted Effect probably benign
Transcript: ENSMUST00000065870
AA Change: E242G

PolyPhen 2 Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)
SMART Domains Protein: ENSMUSP00000065447
Gene: ENSMUSG00000059810
AA Change: E242G

DomainStartEndE-ValueType
C2 47 150 7.98e-15 SMART
PDZ 203 272 8.09e-10 SMART
low complexity region 465 475 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000084521
AA Change: E65G

PolyPhen 2 Score 0.044 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000081569
Gene: ENSMUSG00000059810
AA Change: E65G

DomainStartEndE-ValueType
PDZ 26 95 8.09e-10 SMART
low complexity region 288 298 N/A INTRINSIC
internal_repeat_1 407 447 2.05e-9 PROSPERO
internal_repeat_1 456 501 2.05e-9 PROSPERO
low complexity region 645 674 N/A INTRINSIC
RGS 841 957 3.66e-53 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000098031
AA Change: E234G

PolyPhen 2 Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)
SMART Domains Protein: ENSMUSP00000095639
Gene: ENSMUSG00000059810
AA Change: E234G

DomainStartEndE-ValueType
C2 39 142 7.98e-15 SMART
PDZ 195 264 8.09e-10 SMART
low complexity region 457 467 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000107424
AA Change: E65G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000103047
Gene: ENSMUSG00000059810
AA Change: E65G

DomainStartEndE-ValueType
PDZ 26 95 8.09e-10 SMART
low complexity region 288 298 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the regulator of G-protein signaling (RGS) family. This protein is a GTPase-activating protein that inhibits G-protein-mediated signal transduction. Alternative splicing and the use of alternative promoters results in multiple transcript variants encoding different isoforms. Long isoforms are largely cytosolic and plasma membrane-associated with a function in Wnt signaling and in the epithelial mesenchymal transition, while shorter N-terminally-truncated isoforms can be nuclear. [provided by RefSeq, Jan 2013]
PHENOTYPE: Mice homozygous for a targeted allele exhibit impaired T cell migration in model of Th2-mediated airway inflammation. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 80 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgre1 T A 17: 57,756,933 (GRCm39) V730E probably damaging Het
Agbl1 G A 7: 76,069,814 (GRCm39) D449N not run Het
Agr2 A T 12: 36,047,452 (GRCm39) E96V probably benign Het
Atp1a2 A C 1: 172,114,862 (GRCm39) S308A probably benign Het
Birc7 T C 2: 180,571,150 (GRCm39) S71P possibly damaging Het
Brme1 T G 8: 84,893,981 (GRCm39) S383A probably benign Het
Camk2g T C 14: 20,829,275 (GRCm39) I73V probably damaging Het
Carf C A 1: 60,167,198 (GRCm39) T177K possibly damaging Het
Ccdc191 C T 16: 43,767,820 (GRCm39) Q665* probably null Het
Cd79a A T 7: 24,598,567 (GRCm39) T39S possibly damaging Het
Ces5a C A 8: 94,262,369 (GRCm39) probably benign Het
Dkk2 C A 3: 131,880,790 (GRCm39) T145N probably benign Het
Dot1l C T 10: 80,609,007 (GRCm39) A188V probably damaging Het
Egfr T A 11: 16,846,967 (GRCm39) V788D probably damaging Het
Esyt3 T A 9: 99,240,117 (GRCm39) H109L probably benign Het
Fam234b C T 6: 135,188,899 (GRCm39) T168I probably benign Het
Fan1 G T 7: 63,998,714 (GRCm39) S936Y probably damaging Het
Fat2 T C 11: 55,194,745 (GRCm39) E1098G probably damaging Het
Fcgbp A G 7: 27,806,710 (GRCm39) D2226G possibly damaging Het
Flacc1 T G 1: 58,730,911 (GRCm39) E48D possibly damaging Het
Flvcr2 T C 12: 85,793,831 (GRCm39) V69A probably benign Het
Foxb2 T A 19: 16,850,436 (GRCm39) H190L unknown Het
Fut4 C T 9: 14,662,602 (GRCm39) V231M possibly damaging Het
Gtf2a1 G A 12: 91,542,426 (GRCm39) A91V probably benign Het
Hip1 A G 5: 135,443,151 (GRCm39) S961P probably damaging Het
Hsf2bp C T 17: 32,165,708 (GRCm39) V296M probably benign Het
Hspbp1 G T 7: 4,687,577 (GRCm39) H11Q probably benign Het
Ighv1-84 C T 12: 115,944,432 (GRCm39) E81K probably benign Het
Isg20l2 T C 3: 87,839,485 (GRCm39) L232P possibly damaging Het
Isx A G 8: 75,619,392 (GRCm39) Y181C probably benign Het
Kif9 A G 9: 110,348,109 (GRCm39) Y644C probably damaging Het
Lin7c T A 2: 109,727,682 (GRCm39) V177D probably benign Het
Lpin3 T C 2: 160,739,220 (GRCm39) S343P probably benign Het
Mat1a A T 14: 40,842,141 (GRCm39) Q246L probably benign Het
Mlkl T C 8: 112,060,162 (GRCm39) I75V probably benign Het
Ndufa7 T A 17: 34,057,140 (GRCm39) S107T probably damaging Het
Niban3 T A 8: 72,057,671 (GRCm39) C516S possibly damaging Het
Nip7 T A 8: 107,783,968 (GRCm39) C69* probably null Het
Nipa2 A T 7: 55,583,089 (GRCm39) W219R probably damaging Het
Oas2 A C 5: 120,887,775 (GRCm39) S22A unknown Het
Obscn A G 11: 59,022,483 (GRCm39) V754A probably benign Het
Or4a76 G A 2: 89,461,012 (GRCm39) P77S probably damaging Het
Osbpl1a C T 18: 13,066,642 (GRCm39) C39Y probably damaging Het
Pcdhb16 A T 18: 37,612,606 (GRCm39) Y522F probably benign Het
Pced1a T G 2: 130,261,744 (GRCm39) D303A possibly damaging Het
Peli1 T A 11: 21,098,190 (GRCm39) Y308* probably null Het
Pfas T A 11: 68,879,481 (GRCm39) R243W Het
Pik3r5 C A 11: 68,383,416 (GRCm39) Q412K probably benign Het
Pkd1l1 A T 11: 8,852,428 (GRCm39) I1135N Het
Prune1 C A 3: 95,189,021 (GRCm39) probably benign Het
Ptpn4 T A 1: 119,587,564 (GRCm39) K926N probably damaging Het
Ptpre A G 7: 135,269,329 (GRCm39) N277S probably benign Het
Raver2 A T 4: 100,964,410 (GRCm39) D255V possibly damaging Het
Rgs20 A G 1: 4,980,857 (GRCm39) V187A probably benign Het
Rims2 T G 15: 39,381,235 (GRCm39) S1055R probably benign Het
Rnf146 T C 10: 29,223,640 (GRCm39) D82G probably benign Het
Rpgrip1 A G 14: 52,378,016 (GRCm39) S455G probably benign Het
Samm50 T C 15: 84,080,057 (GRCm39) probably null Het
Sh3bgr A G 16: 96,007,122 (GRCm39) K31E probably benign Het
Slc39a8 T C 3: 135,592,672 (GRCm39) I449T probably damaging Het
Slc5a3 A T 16: 91,875,905 (GRCm39) Y654F probably benign Het
Spata1 T A 3: 146,181,977 (GRCm39) L264F possibly damaging Het
Spats2l A T 1: 57,838,512 (GRCm39) probably benign Het
Stard13 A C 5: 150,971,064 (GRCm39) S848A probably damaging Het
Stat2 A G 10: 128,112,434 (GRCm39) S25G possibly damaging Het
Tet2 C T 3: 133,186,050 (GRCm39) R1129Q possibly damaging Het
Tmem232 T C 17: 65,563,384 (GRCm39) T670A probably benign Het
Tmem266 T C 9: 55,303,883 (GRCm39) L3P unknown Het
Tns3 A T 11: 8,442,793 (GRCm39) D523E probably benign Het
Trim3 A T 7: 105,267,015 (GRCm39) S455T probably damaging Het
Trim31 T C 17: 37,220,554 (GRCm39) V490A probably damaging Het
Trmt11 A C 10: 30,466,039 (GRCm39) N168K probably benign Het
Trpc4 G A 3: 54,198,653 (GRCm39) V526M probably damaging Het
Ttn C A 2: 76,749,482 (GRCm39) D3856Y possibly damaging Het
Tulp2 G A 7: 45,169,227 (GRCm39) D377N probably damaging Het
Ubl7 A G 9: 57,821,875 (GRCm39) T75A probably damaging Het
Ugt2b34 T G 5: 87,049,134 (GRCm39) D297A possibly damaging Het
Usp34 A T 11: 23,314,458 (GRCm39) H800L possibly damaging Het
Utp3 C A 5: 88,703,412 (GRCm39) L314M probably damaging Het
Zer1 A G 2: 30,003,337 (GRCm39) Y27H probably damaging Het
Other mutations in Rgs3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00510:Rgs3 APN 4 62,619,417 (GRCm39) missense possibly damaging 0.87
IGL00918:Rgs3 APN 4 62,619,304 (GRCm39) missense probably damaging 1.00
IGL01594:Rgs3 APN 4 62,537,981 (GRCm39) missense probably damaging 0.99
IGL01761:Rgs3 APN 4 62,570,946 (GRCm39) splice site probably benign
IGL02995:Rgs3 APN 4 62,544,084 (GRCm39) missense possibly damaging 0.95
IGL03365:Rgs3 APN 4 62,607,912 (GRCm39) missense probably benign
R0098:Rgs3 UTSW 4 62,544,143 (GRCm39) missense probably damaging 1.00
R0098:Rgs3 UTSW 4 62,544,143 (GRCm39) missense probably damaging 1.00
R0158:Rgs3 UTSW 4 62,542,121 (GRCm39) missense probably damaging 1.00
R0609:Rgs3 UTSW 4 62,544,173 (GRCm39) missense probably damaging 1.00
R0633:Rgs3 UTSW 4 62,544,143 (GRCm39) missense probably damaging 1.00
R0637:Rgs3 UTSW 4 62,564,910 (GRCm39) splice site probably benign
R0893:Rgs3 UTSW 4 62,523,798 (GRCm39) splice site probably null
R1612:Rgs3 UTSW 4 62,544,172 (GRCm39) missense probably damaging 0.99
R1929:Rgs3 UTSW 4 62,620,384 (GRCm39) missense probably damaging 1.00
R2202:Rgs3 UTSW 4 62,608,741 (GRCm39) missense probably damaging 1.00
R2239:Rgs3 UTSW 4 62,544,124 (GRCm39) missense probably benign 0.30
R2380:Rgs3 UTSW 4 62,544,124 (GRCm39) missense probably benign 0.30
R2974:Rgs3 UTSW 4 62,558,957 (GRCm39) missense probably damaging 1.00
R4871:Rgs3 UTSW 4 62,549,532 (GRCm39) missense probably benign 0.01
R5229:Rgs3 UTSW 4 62,620,424 (GRCm39) missense probably damaging 1.00
R5372:Rgs3 UTSW 4 62,570,934 (GRCm39) intron probably benign
R5597:Rgs3 UTSW 4 62,542,082 (GRCm39) missense probably damaging 1.00
R6006:Rgs3 UTSW 4 62,542,143 (GRCm39) missense probably damaging 1.00
R6056:Rgs3 UTSW 4 62,544,143 (GRCm39) missense probably damaging 0.96
R6732:Rgs3 UTSW 4 62,521,180 (GRCm39) missense probably benign 0.00
R6962:Rgs3 UTSW 4 62,618,952 (GRCm39) intron probably benign
R7141:Rgs3 UTSW 4 62,608,724 (GRCm39) missense probably damaging 1.00
R7156:Rgs3 UTSW 4 62,535,363 (GRCm39) missense probably damaging 0.99
R7193:Rgs3 UTSW 4 62,533,573 (GRCm39) missense probably damaging 0.99
R7660:Rgs3 UTSW 4 62,619,349 (GRCm39) missense possibly damaging 0.94
R7697:Rgs3 UTSW 4 62,575,379 (GRCm39) missense probably benign 0.00
R8025:Rgs3 UTSW 4 62,608,831 (GRCm39) missense probably damaging 0.97
R8059:Rgs3 UTSW 4 62,521,214 (GRCm39) splice site probably benign
R8242:Rgs3 UTSW 4 62,538,022 (GRCm39) missense probably benign
R8413:Rgs3 UTSW 4 62,544,254 (GRCm39) missense possibly damaging 0.54
R8489:Rgs3 UTSW 4 62,544,733 (GRCm39) missense probably damaging 1.00
R8501:Rgs3 UTSW 4 62,521,193 (GRCm39) missense possibly damaging 0.85
R8880:Rgs3 UTSW 4 62,543,373 (GRCm39) missense probably damaging 1.00
R9065:Rgs3 UTSW 4 62,620,465 (GRCm39) missense probably benign 0.05
R9094:Rgs3 UTSW 4 62,500,240 (GRCm39) missense probably damaging 1.00
R9318:Rgs3 UTSW 4 62,559,019 (GRCm39) missense probably benign 0.05
R9483:Rgs3 UTSW 4 62,575,354 (GRCm39) nonsense probably null
R9498:Rgs3 UTSW 4 62,575,412 (GRCm39) missense probably damaging 1.00
R9522:Rgs3 UTSW 4 62,523,729 (GRCm39) missense probably benign 0.12
Z1177:Rgs3 UTSW 4 62,549,451 (GRCm39) missense possibly damaging 0.67
Predicted Primers PCR Primer
(F):5'- GAAGGCCTTTGATCAACGCC -3'
(R):5'- CTGAGGAGCGATGTAAATTGC -3'

Sequencing Primer
(F):5'- AGTTCAGCACCTCTGTGTGGAAC -3'
(R):5'- CGATGTAAATTGCTCACAGCTGG -3'
Posted On 2019-10-07