Incidental Mutation 'R9626:Ppp1r3g'
ID 725170
Institutional Source Beutler Lab
Gene Symbol Ppp1r3g
Ensembl Gene ENSMUSG00000050423
Gene Name protein phosphatase 1, regulatory subunit 3G
Synonyms 1600032L17Rik
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # R9626 (G1)
Quality Score 225.009
Status Not validated
Chromosome 13
Chromosomal Location 36142822-36154371 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 36153612 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Lysine at position 344 (T344K)
Ref Sequence ENSEMBL: ENSMUSP00000122712 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000132661] [ENSMUST00000225537]
AlphaFold Q9CW07
Predicted Effect probably benign
Transcript: ENSMUST00000132661
AA Change: T344K

PolyPhen 2 Score 0.081 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000122712
Gene: ENSMUSG00000050423
AA Change: T344K

DomainStartEndE-ValueType
low complexity region 88 102 N/A INTRINSIC
Pfam:CBM_21 202 339 9.2e-29 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000225537
AA Change: T344K

PolyPhen 2 Score 0.081 (Sensitivity: 0.93; Specificity: 0.85)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aass T A 6: 23,127,502 (GRCm39) N37I unknown Het
Abca9 T A 11: 110,011,606 (GRCm39) T1146S probably benign Het
Acnat2 G A 4: 49,380,179 (GRCm39) H400Y probably damaging Het
Adgrd1 T C 5: 129,275,721 (GRCm39) S768P probably damaging Het
Arap2 T A 5: 62,906,878 (GRCm39) H47L probably benign Het
Atxn1 T A 13: 45,710,796 (GRCm39) N712I possibly damaging Het
Bri3bp T A 5: 125,531,572 (GRCm39) S173T probably damaging Het
Camta1 A T 4: 151,168,287 (GRCm39) S254R probably damaging Het
Card9 T C 2: 26,247,294 (GRCm39) E285G probably benign Het
Celf2 G A 2: 6,590,835 (GRCm39) A320V probably benign Het
Celsr3 T C 9: 108,726,521 (GRCm39) I3250T probably damaging Het
Cfap46 C T 7: 139,230,805 (GRCm39) R941H Het
Cntrob T C 11: 69,202,167 (GRCm39) H475R possibly damaging Het
Dcaf6 G A 1: 165,227,264 (GRCm39) R288* probably null Het
Ebna1bp2 G A 4: 118,478,371 (GRCm39) probably benign Het
Erich3 A T 3: 154,444,730 (GRCm39) D302V probably benign Het
Fbxo48 T A 11: 16,904,333 (GRCm39) *162K probably null Het
Fyttd1 T C 16: 32,725,915 (GRCm39) L290S probably damaging Het
Gcc1 T C 6: 28,418,917 (GRCm39) D472G probably damaging Het
Gjb4 C T 4: 127,246,081 (GRCm39) probably benign Het
Gm5157 G T 7: 20,919,396 (GRCm39) T49K probably damaging Het
Gpr143 GTTTTTT GTTTTTTT X: 151,578,627 (GRCm39) probably null Het
Hnrnpm G T 17: 33,896,264 (GRCm39) D88E probably damaging Het
Hormad2 G A 11: 4,377,372 (GRCm39) P22L probably damaging Het
Hunk C T 16: 90,272,791 (GRCm39) T365M probably damaging Het
Lamb1 A G 12: 31,354,669 (GRCm39) D972G probably benign Het
Mamdc4 A G 2: 25,458,273 (GRCm39) L379P probably damaging Het
Mcrs1 A G 15: 99,146,353 (GRCm39) L179P probably damaging Het
Mterf2 C T 10: 84,956,295 (GRCm39) A110T probably benign Het
Mucl1 A G 15: 103,783,934 (GRCm39) S91P possibly damaging Het
Myo1d C A 11: 80,448,296 (GRCm39) G943V possibly damaging Het
Ndst4 A C 3: 125,476,829 (GRCm39) D18A probably damaging Het
Ndufv1 A T 19: 4,058,064 (GRCm39) C382* probably null Het
Npc1l1 T C 11: 6,177,854 (GRCm39) K519E probably benign Het
Nphs1 A G 7: 30,166,991 (GRCm39) K747E probably benign Het
Nubp2 C G 17: 25,103,374 (GRCm39) probably null Het
Odad2 G T 18: 7,211,422 (GRCm39) C817* probably null Het
Or13a19 T C 7: 139,903,236 (GRCm39) V208A probably benign Het
Or5b97 A T 19: 12,878,600 (GRCm39) D181E possibly damaging Het
Or7a36 T G 10: 78,820,213 (GRCm39) D196E probably benign Het
Or7a40 A G 16: 16,491,491 (GRCm39) M118T probably damaging Het
Or8b48 A G 9: 38,492,977 (GRCm39) T135A probably benign Het
Pcdhac2 T G 18: 37,279,555 (GRCm39) L845R probably damaging Het
Pcdhb14 A C 18: 37,581,787 (GRCm39) T298P probably damaging Het
Phldb2 A T 16: 45,592,547 (GRCm39) L957Q possibly damaging Het
Pole A G 5: 110,459,959 (GRCm39) D1121G possibly damaging Het
Prpf8 A G 11: 75,385,681 (GRCm39) K954R possibly damaging Het
Prr15l C A 11: 96,825,440 (GRCm39) Y23* probably null Het
Sap18b A G 8: 96,552,098 (GRCm39) E36G possibly damaging Het
Slc46a2 A T 4: 59,914,241 (GRCm39) F227L probably benign Het
Spata13 C T 14: 60,944,349 (GRCm39) P581S probably benign Het
Spmip4 T A 6: 50,550,930 (GRCm39) K506N Het
Ssc5d C A 7: 4,946,568 (GRCm39) T974K probably benign Het
Tenm4 C A 7: 96,545,345 (GRCm39) R2491S probably damaging Het
Tex2 T C 11: 106,437,579 (GRCm39) E697G unknown Het
Tmem44 A T 16: 30,366,226 (GRCm39) F67I possibly damaging Het
Trpm6 A T 19: 18,790,846 (GRCm39) Q627L probably damaging Het
Ttc39a A G 4: 109,278,570 (GRCm39) D77G possibly damaging Het
Ttc9 A G 12: 81,710,301 (GRCm39) I198V probably benign Het
Ttn C T 2: 76,661,550 (GRCm39) V11942M unknown Het
Uqcrc2 T A 7: 120,237,118 (GRCm39) Y55* probably null Het
Vmn1r160 A T 7: 22,571,273 (GRCm39) M209L probably benign Het
Vmn2r50 A T 7: 9,771,960 (GRCm39) C580* probably null Het
Vmn2r96 A G 17: 18,793,758 (GRCm39) E34G probably benign Het
Zmynd8 C T 2: 165,654,268 (GRCm39) probably null Het
Other mutations in Ppp1r3g
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01946:Ppp1r3g APN 13 36,152,978 (GRCm39) missense possibly damaging 0.90
IGL02890:Ppp1r3g APN 13 36,153,314 (GRCm39) missense probably damaging 0.98
R0413:Ppp1r3g UTSW 13 36,153,331 (GRCm39) missense probably damaging 1.00
R1065:Ppp1r3g UTSW 13 36,153,418 (GRCm39) missense probably benign 0.07
R4497:Ppp1r3g UTSW 13 36,153,603 (GRCm39) missense probably benign 0.15
R5677:Ppp1r3g UTSW 13 36,153,245 (GRCm39) missense probably damaging 1.00
R6705:Ppp1r3g UTSW 13 36,152,880 (GRCm39) missense probably benign 0.08
R8832:Ppp1r3g UTSW 13 36,153,143 (GRCm39) nonsense probably null
R9127:Ppp1r3g UTSW 13 36,152,621 (GRCm39) missense probably benign
R9287:Ppp1r3g UTSW 13 36,152,834 (GRCm39) missense possibly damaging 0.92
X0027:Ppp1r3g UTSW 13 36,153,206 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GTCAGGGGACTCTGGATCAAAG -3'
(R):5'- TGAGAACACTGCCAGAGCTTG -3'

Sequencing Primer
(F):5'- CTCTGGATCAAAGGCTGAGG -3'
(R):5'- CAGAGCTTGCCGTGAATCTG -3'
Posted On 2022-09-12