Incidental Mutation 'R9643:Ppm1m'
ID 726668
Institutional Source Beutler Lab
Gene Symbol Ppm1m
Ensembl Gene ENSMUSG00000020253
Gene Name protein phosphatase 1M
Synonyms PP2C eta, 2810423O19Rik
MMRRC Submission
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R9643 (G1)
Quality Score 225.009
Status Not validated
Chromosome 9
Chromosomal Location 106072152-106076432 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 106075104 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Histidine at position 147 (R147H)
Ref Sequence ENSEMBL: ENSMUSP00000117908 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076258] [ENSMUST00000140761]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000076258
AA Change: R91H

PolyPhen 2 Score 0.968 (Sensitivity: 0.77; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000075607
Gene: ENSMUSG00000020253
AA Change: R91H

DomainStartEndE-ValueType
PP2Cc 14 394 7.38e-44 SMART
PP2C_SIG 50 396 1.51e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000136431
SMART Domains Protein: ENSMUSP00000118165
Gene: ENSMUSG00000020253

DomainStartEndE-ValueType
PP2Cc 2 200 1.93e-1 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000140761
AA Change: R147H

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000117908
Gene: ENSMUSG00000020253
AA Change: R147H

DomainStartEndE-ValueType
PP2Cc 60 450 8.04e-45 SMART
PP2C_SIG 106 452 1.51e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000213197
Predicted Effect probably benign
Transcript: ENSMUST00000215742
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
Allele List at MGI

All alleles(8) : Targeted(2) Gene trapped(6)

Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik A G 12: 71,211,189 (GRCm39) D641G possibly damaging Het
4921539E11Rik T C 4: 103,092,666 (GRCm39) E272G unknown Het
Abca16 C T 7: 120,065,023 (GRCm39) T560I possibly damaging Het
Adcy3 A G 12: 4,259,455 (GRCm39) R911G probably damaging Het
Adgra2 A G 8: 27,612,031 (GRCm39) T1327A possibly damaging Het
Aldh9a1 T C 1: 167,184,904 (GRCm39) V272A possibly damaging Het
Ankfn1 T A 11: 89,396,167 (GRCm39) H193L probably benign Het
Asb1 A G 1: 91,480,116 (GRCm39) R280G probably benign Het
Atg14 G T 14: 47,788,780 (GRCm39) A191E probably damaging Het
Bcl9 G T 3: 97,112,960 (GRCm39) P1165Q possibly damaging Het
Cdk8 G A 5: 146,235,664 (GRCm39) A264T probably damaging Het
Cep152 G A 2: 125,406,150 (GRCm39) Q1461* probably null Het
Cep170b G T 12: 112,704,045 (GRCm39) W659L probably damaging Het
Cep57l1 T C 10: 41,597,626 (GRCm39) E335G probably damaging Het
Cpt1b T A 15: 89,303,229 (GRCm39) T609S possibly damaging Het
Cyp2c50 A T 19: 40,086,512 (GRCm39) I359F probably damaging Het
Dpf1 T A 7: 29,013,742 (GRCm39) N272K probably damaging Het
Fsip2 A G 2: 82,821,984 (GRCm39) T5906A possibly damaging Het
Gin1 A T 1: 97,712,498 (GRCm39) R220S probably benign Het
Gm30083 T C 14: 33,736,861 (GRCm39) Y32C probably benign Het
Gm45861 A G 8: 27,994,083 (GRCm39) E445G unknown Het
Golga2 T C 2: 32,193,874 (GRCm39) S567P probably damaging Het
Gpr89 A G 3: 96,780,813 (GRCm39) V353A probably damaging Het
Grin2d T C 7: 45,506,948 (GRCm39) K509R possibly damaging Het
Hip1r T C 5: 124,139,319 (GRCm39) I904T probably damaging Het
Ikbke T A 1: 131,187,022 (GRCm39) probably null Het
Il1r1 T A 1: 40,341,532 (GRCm39) C315S probably damaging Het
Ireb2 T A 9: 54,789,730 (GRCm39) F135I possibly damaging Het
Jakmip3 C T 7: 138,621,915 (GRCm39) L272F probably damaging Het
Kntc1 T A 5: 123,949,440 (GRCm39) F1937Y probably damaging Het
Krtap4-16 G A 11: 99,742,271 (GRCm39) T43I unknown Het
Lats2 A G 14: 57,936,875 (GRCm39) V538A possibly damaging Het
Megf8 T A 7: 25,046,907 (GRCm39) W1597R probably damaging Het
Mideas A T 12: 84,219,885 (GRCm39) D356E probably benign Het
Mtus2 A T 5: 148,014,025 (GRCm39) T273S probably benign Het
Nsun6 T A 2: 15,047,106 (GRCm39) E81D probably benign Het
Or13c7 G A 4: 43,855,183 (GRCm39) M291I probably benign Het
Or4c125 A T 2: 89,170,517 (GRCm39) I43K probably damaging Het
Or56a41 A G 7: 104,740,445 (GRCm39) F134L probably benign Het
Or8c10 A G 9: 38,278,912 (GRCm39) I13M probably damaging Het
Or8k23 A G 2: 86,186,408 (GRCm39) F106S probably benign Het
Oxsm T C 14: 16,241,000 (GRCm38) T350A probably damaging Het
Pard3 G A 8: 128,115,900 (GRCm39) R663Q possibly damaging Het
Pcdh15 T A 10: 74,479,335 (GRCm39) I482N probably benign Het
Pcsk2 G A 2: 143,655,501 (GRCm39) D562N probably damaging Het
Pdzk1ip1 T C 4: 114,950,177 (GRCm39) M146T probably benign Het
Plch1 T A 3: 63,660,747 (GRCm39) T279S Het
Plec C T 15: 76,058,177 (GRCm39) R3920Q probably damaging Het
Polr2g A T 19: 8,774,631 (GRCm39) V84E probably damaging Het
Ppp2r2c G T 5: 37,080,383 (GRCm39) V48L probably damaging Het
Pramel25 T A 4: 143,521,855 (GRCm39) C490* probably null Het
Prcp A T 7: 92,524,598 (GRCm39) T18S probably benign Het
Rapsn A G 2: 90,872,268 (GRCm39) S201G probably damaging Het
Rragd A G 4: 33,012,998 (GRCm39) T332A probably benign Het
Scrn2 A G 11: 96,921,342 (GRCm39) D34G probably damaging Het
Serpinb6c T C 13: 34,079,303 (GRCm39) T130A probably benign Het
Setd1b G A 5: 123,298,401 (GRCm39) G1479D probably damaging Het
Shd T A 17: 56,283,268 (GRCm39) L299Q probably damaging Het
Slc5a4b C T 10: 75,945,896 (GRCm39) V55I probably benign Het
Smg1 C A 7: 117,755,933 (GRCm39) R2405L unknown Het
Stxbp2 A T 8: 3,686,392 (GRCm39) M332L Het
Tedc2 A G 17: 24,435,328 (GRCm39) C354R probably benign Het
Tek A T 4: 94,692,523 (GRCm39) R210S possibly damaging Het
Tnk2 T A 16: 32,489,018 (GRCm39) M286K probably damaging Het
Ttc21a G A 9: 119,771,686 (GRCm39) V162I probably benign Het
Usf3 T A 16: 44,042,170 (GRCm39) C2217S possibly damaging Het
Wdr72 C T 9: 74,118,041 (GRCm39) P930S probably damaging Het
Zan A G 5: 137,456,812 (GRCm39) V1308A unknown Het
Zfp521 C T 18: 13,978,922 (GRCm39) R497Q probably damaging Het
Zfp799 T A 17: 33,039,435 (GRCm39) K277M probably damaging Het
Zfp949 C T 9: 88,436,500 (GRCm39) probably benign Het
Other mutations in Ppm1m
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02003:Ppm1m APN 9 106,076,356 (GRCm39) missense probably damaging 0.96
IGL02090:Ppm1m APN 9 106,074,001 (GRCm39) critical splice donor site probably null
IGL02644:Ppm1m APN 9 106,074,082 (GRCm39) missense probably damaging 1.00
IGL02691:Ppm1m APN 9 106,072,568 (GRCm39) missense probably damaging 1.00
IGL03094:Ppm1m APN 9 106,073,610 (GRCm39) missense probably damaging 1.00
R0047:Ppm1m UTSW 9 106,073,895 (GRCm39) nonsense probably null
R0047:Ppm1m UTSW 9 106,073,895 (GRCm39) nonsense probably null
R0361:Ppm1m UTSW 9 106,075,325 (GRCm39) missense probably damaging 1.00
R0452:Ppm1m UTSW 9 106,074,501 (GRCm39) missense probably damaging 1.00
R3053:Ppm1m UTSW 9 106,075,874 (GRCm39) missense probably benign
R4654:Ppm1m UTSW 9 106,073,601 (GRCm39) missense probably damaging 1.00
R5121:Ppm1m UTSW 9 106,073,004 (GRCm39) missense probably benign 0.03
R5450:Ppm1m UTSW 9 106,074,041 (GRCm39) missense probably benign 0.02
R5516:Ppm1m UTSW 9 106,075,138 (GRCm39) missense probably damaging 0.98
R6278:Ppm1m UTSW 9 106,074,427 (GRCm39) missense probably damaging 1.00
R6533:Ppm1m UTSW 9 106,074,069 (GRCm39) unclassified probably benign
R6746:Ppm1m UTSW 9 106,075,351 (GRCm39) nonsense probably null
R7466:Ppm1m UTSW 9 106,073,356 (GRCm39) missense probably damaging 0.99
R7486:Ppm1m UTSW 9 106,073,810 (GRCm39) missense probably damaging 1.00
R7892:Ppm1m UTSW 9 106,075,895 (GRCm39) missense probably benign
R7936:Ppm1m UTSW 9 106,075,144 (GRCm39) missense probably damaging 1.00
R8815:Ppm1m UTSW 9 106,076,237 (GRCm39) unclassified probably benign
X0022:Ppm1m UTSW 9 106,075,321 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- TGGTGTGCCCTTATACCTGG -3'
(R):5'- TCATGTCCTAGTTCGGGCTG -3'

Sequencing Primer
(F):5'- ACTTCTTTAAGTCCCTGGGGG -3'
(R):5'- CACTGTTTGATGGGCATG -3'
Posted On 2022-10-06