Incidental Mutation 'R7475:Ppp1r21'
ID 579454
Institutional Source Beutler Lab
Gene Symbol Ppp1r21
Ensembl Gene ENSMUSG00000034709
Gene Name protein phosphatase 1, regulatory subunit 21
Synonyms Ccdc128, Klraq1, 1110018J12Rik
MMRRC Submission 045549-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.261) question?
Stock # R7475 (G1)
Quality Score 225.009
Status Validated
Chromosome 17
Chromosomal Location 88837552-88895795 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 88863031 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Tryptophan at position 257 (G257W)
Ref Sequence ENSEMBL: ENSMUSP00000048443 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000038551]
AlphaFold Q3TDD9
Predicted Effect probably benign
Transcript: ENSMUST00000038551
AA Change: G257W

PolyPhen 2 Score 0.067 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000048443
Gene: ENSMUSG00000034709
AA Change: G257W

DomainStartEndE-ValueType
KLRAQ 11 112 8.01e-51 SMART
coiled coil region 136 211 N/A INTRINSIC
Pfam:TTKRSYEDQ 255 771 1.8e-273 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency 99% (77/78)
Allele List at MGI
Other mutations in this stock
Total: 77 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc5 G T 16: 20,218,739 (GRCm39) N214K probably benign Het
Abcf1 A G 17: 36,274,459 (GRCm39) probably null Het
Agxt2 A T 15: 10,409,623 (GRCm39) M508L probably benign Het
Akr1c21 A T 13: 4,626,318 (GRCm39) Y114F probably benign Het
Amz1 T C 5: 140,729,941 (GRCm39) probably null Het
Ank1 G T 8: 23,622,646 (GRCm39) A1732S probably benign Het
Atg16l1 T C 1: 87,687,805 (GRCm39) S50P possibly damaging Het
AW551984 A G 9: 39,509,236 (GRCm39) S302P probably damaging Het
Ccn6 T A 10: 39,034,296 (GRCm39) Y102F probably damaging Het
Ces3a T A 8: 105,780,322 (GRCm39) probably null Het
Dedd C A 1: 171,167,881 (GRCm39) P185Q probably benign Het
Fam186a A T 15: 99,845,395 (GRCm39) V283E unknown Het
Fat2 C A 11: 55,194,479 (GRCm39) V1187F probably benign Het
Fbxw11 T C 11: 32,661,999 (GRCm39) probably null Het
Fcgbp C T 7: 27,802,401 (GRCm39) T1443I probably damaging Het
Foxj2 A G 6: 122,814,801 (GRCm39) D279G probably benign Het
Gbp5 A G 3: 142,207,122 (GRCm39) D97G probably damaging Het
Gm49368 A T 7: 127,707,154 (GRCm39) T661S possibly damaging Het
Gria4 T G 9: 4,513,330 (GRCm39) T260P probably damaging Het
Gtf2ird2 T A 5: 134,230,267 (GRCm39) D195E possibly damaging Het
Hectd4 T A 5: 121,496,196 (GRCm39) probably null Het
Ifngr2 G A 16: 91,354,797 (GRCm39) C32Y unknown Het
Ikzf5 A T 7: 130,993,788 (GRCm39) C280S probably benign Het
Ints9 G T 14: 65,263,914 (GRCm39) E395D probably null Het
Isoc2b T C 7: 4,854,084 (GRCm39) D96G probably benign Het
Jmjd1c T G 10: 67,061,092 (GRCm39) S967R probably benign Het
Kcnj3 A T 2: 55,327,338 (GRCm39) K42N probably benign Het
Kiz T C 2: 146,733,006 (GRCm39) V394A possibly damaging Het
Knl1 A T 2: 118,918,027 (GRCm39) H1795L probably damaging Het
Lmntd2 A G 7: 140,790,602 (GRCm39) probably null Het
Loxhd1 C A 18: 77,500,001 (GRCm39) D1690E possibly damaging Het
Lrp1b T C 2: 41,234,588 (GRCm39) D1121G Het
Map3k2 T C 18: 32,333,015 (GRCm39) V63A possibly damaging Het
Mcc G T 18: 44,609,303 (GRCm39) A499D probably damaging Het
Mcpt9 T A 14: 56,264,400 (GRCm39) I232F probably damaging Het
Meltf A G 16: 31,700,756 (GRCm39) K92R probably benign Het
Mff T A 1: 82,723,159 (GRCm39) probably null Het
Mrgpra3 T A 7: 47,239,695 (GRCm39) Y77F probably damaging Het
Mylk G A 16: 34,734,446 (GRCm39) probably null Het
Ndufv2 A G 17: 66,394,532 (GRCm39) V111A possibly damaging Het
Nkd2 T C 13: 73,973,861 (GRCm39) E99G probably damaging Het
Nlk C A 11: 78,474,225 (GRCm39) G358V probably damaging Het
Nnmt A T 9: 48,503,532 (GRCm39) C165S probably damaging Het
Nxpe4 T A 9: 48,304,640 (GRCm39) C242* probably null Het
Oas1b A T 5: 120,955,705 (GRCm39) N162I probably damaging Het
Or4s2 A G 2: 88,473,554 (GRCm39) I148V probably benign Het
Otog A G 7: 45,916,700 (GRCm39) N879S probably damaging Het
Pcsk7 T A 9: 45,838,923 (GRCm39) Y612N probably damaging Het
Peg10 CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG CCACATCAGGATCCACATCAGGATGCACATCAG 6: 4,756,398 (GRCm39) probably benign Het
Pgbd5 T C 8: 125,160,750 (GRCm39) D39G probably benign Het
Pkhd1l1 C T 15: 44,368,581 (GRCm39) Q800* probably null Het
Pkn3 T C 2: 29,977,122 (GRCm39) S621P probably benign Het
Polr3c T C 3: 96,622,501 (GRCm39) I385V probably benign Het
Prkn A G 17: 11,653,501 (GRCm39) D199G probably benign Het
Pxylp1 C T 9: 96,738,420 (GRCm39) probably null Het
Rasgrp1 T C 2: 117,116,589 (GRCm39) T613A probably benign Het
Robo3 C T 9: 37,336,674 (GRCm39) V387I probably benign Het
Rxfp2 T A 5: 149,973,046 (GRCm39) Y174N possibly damaging Het
Sec24a T C 11: 51,604,379 (GRCm39) M746V probably damaging Het
Sema4f T A 6: 82,891,355 (GRCm39) E571D possibly damaging Het
Septin3 T C 15: 82,170,657 (GRCm39) V217A probably benign Het
Serpinb1b A C 13: 33,277,548 (GRCm39) K260N probably benign Het
Sin3b A G 8: 73,476,500 (GRCm39) T645A possibly damaging Het
Sobp C T 10: 42,897,830 (GRCm39) R585Q probably damaging Het
Specc1l T A 10: 75,082,281 (GRCm39) L559Q possibly damaging Het
Srxn1 C T 2: 151,947,573 (GRCm39) probably benign Het
Sspo G A 6: 48,432,794 (GRCm39) R890Q probably benign Het
Stard9 A G 2: 120,518,591 (GRCm39) D505G probably damaging Het
Tjp1 A T 7: 64,972,087 (GRCm39) I653K probably damaging Het
Tnks C T 8: 35,298,866 (GRCm39) E1296K probably damaging Het
Ttbk2 A T 2: 120,579,121 (GRCm39) I667N probably benign Het
Usp24 T C 4: 106,199,550 (GRCm39) S165P possibly damaging Het
Usp46 T A 5: 74,189,598 (GRCm39) K109* probably null Het
Vmn1r191 A G 13: 22,362,942 (GRCm39) C271R probably benign Het
Zfp592 T C 7: 80,673,200 (GRCm39) S55P probably damaging Het
Zmynd15 T C 11: 70,351,867 (GRCm39) S158P probably benign Het
Zscan22 T G 7: 12,640,664 (GRCm39) C303G probably damaging Het
Other mutations in Ppp1r21
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01753:Ppp1r21 APN 17 88,869,530 (GRCm39) splice site probably benign
IGL02366:Ppp1r21 APN 17 88,855,090 (GRCm39) missense probably damaging 0.99
IGL02604:Ppp1r21 APN 17 88,880,171 (GRCm39) missense probably benign 0.00
IGL02680:Ppp1r21 APN 17 88,891,290 (GRCm39) missense probably benign 0.00
R0266:Ppp1r21 UTSW 17 88,876,500 (GRCm39) splice site probably benign
R0436:Ppp1r21 UTSW 17 88,873,117 (GRCm39) missense possibly damaging 0.96
R1398:Ppp1r21 UTSW 17 88,850,307 (GRCm39) missense probably damaging 1.00
R1472:Ppp1r21 UTSW 17 88,866,033 (GRCm39) missense probably damaging 1.00
R1599:Ppp1r21 UTSW 17 88,880,055 (GRCm39) missense probably benign 0.00
R1677:Ppp1r21 UTSW 17 88,858,097 (GRCm39) missense probably benign 0.04
R1760:Ppp1r21 UTSW 17 88,869,653 (GRCm39) missense possibly damaging 0.78
R2571:Ppp1r21 UTSW 17 88,852,810 (GRCm39) missense probably benign 0.06
R3700:Ppp1r21 UTSW 17 88,889,882 (GRCm39) missense possibly damaging 0.88
R3786:Ppp1r21 UTSW 17 88,884,555 (GRCm39) splice site probably null
R3959:Ppp1r21 UTSW 17 88,857,244 (GRCm39) missense probably damaging 1.00
R4649:Ppp1r21 UTSW 17 88,856,941 (GRCm39) missense probably benign
R4654:Ppp1r21 UTSW 17 88,866,227 (GRCm39) missense probably benign 0.01
R4724:Ppp1r21 UTSW 17 88,863,019 (GRCm39) nonsense probably null
R4766:Ppp1r21 UTSW 17 88,880,043 (GRCm39) missense probably benign 0.00
R4933:Ppp1r21 UTSW 17 88,855,049 (GRCm39) missense probably benign 0.07
R4934:Ppp1r21 UTSW 17 88,852,804 (GRCm39) missense probably damaging 0.98
R4934:Ppp1r21 UTSW 17 88,852,803 (GRCm39) missense probably damaging 1.00
R4992:Ppp1r21 UTSW 17 88,876,508 (GRCm39) missense probably benign 0.44
R5109:Ppp1r21 UTSW 17 88,866,268 (GRCm39) missense probably damaging 1.00
R5372:Ppp1r21 UTSW 17 88,858,103 (GRCm39) missense probably benign 0.21
R5861:Ppp1r21 UTSW 17 88,889,937 (GRCm39) missense probably damaging 1.00
R6200:Ppp1r21 UTSW 17 88,876,613 (GRCm39) missense possibly damaging 0.65
R6369:Ppp1r21 UTSW 17 88,889,840 (GRCm39) splice site probably null
R7060:Ppp1r21 UTSW 17 88,887,972 (GRCm39) missense probably damaging 1.00
R7154:Ppp1r21 UTSW 17 88,862,314 (GRCm39) missense probably damaging 0.99
R7390:Ppp1r21 UTSW 17 88,856,958 (GRCm39) missense probably benign 0.26
R7470:Ppp1r21 UTSW 17 88,869,649 (GRCm39) missense probably damaging 1.00
R7657:Ppp1r21 UTSW 17 88,863,110 (GRCm39) missense probably damaging 1.00
R8021:Ppp1r21 UTSW 17 88,856,935 (GRCm39) missense probably benign 0.00
R8081:Ppp1r21 UTSW 17 88,866,272 (GRCm39) missense probably damaging 1.00
R9272:Ppp1r21 UTSW 17 88,866,086 (GRCm39) missense possibly damaging 0.69
R9377:Ppp1r21 UTSW 17 88,852,815 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- AGAATTGAGTTATGGGATGTCTTCCT -3'
(R):5'- GAGTCCCTATTTGTTGTCCCCA -3'

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