Incidental Mutation 'R7134:Plcb3'
ID 552960
Institutional Source Beutler Lab
Gene Symbol Plcb3
Ensembl Gene ENSMUSG00000024960
Gene Name phospholipase C, beta 3
Synonyms
MMRRC Submission 045219-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.671) question?
Stock # R7134 (G1)
Quality Score 225.009
Status Validated
Chromosome 19
Chromosomal Location 6931081-6951738 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 6942698 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Glutamine at position 222 (L222Q)
Ref Sequence ENSEMBL: ENSMUSP00000025912 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025912]
AlphaFold P51432
Predicted Effect probably damaging
Transcript: ENSMUST00000025912
AA Change: L222Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000025912
Gene: ENSMUSG00000024960
AA Change: L222Q

DomainStartEndE-ValueType
Pfam:EF-hand_like 225 316 6.6e-23 PFAM
PLCXc 317 468 4.26e-73 SMART
low complexity region 488 515 N/A INTRINSIC
low complexity region 553 578 N/A INTRINSIC
PLCYc 591 707 3.88e-76 SMART
C2 728 826 4.52e-14 SMART
low complexity region 917 936 N/A INTRINSIC
Pfam:PLC-beta_C 1029 1202 5.5e-57 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 99% (84/85)
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 phosphoinositide phospholipase C beta enzyme family that catalyze the production of the secondary messengers diacylglycerol and inositol 1,4,5-triphosphate from phosphatidylinositol in G-protein-linked receptor-mediated signal transduction. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]
PHENOTYPE: Mice homozygous for one targeted mutation die at E2.5 and exhibit poor embryonic organization and hypocellularity. Mice homozygous for a second targeted mutation survive to adulthood and exhibit an increased antinocieptive response to opioids. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 86 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcf1 A G 17: 36,270,144 (GRCm39) F638S possibly damaging Het
Actl6b T A 5: 137,562,762 (GRCm39) N159K probably damaging Het
Adam6a T G 12: 113,508,655 (GRCm39) S343A probably benign Het
Ankrd17 G A 5: 90,380,173 (GRCm39) T2505I probably damaging Het
Ankrd17 T C 5: 90,433,382 (GRCm39) T728A probably benign Het
Asap2 G T 12: 21,315,964 (GRCm39) E919* probably null Het
Atp10b A T 11: 43,136,291 (GRCm39) I1140F probably damaging Het
Cep126 A T 9: 8,103,383 (GRCm39) V209E probably damaging Het
Cfap65 C T 1: 74,965,792 (GRCm39) R406Q probably benign Het
Cldn1 T C 16: 26,190,376 (GRCm39) M1V probably null Het
Cryl1 C T 14: 57,512,956 (GRCm39) D304N probably benign Het
D3Ertd751e T C 3: 41,708,212 (GRCm39) probably null Het
D630044L22Rik A T 17: 26,181,090 (GRCm39) M156L probably benign Het
Ddx21 T C 10: 62,427,634 (GRCm39) D423G possibly damaging Het
Dock2 T A 11: 34,260,363 (GRCm39) M993L probably benign Het
Dusp29 A T 14: 21,727,129 (GRCm39) I173N probably damaging Het
Eif4g1 C T 16: 20,500,252 (GRCm39) A675V probably damaging Het
Eml1 C T 12: 108,472,810 (GRCm39) S206L probably benign Het
Farp2 A C 1: 93,531,181 (GRCm39) I560L probably benign Het
Fbn1 A T 2: 125,223,969 (GRCm39) D593E probably benign Het
Fetub A G 16: 22,748,007 (GRCm39) D61G possibly damaging Het
Fpgs T C 2: 32,576,641 (GRCm39) K329E probably benign Het
Fpgt T C 3: 154,797,120 (GRCm39) Y45C probably damaging Het
Gas2l1 A T 11: 5,011,106 (GRCm39) C574* probably null Het
Gm9747 G T 1: 82,211,837 (GRCm39) C12F unknown Het
H2-T23 T C 17: 36,342,709 (GRCm39) Y143C probably damaging Het
Hhip A T 8: 80,719,142 (GRCm39) S462T probably benign Het
Hnf1a C T 5: 115,091,446 (GRCm39) G416R probably damaging Het
Hoxa5 C T 6: 52,181,023 (GRCm39) C103Y probably damaging Het
Kansl3 G T 1: 36,390,848 (GRCm39) D395E possibly damaging Het
Marchf10 A G 11: 105,299,502 (GRCm39) S116P probably benign Het
Med12l C T 3: 59,001,180 (GRCm39) Q748* probably null Het
Mroh7 T A 4: 106,577,791 (GRCm39) N296Y probably damaging Het
Mtbp T G 15: 55,421,961 (GRCm39) D61E probably benign Het
Muc5b A T 7: 141,411,391 (GRCm39) I1446L unknown Het
Myh15 T C 16: 48,901,705 (GRCm39) V266A possibly damaging Het
Nap1l1 G A 10: 111,330,655 (GRCm39) probably null Het
Napsa A G 7: 44,235,159 (GRCm39) T315A probably benign Het
Nlrc5 A T 8: 95,206,350 (GRCm39) I734F probably damaging Het
Nnt A G 13: 119,531,198 (GRCm39) V183A probably damaging Het
Nploc4 A T 11: 120,276,614 (GRCm39) D477E probably benign Het
Nrip3 A G 7: 109,364,695 (GRCm39) S144P probably damaging Het
Ntng1 A T 3: 109,842,445 (GRCm39) F109L probably benign Het
Or5p61 A G 7: 107,758,883 (GRCm39) Y66H probably damaging Het
Or5v1 T A 17: 37,809,776 (GRCm39) V78D probably damaging Het
Or6aa1 G A 7: 86,044,752 (GRCm39) probably benign Het
Or8b36 A G 9: 37,937,795 (GRCm39) E231G probably benign Het
Pacsin1 G A 17: 27,921,707 (GRCm39) D30N probably damaging Het
Pbld2 A T 10: 62,860,368 (GRCm39) probably benign Het
Pcnx4 C T 12: 72,613,750 (GRCm39) T565I probably damaging Het
Pdzk1 A T 3: 96,763,246 (GRCm39) T225S probably benign Het
Phyhip T G 14: 70,704,639 (GRCm39) I286S probably benign Het
Pkd1 T A 17: 24,813,086 (GRCm39) Y3903N probably damaging Het
Plcd4 T A 1: 74,593,662 (GRCm39) H262Q probably benign Het
Plekhh1 C T 12: 79,109,390 (GRCm39) A474V probably benign Het
Plppr3 T C 10: 79,701,537 (GRCm39) E435G probably damaging Het
Poln T A 5: 34,276,340 (GRCm39) N305I possibly damaging Het
Pou3f2 T C 4: 22,486,874 (GRCm39) T420A probably benign Het
Ppdpf T C 2: 180,829,523 (GRCm39) Y17H probably damaging Het
Prrx2 C A 2: 30,768,485 (GRCm39) T104K probably damaging Het
Ptprj A T 2: 90,294,822 (GRCm39) L462H probably benign Het
Radil T C 5: 142,471,304 (GRCm39) T991A probably damaging Het
Rbsn T C 6: 92,178,608 (GRCm39) E147G probably damaging Het
Ror2 C T 13: 53,300,742 (GRCm39) V35M probably benign Het
Rps6ka1 T C 4: 133,599,373 (GRCm39) Q18R probably benign Het
Setbp1 T A 18: 78,902,734 (GRCm39) D311V possibly damaging Het
Setd2 C T 9: 110,377,865 (GRCm39) S560L possibly damaging Het
Slc12a5 A T 2: 164,816,878 (GRCm39) I134F probably damaging Het
Speer1h C T 5: 11,647,706 (GRCm39) T148I possibly damaging Het
Svil A G 18: 5,116,080 (GRCm39) D2035G probably damaging Het
Syngap1 T C 17: 27,178,985 (GRCm39) Y665H probably damaging Het
Tbc1d9b T C 11: 50,043,519 (GRCm39) Y547H possibly damaging Het
Tgm2 A G 2: 157,980,812 (GRCm39) V83A probably benign Het
Tmem233 T C 5: 116,189,429 (GRCm39) I117V probably benign Het
Tsen34 A G 7: 3,703,640 (GRCm39) T293A probably damaging Het
Ttn A G 2: 76,709,023 (GRCm39) V8752A unknown Het
Ubac1 A G 2: 25,904,974 (GRCm39) V88A probably benign Het
Uchl4 T C 9: 64,142,621 (GRCm39) V34A probably damaging Het
Ugt2a2 C T 5: 87,608,435 (GRCm39) R468H probably benign Het
Vmn2r102 A T 17: 19,897,749 (GRCm39) T255S probably benign Het
Wdr6 T A 9: 108,450,564 (GRCm39) N988I probably damaging Het
Wnk1 A T 6: 119,903,389 (GRCm39) I2359N unknown Het
Ybey A G 10: 76,304,025 (GRCm39) V59A probably benign Het
Zfp268 T A 4: 145,349,375 (GRCm39) C271S possibly damaging Het
Zfp397 A G 18: 24,090,122 (GRCm39) N142S probably benign Het
Zfy1 A T Y: 725,788 (GRCm39) V659E probably damaging Het
Other mutations in Plcb3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01092:Plcb3 APN 19 6,932,690 (GRCm39) missense probably benign 0.27
IGL01370:Plcb3 APN 19 6,940,192 (GRCm39) missense probably damaging 0.99
IGL01385:Plcb3 APN 19 6,935,276 (GRCm39) missense probably benign
IGL01511:Plcb3 APN 19 6,933,211 (GRCm39) missense probably damaging 0.99
IGL02182:Plcb3 APN 19 6,946,988 (GRCm39) missense probably benign 0.22
IGL02240:Plcb3 APN 19 6,935,448 (GRCm39) splice site probably benign
IGL02350:Plcb3 APN 19 6,935,546 (GRCm39) missense probably damaging 1.00
IGL02357:Plcb3 APN 19 6,935,546 (GRCm39) missense probably damaging 1.00
IGL02550:Plcb3 APN 19 6,937,544 (GRCm39) nonsense probably null
IGL02866:Plcb3 APN 19 6,935,044 (GRCm39) missense probably damaging 1.00
IGL03180:Plcb3 APN 19 6,933,521 (GRCm39) missense probably benign 0.44
IGL03327:Plcb3 APN 19 6,932,420 (GRCm39) missense probably benign
IGL03346:Plcb3 APN 19 6,932,420 (GRCm39) missense probably benign
Multifarious UTSW 19 6,932,071 (GRCm39) critical splice donor site probably null
R0042:Plcb3 UTSW 19 6,943,788 (GRCm39) missense probably damaging 1.00
R0125:Plcb3 UTSW 19 6,936,276 (GRCm39) missense probably damaging 1.00
R0240:Plcb3 UTSW 19 6,940,363 (GRCm39) missense probably benign 0.16
R0240:Plcb3 UTSW 19 6,940,363 (GRCm39) missense probably benign 0.16
R0724:Plcb3 UTSW 19 6,940,760 (GRCm39) missense probably damaging 1.00
R0781:Plcb3 UTSW 19 6,939,281 (GRCm39) nonsense probably null
R0945:Plcb3 UTSW 19 6,932,246 (GRCm39) missense probably damaging 1.00
R1110:Plcb3 UTSW 19 6,939,281 (GRCm39) nonsense probably null
R1414:Plcb3 UTSW 19 6,940,385 (GRCm39) missense probably damaging 1.00
R1454:Plcb3 UTSW 19 6,932,414 (GRCm39) missense possibly damaging 0.64
R1533:Plcb3 UTSW 19 6,935,041 (GRCm39) missense possibly damaging 0.70
R1652:Plcb3 UTSW 19 6,932,664 (GRCm39) missense probably benign 0.00
R1795:Plcb3 UTSW 19 6,933,381 (GRCm39) unclassified probably benign
R1870:Plcb3 UTSW 19 6,940,353 (GRCm39) missense probably benign 0.04
R1934:Plcb3 UTSW 19 6,941,977 (GRCm39) missense probably damaging 1.00
R3980:Plcb3 UTSW 19 6,943,803 (GRCm39) missense probably damaging 1.00
R4397:Plcb3 UTSW 19 6,943,193 (GRCm39) missense probably damaging 0.96
R4533:Plcb3 UTSW 19 6,933,640 (GRCm39) missense probably benign 0.08
R4576:Plcb3 UTSW 19 6,936,415 (GRCm39) splice site probably benign
R4815:Plcb3 UTSW 19 6,940,352 (GRCm39) missense possibly damaging 0.59
R4903:Plcb3 UTSW 19 6,933,211 (GRCm39) missense probably damaging 0.99
R5093:Plcb3 UTSW 19 6,943,578 (GRCm39) missense probably damaging 1.00
R5555:Plcb3 UTSW 19 6,943,587 (GRCm39) missense probably benign 0.19
R5593:Plcb3 UTSW 19 6,932,117 (GRCm39) missense possibly damaging 0.94
R5626:Plcb3 UTSW 19 6,932,643 (GRCm39) missense probably benign 0.24
R5661:Plcb3 UTSW 19 6,940,588 (GRCm39) missense probably damaging 1.00
R5713:Plcb3 UTSW 19 6,935,060 (GRCm39) missense probably damaging 0.99
R5741:Plcb3 UTSW 19 6,931,790 (GRCm39) nonsense probably null
R6025:Plcb3 UTSW 19 6,933,547 (GRCm39) missense probably benign 0.03
R6063:Plcb3 UTSW 19 6,940,202 (GRCm39) missense possibly damaging 0.69
R6155:Plcb3 UTSW 19 6,943,533 (GRCm39) missense probably damaging 1.00
R6157:Plcb3 UTSW 19 6,943,533 (GRCm39) missense probably damaging 1.00
R6178:Plcb3 UTSW 19 6,932,071 (GRCm39) critical splice donor site probably null
R7085:Plcb3 UTSW 19 6,937,501 (GRCm39) missense possibly damaging 0.80
R7117:Plcb3 UTSW 19 6,941,746 (GRCm39) missense probably damaging 1.00
R7153:Plcb3 UTSW 19 6,935,452 (GRCm39) critical splice donor site probably null
R7316:Plcb3 UTSW 19 6,943,753 (GRCm39) critical splice donor site probably null
R7366:Plcb3 UTSW 19 6,939,389 (GRCm39) missense probably benign
R7399:Plcb3 UTSW 19 6,940,235 (GRCm39) missense probably benign
R7736:Plcb3 UTSW 19 6,946,991 (GRCm39) missense probably benign 0.00
R8057:Plcb3 UTSW 19 6,936,267 (GRCm39) missense probably damaging 0.99
R8057:Plcb3 UTSW 19 6,932,463 (GRCm39) missense probably benign
R8376:Plcb3 UTSW 19 6,944,071 (GRCm39) missense probably damaging 0.99
R9103:Plcb3 UTSW 19 6,936,288 (GRCm39) missense probably benign 0.06
R9292:Plcb3 UTSW 19 6,942,042 (GRCm39) missense probably damaging 1.00
R9366:Plcb3 UTSW 19 6,937,658 (GRCm39) critical splice donor site probably null
Predicted Primers PCR Primer
(F):5'- ACCTGTGGCAAAGGGATGAC -3'
(R):5'- CCTGTGGCCTCAACTTCAAC -3'

Sequencing Primer
(F):5'- AACCACATGAGTACCCTGGGTG -3'
(R):5'- CAACTTCAACCGAGTGTGTG -3'
Posted On 2019-05-15