Incidental Mutation 'R2869:Plcl1'
ID 266413
Institutional Source Beutler Lab
Gene Symbol Plcl1
Ensembl Gene ENSMUSG00000038349
Gene Name phospholipase C-like 1
Synonyms C230017K02Rik, PRIP-1, PLC-L
MMRRC Submission 040457-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.877) question?
Stock # R2869 (G1)
Quality Score 225
Status Not validated
Chromosome 1
Chromosomal Location 55445080-55793444 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 55736309 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Valine at position 550 (D550V)
Ref Sequence ENSEMBL: ENSMUSP00000037854 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042986]
AlphaFold Q3USB7
Predicted Effect probably benign
Transcript: ENSMUST00000042986
AA Change: D550V

PolyPhen 2 Score 0.095 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000037854
Gene: ENSMUSG00000038349
AA Change: D550V

DomainStartEndE-ValueType
low complexity region 21 41 N/A INTRINSIC
low complexity region 49 60 N/A INTRINSIC
PH 115 226 6.98e-4 SMART
low complexity region 301 310 N/A INTRINSIC
Pfam:EF-hand_like 316 398 5.9e-27 PFAM
PLCXc 399 543 2.13e-82 SMART
low complexity region 550 564 N/A INTRINSIC
PLCYc 586 702 2.15e-69 SMART
C2 723 829 1.02e-21 SMART
low complexity region 1080 1092 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000187059
Meta Mutation Damage Score 0.0797 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.7%
Validation Efficiency
MGI Phenotype PHENOTYPE: Homozygous null mutants display impaired motor coordination and decreased sensitivity to the sedative diazepam. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Als2 A G 1: 59,250,296 (GRCm39) S483P probably damaging Het
C030034I22Rik T A 17: 69,725,106 (GRCm39) noncoding transcript Het
Carmil1 G A 13: 24,229,051 (GRCm39) silent Het
Ccl27a C T 4: 41,769,640 (GRCm39) R73Q probably benign Het
Cd6 A G 19: 10,771,990 (GRCm39) I307T possibly damaging Het
Dennd2b A T 7: 109,156,637 (GRCm39) Y38N probably benign Het
Dhx57 A T 17: 80,558,805 (GRCm39) D1051E probably benign Het
Eif4enif1 C T 11: 3,192,586 (GRCm39) P805S probably damaging Het
Fan1 A G 7: 64,012,938 (GRCm39) I668T probably benign Het
Frmpd4 A T X: 166,260,243 (GRCm39) D1166E probably benign Homo
Gbp11 C T 5: 105,478,866 (GRCm39) D191N probably benign Het
Ggt6 A T 11: 72,328,187 (GRCm39) N229I probably benign Het
Gm26902 T A 19: 34,452,210 (GRCm39) H106L probably benign Het
Gm37340 G A 2: 6,955,739 (GRCm39) probably benign Het
Gm9874 A T 17: 30,704,763 (GRCm39) probably benign Het
Gria2 G A 3: 80,609,799 (GRCm39) T670I probably damaging Het
Gsdme A T 6: 50,185,157 (GRCm39) C432* probably null Het
Habp2 T A 19: 56,276,423 (GRCm39) probably benign Het
Hmcn1 A T 1: 150,614,467 (GRCm39) V1313D possibly damaging Het
Kcnb1 A G 2: 166,947,855 (GRCm39) L331P probably damaging Het
Klf8 A T X: 152,165,678 (GRCm39) E82D probably damaging Homo
Krt13 A G 11: 100,008,475 (GRCm39) S421P unknown Het
Lactbl1 G A 4: 136,354,097 (GRCm39) C37Y probably damaging Het
Lzts2 C A 19: 45,012,534 (GRCm39) S321* probably null Het
Marchf8 C T 6: 116,378,106 (GRCm39) probably benign Het
Meikin T C 11: 54,264,333 (GRCm39) V103A possibly damaging Het
Mki67 G A 7: 135,309,878 (GRCm39) P191L probably benign Het
Mlxip A G 5: 123,590,730 (GRCm39) M878V probably benign Het
Mpp7 G A 18: 7,461,678 (GRCm39) P65L possibly damaging Het
Myo9b G A 8: 71,786,981 (GRCm39) R721Q probably benign Het
Nav1 A G 1: 135,388,495 (GRCm39) silent Het
Nbn T A 4: 15,963,810 (GRCm39) D70E probably damaging Het
Nell1 A T 7: 49,899,405 (GRCm39) probably benign Het
Nomo1 C A 7: 45,696,361 (GRCm39) T293N probably damaging Het
Notum A G 11: 120,551,022 (GRCm39) V48A probably benign Het
Nwd2 A T 5: 63,957,671 (GRCm39) I334L probably benign Het
Or10z1 T C 1: 174,078,092 (GRCm39) S134G probably benign Het
Or4k2 T C 14: 50,423,811 (GRCm39) T288A probably benign Het
Or6c211 A T 10: 129,505,628 (GRCm39) C253* probably null Het
Ostc T C 3: 130,497,157 (GRCm39) N80S probably damaging Het
Otud4 T A 8: 80,387,702 (GRCm39) N300K possibly damaging Het
Palmd T C 3: 116,717,400 (GRCm39) R366G possibly damaging Het
Parp1 A G 1: 180,401,230 (GRCm39) D45G probably damaging Het
Pes1 C A 11: 3,926,834 (GRCm39) T372K probably benign Het
Ppp1r7 T A 1: 93,285,585 (GRCm39) probably null Het
Prdx4 A G X: 154,123,460 (GRCm39) V15A probably benign Homo
Psmb8 T C 17: 34,419,144 (GRCm39) I146T probably damaging Het
Psmd13 A T 7: 140,466,968 (GRCm39) T116S probably damaging Het
Pzp A T 6: 128,462,519 (GRCm39) probably null Het
Serinc2 A G 4: 130,159,005 (GRCm39) S29P probably damaging Het
Slc39a8 T A 3: 135,592,554 (GRCm39) probably null Het
Sppl2c C T 11: 104,078,141 (GRCm39) P314S probably benign Het
St7 C T 6: 17,819,276 (GRCm39) P60L probably damaging Het
Stx3 A T 19: 11,766,938 (GRCm39) V91D probably damaging Het
Taf6l A G 19: 8,755,992 (GRCm39) probably benign Het
Tafa2 A T 10: 123,540,270 (GRCm39) H42L possibly damaging Het
Tnni3k C T 3: 154,644,387 (GRCm39) probably null Het
Tprg1 T C 16: 25,231,590 (GRCm39) W189R probably damaging Het
Trim32 A G 4: 65,532,694 (GRCm39) D417G probably damaging Het
Vmn2r68 A C 7: 84,882,834 (GRCm39) M306R probably benign Het
Vwa7 G A 17: 35,240,218 (GRCm39) M395I probably damaging Het
Ybx3 G A 6: 131,347,376 (GRCm39) A253V probably damaging Het
Zfp53 A T 17: 21,728,340 (GRCm39) E124D probably benign Het
Zzz3 T A 3: 152,152,481 (GRCm39) silent Het
Other mutations in Plcl1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00233:Plcl1 APN 1 55,445,695 (GRCm39) missense probably benign
IGL00491:Plcl1 APN 1 55,752,657 (GRCm39) critical splice donor site probably null
IGL00753:Plcl1 APN 1 55,735,897 (GRCm39) missense probably damaging 1.00
IGL01415:Plcl1 APN 1 55,735,555 (GRCm39) missense possibly damaging 0.92
IGL03024:Plcl1 APN 1 55,734,946 (GRCm39) missense probably damaging 1.00
K3955:Plcl1 UTSW 1 55,737,098 (GRCm39) missense possibly damaging 0.78
PIT4791001:Plcl1 UTSW 1 55,741,090 (GRCm39) missense probably benign 0.03
R0066:Plcl1 UTSW 1 55,752,634 (GRCm39) missense probably damaging 0.99
R0066:Plcl1 UTSW 1 55,752,634 (GRCm39) missense probably damaging 0.99
R0083:Plcl1 UTSW 1 55,737,098 (GRCm39) missense possibly damaging 0.78
R0086:Plcl1 UTSW 1 55,754,742 (GRCm39) missense probably damaging 1.00
R0092:Plcl1 UTSW 1 55,735,924 (GRCm39) missense probably damaging 0.98
R0108:Plcl1 UTSW 1 55,737,098 (GRCm39) missense possibly damaging 0.78
R1716:Plcl1 UTSW 1 55,734,997 (GRCm39) missense probably damaging 0.99
R2061:Plcl1 UTSW 1 55,790,504 (GRCm39) missense probably benign 0.01
R2128:Plcl1 UTSW 1 55,736,997 (GRCm39) missense probably damaging 1.00
R2869:Plcl1 UTSW 1 55,736,309 (GRCm39) missense probably benign 0.09
R2870:Plcl1 UTSW 1 55,736,309 (GRCm39) missense probably benign 0.09
R2870:Plcl1 UTSW 1 55,736,309 (GRCm39) missense probably benign 0.09
R2872:Plcl1 UTSW 1 55,736,309 (GRCm39) missense probably benign 0.09
R2872:Plcl1 UTSW 1 55,736,309 (GRCm39) missense probably benign 0.09
R2873:Plcl1 UTSW 1 55,736,309 (GRCm39) missense probably benign 0.09
R3819:Plcl1 UTSW 1 55,735,758 (GRCm39) missense probably benign
R3974:Plcl1 UTSW 1 55,737,374 (GRCm39) missense probably benign 0.30
R3975:Plcl1 UTSW 1 55,737,374 (GRCm39) missense probably benign 0.30
R4214:Plcl1 UTSW 1 55,790,494 (GRCm39) nonsense probably null
R4400:Plcl1 UTSW 1 55,754,736 (GRCm39) missense probably damaging 1.00
R4452:Plcl1 UTSW 1 55,736,045 (GRCm39) missense probably benign 0.00
R4615:Plcl1 UTSW 1 55,737,293 (GRCm39) missense probably benign 0.00
R5060:Plcl1 UTSW 1 55,735,671 (GRCm39) missense possibly damaging 0.84
R5422:Plcl1 UTSW 1 55,736,543 (GRCm39) missense probably benign 0.00
R5568:Plcl1 UTSW 1 55,735,309 (GRCm39) missense possibly damaging 0.82
R5781:Plcl1 UTSW 1 55,735,148 (GRCm39) missense possibly damaging 0.92
R5809:Plcl1 UTSW 1 55,735,160 (GRCm39) missense probably damaging 1.00
R6009:Plcl1 UTSW 1 55,735,405 (GRCm39) missense probably damaging 1.00
R6339:Plcl1 UTSW 1 55,735,474 (GRCm39) missense probably damaging 1.00
R6431:Plcl1 UTSW 1 55,736,411 (GRCm39) missense probably benign 0.03
R6534:Plcl1 UTSW 1 55,735,907 (GRCm39) missense probably damaging 1.00
R6565:Plcl1 UTSW 1 55,737,117 (GRCm39) nonsense probably null
R6678:Plcl1 UTSW 1 55,734,935 (GRCm39) missense probably benign 0.13
R6773:Plcl1 UTSW 1 55,790,461 (GRCm39) missense probably benign 0.03
R6925:Plcl1 UTSW 1 55,445,757 (GRCm39) nonsense probably null
R7168:Plcl1 UTSW 1 55,736,622 (GRCm39) missense probably damaging 1.00
R7256:Plcl1 UTSW 1 55,737,377 (GRCm39) missense probably benign 0.45
R7522:Plcl1 UTSW 1 55,735,523 (GRCm39) missense probably benign 0.31
R7527:Plcl1 UTSW 1 55,736,273 (GRCm39) missense probably damaging 1.00
R7536:Plcl1 UTSW 1 55,752,640 (GRCm39) nonsense probably null
R7585:Plcl1 UTSW 1 55,445,608 (GRCm39) missense probably benign 0.00
R7591:Plcl1 UTSW 1 55,736,608 (GRCm39) missense probably benign 0.01
R7689:Plcl1 UTSW 1 55,736,627 (GRCm39) missense probably damaging 1.00
R7960:Plcl1 UTSW 1 55,736,443 (GRCm39) missense possibly damaging 0.48
R8029:Plcl1 UTSW 1 55,735,237 (GRCm39) missense probably benign 0.26
R8241:Plcl1 UTSW 1 55,734,976 (GRCm39) missense probably benign 0.01
R8323:Plcl1 UTSW 1 55,736,895 (GRCm39) missense possibly damaging 0.58
R9000:Plcl1 UTSW 1 55,736,990 (GRCm39) missense probably damaging 1.00
R9331:Plcl1 UTSW 1 55,736,030 (GRCm39) missense possibly damaging 0.95
R9358:Plcl1 UTSW 1 55,735,810 (GRCm39) missense probably damaging 1.00
R9432:Plcl1 UTSW 1 55,445,587 (GRCm39) missense probably benign
R9452:Plcl1 UTSW 1 55,734,992 (GRCm39) missense probably damaging 1.00
R9652:Plcl1 UTSW 1 55,735,450 (GRCm39) missense probably benign 0.00
R9802:Plcl1 UTSW 1 55,735,241 (GRCm39) missense probably damaging 0.98
Z1176:Plcl1 UTSW 1 55,790,443 (GRCm39) nonsense probably null
Z1176:Plcl1 UTSW 1 55,735,199 (GRCm39) missense probably benign 0.20
Z1177:Plcl1 UTSW 1 55,736,043 (GRCm39) missense possibly damaging 0.72
Predicted Primers PCR Primer
(F):5'- GAATCACTGCTCTCTGCCTCAG -3'
(R):5'- ATTCATTGGCAATCCGGCTG -3'

Sequencing Primer
(F):5'- TGCCTCAGCAGAAAGTCATG -3'
(R):5'- GAACACATTTCCCAGTAGTTTTGG -3'
Posted On 2015-02-18