Incidental Mutation 'R4630:Pld4'
ID 349134
Institutional Source Beutler Lab
Gene Symbol Pld4
Ensembl Gene ENSMUSG00000052160
Gene Name phospholipase D family member 4
Synonyms thss
MMRRC Submission 041895-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4630 (G1)
Quality Score 225
Status Validated
Chromosome 12
Chromosomal Location 112727089-112735420 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 112731498 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Aspartic acid at position 217 (V217D)
Ref Sequence ENSEMBL: ENSMUSP00000067002 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063888]
AlphaFold Q8BG07
Predicted Effect probably damaging
Transcript: ENSMUST00000063888
AA Change: V217D

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000067002
Gene: ENSMUSG00000052160
AA Change: V217D

DomainStartEndE-ValueType
transmembrane domain 35 57 N/A INTRINSIC
low complexity region 113 124 N/A INTRINSIC
PLDc 207 234 1.64e-10 SMART
Pfam:PLDc_3 237 414 5.5e-41 PFAM
PLDc 421 447 4.66e-6 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000220826
Predicted Effect noncoding transcript
Transcript: ENSMUST00000221115
Predicted Effect noncoding transcript
Transcript: ENSMUST00000221811
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222886
Meta Mutation Damage Score 0.9216 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.2%
Validation Efficiency 97% (74/76)
MGI Phenotype PHENOTYPE: A spontaneous mutation that introduces a stop codon at residue 46 of 503 results in smaller body size and thin fur. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3110070M22Rik A T 13: 119,624,622 (GRCm39) probably benign Het
Alkbh2 C T 5: 114,262,287 (GRCm39) E148K probably damaging Het
Aopep T C 13: 63,215,906 (GRCm39) S393P probably benign Het
BC024139 T G 15: 76,009,294 (GRCm39) Q240P probably benign Het
Bckdha A T 7: 25,330,884 (GRCm39) I44N probably damaging Het
Brpf1 T C 6: 113,286,867 (GRCm39) Y32H probably damaging Het
Catip A G 1: 74,408,072 (GRCm39) probably benign Het
Ccdc138 T C 10: 58,409,477 (GRCm39) L602P probably damaging Het
Cilp A T 9: 65,187,162 (GRCm39) T1086S probably benign Het
Comp A T 8: 70,827,032 (GRCm39) I58F possibly damaging Het
Crygs T C 16: 22,624,268 (GRCm39) E113G possibly damaging Het
Dnmt3b C T 2: 153,512,235 (GRCm39) R319* probably null Het
Eif3a A G 19: 60,758,366 (GRCm39) I804T unknown Het
Eif3a A T 19: 60,766,424 (GRCm39) H301Q probably benign Het
Elf3 A T 1: 135,184,478 (GRCm39) probably benign Het
Fads2b C A 2: 85,348,990 (GRCm39) G41* probably null Het
Gm10384 A G 15: 36,872,017 (GRCm39) noncoding transcript Het
Gm11627 T A 11: 102,469,657 (GRCm39) probably benign Het
Gpr183 A T 14: 122,192,261 (GRCm39) Y87N probably damaging Het
Gpr183 G C 14: 122,192,262 (GRCm39) Y86* probably null Het
Gpr26 T C 7: 131,568,709 (GRCm39) V18A probably damaging Het
Herc1 T A 9: 66,340,996 (GRCm39) probably null Het
Hint2 C T 4: 43,656,396 (GRCm39) probably benign Het
Jag1 A T 2: 136,927,899 (GRCm39) D837E probably damaging Het
Jmjd1c C A 10: 66,993,753 (GRCm39) S78* probably null Het
Kcnd3 C T 3: 105,566,082 (GRCm39) A421V probably damaging Het
Krt1 C T 15: 101,754,622 (GRCm39) G543S unknown Het
Lalba T C 15: 98,380,549 (GRCm39) M2V probably benign Het
Lama1 T A 17: 68,101,295 (GRCm39) D1929E probably benign Het
Macf1 T C 4: 123,367,432 (GRCm39) K878R possibly damaging Het
Mboat4 T C 8: 34,591,108 (GRCm39) S182P probably damaging Het
Muc5b A T 7: 141,411,721 (GRCm39) T1556S unknown Het
Myo1g T C 11: 6,469,047 (GRCm39) Y85C probably damaging Het
Ncapd2 C A 6: 125,156,196 (GRCm39) probably null Het
Nox3 T C 17: 3,744,257 (GRCm39) D96G possibly damaging Het
Or10a48 T C 7: 108,424,802 (GRCm39) M135V probably damaging Het
Or1e17 T C 11: 73,831,822 (GRCm39) L250P probably damaging Het
Or6c212 A G 10: 129,559,350 (GRCm39) L21P probably damaging Het
Pacs1 C T 19: 5,206,384 (GRCm39) probably null Het
Pgap4 C G 4: 49,586,254 (GRCm39) V305L probably benign Het
Pgm5 C A 19: 24,812,110 (GRCm39) G141* probably null Het
Pik3r4 A G 9: 105,532,098 (GRCm39) M557V probably benign Het
Pphln1-ps1 T C 16: 13,495,278 (GRCm39) S126P probably damaging Het
Ppp1r3c T C 19: 36,710,915 (GRCm39) E285G probably benign Het
Pradc1 T A 6: 85,424,275 (GRCm39) M24L possibly damaging Het
Prepl T C 17: 85,390,659 (GRCm39) T100A probably benign Het
Rmi2 C T 16: 10,704,073 (GRCm39) T138I probably benign Het
Rtkn A T 6: 83,129,163 (GRCm39) K540* probably null Het
Sag C A 1: 87,762,340 (GRCm39) T335K probably damaging Het
Setd4 A G 16: 93,388,114 (GRCm39) L124P probably benign Het
Sh3gl2 A G 4: 85,297,646 (GRCm39) D208G probably damaging Het
Sult4a1 T C 15: 83,989,779 (GRCm39) T8A possibly damaging Het
Tert A G 13: 73,797,110 (GRCm39) D1116G probably damaging Het
Tlr4 A G 4: 66,757,477 (GRCm39) E90G probably benign Het
Tmem123 T C 9: 7,791,393 (GRCm39) L164P probably damaging Het
Top2b T G 14: 16,409,189 (GRCm38) I777M probably damaging Het
Trak1 G A 9: 121,283,491 (GRCm39) R419Q probably benign Het
Trp53bp1 G T 2: 121,038,368 (GRCm39) A1490D probably damaging Het
Ttc16 T C 2: 32,665,389 (GRCm39) probably benign Het
Tyw5 T A 1: 57,427,686 (GRCm39) Q306L probably damaging Het
Ube2j2 T A 4: 156,039,715 (GRCm39) I14N probably damaging Het
Vmn2r103 T C 17: 20,013,958 (GRCm39) I250T probably benign Het
Zar1 A G 5: 72,738,249 (GRCm39) V51A probably benign Het
Zbtb38 T G 9: 96,570,904 (GRCm39) N60T probably damaging Het
Zfp354a T C 11: 50,961,045 (GRCm39) S417P probably damaging Het
Zfp410 A T 12: 84,372,510 (GRCm39) D112V probably damaging Het
Zfp518a C T 19: 40,901,423 (GRCm39) Q451* probably null Het
Zfp64 T C 2: 168,768,463 (GRCm39) N383S possibly damaging Het
Zfp687 A T 3: 94,919,799 (GRCm39) probably null Het
Other mutations in Pld4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00570:Pld4 APN 12 112,729,925 (GRCm39) missense probably benign 0.01
IGL01839:Pld4 APN 12 112,731,513 (GRCm39) missense probably damaging 1.00
IGL01954:Pld4 APN 12 112,734,355 (GRCm39) critical splice donor site probably null
IGL02253:Pld4 APN 12 112,733,141 (GRCm39) missense probably damaging 1.00
IGL03149:Pld4 APN 12 112,733,263 (GRCm39) missense probably benign 0.00
IGL03278:Pld4 APN 12 112,733,165 (GRCm39) missense probably damaging 0.98
IGL03349:Pld4 APN 12 112,734,313 (GRCm39) missense probably benign 0.01
Lipodicum UTSW 12 112,731,498 (GRCm39) missense probably damaging 1.00
PIT4403001:Pld4 UTSW 12 112,734,256 (GRCm39) missense probably damaging 1.00
PIT4468001:Pld4 UTSW 12 112,734,256 (GRCm39) missense probably damaging 1.00
R0052:Pld4 UTSW 12 112,734,291 (GRCm39) missense probably benign 0.03
R1078:Pld4 UTSW 12 112,729,876 (GRCm39) missense probably benign
R1756:Pld4 UTSW 12 112,729,826 (GRCm39) splice site probably null
R2006:Pld4 UTSW 12 112,734,923 (GRCm39) missense possibly damaging 0.89
R2037:Pld4 UTSW 12 112,734,992 (GRCm39) missense probably damaging 1.00
R3738:Pld4 UTSW 12 112,734,469 (GRCm39) missense probably benign 0.07
R4911:Pld4 UTSW 12 112,730,951 (GRCm39) missense probably benign 0.01
R5008:Pld4 UTSW 12 112,734,484 (GRCm39) missense possibly damaging 0.89
R5263:Pld4 UTSW 12 112,731,465 (GRCm39) missense probably damaging 1.00
R5310:Pld4 UTSW 12 112,735,046 (GRCm39) missense probably damaging 1.00
R5386:Pld4 UTSW 12 112,730,422 (GRCm39) nonsense probably null
R5513:Pld4 UTSW 12 112,728,988 (GRCm39) missense probably benign
R5788:Pld4 UTSW 12 112,730,551 (GRCm39) missense probably benign
R6085:Pld4 UTSW 12 112,733,320 (GRCm39) missense probably benign 0.01
R6157:Pld4 UTSW 12 112,734,535 (GRCm39) missense probably damaging 1.00
R6702:Pld4 UTSW 12 112,731,485 (GRCm39) missense probably damaging 1.00
R6767:Pld4 UTSW 12 112,730,549 (GRCm39) missense possibly damaging 0.51
R6962:Pld4 UTSW 12 112,733,288 (GRCm39) missense probably benign 0.00
R7864:Pld4 UTSW 12 112,731,557 (GRCm39) missense probably damaging 1.00
R8792:Pld4 UTSW 12 112,729,924 (GRCm39) missense probably benign 0.00
R8826:Pld4 UTSW 12 112,733,210 (GRCm39) missense possibly damaging 0.95
R9790:Pld4 UTSW 12 112,734,862 (GRCm39) missense probably damaging 1.00
R9791:Pld4 UTSW 12 112,734,862 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AACAGCCTTGATCAGTGGGG -3'
(R):5'- CAAGGTTCTGCTTGCTAACTCC -3'

Sequencing Primer
(F):5'- AGCCTTGATCAGTGGGGTCATTC -3'
(R):5'- TGCTAACTCCTCCCAGTACCAG -3'
Posted On 2015-10-08