Incidental Mutation 'IGL02692:Pla2g2e'
ID 303813
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Pla2g2e
Ensembl Gene ENSMUSG00000028751
Gene Name phospholipase A2, group IIE
Synonyms mGIIEsPLA2s
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02692
Quality Score
Status
Chromosome 4
Chromosomal Location 138605253-138610125 bp(+) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) G to T at 138609870 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000101430 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030531] [ENSMUST00000105803] [ENSMUST00000105804]
AlphaFold Q9QUL3
Predicted Effect probably benign
Transcript: ENSMUST00000030531
SMART Domains Protein: ENSMUSP00000030531
Gene: ENSMUSG00000028751

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
PA2c 20 136 9.74e-55 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000105803
SMART Domains Protein: ENSMUSP00000101429
Gene: ENSMUSG00000028751

DomainStartEndE-ValueType
low complexity region 44 59 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000105804
SMART Domains Protein: ENSMUSP00000101430
Gene: ENSMUSG00000028751

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
PA2c 20 136 9.74e-55 SMART
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit normal IgE antigen-dependent passive cutaneous anaphylaxis. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017N19Rik A C 10: 100,439,410 (GRCm39) S72R probably benign Het
4930544G11Rik T C 6: 65,929,792 (GRCm39) V9A probably damaging Het
Actl11 A G 9: 107,806,507 (GRCm39) N277D probably benign Het
Adam2 T A 14: 66,311,536 (GRCm39) I57F probably damaging Het
Adgrf1 T C 17: 43,614,669 (GRCm39) F251S probably damaging Het
Anapc15-ps T C 10: 95,509,089 (GRCm39) I64V probably benign Het
Anapc4 T C 5: 53,021,871 (GRCm39) V651A probably damaging Het
Atl2 T C 17: 80,172,482 (GRCm39) N163D probably benign Het
B4galnt3 G A 6: 120,187,272 (GRCm39) R708C probably damaging Het
Capza2 C T 6: 17,654,115 (GRCm39) Q56* probably null Het
Cspg4 T A 9: 56,794,738 (GRCm39) H824Q probably benign Het
Dock7 G A 4: 98,875,623 (GRCm39) P1106S probably damaging Het
Fat4 A G 3: 39,005,235 (GRCm39) Y1878C probably damaging Het
Grk2 A T 19: 4,340,716 (GRCm39) probably benign Het
Lmbrd2 G A 15: 9,149,155 (GRCm39) V13I possibly damaging Het
Loxhd1 G T 18: 77,444,609 (GRCm39) C336F probably damaging Het
Morc1 T A 16: 48,330,596 (GRCm39) F355L probably null Het
Mov10 C A 3: 104,708,119 (GRCm39) E503* probably null Het
Nt5dc3 T A 10: 86,640,642 (GRCm39) probably null Het
Or2w3b A G 11: 58,623,343 (GRCm39) V216A probably benign Het
Phf20 T A 2: 156,140,498 (GRCm39) M724K probably damaging Het
Polq T A 16: 36,880,989 (GRCm39) V772E probably damaging Het
Rhoh A G 5: 66,050,143 (GRCm39) R138G probably benign Het
Rnf123 G A 9: 107,945,501 (GRCm39) R390* probably null Het
Septin7 A G 9: 25,207,786 (GRCm39) probably benign Het
Serpina9 A C 12: 103,974,665 (GRCm39) F163V probably damaging Het
Slc2a13 A T 15: 91,205,861 (GRCm39) F442Y probably benign Het
Slc34a1 G A 13: 55,551,049 (GRCm39) probably benign Het
Slc6a11 T C 6: 114,139,100 (GRCm39) F236S probably damaging Het
Usp1 A G 4: 98,817,197 (GRCm39) K130E probably benign Het
Zfp386 A G 12: 116,022,855 (GRCm39) E156G probably damaging Het
Zfp957 C T 14: 79,450,825 (GRCm39) V325I unknown Het
Other mutations in Pla2g2e
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01688:Pla2g2e APN 4 138,606,781 (GRCm39) intron probably benign
IGL02829:Pla2g2e APN 4 138,607,747 (GRCm39) nonsense probably null
R0729:Pla2g2e UTSW 4 138,608,046 (GRCm39) missense possibly damaging 0.82
R3615:Pla2g2e UTSW 4 138,607,685 (GRCm39) missense probably benign 0.00
R3616:Pla2g2e UTSW 4 138,607,685 (GRCm39) missense probably benign 0.00
R5053:Pla2g2e UTSW 4 138,607,686 (GRCm39) missense possibly damaging 0.90
R6325:Pla2g2e UTSW 4 138,607,736 (GRCm39) missense probably damaging 1.00
R6597:Pla2g2e UTSW 4 138,607,984 (GRCm39) missense unknown
R6991:Pla2g2e UTSW 4 138,607,986 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16