Incidental Mutation 'IGL03038:Gstm3'
ID 408772
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gstm3
Ensembl Gene ENSMUSG00000004038
Gene Name glutathione S-transferase, mu 3
Synonyms mGSTM5, Fsc2
Accession Numbers
Essential gene? Probably non essential (E-score: 0.080) question?
Stock # IGL03038
Quality Score
Status
Chromosome 3
Chromosomal Location 107871019-107876484 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 107873485 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 162 (D162G)
Ref Sequence ENSEMBL: ENSMUSP00000004136 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000004136]
AlphaFold P19639
Predicted Effect possibly damaging
Transcript: ENSMUST00000004136
AA Change: D162G

PolyPhen 2 Score 0.752 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000004136
Gene: ENSMUSG00000004038
AA Change: D162G

DomainStartEndE-ValueType
Pfam:GST_N 3 82 6.6e-22 PFAM
Pfam:GST_C_3 41 190 7.7e-11 PFAM
Pfam:GST_C 104 191 1.6e-17 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acadsb T C 7: 131,030,185 (GRCm39) Y111H probably damaging Het
Arhgef6 C T X: 56,290,966 (GRCm39) V262I probably benign Het
Arsk C A 13: 76,213,632 (GRCm39) probably benign Het
Ces1b T C 8: 93,793,680 (GRCm39) E303G probably benign Het
Chst9 T C 18: 15,628,360 (GRCm39) Q55R probably benign Het
Cntnap3 A T 13: 64,888,839 (GRCm39) D1153E possibly damaging Het
D130043K22Rik A G 13: 25,063,602 (GRCm39) E681G probably damaging Het
Fhad1 T C 4: 141,729,805 (GRCm39) E66G probably benign Het
Flii T C 11: 60,615,658 (GRCm39) T69A probably benign Het
Foxl1 A C 8: 121,855,158 (GRCm39) E153A probably damaging Het
Gtpbp3 G A 8: 71,941,947 (GRCm39) V96I possibly damaging Het
Insig2 G A 1: 121,247,403 (GRCm39) T56I probably damaging Het
Kif13a A G 13: 46,926,314 (GRCm39) L264P probably damaging Het
Lama3 T G 18: 12,552,307 (GRCm39) C420G probably damaging Het
Lrp2 C T 2: 69,305,808 (GRCm39) G2918S probably damaging Het
Lrrc8b T C 5: 105,629,358 (GRCm39) L568P probably damaging Het
Lyl1 C T 8: 85,429,300 (GRCm39) P3L possibly damaging Het
Malrd1 G A 2: 16,132,778 (GRCm39) D1900N unknown Het
Mastl C A 2: 23,030,627 (GRCm39) probably benign Het
Med24 T G 11: 98,607,010 (GRCm39) T276P possibly damaging Het
Naip1 A C 13: 100,573,841 (GRCm39) Y239* probably null Het
Nhsl2 A G X: 101,122,491 (GRCm39) K765E probably damaging Het
Npy A G 6: 49,800,588 (GRCm39) N4S probably benign Het
Nsun2 A G 13: 69,767,703 (GRCm39) D188G probably damaging Het
Or6c88 A G 10: 129,406,790 (GRCm39) T89A probably benign Het
Pde1a C A 2: 79,718,290 (GRCm39) probably benign Het
Pik3cb G A 9: 98,947,650 (GRCm39) A509V probably damaging Het
Pou2f2 C T 7: 24,796,577 (GRCm39) S315N probably damaging Het
Prdm2 A C 4: 142,860,571 (GRCm39) S906R probably damaging Het
Prkaca C A 8: 84,721,580 (GRCm39) Q300K probably benign Het
Prox2 T C 12: 85,142,038 (GRCm39) D55G possibly damaging Het
Ryr3 T A 2: 112,498,465 (GRCm39) T3612S possibly damaging Het
S1pr1 T A 3: 115,506,343 (GRCm39) I84L possibly damaging Het
Slc47a1 C T 11: 61,243,918 (GRCm39) V384M probably benign Het
Slc6a20b T C 9: 123,426,394 (GRCm39) N497S possibly damaging Het
Spen C A 4: 141,265,550 (GRCm39) R3L unknown Het
Stxbp2 A T 8: 3,691,971 (GRCm39) I538F probably benign Het
Ttll6 T C 11: 96,042,786 (GRCm39) F444S probably damaging Het
Vwce T A 19: 10,624,035 (GRCm39) Y309N possibly damaging Het
Vwf T C 6: 125,581,120 (GRCm39) L586P possibly damaging Het
Wdr35 T C 12: 9,024,185 (GRCm39) probably benign Het
Other mutations in Gstm3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01585:Gstm3 APN 3 107,873,474 (GRCm39) missense probably benign 0.42
IGL01637:Gstm3 APN 3 107,874,949 (GRCm39) missense probably damaging 1.00
IGL01937:Gstm3 APN 3 107,874,973 (GRCm39) missense probably damaging 0.98
IGL01945:Gstm3 APN 3 107,874,973 (GRCm39) missense probably damaging 0.98
IGL02307:Gstm3 APN 3 107,874,929 (GRCm39) missense probably damaging 0.98
IGL02820:Gstm3 APN 3 107,876,074 (GRCm39) splice site probably benign
IGL03108:Gstm3 APN 3 107,875,080 (GRCm39) critical splice donor site probably null
IGL03271:Gstm3 APN 3 107,873,513 (GRCm39) missense possibly damaging 0.47
IGL03097:Gstm3 UTSW 3 107,876,117 (GRCm39) missense probably benign
R0009:Gstm3 UTSW 3 107,875,156 (GRCm39) missense probably damaging 1.00
R0883:Gstm3 UTSW 3 107,873,586 (GRCm39) splice site probably benign
R1623:Gstm3 UTSW 3 107,875,151 (GRCm39) missense possibly damaging 0.80
R2108:Gstm3 UTSW 3 107,873,450 (GRCm39) missense probably damaging 0.99
R3005:Gstm3 UTSW 3 107,874,923 (GRCm39) missense probably benign 0.03
R3802:Gstm3 UTSW 3 107,871,551 (GRCm39) missense probably benign 0.03
R3803:Gstm3 UTSW 3 107,871,551 (GRCm39) missense probably benign 0.03
R3804:Gstm3 UTSW 3 107,871,551 (GRCm39) missense probably benign 0.03
R4604:Gstm3 UTSW 3 107,875,513 (GRCm39) missense possibly damaging 0.73
R4837:Gstm3 UTSW 3 107,871,531 (GRCm39) missense probably benign
R6593:Gstm3 UTSW 3 107,875,511 (GRCm39) missense probably benign 0.01
R6963:Gstm3 UTSW 3 107,874,940 (GRCm39) missense probably benign 0.01
R7790:Gstm3 UTSW 3 107,876,555 (GRCm39) start gained probably benign
R9245:Gstm3 UTSW 3 107,874,956 (GRCm39) missense probably benign 0.01
R9465:Gstm3 UTSW 3 107,873,431 (GRCm39) missense possibly damaging 0.78
R9753:Gstm3 UTSW 3 107,875,493 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02