Incidental Mutation 'IGL03108:Gstm3'
ID 419092
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 # IGL03108
Quality Score
Status
Chromosome 3
Chromosomal Location 107871019-107876484 bp(-) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) A to T at 107875080 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000004136 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000004136]
AlphaFold P19639
Predicted Effect probably null
Transcript: ENSMUST00000004136
SMART Domains Protein: ENSMUSP00000004136
Gene: ENSMUSG00000004038

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: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrv1 C A 13: 81,707,648 (GRCm39) V1253F probably damaging Het
Apbb2 A G 5: 66,557,574 (GRCm39) W296R probably damaging Het
Armh3 G A 19: 45,808,792 (GRCm39) T633I probably damaging Het
Btbd3 T C 2: 138,126,043 (GRCm39) V409A possibly damaging Het
C130050O18Rik A T 5: 139,400,820 (GRCm39) D291V probably damaging Het
Catsper3 A G 13: 55,955,848 (GRCm39) N318D probably benign Het
Chd1 T A 17: 15,945,543 (GRCm39) D22E possibly damaging Het
Chrnb2 G A 3: 89,670,681 (GRCm39) probably benign Het
Col24a1 G A 3: 145,029,162 (GRCm39) G550D probably damaging Het
Cryl1 T C 14: 57,550,534 (GRCm39) D110G probably damaging Het
Deaf1 A G 7: 140,902,874 (GRCm39) I150T probably damaging Het
Eif3a A T 19: 60,770,747 (GRCm39) D33E possibly damaging Het
Fabp12 C A 3: 10,315,114 (GRCm39) G78C probably benign Het
Fat1 A G 8: 45,476,651 (GRCm39) D1899G probably damaging Het
Galnt13 G A 2: 54,744,660 (GRCm39) V120I probably benign Het
Ganab G A 19: 8,889,840 (GRCm39) A635T probably damaging Het
Gm17509 G A 13: 117,357,380 (GRCm39) probably benign Het
Hfm1 T A 5: 107,043,800 (GRCm39) probably benign Het
Hoxd13 A C 2: 74,500,440 (GRCm39) D327A probably damaging Het
Ints4 G T 7: 97,140,137 (GRCm39) probably null Het
Kcna10 A T 3: 107,102,259 (GRCm39) T297S probably benign Het
Ldb2 G A 5: 44,699,057 (GRCm39) T127I probably damaging Het
Mapk7 T C 11: 61,382,498 (GRCm39) D68G probably damaging Het
Msh3 A T 13: 92,357,596 (GRCm39) probably benign Het
Muc6 A G 7: 141,217,402 (GRCm39) S2359P possibly damaging Het
Mup6 A T 4: 60,005,990 (GRCm39) I161F possibly damaging Het
Nup160 G A 2: 90,534,169 (GRCm39) V665I probably benign Het
Or13a22 A G 7: 140,073,034 (GRCm39) N161S possibly damaging Het
Or14a258 T C 7: 86,034,929 (GRCm39) Y313C possibly damaging Het
Or4e5 T A 14: 52,727,533 (GRCm39) D296V probably damaging Het
Otog G A 7: 45,900,762 (GRCm39) V352I probably damaging Het
Oxct1 T A 15: 4,064,764 (GRCm39) V34D probably benign Het
Pcdhb21 T A 18: 37,648,944 (GRCm39) probably null Het
Pcdhb8 T G 18: 37,490,299 (GRCm39) V659G probably damaging Het
Plxnb2 T C 15: 89,042,234 (GRCm39) N1590S probably benign Het
Rnf168 G T 16: 32,097,099 (GRCm39) R56L possibly damaging Het
Scn8a C T 15: 100,872,496 (GRCm39) P362S probably benign Het
Slc1a3 T A 15: 8,668,562 (GRCm39) I468F probably damaging Het
Slc39a14 G A 14: 70,556,368 (GRCm39) R3W probably damaging Het
Slc7a6 T A 8: 106,921,149 (GRCm39) N373K probably damaging Het
Snrnp200 T C 2: 127,080,087 (GRCm39) S1955P possibly damaging Het
Stat5a T A 11: 100,753,965 (GRCm39) Y98* probably null Het
Thsd7b G T 1: 130,138,013 (GRCm39) G1564C probably damaging Het
Zc3h13 T C 14: 75,569,206 (GRCm39) V1351A possibly damaging 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
IGL03038:Gstm3 APN 3 107,873,485 (GRCm39) missense possibly damaging 0.75
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