Incidental Mutation 'IGL02951:Gsta1'
ID365980
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gsta1
Ensembl Gene ENSMUSG00000074183
Gene Nameglutathione S-transferase, alpha 1 (Ya)
SynonymsGst2-1
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.129) question?
Stock #IGL02951
Quality Score
Status
Chromosome9
Chromosomal Location78230656-78242684 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) A to T at 78242537 bp
ZygosityHeterozygous
Amino Acid Change Lysine to Stop codon at position 211 (K211*)
Ref Sequence ENSEMBL: ENSMUSP00000096139 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098537]
PDB Structure CRYSTAL STRUCTURE OF MGSTA1-1 IN COMPLEX WITH GSH [X-RAY DIFFRACTION]
CRYSTAL STRUCTURE OF MGSTA1-1 IN COMPLEX WITH GLUTATHIONE CONJUGATE OF BENZO[A]PYRENE EPOXIDE [X-RAY DIFFRACTION]
Predicted Effect probably null
Transcript: ENSMUST00000098537
AA Change: K211*
SMART Domains Protein: ENSMUSP00000096139
Gene: ENSMUSG00000074183
AA Change: K211*

DomainStartEndE-ValueType
Pfam:GST_N 5 77 6.7e-23 PFAM
Pfam:GST_C 99 192 2.8e-21 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000127192
Predicted Effect noncoding transcript
Transcript: ENSMUST00000214261
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2610028H24Rik C A 10: 76,454,702 probably benign Het
Acot10 G A 15: 20,665,782 T291I probably benign Het
Atp13a3 A G 16: 30,338,621 probably null Het
Atp2a1 C T 7: 126,450,227 V548M possibly damaging Het
Bsn G A 9: 108,115,613 S980L probably damaging Het
Ccdc158 A G 5: 92,650,006 M425T probably damaging Het
Cdh23 A G 10: 60,311,364 L2733S probably damaging Het
Chd3 C T 11: 69,361,048 probably null Het
Dock2 T C 11: 34,310,448 probably benign Het
Elfn2 T C 15: 78,671,882 K822E probably damaging Het
Eps15l1 G A 8: 72,358,396 S764L probably benign Het
Etl4 C A 2: 20,801,537 probably benign Het
Faap24 C A 7: 35,392,951 K180N probably damaging Het
Fam205a1 C T 4: 42,850,696 E487K probably benign Het
Fhod1 G A 8: 105,331,230 R888W probably damaging Het
Fus T C 7: 127,981,837 probably benign Het
Gm3453 T C 14: 5,976,168 E201G possibly damaging Het
Gm5346 T G 8: 43,627,088 H33P possibly damaging Het
Gnpat G T 8: 124,870,905 D69Y probably benign Het
Gpaa1 T A 15: 76,332,819 probably benign Het
Lct G T 1: 128,300,211 Q1182K probably damaging Het
Mroh1 T C 15: 76,427,636 L523P probably damaging Het
Mrpl46 A G 7: 78,775,452 probably benign Het
Mst1r G T 9: 107,908,204 V354F possibly damaging Het
Myo15b A G 11: 115,881,301 D299G probably damaging Het
Myo6 G A 9: 80,264,234 V506I possibly damaging Het
Nadk A C 4: 155,587,476 K271Q probably benign Het
Nbas A G 12: 13,362,541 R954G probably benign Het
Nbr1 T A 11: 101,571,979 probably null Het
Nup88 T C 11: 70,944,872 D587G possibly damaging Het
Oas1a A T 5: 120,905,664 F135Y probably damaging Het
Obscn A G 11: 58,994,513 probably benign Het
Odf3l2 T C 10: 79,639,977 N251S probably benign Het
Olfr1290 T G 2: 111,490,120 I13L probably benign Het
Parp14 G A 16: 35,858,533 T355I probably benign Het
Pdgfd G T 9: 6,288,494 L43F probably damaging Het
Pou5f2 T C 13: 78,025,118 S60P probably benign Het
Prp2 A G 6: 132,599,825 N25S unknown Het
Ptprq A T 10: 107,667,460 F779Y probably benign Het
Rims2 C T 15: 39,534,938 R1078C probably damaging Het
Rnf38 G T 4: 44,129,619 S425* probably null Het
Rps21 T A 2: 180,258,047 I59N probably damaging Het
Scn5a A T 9: 119,495,685 F1359Y probably damaging Het
Slc35b2 A G 17: 45,564,768 E67G probably damaging Het
Slc37a2 A G 9: 37,255,315 F15L probably benign Het
Snapc4 A C 2: 26,370,835 N465K probably benign Het
Stxbp2 A T 8: 3,641,971 I538F probably benign Het
Taco1 A G 11: 106,069,527 N98S probably benign Het
Tcea3 T C 4: 136,257,988 probably null Het
Thada T C 17: 84,444,028 S507G probably benign Het
Tmem132b T A 5: 125,787,547 C906S probably damaging Het
Trpm2 A T 10: 77,929,278 I963N possibly damaging Het
Usp10 A G 8: 119,947,086 T397A probably benign Het
Usp3 G A 9: 66,542,550 R160* probably null Het
Utp15 T C 13: 98,257,952 Y144C probably damaging Het
Xpc G A 6: 91,506,849 R172W probably damaging Het
Other mutations in Gsta1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1102:Gsta1 UTSW 9 78242495 missense probably damaging 1.00
R1483:Gsta1 UTSW 9 78242493 missense probably damaging 1.00
R1566:Gsta1 UTSW 9 78242459 nonsense probably null
R6130:Gsta1 UTSW 9 78242565 missense probably damaging 0.99
R7910:Gsta1 UTSW 9 78232295 missense probably damaging 1.00
Z1177:Gsta1 UTSW 9 78232242 start codon destroyed probably null 1.00
Posted On2015-12-18