Incidental Mutation 'R3150:Gfod2'
ID271632
Institutional Source Beutler Lab
Gene Symbol Gfod2
Ensembl Gene ENSMUSG00000013150
Gene Nameglucose-fructose oxidoreductase domain containing 2
Synonyms
MMRRC Submission 040602-MU
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R3150 (G1)
Quality Score225
Status Not validated
Chromosome8
Chromosomal Location105713854-105758664 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 105717221 bp
ZygosityHeterozygous
Amino Acid Change Glycine to Aspartic acid at position 230 (G230D)
Ref Sequence ENSEMBL: ENSMUSP00000013294 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000013294] [ENSMUST00000155038]
Predicted Effect probably benign
Transcript: ENSMUST00000013294
AA Change: G230D

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000013294
Gene: ENSMUSG00000013150
AA Change: G230D

DomainStartEndE-ValueType
Pfam:GFO_IDH_MocA 6 119 3.7e-14 PFAM
low complexity region 169 180 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000155038
SMART Domains Protein: ENSMUSP00000122772
Gene: ENSMUSG00000013150

DomainStartEndE-ValueType
Pfam:GFO_IDH_MocA 6 92 6.7e-10 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9530053A07Rik C A 7: 28,154,195 T1528N probably benign Het
Akna A T 4: 63,395,353 S178T possibly damaging Het
BC067074 A T 13: 113,351,760 Q105H probably damaging Het
Cabin1 A G 10: 75,656,911 L1850P probably damaging Het
Ccdc178 G T 18: 22,067,652 A416E possibly damaging Het
Ces1g C T 8: 93,325,816 V282I probably benign Het
Col4a3 T G 1: 82,657,137 probably null Het
Crat C T 2: 30,413,859 probably null Het
Csf2ra C A 19: 61,227,320 A16S possibly damaging Het
Cyp4f18 T C 8: 71,993,200 D317G possibly damaging Het
Ddb1 T A 19: 10,612,982 M291K probably benign Het
Git2 A G 5: 114,730,349 S257P probably damaging Het
Gm5592 A G 7: 41,288,380 E362G probably benign Het
Gpatch2l A G 12: 86,244,315 T91A possibly damaging Het
Hjurp A G 1: 88,266,561 probably benign Het
Hnrnph1 T A 11: 50,385,792 V439E probably benign Het
Itgad C A 7: 128,190,981 H651N possibly damaging Het
Map3k20 C T 2: 72,371,992 T189M probably damaging Het
Mapk11 T C 15: 89,145,450 probably null Het
Mrc2 G A 11: 105,348,431 probably null Het
Nmral1 G A 16: 4,716,469 T36I probably damaging Het
Olfr1231 C T 2: 89,303,218 V125M possibly damaging Het
Olfr1475 A G 19: 13,479,460 V246A probably damaging Het
Olfr860 A G 9: 19,846,214 I135T possibly damaging Het
Padi6 A G 4: 140,735,389 L307P probably damaging Het
Pkd1 G T 17: 24,579,791 R2691L probably benign Het
Ppp2r2a G A 14: 67,023,765 R169W probably damaging Het
Prdm1 A T 10: 44,458,492 probably null Het
Robo1 C T 16: 72,970,269 P443L possibly damaging Het
Rtn4 CGAGGAGGAGGAGGAGGA CGAGGAGGAGGAGGA 11: 29,693,308 probably benign Het
Shprh A G 10: 11,170,030 H865R probably damaging Het
Spats1 A T 17: 45,464,554 S15T probably damaging Het
Srgap2 T C 1: 131,292,589 T216A probably benign Het
Sry ACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG ACTGCTGCTGCTGCTGCTGCTGCTGCTGCTG Y: 2,662,944 probably benign Het
Tie1 G A 4: 118,475,825 A902V probably damaging Het
Usp22 T C 11: 61,160,581 Q312R probably damaging Het
Vmn2r32 T C 7: 7,472,555 Y443C probably benign Het
Vps13d A C 4: 145,086,790 D3274E probably damaging Het
Wdr62 A T 7: 30,271,670 N167K possibly damaging Het
Xpo5 A G 17: 46,242,247 probably null Het
Zswim7 A T 11: 62,273,785 I43N possibly damaging Het
Zswim9 T C 7: 13,277,270 T51A possibly damaging Het
Other mutations in Gfod2
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1974:Gfod2 UTSW 8 105717510 missense possibly damaging 0.69
R4357:Gfod2 UTSW 8 105717545 missense possibly damaging 0.93
R4358:Gfod2 UTSW 8 105717545 missense possibly damaging 0.93
R4359:Gfod2 UTSW 8 105717545 missense possibly damaging 0.93
R4578:Gfod2 UTSW 8 105728246 start codon destroyed probably null 0.77
R4985:Gfod2 UTSW 8 105728011 missense probably damaging 1.00
R6913:Gfod2 UTSW 8 105717363 missense possibly damaging 0.90
R7062:Gfod2 UTSW 8 105722876 intron probably benign
R7851:Gfod2 UTSW 8 105728130 missense probably benign 0.44
R8299:Gfod2 UTSW 8 105728162 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TAAAGCAGTGGGACATCCTG -3'
(R):5'- CTGGATCTGTGACGAGCTTATG -3'

Sequencing Primer
(F):5'- AGTGGGACATCCTGGGGAC -3'
(R):5'- CACTTGACTGGCCAGAAA -3'
Posted On2015-03-25