Incidental Mutation 'IGL02672:Foxred2'
ID 302976
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Foxred2
Ensembl Gene ENSMUSG00000016552
Gene Name FAD-dependent oxidoreductase domain containing 2
Synonyms D15Bwg0759e, A430097D04Rik, LOC239554
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02672
Quality Score
Status
Chromosome 15
Chromosomal Location 77824722-77840922 bp(-) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) A to G at 77829777 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000113403 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000016696] [ENSMUST00000117725]
AlphaFold Q3USW5
Predicted Effect probably null
Transcript: ENSMUST00000016696
SMART Domains Protein: ENSMUSP00000016696
Gene: ENSMUSG00000016552

DomainStartEndE-ValueType
signal peptide 1 17 N/A INTRINSIC
Pfam:Pyr_redox_2 22 243 2.9e-11 PFAM
Pfam:Pyr_redox_3 25 240 9.3e-35 PFAM
Pfam:NAD_binding_8 26 84 3.3e-6 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000117725
SMART Domains Protein: ENSMUSP00000113403
Gene: ENSMUSG00000016552

DomainStartEndE-ValueType
signal peptide 1 17 N/A INTRINSIC
Pfam:Pyr_redox_2 23 478 3.4e-9 PFAM
Pfam:Pyr_redox_3 25 240 6.2e-37 PFAM
Pfam:NAD_binding_8 26 90 4.8e-7 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000140096
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agrn C T 4: 156,259,018 (GRCm39) probably benign Het
Alpi A G 1: 87,028,994 (GRCm39) L60P probably damaging Het
Arpc1a A C 5: 145,041,697 (GRCm39) I327L probably damaging Het
Col5a1 C T 2: 27,864,727 (GRCm39) A737V unknown Het
Dcaf7 T C 11: 105,945,684 (GRCm39) probably benign Het
Dnah9 T G 11: 65,818,427 (GRCm39) I3304L probably benign Het
Dpp10 T A 1: 123,304,376 (GRCm39) H508L probably benign Het
Dync1i1 A G 6: 5,767,034 (GRCm39) D86G probably benign Het
Enpp7 T C 11: 118,883,166 (GRCm39) probably null Het
Fbxw9 C A 8: 85,792,682 (GRCm39) probably null Het
Gas2l2 C T 11: 83,315,957 (GRCm39) R254H probably damaging Het
Gatad2b C T 3: 90,249,198 (GRCm39) L79F possibly damaging Het
Igf1r A T 7: 67,839,781 (GRCm39) D696V probably benign Het
Kcnk5 A G 14: 20,196,580 (GRCm39) I96T probably damaging Het
Lrrc8c C T 5: 105,755,224 (GRCm39) T333M possibly damaging Het
Mcm10 T C 2: 5,006,092 (GRCm39) T417A probably benign Het
Mesp2 T C 7: 79,461,145 (GRCm39) S157P probably benign Het
Naca A G 10: 127,876,152 (GRCm39) probably benign Het
Or5t17 A T 2: 86,832,417 (GRCm39) M35L probably benign Het
Osgepl1 A G 1: 53,359,270 (GRCm39) T260A probably benign Het
Otop1 T C 5: 38,435,170 (GRCm39) probably null Het
Pdk1 T C 2: 71,726,096 (GRCm39) S335P probably damaging Het
Phkb A G 8: 86,668,987 (GRCm39) N338S probably benign Het
Pogz G A 3: 94,763,410 (GRCm39) V61I probably benign Het
Ppp4r1 A G 17: 66,147,942 (GRCm39) Y928C probably damaging Het
Rab17 T C 1: 90,886,940 (GRCm39) E160G probably damaging Het
Rasgrp3 T A 17: 75,803,412 (GRCm39) F70Y probably benign Het
Rere T A 4: 150,594,483 (GRCm39) N364K unknown Het
Ryr1 A T 7: 28,703,944 (GRCm39) probably benign Het
Sae1 A G 7: 16,104,273 (GRCm39) V112A probably damaging Het
Serpinb6d C T 13: 33,855,372 (GRCm39) H349Y probably benign Het
Slc12a1 T C 2: 125,012,596 (GRCm39) V286A probably damaging Het
Smad3 A T 9: 63,575,009 (GRCm39) probably null Het
Sox8 T A 17: 25,787,963 (GRCm39) D162V probably damaging Het
Sptbn1 A G 11: 30,087,239 (GRCm39) F1067L probably damaging Het
Tmprss3 T C 17: 31,409,981 (GRCm39) Y211C probably damaging Het
Top2b T C 14: 16,409,166 (GRCm38) probably benign Het
Tpp1 A T 7: 105,396,168 (GRCm39) H510Q probably benign Het
Ugcg T A 4: 59,218,587 (GRCm39) probably benign Het
Vmn2r96 T A 17: 18,818,376 (GRCm39) I651N probably benign Het
Wdr25 A T 12: 108,864,007 (GRCm39) K51* probably null Het
Other mutations in Foxred2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01394:Foxred2 APN 15 77,839,820 (GRCm39) missense probably benign 0.30
IGL01479:Foxred2 APN 15 77,836,489 (GRCm39) splice site probably null
IGL01748:Foxred2 APN 15 77,836,546 (GRCm39) missense probably damaging 1.00
IGL02160:Foxred2 APN 15 77,839,850 (GRCm39) missense probably benign 0.03
IGL02328:Foxred2 APN 15 77,840,032 (GRCm39) missense probably damaging 1.00
IGL02630:Foxred2 APN 15 77,831,362 (GRCm39) missense probably benign 0.05
soma UTSW 15 77,837,558 (GRCm39) missense possibly damaging 0.78
R0271:Foxred2 UTSW 15 77,827,590 (GRCm39) missense possibly damaging 0.68
R1386:Foxred2 UTSW 15 77,832,721 (GRCm39) critical splice acceptor site probably null
R1581:Foxred2 UTSW 15 77,839,961 (GRCm39) missense possibly damaging 0.94
R4399:Foxred2 UTSW 15 77,839,880 (GRCm39) missense probably benign 0.06
R4399:Foxred2 UTSW 15 77,837,558 (GRCm39) missense possibly damaging 0.78
R4528:Foxred2 UTSW 15 77,827,449 (GRCm39) missense probably benign 0.01
R4937:Foxred2 UTSW 15 77,840,035 (GRCm39) missense probably damaging 1.00
R5165:Foxred2 UTSW 15 77,840,212 (GRCm39) missense probably damaging 1.00
R5318:Foxred2 UTSW 15 77,836,598 (GRCm39) missense probably benign 0.00
R5893:Foxred2 UTSW 15 77,831,344 (GRCm39) missense probably damaging 1.00
R6336:Foxred2 UTSW 15 77,839,964 (GRCm39) missense probably damaging 0.99
R6370:Foxred2 UTSW 15 77,827,506 (GRCm39) missense probably benign 0.01
R6426:Foxred2 UTSW 15 77,837,508 (GRCm39) missense probably damaging 1.00
R6826:Foxred2 UTSW 15 77,831,285 (GRCm39) missense probably benign 0.01
R6891:Foxred2 UTSW 15 77,839,909 (GRCm39) missense probably damaging 1.00
R6934:Foxred2 UTSW 15 77,836,530 (GRCm39) nonsense probably null
R7193:Foxred2 UTSW 15 77,836,230 (GRCm39) missense probably damaging 1.00
R7821:Foxred2 UTSW 15 77,827,550 (GRCm39) missense probably benign 0.01
R8401:Foxred2 UTSW 15 77,836,191 (GRCm39) missense probably damaging 0.98
R8540:Foxred2 UTSW 15 77,836,212 (GRCm39) missense probably damaging 1.00
R8844:Foxred2 UTSW 15 77,832,677 (GRCm39) missense probably benign 0.00
R8916:Foxred2 UTSW 15 77,837,514 (GRCm39) missense probably damaging 1.00
R8963:Foxred2 UTSW 15 77,829,805 (GRCm39) missense probably benign 0.20
R9104:Foxred2 UTSW 15 77,836,517 (GRCm39) missense probably damaging 1.00
R9153:Foxred2 UTSW 15 77,839,787 (GRCm39) critical splice donor site probably null
R9205:Foxred2 UTSW 15 77,836,206 (GRCm39) missense probably damaging 1.00
R9612:Foxred2 UTSW 15 77,836,206 (GRCm39) missense probably damaging 1.00
Z1088:Foxred2 UTSW 15 77,836,203 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16