Incidental Mutation 'IGL02496:Nme9'
ID 295831
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Nme9
Ensembl Gene ENSMUSG00000046242
Gene Name NME/NM23 family member 9
Synonyms Txndc6
Accession Numbers
Essential gene? Probably non essential (E-score: 0.118) question?
Stock # IGL02496
Quality Score
Chromosome 9
Chromosomal Location 99451475-99474751 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 99469631 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Cysteine to Arginine at position 223 (C223R)
Ref Sequence ENSEMBL: ENSMUSP00000150820 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000163199]
AlphaFold A0A1L1SUL6
Predicted Effect noncoding transcript
Transcript: ENSMUST00000056103
Predicted Effect probably damaging
Transcript: ENSMUST00000163199
AA Change: C223R

PolyPhen 2 Score 0.971 (Sensitivity: 0.77; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000127845
Gene: ENSMUSG00000046242
AA Change: C223R

Pfam:Thioredoxin 1 76 6.3e-9 PFAM
NDK 97 241 9.98e-55 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000163199
AA Change: C223R

PolyPhen 2 Score 0.971 (Sensitivity: 0.77; Specificity: 0.96)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 70 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca12 T G 1: 71,288,553 (GRCm38) H1456P possibly damaging Het
Abcg1 C A 17: 31,105,604 (GRCm38) H274Q probably damaging Het
Adamts4 G A 1: 171,250,943 (GRCm38) R44Q probably benign Het
Amigo2 A T 15: 97,245,613 (GRCm38) C309* probably null Het
Ccdc88c A C 12: 100,953,293 (GRCm38) S446A probably benign Het
Cd9 A T 6: 125,472,495 (GRCm38) V28E probably damaging Het
Cops2 A T 2: 125,836,243 (GRCm38) probably benign Het
Csn1s1 C T 5: 87,677,594 (GRCm38) probably benign Het
Cul9 G T 17: 46,540,376 (GRCm38) R373S possibly damaging Het
D630045J12Rik G T 6: 38,149,705 (GRCm38) H1457N probably damaging Het
Dnah9 A G 11: 66,029,363 (GRCm38) S2235P probably damaging Het
Efr3b C T 12: 3,983,391 (GRCm38) V139I probably benign Het
Fbxo10 A T 4: 45,043,883 (GRCm38) W647R probably damaging Het
Flnb T A 14: 7,930,919 (GRCm38) probably benign Het
Flnc G T 6: 29,440,685 (GRCm38) V301L probably damaging Het
Hfm1 T C 5: 106,901,761 (GRCm38) S445G probably benign Het
Hif3a A G 7: 17,039,678 (GRCm38) probably benign Het
Hsd17b4 T C 18: 50,155,153 (GRCm38) Y217H probably damaging Het
Iba57 T C 11: 59,158,946 (GRCm38) T192A probably benign Het
Igkv5-48 A T 6: 69,726,687 (GRCm38) I78N probably damaging Het
Inhbe A T 10: 127,350,928 (GRCm38) W128R probably damaging Het
Ism1 T C 2: 139,757,201 (GRCm38) C365R probably damaging Het
Kif19a A T 11: 114,779,644 (GRCm38) T127S probably damaging Het
Kmt2d C A 15: 98,857,558 (GRCm38) probably benign Het
Mmp20 A G 9: 7,654,041 (GRCm38) R321G probably damaging Het
Msl2 T C 9: 101,100,655 (GRCm38) M76T possibly damaging Het
Nucb1 G T 7: 45,495,043 (GRCm38) probably benign Het
Ocrl G A X: 47,933,438 (GRCm38) D262N probably benign Het
Olfr1450 T A 19: 12,954,192 (GRCm38) I201N possibly damaging Het
Olfr449 A C 6: 42,838,804 (GRCm38) I308L probably benign Het
Olfr46 A C 7: 140,610,168 (GRCm38) M1L probably benign Het
P4ha1 A G 10: 59,371,002 (GRCm38) probably null Het
Parp8 T C 13: 116,862,302 (GRCm38) probably benign Het
Pcdhb6 A G 18: 37,335,454 (GRCm38) D476G probably damaging Het
Pikfyve A G 1: 65,264,376 (GRCm38) E1685G possibly damaging Het
Plod2 T A 9: 92,607,094 (GRCm38) L714Q probably damaging Het
Plscr2 A G 9: 92,289,663 (GRCm38) I103V probably benign Het
Plscr3 C A 11: 69,847,383 (GRCm38) probably benign Het
Pmaip1 A G 18: 66,463,299 (GRCm38) R80G probably damaging Het
Ppm1d C T 11: 85,339,666 (GRCm38) P370L possibly damaging Het
Prr36 C A 8: 4,216,407 (GRCm38) E48* probably null Het
Ptgir G A 7: 16,907,484 (GRCm38) V234I possibly damaging Het
Ptk7 A T 17: 46,590,144 (GRCm38) V219E probably benign Het
Rab39b T A X: 75,575,003 (GRCm38) I74F probably damaging Het
Rasal2 A T 1: 157,149,879 (GRCm38) M1075K possibly damaging Het
Rpl37a G A 1: 72,711,726 (GRCm38) A20T probably null Het
Serpinb10 A C 1: 107,538,425 (GRCm38) probably null Het
Sipa1l1 T A 12: 82,425,094 (GRCm38) Y1283N probably damaging Het
Slc22a23 T A 13: 34,344,485 (GRCm38) I105F possibly damaging Het
Slc25a20 T A 9: 108,682,400 (GRCm38) I221N probably damaging Het
Smarcal1 A T 1: 72,620,088 (GRCm38) H691L probably damaging Het
Smo A C 6: 29,758,481 (GRCm38) T542P probably damaging Het
Spats2 T A 15: 99,173,448 (GRCm38) I51N probably damaging Het
Spon1 G T 7: 114,036,662 (GRCm38) V704L probably benign Het
St5 C A 7: 109,556,235 (GRCm38) R436L possibly damaging Het
Tex9 T A 9: 72,482,492 (GRCm38) Q112L probably benign Het
Tgfbr2 T C 9: 116,090,418 (GRCm38) E580G probably benign Het
Top2b T A 14: 16,387,335 (GRCm38) V141E probably benign Het
Trhde A T 10: 114,800,561 (GRCm38) L247* probably null Het
Umodl1 G T 17: 30,998,654 (GRCm38) V1145F probably damaging Het
Vasp C A 7: 19,258,823 (GRCm38) probably benign Het
Vmn1r8 G T 6: 57,036,571 (GRCm38) L202F probably damaging Het
Vmn2r111 T C 17: 22,568,856 (GRCm38) T505A probably benign Het
Wdr27 A G 17: 14,892,431 (GRCm38) probably benign Het
Wfdc1 T G 8: 119,680,170 (GRCm38) V109G probably damaging Het
Zan C A 5: 137,464,794 (GRCm38) E708* probably null Het
Zbtb1 T A 12: 76,385,395 (GRCm38) F52I possibly damaging Het
Zfp236 A G 18: 82,629,992 (GRCm38) S1015P probably damaging Het
Zfp532 T C 18: 65,624,042 (GRCm38) S349P probably damaging Het
Znfx1 A T 2: 167,047,630 (GRCm38) C731S possibly damaging Het
Other mutations in Nme9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02573:Nme9 APN 9 99,470,855 (GRCm38) missense probably benign 0.45
R1900:Nme9 UTSW 9 99,459,774 (GRCm38) missense probably damaging 0.96
R4091:Nme9 UTSW 9 99,464,527 (GRCm38) missense possibly damaging 0.71
R5079:Nme9 UTSW 9 99,459,702 (GRCm38) missense probably damaging 1.00
R6400:Nme9 UTSW 9 99,469,707 (GRCm38) missense possibly damaging 0.88
R7611:Nme9 UTSW 9 99,470,790 (GRCm38) missense probably benign 0.19
R7659:Nme9 UTSW 9 99,470,857 (GRCm38) missense possibly damaging 0.73
R8791:Nme9 UTSW 9 99,468,248 (GRCm38) missense probably damaging 1.00
R9284:Nme9 UTSW 9 99,456,268 (GRCm38) critical splice donor site probably null
R9361:Nme9 UTSW 9 99,459,722 (GRCm38) missense probably damaging 1.00
Z1176:Nme9 UTSW 9 99,470,795 (GRCm38) missense possibly damaging 0.73
Posted On 2015-04-16