Incidental Mutation 'IGL01577:Gm7168'
ID 91294
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7168
Ensembl Gene ENSMUSG00000067941
Gene Name predicted gene 7168
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # IGL01577
Quality Score
Status
Chromosome 17
Chromosomal Location 14168635-14170940 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 14169649 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Tryptophan at position 339 (R339W)
Ref Sequence ENSEMBL: ENSMUSP00000094997 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000088809]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000088809
AA Change: R339W

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000094997
Gene: ENSMUSG00000067941
AA Change: R339W

DomainStartEndE-ValueType
low complexity region 6 20 N/A INTRINSIC
S_TKc 28 276 5.25e-91 SMART
UBA 296 333 4.39e-2 SMART
low complexity region 436 451 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actr8 A G 14: 29,709,232 (GRCm39) T279A probably benign Het
Adamts9 T G 6: 92,835,128 (GRCm39) probably benign Het
Apba3 G A 10: 81,108,053 (GRCm39) G403D probably damaging Het
Atp13a4 C T 16: 29,260,102 (GRCm39) V235I possibly damaging Het
Brca2 T A 5: 150,465,085 (GRCm39) C1616* probably null Het
Ccdc7a T A 8: 129,715,244 (GRCm39) E280V probably damaging Het
Cdc42bpb A G 12: 111,268,477 (GRCm39) I1241T possibly damaging Het
Cplx4 G T 18: 66,103,015 (GRCm39) A35E probably damaging Het
Cyp2j8 T G 4: 96,367,308 (GRCm39) D270A probably damaging Het
Cyp7a1 T C 4: 6,273,618 (GRCm39) D96G probably damaging Het
Ddx11 G A 17: 66,446,398 (GRCm39) R429H possibly damaging Het
Depdc5 C A 5: 33,113,241 (GRCm39) T419N possibly damaging Het
Diaph3 A C 14: 87,143,467 (GRCm39) I737R probably damaging Het
Elf2 C T 3: 51,163,773 (GRCm39) probably benign Het
Epha6 T A 16: 59,777,289 (GRCm39) I673L possibly damaging Het
Ephx1 A G 1: 180,829,545 (GRCm39) M1T probably null Het
Fndc3a A T 14: 72,827,298 (GRCm39) M84K probably damaging Het
Gad2 T C 2: 22,571,292 (GRCm39) probably benign Het
Gba2 G A 4: 43,573,753 (GRCm39) Q180* probably null Het
Gga2 A G 7: 121,589,006 (GRCm39) Y574H probably damaging Het
Hdac10 T C 15: 89,010,416 (GRCm39) E302G possibly damaging Het
Ighv1-72 A G 12: 115,721,893 (GRCm39) V21A possibly damaging Het
Kif15 A G 9: 122,825,399 (GRCm39) E774G probably benign Het
Lig3 A G 11: 82,674,303 (GRCm39) N43S probably benign Het
Nmnat1 T A 4: 149,554,135 (GRCm39) D135V possibly damaging Het
Or1s2 A G 19: 13,758,162 (GRCm39) Y62C probably damaging Het
Or52n2 A G 7: 104,542,730 (GRCm39) F35S probably benign Het
Pak6 A C 2: 118,524,129 (GRCm39) K428T probably benign Het
Pou2f3 G A 9: 43,058,178 (GRCm39) Q56* probably null Het
Prep T C 10: 44,948,144 (GRCm39) probably benign Het
Psd4 C T 2: 24,293,234 (GRCm39) P700S probably damaging Het
Rad18 A T 6: 112,642,302 (GRCm39) probably benign Het
Rbbp5 A G 1: 132,420,393 (GRCm39) K209E possibly damaging Het
Smurf1 G A 5: 144,829,998 (GRCm39) T335I probably damaging Het
Tbcd G A 11: 121,387,838 (GRCm39) R72Q probably damaging Het
Tsga10 T C 1: 37,874,538 (GRCm39) T116A possibly damaging Het
Unc80 A G 1: 66,569,127 (GRCm39) probably null Het
Vmn1r87 C A 7: 12,865,775 (GRCm39) V171F probably benign Het
Ythdc2 A T 18: 44,991,349 (GRCm39) M786L probably benign Het
Zmym6 C A 4: 126,999,223 (GRCm39) T469K probably damaging Het
Other mutations in Gm7168
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01298:Gm7168 APN 17 14,170,120 (GRCm39) missense probably benign 0.00
IGL01392:Gm7168 APN 17 14,169,169 (GRCm39) missense probably benign
IGL01691:Gm7168 APN 17 14,169,140 (GRCm39) missense probably damaging 0.96
R0064:Gm7168 UTSW 17 14,170,121 (GRCm39) missense probably benign 0.21
R0611:Gm7168 UTSW 17 14,169,797 (GRCm39) missense probably benign
R0737:Gm7168 UTSW 17 14,169,245 (GRCm39) missense probably damaging 1.00
R1789:Gm7168 UTSW 17 14,169,846 (GRCm39) missense probably benign 0.03
R2864:Gm7168 UTSW 17 14,170,117 (GRCm39) missense probably benign 0.42
R2865:Gm7168 UTSW 17 14,170,117 (GRCm39) missense probably benign 0.42
R4179:Gm7168 UTSW 17 14,169,265 (GRCm39) missense probably benign 0.00
R4652:Gm7168 UTSW 17 14,170,069 (GRCm39) missense possibly damaging 0.88
R5174:Gm7168 UTSW 17 14,168,717 (GRCm39) missense probably damaging 1.00
R5722:Gm7168 UTSW 17 14,169,824 (GRCm39) missense probably benign
R6180:Gm7168 UTSW 17 14,168,858 (GRCm39) missense probably damaging 0.98
R7195:Gm7168 UTSW 17 14,169,622 (GRCm39) missense probably benign 0.01
R7366:Gm7168 UTSW 17 14,170,147 (GRCm39) missense probably damaging 1.00
R7490:Gm7168 UTSW 17 14,169,275 (GRCm39) missense probably benign 0.01
R7748:Gm7168 UTSW 17 14,168,914 (GRCm39) missense probably benign 0.03
R8113:Gm7168 UTSW 17 14,169,238 (GRCm39) nonsense probably null
R8201:Gm7168 UTSW 17 14,170,042 (GRCm39) missense probably benign
R9197:Gm7168 UTSW 17 14,169,489 (GRCm39) missense probably benign 0.13
R9260:Gm7168 UTSW 17 14,169,488 (GRCm39) missense probably benign 0.01
R9520:Gm7168 UTSW 17 14,169,506 (GRCm39) missense probably benign
X0020:Gm7168 UTSW 17 14,169,998 (GRCm39) missense probably benign 0.04
Z1177:Gm7168 UTSW 17 14,170,019 (GRCm39) missense probably benign 0.22
Z1177:Gm7168 UTSW 17 14,169,932 (GRCm39) missense probably damaging 1.00
Z1177:Gm7168 UTSW 17 14,169,344 (GRCm39) missense probably damaging 1.00
Posted On 2013-12-09