Incidental Mutation 'R8108:Impact'
ID 630770
Institutional Source Beutler Lab
Gene Symbol Impact
Ensembl Gene ENSMUSG00000024423
Gene Name impact, RWD domain protein
Synonyms E430016J11Rik
MMRRC Submission
Accession Numbers
Is this an essential gene? Possibly essential (E-score: 0.541) question?
Stock # R8108 (G1)
Quality Score 225.009
Status Validated
Chromosome 18
Chromosomal Location 12972252-12992948 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to G at 12984331 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Leucine to Valine at position 154 (L154V)
Ref Sequence ENSEMBL: ENSMUSP00000025290 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025290]
AlphaFold O55091
Predicted Effect probably benign
Transcript: ENSMUST00000025290
AA Change: L154V

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000025290
Gene: ENSMUSG00000024423
AA Change: L154V

DomainStartEndE-ValueType
RWD 14 116 7.86e-29 SMART
low complexity region 126 139 N/A INTRINSIC
low complexity region 160 171 N/A INTRINSIC
Pfam:UPF0029 180 288 8.5e-36 PFAM
low complexity region 306 315 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 99.0%
  • 20x: 97.3%
Validation Efficiency 99% (72/73)
Allele List at MGI
Other mutations in this stock
Total: 73 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acot1 T A 12: 84,017,361 H414Q probably benign Het
Actrt2 A T 4: 154,667,036 D214E probably benign Het
Ccdc7a T C 8: 128,980,153 T332A unknown Het
Chd9 C T 8: 90,933,224 H271Y unknown Het
Depdc5 T G 5: 32,945,049 D966E probably benign Het
Dolpp1 A G 2: 30,396,246 Y119C probably benign Het
Dscam G C 16: 96,643,879 D1537E probably benign Het
Dusp16 A G 6: 134,739,873 I157T probably benign Het
Dyrk2 T C 10: 118,859,829 D508G probably benign Het
Endov T C 11: 119,507,411 V334A probably benign Het
Ep400 A T 5: 110,687,883 V1956E unknown Het
Erich3 A T 3: 154,720,115 Y83F possibly damaging Het
Fbrsl1 T C 5: 110,378,379 probably null Het
Gm1110 T C 9: 26,920,661 I65V probably damaging Het
Gm28374 A G 19: 6,082,200 V19A Het
Gm436 A T 4: 144,670,669 N164K probably benign Het
Gpr107 C A 2: 31,184,869 H336Q probably damaging Het
Gpr137b T C 13: 13,359,406 Y355C Het
Grm1 C A 10: 10,720,132 R584L probably benign Het
Gse1 T C 8: 120,229,810 S347P unknown Het
Ier3ip1 T A 18: 76,940,525 I69K possibly damaging Het
Katnb1 T C 8: 95,093,945 F141S possibly damaging Het
Kifap3 T A 1: 163,797,362 N162K probably damaging Het
Klhl5 A G 5: 65,148,587 probably null Het
Klre1 A G 6: 129,584,222 D182G probably benign Het
Krt42 T A 11: 100,266,957 Y227F probably benign Het
Lhcgr T A 17: 88,742,050 K683* probably null Het
Lrrc37a G A 11: 103,503,057 S514F probably benign Het
Lrrc9 G T 12: 72,454,059 L186F probably damaging Het
Metrn A G 17: 25,795,030 V274A probably benign Het
Mettl25 A T 10: 105,823,179 F414L possibly damaging Het
Mixl1 A G 1: 180,696,702 V104A probably damaging Het
Myo9b T A 8: 71,348,342 M1047K probably damaging Het
Nbea G A 3: 55,819,315 A2081V probably benign Het
Ndufs1 A T 1: 63,150,012 D551E possibly damaging Het
Nectin3 T C 16: 46,464,121 T67A possibly damaging Het
Nme8 C T 13: 19,650,960 V519I probably benign Het
Npat G T 9: 53,571,129 G1379V probably benign Het
Obscn T A 11: 59,061,634 T3870S probably benign Het
Olfr1000 T C 2: 85,608,749 R54G possibly damaging Het
Olfr1288 T C 2: 111,479,234 V150A possibly damaging Het
Olfr177 T C 16: 58,872,236 M305V probably benign Het
Olfr379-ps1 T A 11: 73,433,854 H124L unknown Het
Olfr871 T A 9: 20,212,451 M34K possibly damaging Het
Olfr910 A G 9: 38,539,410 N172D probably damaging Het
Parp8 A T 13: 116,867,073 Y769* probably null Het
Pcnx C T 12: 81,918,819 R59* probably null Het
Pdzd2 G A 15: 12,373,506 S2181L probably benign Het
Phldb1 T C 9: 44,711,161 E65G probably damaging Het
Ppif C T 14: 25,698,326 T157M probably damaging Het
Ppp3ca T A 3: 136,932,225 probably null Het
Proser1 T A 3: 53,472,088 probably null Het
Reg3d T A 6: 78,376,079 K174* probably null Het
Rubcn A T 16: 32,856,950 L55Q probably damaging Het
Sec14l3 T C 11: 4,066,198 L39P probably damaging Het
Ska3 A G 14: 57,826,102 I4T probably damaging Het
Slc30a10 A G 1: 185,464,154 I338V possibly damaging Het
Slc35g1 C G 19: 38,402,829 S186R probably damaging Het
Slc35g1 T A 19: 38,402,831 L187H probably damaging Het
Spata5 T C 3: 37,431,782 S218P probably benign Het
Tbc1d5 T C 17: 50,742,086 I659V probably benign Het
Tbl3 G T 17: 24,700,916 D751E probably benign Het
Tdrd3 T A 14: 87,486,266 D311E possibly damaging Het
Tenm4 T C 7: 96,854,728 F1335S probably benign Het
Tm2d1 A T 4: 98,375,023 C83S probably damaging Het
Tnfrsf22 A T 7: 143,638,373 V192D unknown Het
Trpm6 A G 19: 18,811,790 T575A probably damaging Het
Uri1 T C 7: 37,981,673 D102G possibly damaging Het
Vmn2r1 T A 3: 64,103,050 C570S probably damaging Het
Vps13a C T 19: 16,640,787 V2906I probably damaging Het
Zfp472 T C 17: 32,978,003 Y351H possibly damaging Het
Zfp874a G T 13: 67,443,234 Y110* probably null Het
Zfp986 T A 4: 145,899,305 N178K probably benign Het
Other mutations in Impact
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01531:Impact APN 18 12976019 missense probably benign 0.00
IGL01960:Impact APN 18 12974758 missense probably benign 0.13
R1056:Impact UTSW 18 12976524 missense probably benign 0.14
R1552:Impact UTSW 18 12984280 missense probably benign 0.25
R4111:Impact UTSW 18 12976033 critical splice donor site probably null
R4734:Impact UTSW 18 12985289 missense probably damaging 1.00
R4885:Impact UTSW 18 12986373 missense probably damaging 1.00
R5566:Impact UTSW 18 12974762 missense probably damaging 0.98
R5601:Impact UTSW 18 12976007 missense probably benign 0.44
R5966:Impact UTSW 18 12990544 missense probably benign 0.00
R6974:Impact UTSW 18 12982112 missense probably damaging 1.00
R7168:Impact UTSW 18 12986313 splice site probably null
R8460:Impact UTSW 18 12976507 missense probably benign 0.00
R8474:Impact UTSW 18 12974741 missense probably damaging 1.00
R8897:Impact UTSW 18 12990494 missense probably benign 0.10
Z1177:Impact UTSW 18 12988366 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ATGGTGTGTAGAGATCAAGACCC -3'
(R):5'- ATGTACCCCTGTAGTCCCAG -3'

Sequencing Primer
(F):5'- TCACTGTATGGCCTAGAACTAGC -3'
(R):5'- CTCTACCGAGTGAGTTCCAGGATAG -3'
Posted On 2020-06-30