Incidental Mutation 'R6545:Gm19410'
ID 521109
Institutional Source Beutler Lab
Gene Symbol Gm19410
Ensembl Gene ENSMUSG00000109372
Gene Name predicted gene, 19410
Synonyms
MMRRC Submission 044671-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.145) question?
Stock # R6545 (G1)
Quality Score 225.009
Status Validated
Chromosome 8
Chromosomal Location 36232944-36285201 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 36257652 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Glycine at position 697 (R697G)
Ref Sequence ENSEMBL: ENSMUSP00000147162 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000207505]
AlphaFold A0A140LJC7
Predicted Effect possibly damaging
Transcript: ENSMUST00000207505
AA Change: R697G

PolyPhen 2 Score 0.930 (Sensitivity: 0.81; Specificity: 0.94)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.3%
  • 20x: 97.6%
Validation Efficiency 95% (42/44)
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ago1 C T 4: 126,348,145 (GRCm39) A58T possibly damaging Het
Ago4 T A 4: 126,405,811 (GRCm39) Q366L probably benign Het
Card10 C A 15: 78,661,010 (GRCm39) G950V probably damaging Het
Ceacam1 A T 7: 25,173,279 (GRCm39) V303D probably damaging Het
Cfap54 C T 10: 92,672,319 (GRCm39) R2917H probably benign Het
Cit A G 5: 115,984,493 (GRCm39) S22G probably null Het
Cog4 A G 8: 111,607,577 (GRCm39) E666G probably damaging Het
Crocc2 A G 1: 93,140,659 (GRCm39) D1103G probably benign Het
Cttnbp2 A T 6: 18,405,278 (GRCm39) probably null Het
Dctn3 T C 4: 41,723,084 (GRCm39) E16G probably damaging Het
Dnah6 A G 6: 73,021,715 (GRCm39) S3536P probably damaging Het
Eef2 T A 10: 81,016,948 (GRCm39) I675N probably damaging Het
Gga3 A G 11: 115,477,995 (GRCm39) F531S possibly damaging Het
Gm3173 T A 14: 15,728,395 (GRCm39) M18K possibly damaging Het
Gm5800 A T 14: 51,949,419 (GRCm39) S175R possibly damaging Het
Gria2 T C 3: 80,648,451 (GRCm39) K95R probably damaging Het
Gstm6 A G 3: 107,849,681 (GRCm39) I76T probably damaging Het
Harbi1 T G 2: 91,542,640 (GRCm39) Y34D probably damaging Het
Hectd2 C A 19: 36,564,778 (GRCm39) Q20K probably benign Het
Inpp5f C A 7: 128,296,280 (GRCm39) A250D possibly damaging Het
Irf9 T C 14: 55,842,684 (GRCm39) F59L probably damaging Het
Itgam T A 7: 127,707,044 (GRCm39) M625K probably damaging Het
Kcnh5 C T 12: 75,054,432 (GRCm39) R504Q probably damaging Het
Lama2 T C 10: 27,052,793 (GRCm39) T1389A probably benign Het
Lin54 T A 5: 100,632,996 (GRCm39) probably null Het
Mettl23 A G 11: 116,740,042 (GRCm39) D171G possibly damaging Het
Mgll A G 6: 88,802,685 (GRCm39) N296S probably benign Het
Mpv17 T A 5: 31,302,041 (GRCm39) probably benign Het
Myof A T 19: 37,930,745 (GRCm39) M1001K possibly damaging Het
Myom1 A T 17: 71,389,300 (GRCm39) Q850L probably benign Het
Or10ab5 A T 7: 108,245,662 (GRCm39) N40K probably damaging Het
Pias2 A G 18: 77,217,781 (GRCm39) I328V possibly damaging Het
Polh G A 17: 46,493,685 (GRCm39) P311S possibly damaging Het
Prss34 A T 17: 25,517,809 (GRCm39) R61S probably benign Het
Rassf2 A T 2: 131,840,237 (GRCm39) M280K probably damaging Het
Rpsa A G 9: 119,959,323 (GRCm39) H47R probably benign Het
Rtp3 A G 9: 110,815,894 (GRCm39) V219A possibly damaging Het
Smarcc2 T C 10: 128,319,997 (GRCm39) I790T probably benign Het
Stag3 A G 5: 138,296,614 (GRCm39) T491A possibly damaging Het
Svil C T 18: 5,108,621 (GRCm39) H2007Y probably benign Het
Togaram1 T G 12: 65,024,981 (GRCm39) C750G possibly damaging Het
Vmn2r13 A T 5: 109,304,806 (GRCm39) probably null Het
Vmn2r4 A T 3: 64,313,777 (GRCm39) D401E possibly damaging Het
Wdr97 C T 15: 76,247,578 (GRCm39) R1585C probably damaging Het
Wsb1 A T 11: 79,141,881 (GRCm39) D45E probably damaging Het
Zfp808 T A 13: 62,319,709 (GRCm39) Y313N probably benign Het
Other mutations in Gm19410
AlleleSourceChrCoordTypePredicted EffectPPH Score
BB009:Gm19410 UTSW 8 36,262,753 (GRCm39) missense probably damaging 0.98
BB019:Gm19410 UTSW 8 36,262,753 (GRCm39) missense probably damaging 0.98
R0046:Gm19410 UTSW 8 36,269,799 (GRCm39) missense probably benign 0.31
R6026:Gm19410 UTSW 8 36,279,580 (GRCm39) missense probably benign 0.03
R6039:Gm19410 UTSW 8 36,276,518 (GRCm39) missense probably benign 0.44
R6039:Gm19410 UTSW 8 36,276,518 (GRCm39) missense probably benign 0.44
R6185:Gm19410 UTSW 8 36,274,664 (GRCm39) missense possibly damaging 0.87
R6239:Gm19410 UTSW 8 36,245,918 (GRCm39) missense probably damaging 0.98
R6303:Gm19410 UTSW 8 36,274,714 (GRCm39) missense possibly damaging 0.96
R6377:Gm19410 UTSW 8 36,270,736 (GRCm39) nonsense probably null
R6700:Gm19410 UTSW 8 36,274,664 (GRCm39) missense possibly damaging 0.87
R6720:Gm19410 UTSW 8 36,274,730 (GRCm39) missense probably benign 0.12
R6795:Gm19410 UTSW 8 36,262,676 (GRCm39) missense probably damaging 0.98
R6808:Gm19410 UTSW 8 36,239,733 (GRCm39) missense probably damaging 0.99
R6810:Gm19410 UTSW 8 36,239,733 (GRCm39) missense probably damaging 0.99
R6811:Gm19410 UTSW 8 36,239,733 (GRCm39) missense probably damaging 0.99
R6966:Gm19410 UTSW 8 36,285,127 (GRCm39) missense possibly damaging 0.84
R7264:Gm19410 UTSW 8 36,252,920 (GRCm39) missense probably benign 0.01
R7267:Gm19410 UTSW 8 36,281,997 (GRCm39) missense possibly damaging 0.80
R7355:Gm19410 UTSW 8 36,274,226 (GRCm39) missense probably benign 0.00
R7423:Gm19410 UTSW 8 36,271,761 (GRCm39) missense probably benign 0.28
R7494:Gm19410 UTSW 8 36,262,684 (GRCm39) missense probably damaging 0.99
R7516:Gm19410 UTSW 8 36,263,433 (GRCm39) missense probably benign 0.30
R7517:Gm19410 UTSW 8 36,240,772 (GRCm39) missense possibly damaging 0.45
R7526:Gm19410 UTSW 8 36,257,766 (GRCm39) missense probably damaging 0.98
R7527:Gm19410 UTSW 8 36,269,386 (GRCm39) missense probably damaging 0.99
R7545:Gm19410 UTSW 8 36,269,779 (GRCm39) missense probably damaging 0.99
R7549:Gm19410 UTSW 8 36,266,500 (GRCm39) missense probably benign 0.20
R7564:Gm19410 UTSW 8 36,274,151 (GRCm39) missense probably benign 0.00
R7615:Gm19410 UTSW 8 36,263,513 (GRCm39) missense probably damaging 1.00
R7622:Gm19410 UTSW 8 36,277,501 (GRCm39) missense possibly damaging 0.91
R7655:Gm19410 UTSW 8 36,276,253 (GRCm39) missense probably benign
R7656:Gm19410 UTSW 8 36,276,253 (GRCm39) missense probably benign
R7703:Gm19410 UTSW 8 36,266,539 (GRCm39) missense probably damaging 0.98
R7750:Gm19410 UTSW 8 36,274,652 (GRCm39) missense possibly damaging 0.68
R7760:Gm19410 UTSW 8 36,269,491 (GRCm39) missense probably damaging 0.99
R7837:Gm19410 UTSW 8 36,276,134 (GRCm39) missense possibly damaging 0.91
R7932:Gm19410 UTSW 8 36,262,753 (GRCm39) missense probably damaging 0.98
R7942:Gm19410 UTSW 8 36,238,940 (GRCm39) missense probably damaging 0.98
R7970:Gm19410 UTSW 8 36,282,801 (GRCm39) missense probably benign 0.00
R8088:Gm19410 UTSW 8 36,273,995 (GRCm39) missense probably benign 0.45
R8228:Gm19410 UTSW 8 36,252,992 (GRCm39) missense possibly damaging 0.53
R8382:Gm19410 UTSW 8 36,276,302 (GRCm39) missense probably damaging 0.99
R8757:Gm19410 UTSW 8 36,276,119 (GRCm39) missense possibly damaging 0.83
R8879:Gm19410 UTSW 8 36,239,022 (GRCm39) missense probably damaging 0.99
R9010:Gm19410 UTSW 8 36,282,011 (GRCm39) missense probably benign 0.02
R9060:Gm19410 UTSW 8 36,269,480 (GRCm39) missense probably damaging 1.00
R9088:Gm19410 UTSW 8 36,240,766 (GRCm39) missense probably damaging 1.00
R9104:Gm19410 UTSW 8 36,247,621 (GRCm39) missense probably damaging 0.99
R9186:Gm19410 UTSW 8 36,282,629 (GRCm39) missense possibly damaging 0.90
R9290:Gm19410 UTSW 8 36,269,386 (GRCm39) missense probably damaging 0.99
R9334:Gm19410 UTSW 8 36,270,722 (GRCm39) nonsense probably null
R9398:Gm19410 UTSW 8 36,272,356 (GRCm39) missense probably benign 0.00
R9439:Gm19410 UTSW 8 36,248,810 (GRCm39) missense probably damaging 0.96
R9445:Gm19410 UTSW 8 36,239,652 (GRCm39) missense possibly damaging 0.75
R9511:Gm19410 UTSW 8 36,257,848 (GRCm39) missense probably damaging 0.99
R9520:Gm19410 UTSW 8 36,262,637 (GRCm39) missense probably benign 0.15
R9523:Gm19410 UTSW 8 36,257,608 (GRCm39) missense probably benign 0.01
R9669:Gm19410 UTSW 8 36,247,493 (GRCm39) missense possibly damaging 0.45
R9711:Gm19410 UTSW 8 36,279,493 (GRCm39) missense possibly damaging 0.85
R9728:Gm19410 UTSW 8 36,247,594 (GRCm39) missense possibly damaging 0.95
R9759:Gm19410 UTSW 8 36,252,938 (GRCm39) missense possibly damaging 0.53
Z1176:Gm19410 UTSW 8 36,259,765 (GRCm39) missense possibly damaging 0.79
Z1177:Gm19410 UTSW 8 36,276,119 (GRCm39) missense possibly damaging 0.83
Predicted Primers PCR Primer
(F):5'- GGCAGTAGGAGGCTCATGATAC -3'
(R):5'- AAAGCCATCCGAGTGTCTGC -3'

Sequencing Primer
(F):5'- CATGATACAAAGAAGTGTCTGCTCG -3'
(R):5'- ATCCGAGTGTCTGCTGCCC -3'
Posted On 2018-06-06