Incidental Mutation 'R6456:Gm11127'
ID520228
Institutional Source Beutler Lab
Gene Symbol Gm11127
Ensembl Gene ENSMUSG00000079492
Gene Namepredicted gene 11127
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.061) question?
Stock #R6456 (G1)
Quality Score225.009
Status Not validated
Chromosome17
Chromosomal Location36055816-36058371 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 36056610 bp
ZygosityHeterozygous
Amino Acid Change Tyrosine to Asparagine at position 279 (Y279N)
Ref Sequence ENSEMBL: ENSMUSP00000109371 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000097331] [ENSMUST00000113742]
Predicted Effect probably benign
Transcript: ENSMUST00000097331
SMART Domains Protein: ENSMUSP00000094943
Gene: ENSMUSG00000073407

DomainStartEndE-ValueType
transmembrane domain 15 37 N/A INTRINSIC
low complexity region 103 115 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000113742
AA Change: Y279N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000109371
Gene: ENSMUSG00000079492
AA Change: Y279N

DomainStartEndE-ValueType
signal peptide 1 23 N/A INTRINSIC
Pfam:MHC_I 26 204 6.4e-81 PFAM
IGc1 220 291 2.53e-23 SMART
transmembrane domain 306 328 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.5%
  • 10x: 97.4%
  • 20x: 91.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931408C20Rik T A 1: 26,685,169 H310L probably damaging Het
9930021J03Rik G A 19: 29,716,514 P1860S possibly damaging Het
Abca13 A T 11: 9,290,474 H779L possibly damaging Het
Abca7 T C 10: 80,015,150 V2097A probably null Het
Adam8 A G 7: 139,986,788 S524P possibly damaging Het
Anapc2 T C 2: 25,280,195 M575T probably damaging Het
Arhgap42 T A 9: 9,005,822 I736L probably benign Het
AU040320 A G 4: 126,842,491 N789S probably benign Het
Bmi1 A G 2: 18,682,247 Y46C probably damaging Het
Ccdc125 T C 13: 100,696,309 S465P possibly damaging Het
Cd180 C T 13: 102,702,836 L76F probably damaging Het
Cep135 T C 5: 76,591,724 probably benign Het
Col6a5 G A 9: 105,945,477 T227I unknown Het
Cyp4a29 G T 4: 115,251,184 M368I probably benign Het
Ddx28 T A 8: 106,010,368 I353F possibly damaging Het
Ddx58 T A 4: 40,213,838 N607Y possibly damaging Het
Dhx40 G A 11: 86,784,974 T198M probably damaging Het
Fam71f1 A G 6: 29,334,046 N299S probably benign Het
Fat4 G A 3: 38,983,979 V3927M possibly damaging Het
Gm10226 G T 17: 21,692,025 G56* probably null Het
Itsn2 T G 12: 4,629,923 probably benign Het
Lrrc8a A G 2: 30,255,474 D100G probably benign Het
Madd T C 2: 91,178,191 H122R probably benign Het
Mfsd4b3 C G 10: 39,947,320 V315L probably benign Het
Mki67 C G 7: 135,699,475 A1277P possibly damaging Het
Nlrp9b T A 7: 20,048,778 N872K probably damaging Het
Npas1 T C 7: 16,461,926 T274A probably benign Het
Nrm A T 17: 35,865,400 probably null Het
Olfr418 A T 1: 173,270,538 D121V probably damaging Het
Pdilt T A 7: 119,500,483 L187F probably damaging Het
Pkdcc T C 17: 83,220,119 I242T probably damaging Het
Plch2 C A 4: 154,993,002 D535Y probably damaging Het
Pmpca T A 2: 26,395,167 I468N probably damaging Het
Prpf4 T C 4: 62,414,632 probably null Het
Rcc1 A G 4: 132,334,116 S361P probably benign Het
Rnf213 A G 11: 119,459,966 I3876V probably benign Het
Sall2 T A 14: 52,313,593 Q715L probably damaging Het
Sall2 G A 14: 52,313,594 Q713* probably null Het
Sin3a A G 9: 57,113,701 S1004G possibly damaging Het
Sltm C T 9: 70,542,987 T23M probably damaging Het
Sspo A G 6: 48,451,806 E385G probably benign Het
Syne3 G T 12: 104,940,704 R775S possibly damaging Het
Szt2 A T 4: 118,376,697 probably benign Het
Tlk2 T C 11: 105,221,273 S151P probably benign Het
Trabd2b C T 4: 114,586,560 R305C probably damaging Het
Ttc21b T C 2: 66,188,331 Q1244R probably damaging Het
Vmn2r125 A G 4: 156,351,062 N245S probably benign Het
Wdr34 T C 2: 30,032,767 S323G probably benign Het
Wdr64 G A 1: 175,785,609 probably null Het
Wdr70 G A 15: 7,885,637 T550M possibly damaging Het
Wdr78 A C 4: 103,049,549 M689R probably benign Het
Other mutations in Gm11127
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01859:Gm11127 APN 17 36058011 missense possibly damaging 0.78
IGL02007:Gm11127 APN 17 36056330 missense possibly damaging 0.50
R1075:Gm11127 UTSW 17 36056146 missense probably benign 0.05
R1829:Gm11127 UTSW 17 36058004 missense probably damaging 1.00
R1944:Gm11127 UTSW 17 36058005 missense probably damaging 1.00
R4117:Gm11127 UTSW 17 36057604 missense probably damaging 1.00
R4584:Gm11127 UTSW 17 36057667 missense probably damaging 1.00
R4626:Gm11127 UTSW 17 36057896 frame shift probably null
R4649:Gm11127 UTSW 17 36057876 missense possibly damaging 0.90
R4864:Gm11127 UTSW 17 36058361 utr 3 prime probably benign
R5412:Gm11127 UTSW 17 36056044 missense probably benign 0.01
R5430:Gm11127 UTSW 17 36056075 missense probably benign 0.00
R5547:Gm11127 UTSW 17 36057904 missense possibly damaging 0.63
R5896:Gm11127 UTSW 17 36056344 missense probably benign 0.01
R5974:Gm11127 UTSW 17 36056785 missense probably benign 0.05
R7073:Gm11127 UTSW 17 36058343 missense unknown
R7217:Gm11127 UTSW 17 36056343 missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- ACCATGTTAGAGTCGGTGGATG -3'
(R):5'- CAAGCACCTGCAGTTTCCAG -3'

Sequencing Primer
(F):5'- TCGGTGGATGGAAGAGGCTC -3'
(R):5'- CTGCAGTTTCCAGGAAGAATG -3'
Posted On2018-06-06