Incidental Mutation 'R4843:Gm11146'
Institutional Source Beutler Lab
Gene Symbol Gm11146
Ensembl Gene ENSMUSG00000079546
Gene Namepredicted gene 11146
MMRRC Submission 042456-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.103) question?
Stock #R4843 (G1)
Quality Score213
Status Validated
Chromosomal Location77588578-77602094 bp(-) (GRCm38)
Type of Mutationintron
DNA Base Change (assembly) A to C at 77595256 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000109869 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000114231]
Predicted Effect noncoding transcript
Transcript: ENSMUST00000068704
SMART Domains Protein: ENSMUSP00000070456
Gene: ENSMUSG00000052450

low complexity region 23 42 N/A INTRINSIC
low complexity region 105 116 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000083596
Predicted Effect noncoding transcript
Transcript: ENSMUST00000083623
Predicted Effect probably benign
Transcript: ENSMUST00000114231
Predicted Effect noncoding transcript
Transcript: ENSMUST00000170849
SMART Domains Protein: ENSMUSP00000127794
Gene: ENSMUSG00000090386

transmembrane domain 20 42 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182398
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182601
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182656
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182820
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182986
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183099
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183327
Predicted Effect noncoding transcript
Transcript: ENSMUST00000194553
Predicted Effect noncoding transcript
Transcript: ENSMUST00000231957
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.6%
  • 20x: 93.1%
Validation Efficiency 95% (58/61)
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acp1 T A 12: 30,896,145 K124* probably null Het
Actl11 G T 9: 107,929,492 C338F possibly damaging Het
Adam5 G A 8: 24,813,536 S125F probably damaging Het
Ap2s1 C A 7: 16,743,346 A44D possibly damaging Het
AW554918 T C 18: 25,340,000 V84A probably benign Het
Bsn G A 9: 108,107,189 T3222M unknown Het
Car15 A G 16: 17,836,608 Y155H possibly damaging Het
Cdca2 G T 14: 67,676,976 P945T probably damaging Het
Cdh16 A G 8: 104,621,540 F182L probably damaging Het
Cers6 G A 2: 69,068,659 A214T probably benign Het
Ces1g A T 8: 93,331,265 M136K probably damaging Het
Cnppd1 A G 1: 75,136,442 V394A probably benign Het
Cyp3a59 A T 5: 146,096,261 I148F possibly damaging Het
Dnah1 G A 14: 31,264,963 A3624V probably damaging Het
Exoc3l4 T C 12: 111,428,053 probably benign Het
Fap G T 2: 62,544,374 P227Q probably damaging Het
Fbxw10 G A 11: 62,847,325 R15H possibly damaging Het
Gm11011 T C 2: 169,587,320 probably benign Het
Grip1 G A 10: 119,930,015 R84Q probably damaging Het
Hipk2 A G 6: 38,819,257 C19R possibly damaging Het
Hmgcll1 A G 9: 76,072,634 D102G possibly damaging Het
Ighv16-1 A T 12: 114,068,884 Y99* probably null Het
Kank1 T G 19: 25,431,007 S1283R probably damaging Het
Kcnip1 T A 11: 33,644,504 H95L probably benign Het
L3mbtl3 A T 10: 26,331,879 L314Q unknown Het
Marveld3 C A 8: 109,962,070 R13L possibly damaging Het
Mtrf1l G T 10: 5,823,696 P23Q possibly damaging Het
Npdc1 G A 2: 25,408,945 D284N probably damaging Het
Olfr494 G A 7: 108,368,143 A218T probably benign Het
Olfr786 G T 10: 129,437,447 V212L probably benign Het
Paqr7 A G 4: 134,506,967 Y45C probably damaging Het
Plod3 G A 5: 136,991,000 W428* probably null Het
Pnisr T A 4: 21,857,400 probably benign Het
Ppip5k1 C A 2: 121,326,887 R1046L probably damaging Het
Ppp1r12b G T 1: 134,955,733 A17E probably benign Het
Prmt5 A T 14: 54,516,125 I99N probably benign Het
Ripk2 T C 4: 16,155,073 T149A probably damaging Het
Rpf2 C A 10: 40,247,002 probably benign Het
Rtf1 T A 2: 119,705,536 D190E possibly damaging Het
Shank2 T A 7: 144,031,409 M49K probably benign Het
Snd1 T G 6: 28,668,643 V443G probably damaging Het
Spag9 T C 11: 94,097,818 F555L probably damaging Het
Srfbp1 A G 18: 52,488,677 K270R probably benign Het
Tenm2 T A 11: 36,024,020 N2230I probably damaging Het
Tmem106a T C 11: 101,586,195 probably benign Het
Tpsg1 A T 17: 25,370,617 probably benign Het
Trank1 A G 9: 111,366,078 S1057G probably benign Het
Unc13d G A 11: 116,074,259 T220M probably damaging Het
Vmn1r68 T C 7: 10,527,977 T65A probably benign Het
Vps50 T C 6: 3,536,974 probably null Het
Washc5 A G 15: 59,350,371 I85T possibly damaging Het
Zfp677 C T 17: 21,392,526 T2I probably benign Het
Zxdc A G 6: 90,382,272 T629A possibly damaging Het
Other mutations in Gm11146
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02119:Gm11146 APN 16 77588610 splice site probably null
R0392:Gm11146 UTSW 16 77597166 intron probably benign
R1302:Gm11146 UTSW 16 77602082 missense unknown
R2055:Gm11146 UTSW 16 77595081 intron probably benign
Predicted Primers PCR Primer

Sequencing Primer
Posted On2016-03-01