Incidental Mutation 'R5368:Gm9762'
ID 429465
Institutional Source Beutler Lab
Gene Symbol Gm9762
Ensembl Gene ENSMUSG00000037096
Gene Name predicted pseudogene 9762
MMRRC Submission 043204-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.339) question?
Stock # R5368 (G1)
Quality Score 225
Status Validated
Chromosome 3
Chromosomal Location 78966359-78966799 bp(-) (GRCm38)
Type of Mutation exon
DNA Base Change (assembly) T to A at 78966435 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000036976
Meta Mutation Damage Score 0.8574 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.3%
Validation Efficiency 97% (61/63)
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933402N03Rik T A 7: 131,139,196 (GRCm38) H97L possibly damaging Het
Abca9 T A 11: 110,145,546 (GRCm38) N579I probably damaging Het
Acbd3 A T 1: 180,722,095 (GRCm38) probably benign Het
Ankrd50 A T 3: 38,455,050 (GRCm38) I1056N probably damaging Het
Ceacam18 T C 7: 43,642,034 (GRCm38) V300A probably benign Het
Cfap46 C A 7: 139,627,473 (GRCm38) R1843S possibly damaging Het
D430041D05Rik A G 2: 104,248,284 (GRCm38) V1229A probably damaging Het
Dbx2 G A 15: 95,640,641 (GRCm38) S206L probably benign Het
Dnah11 A T 12: 117,954,893 (GRCm38) D1530E probably damaging Het
Ecm2 A C 13: 49,520,943 (GRCm38) T280P probably benign Het
Emc2 G A 15: 43,511,811 (GRCm38) probably null Het
Epb42 C T 2: 121,019,462 (GRCm38) V689I probably benign Het
Fam114a1 T A 5: 65,006,109 (GRCm38) M209K possibly damaging Het
Fam117a C T 11: 95,375,633 (GRCm38) S193F probably damaging Het
Foxp2 A T 6: 15,377,914 (GRCm38) probably benign Het
Frmd6 T A 12: 70,864,100 (GRCm38) C19* probably null Het
Fyb1 A G 15: 6,580,678 (GRCm38) probably null Het
Gata6 C A 18: 11,063,059 (GRCm38) H442Q possibly damaging Het
Gldc A G 19: 30,158,521 (GRCm38) S160P probably benign Het
Gm3952 A G 8: 128,745,974 (GRCm38) S1626P possibly damaging Het
Gtpbp2 T C 17: 46,166,304 (GRCm38) probably benign Het
Hgd A T 16: 37,589,751 (GRCm38) T50S probably benign Het
Itpr1 C T 6: 108,387,498 (GRCm38) T22M probably damaging Het
Kif26b G A 1: 178,915,884 (GRCm38) E1182K probably damaging Het
Kirrel3 A G 9: 35,007,738 (GRCm38) E230G probably damaging Het
Leng8 A G 7: 4,139,988 (GRCm38) Y88C probably damaging Het
Lpo T C 11: 87,821,069 (GRCm38) D54G possibly damaging Het
Lypd2 G T 15: 74,733,059 (GRCm38) A29E probably benign Het
Mdn1 C T 4: 32,723,690 (GRCm38) P2542L probably damaging Het
Mical3 T C 6: 120,959,473 (GRCm38) Y1364C probably damaging Het
Mroh2b A G 15: 4,905,572 (GRCm38) N163S probably damaging Het
Mtf1 G A 4: 124,825,079 (GRCm38) C295Y probably damaging Het
Nbn T A 4: 15,969,391 (GRCm38) L212Q probably damaging Het
Obscn A T 11: 59,069,026 (GRCm38) probably null Het
Or10ag56 T A 2: 87,308,782 (GRCm38) probably null Het
Or4c110 A G 2: 89,002,091 (GRCm38) S66P probably damaging Het
Peli1 A G 11: 21,148,389 (GRCm38) T375A probably damaging Het
Picalm T C 7: 90,207,595 (GRCm38) *611Q probably null Het
Plch1 G T 3: 63,701,973 (GRCm38) Q938K possibly damaging Het
Plxnb2 A G 15: 89,159,593 (GRCm38) V1352A possibly damaging Het
Pmepa1 G A 2: 173,228,322 (GRCm38) R147W probably damaging Het
Prdm16 T G 4: 154,345,391 (GRCm38) K373Q probably damaging Het
Qki T G 17: 10,239,035 (GRCm38) E135A probably damaging Het
Rad50 T C 11: 53,684,246 (GRCm38) K556E probably benign Het
Scara5 CG C 14: 65,759,662 (GRCm38) probably null Het
Sin3a T A 9: 57,110,800 (GRCm38) D834E possibly damaging Het
Smg8 G A 11: 87,080,260 (GRCm38) S895L probably benign Het
Sorl1 T C 9: 41,979,390 (GRCm38) I1944M probably benign Het
Stam2 G A 2: 52,736,293 (GRCm38) probably benign Het
Tmprss7 A T 16: 45,660,889 (GRCm38) W645R probably damaging Het
Tns1 T C 1: 73,941,017 (GRCm38) M1111V probably benign Het
Ttn A T 2: 76,811,243 (GRCm38) L5176Q possibly damaging Het
Ttn A C 2: 76,778,382 (GRCm38) D17763E probably damaging Het
Ubr4 G A 4: 139,397,528 (GRCm38) probably benign Het
Usp31 T C 7: 121,661,365 (GRCm38) H637R probably damaging Het
Vps50 A C 6: 3,567,739 (GRCm38) E545A possibly damaging Het
Wdfy3 G T 5: 101,872,858 (GRCm38) L2527M probably damaging Het
Wfdc2 T C 2: 164,563,434 (GRCm38) V85A possibly damaging Het
Other mutations in Gm9762
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4697:Gm9762 UTSW 3 78,966,550 (GRCm38) exon noncoding transcript
R4754:Gm9762 UTSW 3 78,966,421 (GRCm38) exon noncoding transcript
R5119:Gm9762 UTSW 3 78,966,400 (GRCm38) exon noncoding transcript
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2016-09-06