Incidental Mutation 'R5789:Gm16551'
ID 448217
Institutional Source Beutler Lab
Gene Symbol Gm16551
Ensembl Gene ENSMUSG00000066477
Gene Name predicted gene 16551
Synonyms
MMRRC Submission 043383-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.146) question?
Stock # R5789 (G1)
Quality Score 225
Status Validated
Chromosome 9
Chromosomal Location 74755719-74760154 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to A at 74756535 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160017
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160842
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160950
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160979
Predicted Effect noncoding transcript
Transcript: ENSMUST00000161862
Predicted Effect noncoding transcript
Transcript: ENSMUST00000162089
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188354
Meta Mutation Damage Score 0.0852 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.6%
  • 20x: 96.0%
Validation Efficiency 97% (61/63)
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb11 A G 2: 69,076,108 (GRCm39) F1200S probably damaging Het
Ahnak A T 19: 8,979,685 (GRCm39) D323V probably benign Het
Aloxe3 T C 11: 69,017,265 (GRCm39) Y13H probably damaging Het
Aqp1 A G 6: 55,313,746 (GRCm39) I91V probably benign Het
C9orf72 T A 4: 35,226,112 (GRCm39) probably benign Het
Carmil1 A G 13: 24,305,831 (GRCm39) S318P probably damaging Het
Cdan1 A G 2: 120,560,016 (GRCm39) F383L probably benign Het
Ciao3 T C 17: 26,000,177 (GRCm39) C303R probably benign Het
Col6a2 T A 10: 76,440,223 (GRCm39) E606V probably damaging Het
Col6a5 T C 9: 105,741,807 (GRCm39) T2371A possibly damaging Het
Cops3 T C 11: 59,721,106 (GRCm39) probably benign Het
Coq7 G T 7: 118,128,929 (GRCm39) H35Q possibly damaging Het
Cp T A 3: 20,011,454 (GRCm39) F3I probably benign Het
D630003M21Rik C T 2: 158,058,734 (GRCm39) E389K possibly damaging Het
Dclre1c A T 2: 3,438,993 (GRCm39) Q51L probably damaging Het
Dhx37 A C 5: 125,498,103 (GRCm39) I702S possibly damaging Het
Dnah3 G T 7: 119,542,822 (GRCm39) A3530D possibly damaging Het
Dnajc13 T C 9: 104,091,387 (GRCm39) R635G probably damaging Het
Dnhd1 A G 7: 105,354,217 (GRCm39) S3066G possibly damaging Het
Doc2b T A 11: 75,676,941 (GRCm39) H144L probably damaging Het
Eif2b3 T A 4: 116,885,692 (GRCm39) I78N probably damaging Het
Enpp1 A T 10: 24,523,137 (GRCm39) H767Q probably benign Het
Fam180a C A 6: 35,290,461 (GRCm39) *174L probably null Het
Gabra1 A T 11: 42,073,742 (GRCm39) probably benign Het
Gfral C T 9: 76,104,328 (GRCm39) R228Q probably benign Het
Ifi213 C A 1: 173,396,360 (GRCm39) probably benign Het
Inpp4a T C 1: 37,411,410 (GRCm39) V358A possibly damaging Het
Kmt2a T C 9: 44,731,201 (GRCm39) probably benign Het
Mrgprb13 A T 7: 47,961,946 (GRCm39) noncoding transcript Het
Mtrex A T 13: 113,027,819 (GRCm39) N680K probably benign Het
Nckap5 A G 1: 125,955,439 (GRCm39) F371S probably damaging Het
Nudcd1 G A 15: 44,251,879 (GRCm39) Q428* probably null Het
Pcdhgc5 C A 18: 37,954,559 (GRCm39) P611Q probably damaging Het
Plekhb1 A T 7: 100,294,793 (GRCm39) Y193* probably null Het
Prrt1 T C 17: 34,850,931 (GRCm39) probably null Het
Ptpn12 G A 5: 21,194,013 (GRCm39) T753I possibly damaging Het
Samsn1 T C 16: 75,673,336 (GRCm39) D180G probably damaging Het
Sh2d2a T A 3: 87,756,820 (GRCm39) probably benign Het
Slc12a2 T A 18: 58,045,091 (GRCm39) probably null Het
Socs3 T A 11: 117,858,608 (GRCm39) Q150L probably benign Het
Supt6 A G 11: 78,124,412 (GRCm39) V23A unknown Het
Tcf12 T C 9: 71,792,518 (GRCm39) Y119C probably damaging Het
Them5 A G 3: 94,253,908 (GRCm39) E210G probably damaging Het
Tmem135 A G 7: 88,845,330 (GRCm39) F167S possibly damaging Het
Tmem170 A G 8: 112,593,032 (GRCm39) V134A possibly damaging Het
Trbv20 A G 6: 41,165,725 (GRCm39) Y50C probably damaging Het
Uroc1 A G 6: 90,321,179 (GRCm39) M252V probably damaging Het
Wasf1 G A 10: 40,802,570 (GRCm39) R75Q probably damaging Het
Xpnpep3 T A 15: 81,300,065 (GRCm39) probably benign Het
Yars1 C T 4: 129,090,690 (GRCm39) T78M probably damaging Het
Zdhhc16 T A 19: 41,926,572 (GRCm39) H98Q probably damaging Het
Zfp90 T C 8: 107,150,605 (GRCm39) L106P probably benign Het
Zscan22 T G 7: 12,637,853 (GRCm39) S82A probably benign Het
Other mutations in Gm16551
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4744:Gm16551 UTSW 9 74,758,153 (GRCm39) unclassified noncoding transcript
Predicted Primers PCR Primer
(F):5'- TGGGATTGAGGACCTAAAATTAAGC -3'
(R):5'- TTTGCTGCTTTAAACTCGCGG -3'

Sequencing Primer
(F):5'- TTGAGGACCTAAAATTAAGCTCTTC -3'
(R):5'- GGGAGGACCTGTTACCCAC -3'
Posted On 2016-12-15