Incidental Mutation 'R4642:Gm16391'
ID 351702
Institutional Source Beutler Lab
Gene Symbol Gm16391
Ensembl Gene ENSMUSG00000066958
Gene Name predicted pseudogene 16391
Synonyms
MMRRC Submission 041904-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.191) question?
Stock # R4642 (G1)
Quality Score 225
Status Validated
Chromosome 17
Chromosomal Location 76591410-76591856 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to G at 76591826 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: ENSMUST00000086601
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.3%
Validation Efficiency 96% (46/48)
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abce1 T C 8: 80,415,982 (GRCm39) T387A probably damaging Het
Acaca A T 11: 84,171,287 (GRCm39) T3S probably damaging Het
Adamts16 G A 13: 70,927,637 (GRCm39) probably benign Het
Cacna1g A G 11: 94,308,920 (GRCm39) I1631T probably damaging Het
Camk1g T A 1: 193,038,667 (GRCm39) D85V probably damaging Het
Caskin1 G A 17: 24,725,602 (GRCm39) S1296N probably benign Het
Ccbe1 A T 18: 66,424,654 (GRCm39) probably benign Het
Ccdc184 T G 15: 98,066,537 (GRCm39) V114G probably benign Het
Cpxm2 C T 7: 131,672,610 (GRCm39) R313H probably benign Het
Crebrf G T 17: 26,962,035 (GRCm39) E377D probably benign Het
Dcstamp T C 15: 39,618,118 (GRCm39) F176L probably benign Het
Dnah2 T C 11: 69,387,385 (GRCm39) D947G probably benign Het
Erbb4 A G 1: 68,289,791 (GRCm39) I750T probably damaging Het
Gas2l3 CACTCGTCATACT CACT 10: 89,266,820 (GRCm39) probably benign Het
Gm973 A T 1: 59,597,273 (GRCm39) E434D probably damaging Het
Hdac7 T C 15: 97,704,397 (GRCm39) E491G probably damaging Het
Hyal5 A G 6: 24,876,621 (GRCm39) N165D probably benign Het
Ly86 A T 13: 37,560,877 (GRCm39) R79S possibly damaging Het
Mapk7 A G 11: 61,381,727 (GRCm39) I13T probably damaging Het
Medag T A 5: 149,335,444 (GRCm39) M1K probably null Het
Myh9 T C 15: 77,646,151 (GRCm39) D1944G probably benign Het
Nadk2 T C 15: 9,092,810 (GRCm39) W206R possibly damaging Het
Or7g18 T A 9: 18,787,463 (GRCm39) M280K probably damaging Het
Pcdhb11 T A 18: 37,555,021 (GRCm39) F117Y probably benign Het
Pdzd8 C T 19: 59,293,662 (GRCm39) E396K probably damaging Het
Piezo1 T A 8: 123,222,193 (GRCm39) Y541F probably damaging Het
Polr3h T C 15: 81,806,667 (GRCm39) I51V probably benign Het
Prune2 T C 19: 16,998,019 (GRCm39) probably null Het
Pyroxd1 C G 6: 142,300,467 (GRCm39) S199* probably null Het
Rars2 T G 4: 34,656,229 (GRCm39) V461G probably damaging Het
Rasgrp3 T C 17: 75,805,443 (GRCm39) C145R possibly damaging Het
Ryr1 T C 7: 28,785,463 (GRCm39) T1743A possibly damaging Het
Sac3d1 G A 19: 6,166,434 (GRCm39) A325V possibly damaging Het
Shank1 A T 7: 43,962,565 (GRCm39) D93V unknown Het
Smg1 T C 7: 117,753,487 (GRCm39) probably benign Het
Tbl1xr1 A T 3: 22,242,584 (GRCm39) N38I probably damaging Het
Ufc1 A G 1: 171,117,467 (GRCm39) I82T probably benign Het
Uggt2 A T 14: 119,272,347 (GRCm39) M434K probably benign Het
Unc80 G A 1: 66,710,873 (GRCm39) probably null Het
Zan T A 5: 137,462,450 (GRCm39) T910S unknown Het
Zfp64 A G 2: 168,776,851 (GRCm39) C256R probably benign Het
Other mutations in Gm16391
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1826:Gm16391 UTSW 17 76,591,418 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- AGGCGATTTCTGCCTCCAAAG -3'
(R):5'- GGGCCAATTTCATGGAACTG -3'

Sequencing Primer
(F):5'- AAGAGGGCGAATCTGTGATGTCC -3'
(R):5'- CCAATTTCATGGAACTGGTGAAAAG -3'
Posted On 2015-10-08