Incidental Mutation 'R2867:Gm42542'
ID 253333
Institutional Source Beutler Lab
Gene Symbol Gm42542
Ensembl Gene
Gene Name predicted gene 42542
Synonyms
MMRRC Submission 040456-MU
Accession Numbers
Essential gene? Not available question?
Stock # R2867 (G1)
Quality Score 225
Status Not validated
Chromosome 6
Chromosomal Location 68870564-68870966 bp(-) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) T to C at 68872634 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000114214
Predicted Effect probably null
Transcript: ENSMUST00000114214
Predicted Effect noncoding transcript
Transcript: ENSMUST00000197978
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.6%
  • 3x: 98.6%
  • 10x: 94.8%
  • 20x: 82.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adss2 T C 1: 177,595,378 (GRCm39) probably null Het
Arid3c T C 4: 41,725,958 (GRCm39) D215G probably damaging Het
Birc2 A C 9: 7,834,478 (GRCm39) M1R probably null Het
Cpz T C 5: 35,659,705 (GRCm39) K647E probably benign Het
Cyp7a1 T C 4: 6,272,493 (GRCm39) E240G probably damaging Het
Dnaaf11 A T 15: 66,310,257 (GRCm39) L337* probably null Het
Epha6 T C 16: 59,780,659 (GRCm39) probably null Het
Grin2b A G 6: 135,710,637 (GRCm39) F970L probably damaging Het
Kcnma1 A T 14: 23,423,275 (GRCm39) N682K probably benign Het
Kif20b A G 19: 34,917,528 (GRCm39) E631G probably damaging Het
Lctl T C 9: 64,045,150 (GRCm39) S550P probably benign Het
Mapk10 C T 5: 103,186,548 (GRCm39) D25N probably benign Het
Mslnl G A 17: 25,961,908 (GRCm39) V128M probably damaging Het
N4bp1 T C 8: 87,588,033 (GRCm39) N302D probably benign Het
Pcdh7 A T 5: 57,879,236 (GRCm39) K930N probably damaging Het
Pramel16 T A 4: 143,675,456 (GRCm39) I457L probably benign Het
Proca1 A T 11: 78,095,806 (GRCm39) N146I probably damaging Het
Ryr2 A T 13: 11,776,235 (GRCm39) W1101R probably damaging Het
Slc35d3 T C 10: 19,725,209 (GRCm39) T216A probably benign Het
Thnsl2 C A 6: 71,108,945 (GRCm39) D289Y probably damaging Het
Tigd4 A G 3: 84,501,259 (GRCm39) N59D possibly damaging Het
Togaram2 T C 17: 72,016,592 (GRCm39) S649P probably benign Het
Tradd G T 8: 105,986,145 (GRCm39) F182L probably benign Het
Trav17 A T 14: 54,044,383 (GRCm39) Y50F probably benign Het
Usp37 A T 1: 74,489,691 (GRCm39) D808E probably damaging Het
Usp42 G A 5: 143,701,219 (GRCm39) P935S possibly damaging Het
Vmn2r23 A G 6: 123,690,123 (GRCm39) D333G possibly damaging Het
Zfpm2 C T 15: 40,962,785 (GRCm39) A149V probably benign Het
Other mutations in Gm42542
AlleleSourceChrCoordTypePredicted EffectPPH Score
H8786:Gm42542 UTSW 6 68,872,634 (GRCm39) critical splice donor site probably null
Predicted Primers PCR Primer
(F):5'- GAGGAACACTGGACTATGTTCCTAG -3'
(R):5'- CACTGGACCTCAACTGTCATC -3'

Sequencing Primer
(F):5'- CAAAATGTTTCTTGTGACTTCTGTTC -3'
(R):5'- TGGACCTCAACTGTCATCAAAGATG -3'
Posted On 2014-12-04