Incidental Mutation 'R3124:Iglc3'
ID 477975
Institutional Source Beutler Lab
Gene Symbol Iglc3
Ensembl Gene ENSMUSG00000105547
Gene Name immunoglobulin lambda constant 3
Synonyms
MMRRC Submission 040597-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.108) question?
Stock # R3124 (G1)
Quality Score 225
Status Not validated
Chromosome 16
Chromosomal Location 18884115-18884431 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 18884345 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: ENSMUST00000198927
Predicted Effect probably benign
Transcript: ENSMUST00000199490
Predicted Effect probably benign
Transcript: ENSMUST00000200074
Predicted Effect probably benign
Transcript: ENSMUST00000200211
Predicted Effect unknown
Transcript: ENSMUST00000200235
AA Change: I29V
Predicted Effect probably benign
Transcript: ENSMUST00000200568
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.5%
Validation Efficiency 100% (40/40)
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd16b G A 2: 181,136,319 (GRCm39) R407H possibly damaging Het
Bag4 C T 8: 26,259,516 (GRCm39) A228T probably benign Het
Cadm1 A G 9: 47,710,775 (GRCm39) E226G possibly damaging Het
Caskin2 T C 11: 115,695,623 (GRCm39) D246G probably damaging Het
Cd80 T A 16: 38,294,255 (GRCm39) V46E probably damaging Het
Ctr9 C T 7: 110,652,653 (GRCm39) R984C unknown Het
Dach2 T C X: 112,729,664 (GRCm39) I417T possibly damaging Het
Dcaf8l A T X: 88,448,327 (GRCm39) Y601N probably benign Het
Drd3 T C 16: 43,643,155 (GRCm39) F464L probably damaging Het
Dyrk1a G A 16: 94,469,660 (GRCm39) probably benign Het
Fam227b T C 2: 125,966,006 (GRCm39) T140A probably benign Het
Fam91a1 A G 15: 58,293,738 (GRCm39) I101V probably benign Het
Fem1b T C 9: 62,703,836 (GRCm39) I475V probably benign Het
Glra3 A G 8: 56,578,244 (GRCm39) R434G possibly damaging Het
Hsd17b12 C T 2: 93,864,303 (GRCm39) R268Q probably benign Het
Khdrbs2 C A 1: 32,558,858 (GRCm39) R408L probably damaging Het
Loxhd1 A G 18: 77,518,774 (GRCm39) D1860G probably damaging Het
Mcpt8 A T 14: 56,321,398 (GRCm39) I22K probably damaging Het
Myo1h A G 5: 114,466,860 (GRCm39) I303V probably benign Het
Nipsnap2 G A 5: 129,825,098 (GRCm39) probably null Het
Nop2 G A 6: 125,109,164 (GRCm39) probably benign Het
Polr2a A T 11: 69,626,536 (GRCm39) S1566T possibly damaging Het
Pthlh A T 6: 147,164,789 (GRCm39) V27E probably damaging Het
Ralgps1 T C 2: 33,048,968 (GRCm39) T314A possibly damaging Het
Robo4 CGG CG 9: 37,322,786 (GRCm39) probably null Het
Skil A G 3: 31,151,487 (GRCm39) N3S probably benign Het
Tas2r129 A G 6: 132,928,411 (GRCm39) N116S probably damaging Het
Tas2r140 T A 6: 133,032,204 (GRCm39) I185L probably benign Het
Tnpo1 GCACCTCTGCTTCCTC GCACCTCTGCTTCCTCACCTCTGCTTCCTC 13: 99,003,637 (GRCm39) probably null Het
Togaram1 G T 12: 65,013,118 (GRCm39) R123L probably damaging Het
Trappc9 G A 15: 72,897,816 (GRCm39) R377W probably damaging Het
Trim12a G T 7: 103,950,063 (GRCm39) T292K probably benign Het
Trim9 C T 12: 70,295,167 (GRCm39) G648R probably damaging Het
Trmt13 T C 3: 116,383,893 (GRCm39) I104V probably benign Het
Vav3 G A 3: 109,535,484 (GRCm39) probably null Het
Vmn1r87 A G 7: 12,865,493 (GRCm39) Y265H probably damaging Het
Zfp574 G T 7: 24,781,026 (GRCm39) A683S possibly damaging Het
Other mutations in Iglc3
AlleleSourceChrCoordTypePredicted EffectPPH Score
R5652:Iglc3 UTSW 16 18,884,420 (GRCm39) unclassified probably benign
R6890:Iglc3 UTSW 16 18,884,258 (GRCm39) unclassified probably benign
R7247:Iglc3 UTSW 16 18,884,191 (GRCm39) missense
R7863:Iglc3 UTSW 16 18,884,248 (GRCm39) missense not run
Predicted Primers
Posted On 2017-05-15