Incidental Mutation 'R6890:Iglc3'
ID 537174
Institutional Source Beutler Lab
Gene Symbol Iglc3
Ensembl Gene ENSMUSG00000105547
Gene Name immunoglobulin lambda constant 3
Synonyms
MMRRC Submission 044984-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.108) question?
Stock # R6890 (G1)
Quality Score 225.009
Status Validated
Chromosome 16
Chromosomal Location 18884115-18884431 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to A at 18884258 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000199490
Predicted Effect probably benign
Transcript: ENSMUST00000200074
Predicted Effect probably benign
Transcript: ENSMUST00000200211
Predicted Effect
Predicted Effect probably benign
Transcript: ENSMUST00000200568
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.4%
  • 20x: 98.0%
Validation Efficiency 100% (39/39)
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Alg3 T C 16: 20,424,736 (GRCm39) T270A possibly damaging Het
Ambp G C 4: 63,068,596 (GRCm39) H140Q probably benign Het
Arhgef10 T C 8: 14,978,786 (GRCm39) C18R probably benign Het
Arhgef10l A G 4: 140,271,730 (GRCm39) F548S probably damaging Het
Armh3 A G 19: 45,948,796 (GRCm39) Y228H probably damaging Het
Cdhr1 T C 14: 36,807,602 (GRCm39) D346G probably damaging Het
Col18a1 T A 10: 76,949,318 (GRCm39) probably benign Het
Col1a2 T A 6: 4,539,587 (GRCm39) L1285Q unknown Het
Cspg5 T C 9: 110,075,852 (GRCm39) L196P probably damaging Het
Dusp10 T G 1: 183,801,393 (GRCm39) Y387D probably damaging Het
Epb41 A T 4: 131,663,140 (GRCm39) D681E probably damaging Het
Eps8 A G 6: 137,489,255 (GRCm39) V381A probably damaging Het
Fbxw16 A T 9: 109,265,810 (GRCm39) S336R probably benign Het
Gm49368 A G 7: 127,680,901 (GRCm39) R277G probably benign Het
Gsg1 C T 6: 135,214,418 (GRCm39) V320I probably benign Het
Klc4 A T 17: 46,942,769 (GRCm39) N598K probably benign Het
Malsu1 A G 6: 49,052,185 (GRCm39) Y135C probably damaging Het
Mapkbp1 T C 2: 119,846,283 (GRCm39) I477T probably damaging Het
Mtss1 G T 15: 58,823,508 (GRCm39) S286R probably damaging Het
Naip2 A C 13: 100,298,549 (GRCm39) S496A probably benign Het
Niban3 T A 8: 72,058,315 (GRCm39) V540D probably damaging Het
Npepps A T 11: 97,158,470 (GRCm39) C98* probably null Het
Nphp3 A C 9: 103,919,153 (GRCm39) Y1267S probably damaging Het
Npr3 A G 15: 11,883,478 (GRCm39) V317A possibly damaging Het
Nsun6 A G 2: 15,053,788 (GRCm39) I7T probably damaging Het
Or13p4 A G 4: 118,546,728 (GRCm39) V307A possibly damaging Het
Or51ai2 A T 7: 103,587,066 (GRCm39) T160S possibly damaging Het
Or5b121 C T 19: 13,507,445 (GRCm39) T180I probably damaging Het
Pcnx1 A G 12: 82,018,150 (GRCm39) H1330R probably benign Het
Rad17 T C 13: 100,773,592 (GRCm39) I201V probably benign Het
Slc26a4 G A 12: 31,599,950 (GRCm39) T126M possibly damaging Het
Slitrk6 A T 14: 110,988,528 (GRCm39) L393* probably null Het
Snx2 A G 18: 53,345,951 (GRCm39) H378R probably damaging Het
Tex21 A G 12: 76,286,229 (GRCm39) probably null Het
Trio A T 15: 27,919,374 (GRCm39) probably benign Het
Vpreb1b T C 16: 17,798,820 (GRCm39) I102T probably damaging Het
Zfp617 T G 8: 72,686,010 (GRCm39) H113Q probably benign Het
Zgpat T A 2: 181,020,304 (GRCm39) I237N probably damaging Het
Other mutations in Iglc3
AlleleSourceChrCoordTypePredicted EffectPPH Score
R3124:Iglc3 UTSW 16 18,884,345 (GRCm39) unclassified probably benign
R5652:Iglc3 UTSW 16 18,884,420 (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 PCR Primer
(F):5'- GTATAGAGAAGAGACCCCACTCTG -3'
(R):5'- TTCATTCACACAGGTCAGCCC -3'

Sequencing Primer
(F):5'- TACAGCTGCAGGGTTCCTAG -3'
(R):5'- GGTCAGCCCAAGTCCACTC -3'
Posted On 2018-10-18