Incidental Mutation 'R8838:Iglv3'
ID 674294
Institutional Source Beutler Lab
Gene Symbol Iglv3
Ensembl Gene ENSMUSG00000076939
Gene Name immunoglobulin lambda variable 3
Synonyms
MMRRC Submission 068666-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.066) question?
Stock # R8838 (G1)
Quality Score 225.009
Status Validated
Chromosome 16
Chromosomal Location 19059958-19060429 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 19060132 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 65 (Y65*)
Ref Sequence ENSEMBL: ENSMUSP00000100465 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103751]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000103751
AA Change: Y65*
SMART Domains Protein: ENSMUSP00000100465
Gene: ENSMUSG00000076939
AA Change: Y65*

DomainStartEndE-ValueType
IGv 36 113 8.97e-15 SMART
Meta Mutation Damage Score 0.9756 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.2%
Validation Efficiency 100% (52/52)
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8a T A 11: 109,920,881 (GRCm39) I1498F probably damaging Het
Aco2 T A 15: 81,796,128 (GRCm39) N508K probably damaging Het
Aff4 T C 11: 53,297,465 (GRCm39) S896P possibly damaging Het
Anapc2 T G 2: 25,163,546 (GRCm39) V261G probably benign Het
Atm A G 9: 53,427,851 (GRCm39) S420P probably damaging Het
Bag6 C T 17: 35,363,367 (GRCm39) R736C probably damaging Het
Brca2 A G 5: 150,465,005 (GRCm39) T1590A possibly damaging Het
Cacna2d3 C T 14: 28,691,220 (GRCm39) C35Y probably benign Het
Cep170b G A 12: 112,710,159 (GRCm39) R1433H probably damaging Het
Cmtm2a A G 8: 105,008,036 (GRCm39) C138R probably damaging Het
Cntnap5c T A 17: 58,198,964 (GRCm39) V86E Het
Cog7 A G 7: 121,549,106 (GRCm39) I385T probably damaging Het
Col28a1 A T 6: 8,091,839 (GRCm39) probably null Het
Dkk3 T C 7: 111,717,542 (GRCm39) E309G probably benign Het
Dnah10 T C 5: 124,842,614 (GRCm39) V1411A probably benign Het
Enox1 G T 14: 77,819,950 (GRCm39) R235L probably benign Het
Foxn1 T C 11: 78,252,438 (GRCm39) N317D possibly damaging Het
Grip2 G A 6: 91,762,721 (GRCm39) probably benign Het
Hmmr T C 11: 40,604,854 (GRCm39) T406A probably benign Het
Hpcal1 G A 12: 17,836,197 (GRCm39) R9H probably benign Het
Itgal A G 7: 126,910,433 (GRCm39) Y514C probably damaging Het
Kcnk9 T C 15: 72,418,019 (GRCm39) E37G possibly damaging Het
Klhl40 A G 9: 121,609,107 (GRCm39) D424G probably benign Het
Lbr A G 1: 181,648,294 (GRCm39) L389P possibly damaging Het
Ly9 A G 1: 171,421,569 (GRCm39) Y561H probably damaging Het
Mcoln3 T C 3: 145,845,126 (GRCm39) F441L probably damaging Het
Muc20 G T 16: 32,613,829 (GRCm39) T516K possibly damaging Het
Naa35 T C 13: 59,775,775 (GRCm39) M551T probably benign Het
Nkx6-2 T A 7: 139,161,868 (GRCm39) T170S probably damaging Het
Nlrp4c T A 7: 6,069,337 (GRCm39) F413I Het
Or10w1 G A 19: 13,632,371 (GRCm39) V193M probably damaging Het
Or1s2 C A 19: 13,758,381 (GRCm39) T133K probably benign Het
Or6c1b T G 10: 129,273,065 (GRCm39) L128R probably damaging Het
Or8k22 T C 2: 86,163,317 (GRCm39) K128E possibly damaging Het
Pcdhga10 C T 18: 37,881,952 (GRCm39) T571I possibly damaging Het
Pla2g4a A T 1: 149,747,256 (GRCm39) M310K probably benign Het
Plaa T C 4: 94,471,791 (GRCm39) T353A probably benign Het
Rapgef1 T C 2: 29,627,458 (GRCm39) F1172S possibly damaging Het
Rfx2 T C 17: 57,087,877 (GRCm39) T505A possibly damaging Het
Rfx4 T C 10: 84,676,758 (GRCm39) V216A probably damaging Het
Rps6kb2 G T 19: 4,211,183 (GRCm39) A114D probably damaging Het
Sdc2 T A 15: 33,023,897 (GRCm39) L92* probably null Het
Slc18b1 A G 10: 23,696,764 (GRCm39) Y319C probably benign Het
Slc22a15 A T 3: 101,790,849 (GRCm39) Y219N probably damaging Het
Tarbp1 A T 8: 127,177,569 (GRCm39) probably benign Het
Tfap2d T C 1: 19,175,036 (GRCm39) L163P possibly damaging Het
Trank1 A G 9: 111,193,973 (GRCm39) I666V probably benign Het
Trav14-1 G T 14: 53,792,009 (GRCm39) A120S probably damaging Het
Trps1 T A 15: 50,753,007 (GRCm39) N20I probably benign Het
Txndc16 A G 14: 45,378,028 (GRCm39) Y682H probably damaging Het
Ube4a A T 9: 44,837,261 (GRCm39) D991E probably damaging Het
Zswim4 C T 8: 84,940,699 (GRCm39) R800Q probably damaging Het
Other mutations in Iglv3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02140:Iglv3 APN 16 19,060,160 (GRCm39) missense probably damaging 1.00
IGL02209:Iglv3 APN 16 19,060,420 (GRCm39) missense probably benign 0.05
R6241:Iglv3 UTSW 16 19,059,968 (GRCm39) missense possibly damaging 0.81
R6814:Iglv3 UTSW 16 19,060,034 (GRCm39) missense probably damaging 1.00
R6872:Iglv3 UTSW 16 19,060,034 (GRCm39) missense probably damaging 1.00
R9158:Iglv3 UTSW 16 19,060,012 (GRCm39) missense probably damaging 0.99
R9585:Iglv3 UTSW 16 19,059,960 (GRCm39) makesense probably null
R9609:Iglv3 UTSW 16 19,060,221 (GRCm39) missense probably damaging 1.00
Z1177:Iglv3 UTSW 16 19,060,202 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TTCCCTACGAGTCCAAGAGG -3'
(R):5'- TTGCTCAGGTCAGGAGAACC -3'

Sequencing Primer
(F):5'- CCAAGAGGATTGCTAGACTATCTAC -3'
(R):5'- GTCAGGAGAACCATTTGTACCCTG -3'
Posted On 2021-07-15