Incidental Mutation 'R5513:Igkv2-137'
ID440173
Institutional Source Beutler Lab
Gene Symbol Igkv2-137
Ensembl Gene ENSMUSG00000076501
Gene Nameimmunoglobulin kappa chain variable 2-137
SynonymsGm16955
MMRRC Submission 043073-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.164) question?
Stock #R5513 (G1)
Quality Score225
Status Validated
Chromosome6
Chromosomal Location67555636-67556216 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 67556014 bp
ZygosityHeterozygous
Amino Acid Change Glycine to Serine at position 54 (G54S)
Ref Sequence ENSEMBL: ENSMUSP00000100103 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103302]
Predicted Effect possibly damaging
Transcript: ENSMUST00000103302
AA Change: G54S

PolyPhen 2 Score 0.875 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000100103
Gene: ENSMUSG00000076501
AA Change: G54S

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
IGv 38 115 2.35e-18 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000199480
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.8%
Validation Efficiency 97% (59/61)
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310035C23Rik G A 1: 105,750,973 V1130I probably damaging Het
Abtb2 A T 2: 103,709,278 probably null Het
Akr1b3 C A 6: 34,316,646 probably benign Het
Alppl2 T A 1: 87,087,338 N434Y probably benign Het
Ampd2 A G 3: 108,075,667 I648T possibly damaging Het
Ankrd11 T C 8: 122,892,520 E1510G probably benign Het
Ano2 A C 6: 126,039,322 K939N possibly damaging Het
Arhgef5 A G 6: 43,272,339 Y8C probably damaging Het
Aspm A T 1: 139,482,398 I2609F probably damaging Het
Camsap2 A T 1: 136,280,863 S964T probably benign Het
Cd22 C T 7: 30,867,025 R823Q probably damaging Het
Cd74 T C 18: 60,811,305 C196R probably damaging Het
Cfap73 A T 5: 120,631,712 I82N probably damaging Het
Cidec A T 6: 113,428,179 Y177N probably damaging Het
Crb1 C T 1: 139,236,821 probably null Het
Cts7 T C 13: 61,355,584 K189E possibly damaging Het
Cyp2c68 A T 19: 39,703,406 Y358N probably damaging Het
Dab2ip A T 2: 35,710,254 H294L probably benign Het
Dnah6 T C 6: 73,190,419 D502G probably null Het
Dnah8 T A 17: 30,752,916 M2768K probably damaging Het
Etl4 C A 2: 20,743,827 S405R probably damaging Het
Fsip2 G T 2: 82,950,908 L19F probably damaging Het
Fsip2 T A 2: 82,985,198 N3758K possibly damaging Het
Fsip2 C G 2: 82,950,912 Q217E probably benign Het
Gm12689 T C 4: 99,296,165 I85T unknown Het
Hivep2 A T 10: 14,132,673 K1672* probably null Het
Ints8 A G 4: 11,248,303 V105A possibly damaging Het
Lrba C T 3: 86,542,641 S2089F probably damaging Het
Lrrc8b A G 5: 105,485,984 K774R probably damaging Het
Mcm4 T A 16: 15,630,514 Y393F probably benign Het
Mki67 A G 7: 135,707,750 L324P probably damaging Het
Olfr12 T C 1: 92,620,380 V158A probably benign Het
Olfr1428 A G 19: 12,109,381 L55P probably damaging Het
Olfr1441 G A 19: 12,422,683 V125I probably benign Het
Olfr665 A T 7: 104,881,499 H264L probably damaging Het
Pld4 A G 12: 112,762,554 E19G probably benign Het
Plvap T C 8: 71,511,529 E63G probably damaging Het
Ppig A G 2: 69,750,359 T746A probably benign Het
Prdm2 GCTCCTCCTCCTCCTCCTCCTCCTC GCTCCTCCTCCTCCTCCTCCTC 4: 143,135,893 probably benign Het
Rbm15b A G 9: 106,886,117 L284P probably benign Het
Rhbdl3 T C 11: 80,331,842 V239A probably damaging Het
Sae1 T C 7: 16,366,856 E197G probably benign Het
Sdhaf2 C T 19: 10,517,030 R105H probably damaging Het
Senp3 T C 11: 69,677,139 D425G probably benign Het
Slc35e2 C T 4: 155,610,026 P10L probably benign Het
Slc46a1 T C 11: 78,466,550 F143S probably benign Het
Tom1 T A 8: 75,057,220 N52K probably damaging Het
Vmn1r11 A T 6: 57,137,632 T94S probably damaging Het
Zfp236 A G 18: 82,658,022 I390T probably damaging Het
Zfp709 A T 8: 71,890,056 H443L probably damaging Het
Zfp960 C T 17: 17,087,734 P237S possibly damaging Het
Other mutations in Igkv2-137
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03268:Igkv2-137 APN 6 67556108 missense probably benign 0.18
R3914:Igkv2-137 UTSW 6 67555984 missense probably damaging 1.00
R4692:Igkv2-137 UTSW 6 67555987 missense possibly damaging 0.87
R8320:Igkv2-137 UTSW 6 67556170 frame shift probably null
R8321:Igkv2-137 UTSW 6 67556170 frame shift probably null
Predicted Primers PCR Primer
(F):5'- TCAGTGACTAGGAAGTTGCTAAAG -3'
(R):5'- GGGCTGTATCACTGTGAAAGG -3'

Sequencing Primer
(F):5'- GTAACACAGTGTCATCATGTTTGTG -3'
(R):5'- GGCTGTATCACTGTGAAAGGATATTC -3'
Posted On2016-11-08