Incidental Mutation 'R9133:Igkv4-92'
ID 693771
Institutional Source Beutler Lab
Gene Symbol Igkv4-92
Ensembl Gene ENSMUSG00000076531
Gene Name immunoglobulin kappa variable 4-92
Synonyms LOC384410, IgVk ay4
MMRRC Submission 068930-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.242) question?
Stock # R9133 (G1)
Quality Score 225.009
Status Validated
Chromosome 6
Chromosomal Location 68732022-68732577 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 68732248 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Asparagine at position 42 (T42N)
Ref Sequence ENSEMBL: ENSMUSP00000100133 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103332]
AlphaFold A0A0B4J1I2
Predicted Effect probably damaging
Transcript: ENSMUST00000103332
AA Change: T42N

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000100133
Gene: ENSMUSG00000076531
AA Change: T42N

DomainStartEndE-ValueType
IGv 38 111 5.88e-10 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency 100% (65/65)
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acat3 T A 17: 13,159,176 (GRCm39) R4S probably benign Het
Adamdec1 A T 14: 68,814,547 (GRCm39) C143* probably null Het
Adck5 A G 15: 76,460,612 (GRCm39) probably benign Het
Aebp2 A G 6: 140,579,441 (GRCm39) D226G probably damaging Het
Ascc3 A G 10: 50,630,175 (GRCm39) I1755V possibly damaging Het
Aspm C T 1: 139,419,266 (GRCm39) T2977M probably damaging Het
Cacna1a A G 8: 85,276,152 (GRCm39) S582G probably damaging Het
Card14 T C 11: 119,231,835 (GRCm39) F801S probably damaging Het
Casp16 T A 17: 23,771,003 (GRCm39) D134V probably damaging Het
Cmya5 A G 13: 93,234,108 (GRCm39) S327P possibly damaging Het
Cutc A T 19: 43,755,727 (GRCm39) D229V possibly damaging Het
Cyp21a1 C A 17: 35,023,419 (GRCm39) probably benign Het
Dnah10 A G 5: 124,859,423 (GRCm39) K2130R probably damaging Het
Dsc1 C T 18: 20,234,904 (GRCm39) S250N probably benign Het
Edc4 T C 8: 106,611,778 (GRCm39) probably null Het
Efcab8 G C 2: 153,646,861 (GRCm39) V397L unknown Het
Ehmt1 A T 2: 24,729,635 (GRCm39) I642K possibly damaging Het
Gjd2 T C 2: 113,842,039 (GRCm39) Q146R probably benign Het
Gm26661 A G 14: 7,791,936 (GRCm38) H117R unknown Het
H2-Oa T A 17: 34,313,505 (GRCm39) D185E probably damaging Het
Hjurp A T 1: 88,202,772 (GRCm39) Y71N possibly damaging Het
Hyal6 A G 6: 24,734,585 (GRCm39) R173G possibly damaging Het
Ica1 A T 6: 8,659,921 (GRCm39) V125D probably benign Het
Ift172 T C 5: 31,442,867 (GRCm39) T140A probably benign Het
Ighv9-4 T A 12: 114,263,883 (GRCm39) I17F probably benign Het
Kctd16 C A 18: 40,392,069 (GRCm39) P219Q probably damaging Het
Kdm5b A T 1: 134,530,323 (GRCm39) I445F probably benign Het
Ksr2 A G 5: 117,841,319 (GRCm39) T598A probably benign Het
Lrrn1 C T 6: 107,544,568 (GRCm39) T122I probably damaging Het
Mars2 A G 1: 55,276,721 (GRCm39) D108G possibly damaging Het
Ms4a14 A G 19: 11,281,038 (GRCm39) W507R Het
Ncoa3 A G 2: 165,910,381 (GRCm39) T1266A possibly damaging Het
Neb T C 2: 52,083,256 (GRCm39) K5650E possibly damaging Het
Nlrp4f T A 13: 65,332,883 (GRCm39) K92* probably null Het
Nme4 G T 17: 26,314,389 (GRCm39) A13E probably benign Het
Nova1 G T 12: 46,865,524 (GRCm39) A4E unknown Het
Nphs1 G T 7: 30,160,092 (GRCm39) E124* probably null Het
Or10d4 T A 9: 39,580,974 (GRCm39) I207N possibly damaging Het
Or10d4b T A 9: 39,534,809 (GRCm39) L128* probably null Het
Or5d14 T C 2: 87,880,782 (GRCm39) Y62C probably damaging Het
Pde8a C T 7: 80,982,619 (GRCm39) T746I probably damaging Het
Peg3 GTGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTC GTGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTC 7: 6,712,167 (GRCm39) probably benign Het
Ranbp2 T C 10: 58,313,050 (GRCm39) S1257P probably damaging Het
Ranbp3 T C 17: 57,003,791 (GRCm39) probably null Het
Rasgrf1 A G 9: 89,793,600 (GRCm39) T126A probably benign Het
Rexo5 T G 7: 119,444,667 (GRCm39) L714R probably damaging Het
Rhobtb3 A G 13: 76,020,512 (GRCm39) Y597H probably damaging Het
Riox1 C G 12: 83,998,221 (GRCm39) Y252* probably null Het
Sh2d3c T C 2: 32,634,778 (GRCm39) Y186H possibly damaging Het
Slc16a7 T A 10: 125,066,536 (GRCm39) T368S probably benign Het
Slc25a26 G A 6: 94,511,143 (GRCm39) V107I Het
Slc4a5 A T 6: 83,203,217 (GRCm39) Y39F possibly damaging Het
Smarcad1 A G 6: 65,049,035 (GRCm39) K254E probably damaging Het
Sspo G T 6: 48,434,747 (GRCm39) V1080L possibly damaging Het
Thsd7b A T 1: 129,843,382 (GRCm39) T865S probably benign Het
Top1 C T 2: 160,545,591 (GRCm39) Q320* probably null Het
Trank1 T A 9: 111,220,770 (GRCm39) N2502K possibly damaging Het
Urad T C 5: 147,252,251 (GRCm39) H67R probably damaging Het
Vamp5 A C 6: 72,357,362 (GRCm39) probably null Het
Vmn1r62 A G 7: 5,679,062 (GRCm39) I248V probably benign Het
Wwc2 G T 8: 48,305,007 (GRCm39) Q873K unknown Het
Zcchc2 C A 1: 105,958,535 (GRCm39) S1002Y probably damaging Het
Zdhhc14 G A 17: 5,803,283 (GRCm39) R462H probably benign Het
Zfp788 A G 7: 41,299,484 (GRCm39) N707D Het
Zfp964 A G 8: 70,115,783 (GRCm39) T128A probably benign Het
Zkscan16 T C 4: 58,957,722 (GRCm39) L668S possibly damaging Het
Other mutations in Igkv4-92
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02147:Igkv4-92 APN 6 68,732,236 (GRCm39) missense probably damaging 1.00
IGL02171:Igkv4-92 APN 6 68,732,573 (GRCm39) missense probably benign 0.01
R4981:Igkv4-92 UTSW 6 68,732,028 (GRCm39) missense possibly damaging 0.80
R5135:Igkv4-92 UTSW 6 68,732,538 (GRCm39) missense probably benign
R5418:Igkv4-92 UTSW 6 68,732,564 (GRCm39) missense possibly damaging 0.49
R9005:Igkv4-92 UTSW 6 68,732,081 (GRCm39) missense probably benign
R9361:Igkv4-92 UTSW 6 68,732,090 (GRCm39) missense possibly damaging 0.94
Predicted Primers PCR Primer
(F):5'- CCTGCATGCAGCTGATTGTC -3'
(R):5'- GAATCCAAGACTCTTTACATTGGGG -3'

Sequencing Primer
(F):5'- TTGTCAGAGTGTAAGAGCTCTCAGAC -3'
(R):5'- ACATTGGGGGAAGTTTGAGTCTAAG -3'
Posted On 2022-01-20