Incidental Mutation 'R6771:Ighv2-9'
ID 532180
Institutional Source Beutler Lab
Gene Symbol Ighv2-9
Ensembl Gene ENSMUSG00000096638
Gene Name immunoglobulin heavy variable 2-9
Synonyms Gm16700
MMRRC Submission 044887-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.118) question?
Stock # R6771 (G1)
Quality Score 225.009
Status Validated
Chromosome 12
Chromosomal Location 113842717-113843008 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 113842807 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Arginine at position 87 (S87R)
Ref Sequence ENSEMBL: ENSMUSP00000100232 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103451]
AlphaFold A0A075B5Q5
Predicted Effect probably damaging
Transcript: ENSMUST00000103451
AA Change: S87R

PolyPhen 2 Score 0.985 (Sensitivity: 0.74; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000100232
Gene: ENSMUSG00000096638
AA Change: S87R

DomainStartEndE-ValueType
low complexity region 2 13 N/A INTRINSIC
IGv 36 116 1.05e-29 SMART
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.7%
  • 20x: 96.3%
Validation Efficiency 95% (37/39)
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd8 G T 8: 71,914,105 (GRCm39) H174Q probably damaging Het
Apoa4 G A 9: 46,154,465 (GRCm39) M355I probably benign Het
Apol8 A T 15: 77,637,258 (GRCm39) probably null Het
Arvcf A G 16: 18,222,614 (GRCm39) T792A probably benign Het
Atp10b T C 11: 43,094,079 (GRCm39) probably null Het
Atp9a A T 2: 168,516,820 (GRCm39) Y340N probably damaging Het
C1rb T G 6: 124,554,364 (GRCm39) S382A probably benign Het
Clmn A G 12: 104,740,041 (GRCm39) V962A probably benign Het
Csmd1 A G 8: 16,121,408 (GRCm39) V1763A possibly damaging Het
Ctnnd1 A T 2: 84,450,454 (GRCm39) D255E probably damaging Het
Ctnnd1 C A 2: 84,450,269 (GRCm39) R317L probably damaging Het
Cyb5a T A 18: 84,889,755 (GRCm39) H61Q probably damaging Het
Dipk1b A G 2: 26,524,875 (GRCm39) R92G probably benign Het
Dmxl2 A T 9: 54,323,808 (GRCm39) I1192N probably damaging Het
Flg T C 3: 93,195,630 (GRCm39) probably benign Het
Fras1 A G 5: 96,746,800 (GRCm39) I623M possibly damaging Het
Ftsj3 T C 11: 106,140,366 (GRCm39) K801E probably damaging Het
Gpr35 T A 1: 92,910,426 (GRCm39) M46K probably damaging Het
Kdm4b C T 17: 56,658,754 (GRCm39) A33V possibly damaging Het
Klhl5 T A 5: 65,321,995 (GRCm39) Y534N probably damaging Het
Marchf8 T C 6: 116,379,004 (GRCm39) S313P probably benign Het
Mccc1 C T 3: 36,043,992 (GRCm39) probably null Het
Memo1 A T 17: 74,508,273 (GRCm39) F270L probably damaging Het
Nxpe3 C A 16: 55,686,471 (GRCm39) G179V probably damaging Het
Or4k15c C A 14: 50,321,446 (GRCm39) A231S probably damaging Het
Or5b120 T A 19: 13,480,318 (GRCm39) F204I possibly damaging Het
Or7g35 C T 9: 19,496,675 (GRCm39) L281F probably benign Het
Otp A G 13: 95,012,294 (GRCm39) D6G probably damaging Het
Ptpn4 T A 1: 119,643,698 (GRCm39) N350I probably benign Het
Pwp2 G A 10: 78,018,222 (GRCm39) probably null Het
Rassf10 A G 7: 112,553,635 (GRCm39) M79V probably benign Het
Rbm12 A T 2: 155,939,375 (GRCm39) I299N possibly damaging Het
Rsf1 GGCG GGCGACGGCTGCG 7: 97,229,113 (GRCm39) probably benign Homo
Scfd2 T C 5: 74,692,117 (GRCm39) H55R probably benign Het
Skic2 G A 17: 35,064,166 (GRCm39) R507* probably null Het
Sp110 C T 1: 85,520,000 (GRCm39) probably null Het
Syde2 G A 3: 145,704,803 (GRCm39) G318E probably damaging Het
Ttn T A 2: 76,538,883 (GRCm39) D34649V possibly damaging Het
Other mutations in Ighv2-9
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4616:Ighv2-9 UTSW 12 113,842,839 (GRCm39) missense probably damaging 0.99
R6769:Ighv2-9 UTSW 12 113,842,930 (GRCm39) missense possibly damaging 0.94
R9704:Ighv2-9 UTSW 12 113,842,746 (GRCm39) missense possibly damaging 0.94
Predicted Primers PCR Primer
(F):5'- GAACTTCTTGGTTCTCAGCGC -3'
(R):5'- ATTGCTTGTCCCCAGGTGTC -3'

Sequencing Primer
(F):5'- GTTCTCAGCGCCCCCTG -3'
(R):5'- TGTCCCAGGTGCAGCTGAAG -3'
Posted On 2018-08-29