Incidental Mutation 'R2401:Ighv8-11'
ID 266143
Institutional Source Beutler Lab
Gene Symbol Ighv8-11
Ensembl Gene ENSMUSG00000095170
Gene Name immunoglobulin heavy variable V8-11
Synonyms
MMRRC Submission 040367-MU
Accession Numbers
Essential gene? Not available question?
Stock # R2401 (G1)
Quality Score 225
Status Not validated
Chromosome 12
Chromosomal Location 115530769-115531069 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to G at 115531223 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000100317 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103536]
AlphaFold A0A075B5X4
Predicted Effect probably benign
Transcript: ENSMUST00000103536
SMART Domains Protein: ENSMUSP00000100317
Gene: ENSMUSG00000095170

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
IGv 36 118 5.7e-29 SMART
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.0%
Validation Efficiency 100% (40/40)
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca14 T C 7: 119,882,312 (GRCm39) L1158P probably damaging Het
Acnat1 A T 4: 49,451,077 (GRCm39) N11K possibly damaging Het
Ammecr1l T A 18: 31,909,056 (GRCm39) I217N possibly damaging Het
Ankrd11 G A 8: 123,635,473 (GRCm39) R54* probably null Het
Ccdc178 C T 18: 22,264,471 (GRCm39) probably null Het
Clcn7 T C 17: 25,372,114 (GRCm39) S425P probably benign Het
Cnmd A G 14: 79,894,045 (GRCm39) V114A probably damaging Het
Col13a1 T C 10: 61,686,941 (GRCm39) T651A unknown Het
Col1a2 G A 6: 4,518,822 (GRCm39) probably benign Het
Cyp3a25 T C 5: 145,923,778 (GRCm39) probably null Het
Dmrta1 A T 4: 89,579,853 (GRCm39) D271V probably benign Het
Efcab3 T A 11: 104,963,144 (GRCm39) probably null Het
Exo5 T C 4: 120,779,194 (GRCm39) I224V probably damaging Het
Fam162b C A 10: 51,463,314 (GRCm39) A118S probably damaging Het
Glb1 A G 9: 114,283,325 (GRCm39) T406A possibly damaging Het
Grk3 T C 5: 113,062,849 (GRCm39) N666S probably benign Het
Hars2 T C 18: 36,922,576 (GRCm39) F370L possibly damaging Het
Iho1 G T 9: 108,290,205 (GRCm39) T133N possibly damaging Het
Inpp4b A T 8: 82,723,968 (GRCm39) D500V probably benign Het
Itgb4 A G 11: 115,897,389 (GRCm39) D1534G possibly damaging Het
Kcnk2 G C 1: 189,072,214 (GRCm39) T38S possibly damaging Het
Kif16b C T 2: 142,598,042 (GRCm39) V527I probably benign Het
Kmt2b A G 7: 30,276,133 (GRCm39) Y1789H probably damaging Het
Lpl A C 8: 69,353,895 (GRCm39) D412A possibly damaging Het
Lrrc27 T G 7: 138,803,529 (GRCm39) L151R probably damaging Het
Muc17 T C 5: 137,190,980 (GRCm39) probably benign Het
Nup205 T A 6: 35,185,069 (GRCm39) Y829* probably null Het
Obscn T C 11: 59,022,472 (GRCm39) R758G possibly damaging Het
Olfm4 A G 14: 80,259,192 (GRCm39) Y447C probably damaging Het
Or4f57 T C 2: 111,790,494 (GRCm39) Y308C probably benign Het
Pcdhb6 T C 18: 37,468,222 (GRCm39) V381A probably benign Het
Prmt2 C T 10: 76,061,249 (GRCm39) W79* probably null Het
Skic2 T C 17: 35,059,361 (GRCm39) M1029V probably benign Het
Stil A G 4: 114,873,483 (GRCm39) R369G probably null Het
Ttc41 T C 10: 86,560,238 (GRCm39) I387T probably benign Het
Tubgcp6 A G 15: 88,987,187 (GRCm39) L1262P probably benign Het
Vmn2r112 T A 17: 22,822,096 (GRCm39) V258E probably damaging Het
Zfp804b T C 5: 6,819,445 (GRCm39) H1206R probably damaging Het
Other mutations in Ighv8-11
AlleleSourceChrCoordTypePredicted EffectPPH Score
R3722:Ighv8-11 UTSW 12 115,530,771 (GRCm39) missense possibly damaging 0.63
R4856:Ighv8-11 UTSW 12 115,530,774 (GRCm39) missense possibly damaging 0.88
R7651:Ighv8-11 UTSW 12 115,531,005 (GRCm39) missense probably benign 0.09
R8690:Ighv8-11 UTSW 12 115,531,164 (GRCm39) critical splice donor site probably benign
Predicted Primers
Posted On 2015-02-05