Incidental Mutation 'R4115:Ighv11-1'
ID 314605
Institutional Source Beutler Lab
Gene Symbol Ighv11-1
Ensembl Gene ENSMUSG00000094533
Gene Name immunoglobulin heavy variable 11-1
Synonyms Gm16611
MMRRC Submission 041630-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.155) question?
Stock # R4115 (G1)
Quality Score 225
Status Not validated
Chromosome 12
Chromosomal Location 113945499-113945794 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 113945685 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 56 (V56A)
Ref Sequence ENSEMBL: ENSMUSP00000100247 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103466]
AlphaFold A0A075B5R6
Predicted Effect probably benign
Transcript: ENSMUST00000103466
AA Change: V56A

PolyPhen 2 Score 0.132 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000100247
Gene: ENSMUSG00000094533
AA Change: V56A

DomainStartEndE-ValueType
IGv 36 117 4.95e-26 SMART
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.3%
  • 20x: 95.3%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ankrd34c A G 9: 89,611,927 (GRCm39) L138P probably damaging Het
Aplp2 C T 9: 31,069,122 (GRCm39) R569Q probably benign Het
BC035044 C T 6: 128,867,813 (GRCm39) probably benign Het
Camta2 T C 11: 70,567,300 (GRCm39) M626V possibly damaging Het
Cdh20 G A 1: 110,066,039 (GRCm39) R771Q probably benign Het
Chd3 T G 11: 69,248,343 (GRCm39) I850L possibly damaging Het
Cspg4 T A 9: 56,805,678 (GRCm39) L2163Q probably damaging Het
Cyp2c66 A G 19: 39,165,003 (GRCm39) D328G possibly damaging Het
Dcun1d3 T C 7: 119,458,957 (GRCm39) N26S probably benign Het
Dmxl2 A T 9: 54,354,272 (GRCm39) Y391* probably null Het
Gnl3 T G 14: 30,738,813 (GRCm39) K79Q probably damaging Het
Hat1 A G 2: 71,271,566 (GRCm39) T380A probably benign Het
Hectd1 A T 12: 51,815,506 (GRCm39) L1527* probably null Het
Ism2 A G 12: 87,333,805 (GRCm39) I80T probably benign Het
Itpr2 C T 6: 146,327,008 (GRCm39) V120I probably damaging Het
Kif1a T A 1: 92,980,260 (GRCm39) E823V probably damaging Het
Letm2 T A 8: 26,070,343 (GRCm39) K432* probably null Het
LTO1 G A 7: 144,473,383 (GRCm39) V142M possibly damaging Het
Mc4r T A 18: 66,993,050 (GRCm39) Y21F probably benign Het
Morc3 G A 16: 93,670,227 (GRCm39) D801N probably benign Het
Mycbpap C A 11: 94,403,051 (GRCm39) probably null Het
Nfkbil1 A G 17: 35,440,286 (GRCm39) M129T probably damaging Het
Notch3 C A 17: 32,377,407 (GRCm39) C223F probably damaging Het
Nrcam T C 12: 44,613,109 (GRCm39) V606A possibly damaging Het
Nudcd2 T C 11: 40,627,434 (GRCm39) M118T probably damaging Het
Or1j13 A T 2: 36,369,797 (GRCm39) L115Q probably damaging Het
Pcsk5 C T 19: 17,410,783 (GRCm39) D1870N unknown Het
Pde3b T C 7: 114,120,962 (GRCm39) F696L probably damaging Het
Pde8a T A 7: 80,932,555 (GRCm39) probably null Het
Pgm1 C T 4: 99,819,348 (GRCm39) Q191* probably null Het
Pramel21 A G 4: 143,344,026 (GRCm39) D442G probably benign Het
Psg20 A G 7: 18,419,905 (GRCm39) S5P probably damaging Het
Reps1 C T 10: 17,979,955 (GRCm39) P397S possibly damaging Het
Sec22a A G 16: 35,139,202 (GRCm39) F232S probably damaging Het
Spata13 G T 14: 60,929,927 (GRCm39) G168V probably damaging Het
Spta1 T C 1: 174,067,923 (GRCm39) W2117R probably damaging Het
Sptbn4 C T 7: 27,090,995 (GRCm39) E1399K probably damaging Het
Tek T C 4: 94,737,920 (GRCm39) S657P probably damaging Het
Thoc2l T C 5: 104,667,299 (GRCm39) L607S probably damaging Het
Trpm6 T C 19: 18,809,921 (GRCm39) W1106R probably damaging Het
Tssk3 T C 4: 129,383,300 (GRCm39) Y124C probably damaging Het
Ugt2b1 A G 5: 87,074,273 (GRCm39) W29R probably damaging Het
Vmn2r97 T C 17: 19,148,332 (GRCm39) F76L probably benign Het
Other mutations in Ighv11-1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4703:Ighv11-1 UTSW 12 113,945,622 (GRCm39) missense possibly damaging 0.70
R4989:Ighv11-1 UTSW 12 113,945,768 (GRCm39) missense probably benign
R7767:Ighv11-1 UTSW 12 113,945,722 (GRCm39) missense probably damaging 1.00
R9726:Ighv11-1 UTSW 12 113,945,623 (GRCm39) missense probably benign 0.18
Predicted Primers PCR Primer
(F):5'- ATACGTGGCTGTGTCCTCAG -3'
(R):5'- TCAACATGGAGTGGGAACTG -3'

Sequencing Primer
(F):5'- GATCGCACATTGCTCATCTGCAG -3'
(R):5'- AGTGGGAACTGAGCTTAATTTTC -3'
Posted On 2015-05-14