Incidental Mutation 'R4533:Ighv1-37'
ID333215
Institutional Source Beutler Lab
Gene Symbol Ighv1-37
Ensembl Gene ENSMUSG00000095923
Gene Nameimmunoglobulin heavy variable 1-37
SynonymsGm16716
MMRRC Submission 041773-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.175) question?
Stock #R4533 (G1)
Quality Score225
Status Validated
Chromosome12
Chromosomal Location114896238-114896671 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 114896527 bp
ZygosityHeterozygous
Amino Acid Change Valine to Aspartic acid at position 21 (V21D)
Ref Sequence ENSEMBL: ENSMUSP00000141375 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103514] [ENSMUST00000193950]
Predicted Effect probably damaging
Transcript: ENSMUST00000103514
AA Change: V20D

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000100295
Gene: ENSMUSG00000095923
AA Change: V20D

DomainStartEndE-ValueType
IGv 35 116 3.69e-25 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000193950
AA Change: V21D

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000141375
Gene: ENSMUSG00000095923
AA Change: V21D

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
IGv 36 117 1.5e-27 SMART
Meta Mutation Damage Score 0.038 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.8%
Validation Efficiency 100% (54/54)
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts7 A G 9: 90,180,708 Y405C probably damaging Het
Ago3 A T 4: 126,345,563 S832T probably damaging Het
Akap9 T A 5: 4,043,948 F2157I probably damaging Het
Anapc5 T C 5: 122,791,735 E561G possibly damaging Het
Art5 T C 7: 102,098,338 H78R probably benign Het
Blvra T A 2: 127,090,384 probably null Het
Ccdc171 A G 4: 83,657,342 T488A possibly damaging Het
Crtc3 A T 7: 80,589,795 M603K probably damaging Het
Csmd1 T C 8: 15,931,037 probably null Het
Dbh C A 2: 27,177,331 H409Q possibly damaging Het
Fam122c G A X: 53,293,499 R94H possibly damaging Het
Gm12185 T C 11: 48,907,920 Y582C probably damaging Het
Gm12185 T C 11: 48,908,094 N524S possibly damaging Het
Gm7356 A C 17: 14,001,410 I119R probably damaging Het
Heatr1 T A 13: 12,434,511 D1963E probably benign Het
Itga3 T G 11: 95,057,293 Q602P probably benign Het
Kcmf1 G A 6: 72,849,591 R152C probably damaging Het
Lin54 T C 5: 100,485,403 I141V possibly damaging Het
Mast1 T A 8: 84,921,361 H497L probably damaging Het
Mrpl44 T C 1: 79,776,254 F41S possibly damaging Het
Myo18b T C 5: 112,693,025 R2301G probably damaging Het
Nek1 A T 8: 61,007,213 M58L possibly damaging Het
Olfr726 T C 14: 50,083,699 probably null Het
Orc4 G A 2: 48,937,489 P31S probably benign Het
P3h3 A G 6: 124,854,408 V338A possibly damaging Het
Pcdha7 T C 18: 36,975,407 V495A possibly damaging Het
Plcb3 T C 19: 6,956,272 E895G probably benign Het
Plekha5 A G 6: 140,570,331 E770G probably damaging Het
Ptchd3 C T 11: 121,836,431 S377F probably damaging Het
Ptprj C T 2: 90,439,955 D1266N probably damaging Het
Raly A T 2: 154,865,933 E291V probably damaging Het
Rnf217 C A 10: 31,608,763 C141F possibly damaging Het
Rufy4 T C 1: 74,147,663 C537R probably damaging Het
Slc12a3 A G 8: 94,357,086 M914V probably null Het
Tbc1d9 A G 8: 83,270,918 T1035A probably damaging Het
Tex14 C T 11: 87,536,829 R36* probably null Het
Tiparp A G 3: 65,546,347 D172G probably benign Het
Ttc3 T A 16: 94,466,877 probably benign Het
Uap1 A T 1: 170,143,425 I466N probably damaging Het
Ubr1 T C 2: 120,942,482 T426A possibly damaging Het
Vmn1r77 T A 7: 12,041,829 H177Q probably benign Het
Vmn2r72 T A 7: 85,751,926 H95L probably benign Het
Vwc2l G A 1: 70,882,139 C151Y probably damaging Het
Wdr12 T C 1: 60,078,195 Y414C probably benign Het
Zfp609 A C 9: 65,703,608 V691G probably benign Het
Zmiz1 T C 14: 25,645,660 Y254H probably damaging Het
Other mutations in Ighv1-37
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00979:Ighv1-37 APN 12 114896450 missense probably benign 0.00
R3971:Ighv1-37 UTSW 12 114896459 missense probably damaging 1.00
R4614:Ighv1-37 UTSW 12 114896243 missense probably benign 0.12
R5726:Ighv1-37 UTSW 12 114896674 unclassified probably benign
R6842:Ighv1-37 UTSW 12 114896655 missense probably damaging 0.98
R6985:Ighv1-37 UTSW 12 114896632 missense probably benign 0.00
Z1088:Ighv1-37 UTSW 12 114896624 critical splice donor site probably benign
Predicted Primers PCR Primer
(F):5'- TGTCTACAGTCAATGTGGCCTTG -3'
(R):5'- GATCACTGTCCTCTCCACAG -3'

Sequencing Primer
(F):5'- CCCTTGAACTTCTGGTTGTAGAAAG -3'
(R):5'- GTCCCTGAAGACACTGACTC -3'
Posted On2015-08-18