Incidental Mutation 'R3811:Ighv1-24'
ID473964
Institutional Source Beutler Lab
Gene Symbol Ighv1-24
Ensembl Gene ENSMUSG00000094241
Gene Nameimmunoglobulin heavy variable V1-24
SynonymsIghv1-24, immunoglobulin heavy variable V1-24
MMRRC Submission 040767-MU
Accession Numbers
Is this an essential gene? Possibly essential (E-score: 0.695) question?
Stock #R3811 (G1)
Quality Score106
Status Not validated
Chromosome12
Chromosomal Location114772928-114773361 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 114773065 bp
ZygosityHeterozygous
Amino Acid Change Leucine to Isoleucine at position 72 (L72I)
Ref Sequence ENSEMBL: ENSMUSP00000142245 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103509] [ENSMUST00000191861]
Predicted Effect probably benign
Transcript: ENSMUST00000103509
AA Change: L53I

PolyPhen 2 Score 0.329 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000100290
Gene: ENSMUSG00000094241
AA Change: L53I

DomainStartEndE-ValueType
IGv 17 98 2.16e-17 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000191861
AA Change: L72I

PolyPhen 2 Score 0.329 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000142245
Gene: ENSMUSG00000094241
AA Change: L72I

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
IGv 36 117 8.9e-20 SMART
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.6%
  • 20x: 95.9%
Validation Efficiency 97% (36/37)
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agbl3 G T 6: 34,799,729 S385I probably damaging Het
Arhgap28 G A 17: 67,896,093 P122S probably benign Het
Arid2 T C 15: 96,289,086 V73A probably benign Het
Atp1b1 C T 1: 164,443,305 R35H probably benign Het
Cacybp T C 1: 160,203,652 D202G probably benign Het
Chsy3 C G 18: 59,176,170 P165R probably benign Het
Creb3 C T 4: 43,565,501 Q227* probably null Het
Crnkl1 C A 2: 145,931,306 R140L probably damaging Het
Cyth4 A G 15: 78,604,649 E39G probably damaging Het
Dnah6 T C 6: 73,191,498 T481A probably benign Het
Dock4 T A 12: 40,779,124 I1003N possibly damaging Het
Galntl5 T C 5: 25,186,180 F26L probably benign Het
Glrx5 C G 12: 105,032,888 C63W probably damaging Het
Gm9602 T A 14: 4,776,499 I28N probably damaging Het
Hivep2 A G 10: 14,130,357 T900A probably benign Het
Hmcn1 A G 1: 150,649,577 probably null Het
Ilvbl G A 10: 78,579,035 C244Y probably benign Het
Kat7 A G 11: 95,291,615 probably benign Het
Kcnd3 C T 3: 105,658,766 A421V probably damaging Het
Lamc1 A T 1: 153,262,708 probably null Het
Mall T A 2: 127,708,854 I129F probably damaging Het
Mdn1 A T 4: 32,693,506 K1044* probably null Het
Med23 A T 10: 24,892,592 R77* probably null Het
Med23 G A 10: 24,892,593 probably null Het
Metap2 A T 10: 93,870,164 L252* probably null Het
Olfr1066 A T 2: 86,455,347 V308E probably benign Het
Psmd1 T A 1: 86,132,715 V828D probably damaging Het
Psmd9 C T 5: 123,234,590 probably benign Het
Rbbp5 T C 1: 132,492,587 V59A probably damaging Het
Sco2 T C 15: 89,373,679 probably benign Het
Slc32a1 G T 2: 158,614,736 C437F possibly damaging Het
Spem2 T C 11: 69,817,164 E325G possibly damaging Het
Steap4 A G 5: 7,977,017 T327A probably benign Het
Tsc2 T C 17: 24,629,037 D70G probably benign Het
Txndc5 T C 13: 38,523,405 K99E probably benign Het
Other mutations in Ighv1-24
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01630:Ighv1-24 APN 12 114773053 missense probably benign 0.22
PIT4581001:Ighv1-24 UTSW 12 114773183 missense probably benign
R2892:Ighv1-24 UTSW 12 114773059 missense probably benign 0.08
R3687:Ighv1-24 UTSW 12 114773080 missense probably damaging 1.00
R5071:Ighv1-24 UTSW 12 114773128 missense probably benign 0.17
R6880:Ighv1-24 UTSW 12 114773043 missense possibly damaging 0.85
Predicted Primers
Posted On2017-04-14