Incidental Mutation 'IGL03051:Ighv7-1'
ID 409078
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ighv7-1
Ensembl Gene ENSMUSG00000076665
Gene Name immunoglobulin heavy variable 7-1
Synonyms Gm16698
Accession Numbers
Essential gene? Probably non essential (E-score: 0.077) question?
Stock # IGL03051
Quality Score
Status
Chromosome 12
Chromosomal Location 113860028-113860566 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to T at 113860576 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000100255 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103474]
AlphaFold A0A075B5S2
Predicted Effect probably benign
Transcript: ENSMUST00000103474
SMART Domains Protein: ENSMUSP00000100255
Gene: ENSMUSG00000076665

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
IGv 36 119 6.1e-35 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aak1 G T 6: 86,964,283 (GRCm39) probably benign Het
Abhd14a A T 9: 106,321,128 (GRCm39) F76I possibly damaging Het
Acvr1b A G 15: 101,100,959 (GRCm39) R374G probably damaging Het
Akap13 T A 7: 75,260,233 (GRCm39) C149* probably null Het
Appbp2 A T 11: 85,082,565 (GRCm39) D555E possibly damaging Het
Arhgap25 T C 6: 87,472,896 (GRCm39) Q87R probably null Het
Baz1b T A 5: 135,246,079 (GRCm39) N509K probably benign Het
Ccn4 T A 15: 66,778,399 (GRCm39) C73* probably null Het
Ces5a C A 8: 94,255,226 (GRCm39) G156C probably damaging Het
Chtf18 G A 17: 25,939,938 (GRCm39) R723W probably damaging Het
Clec4e A G 6: 123,266,692 (GRCm39) S6P probably benign Het
Dennd4a A G 9: 64,769,696 (GRCm39) I468V probably damaging Het
Epb41l4a A T 18: 34,007,825 (GRCm39) Y233N probably damaging Het
Fam210b C T 2: 172,194,612 (GRCm39) H155Y probably benign Het
Frmd4b A T 6: 97,272,943 (GRCm39) C770* probably null Het
Gpa33 A G 1: 165,992,790 (GRCm39) H301R probably benign Het
Gpr39 T A 1: 125,605,485 (GRCm39) C138S probably damaging Het
Gtf2i T A 5: 134,271,768 (GRCm39) K858* probably null Het
Iglv1 T C 16: 18,903,973 (GRCm39) T49A possibly damaging Het
Kif17 A C 4: 138,016,565 (GRCm39) D416A probably damaging Het
Mib2 T C 4: 155,741,747 (GRCm39) T431A probably damaging Het
Mpz G A 1: 170,986,380 (GRCm39) R98H probably damaging Het
Naa16 T C 14: 79,606,522 (GRCm39) E337G probably benign Het
Odam G A 5: 88,040,335 (GRCm39) probably benign Het
Or1e1f T A 11: 73,855,860 (GRCm39) L142H probably benign Het
Parp2 T C 14: 51,056,805 (GRCm39) probably benign Het
Pcdh7 T G 5: 58,286,415 (GRCm39) S1164A probably damaging Het
Pkp4 G T 2: 59,142,106 (GRCm39) A470S probably benign Het
Plin4 A T 17: 56,412,417 (GRCm39) M538K possibly damaging Het
Prex2 T C 1: 11,212,889 (GRCm39) V624A probably damaging Het
Rps6ka5 A C 12: 100,582,250 (GRCm39) probably null Het
Simc1 T C 13: 54,674,036 (GRCm39) S795P probably benign Het
Slc35b4 A T 6: 34,137,406 (GRCm39) probably null Het
Stxbp2 A T 8: 3,691,971 (GRCm39) I538F probably benign Het
Syt14 T C 1: 192,615,528 (GRCm39) N486S probably benign Het
Trim59 T C 3: 68,944,206 (GRCm39) N378S probably benign Het
Wdr17 T A 8: 55,104,349 (GRCm39) D908V probably damaging Het
Wdr74 A G 19: 8,716,875 (GRCm39) probably benign Het
Other mutations in Ighv7-1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01637:Ighv7-1 APN 12 113,860,123 (GRCm39) missense possibly damaging 0.78
IGL03006:Ighv7-1 APN 12 113,860,145 (GRCm39) missense probably damaging 1.00
IGL03281:Ighv7-1 APN 12 113,860,571 (GRCm39) unclassified probably benign
R3008:Ighv7-1 UTSW 12 113,860,071 (GRCm39) missense probably damaging 1.00
R5754:Ighv7-1 UTSW 12 113,860,239 (GRCm39) missense probably damaging 0.99
R6172:Ighv7-1 UTSW 12 113,860,183 (GRCm39) missense probably damaging 0.99
R6213:Ighv7-1 UTSW 12 113,860,141 (GRCm39) missense probably damaging 0.99
R7324:Ighv7-1 UTSW 12 113,860,149 (GRCm39) missense probably damaging 1.00
R8399:Ighv7-1 UTSW 12 113,860,532 (GRCm39) missense unknown
R9193:Ighv7-1 UTSW 12 113,860,110 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02