Incidental Mutation 'IGL00538:Ighv1-7'
ID 332562
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ighv1-7
Ensembl Gene ENSMUSG00000095200
Gene Name immunoglobulin heavy variable V1-7
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.121) question?
Stock # IGL00538
Quality Score
Status
Chromosome 12
Chromosomal Location 114502115-114502408 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to A at 114502381 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Stop codon at position 29 (E29*)
Ref Sequence ENSEMBL: ENSMUSP00000100277 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103496]
AlphaFold A0A075B5T7
Predicted Effect probably null
Transcript: ENSMUST00000103496
AA Change: E29*
SMART Domains Protein: ENSMUSP00000100277
Gene: ENSMUSG00000095200
AA Change: E29*

DomainStartEndE-ValueType
IGv 36 117 6.22e-32 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 20 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arl9 T A 5: 77,151,903 (GRCm39) M1K probably null Het
Asf1a T C 10: 53,482,227 (GRCm39) L13P probably damaging Het
Atg2b T G 12: 105,611,175 (GRCm39) H1252P probably benign Het
Cacna2d1 C T 5: 16,451,783 (GRCm39) R216* probably null Het
Cdc42ep3 G A 17: 79,642,884 (GRCm39) A12V possibly damaging Het
Cntn3 G A 6: 102,397,223 (GRCm39) Q117* probably null Het
Cyp3a41b G A 5: 145,515,010 (GRCm39) probably benign Het
Dhx36 T C 3: 62,408,466 (GRCm39) E124G probably benign Het
Galnt7 T A 8: 58,005,556 (GRCm39) T226S possibly damaging Het
H2al3 T A X: 9,716,244 (GRCm39) probably benign Het
Iqcb1 G T 16: 36,678,948 (GRCm39) V421F probably benign Het
Lrrc8c G A 5: 105,755,076 (GRCm39) V284I probably damaging Het
Rpp14 G A 14: 8,083,934 (GRCm38) G30E possibly damaging Het
Samd9l A T 6: 3,376,779 (GRCm39) Y161N probably damaging Het
Slc14a1 A T 18: 78,147,288 (GRCm39) F313Y probably damaging Het
Taco1 T A 11: 105,962,805 (GRCm39) I164N probably damaging Het
Tenm3 G T 8: 48,689,060 (GRCm39) H2176N probably damaging Het
Tmem156 T C 5: 65,231,183 (GRCm39) Y165C probably damaging Het
Trpc7 A T 13: 56,921,622 (GRCm39) N731K possibly damaging Het
Ubox5 T C 2: 130,441,808 (GRCm39) N293S probably damaging Het
Other mutations in Ighv1-7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02020:Ighv1-7 APN 12 114,502,345 (GRCm39) missense probably damaging 1.00
R3862:Ighv1-7 UTSW 12 114,502,266 (GRCm39) missense probably damaging 1.00
R3863:Ighv1-7 UTSW 12 114,502,266 (GRCm39) missense probably damaging 1.00
R3864:Ighv1-7 UTSW 12 114,502,266 (GRCm39) missense probably damaging 1.00
R5632:Ighv1-7 UTSW 12 114,502,501 (GRCm39) critical splice donor site probably benign
R5976:Ighv1-7 UTSW 12 114,502,379 (GRCm39) missense probably benign 0.35
R8040:Ighv1-7 UTSW 12 114,502,390 (GRCm39) missense probably benign 0.24
R8907:Ighv1-7 UTSW 12 114,502,353 (GRCm39) missense probably damaging 1.00
R9442:Ighv1-7 UTSW 12 114,502,198 (GRCm39) missense probably damaging 1.00
Posted On 2015-08-05