Incidental Mutation 'IGL02685:Ighv13-1'
ID 303514
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ighv13-1
Ensembl Gene ENSMUSG00000102497
Gene Name immunoglobulin heavy variable 13-1
Synonyms Gm16931
Accession Numbers
Essential gene? Probably non essential (E-score: 0.186) question?
Stock # IGL02685
Quality Score
Status
Chromosome 12
Chromosomal Location 114231233-114231526 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) C to A at 114231403 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000141480 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103479] [ENSMUST00000195619]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000103479
SMART Domains Protein: ENSMUSP00000100260
Gene: ENSMUSG00000076670

DomainStartEndE-ValueType
IGv 17 99 1.78e-27 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000103480
SMART Domains Protein: ENSMUSP00000100261
Gene: ENSMUSG00000076671

DomainStartEndE-ValueType
IGv 17 98 2.24e-24 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000195594
Predicted Effect probably benign
Transcript: ENSMUST00000195619
SMART Domains Protein: ENSMUSP00000141480
Gene: ENSMUSG00000076670

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
IGv 35 117 7.1e-30 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb5 T C 12: 118,869,682 (GRCm39) Y779C probably damaging Het
Acad10 A G 5: 121,770,672 (GRCm39) F532L probably benign Het
Adgrb3 A T 1: 25,123,323 (GRCm39) probably null Het
Akr1d1 T C 6: 37,507,278 (GRCm39) probably benign Het
Aqp11 A G 7: 97,386,759 (GRCm39) Y146H probably damaging Het
Cdh2 A T 18: 16,779,557 (GRCm39) L168Q probably damaging Het
Ces2f C T 8: 105,679,730 (GRCm39) Q277* probably null Het
Cmya5 G A 13: 93,227,505 (GRCm39) Q2528* probably null Het
Col22a1 A G 15: 71,673,764 (GRCm39) V984A unknown Het
Col5a3 T C 9: 20,683,501 (GRCm39) D1557G unknown Het
Cpb1 A T 3: 20,319,520 (GRCm39) V188E probably damaging Het
Csgalnact1 C A 8: 68,854,144 (GRCm39) G219V probably damaging Het
Ephb1 G T 9: 101,918,302 (GRCm39) Y402* probably null Het
Foxm1 T C 6: 128,350,070 (GRCm39) L319S possibly damaging Het
Gmppb T C 9: 107,927,118 (GRCm39) probably benign Het
Grid2 T G 6: 64,322,800 (GRCm39) M600R possibly damaging Het
Gstm6 T C 3: 107,848,507 (GRCm39) K57E probably benign Het
Hars2 T G 18: 36,924,171 (GRCm39) S422A probably benign Het
Igdcc4 T C 9: 65,041,107 (GRCm39) M1092T possibly damaging Het
Iqgap2 C A 13: 95,807,912 (GRCm39) R785L probably damaging Het
Kalrn G A 16: 34,334,329 (GRCm39) Q8* probably null Het
Mms22l A G 4: 24,591,133 (GRCm39) T1035A probably benign Het
Myo1b A G 1: 51,817,658 (GRCm39) Y535H probably damaging Het
Neb T A 2: 52,065,313 (GRCm39) K6234N possibly damaging Het
Nlrp9c A G 7: 26,084,982 (GRCm39) I199T probably damaging Het
Or10ak7 A T 4: 118,791,134 (GRCm39) F304I possibly damaging Het
Or4c108 T A 2: 88,803,365 (GRCm39) N290I possibly damaging Het
Or52h9 C A 7: 104,202,357 (GRCm39) T77K probably benign Het
Or7g32 T C 9: 19,408,098 (GRCm39) I18T probably benign Het
Osmr T C 15: 6,845,054 (GRCm39) E904G probably benign Het
Pde8b T C 13: 95,162,628 (GRCm39) *831W probably null Het
Prkdc T C 16: 15,653,907 (GRCm39) V3888A possibly damaging Het
Scn9a C A 2: 66,367,637 (GRCm39) S693I probably damaging Het
Sepsecs T C 5: 52,804,534 (GRCm39) T379A probably benign Het
Ska1 T A 18: 74,330,119 (GRCm39) H207L probably benign Het
Slc17a9 C A 2: 180,375,602 (GRCm39) Q175K probably damaging Het
Slc38a2 G A 15: 96,589,306 (GRCm39) T396I probably benign Het
Slc9a4 A C 1: 40,668,742 (GRCm39) H795P probably benign Het
Sorbs2 C T 8: 46,256,877 (GRCm39) T955I probably benign Het
Spata4 A T 8: 55,053,963 (GRCm39) H43L probably benign Het
Ss18l2 G A 9: 121,539,484 (GRCm39) A6T possibly damaging Het
Sult1e1 C T 5: 87,727,765 (GRCm39) W172* probably null Het
Tlcd1 T C 11: 78,070,363 (GRCm39) probably benign Het
Tmc8 T C 11: 117,683,400 (GRCm39) S652P probably damaging Het
Vps37b T C 5: 124,148,874 (GRCm39) S54G probably damaging Het
Wdr26 A T 1: 181,011,345 (GRCm39) S511T possibly damaging Het
Zfhx4 A G 3: 5,477,213 (GRCm39) Y3251C probably damaging Het
Other mutations in Ighv13-1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01637:Ighv13-1 APN 12 114,231,353 (GRCm39) unclassified probably benign
R4731:Ighv13-1 UTSW 12 114,231,252 (GRCm39) unclassified probably benign
Posted On 2015-04-16