Incidental Mutation 'IGL02552:Batf2'
ID 298123
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Batf2
Ensembl Gene ENSMUSG00000039699
Gene Name basic leucine zipper transcription factor, ATF-like 2
Synonyms 4933430F08Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # IGL02552
Quality Score
Status
Chromosome 19
Chromosomal Location 6214424-6222506 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 6221537 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Asparagine at position 116 (Y116N)
Ref Sequence ENSEMBL: ENSMUSP00000045744 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000045042]
AlphaFold Q8R1H8
Predicted Effect probably benign
Transcript: ENSMUST00000045042
AA Change: Y116N

PolyPhen 2 Score 0.432 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000045744
Gene: ENSMUSG00000039699
AA Change: Y116N

DomainStartEndE-ValueType
BRLZ 16 80 6.76e-12 SMART
low complexity region 147 158 N/A INTRINSIC
low complexity region 168 195 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000132750
Predicted Effect noncoding transcript
Transcript: ENSMUST00000134150
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135461
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139326
Predicted Effect noncoding transcript
Transcript: ENSMUST00000141858
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased susceptibility to parasitic infection induced morbidity/mortality. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700006A11Rik A G 3: 124,208,145 (GRCm39) L178S probably damaging Het
Abca12 A G 1: 71,333,906 (GRCm39) Y1199H probably damaging Het
Abcc9 T C 6: 142,551,645 (GRCm39) D1221G possibly damaging Het
Apc T A 18: 34,446,035 (GRCm39) M977K possibly damaging Het
Arhgap30 T A 1: 171,235,324 (GRCm39) L566Q probably damaging Het
Arhgap40 T A 2: 158,388,721 (GRCm39) W552R probably benign Het
Astn1 C T 1: 158,332,965 (GRCm39) S349F possibly damaging Het
Bard1 T C 1: 71,104,815 (GRCm39) probably benign Het
Bltp3b T A 10: 89,642,605 (GRCm39) L10* probably null Het
Cbx6 T C 15: 79,713,094 (GRCm39) H111R probably damaging Het
Cd44 T A 2: 102,679,076 (GRCm39) N242I probably benign Het
Cdnf C T 2: 3,525,012 (GRCm39) Q184* probably null Het
Chd2 C A 7: 73,097,068 (GRCm39) probably benign Het
Cmtm6 G A 9: 114,566,374 (GRCm39) V88M probably damaging Het
Col24a1 C A 3: 145,179,962 (GRCm39) S1151R possibly damaging Het
Csta2 A G 16: 36,073,459 (GRCm39) E15G probably damaging Het
Degs1l T A 1: 180,882,463 (GRCm39) V75E possibly damaging Het
Dnajc2 T C 5: 21,988,061 (GRCm39) D6G probably damaging Het
Eif3a G A 19: 60,751,664 (GRCm39) probably benign Het
Fbn1 C A 2: 125,254,633 (GRCm39) C210F possibly damaging Het
Fmn2 T A 1: 174,523,286 (GRCm39) D1380E probably damaging Het
Fry A T 5: 150,304,375 (GRCm39) K588N probably damaging Het
Gm18856 G A 13: 14,139,805 (GRCm39) probably benign Het
Gpr37 G T 6: 25,688,686 (GRCm39) T137K probably benign Het
Gzmc T C 14: 56,472,039 (GRCm39) M1V probably null Het
Htr5a T C 5: 28,047,958 (GRCm39) V171A probably benign Het
Ints6l T C X: 55,500,557 (GRCm39) probably benign Het
Kcnma1 C T 14: 23,436,327 (GRCm39) probably null Het
Krt35 C T 11: 99,983,899 (GRCm39) G367D probably benign Het
Nlrp1b C T 11: 71,063,057 (GRCm39) V668I possibly damaging Het
Nlrp1b C T 11: 71,072,878 (GRCm39) V322I possibly damaging Het
Ntf3 T C 6: 126,078,823 (GRCm39) N228D probably damaging Het
Nup133 G A 8: 124,655,994 (GRCm39) R496W possibly damaging Het
Or4c10 T C 2: 89,760,903 (GRCm39) V250A probably benign Het
Or51i1 C A 7: 103,671,463 (GRCm39) G21W probably damaging Het
Pah C T 10: 87,414,707 (GRCm39) probably benign Het
Pan2 G T 10: 128,154,896 (GRCm39) W1112L probably damaging Het
Pkn3 G A 2: 29,970,879 (GRCm39) R209Q probably damaging Het
Plaa C T 4: 94,470,717 (GRCm39) probably null Het
Qprt C T 7: 126,708,027 (GRCm39) A135T probably damaging Het
Rbbp6 T G 7: 122,582,204 (GRCm39) S108A probably damaging Het
Smg1 T A 7: 117,795,117 (GRCm39) probably benign Het
Spink5 T A 18: 44,125,235 (GRCm39) C368S possibly damaging Het
Sptan1 T A 2: 29,908,486 (GRCm39) I1734N probably damaging Het
Stk38l C T 6: 146,669,031 (GRCm39) L170F probably damaging Het
Tesmin C T 19: 3,452,483 (GRCm39) probably benign Het
Tjp1 A T 7: 64,949,530 (GRCm39) C1697* probably null Het
Tmco4 T C 4: 138,785,690 (GRCm39) S587P probably benign Het
Tmem208 G A 8: 106,055,329 (GRCm39) probably null Het
Trim30d T C 7: 104,121,623 (GRCm39) Q224R probably damaging Het
Trpm7 T A 2: 126,682,699 (GRCm39) D390V probably damaging Het
Uba7 A G 9: 107,858,589 (GRCm39) I807V probably benign Het
Utp18 C A 11: 93,759,160 (GRCm39) C438F probably damaging Het
Vps13d T C 4: 144,899,707 (GRCm39) K191E possibly damaging Het
Wdr27 A G 17: 15,146,453 (GRCm39) S181P probably damaging Het
Zfp462 T C 4: 55,010,613 (GRCm39) Y860H probably damaging Het
Other mutations in Batf2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02212:Batf2 APN 19 6,221,991 (GRCm39) missense probably damaging 1.00
IGL02966:Batf2 APN 19 6,221,819 (GRCm39) missense probably damaging 0.96
R2429:Batf2 UTSW 19 6,221,538 (GRCm39) missense probably damaging 0.98
R4008:Batf2 UTSW 19 6,221,378 (GRCm39) missense probably damaging 1.00
R4712:Batf2 UTSW 19 6,221,357 (GRCm39) missense probably benign 0.24
R7082:Batf2 UTSW 19 6,221,405 (GRCm39) missense possibly damaging 0.78
R7267:Batf2 UTSW 19 6,221,396 (GRCm39) missense probably benign
R7400:Batf2 UTSW 19 6,221,538 (GRCm39) missense probably damaging 0.98
Posted On 2015-04-16