Incidental Mutation 'IGL01788:Ifna9'
ID 155107
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ifna9
Ensembl Gene ENSMUSG00000095270
Gene Name interferon alpha 9
Synonyms Ifa9
Accession Numbers
Essential gene? Probably non essential (E-score: 0.057) question?
Stock # IGL01788
Quality Score
Status
Chromosome 4
Chromosomal Location 88510050-88510622 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 88510097 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 176 (S176P)
Ref Sequence ENSEMBL: ENSMUSP00000099871 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000102807]
AlphaFold P09235
Predicted Effect probably damaging
Transcript: ENSMUST00000102807
AA Change: S176P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000099871
Gene: ENSMUSG00000095270
AA Change: S176P

DomainStartEndE-ValueType
signal peptide 1 23 N/A INTRINSIC
IFabd 58 175 1.68e-67 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9230009I02Rik T G 11: 50,982,542 (GRCm39) noncoding transcript Het
Acp6 A G 3: 97,073,198 (GRCm39) T80A probably damaging Het
Adamtsl5 T C 10: 80,180,757 (GRCm39) T102A probably benign Het
Adcy6 C A 15: 98,494,400 (GRCm39) E812* probably null Het
Apol6 G A 15: 76,935,216 (GRCm39) V162I possibly damaging Het
Atp6v1h T A 1: 5,220,206 (GRCm39) M396K possibly damaging Het
B3gnt8 A G 7: 25,328,613 (GRCm39) T348A probably damaging Het
Cgnl1 A G 9: 71,562,672 (GRCm39) V869A probably benign Het
Dcaf5 A T 12: 80,395,098 (GRCm39) I357N probably damaging Het
Dennd4a A G 9: 64,749,903 (GRCm39) I165V probably benign Het
Dlgap2 T A 8: 14,893,631 (GRCm39) I982K probably benign Het
Dop1a A T 9: 86,413,772 (GRCm39) H1891L probably benign Het
Fhad1 A C 4: 141,660,113 (GRCm39) S65R probably benign Het
Fn1 A G 1: 71,652,996 (GRCm39) I1331T probably damaging Het
Fto A T 8: 92,136,359 (GRCm39) Y211F probably benign Het
Gm3278 A C 14: 16,080,370 (GRCm39) R60S probably benign Het
Klk1 T C 7: 43,878,407 (GRCm39) I189T probably benign Het
Mcph1 G A 8: 18,682,419 (GRCm39) G519R probably damaging Het
Mcph1 G A 8: 18,682,420 (GRCm39) G519E probably damaging Het
N4bp1 A T 8: 87,587,624 (GRCm39) V438E probably benign Het
Ncapg T A 5: 45,828,423 (GRCm39) V58E probably damaging Het
Nid2 T A 14: 19,858,047 (GRCm39) S1054T probably damaging Het
Nlrp4a A T 7: 26,153,492 (GRCm39) Y681F probably benign Het
Or4f57 T C 2: 111,791,352 (GRCm39) D22G probably benign Het
Or4k15c A G 14: 50,321,959 (GRCm39) Y60H probably damaging Het
Or52e19b C A 7: 103,032,770 (GRCm39) M146I probably benign Het
Or5b94 G A 19: 12,652,442 (GRCm39) R291K probably damaging Het
Papln A T 12: 83,822,236 (GRCm39) T364S probably benign Het
Pcdh18 C A 3: 49,710,371 (GRCm39) E315* probably null Het
Pmel G A 10: 128,553,701 (GRCm39) R445Q probably damaging Het
Ppp1r12b C T 1: 134,821,245 (GRCm39) V182I possibly damaging Het
Ptprn2 A G 12: 116,864,607 (GRCm39) T541A probably damaging Het
Rbl1 A T 2: 157,005,576 (GRCm39) N813K probably benign Het
Sash1 C A 10: 8,609,410 (GRCm39) R713L probably benign Het
Slc13a1 T G 6: 24,134,371 (GRCm39) T171P probably damaging Het
Slc18b1 G T 10: 23,701,899 (GRCm39) E407D probably damaging Het
Slc2a6 G A 2: 26,914,227 (GRCm39) Q297* probably null Het
Vmn1r209 T C 13: 22,989,832 (GRCm39) H286R probably damaging Het
Vmn1r28 C A 6: 58,242,522 (GRCm39) H122N probably benign Het
Wfs1 A G 5: 37,125,980 (GRCm39) Y304H probably benign Het
Zfp512b A G 2: 181,230,556 (GRCm39) S445P possibly damaging Het
Other mutations in Ifna9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02268:Ifna9 APN 4 88,510,591 (GRCm39) nonsense probably null
R0579:Ifna9 UTSW 4 88,510,508 (GRCm39) missense possibly damaging 0.84
R1530:Ifna9 UTSW 4 88,510,409 (GRCm39) missense possibly damaging 0.83
R1663:Ifna9 UTSW 4 88,510,220 (GRCm39) missense probably benign 0.00
R1872:Ifna9 UTSW 4 88,510,492 (GRCm39) missense probably damaging 0.97
R3923:Ifna9 UTSW 4 88,510,508 (GRCm39) missense possibly damaging 0.84
R4534:Ifna9 UTSW 4 88,510,285 (GRCm39) missense possibly damaging 0.76
R4882:Ifna9 UTSW 4 88,510,540 (GRCm39) missense probably benign 0.01
R5440:Ifna9 UTSW 4 88,510,048 (GRCm39) splice site probably null
R6008:Ifna9 UTSW 4 88,510,600 (GRCm39) missense probably null 1.00
R6464:Ifna9 UTSW 4 88,510,487 (GRCm39) missense possibly damaging 0.93
R6584:Ifna9 UTSW 4 88,510,375 (GRCm39) missense probably damaging 0.99
R6899:Ifna9 UTSW 4 88,510,300 (GRCm39) missense probably damaging 1.00
Posted On 2014-02-04