Incidental Mutation 'IGL02644:Ifi202b'
ID 301854
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ifi202b
Ensembl Gene ENSMUSG00000026535
Gene Name interferon activated gene 202B
Synonyms p202
Accession Numbers
Essential gene? Probably non essential (E-score: 0.049) question?
Stock # IGL02644
Quality Score
Status
Chromosome 1
Chromosomal Location 173790134-173810310 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 173799280 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Leucine at position 256 (H256L)
Ref Sequence ENSEMBL: ENSMUSP00000000266 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000000266]
AlphaFold Q9R002
PDB Structure Structural mimicry for functional antagonism [X-RAY DIFFRACTION]
Molecular basis for abrogation of activation of pro-inflammatory cytokines [X-RAY DIFFRACTION]
Crystal structure of p202 HIN1 [X-RAY DIFFRACTION]
Crystal structure of p202 HIN1 in complex with 20-mer dsDNA [X-RAY DIFFRACTION]
p202 HIN1 in complex with 12-mer dsDNA [X-RAY DIFFRACTION]
Crystal structure of the tetrameric p202 HIN2 [X-RAY DIFFRACTION]
Crystal structure of Ifi202 HINa domain in complex with 20bp dsDNA [X-RAY DIFFRACTION]
Predicted Effect probably benign
Transcript: ENSMUST00000000266
AA Change: H256L

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000000266
Gene: ENSMUSG00000026535
AA Change: H256L

DomainStartEndE-ValueType
Pfam:HIN 58 223 4.1e-68 PFAM
Pfam:HIN 256 421 1.5e-61 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrl4 A T 3: 151,198,007 (GRCm39) Y89F probably benign Het
Agl A G 3: 116,580,246 (GRCm39) Y406H probably damaging Het
Ankhd1 G A 18: 36,711,828 (GRCm39) probably null Het
Ankmy1 T C 1: 92,812,776 (GRCm39) D511G probably benign Het
Arid2 T C 15: 96,266,589 (GRCm39) Y546H probably damaging Het
Asap1 G T 15: 63,982,911 (GRCm39) P806T probably damaging Het
Aspa T A 11: 73,212,992 (GRCm39) T117S probably damaging Het
Atp2a3 C A 11: 72,866,165 (GRCm39) H262N probably benign Het
Bspry A T 4: 62,414,565 (GRCm39) H386L probably damaging Het
C1qc T C 4: 136,617,629 (GRCm39) T156A possibly damaging Het
Cfhr4 A G 1: 139,708,905 (GRCm39) M1T probably null Het
Copz2 A T 11: 96,744,257 (GRCm39) probably benign Het
Cybb A G X: 9,333,395 (GRCm39) V23A probably benign Het
D630003M21Rik T A 2: 158,058,730 (GRCm39) D390V possibly damaging Het
Dennd10 T A 19: 60,810,741 (GRCm39) S43T possibly damaging Het
Dpy19l2 G T 9: 24,569,888 (GRCm39) P355Q probably damaging Het
Gcn1 A T 5: 115,713,250 (GRCm39) Q71L probably benign Het
Gpd1l T C 9: 114,732,725 (GRCm39) probably null Het
Hydin A G 8: 111,265,100 (GRCm39) D2761G probably damaging Het
Igkv8-24 T C 6: 70,193,872 (GRCm39) Y112C probably damaging Het
Lama3 G A 18: 12,658,910 (GRCm39) R2022Q probably benign Het
Mroh4 T A 15: 74,482,224 (GRCm39) R675S possibly damaging Het
Mtf1 T G 4: 124,714,028 (GRCm39) C146G probably damaging Het
Nubpl A G 12: 52,317,841 (GRCm39) D178G probably damaging Het
Or7e165 A C 9: 19,695,010 (GRCm39) I194L probably benign Het
Pam16 A G 16: 4,434,697 (GRCm39) S91P probably damaging Het
Pcdhac2 A G 18: 37,278,232 (GRCm39) E404G probably benign Het
Pde7a C A 3: 19,311,031 (GRCm39) probably benign Het
Perm1 G T 4: 156,303,043 (GRCm39) G529V probably damaging Het
Pik3c2a T C 7: 115,972,049 (GRCm39) T794A probably benign Het
Ppfibp1 A G 6: 146,923,938 (GRCm39) Y722C probably damaging Het
Ppm1m A T 9: 106,074,082 (GRCm39) I241N probably damaging Het
Psd T C 19: 46,311,834 (GRCm39) Y282C probably damaging Het
Rpl27 T A 11: 101,336,317 (GRCm39) probably benign Het
Scaf1 A G 7: 44,655,357 (GRCm39) probably benign Het
Sec14l2 A T 11: 4,053,380 (GRCm39) probably benign Het
Smchd1 T A 17: 71,667,016 (GRCm39) probably benign Het
Sptb A T 12: 76,652,391 (GRCm39) D1615E probably damaging Het
Stt3a A C 9: 36,663,649 (GRCm39) C198G possibly damaging Het
Tas2r144 T C 6: 42,192,787 (GRCm39) S176P possibly damaging Het
Tlr13 A G X: 105,200,503 (GRCm39) D80G probably benign Het
Tmco4 A G 4: 138,737,920 (GRCm39) probably benign Het
Tnpo2 T A 8: 85,771,109 (GRCm39) C132S possibly damaging Het
Tubgcp3 T C 8: 12,698,733 (GRCm39) D406G probably damaging Het
Vmn2r125 G A 4: 156,703,294 (GRCm39) R224Q probably benign Het
Zfp524 C A 7: 5,020,479 (GRCm39) D2E probably damaging Het
Other mutations in Ifi202b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01551:Ifi202b APN 1 173,798,928 (GRCm39) missense probably benign 0.00
IGL02019:Ifi202b APN 1 173,802,550 (GRCm39) missense possibly damaging 0.95
IGL02466:Ifi202b APN 1 173,799,875 (GRCm39) missense possibly damaging 0.71
IGL02508:Ifi202b APN 1 173,802,338 (GRCm39) missense probably benign 0.18
IGL02567:Ifi202b APN 1 173,791,370 (GRCm39) missense possibly damaging 0.84
R0282:Ifi202b UTSW 1 173,804,926 (GRCm39) missense probably benign 0.00
R1178:Ifi202b UTSW 1 173,799,788 (GRCm39) missense probably benign 0.02
R3414:Ifi202b UTSW 1 173,791,479 (GRCm39) missense probably benign 0.19
R5739:Ifi202b UTSW 1 173,798,918 (GRCm39) critical splice donor site probably null
R5944:Ifi202b UTSW 1 173,791,365 (GRCm39) missense probably benign 0.00
R6805:Ifi202b UTSW 1 173,802,555 (GRCm39) missense probably damaging 1.00
R7019:Ifi202b UTSW 1 173,791,524 (GRCm39) missense probably benign 0.00
R7291:Ifi202b UTSW 1 173,802,381 (GRCm39) missense probably benign 0.02
R7555:Ifi202b UTSW 1 173,799,787 (GRCm39) missense probably damaging 0.99
R7825:Ifi202b UTSW 1 173,802,616 (GRCm39) missense probably damaging 1.00
R8151:Ifi202b UTSW 1 173,804,923 (GRCm39) missense probably benign 0.00
R8379:Ifi202b UTSW 1 173,802,298 (GRCm39) critical splice donor site probably null
R8887:Ifi202b UTSW 1 173,802,480 (GRCm39) missense probably damaging 1.00
R9177:Ifi202b UTSW 1 173,804,949 (GRCm39) start codon destroyed probably null 0.01
R9642:Ifi202b UTSW 1 173,799,850 (GRCm39) nonsense probably null
Posted On 2015-04-16