Incidental Mutation 'R5844:Ifi205'
ID 450572
Institutional Source Beutler Lab
Gene Symbol Ifi205
Ensembl Gene ENSMUSG00000054203
Gene Name interferon activated gene 205
Synonyms D3
MMRRC Submission 044062-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.074) question?
Stock # R5844 (G1)
Quality Score 225
Status Validated
Chromosome 1
Chromosomal Location 173839564-173859376 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to C at 173854258 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000062409 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059226]
AlphaFold Q8CGE8
Predicted Effect probably null
Transcript: ENSMUST00000059226
SMART Domains Protein: ENSMUSP00000062409
Gene: ENSMUSG00000054203

DomainStartEndE-ValueType
PYRIN 6 84 9.42e-13 SMART
low complexity region 102 112 N/A INTRINSIC
low complexity region 121 134 N/A INTRINSIC
low complexity region 168 185 N/A INTRINSIC
Pfam:HIN 204 372 2e-76 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000192166
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.5%
  • 20x: 95.9%
Validation Efficiency 98% (55/56)
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930407I10Rik A T 15: 81,950,065 (GRCm39) M1321L probably benign Het
Adra1a C T 14: 66,965,183 (GRCm39) T391I probably benign Het
Atf7ip C A 6: 136,583,812 (GRCm39) A1281D probably damaging Het
BC005624 T C 2: 30,866,023 (GRCm39) N141S probably benign Het
Catsperg2 A T 7: 29,397,257 (GRCm39) L1082Q possibly damaging Het
Cavin2 C T 1: 51,328,998 (GRCm39) R152C probably damaging Het
Ccdc33 C T 9: 57,940,489 (GRCm39) probably benign Het
Cfap43 T C 19: 47,784,135 (GRCm39) D466G probably benign Het
Cfap46 C A 7: 139,230,858 (GRCm39) M923I probably damaging Het
Chd1l T A 3: 97,479,883 (GRCm39) K621N probably benign Het
Cnksr1 A G 4: 133,955,575 (GRCm39) probably benign Het
Cym T C 3: 107,127,080 (GRCm39) H25R probably benign Het
Dagla T A 19: 10,248,489 (GRCm39) D57V probably damaging Het
Dnah3 TTCCTC TTC 7: 119,550,244 (GRCm39) probably benign Het
Dse T A 10: 34,029,038 (GRCm39) D684V probably damaging Het
Eml2 G A 7: 18,935,088 (GRCm39) V432I probably damaging Het
Fbxo10 A T 4: 45,058,760 (GRCm39) S326T probably benign Het
Galntl5 G T 5: 25,391,091 (GRCm39) probably benign Het
Grm5 A G 7: 87,453,232 (GRCm39) R290G possibly damaging Het
Gtpbp3 A G 8: 71,945,199 (GRCm39) T425A probably benign Het
Hepacam2 A G 6: 3,476,073 (GRCm39) I284T probably damaging Het
Irs3 T C 5: 137,642,548 (GRCm39) T297A probably benign Het
Kmt2d G A 15: 98,749,990 (GRCm39) probably benign Het
Map4k4 T A 1: 40,039,036 (GRCm39) probably benign Het
Mfsd6 T C 1: 52,697,542 (GRCm39) S782G probably benign Het
Mis18a G A 16: 90,523,969 (GRCm39) silent Het
Mtpn C T 6: 35,489,225 (GRCm39) D100N probably benign Het
Myom2 G A 8: 15,181,182 (GRCm39) probably null Het
Ntaq1 A G 15: 58,017,056 (GRCm39) N157S probably benign Het
Or13a1 A T 6: 116,470,900 (GRCm39) E110V probably damaging Het
Or5g25 A G 2: 85,478,239 (GRCm39) V142A probably benign Het
Pde3b C T 7: 114,108,106 (GRCm39) T568I probably benign Het
Pip4p1 T C 14: 51,166,499 (GRCm39) T160A probably benign Het
Pkhd1 G T 1: 20,451,685 (GRCm39) D2203E probably benign Het
Ppp1r36 A G 12: 76,473,566 (GRCm39) K66E possibly damaging Het
Rfc1 C A 5: 65,451,130 (GRCm39) M319I probably benign Het
Rnd2 C T 11: 101,359,825 (GRCm39) L57F probably damaging Het
Runx1t1 T C 4: 13,881,068 (GRCm39) V456A probably damaging Het
Rxfp2 A G 5: 149,966,589 (GRCm39) K109R probably benign Het
Sgo2a T G 1: 58,055,556 (GRCm39) V580G probably damaging Het
Skint9 T C 4: 112,271,080 (GRCm39) Q110R probably benign Het
Slc38a9 A G 13: 112,868,035 (GRCm39) Y507C probably damaging Het
Smarca4 T A 9: 21,589,238 (GRCm39) probably benign Het
Tmem88 C G 11: 69,288,504 (GRCm39) Q138H probably benign Het
Tns2 C T 15: 102,017,369 (GRCm39) R281C probably damaging Het
Tns3 A C 11: 8,384,580 (GRCm39) F1413V probably damaging Het
Trpm8 T C 1: 88,312,433 (GRCm39) *1105Q probably null Het
Zfp853 C T 5: 143,274,424 (GRCm39) V399M unknown Het
Zim1 T C 7: 6,681,115 (GRCm39) R183G probably benign Het
Zmiz1 T C 14: 25,657,354 (GRCm39) S871P probably damaging Het
Other mutations in Ifi205
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00990:Ifi205 APN 1 173,854,899 (GRCm39) splice site probably benign
IGL02419:Ifi205 APN 1 173,845,180 (GRCm39) missense probably damaging 0.99
IGL02476:Ifi205 APN 1 173,842,627 (GRCm39) missense probably damaging 1.00
IGL03128:Ifi205 APN 1 173,842,652 (GRCm39) missense probably damaging 0.99
IGL03154:Ifi205 APN 1 173,845,232 (GRCm39) splice site probably benign
R0211:Ifi205 UTSW 1 173,855,994 (GRCm39) missense probably benign
R1932:Ifi205 UTSW 1 173,855,980 (GRCm39) missense possibly damaging 0.47
R2397:Ifi205 UTSW 1 173,845,141 (GRCm39) missense possibly damaging 0.64
R3115:Ifi205 UTSW 1 173,855,901 (GRCm39) missense possibly damaging 0.95
R4534:Ifi205 UTSW 1 173,845,207 (GRCm39) missense probably benign 0.16
R4544:Ifi205 UTSW 1 173,854,139 (GRCm39) missense possibly damaging 0.96
R4715:Ifi205 UTSW 1 173,855,887 (GRCm39) missense possibly damaging 0.51
R4977:Ifi205 UTSW 1 173,842,574 (GRCm39) missense probably benign 0.07
R6061:Ifi205 UTSW 1 173,854,830 (GRCm39) missense possibly damaging 0.91
R6510:Ifi205 UTSW 1 173,845,131 (GRCm39) missense probably damaging 1.00
R7032:Ifi205 UTSW 1 173,855,916 (GRCm39) missense possibly damaging 0.80
R7196:Ifi205 UTSW 1 173,854,109 (GRCm39) missense probably damaging 0.96
R7244:Ifi205 UTSW 1 173,845,210 (GRCm39) nonsense probably null
R7419:Ifi205 UTSW 1 173,855,874 (GRCm39) missense possibly damaging 0.71
R7431:Ifi205 UTSW 1 173,855,943 (GRCm39) missense probably benign
R7660:Ifi205 UTSW 1 173,855,814 (GRCm39) missense probably benign 0.27
R7787:Ifi205 UTSW 1 173,842,644 (GRCm39) missense probably damaging 1.00
R7787:Ifi205 UTSW 1 173,842,640 (GRCm39) missense probably damaging 1.00
R9069:Ifi205 UTSW 1 173,855,841 (GRCm39) missense probably benign
R9163:Ifi205 UTSW 1 173,844,988 (GRCm39) missense possibly damaging 0.88
R9348:Ifi205 UTSW 1 173,844,997 (GRCm39) missense probably benign 0.24
R9376:Ifi205 UTSW 1 173,854,221 (GRCm39) missense probably benign
R9477:Ifi205 UTSW 1 173,854,155 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- GAAAGCTTGTACCTTAGCCGAAG -3'
(R):5'- CAGGTAGAACGATGGTTGTTGC -3'

Sequencing Primer
(F):5'- CGAAGGAATGTTAGATGAAGCC -3'
(R):5'- GAACGATGGTTGTTGCATATTTACAC -3'
Posted On 2016-12-20