Incidental Mutation 'IGL00906:Ifi204'
ID 26612
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ifi204
Ensembl Gene ENSMUSG00000073489
Gene Name interferon activated gene 204
Synonyms p204
Accession Numbers
Essential gene? Probably non essential (E-score: 0.172) question?
Stock # IGL00906
Quality Score
Status
Chromosome 1
Chromosomal Location 173574859-173594509 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 173587197 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000106845 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000111214]
AlphaFold P0DOV2
Predicted Effect probably benign
Transcript: ENSMUST00000111214
SMART Domains Protein: ENSMUSP00000106845
Gene: ENSMUSG00000073489

DomainStartEndE-ValueType
PYRIN 6 84 8.33e-14 SMART
low complexity region 120 154 N/A INTRINSIC
low complexity region 190 206 N/A INTRINSIC
Pfam:HIN 225 393 6.2e-78 PFAM
Pfam:HIN 429 595 9.8e-78 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000192414
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aacs A G 5: 125,580,338 (GRCm39) E221G probably benign Het
Alb A G 5: 90,619,932 (GRCm39) N453S probably benign Het
Bckdha C T 7: 25,332,767 (GRCm39) V183M probably benign Het
Brpf3 A G 17: 29,055,674 (GRCm39) probably benign Het
Ccdc163 T C 4: 116,567,487 (GRCm39) probably null Het
Ccdc178 A T 18: 22,268,225 (GRCm39) C87* probably null Het
Cfhr4 A T 1: 139,659,312 (GRCm39) V739E probably damaging Het
Clca4a A G 3: 144,660,700 (GRCm39) V708A probably damaging Het
Cyfip2 A G 11: 46,091,512 (GRCm39) V1136A possibly damaging Het
Dnah11 A C 12: 117,874,937 (GRCm39) L3976R probably damaging Het
Erich1 A G 8: 14,083,770 (GRCm39) probably benign Het
Fam228a A T 12: 4,782,773 (GRCm39) Y107N possibly damaging Het
Iars2 A T 1: 185,028,600 (GRCm39) probably benign Het
Ifih1 A T 2: 62,476,168 (GRCm39) I36N probably benign Het
Jak1 C T 4: 101,011,826 (GRCm39) G1092D probably damaging Het
Kir3dl2 G A X: 135,357,097 (GRCm39) P122S probably damaging Het
Nacc2 T C 2: 25,951,678 (GRCm39) T386A probably damaging Het
Nrf1 C T 6: 30,098,477 (GRCm39) T135M probably damaging Het
Or4k15 A G 14: 50,364,214 (GRCm39) Y60C probably damaging Het
Or51i2 G A 7: 103,689,051 (GRCm39) G16D probably damaging Het
Pcca A C 14: 122,927,545 (GRCm39) D436A probably benign Het
Pcdhb11 A T 18: 37,555,174 (GRCm39) Q168L possibly damaging Het
Pdgfra A G 5: 75,340,834 (GRCm39) I598V probably benign Het
Pla2g6 C T 15: 79,171,947 (GRCm39) V637I probably damaging Het
Plac1 A C X: 52,159,593 (GRCm39) V39G probably damaging Het
Pparg A G 6: 115,416,822 (GRCm39) E5G probably damaging Het
Ppp1r9a A G 6: 5,157,023 (GRCm39) D967G possibly damaging Het
Rel T C 11: 23,694,266 (GRCm39) T322A probably benign Het
Sgk3 A G 1: 9,947,470 (GRCm39) T137A probably benign Het
Sgpp2 A G 1: 78,367,184 (GRCm39) R106G probably benign Het
Slc27a5 T A 7: 12,724,984 (GRCm39) M459L probably benign Het
Snx21 T C 2: 164,628,140 (GRCm39) L52P probably damaging Het
Srarp G A 4: 141,160,584 (GRCm39) T83M probably benign Het
Sstr2 A G 11: 113,515,821 (GRCm39) R247G probably benign Het
Tnpo3 G A 6: 29,589,047 (GRCm39) S101L probably damaging Het
Zan A G 5: 137,387,622 (GRCm39) I4863T unknown Het
Other mutations in Ifi204
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01922:Ifi204 APN 1 173,589,288 (GRCm39) missense possibly damaging 0.51
IGL02296:Ifi204 APN 1 173,576,880 (GRCm39) missense possibly damaging 0.93
IGL02419:Ifi204 APN 1 173,576,946 (GRCm39) missense possibly damaging 0.71
IGL02505:Ifi204 APN 1 173,583,220 (GRCm39) missense probably benign 0.04
R0938:Ifi204 UTSW 1 173,579,311 (GRCm39) missense possibly damaging 0.85
R1363:Ifi204 UTSW 1 173,576,862 (GRCm39) missense probably benign 0.00
R1834:Ifi204 UTSW 1 173,575,172 (GRCm39) missense unknown
R2031:Ifi204 UTSW 1 173,580,343 (GRCm39) missense probably damaging 1.00
R2254:Ifi204 UTSW 1 173,589,296 (GRCm39) missense possibly damaging 0.95
R2379:Ifi204 UTSW 1 173,583,559 (GRCm39) nonsense probably null
R2408:Ifi204 UTSW 1 173,583,198 (GRCm39) missense possibly damaging 0.80
R3011:Ifi204 UTSW 1 173,579,217 (GRCm39) missense probably benign 0.01
R3617:Ifi204 UTSW 1 173,583,283 (GRCm39) missense possibly damaging 0.51
R3894:Ifi204 UTSW 1 173,576,774 (GRCm39) missense possibly damaging 0.86
R3916:Ifi204 UTSW 1 173,583,341 (GRCm39) missense possibly damaging 0.95
R4656:Ifi204 UTSW 1 173,587,927 (GRCm39) intron probably benign
R4657:Ifi204 UTSW 1 173,587,927 (GRCm39) intron probably benign
R4694:Ifi204 UTSW 1 173,576,825 (GRCm39) missense probably damaging 0.99
R4703:Ifi204 UTSW 1 173,587,927 (GRCm39) intron probably benign
R4704:Ifi204 UTSW 1 173,587,927 (GRCm39) intron probably benign
R4894:Ifi204 UTSW 1 173,587,808 (GRCm39) missense probably damaging 0.98
R4947:Ifi204 UTSW 1 173,583,316 (GRCm39) missense probably damaging 0.98
R5023:Ifi204 UTSW 1 173,579,306 (GRCm39) missense possibly damaging 0.93
R5036:Ifi204 UTSW 1 173,580,311 (GRCm39) missense possibly damaging 0.79
R5119:Ifi204 UTSW 1 173,583,234 (GRCm39) missense probably damaging 1.00
R5194:Ifi204 UTSW 1 173,576,910 (GRCm39) missense possibly damaging 0.86
R5762:Ifi204 UTSW 1 173,580,325 (GRCm39) missense probably damaging 0.98
R6063:Ifi204 UTSW 1 173,579,223 (GRCm39) missense probably benign 0.03
R6808:Ifi204 UTSW 1 173,589,269 (GRCm39) missense probably benign 0.27
R7311:Ifi204 UTSW 1 173,587,134 (GRCm39) missense probably benign 0.26
R7338:Ifi204 UTSW 1 173,587,703 (GRCm39) missense possibly damaging 0.67
R7430:Ifi204 UTSW 1 173,583,247 (GRCm39) missense probably benign 0.43
R7528:Ifi204 UTSW 1 173,579,406 (GRCm39) missense probably benign 0.06
R7985:Ifi204 UTSW 1 173,587,772 (GRCm39) missense possibly damaging 0.50
R8021:Ifi204 UTSW 1 173,586,919 (GRCm39) intron probably benign
R8137:Ifi204 UTSW 1 173,589,188 (GRCm39) missense possibly damaging 0.65
R8141:Ifi204 UTSW 1 173,583,189 (GRCm39) missense possibly damaging 0.81
R8191:Ifi204 UTSW 1 173,579,226 (GRCm39) missense possibly damaging 0.71
R8487:Ifi204 UTSW 1 173,587,839 (GRCm39) missense probably damaging 0.99
R9075:Ifi204 UTSW 1 173,589,282 (GRCm39) missense possibly damaging 0.95
R9124:Ifi204 UTSW 1 173,579,193 (GRCm39) critical splice donor site probably null
R9311:Ifi204 UTSW 1 173,589,215 (GRCm39) missense possibly damaging 0.45
R9498:Ifi204 UTSW 1 173,583,537 (GRCm39) missense possibly damaging 0.81
R9712:Ifi204 UTSW 1 173,576,924 (GRCm39) missense probably damaging 0.99
Z1176:Ifi204 UTSW 1 173,579,194 (GRCm39) missense probably null 0.00
Posted On 2013-04-17