Incidental Mutation 'IGL02954:Gm17334'
ID 365050
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm17334
Ensembl Gene ENSMUSG00000091191
Gene Name predicted gene, 17334
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.328) question?
Stock # IGL02954
Quality Score
Status
Chromosome 11
Chromosomal Location 53660878-53664021 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) A to G at 53663654 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000118795 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000019043] [ENSMUST00000108920] [ENSMUST00000108922] [ENSMUST00000123376] [ENSMUST00000133291] [ENSMUST00000138913] [ENSMUST00000170390] [ENSMUST00000140866] [ENSMUST00000142221]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000019043
SMART Domains Protein: ENSMUSP00000019043
Gene: ENSMUSG00000018899

DomainStartEndE-ValueType
IRF 1 114 6.75e-62 SMART
low complexity region 120 138 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000108920
SMART Domains Protein: ENSMUSP00000104548
Gene: ENSMUSG00000018899

DomainStartEndE-ValueType
IRF 1 114 6.75e-62 SMART
low complexity region 120 138 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000108922
SMART Domains Protein: ENSMUSP00000104550
Gene: ENSMUSG00000018899

DomainStartEndE-ValueType
IRF 1 114 6.75e-62 SMART
low complexity region 120 138 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000123376
SMART Domains Protein: ENSMUSP00000122101
Gene: ENSMUSG00000018899

DomainStartEndE-ValueType
IRF 1 114 6.75e-62 SMART
low complexity region 120 138 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000128336
Predicted Effect probably benign
Transcript: ENSMUST00000133291
SMART Domains Protein: ENSMUSP00000116656
Gene: ENSMUSG00000018899

DomainStartEndE-ValueType
IRF 1 114 6.75e-62 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000138913
SMART Domains Protein: ENSMUSP00000118314
Gene: ENSMUSG00000018899

DomainStartEndE-ValueType
IRF 1 62 2.41e-8 SMART
Predicted Effect unknown
Transcript: ENSMUST00000170390
AA Change: V69A
Predicted Effect probably benign
Transcript: ENSMUST00000140866
SMART Domains Protein: ENSMUSP00000114315
Gene: ENSMUSG00000018899

DomainStartEndE-ValueType
IRF 1 114 6.75e-62 SMART
low complexity region 120 138 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153054
Predicted Effect probably benign
Transcript: ENSMUST00000142221
SMART Domains Protein: ENSMUSP00000118795
Gene: ENSMUSG00000018899

DomainStartEndE-ValueType
Pfam:IRF 5 48 4.8e-11 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb1a G T 5: 8,782,341 (GRCm39) R908L probably benign Het
Abcc9 T C 6: 142,592,007 (GRCm39) N774S probably damaging Het
Alpk2 C T 18: 65,439,207 (GRCm39) V729I probably benign Het
Atf3 T C 1: 190,903,852 (GRCm39) N125D probably damaging Het
Bcat1 C T 6: 144,964,945 (GRCm39) G215D probably damaging Het
Bptf G T 11: 106,945,575 (GRCm39) Q2555K possibly damaging Het
Cthrc1 A G 15: 38,940,389 (GRCm39) probably benign Het
Cyp2c38 A G 19: 39,379,520 (GRCm39) M443T probably damaging Het
D6Wsu163e C T 6: 126,951,441 (GRCm39) probably benign Het
Dgkg T A 16: 22,441,003 (GRCm39) E3D probably benign Het
Dnah8 G T 17: 30,923,809 (GRCm39) R1259L probably benign Het
Dnah9 A G 11: 66,009,793 (GRCm39) L698P probably damaging Het
Ebag9 A C 15: 44,493,601 (GRCm39) H141P probably benign Het
Emilin2 T C 17: 71,563,526 (GRCm39) R840G probably benign Het
Faap100 A T 11: 120,262,957 (GRCm39) H800Q probably damaging Het
Fh1 A T 1: 175,437,301 (GRCm39) I266N probably damaging Het
Fkbp15 A G 4: 62,239,302 (GRCm39) probably benign Het
Gm5773 G T 3: 93,680,358 (GRCm39) W10L probably benign Het
Gng13 T C 17: 25,937,726 (GRCm39) Y18H probably damaging Het
Hivep3 T C 4: 119,990,838 (GRCm39) S2113P probably damaging Het
Ift81 A T 5: 122,748,248 (GRCm39) probably benign Het
Irak3 A C 10: 120,012,147 (GRCm39) L206V probably damaging Het
Kcng4 C T 8: 120,359,792 (GRCm39) A195T probably benign Het
Lrrc40 G A 3: 157,747,302 (GRCm39) probably benign Het
Nars2 T G 7: 96,689,100 (GRCm39) probably null Het
Nol8 T C 13: 49,814,648 (GRCm39) V234A probably benign Het
Or12j4 A T 7: 140,046,353 (GRCm39) K80* probably null Het
Or1o4 T A 17: 37,591,195 (GRCm39) N39Y probably damaging Het
Patz1 A G 11: 3,241,761 (GRCm39) Y383C probably damaging Het
Pdcd5 T C 7: 35,343,089 (GRCm39) Y152C probably damaging Het
Phkg1 A G 5: 129,894,910 (GRCm39) W214R probably damaging Het
Plxna1 A G 6: 89,301,649 (GRCm39) L1459P probably damaging Het
Pspc1 G A 14: 57,009,217 (GRCm39) P206S probably benign Het
St7 A T 6: 17,848,030 (GRCm39) N198I probably damaging Het
Supt3 A G 17: 45,349,015 (GRCm39) D249G probably damaging Het
Taf1c T C 8: 120,327,225 (GRCm39) Y418C probably damaging Het
Tdrd6 A G 17: 43,938,153 (GRCm39) V965A possibly damaging Het
Ugt2b35 A G 5: 87,159,180 (GRCm39) N458S probably benign Het
Vmn1r8 A G 6: 57,013,315 (GRCm39) Y122C probably benign Het
Other mutations in Gm17334
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2074:Gm17334 UTSW 11 53,663,654 (GRCm39) intron probably benign
R6431:Gm17334 UTSW 11 53,663,564 (GRCm39) intron probably benign
R7847:Gm17334 UTSW 11 53,663,564 (GRCm39) intron probably benign
R9571:Gm17334 UTSW 11 53,663,760 (GRCm39) missense unknown
Posted On 2015-12-18