Incidental Mutation 'IGL01819:Iqcf5'
ID 154483
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Iqcf5
Ensembl Gene ENSMUSG00000066382
Gene Name IQ motif containing F5
Synonyms 1700007L12Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.054) question?
Stock # IGL01819
Quality Score
Chromosome 9
Chromosomal Location 106391772-106393202 bp(+) (GRCm39)
Type of Mutation makesense
DNA Base Change (assembly) T to A at 106393189 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Stop codon to Arginine at position 149 (*149R)
Ref Sequence ENSEMBL: ENSMUSP00000082194 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000085113]
AlphaFold Q9DAL7
Predicted Effect probably null
Transcript: ENSMUST00000085113
AA Change: *149R
SMART Domains Protein: ENSMUSP00000082194
Gene: ENSMUSG00000066382
AA Change: *149R

IQ 10 32 8.38e-4 SMART
IQ 66 88 9.85e-1 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000189866
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adora2b A G 11: 62,156,010 (GRCm39) N153S possibly damaging Het
Afm C T 5: 90,672,765 (GRCm39) T200I probably benign Het
Cyp2c67 T C 19: 39,604,165 (GRCm39) D397G probably damaging Het
Dnah9 A G 11: 65,998,952 (GRCm39) V1032A probably benign Het
Elovl7 T G 13: 108,410,854 (GRCm39) V143G probably damaging Het
Fhl4 T C 10: 84,934,734 (GRCm39) K16E probably damaging Het
Golga1 C T 2: 38,924,161 (GRCm39) C383Y probably benign Het
Gucy1a2 C T 9: 3,865,409 (GRCm39) R628* probably null Het
Hectd4 A G 5: 121,466,481 (GRCm39) D2432G possibly damaging Het
Kcnab1 T A 3: 65,226,875 (GRCm39) Y185N probably damaging Het
Lars1 G T 18: 42,335,615 (GRCm39) T1167K probably benign Het
Mib2 A T 4: 155,739,715 (GRCm39) probably null Het
Mrps2 T C 2: 28,358,348 (GRCm39) V46A probably benign Het
Myo18b T C 5: 113,025,916 (GRCm39) T45A unknown Het
Myo1e C T 9: 70,250,322 (GRCm39) probably benign Het
Or10ag59 A G 2: 87,405,823 (GRCm39) I132V probably damaging Het
Or4k39 T A 2: 111,239,078 (GRCm39) V106E probably damaging Het
Osbp2 A T 11: 3,667,127 (GRCm39) I8N probably damaging Het
Pcdhb22 A T 18: 37,652,974 (GRCm39) N481Y probably damaging Het
Pde3a T C 6: 141,433,263 (GRCm39) W765R probably damaging Het
Phf11c T C 14: 59,630,586 (GRCm39) T40A probably benign Het
Pih1d2 T A 9: 50,533,177 (GRCm39) S268R probably benign Het
Pkd1l2 T C 8: 117,724,913 (GRCm39) N2333D probably damaging Het
Prex1 A G 2: 166,463,165 (GRCm39) I62T probably damaging Het
Ptcd2 T C 13: 99,463,219 (GRCm39) N245S possibly damaging Het
Ripor3 C A 2: 167,822,763 (GRCm39) V933F probably damaging Het
Sanbr A G 11: 23,534,561 (GRCm39) S105P probably benign Het
Sphk2 A G 7: 45,360,480 (GRCm39) probably null Het
Tfcp2 T G 15: 100,402,320 (GRCm39) E492D probably benign Het
Ttn C T 2: 76,629,106 (GRCm39) V14411I possibly damaging Het
Utp20 T C 10: 88,628,549 (GRCm39) Q915R probably damaging Het
Vmn2r45 C A 7: 8,488,556 (GRCm39) S158I probably benign Het
Other mutations in Iqcf5
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6352:Iqcf5 UTSW 9 106,392,929 (GRCm39) missense possibly damaging 0.57
R7017:Iqcf5 UTSW 9 106,392,863 (GRCm39) missense possibly damaging 0.90
R7120:Iqcf5 UTSW 9 106,392,995 (GRCm39) missense probably damaging 1.00
R7988:Iqcf5 UTSW 9 106,393,020 (GRCm39) missense possibly damaging 0.84
R9660:Iqcf5 UTSW 9 106,393,168 (GRCm39) missense probably damaging 1.00
R9728:Iqcf5 UTSW 9 106,393,168 (GRCm39) missense probably damaging 1.00
Posted On 2014-02-04