Incidental Mutation 'IGL01819:Iqcf5'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Iqcf5
Ensembl Gene ENSMUSG00000066382
Gene NameIQ motif containing F5
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.056) question?
Stock #IGL01819
Quality Score
Chromosomal Location106514573-106516010 bp(+) (GRCm38)
Type of Mutationmakesense
DNA Base Change (assembly) T to A at 106515990 bp
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]
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
0610010F05Rik A G 11: 23,584,561 S105P probably benign Het
Adora2b A G 11: 62,265,184 N153S possibly damaging Het
Afm C T 5: 90,524,906 T200I probably benign Het
Cyp2c67 T C 19: 39,615,721 D397G probably damaging Het
Dnah9 A G 11: 66,108,126 V1032A probably benign Het
Elovl7 T G 13: 108,274,320 V143G probably damaging Het
Fhl4 T C 10: 85,098,870 K16E probably damaging Het
Golga1 C T 2: 39,034,149 C383Y probably benign Het
Gucy1a2 C T 9: 3,865,409 R628* probably null Het
Hectd4 A G 5: 121,328,418 D2432G possibly damaging Het
Kcnab1 T A 3: 65,319,454 Y185N probably damaging Het
Lars G T 18: 42,202,550 T1167K probably benign Het
Mib2 A T 4: 155,655,258 probably null Het
Mrps2 T C 2: 28,468,336 V46A probably benign Het
Myo18b T C 5: 112,878,050 T45A unknown Het
Myo1e C T 9: 70,343,040 probably benign Het
Olfr1129 A G 2: 87,575,479 I132V probably damaging Het
Olfr1285 T A 2: 111,408,733 V106E probably damaging Het
Osbp2 A T 11: 3,717,127 I8N probably damaging Het
Pcdhb22 A T 18: 37,519,921 N481Y probably damaging Het
Pde3a T C 6: 141,487,537 W765R probably damaging Het
Phf11c T C 14: 59,393,137 T40A probably benign Het
Pih1d2 T A 9: 50,621,877 S268R probably benign Het
Pkd1l2 T C 8: 116,998,174 N2333D probably damaging Het
Prex1 A G 2: 166,621,245 I62T probably damaging Het
Ptcd2 T C 13: 99,326,711 N245S possibly damaging Het
Ripor3 C A 2: 167,980,843 V933F probably damaging Het
Sphk2 A G 7: 45,711,056 probably null Het
Tfcp2 T G 15: 100,504,439 E492D probably benign Het
Ttn C T 2: 76,798,762 V14411I possibly damaging Het
Utp20 T C 10: 88,792,687 Q915R probably damaging Het
Vmn2r45 C A 7: 8,485,557 S158I probably benign Het
Other mutations in Iqcf5
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6352:Iqcf5 UTSW 9 106515730 missense possibly damaging 0.57
R7017:Iqcf5 UTSW 9 106515664 missense possibly damaging 0.90
R7120:Iqcf5 UTSW 9 106515796 missense probably damaging 1.00
R7988:Iqcf5 UTSW 9 106515821 missense possibly damaging 0.84
Posted On2014-02-04