Incidental Mutation 'IGL01819:Iqcf5'
ID154483
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Iqcf5
Ensembl Gene ENSMUSG00000066382
Gene NameIQ motif containing F5
Synonyms1700007L12Rik
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.056) question?
Stock #IGL01819
Quality Score
Status
Chromosome9
Chromosomal Location106514573-106516010 bp(+) (GRCm38)
Type of Mutationmakesense
DNA Base Change (assembly) T to A at 106515990 bp
ZygosityHeterozygous
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

DomainStartEndE-ValueType
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