Incidental Mutation 'IGL01329:Iqcf4'
ID 74427
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Iqcf4
Ensembl Gene ENSMUSG00000041009
Gene Name IQ motif containing F4
Synonyms 1700042N06Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.049) question?
Stock # IGL01329
Quality Score
Status
Chromosome 9
Chromosomal Location 106445518-106448166 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 106447832 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Glutamic Acid at position 26 (K26E)
Ref Sequence ENSEMBL: ENSMUSP00000082192 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000085111]
AlphaFold Q6P8Y2
Predicted Effect probably benign
Transcript: ENSMUST00000085111
AA Change: K26E

PolyPhen 2 Score 0.119 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000082192
Gene: ENSMUSG00000041009
AA Change: K26E

DomainStartEndE-ValueType
coiled coil region 14 41 N/A INTRINSIC
IQ 66 88 2.72e-3 SMART
IQ 89 111 2.32e2 SMART
IQ 122 144 9.33e-2 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb4 T C 5: 8,944,166 (GRCm39) probably null Het
Ankib1 A T 5: 3,784,194 (GRCm39) probably benign Het
Birc2 T C 9: 7,860,733 (GRCm39) Y195C probably damaging Het
Cand2 T C 6: 115,759,755 (GRCm39) I142T probably benign Het
Cdh15 T C 8: 123,592,062 (GRCm39) probably benign Het
Ceacam5 G A 7: 17,479,534 (GRCm39) G217D probably damaging Het
Cfap54 T A 10: 92,917,385 (GRCm39) H25L unknown Het
Cfap95 A G 19: 23,630,100 (GRCm39) probably benign Het
Col22a1 A G 15: 71,778,889 (GRCm39) V266A probably benign Het
D3Ertd751e A G 3: 41,703,132 (GRCm39) D69G probably benign Het
Dnah3 T C 7: 119,622,164 (GRCm39) I1518V probably damaging Het
Entpd8 A G 2: 24,974,358 (GRCm39) K381R probably benign Het
Fli1 T A 9: 32,335,397 (GRCm39) K345I probably damaging Het
G6pd2 T C 5: 61,967,281 (GRCm39) V352A probably damaging Het
Gbp11 C T 5: 105,475,482 (GRCm39) probably null Het
Gm11992 A G 11: 9,018,383 (GRCm39) *292W probably null Het
Ifnar2 T A 16: 91,188,599 (GRCm39) probably benign Het
Impg1 T C 9: 80,230,111 (GRCm39) K661R probably benign Het
Inf2 G T 12: 112,578,290 (GRCm39) E651* probably null Het
Ints1 A G 5: 139,753,258 (GRCm39) probably benign Het
Map4k3 A G 17: 80,951,613 (GRCm39) V289A probably benign Het
Mis18bp1 T C 12: 65,205,215 (GRCm39) K319R possibly damaging Het
Nubpl T C 12: 52,352,638 (GRCm39) V291A probably damaging Het
Or4f56 A G 2: 111,703,295 (GRCm39) F302L probably benign Het
Or4k15c C T 14: 50,321,454 (GRCm39) R228H probably benign Het
Or8b57 A G 9: 40,003,324 (GRCm39) S313P possibly damaging Het
Or8k38 T C 2: 86,488,551 (GRCm39) N84D probably benign Het
Otof A G 5: 30,598,723 (GRCm39) S29P probably benign Het
Pcca A G 14: 122,927,545 (GRCm39) D436G possibly damaging Het
Rasef T A 4: 73,645,882 (GRCm39) T496S probably damaging Het
Saa2 A G 7: 46,402,896 (GRCm39) D49G probably benign Het
Scart1 T A 7: 139,804,552 (GRCm39) probably null Het
Scn2a A G 2: 65,547,852 (GRCm39) I1015V probably benign Het
Sim2 T C 16: 93,907,119 (GRCm39) Y154H possibly damaging Het
Spag17 A G 3: 100,002,865 (GRCm39) H1863R probably benign Het
Supt16 C T 14: 52,414,489 (GRCm39) E438K probably benign Het
Svil A G 18: 5,064,501 (GRCm39) E1111G probably benign Het
Trabd2b T C 4: 114,266,322 (GRCm39) V112A probably damaging Het
Vmn1r205 T C 13: 22,776,273 (GRCm39) I276M probably benign Het
Vps13d A T 4: 144,882,776 (GRCm39) I939N possibly damaging Het
Zc3h11a T C 1: 133,553,600 (GRCm39) M515V probably benign Het
Zfp457 T C 13: 67,442,330 (GRCm39) T82A possibly damaging Het
Other mutations in Iqcf4
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0781:Iqcf4 UTSW 9 106,445,860 (GRCm39) missense probably benign 0.06
R1764:Iqcf4 UTSW 9 106,445,893 (GRCm39) missense probably benign 0.12
R4525:Iqcf4 UTSW 9 106,447,827 (GRCm39) missense possibly damaging 0.51
R4703:Iqcf4 UTSW 9 106,445,519 (GRCm39) splice site probably null
R5823:Iqcf4 UTSW 9 106,445,800 (GRCm39) missense probably benign 0.00
R6298:Iqcf4 UTSW 9 106,445,874 (GRCm39) missense probably benign 0.25
R7773:Iqcf4 UTSW 9 106,445,812 (GRCm39) missense probably benign 0.08
R7780:Iqcf4 UTSW 9 106,445,860 (GRCm39) missense possibly damaging 0.93
R7818:Iqcf4 UTSW 9 106,447,738 (GRCm39) nonsense probably null
R8694:Iqcf4 UTSW 9 106,448,111 (GRCm39) start gained probably benign
R9435:Iqcf4 UTSW 9 106,445,652 (GRCm39) missense possibly damaging 0.95
RF003:Iqcf4 UTSW 9 106,447,806 (GRCm39) small insertion probably benign
RF007:Iqcf4 UTSW 9 106,447,808 (GRCm39) small insertion probably benign
RF016:Iqcf4 UTSW 9 106,447,808 (GRCm39) small insertion probably benign
RF028:Iqcf4 UTSW 9 106,447,813 (GRCm39) small insertion probably benign
RF031:Iqcf4 UTSW 9 106,447,814 (GRCm39) small insertion probably benign
RF036:Iqcf4 UTSW 9 106,447,810 (GRCm39) small insertion probably benign
RF041:Iqcf4 UTSW 9 106,447,812 (GRCm39) nonsense probably null
RF042:Iqcf4 UTSW 9 106,447,804 (GRCm39) small insertion probably benign
RF043:Iqcf4 UTSW 9 106,447,812 (GRCm39) small insertion probably benign
RF045:Iqcf4 UTSW 9 106,447,809 (GRCm39) small insertion probably benign
RF046:Iqcf4 UTSW 9 106,447,809 (GRCm39) small insertion probably benign
RF047:Iqcf4 UTSW 9 106,447,811 (GRCm39) small insertion probably benign
RF063:Iqcf4 UTSW 9 106,447,816 (GRCm39) small insertion probably benign
Posted On 2013-10-07