Incidental Mutation 'RF031:Iqcf4'
ID 604373
Institutional Source Beutler Lab
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 # RF031 (G1)
Quality Score 122.467
Status Not validated
Chromosome 9
Chromosomal Location 106445518-106448166 bp(-) (GRCm39)
Type of Mutation small insertion (12 aa in frame mutation)
DNA Base Change (assembly) TTTCCTTTT to TTTCCTTTTCCTTTTCCTTTTCCTTTTCCTTTTCCTCTTCCTTTT at 106447814 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000082192 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000085111]
AlphaFold Q6P8Y2
Predicted Effect probably benign
Transcript: ENSMUST00000085111
SMART Domains Protein: ENSMUSP00000082192
Gene: ENSMUSG00000041009

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
  • 1x: 99.8%
  • 3x: 99.7%
  • 10x: 99.4%
  • 20x: 98.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
AI837181 GCG GCGCCG 19: 5,475,246 (GRCm39) probably benign Het
Blm CTCCTCCTCCTCCTCCTCCTCCTC CTCCTCCTCCTCTTCCTCCTCCTCCTCCTCCTCCTC 7: 80,162,654 (GRCm39) probably benign Het
Blm CCTCCTCCTCC CCTCCTCCTCCTGCTCCTCCTCC 7: 80,162,671 (GRCm39) probably benign Het
Cyb5r4 GGGA GGGATGTGACAGACACACTGCCCATGGA 9: 86,922,498 (GRCm39) probably benign Het
Dcdc2b GCTGC GCTGCCAGGACTGC 4: 129,503,444 (GRCm39) probably benign Het
Dclre1a CTTTGCT C 19: 56,532,564 (GRCm39) probably benign Het
Dctn6 AAATCATGGCTTGCGATCT A 8: 34,572,236 (GRCm39) probably null Het
Elovl5 G T 9: 77,888,755 (GRCm39) probably null Het
Ermn AACT AACTACT 2: 57,938,078 (GRCm39) probably benign Het
Fbrsl1 G GCGTGTGCTGGTC 5: 110,526,017 (GRCm39) probably benign Het
Fgd6 ATT A 10: 93,880,187 (GRCm39) probably null Het
Flywch1 TCACTCACCCACTCCTGGTGT TCACTCACCCACTCCTGGTGTGGGGAGGCTACGCACTCACCCACTCCTGGTGT 17: 23,981,132 (GRCm39) probably null Het
Gab3 TCT TCTGCT X: 74,043,602 (GRCm39) probably benign Het
Gab3 TTC TTCATC X: 74,043,607 (GRCm39) probably benign Het
Gab3 CTT CTTATT X: 74,043,603 (GRCm39) probably null Het
Gm11060 CTGTGTG CTG 2: 104,922,385 (GRCm39) probably null Het
Gm5475 GGTGGAAGGAAAG GG 15: 100,325,029 (GRCm39) probably null Het
Heatr3 TAT TATTAAT 8: 88,883,085 (GRCm39) probably benign Het
Ivl GCTGCTGCTGCTGC G 3: 92,479,625 (GRCm39) probably null Het
Kif12 GGC GGCCTCCACCCGGCGTGC 4: 63,089,662 (GRCm39) probably benign Het
L1td1 AGGAGGAGGAGGAGGAGGAGGAGGGGGAGGAGGAG AGGAGGAGGAG 4: 98,625,026 (GRCm39) probably benign Het
Lca5l CCCTGGCCCCGGCC CCC 16: 95,960,504 (GRCm39) probably null Het
Loricrin ATAGCCG A 3: 91,989,183 (GRCm39) probably benign Het
Mapk7 GGGGCA GGGGCACGGGCA 11: 61,381,060 (GRCm39) probably benign Het
Nf2 AAAAG A 11: 4,779,936 (GRCm39) probably null Het
Nlrp3 GGGTA G 11: 59,449,378 (GRCm39) probably null Het
Nolc1 CAGCAGC CAGCAGCAGGAGCAGC 19: 46,069,810 (GRCm39) probably benign Het
Pdik1l TTTT TTTTGTTTTTGATTT 4: 134,006,685 (GRCm39) probably null Het
Phldb3 CGCCCCCG C 7: 24,325,918 (GRCm39) probably null Het
Setd1a GGTGGTAGT GGTGGTAGTAGTGGTAGT 7: 127,384,483 (GRCm39) probably benign Het
Spmap2l CCCCAGTCCCGCAAGGCCAG CCCCAGTCCCGCAAGGCCAGCGATCCTACCCAGTCCCGCAAGGCCAG 5: 77,164,257 (GRCm39) probably benign Het
Strn CTTACCCCAGTC CTTACCCCAGTCCGTGCTCCCTTACCCCAGTCCGTGATCCATTACCCCAGTC 17: 78,984,706 (GRCm39) probably null Het
Tcof1 TTCCCAGAGATCCCCTTGGC TTCCCAGAGATCCCCTTGGCTGCTGAGATGGGCACTATCCCAGAGATCCCCTTGGC 18: 60,966,637 (GRCm39) probably benign Het
Tcof1 AGC AGCGGC 18: 60,968,817 (GRCm39) probably benign Het
Tedc2 AGGAACCCT AGGAACCCTGGAACCCT 17: 24,435,213 (GRCm39) probably benign Het
Tmem59 T TGTTTGTTG 4: 107,047,729 (GRCm39) probably benign Het
Zfhx3 C CCGCAGCAAA 8: 109,682,730 (GRCm39) probably benign Het
Zfp335 TCGTCGTC TCGTCGTCGTC 2: 164,749,383 (GRCm39) probably benign Het
Other mutations in Iqcf4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01329:Iqcf4 APN 9 106,447,832 (GRCm39) missense probably benign 0.12
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
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
Predicted Primers PCR Primer
(F):5'- TGCATACATTCCATGACCGATC -3'
(R):5'- TGTCTCCAAACATGGGCTGTC -3'

Sequencing Primer
(F):5'- TCCATGACCGATCTATGTTGTAG -3'
(R):5'- CTCCAAACATGGGCTGTCTGTATAG -3'
Posted On 2019-12-04