Incidental Mutation 'IGL02835:Iqcm'
ID 361628
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Iqcm
Ensembl Gene ENSMUSG00000031620
Gene Name IQ motif containing M
Synonyms 1700007B14Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.065) question?
Stock # IGL02835 (G1)
Quality Score
Status
Chromosome 8
Chromosomal Location 76175322-76711131 bp(+) (GRCm39)
Type of Mutation utr 5 prime
DNA Base Change (assembly) T to A at 76281511 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000148495 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034033] [ENSMUST00000121983] [ENSMUST00000212704]
AlphaFold Q149I8
Predicted Effect probably benign
Transcript: ENSMUST00000034033
SMART Domains Protein: ENSMUSP00000034033
Gene: ENSMUSG00000031620

DomainStartEndE-ValueType
IQ 281 303 2.54e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000121983
SMART Domains Protein: ENSMUSP00000112901
Gene: ENSMUSG00000031620

DomainStartEndE-ValueType
IQ 281 303 2.54e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000212704
Coding Region Coverage
  • 1x: 0.0%
  • 3x: 0.0%
  • 10x: 0.0%
  • 20x: 0.0%
Validation Efficiency 98% (57/58)
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700011L22Rik T A 8: 79,937,284 (GRCm39) K208* probably null Het
A530016L24Rik A C 12: 112,461,420 (GRCm39) probably null Het
A830018L16Rik A C 1: 12,042,279 (GRCm39) D433A possibly damaging Het
Abca13 T A 11: 9,401,515 (GRCm39) I3985N probably damaging Het
Abhd17c C T 7: 83,800,731 (GRCm39) D108N probably benign Het
Adam29 C T 8: 56,326,173 (GRCm39) D94N probably damaging Het
Agr2 A G 12: 36,045,903 (GRCm39) D50G probably benign Het
Angptl1 A G 1: 156,686,090 (GRCm39) D392G probably benign Het
Apob A G 12: 8,065,097 (GRCm39) N3989S possibly damaging Het
AU018091 T C 7: 3,218,897 (GRCm39) D12G unknown Het
Cyfip2 A T 11: 46,140,598 (GRCm39) S742T probably benign Het
Dlc1 C T 8: 37,051,055 (GRCm39) S892N probably damaging Het
Dsg1b A G 18: 20,525,071 (GRCm39) N169S possibly damaging Het
Egfem1 T C 3: 29,711,390 (GRCm39) L323P probably damaging Het
Emilin3 G A 2: 160,750,649 (GRCm39) Q320* probably null Het
Fjx1 G A 2: 102,281,092 (GRCm39) A281V possibly damaging Het
Fmn2 T A 1: 174,409,625 (GRCm39) D619E unknown Het
Gm4795 A C 10: 44,882,254 (GRCm39) noncoding transcript Het
Gm5117 T C 8: 32,227,198 (GRCm39) noncoding transcript Het
Gm5250 T C 1: 13,132,418 (GRCm39) noncoding transcript Het
Gtdc1 A T 2: 44,646,324 (GRCm39) Y101* probably null Het
Herc6 T C 6: 57,623,146 (GRCm39) I583T possibly damaging Het
Hyal4 G A 6: 24,765,714 (GRCm39) R356H probably benign Het
Il22ra2 C A 10: 19,502,424 (GRCm39) T81K probably benign Het
Izumo4 G A 10: 80,540,959 (GRCm39) V220I probably benign Het
Kif16b A T 2: 142,554,133 (GRCm39) D899E probably benign Het
Lrp2 A T 2: 69,335,648 (GRCm39) N1358K probably damaging Het
Lrrk2 A G 15: 91,698,863 (GRCm39) probably null Het
Lyst C T 13: 13,835,685 (GRCm39) T1789M possibly damaging Het
Map4k4 A G 1: 40,049,760 (GRCm39) T732A probably damaging Het
Mdh1b A T 1: 63,757,816 (GRCm39) I305N probably damaging Het
Mettl13 A G 1: 162,373,585 (GRCm39) I222T probably damaging Het
Mtcl2 G A 2: 156,883,854 (GRCm39) T363I possibly damaging Het
Muc4 T C 16: 32,584,319 (GRCm39) F2583L probably benign Het
Nbea C T 3: 55,625,290 (GRCm39) R2267Q possibly damaging Het
Ndfip1 T C 18: 38,589,144 (GRCm39) Y178H probably damaging Het
Nin A T 12: 70,103,512 (GRCm39) F243I probably damaging Het
Nlrp10 A T 7: 108,523,869 (GRCm39) I537K possibly damaging Het
Nup155 T C 15: 8,172,614 (GRCm39) Y867H probably damaging Het
Pakap C G 4: 57,883,044 (GRCm39) P837A probably damaging Het
Pik3r4 A C 9: 105,549,905 (GRCm39) I999L probably benign Het
Pitpnm3 G A 11: 71,952,292 (GRCm39) probably benign Het
Pkd1l2 G A 8: 117,792,484 (GRCm39) T436I probably benign Het
Polg2 A T 11: 106,666,266 (GRCm39) V293E probably benign Het
Pramel22 T A 4: 143,380,817 (GRCm39) Y402F probably damaging Het
Prok1 T C 3: 107,144,531 (GRCm39) probably null Het
Ptcd1 T C 5: 145,091,500 (GRCm39) D533G possibly damaging Het
Ptpn13 T C 5: 103,707,891 (GRCm39) V1484A probably damaging Het
Rapgef2 A T 3: 79,000,293 (GRCm39) probably benign Het
Serpinb8 T G 1: 107,530,586 (GRCm39) F121L probably damaging Het
Sh3rf1 T A 8: 61,679,081 (GRCm39) V41E probably damaging Het
Snx13 A G 12: 35,182,126 (GRCm39) N725S possibly damaging Het
Stab1 A T 14: 30,867,981 (GRCm39) probably null Het
Themis A T 10: 28,637,616 (GRCm39) probably benign Het
Trim68 T A 7: 102,327,780 (GRCm39) Y391F probably benign Het
Trmt1 T G 8: 85,423,589 (GRCm39) V327G probably null Het
Vill C T 9: 118,896,513 (GRCm39) T120M probably benign Het
Other mutations in Iqcm
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01895:Iqcm APN 8 76,615,188 (GRCm39) missense probably damaging 1.00
R0056:Iqcm UTSW 8 76,480,014 (GRCm39) missense probably benign
R2146:Iqcm UTSW 8 76,615,241 (GRCm39) missense probably damaging 1.00
R2910:Iqcm UTSW 8 76,441,404 (GRCm39) missense probably benign
R3801:Iqcm UTSW 8 76,396,021 (GRCm39) missense possibly damaging 0.59
R3804:Iqcm UTSW 8 76,396,021 (GRCm39) missense possibly damaging 0.59
R3834:Iqcm UTSW 8 76,304,380 (GRCm39) missense possibly damaging 0.93
R3897:Iqcm UTSW 8 76,480,028 (GRCm39) missense probably damaging 1.00
R4447:Iqcm UTSW 8 76,356,394 (GRCm39) missense probably damaging 0.97
R4448:Iqcm UTSW 8 76,356,394 (GRCm39) missense probably damaging 0.97
R4450:Iqcm UTSW 8 76,356,394 (GRCm39) missense probably damaging 0.97
R4687:Iqcm UTSW 8 76,489,617 (GRCm39) missense probably damaging 1.00
R4810:Iqcm UTSW 8 76,615,281 (GRCm39) missense probably damaging 1.00
R4845:Iqcm UTSW 8 76,472,980 (GRCm39) missense probably damaging 0.99
R4856:Iqcm UTSW 8 76,615,228 (GRCm39) missense possibly damaging 0.95
R4886:Iqcm UTSW 8 76,615,228 (GRCm39) missense possibly damaging 0.95
R5063:Iqcm UTSW 8 76,472,914 (GRCm39) missense probably damaging 1.00
R5460:Iqcm UTSW 8 76,441,417 (GRCm39) missense probably benign
R6403:Iqcm UTSW 8 76,304,624 (GRCm39) critical splice donor site probably null
R6667:Iqcm UTSW 8 76,479,980 (GRCm39) missense probably damaging 1.00
R7187:Iqcm UTSW 8 76,480,044 (GRCm39) missense probably benign 0.22
R7263:Iqcm UTSW 8 76,489,701 (GRCm39) missense probably benign
R7701:Iqcm UTSW 8 76,281,539 (GRCm39) missense probably benign 0.02
R7916:Iqcm UTSW 8 76,304,578 (GRCm39) missense probably benign
R7938:Iqcm UTSW 8 76,304,596 (GRCm39) missense probably benign
R7974:Iqcm UTSW 8 76,281,520 (GRCm39) start codon destroyed probably null 0.66
R8039:Iqcm UTSW 8 76,489,733 (GRCm39) missense probably damaging 1.00
R8311:Iqcm UTSW 8 76,480,118 (GRCm39) splice site probably benign
R8703:Iqcm UTSW 8 76,615,271 (GRCm39) missense probably damaging 1.00
R9175:Iqcm UTSW 8 76,710,867 (GRCm39) missense possibly damaging 0.84
R9475:Iqcm UTSW 8 76,480,083 (GRCm39) missense probably damaging 1.00
RF002:Iqcm UTSW 8 76,304,527 (GRCm39) missense probably benign 0.01
X0018:Iqcm UTSW 8 76,710,840 (GRCm39) nonsense probably null
Posted On 2015-12-18