Incidental Mutation 'R2257:Iqca1l'
ID 243435
Institutional Source Beutler Lab
Gene Symbol Iqca1l
Ensembl Gene ENSMUSG00000038199
Gene Name IQ motif containing with AAA domain 1 like
Synonyms 4931409K22Rik
MMRRC Submission 040257-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.173) question?
Stock # R2257 (G1)
Quality Score 225
Status Validated
Chromosome 5
Chromosomal Location 24748432-24760467 bp(-) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) C to T at 24757038 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000142624 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000088302] [ENSMUST00000198887] [ENSMUST00000200634]
AlphaFold A6H690
Predicted Effect probably benign
Transcript: ENSMUST00000088302
SMART Domains Protein: ENSMUSP00000085642
Gene: ENSMUSG00000038199

DomainStartEndE-ValueType
low complexity region 46 54 N/A INTRINSIC
low complexity region 70 77 N/A INTRINSIC
low complexity region 184 198 N/A INTRINSIC
IQ 205 227 7.58e-2 SMART
coiled coil region 335 382 N/A INTRINSIC
coiled coil region 429 450 N/A INTRINSIC
low complexity region 467 484 N/A INTRINSIC
Pfam:AAA 568 700 1.6e-14 PFAM
low complexity region 819 825 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000198709
Predicted Effect probably benign
Transcript: ENSMUST00000198887
SMART Domains Protein: ENSMUSP00000142918
Gene: ENSMUSG00000038199

DomainStartEndE-ValueType
low complexity region 46 54 N/A INTRINSIC
low complexity region 70 77 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000199185
Predicted Effect probably benign
Transcript: ENSMUST00000200634
SMART Domains Protein: ENSMUSP00000142624
Gene: ENSMUSG00000038199

DomainStartEndE-ValueType
low complexity region 46 54 N/A INTRINSIC
low complexity region 70 77 N/A INTRINSIC
low complexity region 184 198 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.2%
Validation Efficiency 96% (70/73)
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930567H17Rik A T X: 69,438,012 (GRCm39) W94R probably damaging Het
Abcc3 C T 11: 94,254,420 (GRCm39) V693M probably damaging Het
Acp7 A C 7: 28,313,838 (GRCm39) W399G probably damaging Het
Ap1s1 T C 5: 137,070,633 (GRCm39) Y94C possibly damaging Het
Arhgap32 T C 9: 32,158,793 (GRCm39) I186T probably damaging Het
Atg4a A G X: 139,890,984 (GRCm39) I91V probably benign Het
Atp7b T G 8: 22,488,282 (GRCm39) T1102P probably damaging Het
Cabs1 T C 5: 88,128,074 (GRCm39) S242P probably damaging Het
Cass4 T C 2: 172,269,390 (GRCm39) F493L probably damaging Het
Cass4 C T 2: 172,274,478 (GRCm39) P753L probably damaging Het
Cdk14 T A 5: 4,938,924 (GRCm39) M433L probably benign Het
Cep162 C A 9: 87,088,967 (GRCm39) D972Y probably damaging Het
Cfap100 C G 6: 90,390,802 (GRCm39) R184P possibly damaging Het
Cimip3 AC A 17: 47,744,348 (GRCm39) probably benign Het
Clasrp A G 7: 19,320,510 (GRCm39) probably benign Het
Copb1 T A 7: 113,853,110 (GRCm39) D29V possibly damaging Het
Cyp2b9 G A 7: 25,873,030 (GRCm39) probably null Het
Dhx36 C T 3: 62,385,064 (GRCm39) G683S probably damaging Het
Dnaaf11 T A 15: 66,309,436 (GRCm39) probably benign Het
Dnah10 T A 5: 124,838,301 (GRCm39) I1110N probably damaging Het
Dnajc3 C G 14: 119,210,114 (GRCm39) P322A probably benign Het
Eml4 A G 17: 83,785,189 (GRCm39) T785A probably damaging Het
Fam228a T C 12: 4,787,775 (GRCm39) probably benign Het
Fam83e A T 7: 45,378,193 (GRCm39) K406* probably null Het
Fam83e A T 7: 45,378,194 (GRCm39) K406M possibly damaging Het
Fam90a1a T A 8: 22,453,533 (GRCm39) L296Q possibly damaging Het
Fat1 A G 8: 45,403,408 (GRCm39) Y53C probably damaging Het
Fcrl2 T C 3: 87,166,928 (GRCm39) I22V probably damaging Het
Fryl T A 5: 73,230,187 (GRCm39) N1657Y possibly damaging Het
Greb1l A G 18: 10,503,307 (GRCm39) M453V possibly damaging Het
Grm8 A T 6: 27,760,224 (GRCm39) C369S probably damaging Het
Hdc G A 2: 126,458,000 (GRCm39) probably null Het
Hsf3 A T X: 95,363,928 (GRCm39) L191* probably null Het
Kif4 A T X: 99,769,737 (GRCm39) N1126Y probably benign Het
Lat2 T C 5: 134,631,481 (GRCm39) D191G probably damaging Het
Lipt2 C T 7: 99,808,601 (GRCm39) T38I probably benign Het
Lmo7 T C 14: 102,137,566 (GRCm39) L634P probably damaging Het
Magea2 A T X: 153,810,855 (GRCm39) L243Q probably damaging Het
Mctp2 A G 7: 71,835,568 (GRCm39) L543P probably damaging Het
Mgat4a T C 1: 37,529,394 (GRCm39) N24D probably benign Het
Mical3 A T 6: 121,010,696 (GRCm39) S429T possibly damaging Het
Mrps35 A G 6: 146,972,125 (GRCm39) E256G possibly damaging Het
Mybbp1a T A 11: 72,337,021 (GRCm39) S586T probably benign Het
Myo1e G A 9: 70,285,655 (GRCm39) probably null Het
Nob1 A G 8: 108,143,729 (GRCm39) probably benign Het
Nom1 T A 5: 29,642,750 (GRCm39) V417D probably damaging Het
Nphs1 A T 7: 30,167,417 (GRCm39) I782F possibly damaging Het
Numa1 A G 7: 101,649,998 (GRCm39) E1243G probably damaging Het
Or52e7 A G 7: 104,685,026 (GRCm39) Y207C probably benign Het
Or7g27 A G 9: 19,249,789 (GRCm39) E11G probably benign Het
Padi4 G A 4: 140,487,251 (GRCm39) T217I possibly damaging Het
Pias3 C T 3: 96,606,962 (GRCm39) T75I probably benign Het
Ppp1r37 G T 7: 19,295,943 (GRCm39) probably benign Het
Prrc2a G A 17: 35,380,044 (GRCm39) P185L unknown Het
Prss57 C T 10: 79,623,204 (GRCm39) C81Y probably damaging Het
Psen1 C T 12: 83,761,594 (GRCm39) S132L probably damaging Het
Ranbp6 A G 19: 29,788,949 (GRCm39) S468P possibly damaging Het
Sla2 G A 2: 156,717,862 (GRCm39) R137C probably damaging Het
Slc2a9 T C 5: 38,610,542 (GRCm39) T86A probably damaging Het
Slco1a6 A T 6: 142,036,742 (GRCm39) M555K probably benign Het
Thoc1 C A 18: 9,993,466 (GRCm39) D608E possibly damaging Het
Tmem121b A T 6: 120,469,030 (GRCm39) Y562* probably null Het
Tmem121b A G 6: 120,469,032 (GRCm39) Y562H probably damaging Het
Tmprss7 A T 16: 45,506,696 (GRCm39) M122K possibly damaging Het
Tmub1 C A 5: 24,651,922 (GRCm39) G14V possibly damaging Het
Uap1 A T 1: 169,986,312 (GRCm39) probably benign Het
Ugdh A T 5: 65,574,458 (GRCm39) probably benign Het
Vmn2r59 A T 7: 41,661,669 (GRCm39) C715* probably null Het
Vps13a G A 19: 16,659,538 (GRCm39) T1663I possibly damaging Het
Vps13c A C 9: 67,860,228 (GRCm39) I2815L possibly damaging Het
Zc3h3 G T 15: 75,711,415 (GRCm39) Q349K possibly damaging Het
Other mutations in Iqca1l
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01383:Iqca1l APN 5 24,753,292 (GRCm39) missense probably benign 0.03
IGL02110:Iqca1l APN 5 24,753,082 (GRCm39) splice site probably benign
R0329:Iqca1l UTSW 5 24,750,783 (GRCm39) splice site probably null
R0492:Iqca1l UTSW 5 24,759,626 (GRCm39) missense probably damaging 1.00
R0585:Iqca1l UTSW 5 24,755,721 (GRCm39) missense probably benign
R0656:Iqca1l UTSW 5 24,754,760 (GRCm39) missense possibly damaging 0.67
R0894:Iqca1l UTSW 5 24,755,731 (GRCm39) splice site probably null
R1546:Iqca1l UTSW 5 24,760,426 (GRCm39) splice site probably null
R1642:Iqca1l UTSW 5 24,757,686 (GRCm39) missense probably damaging 1.00
R1998:Iqca1l UTSW 5 24,750,004 (GRCm39) missense probably benign 0.01
R2090:Iqca1l UTSW 5 24,755,674 (GRCm39) missense probably benign 0.15
R2186:Iqca1l UTSW 5 24,759,524 (GRCm39) missense probably damaging 1.00
R2237:Iqca1l UTSW 5 24,753,292 (GRCm39) missense probably benign 0.03
R2256:Iqca1l UTSW 5 24,757,038 (GRCm39) utr 3 prime probably benign
R3078:Iqca1l UTSW 5 24,751,664 (GRCm39) missense probably benign
R3522:Iqca1l UTSW 5 24,754,624 (GRCm39) critical splice donor site probably null
R3910:Iqca1l UTSW 5 24,750,440 (GRCm39) splice site probably benign
R3911:Iqca1l UTSW 5 24,750,440 (GRCm39) splice site probably benign
R4333:Iqca1l UTSW 5 24,749,368 (GRCm39) missense probably damaging 1.00
R4335:Iqca1l UTSW 5 24,749,368 (GRCm39) missense probably damaging 1.00
R4500:Iqca1l UTSW 5 24,753,275 (GRCm39) missense possibly damaging 0.85
R4761:Iqca1l UTSW 5 24,756,981 (GRCm39) missense probably benign
R4773:Iqca1l UTSW 5 24,755,596 (GRCm39) critical splice donor site probably null
R4880:Iqca1l UTSW 5 24,754,750 (GRCm39) missense probably benign
R5614:Iqca1l UTSW 5 24,755,140 (GRCm39) missense probably benign 0.03
R5839:Iqca1l UTSW 5 24,757,024 (GRCm39) missense probably damaging 0.98
R5847:Iqca1l UTSW 5 24,749,164 (GRCm39) missense probably benign 0.16
R7061:Iqca1l UTSW 5 24,750,063 (GRCm39) missense probably benign 0.00
R7131:Iqca1l UTSW 5 24,753,954 (GRCm39) missense possibly damaging 0.81
R7156:Iqca1l UTSW 5 24,757,648 (GRCm39) missense probably benign 0.05
R7248:Iqca1l UTSW 5 24,749,269 (GRCm39) missense probably benign 0.00
R7480:Iqca1l UTSW 5 24,751,904 (GRCm39) missense probably damaging 1.00
R7693:Iqca1l UTSW 5 24,751,626 (GRCm39) missense probably benign 0.01
R7782:Iqca1l UTSW 5 24,749,224 (GRCm39) missense probably damaging 0.98
R7814:Iqca1l UTSW 5 24,750,420 (GRCm39) missense possibly damaging 0.95
R7898:Iqca1l UTSW 5 24,758,643 (GRCm39) missense probably damaging 1.00
R8024:Iqca1l UTSW 5 24,755,634 (GRCm39) missense possibly damaging 0.70
R8172:Iqca1l UTSW 5 24,748,608 (GRCm39) missense probably benign
R8281:Iqca1l UTSW 5 24,754,008 (GRCm39) missense probably benign 0.02
R8511:Iqca1l UTSW 5 24,750,906 (GRCm39) missense possibly damaging 0.95
R8888:Iqca1l UTSW 5 24,755,628 (GRCm39) missense probably benign 0.20
R8895:Iqca1l UTSW 5 24,755,628 (GRCm39) missense probably benign 0.20
R9246:Iqca1l UTSW 5 24,753,969 (GRCm39) missense probably benign 0.22
R9450:Iqca1l UTSW 5 24,754,447 (GRCm39) missense probably benign 0.13
X0063:Iqca1l UTSW 5 24,754,763 (GRCm39) splice site probably null
Z1177:Iqca1l UTSW 5 24,755,793 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- AAACCCAGTGAGTTCCCTGTC -3'
(R):5'- GCCCAGTTTCTTAAGGTCAAAAC -3'

Sequencing Primer
(F):5'- AACCCAGTGAGTTCCCTGTCTTTATG -3'
(R):5'- AAGACCACTGGCTGTTCTTG -3'
Posted On 2014-10-16