Incidental Mutation 'R4773:Iqca1l'
ID 367659
Institutional Source Beutler Lab
Gene Symbol Iqca1l
Ensembl Gene ENSMUSG00000038199
Gene Name IQ motif containing with AAA domain 1 like
Synonyms 4931409K22Rik
MMRRC Submission 042411-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.173) question?
Stock # R4773 (G1)
Quality Score 225
Status Validated
Chromosome 5
Chromosomal Location 24748432-24760467 bp(-) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) A to G at 24755596 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000085642 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000088302] [ENSMUST00000198887] [ENSMUST00000200634]
AlphaFold A6H690
Predicted Effect probably null
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
Meta Mutation Damage Score 0.9478 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 94.2%
Validation Efficiency 100% (89/89)
Allele List at MGI
Other mutations in this stock
Total: 82 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9230009I02Rik A G 11: 50,982,089 (GRCm39) noncoding transcript Het
Actl7b T C 4: 56,740,972 (GRCm39) I129V probably benign Het
Adipor2 A G 6: 119,336,047 (GRCm39) L225P probably benign Het
Arhgap25 A G 6: 87,473,053 (GRCm39) F35L probably benign Het
Asah2 A T 19: 32,030,258 (GRCm39) M138K probably damaging Het
Asxl1 T A 2: 153,243,905 (GRCm39) M1486K probably damaging Het
B4galt4 T A 16: 38,572,658 (GRCm39) S114R probably benign Het
Brpf3 T G 17: 29,040,233 (GRCm39) S885A probably benign Het
Cacna1g G T 11: 94,302,298 (GRCm39) H1944N possibly damaging Het
Cby2 T A 14: 75,820,546 (GRCm39) Y393F probably damaging Het
Ccdc110 G A 8: 46,396,245 (GRCm39) C712Y probably damaging Het
Ccdc175 A T 12: 72,182,822 (GRCm39) I399N probably damaging Het
Cct8l1 A T 5: 25,722,754 (GRCm39) T490S probably benign Het
Cd109 CATTTATTTATTTATTTATTTATTTATTTATTTAT CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT 9: 78,619,782 (GRCm39) probably benign Het
Copa A G 1: 171,932,787 (GRCm39) N371D probably damaging Het
Cpeb1 A T 7: 81,005,695 (GRCm39) H381Q probably benign Het
Cyp2d40 T A 15: 82,645,763 (GRCm39) I81F possibly damaging Het
Dscc1 A T 15: 54,943,654 (GRCm39) D405E probably benign Het
Ece1 A G 4: 137,672,464 (GRCm39) D369G probably benign Het
Exd2 T C 12: 80,522,592 (GRCm39) V17A possibly damaging Het
Fam111a A T 19: 12,565,772 (GRCm39) N507I possibly damaging Het
Flnc T C 6: 29,445,038 (GRCm39) V719A possibly damaging Het
Fscb C T 12: 64,520,464 (GRCm39) G334D probably damaging Het
Glud1 T C 14: 34,043,782 (GRCm39) probably null Het
Gm8126 T A 14: 43,119,072 (GRCm39) Y180* probably null Het
Grip2 G A 6: 91,759,413 (GRCm39) P347L possibly damaging Het
H1f3 T C 13: 23,739,576 (GRCm39) S105P probably damaging Het
H60b C T 10: 22,164,644 (GRCm39) probably benign Het
Itga6 T C 2: 71,652,788 (GRCm39) V217A probably benign Het
Kndc1 G A 7: 139,503,946 (GRCm39) W1083* probably null Het
Limch1 A T 5: 67,184,850 (GRCm39) D613V probably damaging Het
Lpl T A 8: 69,349,403 (GRCm39) C310S probably damaging Het
Marchf1 T A 8: 66,839,876 (GRCm39) C220S probably benign Het
Mbd5 A C 2: 49,164,623 (GRCm39) H308P probably damaging Het
Med13 T C 11: 86,167,746 (GRCm39) D2003G probably damaging Het
Mettl16 T A 11: 74,708,127 (GRCm39) V442D possibly damaging Het
Mstn A T 1: 53,101,267 (GRCm39) T115S probably benign Het
Mtcl2 G T 2: 156,872,489 (GRCm39) Q953K probably benign Het
Nfil3 A G 13: 53,122,050 (GRCm39) S285P probably damaging Het
Odad4 C A 11: 100,440,742 (GRCm39) N74K probably benign Het
Or10j3 A C 1: 173,031,796 (GRCm39) Y291S probably damaging Het
Or51a24 A G 7: 103,733,502 (GRCm39) S262P probably damaging Het
Otof A G 5: 30,552,026 (GRCm39) V321A probably benign Het
Pcdha8 G T 18: 37,127,626 (GRCm39) A703S probably damaging Het
Pcdhb18 A G 18: 37,623,507 (GRCm39) Y279C probably damaging Het
Pdgfa T C 5: 138,979,051 (GRCm39) D51G probably benign Het
Pdzd8 A G 19: 59,289,292 (GRCm39) Y703H probably damaging Het
Pecr G T 1: 72,306,594 (GRCm39) P229Q probably damaging Het
Phkg1 G T 5: 129,902,114 (GRCm39) probably null Het
Plxnb2 A T 15: 89,051,150 (GRCm39) H356Q probably benign Het
Polr1b T C 2: 128,947,248 (GRCm39) I191T probably benign Het
Ppp4r3a A G 12: 101,049,026 (GRCm39) L35P possibly damaging Het
Rasa2 C T 9: 96,426,470 (GRCm39) G792D probably benign Het
Rps11-ps4 T C 12: 51,344,406 (GRCm39) noncoding transcript Het
Sema3g A G 14: 30,942,666 (GRCm39) D89G probably benign Het
Shroom3 G T 5: 93,090,945 (GRCm39) V1151F probably damaging Het
Slfn8 A G 11: 82,908,219 (GRCm39) V108A probably damaging Het
Smg9 T A 7: 24,107,019 (GRCm39) M221K possibly damaging Het
Sos1 A G 17: 80,705,660 (GRCm39) S1304P probably damaging Het
Sqle C A 15: 59,189,688 (GRCm39) A110E possibly damaging Het
Stab2 G A 10: 86,743,235 (GRCm39) Q1154* probably null Het
Taf4b A G 18: 14,937,577 (GRCm39) T217A probably benign Het
Tex15 T C 8: 34,072,760 (GRCm39) V2769A probably benign Het
Tmem156 A T 5: 65,237,502 (GRCm39) C53S probably damaging Het
Tmtc3 T A 10: 100,293,001 (GRCm39) K452N possibly damaging Het
Tns2 C T 15: 102,017,369 (GRCm39) R281C probably damaging Het
Tph1 T C 7: 46,306,376 (GRCm39) E195G probably damaging Het
Trpc6 T A 9: 8,609,852 (GRCm39) Y107N possibly damaging Het
Tsga10 G A 1: 37,874,606 (GRCm39) T93I probably damaging Het
Ttn T A 2: 76,571,778 (GRCm39) N26372Y probably damaging Het
Tubd1 T C 11: 86,446,128 (GRCm39) L256P possibly damaging Het
Txnrd2 C G 16: 18,259,569 (GRCm39) A126G probably benign Het
Vmn1r210 T G 13: 23,011,374 (GRCm39) K304T probably benign Het
Vps25 T C 11: 101,149,655 (GRCm39) S160P probably benign Het
Vrk3 T A 7: 44,424,900 (GRCm39) D438E probably benign Het
Vwa5b1 A G 4: 138,309,066 (GRCm39) L708P probably benign Het
Washc3 C T 10: 88,055,124 (GRCm39) Q105* probably null Het
Wdr83os T A 8: 85,807,410 (GRCm39) probably benign Het
Wwc1 T C 11: 35,758,123 (GRCm39) H741R probably benign Het
Zan T C 5: 137,434,575 (GRCm39) probably benign Het
Zdhhc4 A T 5: 143,311,931 (GRCm39) L14I possibly damaging Het
Zfp568 T A 7: 29,697,195 (GRCm39) D38E probably 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
R2257: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
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'- GGTGAGAATGCTATGGGATCATTC -3'
(R):5'- TTAACCAGGCCTTCCTAGGG -3'

Sequencing Primer
(F):5'- GCTATGGGATCATTCAAGACACTC -3'
(R):5'- CTAGGGGAGGAGTCACGG -3'
Posted On 2015-12-29