Incidental Mutation 'IGL02901:Iqub'
ID 363600
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Iqub
Ensembl Gene ENSMUSG00000046192
Gene Name IQ motif and ubiquitin domain containing
Synonyms 4932408B21Rik, Trs4
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02901
Quality Score
Status
Chromosome 6
Chromosomal Location 24444864-24515066 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 24454194 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 563 (L563P)
Ref Sequence ENSEMBL: ENSMUSP00000051177 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000052277]
AlphaFold Q8CDK3
Predicted Effect probably damaging
Transcript: ENSMUST00000052277
AA Change: L563P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000051177
Gene: ENSMUSG00000046192
AA Change: L563P

DomainStartEndE-ValueType
PDB:2DAF|A 119 216 1e-38 PDB
Blast:UBQ 129 199 3e-26 BLAST
low complexity region 218 229 N/A INTRINSIC
low complexity region 289 306 N/A INTRINSIC
IQ 333 355 1.74e-1 SMART
low complexity region 357 383 N/A INTRINSIC
low complexity region 735 742 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI

All alleles(2) : Targeted, knock-out(2)

Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adra1d A T 2: 131,403,524 (GRCm39) Y189N probably damaging Het
Ahdc1 A G 4: 132,792,245 (GRCm39) D1162G possibly damaging Het
Alpk2 A G 18: 65,439,482 (GRCm39) M637T probably benign Het
Arvcf G A 16: 18,216,992 (GRCm39) A440T probably damaging Het
BC051665 A T 13: 60,932,532 (GRCm39) V51E probably damaging Het
Clca3a2 A T 3: 144,522,529 (GRCm39) V164E probably damaging Het
Cox6a2 A C 7: 127,805,454 (GRCm39) L5R probably damaging Het
Cpsf1 A T 15: 76,483,696 (GRCm39) L849* probably null Het
Dclk1 A G 3: 55,395,208 (GRCm39) probably benign Het
Fam120b T A 17: 15,627,964 (GRCm39) probably benign Het
Itgb3 A T 11: 104,528,772 (GRCm39) I300F probably benign Het
Mdga2 A G 12: 66,844,583 (GRCm39) probably benign Het
Mfsd6 A G 1: 52,747,632 (GRCm39) I411T probably benign Het
Misp A T 10: 79,662,771 (GRCm39) Y396F possibly damaging Het
Nhsl2 T A X: 101,122,849 (GRCm39) V884D probably benign Het
Nxf7 A T X: 134,487,984 (GRCm39) probably null Het
Or10al4 T A 17: 38,037,311 (GRCm39) I132K probably damaging Het
Or4b12 G A 2: 90,096,052 (GRCm39) H241Y probably damaging Het
Palld T A 8: 62,330,029 (GRCm39) K283* probably null Het
Pkd1l2 G A 8: 117,792,484 (GRCm39) T436I probably benign Het
Proc T G 18: 32,256,678 (GRCm39) T330P possibly damaging Het
Prpf38a T C 4: 108,425,615 (GRCm39) D221G probably damaging Het
Prss55 T A 14: 64,314,576 (GRCm39) N198I probably damaging Het
Rabggta A G 14: 55,959,138 (GRCm39) S10P probably benign Het
Sbk2 A G 7: 4,960,289 (GRCm39) Y294H possibly damaging Het
Smyd1 A G 6: 71,215,614 (GRCm39) V115A probably benign Het
Trpm7 A G 2: 126,649,207 (GRCm39) probably null Het
Ttc21a A G 9: 119,787,347 (GRCm39) N751S probably damaging Het
Upk1a A T 7: 30,303,204 (GRCm39) M241K possibly damaging Het
Vmn2r71 A C 7: 85,268,470 (GRCm39) E224D probably benign Het
Vmn2r81 C T 10: 79,106,564 (GRCm39) T514I probably damaging Het
Zkscan16 T C 4: 58,946,283 (GRCm39) W53R probably damaging Het
Other mutations in Iqub
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01015:Iqub APN 6 24,501,005 (GRCm39) splice site probably benign
IGL01447:Iqub APN 6 24,505,627 (GRCm39) missense probably benign 0.01
IGL01621:Iqub APN 6 24,446,211 (GRCm39) missense probably benign 0.45
IGL01702:Iqub APN 6 24,500,312 (GRCm39) missense probably benign 0.13
IGL01917:Iqub APN 6 24,479,318 (GRCm39) missense probably damaging 0.97
IGL02411:Iqub APN 6 24,449,810 (GRCm39) missense probably damaging 0.98
IGL02580:Iqub APN 6 24,501,398 (GRCm39) missense probably benign 0.06
IGL02704:Iqub APN 6 24,505,909 (GRCm39) splice site probably benign
D4043:Iqub UTSW 6 24,505,750 (GRCm39) missense possibly damaging 0.81
R0304:Iqub UTSW 6 24,454,290 (GRCm39) missense probably damaging 0.99
R0391:Iqub UTSW 6 24,446,154 (GRCm39) missense probably benign 0.00
R0453:Iqub UTSW 6 24,450,829 (GRCm39) missense probably damaging 1.00
R0464:Iqub UTSW 6 24,479,262 (GRCm39) nonsense probably null
R0465:Iqub UTSW 6 24,503,783 (GRCm39) missense probably damaging 1.00
R0479:Iqub UTSW 6 24,505,809 (GRCm39) missense probably benign 0.28
R0606:Iqub UTSW 6 24,501,260 (GRCm39) splice site probably benign
R1146:Iqub UTSW 6 24,505,627 (GRCm39) missense possibly damaging 0.89
R1146:Iqub UTSW 6 24,505,627 (GRCm39) missense possibly damaging 0.89
R1238:Iqub UTSW 6 24,505,884 (GRCm39) missense probably benign 0.03
R1452:Iqub UTSW 6 24,491,558 (GRCm39) missense probably benign 0.13
R1927:Iqub UTSW 6 24,491,670 (GRCm39) missense probably benign 0.11
R3195:Iqub UTSW 6 24,462,036 (GRCm39) splice site probably benign
R4438:Iqub UTSW 6 24,505,867 (GRCm39) missense probably benign 0.01
R4577:Iqub UTSW 6 24,501,290 (GRCm39) missense probably damaging 0.99
R4671:Iqub UTSW 6 24,479,183 (GRCm39) missense probably benign 0.00
R4860:Iqub UTSW 6 24,450,841 (GRCm39) missense probably damaging 0.99
R4860:Iqub UTSW 6 24,450,841 (GRCm39) missense probably damaging 0.99
R4906:Iqub UTSW 6 24,501,368 (GRCm39) missense probably damaging 0.99
R5605:Iqub UTSW 6 24,505,620 (GRCm39) missense probably benign
R5772:Iqub UTSW 6 24,454,250 (GRCm39) missense possibly damaging 0.64
R5801:Iqub UTSW 6 24,449,768 (GRCm39) missense probably benign 0.11
R5853:Iqub UTSW 6 24,491,601 (GRCm39) missense probably benign 0.00
R6423:Iqub UTSW 6 24,491,528 (GRCm39) missense probably damaging 0.98
R6475:Iqub UTSW 6 24,449,744 (GRCm39) missense probably damaging 1.00
R6476:Iqub UTSW 6 24,449,744 (GRCm39) missense probably damaging 1.00
R6477:Iqub UTSW 6 24,449,744 (GRCm39) missense probably damaging 1.00
R6701:Iqub UTSW 6 24,449,744 (GRCm39) missense probably damaging 1.00
R6702:Iqub UTSW 6 24,449,744 (GRCm39) missense probably damaging 1.00
R6703:Iqub UTSW 6 24,449,744 (GRCm39) missense probably damaging 1.00
R6860:Iqub UTSW 6 24,505,737 (GRCm39) missense possibly damaging 0.81
R7331:Iqub UTSW 6 24,500,393 (GRCm39) missense possibly damaging 0.73
R7530:Iqub UTSW 6 24,450,622 (GRCm39) missense probably benign 0.00
R7997:Iqub UTSW 6 24,501,413 (GRCm39) missense possibly damaging 0.86
R8050:Iqub UTSW 6 24,503,784 (GRCm39) missense possibly damaging 0.95
R8141:Iqub UTSW 6 24,491,608 (GRCm39) missense probably benign 0.00
R8153:Iqub UTSW 6 24,450,789 (GRCm39) nonsense probably null
R8163:Iqub UTSW 6 24,449,714 (GRCm39) missense probably benign 0.01
R8702:Iqub UTSW 6 24,461,914 (GRCm39) missense probably damaging 1.00
R8824:Iqub UTSW 6 24,479,307 (GRCm39) nonsense probably null
R8899:Iqub UTSW 6 24,505,768 (GRCm39) missense probably benign 0.00
R9075:Iqub UTSW 6 24,446,124 (GRCm39) missense probably damaging 1.00
R9186:Iqub UTSW 6 24,450,766 (GRCm39) missense possibly damaging 0.92
R9240:Iqub UTSW 6 24,505,622 (GRCm39) missense probably benign
R9256:Iqub UTSW 6 24,446,198 (GRCm39) missense possibly damaging 0.92
X0025:Iqub UTSW 6 24,500,383 (GRCm39) missense probably damaging 0.96
Z1088:Iqub UTSW 6 24,500,242 (GRCm39) splice site probably null
Posted On 2015-12-18