Incidental Mutation 'R2094:Iws1'
ID 232004
Institutional Source Beutler Lab
Gene Symbol Iws1
Ensembl Gene ENSMUSG00000024384
Gene Name IWS1, SUPT6 interacting protein
Synonyms 1700069O15Rik
MMRRC Submission 040098-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.957) question?
Stock # R2094 (G1)
Quality Score 225
Status Validated
Chromosome 18
Chromosomal Location 32200794-32237381 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 32217719 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 441 (E441G)
Ref Sequence ENSEMBL: ENSMUSP00000148514 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025243] [ENSMUST00000212675]
AlphaFold Q8C1D8
Predicted Effect probably damaging
Transcript: ENSMUST00000025243
AA Change: E441G

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000025243
Gene: ENSMUSG00000024384
AA Change: E441G

DomainStartEndE-ValueType
low complexity region 21 32 N/A INTRINSIC
low complexity region 73 86 N/A INTRINSIC
low complexity region 92 109 N/A INTRINSIC
internal_repeat_2 112 179 9.21e-13 PROSPERO
internal_repeat_1 118 184 9.82e-20 PROSPERO
internal_repeat_1 183 296 9.82e-20 PROSPERO
internal_repeat_2 229 316 9.21e-13 PROSPERO
low complexity region 320 332 N/A INTRINSIC
low complexity region 357 373 N/A INTRINSIC
low complexity region 384 404 N/A INTRINSIC
low complexity region 407 418 N/A INTRINSIC
low complexity region 422 442 N/A INTRINSIC
low complexity region 528 540 N/A INTRINSIC
Pfam:Med26 584 636 4.8e-19 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212115
Predicted Effect probably benign
Transcript: ENSMUST00000212280
Predicted Effect probably benign
Transcript: ENSMUST00000212458
Predicted Effect probably damaging
Transcript: ENSMUST00000212675
AA Change: E441G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably benign
Transcript: ENSMUST00000213074
Meta Mutation Damage Score 0.1247 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.4%
Validation Efficiency 100% (56/56)
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A130010J15Rik A G 1: 192,857,154 (GRCm39) I169V probably benign Het
Arrdc5 A G 17: 56,604,856 (GRCm39) S144P probably benign Het
Astn1 A G 1: 158,495,179 (GRCm39) M92V probably benign Het
Atg5 A G 10: 44,195,544 (GRCm39) I189M probably damaging Het
Atmin A G 8: 117,684,277 (GRCm39) T646A probably damaging Het
Atp1a2 G A 1: 172,115,000 (GRCm39) R262W probably damaging Het
Atp6v1g2 A G 17: 35,455,785 (GRCm39) K16E probably damaging Het
Bex6 G A 16: 32,005,278 (GRCm39) E29K possibly damaging Het
Casd1 A G 6: 4,608,705 (GRCm39) Y101C probably damaging Het
Ccdc168 A C 1: 44,098,890 (GRCm39) I736S probably benign Het
Cdx1 T C 18: 61,168,984 (GRCm39) D70G possibly damaging Het
Cebpz T C 17: 79,242,983 (GRCm39) T224A probably benign Het
Cep170b T C 12: 112,702,164 (GRCm39) V319A possibly damaging Het
Chrna2 C T 14: 66,386,912 (GRCm39) R353W possibly damaging Het
Chst5 A T 8: 112,617,176 (GRCm39) V148E probably benign Het
Clhc1 T A 11: 29,507,771 (GRCm39) W162R probably benign Het
Csmd1 T A 8: 16,129,992 (GRCm39) Q1710L probably damaging Het
Ddb1 A C 19: 10,590,300 (GRCm39) M276L probably benign Het
Dot1l C T 10: 80,621,712 (GRCm39) R455C probably damaging Het
Dync2h1 A G 9: 7,148,735 (GRCm39) V903A probably benign Het
Eno1b T C 18: 48,180,542 (GRCm39) V240A possibly damaging Het
Erich1 T G 8: 14,140,527 (GRCm39) probably benign Het
Ermp1 A C 19: 29,617,328 (GRCm39) S227A probably benign Het
Etv1 C A 12: 38,885,115 (GRCm39) P143Q probably null Het
Gimap8 A T 6: 48,627,502 (GRCm39) I159F probably benign Het
Gpr4 G A 7: 18,956,503 (GRCm39) V142M possibly damaging Het
Gucy1a1 C T 3: 82,020,639 (GRCm39) C86Y probably benign Het
Ifngr2 T G 16: 91,358,667 (GRCm39) probably null Het
Insrr A T 3: 87,710,488 (GRCm39) N398I probably damaging Het
Larp7-ps A G 4: 92,079,893 (GRCm39) S32P probably damaging Het
Megf10 A T 18: 57,414,785 (GRCm39) K732* probably null Het
Mprip T A 11: 59,640,334 (GRCm39) probably benign Het
Mrgprb8 T C 7: 48,038,953 (GRCm39) V208A probably benign Het
Msc G C 1: 14,825,908 (GRCm39) P22R probably benign Het
Opcml G A 9: 28,812,886 (GRCm39) E193K probably damaging Het
Or4k15b A T 14: 50,272,171 (GRCm39) S230T probably damaging Het
Oxsr1 A C 9: 119,123,560 (GRCm39) H71Q probably benign Het
Pkp2 T A 16: 16,064,831 (GRCm39) W452R probably damaging Het
Prrc2b C T 2: 32,072,582 (GRCm39) T20I probably damaging Het
Rasgrp3 T C 17: 75,810,136 (GRCm39) S279P probably damaging Het
Rtl1 T A 12: 109,557,831 (GRCm39) D1336V unknown Het
Serpina3m G T 12: 104,355,529 (GRCm39) K65N probably benign Het
Serpine2 A G 1: 79,788,411 (GRCm39) V182A probably damaging Het
Slc10a1 A G 12: 81,002,822 (GRCm39) V272A possibly damaging Het
Slc25a29 A T 12: 108,793,358 (GRCm39) N73K probably damaging Het
Slit1 G A 19: 41,594,819 (GRCm39) R1184W probably damaging Het
Srrm2 T C 17: 24,031,403 (GRCm39) probably benign Het
Stk11ip A G 1: 75,502,165 (GRCm39) probably benign Het
Tcerg1 A G 18: 42,697,210 (GRCm39) K767R possibly damaging Het
Tmem82 T C 4: 141,343,598 (GRCm39) K224R probably benign Het
Tmprss11g A G 5: 86,647,415 (GRCm39) L41S probably damaging Het
Trim42 T C 9: 97,248,150 (GRCm39) N182S probably benign Het
Ttn T C 2: 76,660,432 (GRCm39) T7430A probably benign Het
Wwp1 T C 4: 19,650,390 (GRCm39) T259A probably benign Het
Other mutations in Iws1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00432:Iws1 APN 18 32,217,741 (GRCm39) missense probably benign 0.07
IGL01432:Iws1 APN 18 32,216,519 (GRCm39) splice site probably benign
IGL01647:Iws1 APN 18 32,230,275 (GRCm39) nonsense probably null
IGL02054:Iws1 APN 18 32,223,595 (GRCm39) critical splice donor site probably null
IGL02189:Iws1 APN 18 32,226,178 (GRCm39) missense probably damaging 1.00
IGL02664:Iws1 APN 18 32,203,217 (GRCm39) missense possibly damaging 0.81
IGL03384:Iws1 APN 18 32,226,203 (GRCm39) missense probably damaging 1.00
IGL03394:Iws1 APN 18 32,221,301 (GRCm39) splice site probably benign
R0352:Iws1 UTSW 18 32,217,258 (GRCm39) missense probably damaging 1.00
R1385:Iws1 UTSW 18 32,223,483 (GRCm39) missense probably benign 0.03
R1486:Iws1 UTSW 18 32,230,309 (GRCm39) missense probably damaging 1.00
R1526:Iws1 UTSW 18 32,213,178 (GRCm39) missense probably benign 0.00
R1529:Iws1 UTSW 18 32,213,334 (GRCm39) missense probably benign
R3774:Iws1 UTSW 18 32,213,048 (GRCm39) missense probably damaging 1.00
R3907:Iws1 UTSW 18 32,212,973 (GRCm39) missense possibly damaging 0.93
R4018:Iws1 UTSW 18 32,203,205 (GRCm39) nonsense probably null
R4423:Iws1 UTSW 18 32,216,503 (GRCm39) missense probably damaging 1.00
R4703:Iws1 UTSW 18 32,213,066 (GRCm39) missense probably benign 0.19
R4979:Iws1 UTSW 18 32,226,320 (GRCm39) unclassified probably benign
R5228:Iws1 UTSW 18 32,221,314 (GRCm39) missense probably damaging 1.00
R5352:Iws1 UTSW 18 32,216,457 (GRCm39) missense probably damaging 1.00
R6428:Iws1 UTSW 18 32,219,343 (GRCm39) missense probably damaging 1.00
R6846:Iws1 UTSW 18 32,219,326 (GRCm39) unclassified probably benign
R6892:Iws1 UTSW 18 32,219,327 (GRCm39) missense probably damaging 0.99
R7163:Iws1 UTSW 18 32,226,277 (GRCm39) missense possibly damaging 0.80
R7540:Iws1 UTSW 18 32,213,536 (GRCm39) missense possibly damaging 0.94
R7605:Iws1 UTSW 18 32,222,540 (GRCm39) missense probably benign 0.01
R7714:Iws1 UTSW 18 32,223,568 (GRCm39) missense probably benign 0.00
R8218:Iws1 UTSW 18 32,226,688 (GRCm39) missense probably benign 0.00
R8229:Iws1 UTSW 18 32,217,740 (GRCm39) missense probably benign
R8728:Iws1 UTSW 18 32,216,334 (GRCm39) missense probably damaging 1.00
R8987:Iws1 UTSW 18 32,226,645 (GRCm39) missense possibly damaging 0.60
R9096:Iws1 UTSW 18 32,216,373 (GRCm39) missense probably benign
R9187:Iws1 UTSW 18 32,213,213 (GRCm39) missense possibly damaging 0.68
R9188:Iws1 UTSW 18 32,213,213 (GRCm39) missense possibly damaging 0.68
R9189:Iws1 UTSW 18 32,213,213 (GRCm39) missense possibly damaging 0.68
R9190:Iws1 UTSW 18 32,213,213 (GRCm39) missense possibly damaging 0.68
R9284:Iws1 UTSW 18 32,213,213 (GRCm39) missense possibly damaging 0.68
R9302:Iws1 UTSW 18 32,213,213 (GRCm39) missense possibly damaging 0.68
R9351:Iws1 UTSW 18 32,213,213 (GRCm39) missense possibly damaging 0.68
R9352:Iws1 UTSW 18 32,213,213 (GRCm39) missense possibly damaging 0.68
R9572:Iws1 UTSW 18 32,203,257 (GRCm39) missense probably damaging 1.00
R9703:Iws1 UTSW 18 32,212,738 (GRCm39) missense probably damaging 0.99
R9758:Iws1 UTSW 18 32,216,347 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GATCATGAACGTGCTCATACAGG -3'
(R):5'- ACTCTTCCCAATCTGGAGCC -3'

Sequencing Primer
(F):5'- CGTGCTCATACAGGTATGGAC -3'
(R):5'- TGGAGCCCCAGATGAGAAAC -3'
Posted On 2014-09-18