Incidental Mutation 'R7199:Bzw2'
ID 560191
Institutional Source Beutler Lab
Gene Symbol Bzw2
Ensembl Gene ENSMUSG00000020547
Gene Name basic leucine zipper and W2 domains 2
Synonyms 1110001I24Rik, HSPC028
MMRRC Submission 045277-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7199 (G1)
Quality Score 225.009
Status Not validated
Chromosome 12
Chromosomal Location 36141834-36206922 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to A at 36180054 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 58 (R58*)
Ref Sequence ENSEMBL: ENSMUSP00000020856 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020856] [ENSMUST00000220763] [ENSMUST00000220828] [ENSMUST00000221388] [ENSMUST00000223382] [ENSMUST00000223474]
AlphaFold Q91VK1
Predicted Effect probably null
Transcript: ENSMUST00000020856
AA Change: R58*
SMART Domains Protein: ENSMUSP00000020856
Gene: ENSMUSG00000020547
AA Change: R58*

DomainStartEndE-ValueType
eIF5C 326 411 3.29e-33 SMART
Predicted Effect probably null
Transcript: ENSMUST00000220763
AA Change: R58*
Predicted Effect probably null
Transcript: ENSMUST00000220828
AA Change: R58*
Predicted Effect probably benign
Transcript: ENSMUST00000221388
Predicted Effect probably null
Transcript: ENSMUST00000223382
AA Change: R58*
Predicted Effect probably null
Transcript: ENSMUST00000223474
AA Change: R58*
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 93 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310034C09Rik A G 16: 88,555,902 (GRCm39) T39A probably damaging Het
Abca3 G A 17: 24,596,681 (GRCm39) G378D probably damaging Het
Abtb2 T C 2: 103,397,565 (GRCm39) V165A possibly damaging Het
Ache A G 5: 137,288,504 (GRCm39) E70G probably damaging Het
Adamtsl4 T C 3: 95,588,119 (GRCm39) T623A probably benign Het
Ahdc1 G A 4: 132,791,935 (GRCm39) V1059I probably benign Het
Ajuba G A 14: 54,810,915 (GRCm39) Q357* probably null Het
Ano7 A T 1: 93,330,700 (GRCm39) D54V Het
Apob A T 12: 8,055,072 (GRCm39) D1357V probably damaging Het
Atad2b T A 12: 5,067,992 (GRCm39) Y997N probably damaging Het
Bhlhe22 C A 3: 18,110,006 (GRCm39) T352K probably damaging Het
Bsn T C 9: 107,992,533 (GRCm39) E1073G probably damaging Het
C7 G T 15: 5,023,725 (GRCm39) S694R probably benign Het
Cbr2 T A 11: 120,621,087 (GRCm39) H170L probably benign Het
Cdcp3 G A 7: 130,837,641 (GRCm39) W512* probably null Het
Cgas C A 9: 78,340,315 (GRCm39) K472N probably benign Het
Ckap2l T C 2: 129,126,975 (GRCm39) N401S probably benign Het
Cldn1 A G 16: 26,190,346 (GRCm39) F11L probably benign Het
Cmtr1 A G 17: 29,895,174 (GRCm39) T118A probably benign Het
Cog6 T C 3: 52,890,610 (GRCm39) E610G probably benign Het
Col3a1 G T 1: 45,371,301 (GRCm39) A451S probably null Het
Cr1l T A 1: 194,799,878 (GRCm39) R265S probably benign Het
Dapk1 T C 13: 60,902,024 (GRCm39) I951T probably benign Het
Dnah9 T C 11: 66,009,770 (GRCm39) N706D probably benign Het
Dpysl5 A T 5: 30,940,539 (GRCm39) T239S probably benign Het
Ect2l T A 10: 18,004,894 (GRCm39) Y913F probably benign Het
Elf5 C A 2: 103,269,641 (GRCm39) A74D possibly damaging Het
Erap1 T C 13: 74,814,258 (GRCm39) V399A probably benign Het
Ercc4 A G 16: 12,965,657 (GRCm39) D763G probably damaging Het
Fam222b T A 11: 78,045,683 (GRCm39) C415S possibly damaging Het
Fat4 A C 3: 39,031,511 (GRCm39) N2432T probably damaging Het
Fbn2 G T 18: 58,186,833 (GRCm39) C1689* probably null Het
Frrs1l T A 4: 56,972,282 (GRCm39) T140S probably damaging Het
Gm5141 A T 13: 62,924,877 (GRCm39) H10Q possibly damaging Het
Inafm1 A T 7: 16,007,079 (GRCm39) L46Q probably damaging Het
Irak2 T C 6: 113,650,045 (GRCm39) L260P probably damaging Het
Kat2b T C 17: 53,977,706 (GRCm39) L751P probably damaging Het
Kcnh1 T A 1: 192,019,913 (GRCm39) I413N probably benign Het
Kirrel1 T C 3: 86,990,695 (GRCm39) D709G probably benign Het
Lama4 T C 10: 38,956,536 (GRCm39) V1153A possibly damaging Het
Lipg A T 18: 75,088,655 (GRCm39) F98L probably benign Het
Lman1 T C 18: 66,127,936 (GRCm39) E236G probably damaging Het
Lrp1 T A 10: 127,409,325 (GRCm39) D1598V probably damaging Het
Lrrc71 T A 3: 87,650,384 (GRCm39) N230Y probably damaging Het
Maneal T C 4: 124,750,983 (GRCm39) S258G possibly damaging Het
Marchf10 T A 11: 105,281,532 (GRCm39) E251V probably damaging Het
Mpdz A G 4: 81,215,570 (GRCm39) I1484T probably damaging Het
Mtcl1 T A 17: 66,647,534 (GRCm39) N1882I probably benign Het
Neb G A 2: 52,110,212 (GRCm39) A212V probably benign Het
Obscn G A 11: 58,903,672 (GRCm39) S7434L probably benign Het
Or14j8 A C 17: 38,263,048 (GRCm39) I289S probably damaging Het
Or1ad8 T A 11: 50,898,223 (GRCm39) C141* probably null Het
Or1j12 A T 2: 36,342,872 (GRCm39) I92F probably damaging Het
Or4k47 T C 2: 111,451,538 (GRCm39) M294V probably benign Het
Or8g2b A G 9: 39,750,753 (GRCm39) M8V probably benign Het
Orc6 T C 8: 86,029,590 (GRCm39) probably null Het
Otogl T G 10: 107,710,394 (GRCm39) E565A possibly damaging Het
Papss1 A G 3: 131,290,899 (GRCm39) Q214R probably benign Het
Pck2 G A 14: 55,786,169 (GRCm39) V653M probably benign Het
Plxna4 G A 6: 32,192,113 (GRCm39) Q826* probably null Het
Pms1 T A 1: 53,295,889 (GRCm39) T161S probably benign Het
Prkar2a C A 9: 108,617,669 (GRCm39) N242K probably damaging Het
Prss1 T A 6: 41,439,690 (GRCm39) I141N probably damaging Het
Puf60 A G 15: 75,943,717 (GRCm39) V235A probably damaging Het
Rapgef6 T A 11: 54,437,252 (GRCm39) F65Y probably benign Het
Rasgef1b T C 5: 99,447,898 (GRCm39) E104G unknown Het
Rcn3 T C 7: 44,734,333 (GRCm39) Y225C probably damaging Het
Rhot1 G C 11: 80,137,560 (GRCm39) W354S probably damaging Het
Rp1 T C 1: 4,417,513 (GRCm39) S1200G possibly damaging Het
Scaper T A 9: 55,745,460 (GRCm39) K603* probably null Het
Selenbp1 G A 3: 94,851,745 (GRCm39) V429I possibly damaging Het
Setd5 T G 6: 113,098,099 (GRCm39) S713A probably benign Het
Shank1 T C 7: 44,002,564 (GRCm39) Y1428H possibly damaging Het
Slc11a1 G T 1: 74,422,830 (GRCm39) W361L possibly damaging Het
Spta1 A T 1: 174,050,837 (GRCm39) D1772V possibly damaging Het
St8sia6 T C 2: 13,661,721 (GRCm39) H370R probably damaging Het
Stkld1 A T 2: 26,842,726 (GRCm39) D566V probably damaging Het
Tango6 T C 8: 107,415,791 (GRCm39) V204A probably benign Het
Tdrd5 G A 1: 156,129,293 (GRCm39) A139V probably damaging Het
Tenm2 A T 11: 36,062,263 (GRCm39) V534E probably damaging Het
Tfip11 A T 5: 112,479,044 (GRCm39) Q204L probably benign Het
Tlr4 A T 4: 66,759,430 (GRCm39) Q741L probably damaging Het
Tmem18 A G 12: 30,638,654 (GRCm39) M111V probably benign Het
Togaram1 A G 12: 65,042,292 (GRCm39) N1167S probably benign Het
Trappc3 C T 4: 126,168,945 (GRCm39) A145V possibly damaging Het
Trbj2-3 T C 6: 41,520,176 (GRCm39) F7S probably damaging Het
Vinac1 A G 2: 128,880,238 (GRCm39) S563P Het
Vmn1r212 T A 13: 23,067,731 (GRCm39) M201L probably benign Het
Xaf1 C A 11: 72,194,201 (GRCm39) C27* probably null Het
Zeb1 T C 18: 5,767,703 (GRCm39) V738A probably benign Het
Zfp524 A T 7: 5,020,883 (GRCm39) H137L probably damaging Het
Zfyve19 A T 2: 119,047,118 (GRCm39) H367L probably damaging Het
Zim1 G A 7: 6,680,872 (GRCm39) Q264* probably null Het
Other mutations in Bzw2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01472:Bzw2 APN 12 36,159,795 (GRCm39) missense probably damaging 1.00
IGL01731:Bzw2 APN 12 36,157,647 (GRCm39) splice site probably null
IGL02071:Bzw2 APN 12 36,157,502 (GRCm39) missense probably benign 0.26
R0003:Bzw2 UTSW 12 36,180,014 (GRCm39) missense probably damaging 1.00
R0462:Bzw2 UTSW 12 36,174,023 (GRCm39) missense probably damaging 1.00
R1615:Bzw2 UTSW 12 36,169,126 (GRCm39) splice site probably benign
R3121:Bzw2 UTSW 12 36,170,788 (GRCm39) splice site probably null
R4353:Bzw2 UTSW 12 36,173,978 (GRCm39) missense probably damaging 1.00
R4649:Bzw2 UTSW 12 36,173,980 (GRCm39) missense probably null 1.00
R5121:Bzw2 UTSW 12 36,154,350 (GRCm39) missense probably damaging 1.00
R6143:Bzw2 UTSW 12 36,170,725 (GRCm39) missense probably benign 0.42
R6408:Bzw2 UTSW 12 36,157,524 (GRCm39) missense possibly damaging 0.65
R7220:Bzw2 UTSW 12 36,173,950 (GRCm39) missense possibly damaging 0.60
R7469:Bzw2 UTSW 12 36,157,550 (GRCm39) missense probably damaging 0.99
R8025:Bzw2 UTSW 12 36,157,517 (GRCm39) missense probably damaging 1.00
R8138:Bzw2 UTSW 12 36,159,819 (GRCm39) missense probably benign
R8363:Bzw2 UTSW 12 36,180,122 (GRCm39) missense probably benign 0.01
R8833:Bzw2 UTSW 12 36,169,069 (GRCm39) missense probably benign 0.01
R8888:Bzw2 UTSW 12 36,173,982 (GRCm39) nonsense probably null
R8895:Bzw2 UTSW 12 36,173,982 (GRCm39) nonsense probably null
R8931:Bzw2 UTSW 12 36,184,943 (GRCm39) missense possibly damaging 0.66
R9377:Bzw2 UTSW 12 36,180,131 (GRCm39) missense probably damaging 1.00
R9494:Bzw2 UTSW 12 36,184,947 (GRCm39) start codon destroyed probably benign 0.21
X0027:Bzw2 UTSW 12 36,154,279 (GRCm39) missense probably damaging 1.00
X0066:Bzw2 UTSW 12 36,164,034 (GRCm39) missense probably benign 0.23
Predicted Primers PCR Primer
(F):5'- AGGTCCATATGCTCCTTTGTGC -3'
(R):5'- GGCCAGTTTCTTTCCAGACTATATG -3'

Sequencing Primer
(F):5'- CTTTCTACTACCTGTGGTGAGTG -3'
(R):5'- ATGGATAAACACATATGCTCACG -3'
Posted On 2019-06-26