Incidental Mutation 'IGL01107:Zbtb11'
ID 52929
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zbtb11
Ensembl Gene ENSMUSG00000022601
Gene Name zinc finger and BTB domain containing 11
Synonyms 9230110G02Rik, ZNF-U69274
Accession Numbers
Essential gene? Probably essential (E-score: 0.972) question?
Stock # IGL01107
Quality Score
Status
Chromosome 16
Chromosomal Location 55794246-55829276 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 55826370 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Histidine at position 800 (Y800H)
Ref Sequence ENSEMBL: ENSMUSP00000056923 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050248] [ENSMUST00000119981]
AlphaFold G5E8B9
Predicted Effect probably damaging
Transcript: ENSMUST00000050248
AA Change: Y800H

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000056923
Gene: ENSMUSG00000022601
AA Change: Y800H

DomainStartEndE-ValueType
low complexity region 136 158 N/A INTRINSIC
low complexity region 161 177 N/A INTRINSIC
BTB 214 312 4.77e-13 SMART
low complexity region 371 399 N/A INTRINSIC
ZnF_C2H2 566 588 1.1e-2 SMART
ZnF_C2H2 594 616 2.09e-3 SMART
low complexity region 623 640 N/A INTRINSIC
ZnF_C2H2 648 670 4.47e-3 SMART
ZnF_C2H2 676 698 8.22e-2 SMART
ZnF_C2H2 704 726 2.27e-4 SMART
ZnF_C2H2 732 754 1.28e-3 SMART
ZnF_C2H2 763 785 2.95e-3 SMART
ZnF_C2H2 791 813 7.67e-2 SMART
ZnF_C2H2 819 843 2.95e-3 SMART
ZnF_C2H2 855 877 1.67e-2 SMART
ZnF_C2H2 883 905 3.02e0 SMART
ZnF_C2H2 911 934 9.58e-3 SMART
low complexity region 979 994 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000119981
SMART Domains Protein: ENSMUSP00000112565
Gene: ENSMUSG00000071533

DomainStartEndE-ValueType
Pfam:PCNP 1 100 6.3e-59 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000184618
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700001O22Rik A T 2: 30,687,948 (GRCm39) F215Y probably damaging Het
2700049A03Rik T C 12: 71,241,242 (GRCm39) probably null Het
Akip1 C T 7: 109,311,045 (GRCm39) T195M probably damaging Het
Arhgef16 T C 4: 154,364,701 (GRCm39) N631S probably benign Het
Brat1 C T 5: 140,702,932 (GRCm39) S544L probably damaging Het
Cfap65 C T 1: 74,958,342 (GRCm39) probably null Het
Defa22 T A 8: 21,653,053 (GRCm39) probably null Het
Dnajc4 C T 19: 6,966,869 (GRCm39) R153H probably benign Het
Dusp11 A G 6: 85,929,352 (GRCm39) probably benign Het
E2f4 T A 8: 106,030,809 (GRCm39) probably benign Het
Ece1 T A 4: 137,665,969 (GRCm39) L271Q probably damaging Het
Fcgrt T C 7: 44,742,752 (GRCm39) D343G probably damaging Het
Igsf10 T C 3: 59,238,945 (GRCm39) E412G probably damaging Het
Il4ra G T 7: 125,175,086 (GRCm39) L431F possibly damaging Het
Ilrun A T 17: 28,005,043 (GRCm39) probably null Het
Krt86 T A 15: 101,373,306 (GRCm39) L200Q probably damaging Het
Lpcat1 T A 13: 73,642,947 (GRCm39) F126I probably damaging Het
Prag1 A G 8: 36,567,085 (GRCm39) T79A probably benign Het
Pramel13 A T 4: 144,119,664 (GRCm39) I301N probably benign Het
Psg29 G T 7: 16,938,850 (GRCm39) L41F probably benign Het
Rai14 C T 15: 10,599,797 (GRCm39) probably benign Het
Reg3a A G 6: 78,360,228 (GRCm39) D136G probably benign Het
Rif1 A G 2: 52,001,315 (GRCm39) T1590A probably benign Het
Rorb A T 19: 18,934,692 (GRCm39) L300* probably null Het
Sin3b T C 8: 73,457,733 (GRCm39) C150R possibly damaging Het
Smarcc1 C A 9: 110,051,005 (GRCm39) H942N probably damaging Het
Tas2r105 A G 6: 131,664,074 (GRCm39) V118A probably benign Het
Tmem131 T C 1: 36,868,662 (GRCm39) S388G probably damaging Het
Ttll9 C A 2: 152,844,809 (GRCm39) probably benign Het
Ush1c A G 7: 45,859,325 (GRCm39) L498P probably damaging Het
Vmn2r100 A G 17: 19,741,618 (GRCm39) Y110C probably damaging Het
Zdhhc20 T A 14: 58,103,046 (GRCm39) E101V probably damaging Het
Other mutations in Zbtb11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00839:Zbtb11 APN 16 55,820,965 (GRCm39) nonsense probably null
IGL01341:Zbtb11 APN 16 55,811,294 (GRCm39) missense possibly damaging 0.68
IGL01510:Zbtb11 APN 16 55,810,706 (GRCm39) missense probably damaging 0.99
IGL01611:Zbtb11 APN 16 55,800,973 (GRCm39) missense probably damaging 1.00
IGL01736:Zbtb11 APN 16 55,818,523 (GRCm39) missense probably damaging 1.00
IGL01834:Zbtb11 APN 16 55,811,371 (GRCm39) missense probably benign 0.35
IGL02427:Zbtb11 APN 16 55,802,713 (GRCm39) missense possibly damaging 0.95
IGL02441:Zbtb11 APN 16 55,794,552 (GRCm39) missense possibly damaging 0.94
IGL02455:Zbtb11 APN 16 55,821,038 (GRCm39) missense probably damaging 1.00
PIT4544001:Zbtb11 UTSW 16 55,818,556 (GRCm39) nonsense probably null
R0987:Zbtb11 UTSW 16 55,811,071 (GRCm39) missense probably benign 0.00
R1414:Zbtb11 UTSW 16 55,810,923 (GRCm39) nonsense probably null
R1437:Zbtb11 UTSW 16 55,811,983 (GRCm39) critical splice donor site probably null
R1570:Zbtb11 UTSW 16 55,811,178 (GRCm39) missense probably benign
R1658:Zbtb11 UTSW 16 55,794,588 (GRCm39) missense possibly damaging 0.71
R1735:Zbtb11 UTSW 16 55,811,045 (GRCm39) missense probably benign
R2048:Zbtb11 UTSW 16 55,818,372 (GRCm39) missense probably damaging 1.00
R2925:Zbtb11 UTSW 16 55,794,447 (GRCm39) missense probably benign 0.00
R4072:Zbtb11 UTSW 16 55,818,427 (GRCm39) missense possibly damaging 0.89
R4075:Zbtb11 UTSW 16 55,818,427 (GRCm39) missense possibly damaging 0.89
R4076:Zbtb11 UTSW 16 55,818,427 (GRCm39) missense possibly damaging 0.89
R5023:Zbtb11 UTSW 16 55,826,428 (GRCm39) missense probably damaging 1.00
R5755:Zbtb11 UTSW 16 55,821,076 (GRCm39) missense probably benign 0.02
R5757:Zbtb11 UTSW 16 55,827,392 (GRCm39) missense probably damaging 1.00
R6218:Zbtb11 UTSW 16 55,818,436 (GRCm39) missense probably benign 0.00
R6313:Zbtb11 UTSW 16 55,810,854 (GRCm39) missense probably benign 0.03
R6461:Zbtb11 UTSW 16 55,827,234 (GRCm39) missense probably damaging 0.99
R6666:Zbtb11 UTSW 16 55,826,615 (GRCm39) missense probably damaging 1.00
R6807:Zbtb11 UTSW 16 55,810,865 (GRCm39) missense probably benign 0.03
R7194:Zbtb11 UTSW 16 55,827,551 (GRCm39) missense probably damaging 1.00
R7424:Zbtb11 UTSW 16 55,810,850 (GRCm39) missense probably benign 0.01
R8022:Zbtb11 UTSW 16 55,826,383 (GRCm39) missense probably damaging 0.99
R8436:Zbtb11 UTSW 16 55,821,022 (GRCm39) nonsense probably null
R8532:Zbtb11 UTSW 16 55,811,252 (GRCm39) missense probably benign 0.03
R8806:Zbtb11 UTSW 16 55,802,637 (GRCm39) missense probably damaging 1.00
R9033:Zbtb11 UTSW 16 55,818,492 (GRCm39) missense probably benign
R9673:Zbtb11 UTSW 16 55,827,336 (GRCm39) missense probably damaging 1.00
RF014:Zbtb11 UTSW 16 55,800,960 (GRCm39) missense probably damaging 0.97
Z1176:Zbtb11 UTSW 16 55,811,865 (GRCm39) nonsense probably null
Posted On 2013-06-21