Incidental Mutation 'IGL02499:Zbtb10'
ID 295959
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zbtb10
Ensembl Gene ENSMUSG00000069114
Gene Name zinc finger and BTB domain containing 10
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.442) question?
Stock # IGL02499
Quality Score
Status
Chromosome 3
Chromosomal Location 9315662-9350393 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 9316800 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Valine at position 204 (G204V)
Ref Sequence ENSEMBL: ENSMUSP00000119386 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000155203]
AlphaFold E9Q8X5
Predicted Effect probably damaging
Transcript: ENSMUST00000155203
AA Change: G204V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000119386
Gene: ENSMUSG00000069114
AA Change: G204V

DomainStartEndE-ValueType
low complexity region 15 32 N/A INTRINSIC
low complexity region 38 54 N/A INTRINSIC
low complexity region 75 82 N/A INTRINSIC
low complexity region 96 111 N/A INTRINSIC
low complexity region 121 137 N/A INTRINSIC
low complexity region 180 222 N/A INTRINSIC
ZnF_TTF 239 321 7.92e-2 SMART
BTB 357 456 4.02e-20 SMART
internal_repeat_1 648 671 2.82e-12 PROSPERO
internal_repeat_1 672 695 2.82e-12 PROSPERO
ZnF_C2H2 714 736 6.78e-3 SMART
ZnF_C2H2 742 764 2.09e-3 SMART
low complexity region 765 777 N/A INTRINSIC
low complexity region 823 842 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A930011G23Rik A G 5: 99,377,236 (GRCm39) S404P probably damaging Het
A930011G23Rik G A 5: 99,377,241 (GRCm39) P402L probably damaging Het
Abcb1a A G 5: 8,776,807 (GRCm39) N835S possibly damaging Het
Abr A T 11: 76,399,916 (GRCm39) F27Y probably benign Het
Adam5 C T 8: 25,271,581 (GRCm39) probably null Het
Alas1 A T 9: 106,118,520 (GRCm39) Y201N probably damaging Het
Aldoart1 T A 4: 72,770,476 (GRCm39) R111W possibly damaging Het
Arhgef25 A G 10: 127,021,460 (GRCm39) Y253H probably damaging Het
Arhgef28 G T 13: 98,090,291 (GRCm39) A1076E possibly damaging Het
Baz2b C T 2: 59,731,840 (GRCm39) R2066K possibly damaging Het
Bdh1 G T 16: 31,256,866 (GRCm39) R5L possibly damaging Het
Brap A G 5: 121,817,934 (GRCm39) Y358C probably damaging Het
Cad T C 5: 31,226,948 (GRCm39) V1235A probably damaging Het
Cadps G T 14: 12,822,725 (GRCm38) S5* probably null Het
Cd200r2 A G 16: 44,734,948 (GRCm39) T220A possibly damaging Het
Cd209e T A 8: 3,904,238 (GRCm39) M6L probably benign Het
Cdh23 G T 10: 60,220,958 (GRCm39) T1265K probably damaging Het
Clec16a T C 16: 10,512,540 (GRCm39) S828P probably benign Het
Dao A G 5: 114,152,002 (GRCm39) K107E possibly damaging Het
Dnah6 T A 6: 72,998,210 (GRCm39) M4071L probably benign Het
Dvl1 T C 4: 155,939,237 (GRCm39) I250T probably benign Het
Dzip3 A C 16: 48,754,213 (GRCm39) L945V probably damaging Het
Gm128 A G 3: 95,147,992 (GRCm39) S101P possibly damaging Het
Gphn T C 12: 78,539,074 (GRCm39) L240P probably benign Het
Hecw2 A G 1: 53,965,647 (GRCm39) I393T probably benign Het
Iigp1c T C 18: 60,378,710 (GRCm39) S82P probably damaging Het
Kat14 A G 2: 144,235,751 (GRCm39) E161G probably benign Het
Kcne3 A C 7: 99,833,610 (GRCm39) I76L probably benign Het
Kcnk18 A T 19: 59,223,614 (GRCm39) Q253L probably benign Het
Kmt2a T C 9: 44,741,806 (GRCm39) probably benign Het
Lrrc73 A G 17: 46,567,915 (GRCm39) probably benign Het
Mki67 A G 7: 135,296,056 (GRCm39) S2993P possibly damaging Het
Mto1 T A 9: 78,368,794 (GRCm39) probably benign Het
Myo9a T A 9: 59,722,669 (GRCm39) probably benign Het
Myt1 G A 2: 181,467,342 (GRCm39) probably benign Het
Ncoa7 T C 10: 30,566,885 (GRCm39) T587A probably benign Het
Nemf T A 12: 69,368,903 (GRCm39) I771F probably damaging Het
Or10k2 T A 8: 84,267,812 (GRCm39) V13D possibly damaging Het
Or5k16 A G 16: 58,736,614 (GRCm39) L130P probably damaging Het
Or8c10 A T 9: 38,278,977 (GRCm39) Y45F probably benign Het
Papln T C 12: 83,827,445 (GRCm39) V761A probably benign Het
Pask A T 1: 93,248,817 (GRCm39) L861* probably null Het
Pcdh18 T A 3: 49,707,896 (GRCm39) R859S probably benign Het
Ppip5k1 C T 2: 121,162,034 (GRCm39) probably null Het
Ptprs A G 17: 56,744,884 (GRCm39) V284A probably damaging Het
Rasgrp4 A T 7: 28,850,928 (GRCm39) probably benign Het
Rp1 T C 1: 4,419,271 (GRCm39) I614V probably benign Het
Sec23ip T C 7: 128,378,640 (GRCm39) I818T probably damaging Het
Skint11 G A 4: 114,051,801 (GRCm39) A50T probably benign Het
Sqor T A 2: 122,650,007 (GRCm39) M417K possibly damaging Het
Tbc1d24 T C 17: 24,426,593 (GRCm39) probably null Het
Tbc1d8b A T X: 138,613,173 (GRCm39) D333V probably damaging Het
Tbx2 T C 11: 85,731,739 (GRCm39) S679P possibly damaging Het
Thbs2 A G 17: 14,904,328 (GRCm39) probably benign Het
Ttn T C 2: 76,689,795 (GRCm39) probably benign Het
Vmn2r28 A T 7: 5,493,568 (GRCm39) I126N probably damaging Het
Zfp426 A C 9: 20,384,414 (GRCm39) probably benign Het
Other mutations in Zbtb10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02174:Zbtb10 APN 3 9,316,872 (GRCm39) missense probably damaging 0.96
IGL02207:Zbtb10 APN 3 9,345,525 (GRCm39) critical splice donor site probably null
IGL02506:Zbtb10 APN 3 9,330,297 (GRCm39) missense probably damaging 0.99
IGL03294:Zbtb10 APN 3 9,346,047 (GRCm39) missense probably benign 0.18
R0510:Zbtb10 UTSW 3 9,329,728 (GRCm39) missense probably damaging 1.00
R1859:Zbtb10 UTSW 3 9,345,446 (GRCm39) missense possibly damaging 0.47
R2342:Zbtb10 UTSW 3 9,330,255 (GRCm39) missense possibly damaging 0.60
R3407:Zbtb10 UTSW 3 9,329,926 (GRCm39) missense probably damaging 1.00
R4161:Zbtb10 UTSW 3 9,345,356 (GRCm39) missense probably damaging 1.00
R4301:Zbtb10 UTSW 3 9,330,220 (GRCm39) missense probably damaging 0.96
R4698:Zbtb10 UTSW 3 9,329,610 (GRCm39) missense possibly damaging 0.87
R5184:Zbtb10 UTSW 3 9,329,731 (GRCm39) missense probably damaging 0.99
R5443:Zbtb10 UTSW 3 9,345,108 (GRCm39) missense probably benign
R5665:Zbtb10 UTSW 3 9,330,252 (GRCm39) missense probably damaging 0.99
R5744:Zbtb10 UTSW 3 9,329,623 (GRCm39) missense probably damaging 1.00
R5862:Zbtb10 UTSW 3 9,330,276 (GRCm39) missense probably damaging 0.98
R5909:Zbtb10 UTSW 3 9,345,109 (GRCm39) missense probably benign 0.14
R6547:Zbtb10 UTSW 3 9,316,763 (GRCm39) missense probably benign 0.38
R6612:Zbtb10 UTSW 3 9,317,125 (GRCm39) missense possibly damaging 0.87
R7457:Zbtb10 UTSW 3 9,316,538 (GRCm39) missense possibly damaging 0.77
R8985:Zbtb10 UTSW 3 9,345,807 (GRCm39) missense probably damaging 1.00
R9191:Zbtb10 UTSW 3 9,330,295 (GRCm39) missense probably damaging 0.98
R9472:Zbtb10 UTSW 3 9,343,355 (GRCm39) missense probably benign 0.25
R9616:Zbtb10 UTSW 3 9,316,473 (GRCm39) missense probably benign 0.01
Z1177:Zbtb10 UTSW 3 9,343,391 (GRCm39) missense probably benign
Posted On 2015-04-16