Incidental Mutation 'R4050:Zbtb26'
ID 314086
Institutional Source Beutler Lab
Gene Symbol Zbtb26
Ensembl Gene ENSMUSG00000050714
Gene Name zinc finger and BTB domain containing 26
Synonyms A630026F21Rik
MMRRC Submission 040968-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.365) question?
Stock # R4050 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 37322180-37333147 bp(-) (GRCm39)
Type of Mutation start codon destroyed
DNA Base Change (assembly) A to C at 37327000 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Arginine at position 1 (M1R)
Ref Sequence ENSEMBL: ENSMUSP00000070071 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000067043] [ENSMUST00000102789] [ENSMUST00000112932]
AlphaFold Q8C8S0
Predicted Effect probably null
Transcript: ENSMUST00000067043
AA Change: M1R

PolyPhen 2 Score 0.457 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000070071
Gene: ENSMUSG00000050714
AA Change: M1R

DomainStartEndE-ValueType
BTB 33 127 4.38e-12 SMART
low complexity region 169 179 N/A INTRINSIC
ZnF_C2H2 273 295 1.36e-2 SMART
ZnF_C2H2 298 320 1.4e-4 SMART
ZnF_C2H2 326 348 2.99e-4 SMART
ZnF_C2H2 354 377 2.09e-3 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000102789
AA Change: M12R

PolyPhen 2 Score 0.720 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000099850
Gene: ENSMUSG00000050714
AA Change: M12R

DomainStartEndE-ValueType
BTB 44 138 4.38e-12 SMART
low complexity region 180 190 N/A INTRINSIC
ZnF_C2H2 284 306 1.36e-2 SMART
ZnF_C2H2 309 331 1.4e-4 SMART
ZnF_C2H2 337 359 2.99e-4 SMART
ZnF_C2H2 365 388 2.09e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000112932
SMART Domains Protein: ENSMUSP00000108554
Gene: ENSMUSG00000066798

DomainStartEndE-ValueType
BTB 33 127 2.67e-16 SMART
Blast:BTB 161 196 1e-5 BLAST
ZnF_C2H2 300 322 7.15e-2 SMART
ZnF_C2H2 325 347 1.58e-3 SMART
ZnF_C2H2 353 375 3.63e-3 SMART
ZnF_C2H2 381 404 8.81e-2 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203522
Meta Mutation Damage Score 0.9694 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.5%
Validation Efficiency 97% (58/60)
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2510039O18Rik A G 4: 148,029,449 (GRCm39) D473G probably damaging Het
Abca1 T A 4: 53,044,144 (GRCm39) Q1826L probably damaging Het
Apob G A 12: 8,065,390 (GRCm39) V4087I probably benign Het
Atp10b G A 11: 43,150,363 (GRCm39) A1354T probably benign Het
Baz1a A G 12: 54,976,404 (GRCm39) V424A probably benign Het
Cdc20b G A 13: 113,200,819 (GRCm39) D180N probably benign Het
Cep57l1 G T 10: 41,605,356 (GRCm39) R130S probably damaging Het
Ddb1 A G 19: 10,605,171 (GRCm39) D1053G probably benign Het
Ddx39a T A 8: 84,448,863 (GRCm39) M246K probably benign Het
Dip2a G A 10: 76,114,441 (GRCm39) T1013M probably damaging Het
Edar G T 10: 58,445,769 (GRCm39) T265N possibly damaging Het
Fcgbpl1 T C 7: 27,852,410 (GRCm39) V1311A possibly damaging Het
Gbp8 T A 5: 105,179,104 (GRCm39) I132F probably damaging Het
Gga1 A G 15: 78,775,691 (GRCm39) D382G probably benign Het
Ggps1 T C 13: 14,228,284 (GRCm39) K300E probably benign Het
Gm10518 C A 1: 179,631,378 (GRCm39) probably benign Het
Gm8074 G A 9: 78,229,618 (GRCm39) noncoding transcript Het
H2-Eb1 T A 17: 34,533,342 (GRCm39) L188Q probably damaging Het
Heatr6 A G 11: 83,646,599 (GRCm39) S95G probably damaging Het
Hnf1a T A 5: 115,108,633 (GRCm39) N91Y probably damaging Het
Ints10 C T 8: 69,280,003 (GRCm39) S710F probably damaging Het
Kazn C T 4: 141,834,215 (GRCm39) E614K unknown Het
Kif26a T A 12: 112,146,350 (GRCm39) M1812K probably benign Het
Lmo7 A T 14: 102,139,713 (GRCm39) K488* probably null Het
Mad1l1 A G 5: 140,118,571 (GRCm39) S457P probably damaging Het
Met A G 6: 17,533,983 (GRCm39) T645A probably benign Het
Mpp4 T C 1: 59,185,903 (GRCm39) probably null Het
Mycl A T 4: 122,890,632 (GRCm39) probably null Het
Ncbp1 G A 4: 46,147,483 (GRCm39) R110H probably damaging Het
Nfasc G T 1: 132,538,043 (GRCm39) probably benign Het
Nup35 A G 2: 80,486,320 (GRCm39) I212V probably benign Het
Or2y8 T G 11: 52,035,961 (GRCm39) Y132S probably damaging Het
Or4p20 A G 2: 88,253,967 (GRCm39) M134T probably damaging Het
Ovgp1 T C 3: 105,893,883 (GRCm39) probably benign Het
Ovgp1 A G 3: 105,893,912 (GRCm39) probably benign Het
Pcgf5 G A 19: 36,420,311 (GRCm39) S181N probably damaging Het
Plk2 C T 13: 110,536,400 (GRCm39) T617I probably damaging Het
Polq A T 16: 36,913,182 (GRCm39) probably null Het
Ppp1r1a A G 15: 103,440,881 (GRCm39) L92P probably damaging Het
Pramel24 T C 4: 143,453,692 (GRCm39) S267P probably benign Het
Prg4 G C 1: 150,330,510 (GRCm39) probably benign Het
Prune1 T C 3: 95,169,542 (GRCm39) K220R possibly damaging Het
Rab3gap2 G A 1: 185,004,840 (GRCm39) probably null Het
Rufy4 T C 1: 74,186,822 (GRCm39) C537R probably damaging Het
Sall3 G A 18: 81,014,697 (GRCm39) A1005V probably benign Het
Samd15 T G 12: 87,247,406 (GRCm39) N30K probably benign Het
Scn8a A T 15: 100,911,294 (GRCm39) K905* probably null Het
Scrib G A 15: 75,923,322 (GRCm39) R1245W possibly damaging Het
Skint4 C T 4: 111,981,811 (GRCm39) S260L probably benign Het
Slc29a2 A T 19: 5,079,481 (GRCm39) M339L possibly damaging Het
Slx9 T C 10: 77,350,164 (GRCm39) R75G possibly damaging Het
Spire1 G T 18: 67,662,101 (GRCm39) probably null Het
Synpo2 T C 3: 122,907,927 (GRCm39) D463G possibly damaging Het
Taf4 C A 2: 179,573,805 (GRCm39) G688C probably damaging Het
Tasor2 A G 13: 3,623,507 (GRCm39) S2148P probably benign Het
Tpte T A 8: 22,856,000 (GRCm39) V600E probably damaging Het
Ttn A G 2: 76,651,510 (GRCm39) V10953A probably benign Het
Vav2 T C 2: 27,178,691 (GRCm39) Y333C probably benign Het
Vav2 A G 2: 27,181,415 (GRCm39) S311P probably damaging Het
Zfp26 G A 9: 20,353,525 (GRCm39) P88L probably benign Het
Zfp324 T C 7: 12,704,794 (GRCm39) F328L probably damaging Het
Other mutations in Zbtb26
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00579:Zbtb26 APN 2 37,326,454 (GRCm39) missense possibly damaging 0.82
IGL00899:Zbtb26 APN 2 37,326,270 (GRCm39) nonsense probably null
IGL01598:Zbtb26 APN 2 37,326,283 (GRCm39) missense probably damaging 1.00
IGL01940:Zbtb26 APN 2 37,325,987 (GRCm39) missense possibly damaging 0.93
IGL02152:Zbtb26 APN 2 37,326,703 (GRCm39) missense possibly damaging 0.95
IGL02867:Zbtb26 APN 2 37,326,261 (GRCm39) missense probably benign 0.00
IGL02889:Zbtb26 APN 2 37,326,261 (GRCm39) missense probably benign 0.00
IGL03081:Zbtb26 APN 2 37,326,612 (GRCm39) missense possibly damaging 0.67
R0138:Zbtb26 UTSW 2 37,326,053 (GRCm39) missense probably benign 0.16
R0328:Zbtb26 UTSW 2 37,326,807 (GRCm39) missense possibly damaging 0.81
R0927:Zbtb26 UTSW 2 37,326,337 (GRCm39) missense possibly damaging 0.91
R1671:Zbtb26 UTSW 2 37,326,377 (GRCm39) missense probably benign 0.00
R1813:Zbtb26 UTSW 2 37,326,347 (GRCm39) missense possibly damaging 0.68
R1896:Zbtb26 UTSW 2 37,326,347 (GRCm39) missense possibly damaging 0.68
R2128:Zbtb26 UTSW 2 37,326,563 (GRCm39) missense probably benign 0.00
R2374:Zbtb26 UTSW 2 37,326,497 (GRCm39) missense probably benign
R4631:Zbtb26 UTSW 2 37,326,968 (GRCm39) missense probably benign 0.00
R4940:Zbtb26 UTSW 2 37,326,781 (GRCm39) missense probably damaging 0.98
R5071:Zbtb26 UTSW 2 37,325,941 (GRCm39) missense probably benign 0.26
R6348:Zbtb26 UTSW 2 37,325,687 (GRCm39) missense probably benign 0.43
R6962:Zbtb26 UTSW 2 37,326,106 (GRCm39) missense possibly damaging 0.71
R6990:Zbtb26 UTSW 2 37,326,557 (GRCm39) missense probably benign 0.00
R7261:Zbtb26 UTSW 2 37,326,667 (GRCm39) missense possibly damaging 0.71
R7981:Zbtb26 UTSW 2 37,326,887 (GRCm39) missense possibly damaging 0.51
R8013:Zbtb26 UTSW 2 37,327,013 (GRCm39) critical splice acceptor site probably null
R8014:Zbtb26 UTSW 2 37,327,013 (GRCm39) critical splice acceptor site probably null
R8872:Zbtb26 UTSW 2 37,326,913 (GRCm39) missense probably damaging 0.99
R8876:Zbtb26 UTSW 2 37,326,896 (GRCm39) missense probably benign
R8905:Zbtb26 UTSW 2 37,326,927 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TTCACCTCTCGGGAATCATTCAG -3'
(R):5'- GGTACAGTTGACACCTGTTAATGG -3'

Sequencing Primer
(F):5'- CTCGGGAATCATTCAGTAAAAACTGG -3'
(R):5'- TGGTAAGAAATAACTTTTAGCAGCC -3'
Posted On 2015-04-30