Incidental Mutation 'R0016:Tasor2'
ID 32713
Institutional Source Beutler Lab
Gene Symbol Tasor2
Ensembl Gene ENSMUSG00000033799
Gene Name transcription activation suppressor family member 2
Synonyms BC016423, Fam208b
MMRRC Submission 038311-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.102) question?
Stock # R0016 (G1)
Quality Score 224
Status Validated (trace)
Chromosome 13
Chromosomal Location 3616035-3661108 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to C at 3635170 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000096069]
AlphaFold Q5DTT3
Predicted Effect possibly damaging
Transcript: ENSMUST00000096069
AA Change: S546A

PolyPhen 2 Score 0.705 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000093774
Gene: ENSMUSG00000033799
AA Change: S546A

DomainStartEndE-ValueType
Pfam:DUF3699 91 167 1.4e-24 PFAM
low complexity region 272 282 N/A INTRINSIC
low complexity region 447 459 N/A INTRINSIC
Pfam:DUF3715 533 695 2.3e-25 PFAM
low complexity region 1156 1168 N/A INTRINSIC
low complexity region 1196 1207 N/A INTRINSIC
low complexity region 1312 1330 N/A INTRINSIC
low complexity region 2012 2021 N/A INTRINSIC
low complexity region 2250 2263 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000222909
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.4%
  • 20x: 93.2%
Validation Efficiency 100% (58/58)
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca12 A C 1: 71,333,959 (GRCm39) V1181G probably benign Het
Adamts12 A T 15: 11,217,915 (GRCm39) I291F probably damaging Het
Aspm G C 1: 139,407,282 (GRCm39) Q2056H probably benign Het
C7 A T 15: 5,076,406 (GRCm39) V122E probably benign Het
Casp12 A T 9: 5,352,844 (GRCm39) Q152L probably null Het
Cdh16 T A 8: 105,344,264 (GRCm39) T92S probably benign Het
Chrd G C 16: 20,553,058 (GRCm39) V162L possibly damaging Het
Cpne8 A G 15: 90,385,608 (GRCm39) probably benign Het
Cspg4b T C 13: 113,502,639 (GRCm39) Y115H probably damaging Het
Cyp2j7 T A 4: 96,090,384 (GRCm39) I347F probably damaging Het
Cyp4a10 A T 4: 115,378,304 (GRCm39) Q130L probably damaging Het
Dach1 C T 14: 98,406,184 (GRCm39) G188R probably damaging Het
Dgkd T C 1: 87,845,674 (GRCm39) S294P probably benign Het
Dnah8 A G 17: 30,882,290 (GRCm39) I621V probably benign Het
Dync2h1 A G 9: 7,144,346 (GRCm39) probably benign Het
Echdc1 A T 10: 29,198,417 (GRCm39) probably benign Het
Elovl3 T A 19: 46,120,597 (GRCm39) F30Y probably damaging Het
Fa2h T C 8: 112,120,146 (GRCm39) Y80C probably damaging Het
Fgd3 C T 13: 49,450,085 (GRCm39) D55N probably benign Het
Fhod1 T C 8: 106,058,287 (GRCm39) E823G possibly damaging Het
Gapvd1 A G 2: 34,589,925 (GRCm39) probably benign Het
Gm17067 A T 7: 42,358,046 (GRCm39) I152K probably benign Het
Gvin3 G A 7: 106,202,453 (GRCm39) L264F probably benign Het
Kif27 A G 13: 58,502,528 (GRCm39) V50A probably damaging Het
Kpna2 T C 11: 106,881,912 (GRCm39) T305A probably benign Het
Krtap22-2 A G 16: 88,807,407 (GRCm39) probably benign Het
Lrp2bp T A 8: 46,465,068 (GRCm39) F62L probably damaging Het
Marf1 G A 16: 13,970,129 (GRCm39) H197Y probably damaging Het
Mob3b A G 4: 35,083,947 (GRCm39) F81L probably benign Het
Mon2 C T 10: 122,871,451 (GRCm39) V389M probably damaging Het
Myef2l A T 3: 10,154,379 (GRCm39) M383L possibly damaging Het
Myh8 A G 11: 67,189,351 (GRCm39) K1176E probably damaging Het
Naf1 T C 8: 67,341,707 (GRCm39) probably benign Het
Nckap1l A G 15: 103,384,063 (GRCm39) T554A probably benign Het
Oog3 A G 4: 143,884,641 (GRCm39) Y432H probably damaging Het
Paxbp1 A T 16: 90,832,924 (GRCm39) probably benign Het
Phf20 A T 2: 156,109,114 (GRCm39) K154* probably null Het
Pip4p1 C T 14: 51,166,351 (GRCm39) R213Q probably damaging Het
Plekhj1 T C 10: 80,632,250 (GRCm39) D74G possibly damaging Het
Plpp4 T C 7: 128,925,148 (GRCm39) C128R probably damaging Het
Rcan3 A T 4: 135,145,689 (GRCm39) probably null Het
Sh3rf1 T A 8: 61,827,172 (GRCm39) M642K probably benign Het
Slc7a1 A G 5: 148,271,393 (GRCm39) V522A probably benign Het
Sorbs1 A G 19: 40,303,182 (GRCm39) probably benign Het
Spry2 C T 14: 106,130,731 (GRCm39) V152M probably benign Het
Srgap2 A G 1: 131,277,200 (GRCm39) M349T possibly damaging Het
Stag3 A G 5: 138,289,643 (GRCm39) H271R possibly damaging Het
Stat4 T C 1: 52,107,939 (GRCm39) V136A probably benign Het
Stc2 A T 11: 31,310,177 (GRCm39) D286E probably benign Het
Stk31 T C 6: 49,414,311 (GRCm39) Y482H probably damaging Het
Ticrr C T 7: 79,343,540 (GRCm39) P1135L probably benign Het
Trim27 A T 13: 21,375,399 (GRCm39) E310V probably benign Het
Uvrag T C 7: 98,641,188 (GRCm39) K284R probably benign Het
Vmn1r78 A C 7: 11,887,279 (GRCm39) S297R probably benign Het
Xylt2 A G 11: 94,560,466 (GRCm39) S270P probably damaging Het
Zfhx3 T C 8: 109,676,810 (GRCm39) M2620T probably benign Het
Zkscan2 C A 7: 123,099,219 (GRCm39) probably benign Het
Zwint T C 10: 72,493,030 (GRCm39) probably benign Het
Other mutations in Tasor2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00330:Tasor2 APN 13 3,624,832 (GRCm39) missense probably benign
IGL00670:Tasor2 APN 13 3,635,241 (GRCm39) missense probably benign 0.14
IGL00957:Tasor2 APN 13 3,627,101 (GRCm39) missense possibly damaging 0.86
IGL01311:Tasor2 APN 13 3,625,885 (GRCm39) missense possibly damaging 0.85
IGL01318:Tasor2 APN 13 3,625,067 (GRCm39) missense possibly damaging 0.66
IGL01767:Tasor2 APN 13 3,626,633 (GRCm39) missense probably benign 0.00
IGL02073:Tasor2 APN 13 3,624,721 (GRCm39) missense probably benign 0.01
IGL02152:Tasor2 APN 13 3,635,371 (GRCm39) missense probably benign
IGL02431:Tasor2 APN 13 3,624,736 (GRCm39) missense possibly damaging 0.85
IGL02478:Tasor2 APN 13 3,624,661 (GRCm39) missense probably benign 0.12
IGL02732:Tasor2 APN 13 3,623,626 (GRCm39) missense probably benign 0.09
IGL02745:Tasor2 APN 13 3,635,140 (GRCm39) missense probably benign 0.23
IGL02800:Tasor2 APN 13 3,635,154 (GRCm39) missense probably benign
IGL02989:Tasor2 APN 13 3,634,820 (GRCm39) missense probably benign 0.01
IGL03124:Tasor2 APN 13 3,624,704 (GRCm39) missense probably benign 0.41
IGL03154:Tasor2 APN 13 3,625,255 (GRCm39) missense possibly damaging 0.56
IGL03216:Tasor2 APN 13 3,624,553 (GRCm39) missense probably damaging 0.98
BB001:Tasor2 UTSW 13 3,644,331 (GRCm39) missense possibly damaging 0.92
BB011:Tasor2 UTSW 13 3,644,331 (GRCm39) missense possibly damaging 0.92
H8562:Tasor2 UTSW 13 3,627,000 (GRCm39) missense probably damaging 0.98
PIT4585001:Tasor2 UTSW 13 3,624,979 (GRCm39) missense possibly damaging 0.55
R0016:Tasor2 UTSW 13 3,635,170 (GRCm39) splice site probably null
R0157:Tasor2 UTSW 13 3,625,550 (GRCm39) missense probably benign 0.06
R0375:Tasor2 UTSW 13 3,646,842 (GRCm39) missense possibly damaging 0.85
R0403:Tasor2 UTSW 13 3,632,052 (GRCm39) nonsense probably null
R0472:Tasor2 UTSW 13 3,638,364 (GRCm39) missense possibly damaging 0.93
R0517:Tasor2 UTSW 13 3,616,964 (GRCm39) missense possibly damaging 0.94
R0586:Tasor2 UTSW 13 3,640,321 (GRCm39) missense probably damaging 0.99
R0600:Tasor2 UTSW 13 3,626,054 (GRCm39) missense probably benign
R0659:Tasor2 UTSW 13 3,624,448 (GRCm39) missense probably damaging 0.99
R1257:Tasor2 UTSW 13 3,625,049 (GRCm39) missense probably benign 0.25
R1375:Tasor2 UTSW 13 3,626,029 (GRCm39) missense probably benign 0.06
R1443:Tasor2 UTSW 13 3,625,543 (GRCm39) missense probably benign 0.00
R1497:Tasor2 UTSW 13 3,620,409 (GRCm39) missense probably damaging 0.96
R1544:Tasor2 UTSW 13 3,640,413 (GRCm39) missense possibly damaging 0.68
R1554:Tasor2 UTSW 13 3,626,374 (GRCm39) missense possibly damaging 0.85
R1629:Tasor2 UTSW 13 3,624,121 (GRCm39) missense possibly damaging 0.84
R1633:Tasor2 UTSW 13 3,631,771 (GRCm39) missense possibly damaging 0.53
R1661:Tasor2 UTSW 13 3,623,860 (GRCm39) missense possibly damaging 0.63
R1673:Tasor2 UTSW 13 3,634,498 (GRCm39) critical splice donor site probably null
R1675:Tasor2 UTSW 13 3,619,507 (GRCm39) missense possibly damaging 0.65
R1781:Tasor2 UTSW 13 3,634,759 (GRCm39) missense possibly damaging 0.95
R1792:Tasor2 UTSW 13 3,640,559 (GRCm39) missense possibly damaging 0.91
R1826:Tasor2 UTSW 13 3,631,759 (GRCm39) missense probably damaging 0.98
R1920:Tasor2 UTSW 13 3,626,612 (GRCm39) missense possibly damaging 0.63
R1983:Tasor2 UTSW 13 3,624,853 (GRCm39) missense possibly damaging 0.92
R2016:Tasor2 UTSW 13 3,626,770 (GRCm39) missense probably benign 0.41
R2017:Tasor2 UTSW 13 3,626,770 (GRCm39) missense probably benign 0.41
R2220:Tasor2 UTSW 13 3,631,872 (GRCm39) missense probably benign 0.00
R2513:Tasor2 UTSW 13 3,632,150 (GRCm39) missense possibly damaging 0.53
R2898:Tasor2 UTSW 13 3,635,122 (GRCm39) missense possibly damaging 0.82
R2904:Tasor2 UTSW 13 3,632,185 (GRCm39) missense possibly damaging 0.53
R3149:Tasor2 UTSW 13 3,624,359 (GRCm39) missense probably damaging 0.98
R3623:Tasor2 UTSW 13 3,645,556 (GRCm39) missense probably benign
R3624:Tasor2 UTSW 13 3,645,556 (GRCm39) missense probably benign
R3725:Tasor2 UTSW 13 3,640,538 (GRCm39) missense probably benign 0.33
R3835:Tasor2 UTSW 13 3,625,292 (GRCm39) missense probably benign 0.01
R3890:Tasor2 UTSW 13 3,646,785 (GRCm39) missense probably damaging 0.96
R4023:Tasor2 UTSW 13 3,634,554 (GRCm39) missense probably damaging 0.99
R4024:Tasor2 UTSW 13 3,634,554 (GRCm39) missense probably damaging 0.99
R4025:Tasor2 UTSW 13 3,634,554 (GRCm39) missense probably damaging 0.99
R4050:Tasor2 UTSW 13 3,623,507 (GRCm39) missense probably benign 0.09
R4308:Tasor2 UTSW 13 3,619,498 (GRCm39) missense probably damaging 0.97
R4484:Tasor2 UTSW 13 3,631,831 (GRCm39) missense probably benign 0.12
R4674:Tasor2 UTSW 13 3,623,686 (GRCm39) missense possibly damaging 0.69
R4718:Tasor2 UTSW 13 3,624,495 (GRCm39) missense probably benign 0.00
R4745:Tasor2 UTSW 13 3,640,069 (GRCm39) missense probably benign 0.26
R4776:Tasor2 UTSW 13 3,620,391 (GRCm39) missense probably damaging 1.00
R4839:Tasor2 UTSW 13 3,634,807 (GRCm39) missense probably damaging 0.96
R4855:Tasor2 UTSW 13 3,616,680 (GRCm39) splice site probably null
R5049:Tasor2 UTSW 13 3,624,000 (GRCm39) missense probably benign 0.00
R5076:Tasor2 UTSW 13 3,626,357 (GRCm39) missense probably benign 0.41
R5287:Tasor2 UTSW 13 3,625,744 (GRCm39) missense probably benign 0.41
R5298:Tasor2 UTSW 13 3,645,613 (GRCm39) splice site probably null
R5379:Tasor2 UTSW 13 3,638,496 (GRCm39) missense probably benign 0.41
R5512:Tasor2 UTSW 13 3,645,517 (GRCm39) missense probably damaging 0.99
R5624:Tasor2 UTSW 13 3,634,996 (GRCm39) missense possibly damaging 0.66
R5750:Tasor2 UTSW 13 3,623,642 (GRCm39) nonsense probably null
R6114:Tasor2 UTSW 13 3,640,081 (GRCm39) missense probably damaging 1.00
R6118:Tasor2 UTSW 13 3,631,891 (GRCm39) missense possibly damaging 0.76
R6119:Tasor2 UTSW 13 3,631,891 (GRCm39) missense possibly damaging 0.76
R6269:Tasor2 UTSW 13 3,631,891 (GRCm39) missense possibly damaging 0.76
R6270:Tasor2 UTSW 13 3,631,891 (GRCm39) missense possibly damaging 0.76
R6271:Tasor2 UTSW 13 3,631,891 (GRCm39) missense possibly damaging 0.76
R6272:Tasor2 UTSW 13 3,631,891 (GRCm39) missense possibly damaging 0.76
R6525:Tasor2 UTSW 13 3,626,540 (GRCm39) nonsense probably null
R6550:Tasor2 UTSW 13 3,640,519 (GRCm39) missense possibly damaging 0.85
R6714:Tasor2 UTSW 13 3,644,189 (GRCm39) missense probably benign 0.00
R6797:Tasor2 UTSW 13 3,626,769 (GRCm39) missense probably benign 0.26
R6967:Tasor2 UTSW 13 3,624,819 (GRCm39) missense probably benign 0.22
R7016:Tasor2 UTSW 13 3,626,857 (GRCm39) missense possibly damaging 0.92
R7219:Tasor2 UTSW 13 3,640,521 (GRCm39) missense probably damaging 0.99
R7454:Tasor2 UTSW 13 3,635,332 (GRCm39) missense probably benign 0.21
R7570:Tasor2 UTSW 13 3,623,621 (GRCm39) missense probably damaging 0.99
R7571:Tasor2 UTSW 13 3,625,292 (GRCm39) missense probably benign 0.01
R7580:Tasor2 UTSW 13 3,624,752 (GRCm39) missense probably damaging 0.99
R7587:Tasor2 UTSW 13 3,618,849 (GRCm39) missense possibly damaging 0.83
R7657:Tasor2 UTSW 13 3,623,777 (GRCm39) missense probably damaging 0.98
R7810:Tasor2 UTSW 13 3,625,714 (GRCm39) missense possibly damaging 0.61
R7909:Tasor2 UTSW 13 3,623,765 (GRCm39) missense possibly damaging 0.93
R7924:Tasor2 UTSW 13 3,644,331 (GRCm39) missense possibly damaging 0.92
R7945:Tasor2 UTSW 13 3,626,085 (GRCm39) missense probably benign
R8005:Tasor2 UTSW 13 3,625,681 (GRCm39) missense probably benign
R8067:Tasor2 UTSW 13 3,619,602 (GRCm39) missense probably benign
R8112:Tasor2 UTSW 13 3,619,516 (GRCm39) missense probably damaging 1.00
R8162:Tasor2 UTSW 13 3,649,691 (GRCm39) missense probably damaging 0.96
R8170:Tasor2 UTSW 13 3,624,881 (GRCm39) nonsense probably null
R8240:Tasor2 UTSW 13 3,624,388 (GRCm39) missense probably benign
R8263:Tasor2 UTSW 13 3,640,016 (GRCm39) missense probably benign 0.03
R8263:Tasor2 UTSW 13 3,625,286 (GRCm39) missense possibly damaging 0.70
R8477:Tasor2 UTSW 13 3,625,079 (GRCm39) missense probably benign 0.18
R9022:Tasor2 UTSW 13 3,626,659 (GRCm39) missense probably benign
R9140:Tasor2 UTSW 13 3,638,441 (GRCm39) missense probably benign 0.04
R9167:Tasor2 UTSW 13 3,624,724 (GRCm39) missense probably benign
R9527:Tasor2 UTSW 13 3,635,191 (GRCm39) missense possibly damaging 0.61
R9535:Tasor2 UTSW 13 3,623,559 (GRCm39) missense possibly damaging 0.69
R9711:Tasor2 UTSW 13 3,649,667 (GRCm39) missense probably benign
X0024:Tasor2 UTSW 13 3,649,837 (GRCm39) missense probably null 0.99
X0025:Tasor2 UTSW 13 3,626,827 (GRCm39) missense probably benign 0.15
X0066:Tasor2 UTSW 13 3,638,441 (GRCm39) missense probably benign 0.04
Z1176:Tasor2 UTSW 13 3,638,429 (GRCm39) missense probably damaging 0.98
Z1176:Tasor2 UTSW 13 3,626,636 (GRCm39) missense probably benign 0.01
Z1177:Tasor2 UTSW 13 3,624,234 (GRCm39) missense probably damaging 0.96
Predicted Primers PCR Primer
(F):5'- AGTTCTGACTTGCATCTGACAATTCCC -3'
(R):5'- TTGTAAGCACATTGAGGACACTCTGG -3'

Sequencing Primer
(F):5'- CGCGTTAAATCTGACTCTGAAC -3'
(R):5'- CACATTGAGGACACTCTGGTATTTTG -3'
Posted On 2013-05-09