Incidental Mutation 'R6119:Tasor2'
ID 485679
Institutional Source Beutler Lab
Gene Symbol Tasor2
Ensembl Gene ENSMUSG00000033799
Gene Name transcription activation suppressor family member 2
Synonyms BC016423, Fam208b
MMRRC Submission 044429-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.102) question?
Stock # R6119 (G1)
Quality Score 225.009
Status Not validated
Chromosome 13
Chromosomal Location 3616035-3661108 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 3631891 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Histidine at position 870 (R870H)
Ref Sequence ENSEMBL: ENSMUSP00000093774 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000096069]
AlphaFold Q5DTT3
Predicted Effect possibly damaging
Transcript: ENSMUST00000096069
AA Change: R870H

PolyPhen 2 Score 0.759 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000093774
Gene: ENSMUSG00000033799
AA Change: R870H

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 benign
Transcript: ENSMUST00000222909
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.5%
  • 10x: 97.7%
  • 20x: 93.2%
Validation Efficiency 100% (53/53)
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310022A10Rik C T 7: 27,265,138 (GRCm39) R97* probably null Het
4930544D05Rik G A 11: 70,507,317 (GRCm39) A121T probably damaging Het
Abtb2 A T 2: 103,532,655 (GRCm39) E484D probably benign Het
Ankk1 A T 9: 49,338,183 (GRCm39) W37R possibly damaging Het
Arhgap11a C A 2: 113,664,695 (GRCm39) M529I probably benign Het
Btd G A 14: 31,363,065 (GRCm39) probably benign Het
Ddx47 T C 6: 135,000,318 (GRCm39) I438T probably benign Het
Dnhd1 A G 7: 105,358,647 (GRCm39) T3379A probably benign Het
Dusp3 A G 11: 101,871,495 (GRCm39) probably benign Het
Dync1h1 A G 12: 110,594,440 (GRCm39) K1289E possibly damaging Het
Egf A T 3: 129,530,421 (GRCm39) I247N probably benign Het
Erich1 A G 8: 14,083,692 (GRCm39) L126P probably benign Het
Fat3 T A 9: 16,287,864 (GRCm39) H553L possibly damaging Het
Gdpgp1 T C 7: 79,888,740 (GRCm39) L257P probably damaging Het
Gimap8 T C 6: 48,635,888 (GRCm39) I551T possibly damaging Het
Gnptab C A 10: 88,267,257 (GRCm39) D449E probably damaging Het
Grb10 T C 11: 11,883,551 (GRCm39) D513G probably damaging Het
Grin1 T G 2: 25,195,170 (GRCm39) D283A probably damaging Het
Gtf2i A T 5: 134,315,911 (GRCm39) probably null Het
Ip6k3 A G 17: 27,367,599 (GRCm39) V199A possibly damaging Het
Kif17 T A 4: 138,015,643 (GRCm39) Y405* probably null Het
Lair1 T C 7: 4,031,895 (GRCm39) M71V probably benign Het
Mamdc2 G A 19: 23,330,679 (GRCm39) T376M probably damaging Het
Msra G A 14: 64,678,183 (GRCm39) R38C probably damaging Het
Mthfd1 A T 12: 76,350,447 (GRCm39) I462F probably damaging Het
Nbr1 A G 11: 101,457,938 (GRCm39) probably null Het
Neb A G 2: 52,110,943 (GRCm39) M181T probably benign Het
Noxo1 A G 17: 24,915,545 (GRCm39) probably benign Het
Optn C A 2: 5,026,134 (GRCm39) probably null Het
Or10ag58 A T 2: 87,265,733 (GRCm39) K301* probably null Het
Or4c103 A G 2: 88,513,935 (GRCm39) I47T probably damaging Het
Or5k17 A T 16: 58,746,895 (GRCm39) I13N possibly damaging Het
Or6c215 G A 10: 129,637,689 (GRCm39) A235V probably damaging Het
Or6c215 C A 10: 129,637,690 (GRCm39) A235S probably damaging Het
Pclo A G 5: 14,727,033 (GRCm39) probably benign Het
Ppp1r16b A G 2: 158,593,047 (GRCm39) I209V probably benign Het
Prss12 A G 3: 123,283,258 (GRCm39) I517V possibly damaging Het
Pwwp3a A G 10: 80,064,865 (GRCm39) K32E probably benign Het
Ripor2 C T 13: 24,798,627 (GRCm39) probably benign Het
Rmnd5b A G 11: 51,516,536 (GRCm39) S274P probably benign Het
Sftpa1 T A 14: 40,854,509 (GRCm39) I32N probably damaging Het
Slc2a12 T A 10: 22,541,246 (GRCm39) I367N probably damaging Het
Sorcs1 T C 19: 50,276,532 (GRCm39) D340G probably damaging Het
Synj1 T C 16: 90,735,877 (GRCm39) K1359E probably benign Het
Tcf12 T A 9: 71,775,547 (GRCm39) E421V probably damaging Het
Tecta A T 9: 42,284,371 (GRCm39) F905I probably benign Het
Tmem106a T A 11: 101,474,576 (GRCm39) C58* probably null Het
Tmem131l A T 3: 83,805,689 (GRCm39) F1585I probably damaging Het
Tnks2 T C 19: 36,856,752 (GRCm39) S208P possibly damaging Het
Trim50 A G 5: 135,382,274 (GRCm39) N42S probably benign Het
Tsc22d2 T A 3: 58,367,674 (GRCm39) probably benign Het
Ttll3 T A 6: 113,371,702 (GRCm39) L23H probably damaging Het
Vmn1r10 A G 6: 57,091,218 (GRCm39) Y270C probably benign Het
Ypel3 T C 7: 126,377,537 (GRCm39) V74A possibly damaging Het
Zfp677 A G 17: 21,618,070 (GRCm39) T376A possibly damaging 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
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
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
Posted On 2017-08-16