Incidental Mutation 'IGL02152:Tasor2'
ID 282057
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tasor2
Ensembl Gene ENSMUSG00000033799
Gene Name transcription activation suppressor family member 2
Synonyms BC016423, Fam208b
Accession Numbers
Essential gene? Probably non essential (E-score: 0.102) question?
Stock # IGL02152
Quality Score
Status
Chromosome 13
Chromosomal Location 3616035-3661108 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 3635371 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Lysine at position 479 (E479K)
Ref Sequence ENSEMBL: ENSMUSP00000093774 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000096069]
AlphaFold Q5DTT3
Predicted Effect probably benign
Transcript: ENSMUST00000096069
AA Change: E479K

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000093774
Gene: ENSMUSG00000033799
AA Change: E479K

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
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700028K03Rik A G 5: 107,695,983 (GRCm39) T140A probably benign Het
4933430I17Rik T C 4: 62,460,991 (GRCm39) Y289H possibly damaging Het
Adamts17 T A 7: 66,774,748 (GRCm39) S956T probably benign Het
Adamts6 A T 13: 104,450,168 (GRCm39) S290C probably null Het
Apaf1 A T 10: 90,897,681 (GRCm39) H267Q probably benign Het
Aplp2 G A 9: 31,122,947 (GRCm39) P26L unknown Het
Arid1b C T 17: 5,364,243 (GRCm39) S1019F probably damaging Het
Armc3 G A 2: 19,290,948 (GRCm39) probably null Het
Ass1 T C 2: 31,382,336 (GRCm39) I169T probably damaging Het
Ccser1 A G 6: 61,288,692 (GRCm39) D285G possibly damaging Het
Cenpf A G 1: 189,381,209 (GRCm39) V2737A probably benign Het
Chrm5 A G 2: 112,310,913 (GRCm39) Y68H probably damaging Het
Cops4 A G 5: 100,681,456 (GRCm39) T164A probably benign Het
Cox4i1 A G 8: 121,399,604 (GRCm39) S72G probably benign Het
Cpox A G 16: 58,494,787 (GRCm39) T275A possibly damaging Het
Cyb5a T C 18: 84,891,281 (GRCm39) I68T probably benign Het
Efna5 T C 17: 62,958,055 (GRCm39) D67G probably benign Het
Enpp3 T C 10: 24,649,900 (GRCm39) E842G probably damaging Het
Fam210b A G 2: 172,193,423 (GRCm39) K79E probably benign Het
Gm4799 T C 10: 82,790,589 (GRCm39) noncoding transcript Het
Gpr146 A T 5: 139,378,467 (GRCm39) R90W probably damaging Het
H2ac10 A G 13: 23,718,451 (GRCm39) H124R probably benign Het
Hal A G 10: 93,339,404 (GRCm39) I498V possibly damaging Het
Hnrnpm C T 17: 33,877,386 (GRCm39) G365R probably damaging Het
Jakmip3 A G 7: 138,627,217 (GRCm39) D407G probably damaging Het
Kank1 A G 19: 25,405,536 (GRCm39) I1185V possibly damaging Het
Kcnj16 A T 11: 110,916,036 (GRCm39) M233L probably benign Het
Klhl5 A T 5: 65,306,143 (GRCm39) Q370L probably damaging Het
L3hypdh C T 12: 72,123,917 (GRCm39) probably null Het
Las1l A G X: 94,996,908 (GRCm39) V130A probably damaging Het
Liat1 A G 11: 75,894,051 (GRCm39) I143V probably benign Het
Lrp2bp A T 8: 46,476,081 (GRCm39) Y274F probably damaging Het
Morc2b T A 17: 33,356,917 (GRCm39) K285M probably damaging Het
Mpp3 A T 11: 101,916,216 (GRCm39) Y45* probably null Het
Muc4 T A 16: 32,598,023 (GRCm39) probably benign Het
Muc5ac T C 7: 141,353,914 (GRCm39) C837R possibly damaging Het
Nr2f6 T A 8: 71,828,810 (GRCm39) I155F probably damaging Het
Nsg1 A G 5: 38,302,145 (GRCm39) F50L probably benign Het
Or14a258 T A 7: 86,035,251 (GRCm39) M206L probably benign Het
Ostf1 C A 19: 18,567,822 (GRCm39) G101C probably damaging Het
Pam C T 1: 97,768,474 (GRCm39) R552Q probably damaging Het
Pkd1l3 A G 8: 110,395,924 (GRCm39) N2108S probably damaging Het
Prkdc A T 16: 15,487,149 (GRCm39) H484L probably benign Het
Pwwp3a A G 10: 80,075,812 (GRCm39) D466G probably damaging Het
Rfx5 G A 3: 94,864,493 (GRCm39) R213Q probably damaging Het
Ryr1 T C 7: 28,751,440 (GRCm39) S3715G possibly damaging Het
Sall2 A G 14: 52,552,971 (GRCm39) S73P probably damaging Het
Sec22c G A 9: 121,513,845 (GRCm39) A264V probably benign Het
Sis A C 3: 72,796,319 (GRCm39) probably benign Het
Spam1 T A 6: 24,800,802 (GRCm39) probably benign Het
Spmip2 T C 3: 79,252,839 (GRCm39) I18T possibly damaging Het
St13 T A 15: 81,250,583 (GRCm39) I318F probably damaging Het
Syne1 T C 10: 5,374,382 (GRCm39) I142V probably damaging Het
Trpm6 A T 19: 18,809,903 (GRCm39) T1100S possibly damaging Het
Ttll6 G A 11: 96,026,366 (GRCm39) W90* probably null Het
Txndc12 T A 4: 108,691,989 (GRCm39) C9* probably null Het
Ubr7 C T 12: 102,734,535 (GRCm39) Q270* probably null Het
Vps33b A G 7: 79,934,817 (GRCm39) S302G probably benign Het
Xylt1 T A 7: 117,233,997 (GRCm39) V508E probably damaging Het
Zbtb26 A T 2: 37,326,703 (GRCm39) L111Q possibly damaging Het
Zfp410 T C 12: 84,379,702 (GRCm39) probably benign Het
Zscan18 A T 7: 12,509,223 (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
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
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
Posted On 2015-04-16