Incidental Mutation 'IGL01351:Tasor'
ID 75365
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tasor
Ensembl Gene ENSMUSG00000040651
Gene Name transcription activation suppressor
Synonyms D14Abb1e, Fam208a, 4933409E02Rik, MommeD6
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # IGL01351
Quality Score
Status
Chromosome 14
Chromosomal Location 27150791-27205512 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 27186258 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 819 (E819G)
Ref Sequence ENSEMBL: ENSMUSP00000022450 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022450]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000022450
AA Change: E819G

PolyPhen 2 Score 0.017 (Sensitivity: 0.95; Specificity: 0.80)
SMART Domains Protein: ENSMUSP00000022450
Gene: ENSMUSG00000040651
AA Change: E819G

DomainStartEndE-ValueType
low complexity region 20 27 N/A INTRINSIC
low complexity region 42 61 N/A INTRINSIC
low complexity region 74 88 N/A INTRINSIC
Pfam:DUF3715 153 314 1.5e-55 PFAM
low complexity region 442 457 N/A INTRINSIC
low complexity region 1087 1102 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223688
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for ENU mutations are not viable past gastrulation. [provided by MGI curators]
Allele List at MGI

All alleles(26) : Gene trapped(26)

Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 T C 11: 9,217,565 (GRCm39) S336P probably benign Het
Abca9 T C 11: 110,039,729 (GRCm39) Y428C probably damaging Het
Alpk1 T C 3: 127,466,011 (GRCm39) Q1165R probably damaging Het
Angel2 C A 1: 190,665,310 (GRCm39) N80K probably benign Het
Bmp6 T C 13: 38,653,610 (GRCm39) S226P probably damaging Het
Ccar2 T C 14: 70,383,311 (GRCm39) T229A probably benign Het
Cdh12 G A 15: 21,237,989 (GRCm39) V75M probably damaging Het
Cdh6 G T 15: 13,034,326 (GRCm39) A778E possibly damaging Het
Corin A T 5: 72,496,334 (GRCm39) C540S probably damaging Het
Cyfip1 C A 7: 55,547,991 (GRCm39) Y530* probably null Het
Dock10 T G 1: 80,570,876 (GRCm39) K327N probably damaging Het
Dpy19l3 A G 7: 35,426,840 (GRCm39) probably benign Het
E2f8 T C 7: 48,516,899 (GRCm39) T827A probably benign Het
Edem3 T C 1: 151,668,136 (GRCm39) V305A possibly damaging Het
Fam170a T C 18: 50,414,845 (GRCm39) W164R probably benign Het
Fbxw14 T C 9: 109,103,640 (GRCm39) D24G possibly damaging Het
Gnmt T C 17: 47,037,606 (GRCm39) D124G probably benign Het
Gpx5 T C 13: 21,471,669 (GRCm39) D178G probably damaging Het
Gsdmd T A 15: 75,736,186 (GRCm39) I105N probably damaging Het
Hps5 C T 7: 46,410,856 (GRCm39) M1113I probably damaging Het
Hyal6 T C 6: 24,734,178 (GRCm39) F37S probably damaging Het
Il17c C T 8: 123,148,862 (GRCm39) T2I probably benign Het
Lyz1 A G 10: 117,127,093 (GRCm39) C48R probably damaging Het
Or52e18 T A 7: 104,609,946 (GRCm39) probably benign Het
Pafah1b3 G A 7: 24,994,570 (GRCm39) R215C possibly damaging Het
Psmb4 A T 3: 94,793,538 (GRCm39) probably null Het
Rnf213 T C 11: 119,373,944 (GRCm39) V5009A probably benign Het
Sema6a T C 18: 47,414,369 (GRCm39) K494E possibly damaging Het
Sfmbt1 T C 14: 30,491,777 (GRCm39) V17A probably benign Het
Speg T A 1: 75,387,920 (GRCm39) probably benign Het
Spint1 A G 2: 119,076,936 (GRCm39) D340G probably damaging Het
Tctn3 T C 19: 40,596,081 (GRCm39) I309V probably benign Het
Tex19.1 T A 11: 121,038,072 (GRCm39) D143E probably damaging Het
Tktl2 A G 8: 66,965,548 (GRCm39) I369V probably benign Het
Tm2d2 A G 8: 25,510,573 (GRCm39) probably benign Het
Traf4 C A 11: 78,056,226 (GRCm39) R14L possibly damaging Het
Zfhx4 A G 3: 5,466,196 (GRCm39) Y2118C probably damaging Het
Zmynd15 C A 11: 70,354,416 (GRCm39) N425K probably benign Het
Other mutations in Tasor
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00093:Tasor APN 14 27,170,163 (GRCm39) missense probably damaging 1.00
IGL00467:Tasor APN 14 27,170,121 (GRCm39) missense probably benign 0.02
IGL01071:Tasor APN 14 27,164,579 (GRCm39) critical splice donor site probably null
IGL01375:Tasor APN 14 27,162,120 (GRCm39) missense probably damaging 1.00
IGL01509:Tasor APN 14 27,181,731 (GRCm39) splice site probably benign
IGL02342:Tasor APN 14 27,198,624 (GRCm39) missense possibly damaging 0.83
IGL03105:Tasor APN 14 27,164,509 (GRCm39) missense probably damaging 0.98
IGL03131:Tasor APN 14 27,183,136 (GRCm39) nonsense probably null
IGL03248:Tasor APN 14 27,198,649 (GRCm39) missense probably damaging 1.00
IGL03383:Tasor APN 14 27,163,918 (GRCm39) missense possibly damaging 0.93
balsam UTSW 14 27,183,107 (GRCm39) missense probably benign 0.01
santa_rosa UTSW 14 27,198,658 (GRCm39) splice site probably null
D4043:Tasor UTSW 14 27,193,949 (GRCm39) missense probably benign 0.07
R0147:Tasor UTSW 14 27,193,725 (GRCm39) missense probably benign 0.23
R0512:Tasor UTSW 14 27,168,363 (GRCm39) missense probably damaging 1.00
R0589:Tasor UTSW 14 27,183,107 (GRCm39) missense probably benign 0.01
R0609:Tasor UTSW 14 27,183,707 (GRCm39) missense probably benign 0.09
R0798:Tasor UTSW 14 27,198,593 (GRCm39) missense probably damaging 1.00
R1107:Tasor UTSW 14 27,201,680 (GRCm39) nonsense probably null
R1205:Tasor UTSW 14 27,183,275 (GRCm39) missense probably damaging 1.00
R1376:Tasor UTSW 14 27,151,338 (GRCm39) missense probably benign 0.00
R1376:Tasor UTSW 14 27,151,338 (GRCm39) missense probably benign 0.00
R1441:Tasor UTSW 14 27,186,217 (GRCm39) nonsense probably null
R1493:Tasor UTSW 14 27,171,926 (GRCm39) missense probably damaging 1.00
R1527:Tasor UTSW 14 27,202,050 (GRCm39) critical splice donor site probably null
R1729:Tasor UTSW 14 27,201,590 (GRCm39) missense probably damaging 1.00
R1752:Tasor UTSW 14 27,193,885 (GRCm39) nonsense probably null
R1960:Tasor UTSW 14 27,201,746 (GRCm39) missense possibly damaging 0.95
R1960:Tasor UTSW 14 27,160,621 (GRCm39) missense probably damaging 1.00
R1965:Tasor UTSW 14 27,164,511 (GRCm39) missense probably damaging 1.00
R2074:Tasor UTSW 14 27,183,170 (GRCm39) missense probably benign 0.03
R2107:Tasor UTSW 14 27,183,744 (GRCm39) critical splice donor site probably null
R2130:Tasor UTSW 14 27,198,571 (GRCm39) missense possibly damaging 0.74
R2130:Tasor UTSW 14 27,168,345 (GRCm39) missense probably damaging 1.00
R2131:Tasor UTSW 14 27,198,571 (GRCm39) missense possibly damaging 0.74
R2133:Tasor UTSW 14 27,198,571 (GRCm39) missense possibly damaging 0.74
R2140:Tasor UTSW 14 27,201,992 (GRCm39) missense probably damaging 1.00
R2184:Tasor UTSW 14 27,188,141 (GRCm39) missense possibly damaging 0.83
R2279:Tasor UTSW 14 27,164,452 (GRCm39) missense probably damaging 1.00
R3979:Tasor UTSW 14 27,199,087 (GRCm39) missense possibly damaging 0.95
R4113:Tasor UTSW 14 27,181,918 (GRCm39) nonsense probably null
R4434:Tasor UTSW 14 27,171,818 (GRCm39) critical splice donor site probably null
R4562:Tasor UTSW 14 27,188,265 (GRCm39) missense possibly damaging 0.67
R4568:Tasor UTSW 14 27,198,658 (GRCm39) splice site probably null
R4754:Tasor UTSW 14 27,183,052 (GRCm39) missense probably benign
R4980:Tasor UTSW 14 27,183,382 (GRCm39) missense probably benign 0.39
R4993:Tasor UTSW 14 27,151,071 (GRCm39) missense possibly damaging 0.88
R5200:Tasor UTSW 14 27,151,183 (GRCm39) missense probably benign 0.41
R5316:Tasor UTSW 14 27,193,992 (GRCm39) missense possibly damaging 0.52
R5599:Tasor UTSW 14 27,201,886 (GRCm39) missense probably benign 0.01
R5678:Tasor UTSW 14 27,151,080 (GRCm39) small insertion probably benign
R5680:Tasor UTSW 14 27,151,080 (GRCm39) small insertion probably benign
R5887:Tasor UTSW 14 27,188,254 (GRCm39) nonsense probably null
R6181:Tasor UTSW 14 27,194,235 (GRCm39) missense probably benign 0.01
R6556:Tasor UTSW 14 27,151,215 (GRCm39) missense probably benign
R6603:Tasor UTSW 14 27,168,343 (GRCm39) missense probably damaging 1.00
R6829:Tasor UTSW 14 27,164,438 (GRCm39) missense possibly damaging 0.90
R6864:Tasor UTSW 14 27,183,115 (GRCm39) missense probably damaging 0.96
R6919:Tasor UTSW 14 27,171,758 (GRCm39) nonsense probably null
R7046:Tasor UTSW 14 27,194,392 (GRCm39) missense probably damaging 1.00
R7057:Tasor UTSW 14 27,183,608 (GRCm39) missense probably damaging 0.97
R7064:Tasor UTSW 14 27,194,288 (GRCm39) missense probably benign 0.09
R7290:Tasor UTSW 14 27,160,610 (GRCm39) missense probably damaging 1.00
R7303:Tasor UTSW 14 27,193,809 (GRCm39) missense probably damaging 1.00
R7439:Tasor UTSW 14 27,193,602 (GRCm39) missense probably damaging 1.00
R7524:Tasor UTSW 14 27,188,160 (GRCm39) missense probably damaging 0.99
R7580:Tasor UTSW 14 27,188,243 (GRCm39) missense probably benign 0.29
R7726:Tasor UTSW 14 27,169,454 (GRCm39) missense probably damaging 0.99
R7771:Tasor UTSW 14 27,189,516 (GRCm39) missense probably damaging 1.00
R7782:Tasor UTSW 14 27,193,901 (GRCm39) missense probably benign 0.07
R7795:Tasor UTSW 14 27,203,340 (GRCm39) missense
R7835:Tasor UTSW 14 27,198,600 (GRCm39) missense probably damaging 1.00
R7954:Tasor UTSW 14 27,169,481 (GRCm39) critical splice donor site probably null
R7981:Tasor UTSW 14 27,168,373 (GRCm39) missense possibly damaging 0.49
R8101:Tasor UTSW 14 27,164,438 (GRCm39) missense possibly damaging 0.90
R8160:Tasor UTSW 14 27,171,913 (GRCm39) missense probably damaging 1.00
R8307:Tasor UTSW 14 27,193,622 (GRCm39) missense probably damaging 1.00
R8913:Tasor UTSW 14 27,188,145 (GRCm39) missense probably damaging 1.00
R9070:Tasor UTSW 14 27,194,484 (GRCm39) missense probably benign 0.14
R9219:Tasor UTSW 14 27,186,344 (GRCm39) missense possibly damaging 0.50
R9420:Tasor UTSW 14 27,163,927 (GRCm39) missense probably damaging 0.99
R9513:Tasor UTSW 14 27,186,271 (GRCm39) nonsense probably null
R9562:Tasor UTSW 14 27,201,766 (GRCm39) critical splice donor site probably null
R9565:Tasor UTSW 14 27,201,766 (GRCm39) critical splice donor site probably null
R9627:Tasor UTSW 14 27,194,123 (GRCm39) missense probably benign
X0002:Tasor UTSW 14 27,194,063 (GRCm39) missense possibly damaging 0.90
Z1176:Tasor UTSW 14 27,199,105 (GRCm39) missense probably damaging 1.00
Z1176:Tasor UTSW 14 27,151,165 (GRCm39) missense probably damaging 0.97
Z1177:Tasor UTSW 14 27,170,207 (GRCm39) missense probably damaging 1.00
Posted On 2013-10-07