Incidental Mutation 'IGL01509:Tasor'
ID 89154
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 # IGL01509
Quality Score
Status
Chromosome 14
Chromosomal Location 27150791-27205512 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 27181731 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
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
SMART Domains Protein: ENSMUSP00000022450
Gene: ENSMUSG00000040651

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: 22 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A4gnt T A 9: 99,495,819 (GRCm39) I85N probably benign Het
Bbof1 T A 12: 84,457,859 (GRCm39) N41K possibly damaging Het
Cdh10 A G 15: 18,986,884 (GRCm39) K372E possibly damaging Het
Clmn T A 12: 104,747,162 (GRCm39) Q795L probably benign Het
Dnai4 G A 4: 102,929,884 (GRCm39) P369L possibly damaging Het
Enox1 T C 14: 77,936,713 (GRCm39) S583P probably damaging Het
Hmcn1 C T 1: 150,485,382 (GRCm39) G4407S probably damaging Het
Ifi206 T A 1: 173,313,142 (GRCm39) M109L probably benign Het
Ighmbp2 A G 19: 3,318,711 (GRCm39) M455T possibly damaging Het
Inpp4b T C 8: 82,617,332 (GRCm39) probably benign Het
Mctp2 A G 7: 71,909,017 (GRCm39) S99P probably benign Het
Mrgprb2 G A 7: 48,202,674 (GRCm39) T17M possibly damaging Het
Ogdhl T A 14: 32,059,716 (GRCm39) M410K probably damaging Het
Pard3b A T 1: 62,200,407 (GRCm39) R315S possibly damaging Het
Pde3b A G 7: 114,117,645 (GRCm39) Q625R probably benign Het
Plxna3 A G X: 73,376,039 (GRCm39) Q355R probably benign Het
Ptprm A T 17: 67,069,208 (GRCm39) F907I possibly damaging Het
Slc16a4 A C 3: 107,218,750 (GRCm39) probably null Het
Vmn1r82 A T 7: 12,039,096 (GRCm39) H123L probably damaging Het
Vmn2r1 T C 3: 64,010,466 (GRCm39) I568T probably benign Het
Zfp7 G A 15: 76,765,333 (GRCm39) V9M probably damaging Het
Zfp759 A G 13: 67,287,658 (GRCm39) N403S 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
IGL01351:Tasor APN 14 27,186,258 (GRCm39) missense probably benign 0.02
IGL01375:Tasor APN 14 27,162,120 (GRCm39) missense probably damaging 1.00
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 2013-12-03