Incidental Mutation 'R1920:Tasor2'
| ID |
212973 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Tasor2
|
| Ensembl Gene |
ENSMUSG00000033799 |
| Gene Name |
transcription activation suppressor family member 2 |
| Synonyms |
BC016423, Fam208b |
| MMRRC Submission |
039938-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.102)
|
| Stock # |
R1920 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
13 |
| Chromosomal Location |
3616035-3661108 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 3626612 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Asparagine
at position 1113
(Y1113N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000093774
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000096069]
|
| AlphaFold |
Q5DTT3 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000096069
AA Change: Y1113N
PolyPhen 2
Score 0.630 (Sensitivity: 0.87; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000093774
Gene: ENSMUSG00000033799
AA Change: Y1113N
| Domain | Start | End | E-Value | Type |
|---|
|
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 |
noncoding transcript
Transcript: ENSMUST00000221059
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000222909
AA Change: Y431N
|
| Meta Mutation Damage Score |
0.1795 |
| Coding Region Coverage |
- 1x: 97.5%
- 3x: 97.0%
- 10x: 95.7%
- 20x: 93.4%
|
| Validation Efficiency |
98% (101/103) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 98 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700056E22Rik |
A |
G |
1: 183,765,828 (GRCm39) |
V77A |
probably benign |
Het |
| Actl7a |
G |
A |
4: 56,744,135 (GRCm39) |
V221M |
probably damaging |
Het |
| Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
| Arhgef10 |
C |
T |
8: 15,006,987 (GRCm39) |
|
probably benign |
Het |
| Asgr2 |
T |
C |
11: 69,989,123 (GRCm39) |
L86P |
possibly damaging |
Het |
| Atp12a |
A |
G |
14: 56,624,308 (GRCm39) |
R919G |
probably benign |
Het |
| Atrn |
A |
G |
2: 130,836,971 (GRCm39) |
Y1145C |
probably damaging |
Het |
| B3gnt5 |
T |
G |
16: 19,588,294 (GRCm39) |
L171R |
probably benign |
Het |
| Bbof1 |
T |
A |
12: 84,457,859 (GRCm39) |
N41K |
possibly damaging |
Het |
| Bdp1 |
A |
T |
13: 100,235,097 (GRCm39) |
W166R |
probably benign |
Het |
| Bean1 |
A |
T |
8: 104,937,742 (GRCm39) |
H107L |
possibly damaging |
Het |
| Brd4 |
T |
C |
17: 32,417,060 (GRCm39) |
|
probably benign |
Het |
| Cadps |
T |
C |
14: 12,465,859 (GRCm38) |
K1017R |
possibly damaging |
Het |
| Cep78 |
G |
A |
19: 15,951,715 (GRCm39) |
|
probably benign |
Het |
| Cfap70 |
C |
T |
14: 20,445,020 (GRCm39) |
A1087T |
probably damaging |
Het |
| Cideb |
A |
G |
14: 55,992,700 (GRCm39) |
V72A |
probably benign |
Het |
| Cpz |
T |
C |
5: 35,675,012 (GRCm39) |
E79G |
probably damaging |
Het |
| Crybg1 |
A |
G |
10: 43,873,544 (GRCm39) |
L1188P |
probably damaging |
Het |
| Cuzd1 |
G |
A |
7: 130,911,425 (GRCm39) |
P518L |
probably benign |
Het |
| Cyp2j5 |
A |
T |
4: 96,551,491 (GRCm39) |
N77K |
probably damaging |
Het |
| Cyp4f39 |
T |
G |
17: 32,702,265 (GRCm39) |
F254C |
probably benign |
Het |
| Dkk1 |
C |
A |
19: 30,524,731 (GRCm39) |
V225L |
probably damaging |
Het |
| Dlg5 |
T |
C |
14: 24,226,639 (GRCm39) |
Y421C |
probably damaging |
Het |
| Dll3 |
T |
C |
7: 27,998,348 (GRCm39) |
T206A |
probably benign |
Het |
| Dnhd1 |
T |
C |
7: 105,362,614 (GRCm39) |
C3766R |
probably benign |
Het |
| Dock9 |
G |
T |
14: 121,820,792 (GRCm39) |
S1534Y |
probably damaging |
Het |
| Dst |
T |
C |
1: 34,200,110 (GRCm39) |
V96A |
probably damaging |
Het |
| F2r |
A |
G |
13: 95,740,698 (GRCm39) |
F279S |
probably damaging |
Het |
| Farp1 |
C |
A |
14: 121,492,908 (GRCm39) |
N503K |
probably benign |
Het |
| Fbxw2 |
G |
A |
2: 34,712,776 (GRCm39) |
T95I |
probably damaging |
Het |
| Fis1 |
A |
G |
5: 136,994,461 (GRCm39) |
T50A |
probably benign |
Het |
| Frzb |
T |
G |
2: 80,276,772 (GRCm39) |
E138A |
probably damaging |
Het |
| Fsip2 |
A |
T |
2: 82,817,164 (GRCm39) |
D4299V |
probably benign |
Het |
| Fyco1 |
C |
T |
9: 123,659,478 (GRCm39) |
D233N |
probably damaging |
Het |
| Gmpr |
A |
G |
13: 45,667,997 (GRCm39) |
|
probably benign |
Het |
| Hc |
C |
T |
2: 34,919,407 (GRCm39) |
|
probably benign |
Het |
| Hnrnpa1 |
T |
C |
15: 103,150,699 (GRCm39) |
M186T |
possibly damaging |
Het |
| Kl |
A |
G |
5: 150,906,132 (GRCm39) |
K501E |
probably benign |
Het |
| Klhl42 |
A |
G |
6: 147,009,427 (GRCm39) |
N422S |
probably damaging |
Het |
| Kmt2d |
C |
G |
15: 98,753,471 (GRCm39) |
K127N |
probably damaging |
Het |
| Kmt2d |
T |
A |
15: 98,753,472 (GRCm39) |
K127M |
probably damaging |
Het |
| Krt39 |
T |
A |
11: 99,405,461 (GRCm39) |
T480S |
probably benign |
Het |
| Lims2 |
T |
A |
18: 32,088,395 (GRCm39) |
C198* |
probably null |
Het |
| Mctp1 |
A |
G |
13: 76,532,729 (GRCm39) |
N26D |
possibly damaging |
Het |
| Mdm4 |
A |
G |
1: 132,931,538 (GRCm39) |
S168P |
probably benign |
Het |
| Myo3a |
A |
G |
2: 22,455,008 (GRCm39) |
Y71C |
probably benign |
Het |
| Nlrp9c |
T |
A |
7: 26,084,319 (GRCm39) |
D420V |
probably damaging |
Het |
| Ntf3 |
A |
T |
6: 126,079,485 (GRCm39) |
I7N |
possibly damaging |
Het |
| Or10ag52 |
G |
A |
2: 87,043,721 (GRCm39) |
G162S |
probably benign |
Het |
| Or13c25 |
G |
T |
4: 52,910,849 (GRCm39) |
T315K |
probably benign |
Het |
| Or4c119 |
A |
G |
2: 88,986,925 (GRCm39) |
V198A |
probably benign |
Het |
| Or8b38 |
T |
C |
9: 37,972,981 (GRCm39) |
Y122H |
probably damaging |
Het |
| Papln |
C |
A |
12: 83,836,028 (GRCm39) |
Y1222* |
probably null |
Het |
| Pgm3 |
T |
G |
9: 86,440,531 (GRCm39) |
I387L |
possibly damaging |
Het |
| Pira12 |
G |
C |
7: 3,900,871 (GRCm39) |
P20R |
probably damaging |
Het |
| Pkd1 |
C |
A |
17: 24,814,131 (GRCm39) |
P4167Q |
probably damaging |
Het |
| Plcb4 |
T |
A |
2: 135,854,947 (GRCm39) |
V1174E |
probably damaging |
Het |
| Polr1b |
A |
G |
2: 128,943,031 (GRCm39) |
N9D |
probably benign |
Het |
| Prkaa2 |
G |
A |
4: 104,893,950 (GRCm39) |
Q456* |
probably null |
Het |
| Ptch2 |
G |
T |
4: 116,965,858 (GRCm39) |
V425L |
probably benign |
Het |
| Ptprh |
A |
T |
7: 4,552,394 (GRCm39) |
S957T |
probably benign |
Het |
| Riok1 |
A |
G |
13: 38,241,177 (GRCm39) |
D444G |
probably benign |
Het |
| Rrbp1 |
A |
T |
2: 143,830,211 (GRCm39) |
V652E |
probably benign |
Het |
| Rrp36 |
C |
T |
17: 46,983,671 (GRCm39) |
R47Q |
possibly damaging |
Het |
| Sec24c |
T |
C |
14: 20,736,955 (GRCm39) |
S304P |
probably damaging |
Het |
| Serpinb6b |
A |
T |
13: 33,158,991 (GRCm39) |
D64V |
possibly damaging |
Het |
| Serpinb9b |
A |
T |
13: 33,223,531 (GRCm39) |
|
probably null |
Het |
| Six6 |
T |
A |
12: 72,988,538 (GRCm39) |
I237N |
probably damaging |
Het |
| Slc25a36 |
A |
T |
9: 96,975,135 (GRCm39) |
M127K |
probably benign |
Het |
| Slc2a10 |
A |
G |
2: 165,356,550 (GRCm39) |
D70G |
probably damaging |
Het |
| Slc2a3 |
T |
A |
6: 122,713,700 (GRCm39) |
I171F |
probably damaging |
Het |
| Smc4 |
A |
G |
3: 68,940,401 (GRCm39) |
T1087A |
probably damaging |
Het |
| Spg21 |
A |
G |
9: 65,391,779 (GRCm39) |
Y242C |
probably damaging |
Het |
| St14 |
A |
G |
9: 31,001,166 (GRCm39) |
V855A |
possibly damaging |
Het |
| Stx2 |
G |
A |
5: 129,065,903 (GRCm39) |
T251M |
probably damaging |
Het |
| Svs3b |
A |
T |
2: 164,097,848 (GRCm39) |
S158T |
probably benign |
Het |
| Synpo |
C |
T |
18: 60,736,661 (GRCm39) |
M428I |
probably benign |
Het |
| Tbc1d31 |
G |
A |
15: 57,775,760 (GRCm39) |
R17H |
probably damaging |
Het |
| Tbl3 |
G |
A |
17: 24,923,477 (GRCm39) |
T284I |
probably benign |
Het |
| Tcof1 |
T |
C |
18: 60,971,927 (GRCm39) |
T127A |
possibly damaging |
Het |
| Tgoln1 |
T |
C |
6: 72,593,084 (GRCm39) |
E132G |
probably benign |
Het |
| Timeless |
T |
C |
10: 128,077,583 (GRCm39) |
I221T |
probably damaging |
Het |
| Tmem176b |
C |
T |
6: 48,815,138 (GRCm39) |
A52T |
possibly damaging |
Het |
| Tmem192 |
C |
T |
8: 65,418,235 (GRCm39) |
L207F |
probably damaging |
Het |
| Trank1 |
T |
C |
9: 111,176,996 (GRCm39) |
|
probably null |
Het |
| Ttc7b |
C |
T |
12: 100,381,389 (GRCm39) |
|
probably null |
Het |
| Tubb5 |
T |
C |
17: 36,146,190 (GRCm39) |
Y340C |
probably benign |
Het |
| Ubr1 |
G |
A |
2: 120,761,449 (GRCm39) |
T576I |
probably benign |
Het |
| Vcan |
T |
C |
13: 89,841,134 (GRCm39) |
E1470G |
probably damaging |
Het |
| Vmn1r200 |
T |
A |
13: 22,579,663 (GRCm39) |
N146K |
probably damaging |
Het |
| Vmn2r120 |
T |
A |
17: 57,831,839 (GRCm39) |
I317F |
probably benign |
Het |
| Vmn2r61 |
T |
C |
7: 41,949,710 (GRCm39) |
I710T |
possibly damaging |
Het |
| Wipf1 |
T |
A |
2: 73,270,499 (GRCm39) |
K61N |
probably benign |
Het |
| Zfp112 |
T |
C |
7: 23,824,662 (GRCm39) |
V210A |
probably benign |
Het |
| Zfp612 |
G |
A |
8: 110,815,095 (GRCm39) |
V101M |
probably benign |
Het |
| Zfp637 |
A |
G |
6: 117,822,681 (GRCm39) |
R270G |
probably damaging |
Het |
| Zfp652 |
A |
G |
11: 95,654,851 (GRCm39) |
E418G |
possibly damaging |
Het |
| Zfp97 |
A |
G |
17: 17,365,265 (GRCm39) |
I255V |
probably benign |
Het |
|
| Other mutations in Tasor2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH 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 |
|
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'- AAAGACATGCTCAAGCCATTCTG -3'
(R):5'- TGCCAGTGTACCAATACATACAG -3'
Sequencing Primer
(F):5'- CTCAAGCCATTCTGAGTCTGTAGAG -3'
(R):5'- CAGTGTACCAATACATACAGAAGTAC -3'
|
| Posted On |
2014-07-14 |
Incidental Mutation