Incidental Mutation 'R1826:Tasor2'
ID |
206831 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Tasor2
|
Ensembl Gene |
ENSMUSG00000033799 |
Gene Name |
transcription activation suppressor family member 2 |
Synonyms |
BC016423, Fam208b |
MMRRC Submission |
039853-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.102)
|
Stock # |
R1826 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
13 |
Chromosomal Location |
3616035-3661108 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 3631759 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Asparagine to Isoleucine
at position 914
(N914I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000093774
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000096069]
|
AlphaFold |
Q5DTT3 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000096069
AA Change: N914I
PolyPhen 2
Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000093774 Gene: ENSMUSG00000033799 AA Change: N914I
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 |
probably benign
Transcript: ENSMUST00000222909
|
Meta Mutation Damage Score |
0.1724 |
Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.8%
- 10x: 95.1%
- 20x: 92.0%
|
Validation Efficiency |
95% (116/122) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc2 |
T |
C |
19: 43,810,453 (GRCm39) |
S917P |
probably benign |
Het |
Acsbg1 |
C |
T |
9: 54,529,840 (GRCm39) |
V256M |
possibly damaging |
Het |
Adam34 |
T |
A |
8: 44,104,379 (GRCm39) |
D422V |
probably damaging |
Het |
Adam6a |
T |
A |
12: 113,509,742 (GRCm39) |
V705E |
possibly damaging |
Het |
Adamts12 |
C |
A |
15: 11,071,606 (GRCm39) |
P50Q |
probably benign |
Het |
Arfgap3 |
C |
T |
15: 83,187,303 (GRCm39) |
|
probably null |
Het |
Aspg |
T |
A |
12: 112,089,852 (GRCm39) |
D463E |
probably damaging |
Het |
Atad2b |
G |
A |
12: 5,024,094 (GRCm39) |
S73N |
probably benign |
Het |
Atp11a |
T |
C |
8: 12,896,154 (GRCm39) |
L788P |
probably damaging |
Het |
B3gnt8 |
T |
C |
7: 25,328,188 (GRCm39) |
F206S |
probably damaging |
Het |
Baz2b |
T |
C |
2: 59,799,077 (GRCm39) |
E349G |
probably benign |
Het |
Bmp2k |
A |
T |
5: 97,209,261 (GRCm39) |
|
probably benign |
Het |
Camta2 |
A |
G |
11: 70,574,134 (GRCm39) |
F128L |
probably damaging |
Het |
Ccdc88a |
A |
T |
11: 29,439,637 (GRCm39) |
Q30L |
possibly damaging |
Het |
Cdh1 |
T |
C |
8: 107,392,898 (GRCm39) |
M794T |
probably benign |
Het |
Cdh5 |
A |
G |
8: 104,857,723 (GRCm39) |
N383S |
possibly damaging |
Het |
Cep85l |
T |
C |
10: 53,224,908 (GRCm39) |
D227G |
possibly damaging |
Het |
Clec4e |
A |
G |
6: 123,260,591 (GRCm39) |
S156P |
probably damaging |
Het |
Col10a1 |
G |
T |
10: 34,270,645 (GRCm39) |
G206C |
probably damaging |
Het |
Col4a2 |
T |
C |
8: 11,363,509 (GRCm39) |
|
probably null |
Het |
Copg2 |
A |
G |
6: 30,789,777 (GRCm39) |
M517T |
probably benign |
Het |
Cyp2f2 |
T |
A |
7: 26,831,987 (GRCm39) |
L414Q |
probably damaging |
Het |
Dact1 |
G |
A |
12: 71,365,118 (GRCm39) |
G596D |
probably damaging |
Het |
Dcaf13 |
T |
C |
15: 38,982,294 (GRCm39) |
C87R |
probably damaging |
Het |
Dchs1 |
T |
G |
7: 105,406,834 (GRCm39) |
T2224P |
probably damaging |
Het |
Dnah12 |
A |
G |
14: 26,432,174 (GRCm39) |
M429V |
probably benign |
Het |
Dppa2 |
G |
A |
16: 48,137,711 (GRCm39) |
R231H |
probably damaging |
Het |
Elavl4 |
T |
C |
4: 110,108,489 (GRCm39) |
D78G |
probably damaging |
Het |
Enthd1 |
T |
C |
15: 80,358,482 (GRCm39) |
E346G |
probably damaging |
Het |
Exoc3l |
A |
T |
8: 106,020,250 (GRCm39) |
I225N |
probably damaging |
Het |
Fasn |
C |
T |
11: 120,699,325 (GRCm39) |
|
probably benign |
Het |
Fbxl7 |
G |
A |
15: 26,552,851 (GRCm39) |
R139C |
possibly damaging |
Het |
Fbxw15 |
C |
A |
9: 109,388,782 (GRCm39) |
|
probably null |
Het |
Flnc |
A |
G |
6: 29,455,184 (GRCm39) |
T1971A |
probably damaging |
Het |
Fnip1 |
T |
G |
11: 54,356,990 (GRCm39) |
V33G |
probably damaging |
Het |
Foxn2 |
A |
G |
17: 88,794,233 (GRCm39) |
E390G |
possibly damaging |
Het |
Fry |
C |
T |
5: 150,360,174 (GRCm39) |
S1940L |
possibly damaging |
Het |
Fzd3 |
A |
T |
14: 65,490,555 (GRCm39) |
D9E |
probably benign |
Het |
Gabrd |
T |
C |
4: 155,470,943 (GRCm39) |
Y255C |
probably damaging |
Het |
Garem1 |
A |
T |
18: 21,262,509 (GRCm39) |
F768L |
probably benign |
Het |
Gas2 |
T |
A |
7: 51,593,421 (GRCm39) |
L167Q |
probably damaging |
Het |
Gm16391 |
A |
G |
17: 76,591,418 (GRCm39) |
|
noncoding transcript |
Het |
Gm1979 |
A |
T |
5: 26,206,240 (GRCm39) |
N113K |
probably damaging |
Het |
Gpr83 |
G |
T |
9: 14,779,629 (GRCm39) |
C269F |
possibly damaging |
Het |
Hdac4 |
T |
A |
1: 91,912,421 (GRCm39) |
N352Y |
probably damaging |
Het |
Hdac9 |
A |
G |
12: 34,479,491 (GRCm39) |
|
probably benign |
Het |
Hhipl2 |
G |
A |
1: 183,217,253 (GRCm39) |
S673N |
probably benign |
Het |
Iffo2 |
T |
A |
4: 139,341,376 (GRCm39) |
S417T |
probably benign |
Het |
Itgb5 |
G |
T |
16: 33,685,930 (GRCm39) |
R90L |
possibly damaging |
Het |
Jade1 |
T |
G |
3: 41,567,648 (GRCm39) |
L572W |
probably damaging |
Het |
Kcnh1 |
T |
A |
1: 192,095,376 (GRCm39) |
M478K |
possibly damaging |
Het |
Kcnma1 |
C |
A |
14: 23,380,997 (GRCm39) |
D903Y |
probably damaging |
Het |
Kcnq4 |
T |
A |
4: 120,561,701 (GRCm39) |
H456L |
probably benign |
Het |
Kif9 |
C |
A |
9: 110,346,701 (GRCm39) |
T613K |
probably benign |
Het |
Krt36 |
T |
G |
11: 99,993,856 (GRCm39) |
|
probably benign |
Het |
Kyat3 |
A |
T |
3: 142,428,940 (GRCm39) |
D89V |
possibly damaging |
Het |
Lnpep |
A |
T |
17: 17,783,098 (GRCm39) |
F568I |
probably damaging |
Het |
Lpl |
T |
C |
8: 69,354,943 (GRCm39) |
F444L |
possibly damaging |
Het |
Lrp1 |
A |
T |
10: 127,389,576 (GRCm39) |
V3153E |
probably damaging |
Het |
Lrrn1 |
A |
T |
6: 107,544,529 (GRCm39) |
N109I |
probably benign |
Het |
Ltn1 |
A |
G |
16: 87,212,504 (GRCm39) |
Y686H |
probably damaging |
Het |
Mcoln2 |
A |
C |
3: 145,881,227 (GRCm39) |
D166A |
possibly damaging |
Het |
Ms4a6b |
A |
T |
19: 11,501,298 (GRCm39) |
I103F |
probably damaging |
Het |
Mtmr10 |
T |
G |
7: 63,987,214 (GRCm39) |
S585A |
probably benign |
Het |
Mx1 |
T |
C |
16: 97,256,837 (GRCm39) |
N114S |
possibly damaging |
Het |
Mysm1 |
A |
T |
4: 94,858,923 (GRCm39) |
N75K |
probably benign |
Het |
Nkx1-1 |
A |
G |
5: 33,591,277 (GRCm39) |
V15A |
unknown |
Het |
Nlrp1a |
G |
A |
11: 71,013,573 (GRCm39) |
T559I |
possibly damaging |
Het |
Nlrp1a |
T |
A |
11: 70,998,806 (GRCm39) |
|
probably benign |
Het |
Oas1f |
A |
G |
5: 120,993,652 (GRCm39) |
K288R |
probably benign |
Het |
Or10q1 |
T |
A |
19: 13,726,711 (GRCm39) |
D80E |
probably benign |
Het |
Or55b3 |
A |
G |
7: 102,126,720 (GRCm39) |
L119P |
probably damaging |
Het |
Or9e1 |
T |
A |
11: 58,732,257 (GRCm39) |
C106S |
probably benign |
Het |
Pcdhb2 |
T |
A |
18: 37,429,038 (GRCm39) |
V337D |
probably damaging |
Het |
Pcdhb5 |
C |
T |
18: 37,454,522 (GRCm39) |
R301* |
probably null |
Het |
Phf12 |
T |
C |
11: 77,915,780 (GRCm39) |
|
probably benign |
Het |
Pik3c2a |
C |
T |
7: 115,967,352 (GRCm39) |
D862N |
probably benign |
Het |
Pkhd1l1 |
T |
A |
15: 44,366,741 (GRCm39) |
L740I |
possibly damaging |
Het |
Ppp1r9a |
A |
T |
6: 5,111,060 (GRCm39) |
|
probably benign |
Het |
Prg4 |
T |
C |
1: 150,327,760 (GRCm39) |
D820G |
probably benign |
Het |
Prmt9 |
C |
T |
8: 78,282,303 (GRCm39) |
Q67* |
probably null |
Het |
Prob1 |
T |
C |
18: 35,786,628 (GRCm39) |
E542G |
possibly damaging |
Het |
Pttg1 |
A |
G |
11: 43,311,193 (GRCm39) |
V188A |
probably damaging |
Het |
Rassf1 |
T |
A |
9: 107,435,392 (GRCm39) |
L260H |
probably damaging |
Het |
Rbm5 |
T |
A |
9: 107,619,613 (GRCm39) |
Q766L |
probably damaging |
Het |
Rbms3 |
T |
A |
9: 116,651,936 (GRCm39) |
Y137F |
probably damaging |
Het |
Rccd1 |
T |
C |
7: 79,969,966 (GRCm39) |
|
probably benign |
Het |
Rnf182 |
G |
A |
13: 43,822,010 (GRCm39) |
W187* |
probably null |
Het |
S100a11 |
A |
T |
3: 93,433,428 (GRCm39) |
I91F |
probably benign |
Het |
Setd4 |
T |
A |
16: 93,388,187 (GRCm39) |
K100* |
probably null |
Het |
Simc1 |
T |
A |
13: 54,672,452 (GRCm39) |
C267S |
probably benign |
Het |
Slc16a1 |
G |
T |
3: 104,558,255 (GRCm39) |
A91S |
probably benign |
Het |
Slc36a1 |
A |
G |
11: 55,111,279 (GRCm39) |
N133S |
probably benign |
Het |
Ssxb16 |
T |
A |
X: 8,746,944 (GRCm39) |
Y133* |
probably null |
Het |
Svil |
C |
T |
18: 5,063,383 (GRCm39) |
P885S |
probably benign |
Het |
Svop |
A |
T |
5: 114,198,117 (GRCm39) |
|
probably null |
Het |
Taar7d |
T |
C |
10: 23,903,474 (GRCm39) |
Y119H |
probably damaging |
Het |
Tgfb3 |
T |
C |
12: 86,108,818 (GRCm39) |
T304A |
probably benign |
Het |
Tmem94 |
C |
A |
11: 115,684,039 (GRCm39) |
C786* |
probably null |
Het |
Tnfrsf4 |
T |
A |
4: 156,100,736 (GRCm39) |
|
probably null |
Het |
Tns1 |
C |
A |
1: 73,992,793 (GRCm39) |
M1I |
probably null |
Het |
Trappc13 |
C |
T |
13: 104,306,327 (GRCm39) |
|
probably null |
Het |
Trim72 |
T |
C |
7: 127,607,016 (GRCm39) |
F182L |
possibly damaging |
Het |
Ttc6 |
T |
C |
12: 57,707,033 (GRCm39) |
S647P |
probably benign |
Het |
Tulp1 |
A |
G |
17: 28,575,341 (GRCm39) |
L400P |
possibly damaging |
Het |
Vegfc |
C |
T |
8: 54,634,347 (GRCm39) |
T342M |
possibly damaging |
Het |
Vit |
T |
A |
17: 78,842,105 (GRCm39) |
V15E |
probably benign |
Het |
Vps13d |
A |
T |
4: 144,881,573 (GRCm39) |
M1334K |
probably damaging |
Het |
Zfp280d |
T |
C |
9: 72,206,062 (GRCm39) |
V23A |
probably damaging |
Het |
Zfp608 |
A |
G |
18: 55,031,648 (GRCm39) |
I764T |
probably benign |
Het |
Zfp94 |
T |
C |
7: 24,008,540 (GRCm39) |
Y33C |
probably damaging |
Het |
Zfyve26 |
T |
A |
12: 79,315,823 (GRCm39) |
I1218F |
probably damaging |
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 |
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 |
|
Predicted Primers |
PCR Primer
(F):5'- CTAGCTGTGGACAATGAGAGAACAC -3'
(R):5'- ACCCTCTGTTGAAGGGTCTG -3'
Sequencing Primer
(F):5'- GGAAGACCCATTTTTTTCCC -3'
(R):5'- TAGACCCTCTGTTGGAGACTAAG -3'
|
Posted On |
2014-06-23 |