Incidental Mutation 'R1544:Tasor2'
| ID |
172051 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Tasor2
|
| Ensembl Gene |
ENSMUSG00000033799 |
| Gene Name |
transcription activation suppressor family member 2 |
| Synonyms |
BC016423, Fam208b |
| MMRRC Submission |
039583-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.102)
|
| Stock # |
R1544 (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 3640413 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Histidine to Glutamine
at position 241
(H241Q)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000093774
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000096069]
|
| AlphaFold |
Q5DTT3 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000096069
AA Change: H241Q
PolyPhen 2
Score 0.682 (Sensitivity: 0.86; Specificity: 0.92)
|
| SMART Domains |
Protein: ENSMUSP00000093774
Gene: ENSMUSG00000033799
AA Change: H241Q
| 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: ENSMUST00000222041
|
| Meta Mutation Damage Score |
0.1795 |
| Coding Region Coverage |
- 1x: 98.9%
- 3x: 97.9%
- 10x: 94.7%
- 20x: 86.9%
|
| Validation Efficiency |
99% (114/115) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 111 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4931406B18Rik |
A |
G |
7: 43,147,543 (GRCm39) |
I182T |
possibly damaging |
Het |
| 4933406P04Rik |
A |
G |
10: 20,187,105 (GRCm39) |
|
probably benign |
Het |
| A730018C14Rik |
A |
G |
12: 112,381,924 (GRCm39) |
|
noncoding transcript |
Het |
| Aacs |
A |
T |
5: 125,593,394 (GRCm39) |
I666F |
possibly damaging |
Het |
| Abcb9 |
C |
T |
5: 124,221,694 (GRCm39) |
V227I |
probably benign |
Het |
| Abcd3 |
T |
C |
3: 121,578,122 (GRCm39) |
Q168R |
probably benign |
Het |
| Adamts4 |
A |
G |
1: 171,080,311 (GRCm39) |
Q288R |
probably benign |
Het |
| Atad2 |
G |
A |
15: 57,966,760 (GRCm39) |
A611V |
probably damaging |
Het |
| Aup1 |
T |
C |
6: 83,032,187 (GRCm39) |
V118A |
possibly damaging |
Het |
| Bend7 |
T |
A |
2: 4,768,122 (GRCm39) |
|
probably benign |
Het |
| Brd4 |
A |
G |
17: 32,417,646 (GRCm39) |
|
probably benign |
Het |
| C4b |
C |
A |
17: 34,957,941 (GRCm39) |
R580L |
probably benign |
Het |
| Cct8 |
G |
T |
16: 87,288,342 (GRCm39) |
|
probably benign |
Het |
| Cfhr4 |
A |
T |
1: 139,664,608 (GRCm39) |
C484S |
probably damaging |
Het |
| Cilp |
T |
C |
9: 65,183,127 (GRCm39) |
Y344H |
probably benign |
Het |
| Clic6 |
A |
T |
16: 92,288,961 (GRCm39) |
|
probably benign |
Het |
| Colgalt2 |
T |
C |
1: 152,360,703 (GRCm39) |
S247P |
probably damaging |
Het |
| Csf2rb |
G |
T |
15: 78,224,955 (GRCm39) |
A212S |
probably benign |
Het |
| Csmd3 |
A |
C |
15: 47,475,294 (GRCm39) |
|
probably null |
Het |
| Cyp26c1 |
A |
G |
19: 37,679,393 (GRCm39) |
D366G |
probably benign |
Het |
| Dhx33 |
A |
G |
11: 70,890,354 (GRCm39) |
S222P |
probably damaging |
Het |
| Dhx40 |
T |
A |
11: 86,697,379 (GRCm39) |
I63F |
possibly damaging |
Het |
| Dipk2b |
A |
C |
X: 18,286,701 (GRCm39) |
L285V |
possibly damaging |
Het |
| Dlgap2 |
T |
A |
8: 14,879,861 (GRCm39) |
|
probably null |
Het |
| Dnah7b |
T |
A |
1: 46,105,957 (GRCm39) |
D20E |
unknown |
Het |
| Dnase2b |
C |
A |
3: 146,290,312 (GRCm39) |
A220S |
probably benign |
Het |
| Dock10 |
T |
C |
1: 80,570,352 (GRCm39) |
E362G |
probably benign |
Het |
| Ect2l |
C |
T |
10: 18,044,182 (GRCm39) |
V226I |
probably benign |
Het |
| Epha10 |
C |
A |
4: 124,779,389 (GRCm39) |
N78K |
probably damaging |
Het |
| Epha3 |
A |
G |
16: 63,593,416 (GRCm39) |
V224A |
probably damaging |
Het |
| Fcgr4 |
C |
A |
1: 170,847,523 (GRCm39) |
D40E |
probably damaging |
Het |
| Fer1l4 |
T |
C |
2: 155,887,553 (GRCm39) |
M548V |
probably benign |
Het |
| Flii |
C |
T |
11: 60,610,518 (GRCm39) |
|
probably null |
Het |
| Flnc |
A |
T |
6: 29,444,079 (GRCm39) |
Y631F |
probably benign |
Het |
| Gm6871 |
A |
C |
7: 41,195,514 (GRCm39) |
|
probably null |
Het |
| Gtf2ird1 |
A |
T |
5: 134,387,772 (GRCm39) |
S1028T |
possibly damaging |
Het |
| Hycc1 |
A |
T |
5: 24,170,139 (GRCm39) |
D403E |
probably benign |
Het |
| Hydin |
A |
G |
8: 111,301,486 (GRCm39) |
H3739R |
probably benign |
Het |
| Iqcg |
A |
T |
16: 32,865,895 (GRCm39) |
N149K |
probably benign |
Het |
| Iqgap3 |
A |
G |
3: 88,006,200 (GRCm39) |
D537G |
probably benign |
Het |
| Itih2 |
T |
G |
2: 10,110,025 (GRCm39) |
D576A |
probably benign |
Het |
| Kcmf1 |
T |
C |
6: 72,825,212 (GRCm39) |
T243A |
probably benign |
Het |
| Kif1a |
A |
G |
1: 93,002,670 (GRCm39) |
|
probably benign |
Het |
| Klf10 |
C |
T |
15: 38,297,030 (GRCm39) |
G337S |
probably damaging |
Het |
| Krt31 |
T |
C |
11: 99,938,699 (GRCm39) |
N298S |
possibly damaging |
Het |
| Lmnb1 |
A |
G |
18: 56,882,823 (GRCm39) |
E556G |
probably benign |
Het |
| Mael |
A |
T |
1: 166,029,859 (GRCm39) |
S354T |
probably benign |
Het |
| Mast3 |
T |
C |
8: 71,238,816 (GRCm39) |
D496G |
probably damaging |
Het |
| Med12l |
A |
G |
3: 59,172,661 (GRCm39) |
T1806A |
possibly damaging |
Het |
| Mms19 |
A |
G |
19: 41,944,260 (GRCm39) |
|
probably null |
Het |
| Moap1 |
A |
T |
12: 102,709,504 (GRCm39) |
M15K |
possibly damaging |
Het |
| Mpv17l |
G |
T |
16: 13,764,683 (GRCm39) |
W70L |
probably damaging |
Het |
| Muc4 |
G |
C |
16: 32,753,919 (GRCm38) |
R1265P |
probably benign |
Het |
| Myo7b |
T |
C |
18: 32,127,962 (GRCm39) |
I577V |
probably benign |
Het |
| Myo9b |
T |
A |
8: 71,743,620 (GRCm39) |
L227Q |
probably damaging |
Het |
| Myom2 |
T |
C |
8: 15,154,059 (GRCm39) |
|
probably benign |
Het |
| Naip6 |
C |
A |
13: 100,452,983 (GRCm39) |
R26L |
probably benign |
Het |
| Nbea |
T |
C |
3: 55,966,248 (GRCm39) |
T405A |
probably damaging |
Het |
| Nrp2 |
T |
A |
1: 62,802,063 (GRCm39) |
I502N |
probably damaging |
Het |
| Nt5el |
A |
T |
13: 105,246,129 (GRCm39) |
H230L |
probably benign |
Het |
| Nufip2 |
G |
A |
11: 77,582,733 (GRCm39) |
E216K |
possibly damaging |
Het |
| Oaf |
A |
G |
9: 43,133,930 (GRCm39) |
Y264H |
probably damaging |
Het |
| Or51a42 |
A |
G |
7: 103,708,431 (GRCm39) |
V126A |
probably damaging |
Het |
| Or5m10 |
T |
C |
2: 85,717,615 (GRCm39) |
L157P |
probably damaging |
Het |
| Or6c217 |
A |
T |
10: 129,738,293 (GRCm39) |
C95* |
probably null |
Het |
| Pax1 |
T |
C |
2: 147,210,321 (GRCm39) |
V352A |
probably damaging |
Het |
| Pkd1l2 |
TGGG |
TGG |
8: 117,764,974 (GRCm39) |
|
probably null |
Het |
| Plxna3 |
G |
A |
X: 73,383,772 (GRCm39) |
|
probably null |
Het |
| Pnpla3 |
T |
C |
15: 84,065,247 (GRCm39) |
V347A |
probably benign |
Het |
| Ppl |
T |
A |
16: 4,920,461 (GRCm39) |
K350* |
probably null |
Het |
| Pramel28 |
T |
C |
4: 143,692,632 (GRCm39) |
D123G |
probably benign |
Het |
| Prb1a |
T |
A |
6: 132,186,424 (GRCm39) |
|
probably null |
Het |
| Prb1a |
C |
A |
6: 132,186,423 (GRCm39) |
|
probably null |
Het |
| Ptpn11 |
G |
A |
5: 121,275,574 (GRCm39) |
H540Y |
probably benign |
Het |
| Ptprz1 |
C |
A |
6: 23,000,747 (GRCm39) |
H946N |
possibly damaging |
Het |
| Pwwp4a |
G |
T |
X: 72,171,261 (GRCm39) |
G218C |
probably damaging |
Het |
| Rad51b |
A |
G |
12: 79,349,317 (GRCm39) |
E51G |
possibly damaging |
Het |
| Rin2 |
T |
C |
2: 145,700,366 (GRCm39) |
V181A |
probably damaging |
Het |
| Rnf157 |
T |
A |
11: 116,245,188 (GRCm39) |
|
probably null |
Het |
| Rnf207 |
A |
G |
4: 152,398,328 (GRCm39) |
|
probably benign |
Het |
| Ror1 |
A |
T |
4: 100,299,183 (GRCm39) |
K852M |
probably damaging |
Het |
| Sbp |
T |
A |
17: 24,164,043 (GRCm39) |
I102K |
probably benign |
Het |
| Scaf8 |
T |
C |
17: 3,195,429 (GRCm39) |
I33T |
probably damaging |
Het |
| Scn5a |
C |
T |
9: 119,315,699 (GRCm39) |
V1670I |
probably damaging |
Het |
| Serhl |
C |
T |
15: 82,989,877 (GRCm39) |
T42M |
probably damaging |
Het |
| Sin3a |
A |
G |
9: 57,011,281 (GRCm39) |
|
probably benign |
Het |
| Slc12a2 |
A |
G |
18: 58,012,374 (GRCm39) |
S166G |
probably benign |
Het |
| Slc15a4 |
G |
A |
5: 127,680,832 (GRCm39) |
H396Y |
probably benign |
Het |
| Slc2a7 |
A |
T |
4: 150,239,143 (GRCm39) |
N123Y |
probably damaging |
Het |
| Smpd3 |
G |
A |
8: 106,992,199 (GRCm39) |
T118M |
possibly damaging |
Het |
| Spns2 |
A |
T |
11: 72,347,193 (GRCm39) |
I427N |
probably benign |
Het |
| Ssmem1 |
T |
A |
6: 30,519,650 (GRCm39) |
S112T |
probably damaging |
Het |
| Stard10 |
A |
T |
7: 100,993,233 (GRCm39) |
D190V |
probably damaging |
Het |
| Stil |
A |
T |
4: 114,881,049 (GRCm39) |
K531M |
probably damaging |
Het |
| Strc |
T |
C |
2: 121,203,219 (GRCm39) |
|
probably null |
Het |
| Svil |
T |
A |
18: 5,046,817 (GRCm39) |
I21N |
possibly damaging |
Het |
| Syt11 |
T |
C |
3: 88,656,110 (GRCm39) |
M14V |
probably benign |
Het |
| Tg |
A |
T |
15: 66,577,081 (GRCm39) |
Q1468L |
probably benign |
Het |
| Tjp1 |
A |
G |
7: 64,952,669 (GRCm39) |
V1555A |
probably benign |
Het |
| Tmprss11d |
A |
C |
5: 86,486,658 (GRCm39) |
S77R |
probably damaging |
Het |
| Tsnaxip1 |
A |
G |
8: 106,554,383 (GRCm39) |
|
probably benign |
Het |
| Tyr |
C |
A |
7: 87,141,914 (GRCm39) |
L138F |
probably damaging |
Het |
| Ubash3b |
A |
G |
9: 40,927,901 (GRCm39) |
V469A |
probably damaging |
Het |
| Ugt8a |
T |
C |
3: 125,709,098 (GRCm39) |
Y4C |
probably benign |
Het |
| Vmn1r201 |
A |
T |
13: 22,658,968 (GRCm39) |
T61S |
probably benign |
Het |
| Vmn1r204 |
A |
G |
13: 22,740,465 (GRCm39) |
H32R |
probably benign |
Het |
| Vmn1r228 |
T |
A |
17: 20,997,285 (GRCm39) |
I78L |
probably benign |
Het |
| Wdr90 |
T |
C |
17: 26,068,284 (GRCm39) |
D1348G |
possibly damaging |
Het |
| Zfp563 |
T |
A |
17: 33,324,187 (GRCm39) |
C261S |
probably benign |
Het |
| Zfp809 |
T |
A |
9: 22,146,395 (GRCm39) |
L28Q |
probably damaging |
Het |
| Znrf3 |
T |
A |
11: 5,239,066 (GRCm39) |
Q99L |
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 |
|
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 |
|
| Predicted Primers |
PCR Primer
(F):5'- AAACCCCGTCTGCAATGCAAGG -3'
(R):5'- GGAGCCTGAGGCAGCTATTTTACTC -3'
Sequencing Primer
(F):5'- TCTGCAATGCAAGGGAACTG -3'
(R):5'- GGCATCTCTTTGAAAGTGATACC -3'
|
| Posted On |
2014-04-13 |
Incidental Mutation