Incidental Mutation 'R0609:Tasor'
ID |
54553 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Tasor
|
Ensembl Gene |
ENSMUSG00000040651 |
Gene Name |
transcription activation suppressor |
Synonyms |
D14Abb1e, Fam208a, 4933409E02Rik, MommeD6 |
MMRRC Submission |
038798-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R0609 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
14 |
Chromosomal Location |
27150791-27205512 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 27183707 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Isoleucine
at position 722
(T722I)
|
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: T722I
PolyPhen 2
Score 0.094 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000022450 Gene: ENSMUSG00000040651 AA Change: T722I
Domain | Start | End | E-Value | Type |
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 |
- 1x: 99.4%
- 3x: 98.9%
- 10x: 97.6%
- 20x: 95.6%
|
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: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930596D02Rik |
A |
T |
14: 35,533,418 (GRCm39) |
|
probably null |
Het |
Abcb4 |
T |
A |
5: 8,997,376 (GRCm39) |
C952S |
probably damaging |
Het |
Adamtsl2 |
A |
G |
2: 26,979,647 (GRCm39) |
D272G |
probably benign |
Het |
Aim2 |
G |
A |
1: 173,289,530 (GRCm39) |
D158N |
probably damaging |
Het |
Aldh3b1 |
C |
T |
19: 3,964,024 (GRCm39) |
R426H |
probably damaging |
Het |
Apoc2 |
A |
G |
7: 19,407,278 (GRCm39) |
S28P |
probably benign |
Het |
Arfgef3 |
G |
A |
10: 18,473,179 (GRCm39) |
T1628I |
probably benign |
Het |
Atp10a |
G |
A |
7: 58,469,488 (GRCm39) |
|
probably null |
Het |
Bcl2 |
G |
A |
1: 106,640,292 (GRCm39) |
R107C |
probably damaging |
Het |
Bmp8b |
T |
A |
4: 123,015,692 (GRCm39) |
D226E |
probably benign |
Het |
Brsk2 |
T |
C |
7: 141,552,229 (GRCm39) |
Y618H |
probably damaging |
Het |
Casp12 |
T |
A |
9: 5,346,554 (GRCm39) |
F27Y |
probably damaging |
Het |
Casp8 |
T |
A |
1: 58,883,951 (GRCm39) |
N439K |
probably benign |
Het |
Ccdc175 |
T |
A |
12: 72,204,281 (GRCm39) |
K253N |
probably benign |
Het |
Cdc42bpa |
A |
G |
1: 179,867,744 (GRCm39) |
H193R |
probably damaging |
Het |
Cdk17 |
T |
C |
10: 93,052,334 (GRCm39) |
M105T |
probably benign |
Het |
Cdon |
C |
A |
9: 35,389,907 (GRCm39) |
P854T |
probably damaging |
Het |
Cep44 |
A |
G |
8: 56,997,187 (GRCm39) |
M117T |
possibly damaging |
Het |
Cep89 |
A |
T |
7: 35,134,955 (GRCm39) |
E674D |
probably damaging |
Het |
Cit |
C |
T |
5: 116,012,002 (GRCm39) |
A203V |
probably damaging |
Het |
Clstn1 |
C |
A |
4: 149,713,757 (GRCm39) |
|
probably null |
Het |
Col7a1 |
T |
A |
9: 108,787,215 (GRCm39) |
D565E |
unknown |
Het |
Cpb1 |
T |
A |
3: 20,316,638 (GRCm39) |
Y304F |
probably damaging |
Het |
Cps1 |
T |
G |
1: 67,211,961 (GRCm39) |
Y710D |
probably damaging |
Het |
Creb3l1 |
T |
C |
2: 91,817,398 (GRCm39) |
T372A |
possibly damaging |
Het |
Dars1 |
A |
G |
1: 128,333,118 (GRCm39) |
V102A |
probably benign |
Het |
Dhx35 |
C |
T |
2: 158,659,335 (GRCm39) |
T168I |
possibly damaging |
Het |
Dnah5 |
T |
C |
15: 28,327,925 (GRCm39) |
S2100P |
probably benign |
Het |
Dst |
T |
C |
1: 34,306,041 (GRCm39) |
|
probably null |
Het |
Egflam |
A |
C |
15: 7,283,004 (GRCm39) |
L351R |
possibly damaging |
Het |
Elp2 |
T |
A |
18: 24,759,213 (GRCm39) |
D523E |
probably benign |
Het |
Exo5 |
C |
A |
4: 120,778,881 (GRCm39) |
G328V |
probably damaging |
Het |
Fut9 |
A |
G |
4: 25,620,811 (GRCm39) |
M1T |
probably null |
Het |
Galnt5 |
A |
G |
2: 57,914,637 (GRCm39) |
N584S |
possibly damaging |
Het |
Gbp3 |
T |
C |
3: 142,273,533 (GRCm39) |
V360A |
probably damaging |
Het |
Gdf6 |
G |
A |
4: 9,859,977 (GRCm39) |
C353Y |
probably damaging |
Het |
Hace1 |
A |
G |
10: 45,524,965 (GRCm39) |
T244A |
probably damaging |
Het |
Hr |
T |
C |
14: 70,797,097 (GRCm39) |
I500T |
probably benign |
Het |
Ifnl2 |
A |
T |
7: 28,208,707 (GRCm39) |
L115Q |
probably damaging |
Het |
Iigp1 |
T |
C |
18: 60,522,896 (GRCm39) |
F5L |
probably benign |
Het |
Inhbb |
A |
G |
1: 119,345,146 (GRCm39) |
L381P |
probably damaging |
Het |
Irx3 |
A |
T |
8: 92,527,721 (GRCm39) |
S50T |
probably benign |
Het |
Ivns1abp |
C |
T |
1: 151,235,896 (GRCm39) |
T363I |
probably benign |
Het |
Izumo1 |
A |
T |
7: 45,272,323 (GRCm39) |
T35S |
probably benign |
Het |
Kank4 |
A |
G |
4: 98,665,342 (GRCm39) |
S651P |
probably damaging |
Het |
Kit |
T |
C |
5: 75,771,539 (GRCm39) |
V232A |
probably benign |
Het |
Klhl11 |
T |
C |
11: 100,354,540 (GRCm39) |
Y427C |
probably damaging |
Het |
Laptm4b |
T |
A |
15: 34,258,835 (GRCm39) |
N36K |
probably damaging |
Het |
Lrrk1 |
T |
C |
7: 65,916,363 (GRCm39) |
|
probably null |
Het |
Mamdc4 |
G |
T |
2: 25,454,205 (GRCm39) |
Q1042K |
probably benign |
Het |
Mical2 |
A |
G |
7: 111,920,647 (GRCm39) |
|
probably null |
Het |
Ms4a3 |
C |
A |
19: 11,608,725 (GRCm39) |
V176F |
possibly damaging |
Het |
Myo3a |
T |
C |
2: 22,338,324 (GRCm39) |
V427A |
probably benign |
Het |
Myo3a |
A |
C |
2: 22,401,110 (GRCm39) |
E626D |
possibly damaging |
Het |
Nckap5 |
A |
T |
1: 125,955,025 (GRCm39) |
L509* |
probably null |
Het |
Ndufa5 |
A |
T |
6: 24,519,248 (GRCm39) |
D64E |
possibly damaging |
Het |
Nedd4l |
T |
C |
18: 65,341,532 (GRCm39) |
Y753H |
probably damaging |
Het |
Nynrin |
T |
C |
14: 56,110,218 (GRCm39) |
V1775A |
probably damaging |
Het |
Oplah |
A |
G |
15: 76,187,192 (GRCm39) |
S570P |
probably benign |
Het |
Or14c39 |
T |
C |
7: 86,344,084 (GRCm39) |
V140A |
possibly damaging |
Het |
Or2ag1b |
A |
T |
7: 106,288,205 (GRCm39) |
H244Q |
probably damaging |
Het |
Or4q3 |
T |
C |
14: 50,583,383 (GRCm39) |
Y141C |
probably damaging |
Het |
Or5t18 |
A |
G |
2: 86,637,205 (GRCm39) |
L46S |
probably damaging |
Het |
Or9r3 |
G |
A |
10: 129,948,449 (GRCm39) |
S70F |
probably damaging |
Het |
Osbpl11 |
C |
A |
16: 33,054,814 (GRCm39) |
Y632* |
probably null |
Het |
Osbpl5 |
A |
T |
7: 143,248,558 (GRCm39) |
L644Q |
probably damaging |
Het |
Pcdhb19 |
T |
C |
18: 37,631,005 (GRCm39) |
W267R |
probably benign |
Het |
Pkhd1l1 |
A |
C |
15: 44,330,820 (GRCm39) |
S132R |
possibly damaging |
Het |
Pramel23 |
A |
T |
4: 143,425,073 (GRCm39) |
D123E |
probably benign |
Het |
Ptpn13 |
T |
A |
5: 103,704,011 (GRCm39) |
S1348T |
probably benign |
Het |
Rc3h1 |
T |
A |
1: 160,757,705 (GRCm39) |
W8R |
probably damaging |
Het |
Rgs3 |
T |
G |
4: 62,544,173 (GRCm39) |
V315G |
probably damaging |
Het |
Rora |
T |
A |
9: 69,269,151 (GRCm39) |
M82K |
probably damaging |
Het |
Rph3al |
T |
C |
11: 75,799,795 (GRCm39) |
I55V |
probably benign |
Het |
Sag |
T |
C |
1: 87,740,713 (GRCm39) |
V45A |
probably damaging |
Het |
Scn3a |
T |
C |
2: 65,366,854 (GRCm39) |
E56G |
probably damaging |
Het |
Sec24c |
T |
G |
14: 20,737,016 (GRCm39) |
V324G |
probably damaging |
Het |
Sptbn1 |
A |
G |
11: 30,088,979 (GRCm39) |
L748S |
probably damaging |
Het |
Stard9 |
A |
T |
2: 120,536,787 (GRCm39) |
D4186V |
probably damaging |
Het |
Stk39 |
T |
C |
2: 68,196,511 (GRCm39) |
E306G |
probably damaging |
Het |
Sycp1 |
C |
A |
3: 102,806,165 (GRCm39) |
|
probably null |
Het |
Taf2 |
A |
C |
15: 54,923,446 (GRCm39) |
L277R |
probably damaging |
Het |
Tbc1d23 |
T |
A |
16: 56,993,469 (GRCm39) |
I566F |
possibly damaging |
Het |
Tekt5 |
T |
C |
16: 10,179,168 (GRCm39) |
T400A |
possibly damaging |
Het |
Tgfbrap1 |
T |
C |
1: 43,099,301 (GRCm39) |
H401R |
probably benign |
Het |
Tie1 |
T |
A |
4: 118,333,344 (GRCm39) |
I841L |
possibly damaging |
Het |
Tln1 |
T |
G |
4: 43,544,645 (GRCm39) |
T1095P |
possibly damaging |
Het |
Tmem147 |
A |
G |
7: 30,427,527 (GRCm39) |
Y72H |
probably benign |
Het |
Tnfaip2 |
A |
G |
12: 111,419,941 (GRCm39) |
N691S |
probably benign |
Het |
Trim24 |
G |
A |
6: 37,934,718 (GRCm39) |
C811Y |
probably damaging |
Het |
Trim30b |
T |
A |
7: 104,007,183 (GRCm39) |
|
probably benign |
Het |
Trpc4 |
T |
G |
3: 54,102,189 (GRCm39) |
L29R |
probably damaging |
Het |
Trpm6 |
A |
T |
19: 18,803,226 (GRCm39) |
I890F |
probably damaging |
Het |
Ttc23l |
C |
T |
15: 10,504,622 (GRCm39) |
E442K |
probably benign |
Het |
Tut7 |
A |
T |
13: 59,947,596 (GRCm39) |
C506* |
probably null |
Het |
Uggt2 |
A |
G |
14: 119,332,748 (GRCm39) |
V62A |
probably damaging |
Het |
Ugt1a6a |
C |
A |
1: 88,066,606 (GRCm39) |
S137R |
probably benign |
Het |
Unc13a |
A |
G |
8: 72,111,111 (GRCm39) |
Y367H |
probably damaging |
Het |
Vmn2r49 |
A |
G |
7: 9,710,233 (GRCm39) |
I833T |
probably benign |
Het |
Vmn2r7 |
T |
C |
3: 64,623,900 (GRCm39) |
D231G |
probably benign |
Het |
Ythdc2 |
A |
T |
18: 44,997,424 (GRCm39) |
M994L |
probably benign |
Het |
Zfp804a |
G |
A |
2: 82,087,932 (GRCm39) |
S587N |
probably damaging |
Het |
Zswim2 |
A |
G |
2: 83,754,003 (GRCm39) |
I219T |
probably benign |
Het |
|
Other mutations in Tasor |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH 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 |
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 |
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 |
|
Predicted Primers |
PCR Primer
(F):5'- TGAACCTGAACAGCAGAAGTCGTC -3'
(R):5'- AGTCAACCAACCACGTCTTTCACTG -3'
Sequencing Primer
(F):5'- AGCAGAAGTCGTCTCATTCTTTG -3'
(R):5'- AGCTCCAGTGTGAAACCCTG -3'
|
Posted On |
2013-07-11 |