Incidental Mutation 'R4859:Trip12'
ID |
372287 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Trip12
|
Ensembl Gene |
ENSMUSG00000026219 |
Gene Name |
thyroid hormone receptor interactor 12 |
Synonyms |
Gtl6, 1110036I07Rik, 6720416K24Rik |
MMRRC Submission |
042470-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R4859 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
84698910-84818237 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 84771531 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Threonine
at position 248
(S248T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000139682
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027421]
[ENSMUST00000185909]
[ENSMUST00000186465]
[ENSMUST00000186648]
[ENSMUST00000186894]
[ENSMUST00000187818]
[ENSMUST00000189496]
[ENSMUST00000190067]
|
AlphaFold |
G5E870 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000027421
AA Change: S206T
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000027421 Gene: ENSMUSG00000026219 AA Change: S206T
Domain | Start | End | E-Value | Type |
low complexity region
|
34 |
39 |
N/A |
INTRINSIC |
low complexity region
|
153 |
172 |
N/A |
INTRINSIC |
low complexity region
|
177 |
188 |
N/A |
INTRINSIC |
low complexity region
|
191 |
215 |
N/A |
INTRINSIC |
low complexity region
|
231 |
247 |
N/A |
INTRINSIC |
low complexity region
|
379 |
391 |
N/A |
INTRINSIC |
low complexity region
|
392 |
406 |
N/A |
INTRINSIC |
low complexity region
|
416 |
427 |
N/A |
INTRINSIC |
SCOP:d1ee4a_
|
446 |
660 |
5e-20 |
SMART |
PDB:1WA5|B
|
447 |
641 |
1e-5 |
PDB |
Pfam:WWE
|
765 |
831 |
7.6e-22 |
PFAM |
low complexity region
|
983 |
1006 |
N/A |
INTRINSIC |
low complexity region
|
1033 |
1047 |
N/A |
INTRINSIC |
low complexity region
|
1062 |
1073 |
N/A |
INTRINSIC |
low complexity region
|
1333 |
1344 |
N/A |
INTRINSIC |
low complexity region
|
1345 |
1362 |
N/A |
INTRINSIC |
Blast:HECTc
|
1363 |
1417 |
8e-8 |
BLAST |
Blast:HECTc
|
1573 |
1629 |
2e-24 |
BLAST |
HECTc
|
1636 |
2025 |
1.29e-177 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000185909
AA Change: S248T
PolyPhen 2
Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000139986 Gene: ENSMUSG00000026219 AA Change: S248T
Domain | Start | End | E-Value | Type |
low complexity region
|
195 |
214 |
N/A |
INTRINSIC |
low complexity region
|
219 |
230 |
N/A |
INTRINSIC |
low complexity region
|
233 |
257 |
N/A |
INTRINSIC |
low complexity region
|
273 |
289 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000186465
AA Change: S206T
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000140224 Gene: ENSMUSG00000026219 AA Change: S206T
Domain | Start | End | E-Value | Type |
low complexity region
|
34 |
39 |
N/A |
INTRINSIC |
low complexity region
|
153 |
172 |
N/A |
INTRINSIC |
low complexity region
|
177 |
188 |
N/A |
INTRINSIC |
low complexity region
|
191 |
215 |
N/A |
INTRINSIC |
low complexity region
|
231 |
247 |
N/A |
INTRINSIC |
low complexity region
|
379 |
391 |
N/A |
INTRINSIC |
low complexity region
|
392 |
406 |
N/A |
INTRINSIC |
low complexity region
|
416 |
427 |
N/A |
INTRINSIC |
SCOP:d1ee4a_
|
446 |
660 |
5e-20 |
SMART |
PDB:1WA5|B
|
447 |
641 |
1e-5 |
PDB |
Pfam:WWE
|
761 |
831 |
2.2e-22 |
PFAM |
low complexity region
|
983 |
1006 |
N/A |
INTRINSIC |
low complexity region
|
1033 |
1047 |
N/A |
INTRINSIC |
low complexity region
|
1062 |
1073 |
N/A |
INTRINSIC |
low complexity region
|
1333 |
1344 |
N/A |
INTRINSIC |
low complexity region
|
1345 |
1362 |
N/A |
INTRINSIC |
Blast:HECTc
|
1363 |
1417 |
8e-8 |
BLAST |
Blast:HECTc
|
1573 |
1629 |
2e-24 |
BLAST |
HECTc
|
1636 |
2025 |
1.29e-177 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000186648
AA Change: S206T
PolyPhen 2
Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000139563 Gene: ENSMUSG00000026219 AA Change: S206T
Domain | Start | End | E-Value | Type |
low complexity region
|
34 |
39 |
N/A |
INTRINSIC |
low complexity region
|
153 |
172 |
N/A |
INTRINSIC |
low complexity region
|
177 |
188 |
N/A |
INTRINSIC |
low complexity region
|
191 |
215 |
N/A |
INTRINSIC |
low complexity region
|
231 |
247 |
N/A |
INTRINSIC |
low complexity region
|
386 |
400 |
N/A |
INTRINSIC |
low complexity region
|
410 |
421 |
N/A |
INTRINSIC |
SCOP:d1ee4a_
|
440 |
654 |
5e-20 |
SMART |
PDB:1WA5|B
|
441 |
635 |
1e-5 |
PDB |
low complexity region
|
950 |
973 |
N/A |
INTRINSIC |
low complexity region
|
1000 |
1014 |
N/A |
INTRINSIC |
low complexity region
|
1029 |
1040 |
N/A |
INTRINSIC |
low complexity region
|
1300 |
1311 |
N/A |
INTRINSIC |
low complexity region
|
1312 |
1329 |
N/A |
INTRINSIC |
Blast:HECTc
|
1330 |
1384 |
7e-8 |
BLAST |
Blast:HECTc
|
1540 |
1596 |
2e-24 |
BLAST |
HECTc
|
1603 |
1992 |
6.2e-180 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000186894
AA Change: S206T
PolyPhen 2
Score 0.024 (Sensitivity: 0.95; Specificity: 0.81)
|
SMART Domains |
Protein: ENSMUSP00000140267 Gene: ENSMUSG00000026219 AA Change: S206T
Domain | Start | End | E-Value | Type |
low complexity region
|
34 |
39 |
N/A |
INTRINSIC |
low complexity region
|
153 |
172 |
N/A |
INTRINSIC |
low complexity region
|
177 |
188 |
N/A |
INTRINSIC |
low complexity region
|
191 |
215 |
N/A |
INTRINSIC |
low complexity region
|
231 |
247 |
N/A |
INTRINSIC |
low complexity region
|
379 |
391 |
N/A |
INTRINSIC |
low complexity region
|
392 |
406 |
N/A |
INTRINSIC |
low complexity region
|
416 |
427 |
N/A |
INTRINSIC |
SCOP:d1ee4a_
|
446 |
660 |
3e-20 |
SMART |
PDB:1WA5|B
|
447 |
641 |
7e-6 |
PDB |
Blast:ARM
|
476 |
516 |
6e-6 |
BLAST |
WWE
|
764 |
839 |
6.9e-25 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000187818
|
SMART Domains |
Protein: ENSMUSP00000140917 Gene: ENSMUSG00000026219
Domain | Start | End | E-Value | Type |
low complexity region
|
34 |
39 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000189496
AA Change: S248T
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000139682 Gene: ENSMUSG00000026219 AA Change: S248T
Domain | Start | End | E-Value | Type |
low complexity region
|
195 |
214 |
N/A |
INTRINSIC |
low complexity region
|
219 |
230 |
N/A |
INTRINSIC |
low complexity region
|
233 |
257 |
N/A |
INTRINSIC |
low complexity region
|
273 |
289 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000190067
|
SMART Domains |
Protein: ENSMUSP00000140817 Gene: ENSMUSG00000026219
Domain | Start | End | E-Value | Type |
low complexity region
|
34 |
39 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000190464
|
Meta Mutation Damage Score |
0.0963 |
Coding Region Coverage |
- 1x: 98.9%
- 3x: 98.1%
- 10x: 95.5%
- 20x: 89.5%
|
Validation Efficiency |
100% (112/112) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is an E3 ubiquitin-protein ligase involved in the degradation of the p19ARF/ARF isoform of CDKN2A, a tumor suppressor. The encoded protein also plays a role in the DNA damage response by regulating the stability of USP7, which regulates tumor suppressor p53. [provided by RefSeq, Jan 2017] PHENOTYPE: Mice homozygous for a targeted allele exhibit complete embryonic lethality during organogenesis associated with embryonic growth retardation and abnormal placenta development. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
T |
A |
8: 41,207,580 (GRCm39) |
V282E |
probably benign |
Het |
Adam26b |
T |
C |
8: 43,973,296 (GRCm39) |
T569A |
possibly damaging |
Het |
Adam6a |
A |
G |
12: 113,509,609 (GRCm39) |
N661D |
probably damaging |
Het |
Adck1 |
G |
A |
12: 88,407,865 (GRCm39) |
A199T |
probably benign |
Het |
Adhfe1 |
A |
G |
1: 9,628,438 (GRCm39) |
Y270C |
probably damaging |
Het |
Aldh16a1 |
C |
T |
7: 44,796,731 (GRCm39) |
R256H |
probably benign |
Het |
Ap5z1 |
T |
C |
5: 142,459,748 (GRCm39) |
M466T |
possibly damaging |
Het |
Aspm |
C |
T |
1: 139,397,131 (GRCm39) |
L908F |
probably damaging |
Het |
Atp8b2 |
T |
A |
3: 89,853,287 (GRCm39) |
T743S |
probably benign |
Het |
Bag2 |
G |
T |
1: 33,786,022 (GRCm39) |
T100K |
probably damaging |
Het |
Camk2a |
A |
G |
18: 61,076,246 (GRCm39) |
|
probably benign |
Het |
Ccdc158 |
A |
G |
5: 92,781,262 (GRCm39) |
Y848H |
probably damaging |
Het |
Ccp110 |
T |
G |
7: 118,324,653 (GRCm39) |
V725G |
possibly damaging |
Het |
Cdh6 |
A |
G |
15: 13,051,418 (GRCm39) |
V405A |
probably benign |
Het |
Ces2g |
T |
C |
8: 105,694,094 (GRCm39) |
|
probably null |
Het |
Cfap157 |
A |
G |
2: 32,667,554 (GRCm39) |
F510L |
probably benign |
Het |
Chd3 |
A |
T |
11: 69,250,722 (GRCm39) |
M669K |
possibly damaging |
Het |
Cnot10 |
C |
T |
9: 114,456,532 (GRCm39) |
A168T |
probably damaging |
Het |
Crybg1 |
A |
G |
10: 43,868,565 (GRCm39) |
V1371A |
probably damaging |
Het |
Dars2 |
A |
G |
1: 160,872,560 (GRCm39) |
L547P |
probably damaging |
Het |
Dis3 |
A |
G |
14: 99,325,226 (GRCm39) |
C483R |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,395,762 (GRCm39) |
L3888Q |
probably damaging |
Het |
Dpysl2 |
A |
T |
14: 67,066,888 (GRCm39) |
Y182N |
probably damaging |
Het |
Eif4g1 |
T |
A |
16: 20,500,923 (GRCm39) |
F509L |
probably benign |
Het |
Evc |
T |
C |
5: 37,458,253 (GRCm39) |
T85A |
probably damaging |
Het |
Farsb |
T |
C |
1: 78,444,609 (GRCm39) |
T283A |
probably benign |
Het |
Fem1al |
G |
T |
11: 29,775,178 (GRCm39) |
A93E |
probably damaging |
Het |
Fgf14 |
C |
A |
14: 124,429,845 (GRCm39) |
R30L |
possibly damaging |
Het |
Gbe1 |
T |
C |
16: 70,275,289 (GRCm39) |
L363P |
probably damaging |
Het |
Gcg |
A |
G |
2: 62,307,189 (GRCm39) |
V124A |
probably damaging |
Het |
Glb1l |
A |
G |
1: 75,176,963 (GRCm39) |
|
probably benign |
Het |
Gm5431 |
T |
C |
11: 48,780,409 (GRCm39) |
E449G |
probably damaging |
Het |
Gon4l |
T |
C |
3: 88,802,655 (GRCm39) |
S1089P |
probably benign |
Het |
Hgd |
T |
C |
16: 37,409,111 (GRCm39) |
L25P |
probably damaging |
Het |
Hnf1a |
T |
C |
5: 115,093,311 (GRCm39) |
H318R |
possibly damaging |
Het |
Hsd17b7 |
A |
C |
1: 169,794,826 (GRCm39) |
V71G |
possibly damaging |
Het |
Hydin |
T |
C |
8: 111,233,126 (GRCm39) |
S1742P |
possibly damaging |
Het |
Insyn2b |
A |
G |
11: 34,353,154 (GRCm39) |
S399G |
probably benign |
Het |
Kank2 |
T |
C |
9: 21,691,078 (GRCm39) |
E552G |
probably benign |
Het |
Kcnq4 |
C |
A |
4: 120,573,810 (GRCm39) |
R217L |
probably damaging |
Het |
Klrg2 |
T |
C |
6: 38,604,540 (GRCm39) |
*201W |
probably null |
Het |
Kndc1 |
T |
C |
7: 139,501,821 (GRCm39) |
S953P |
probably benign |
Het |
Lama2 |
TTTGCGCATT |
TTT |
10: 26,919,639 (GRCm39) |
|
probably null |
Het |
Lonp1 |
A |
G |
17: 56,933,587 (GRCm39) |
V96A |
probably benign |
Het |
Mgat4e |
T |
C |
1: 134,469,478 (GRCm39) |
K189E |
possibly damaging |
Het |
Msantd5f8 |
A |
G |
4: 73,805,457 (GRCm39) |
S351P |
probably damaging |
Het |
Msh2 |
G |
A |
17: 88,026,187 (GRCm39) |
V722I |
possibly damaging |
Het |
Mtcl3 |
A |
C |
10: 29,026,390 (GRCm39) |
M491L |
probably benign |
Het |
N4bp2 |
T |
C |
5: 65,982,641 (GRCm39) |
Y1632H |
probably damaging |
Het |
Nlrc4 |
T |
G |
17: 74,743,032 (GRCm39) |
K862T |
probably damaging |
Het |
Notch4 |
A |
T |
17: 34,806,154 (GRCm39) |
Q1750L |
probably damaging |
Het |
Obscn |
C |
T |
11: 58,972,849 (GRCm39) |
V2066I |
possibly damaging |
Het |
Or2v2 |
T |
C |
11: 49,003,993 (GRCm39) |
K187E |
probably damaging |
Het |
Or4c15 |
T |
A |
2: 88,760,627 (GRCm39) |
I11L |
probably benign |
Het |
Or4f14b |
A |
T |
2: 111,775,156 (GRCm39) |
I215N |
probably damaging |
Het |
Or52d13 |
A |
T |
7: 103,110,243 (GRCm39) |
Y57* |
probably null |
Het |
Or5m8 |
T |
C |
2: 85,823,075 (GRCm39) |
S305P |
probably damaging |
Het |
Pde7a |
T |
A |
3: 19,295,655 (GRCm39) |
|
probably benign |
Het |
Pign |
A |
T |
1: 105,575,892 (GRCm39) |
Y249* |
probably null |
Het |
Ppp1r17 |
A |
T |
6: 56,003,449 (GRCm39) |
E87D |
probably damaging |
Het |
Prss3 |
T |
A |
6: 41,350,857 (GRCm39) |
Q211L |
probably damaging |
Het |
Rapgef6 |
A |
G |
11: 54,526,989 (GRCm39) |
E413G |
probably benign |
Het |
Rnf150 |
A |
G |
8: 83,590,712 (GRCm39) |
H25R |
probably damaging |
Het |
Scamp2 |
T |
C |
9: 57,488,934 (GRCm39) |
|
probably null |
Het |
Scap |
T |
A |
9: 110,203,410 (GRCm39) |
|
probably benign |
Het |
Sdc2 |
A |
C |
15: 33,032,602 (GRCm39) |
K175N |
probably damaging |
Het |
Serpinb6d |
T |
A |
13: 33,851,547 (GRCm39) |
|
probably null |
Het |
Sh3tc2 |
A |
G |
18: 62,146,164 (GRCm39) |
N1181S |
probably benign |
Het |
Slc44a2 |
T |
C |
9: 21,259,441 (GRCm39) |
I46T |
probably damaging |
Het |
Slfn8 |
A |
G |
11: 82,908,540 (GRCm39) |
M1T |
probably null |
Het |
Slitrk6 |
T |
C |
14: 110,989,315 (GRCm39) |
T131A |
probably damaging |
Het |
Spata1 |
C |
G |
3: 146,175,529 (GRCm39) |
D326H |
probably damaging |
Het |
Tbck |
T |
G |
3: 132,507,288 (GRCm39) |
S753R |
probably benign |
Het |
Tdp1 |
A |
G |
12: 99,876,070 (GRCm39) |
I340M |
probably benign |
Het |
Tmprss6 |
T |
A |
15: 78,330,877 (GRCm39) |
Y50F |
probably damaging |
Het |
Trank1 |
T |
A |
9: 111,194,078 (GRCm39) |
S701T |
probably benign |
Het |
Trbv17 |
A |
T |
6: 41,140,223 (GRCm39) |
N26I |
probably benign |
Het |
Vmn2r53 |
T |
G |
7: 12,335,330 (GRCm39) |
Q110P |
probably damaging |
Het |
Vmn2r75 |
A |
G |
7: 85,797,611 (GRCm39) |
V734A |
probably benign |
Het |
Wfdc11 |
A |
T |
2: 164,507,415 (GRCm39) |
M14K |
probably null |
Het |
Xcr1 |
T |
A |
9: 123,685,712 (GRCm39) |
M17L |
probably benign |
Het |
Zbtb40 |
A |
G |
4: 136,716,070 (GRCm39) |
I965T |
probably damaging |
Het |
Zfp760 |
A |
T |
17: 21,942,511 (GRCm39) |
H562L |
probably damaging |
Het |
Zfp760 |
A |
T |
17: 21,942,516 (GRCm39) |
R564* |
probably null |
Het |
Znf41-ps |
T |
A |
4: 145,555,283 (GRCm39) |
|
noncoding transcript |
Het |
Zyg11a |
A |
T |
4: 108,067,387 (GRCm39) |
I41N |
probably damaging |
Het |
|
Other mutations in Trip12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00331:Trip12
|
APN |
1 |
84,708,262 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00430:Trip12
|
APN |
1 |
84,741,582 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00465:Trip12
|
APN |
1 |
84,741,582 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00819:Trip12
|
APN |
1 |
84,731,993 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00900:Trip12
|
APN |
1 |
84,702,485 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL00990:Trip12
|
APN |
1 |
84,729,605 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01087:Trip12
|
APN |
1 |
84,735,580 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01400:Trip12
|
APN |
1 |
84,729,699 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01521:Trip12
|
APN |
1 |
84,743,919 (GRCm39) |
splice site |
probably benign |
|
IGL01619:Trip12
|
APN |
1 |
84,792,631 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01796:Trip12
|
APN |
1 |
84,705,999 (GRCm39) |
missense |
probably benign |
0.42 |
IGL01975:Trip12
|
APN |
1 |
84,792,534 (GRCm39) |
splice site |
probably benign |
|
IGL02190:Trip12
|
APN |
1 |
84,743,791 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02474:Trip12
|
APN |
1 |
84,771,854 (GRCm39) |
missense |
probably benign |
|
IGL02517:Trip12
|
APN |
1 |
84,721,535 (GRCm39) |
unclassified |
probably benign |
|
IGL02631:Trip12
|
APN |
1 |
84,743,729 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02991:Trip12
|
APN |
1 |
84,716,536 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03161:Trip12
|
APN |
1 |
84,738,853 (GRCm39) |
unclassified |
probably benign |
|
IGL03388:Trip12
|
APN |
1 |
84,720,907 (GRCm39) |
missense |
probably damaging |
0.99 |
cardamom
|
UTSW |
1 |
84,726,997 (GRCm39) |
missense |
probably damaging |
0.99 |
pungent
|
UTSW |
1 |
84,771,636 (GRCm39) |
missense |
possibly damaging |
0.70 |
spices
|
UTSW |
1 |
84,771,596 (GRCm39) |
missense |
probably benign |
0.10 |
sulfuric
|
UTSW |
1 |
84,736,771 (GRCm39) |
missense |
probably benign |
0.19 |
Turmeric
|
UTSW |
1 |
84,732,064 (GRCm39) |
missense |
probably benign |
0.07 |
LCD18:Trip12
|
UTSW |
1 |
84,754,482 (GRCm38) |
unclassified |
probably benign |
|
R0090:Trip12
|
UTSW |
1 |
84,709,857 (GRCm39) |
splice site |
probably benign |
|
R0111:Trip12
|
UTSW |
1 |
84,736,854 (GRCm39) |
unclassified |
probably benign |
|
R0471:Trip12
|
UTSW |
1 |
84,703,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R0486:Trip12
|
UTSW |
1 |
84,738,805 (GRCm39) |
nonsense |
probably null |
|
R0557:Trip12
|
UTSW |
1 |
84,702,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R0570:Trip12
|
UTSW |
1 |
84,729,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Trip12
|
UTSW |
1 |
84,735,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R0627:Trip12
|
UTSW |
1 |
84,746,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R0630:Trip12
|
UTSW |
1 |
84,771,636 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0657:Trip12
|
UTSW |
1 |
84,736,771 (GRCm39) |
missense |
probably benign |
0.19 |
R0741:Trip12
|
UTSW |
1 |
84,722,902 (GRCm39) |
missense |
probably benign |
0.09 |
R0862:Trip12
|
UTSW |
1 |
84,721,730 (GRCm39) |
missense |
probably damaging |
0.99 |
R0864:Trip12
|
UTSW |
1 |
84,721,730 (GRCm39) |
missense |
probably damaging |
0.99 |
R1124:Trip12
|
UTSW |
1 |
84,714,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R1252:Trip12
|
UTSW |
1 |
84,754,071 (GRCm39) |
nonsense |
probably null |
|
R1455:Trip12
|
UTSW |
1 |
84,736,821 (GRCm39) |
missense |
probably benign |
0.01 |
R1487:Trip12
|
UTSW |
1 |
84,746,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R1702:Trip12
|
UTSW |
1 |
84,722,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R1781:Trip12
|
UTSW |
1 |
84,708,342 (GRCm39) |
missense |
probably benign |
0.01 |
R1847:Trip12
|
UTSW |
1 |
84,726,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R1854:Trip12
|
UTSW |
1 |
84,705,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Trip12
|
UTSW |
1 |
84,722,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R1926:Trip12
|
UTSW |
1 |
84,727,012 (GRCm39) |
missense |
probably damaging |
0.98 |
R1935:Trip12
|
UTSW |
1 |
84,771,822 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1950:Trip12
|
UTSW |
1 |
84,738,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R1994:Trip12
|
UTSW |
1 |
84,726,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Trip12
|
UTSW |
1 |
84,738,587 (GRCm39) |
nonsense |
probably null |
|
R2391:Trip12
|
UTSW |
1 |
84,792,511 (GRCm39) |
frame shift |
probably null |
|
R2423:Trip12
|
UTSW |
1 |
84,792,511 (GRCm39) |
frame shift |
probably null |
|
R2433:Trip12
|
UTSW |
1 |
84,721,544 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2905:Trip12
|
UTSW |
1 |
84,732,064 (GRCm39) |
missense |
probably benign |
0.07 |
R3040:Trip12
|
UTSW |
1 |
84,719,966 (GRCm39) |
missense |
probably benign |
0.13 |
R3735:Trip12
|
UTSW |
1 |
84,792,511 (GRCm39) |
frame shift |
probably null |
|
R3907:Trip12
|
UTSW |
1 |
84,709,827 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4394:Trip12
|
UTSW |
1 |
84,703,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R4540:Trip12
|
UTSW |
1 |
84,726,997 (GRCm39) |
missense |
probably damaging |
0.99 |
R5240:Trip12
|
UTSW |
1 |
84,771,854 (GRCm39) |
missense |
probably benign |
|
R5278:Trip12
|
UTSW |
1 |
84,739,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R5377:Trip12
|
UTSW |
1 |
84,735,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R5510:Trip12
|
UTSW |
1 |
84,746,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R5542:Trip12
|
UTSW |
1 |
84,727,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R5550:Trip12
|
UTSW |
1 |
84,738,820 (GRCm39) |
missense |
probably damaging |
0.99 |
R5886:Trip12
|
UTSW |
1 |
84,708,179 (GRCm39) |
intron |
probably benign |
|
R5893:Trip12
|
UTSW |
1 |
84,736,884 (GRCm39) |
unclassified |
probably benign |
|
R5914:Trip12
|
UTSW |
1 |
84,741,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R5925:Trip12
|
UTSW |
1 |
84,726,974 (GRCm39) |
nonsense |
probably null |
|
R5985:Trip12
|
UTSW |
1 |
84,703,492 (GRCm39) |
missense |
probably damaging |
0.99 |
R6135:Trip12
|
UTSW |
1 |
84,738,559 (GRCm39) |
missense |
probably benign |
0.00 |
R6158:Trip12
|
UTSW |
1 |
84,738,733 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6419:Trip12
|
UTSW |
1 |
84,771,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R6816:Trip12
|
UTSW |
1 |
84,771,435 (GRCm39) |
missense |
probably damaging |
0.99 |
R7144:Trip12
|
UTSW |
1 |
84,771,435 (GRCm39) |
missense |
probably damaging |
0.99 |
R7194:Trip12
|
UTSW |
1 |
84,771,943 (GRCm39) |
missense |
probably benign |
0.07 |
R7355:Trip12
|
UTSW |
1 |
84,792,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:Trip12
|
UTSW |
1 |
84,728,163 (GRCm39) |
missense |
probably damaging |
0.98 |
R7588:Trip12
|
UTSW |
1 |
84,738,604 (GRCm39) |
missense |
probably damaging |
0.99 |
R7705:Trip12
|
UTSW |
1 |
84,755,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R7818:Trip12
|
UTSW |
1 |
84,738,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R7918:Trip12
|
UTSW |
1 |
84,722,784 (GRCm39) |
missense |
probably damaging |
0.98 |
R8127:Trip12
|
UTSW |
1 |
84,716,463 (GRCm39) |
missense |
probably damaging |
0.99 |
R8221:Trip12
|
UTSW |
1 |
84,743,771 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8336:Trip12
|
UTSW |
1 |
84,743,762 (GRCm39) |
missense |
probably benign |
0.37 |
R8373:Trip12
|
UTSW |
1 |
84,773,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R8719:Trip12
|
UTSW |
1 |
84,722,790 (GRCm39) |
missense |
probably damaging |
0.98 |
R8771:Trip12
|
UTSW |
1 |
84,721,018 (GRCm39) |
unclassified |
probably benign |
|
R8997:Trip12
|
UTSW |
1 |
84,771,596 (GRCm39) |
missense |
probably benign |
0.10 |
R9146:Trip12
|
UTSW |
1 |
84,771,881 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9236:Trip12
|
UTSW |
1 |
84,703,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R9338:Trip12
|
UTSW |
1 |
84,727,019 (GRCm39) |
missense |
probably damaging |
0.99 |
R9391:Trip12
|
UTSW |
1 |
84,773,473 (GRCm39) |
missense |
probably benign |
0.00 |
R9516:Trip12
|
UTSW |
1 |
84,735,215 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Trip12
|
UTSW |
1 |
84,738,508 (GRCm39) |
missense |
probably benign |
0.12 |
X0065:Trip12
|
UTSW |
1 |
84,726,884 (GRCm39) |
missense |
probably benign |
0.21 |
Z1088:Trip12
|
UTSW |
1 |
84,743,889 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- AGGTAGGCTAACTTTGGGGC -3'
(R):5'- CTGCTGGTAGTTCACGGAATCAG -3'
Sequencing Primer
(F):5'- CTAACTTTGGGGCTGAAGCGAG -3'
(R):5'- CTGGTAGTTCACGGAATCAGAAAAG -3'
|
Posted On |
2016-03-01 |