Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933402J07Rik |
G |
A |
8: 88,315,585 (GRCm39) |
R225H |
possibly damaging |
Het |
9330159F19Rik |
A |
T |
10: 29,098,290 (GRCm39) |
H199L |
possibly damaging |
Het |
Acaca |
AC |
A |
11: 84,167,390 (GRCm39) |
|
probably null |
Het |
Adam23 |
G |
A |
1: 63,582,329 (GRCm39) |
V326M |
probably damaging |
Het |
Aldh1a2 |
T |
A |
9: 71,169,023 (GRCm39) |
Y168* |
probably null |
Het |
Ano6 |
A |
G |
15: 95,870,451 (GRCm39) |
K869E |
possibly damaging |
Het |
Aplp2 |
G |
A |
9: 31,088,400 (GRCm39) |
A106V |
probably damaging |
Het |
Arhgdib |
T |
A |
6: 136,906,612 (GRCm39) |
K30* |
probably null |
Het |
Arl11 |
A |
G |
14: 61,548,393 (GRCm39) |
T68A |
probably benign |
Het |
Atg7 |
A |
G |
6: 114,650,638 (GRCm39) |
T83A |
possibly damaging |
Het |
Card9 |
T |
C |
2: 26,249,546 (GRCm39) |
E5G |
probably damaging |
Het |
Cars1 |
A |
G |
7: 143,123,194 (GRCm39) |
V474A |
probably damaging |
Het |
Cd300ld2 |
A |
G |
11: 114,904,601 (GRCm39) |
F89L |
probably benign |
Het |
Celf2 |
T |
A |
2: 6,889,769 (GRCm39) |
M1L |
probably benign |
Het |
Cnot1 |
T |
C |
8: 96,451,205 (GRCm39) |
D2174G |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Cox6b2 |
A |
G |
7: 4,754,937 (GRCm39) |
F74S |
probably damaging |
Het |
Cyp11b1 |
T |
A |
15: 74,710,383 (GRCm39) |
Q306L |
probably benign |
Het |
Ddx3y |
A |
G |
Y: 1,279,543 (GRCm39) |
I107T |
probably benign |
Het |
Dnah5 |
A |
T |
15: 28,326,782 (GRCm39) |
Y1997F |
probably damaging |
Het |
Dync2i1 |
A |
G |
12: 116,189,649 (GRCm39) |
L620P |
probably damaging |
Het |
Epha4 |
A |
T |
1: 77,364,460 (GRCm39) |
I683N |
probably damaging |
Het |
Fam120a |
G |
T |
13: 49,039,219 (GRCm39) |
A979E |
possibly damaging |
Het |
Gmip |
A |
G |
8: 70,266,774 (GRCm39) |
I296M |
probably damaging |
Het |
Gpr37l1 |
A |
G |
1: 135,094,639 (GRCm39) |
S202P |
probably damaging |
Het |
Ifi208 |
C |
A |
1: 173,505,476 (GRCm39) |
D75E |
possibly damaging |
Het |
Il24 |
T |
C |
1: 130,811,680 (GRCm39) |
N132S |
possibly damaging |
Het |
Katnal2 |
A |
G |
18: 77,099,763 (GRCm39) |
C124R |
probably benign |
Het |
Kcnq3 |
A |
T |
15: 65,867,270 (GRCm39) |
L791Q |
probably damaging |
Het |
Kcns3 |
T |
A |
12: 11,141,445 (GRCm39) |
D418V |
probably benign |
Het |
Kif13a |
A |
G |
13: 46,906,089 (GRCm39) |
V618A |
possibly damaging |
Het |
Kif13a |
A |
T |
13: 46,927,154 (GRCm39) |
V1179E |
possibly damaging |
Het |
Lpp |
A |
G |
16: 24,663,874 (GRCm39) |
I259V |
probably benign |
Het |
Mapkapk2 |
A |
G |
1: 130,986,087 (GRCm39) |
|
probably null |
Het |
Marchf7 |
T |
C |
2: 60,065,265 (GRCm39) |
S514P |
probably benign |
Het |
Nr4a2 |
T |
A |
2: 56,999,104 (GRCm39) |
L381F |
probably damaging |
Het |
Nt5dc3 |
A |
G |
10: 86,660,115 (GRCm39) |
D328G |
probably damaging |
Het |
Obox6 |
T |
C |
7: 15,568,445 (GRCm39) |
K144E |
probably damaging |
Het |
Oga |
A |
T |
19: 45,746,845 (GRCm39) |
M735K |
possibly damaging |
Het |
Olfml2b |
G |
A |
1: 170,509,346 (GRCm39) |
V565M |
probably damaging |
Het |
Or1d2 |
T |
C |
11: 74,255,819 (GRCm39) |
V108A |
probably damaging |
Het |
Orc3 |
G |
A |
4: 34,575,114 (GRCm39) |
A590V |
possibly damaging |
Het |
Picalm |
T |
C |
7: 89,809,757 (GRCm39) |
S78P |
possibly damaging |
Het |
Por |
T |
A |
5: 135,758,339 (GRCm39) |
Y105* |
probably null |
Het |
Ppara |
A |
G |
15: 85,682,180 (GRCm39) |
K292R |
probably benign |
Het |
Pramel27 |
T |
C |
4: 143,577,380 (GRCm39) |
F3S |
probably damaging |
Het |
Prss59 |
T |
G |
6: 40,903,096 (GRCm39) |
Y92S |
probably damaging |
Het |
Ralgds |
T |
A |
2: 28,440,558 (GRCm39) |
I844N |
probably damaging |
Het |
Rttn |
T |
C |
18: 89,027,441 (GRCm39) |
Y519H |
probably damaging |
Het |
Scn9a |
A |
G |
2: 66,332,060 (GRCm39) |
V1261A |
probably benign |
Het |
Slc2a2 |
T |
A |
3: 28,767,811 (GRCm39) |
|
probably null |
Het |
Slc5a7 |
T |
C |
17: 54,600,006 (GRCm39) |
M136V |
probably benign |
Het |
Smc4 |
C |
A |
3: 68,941,441 (GRCm39) |
A1232E |
probably damaging |
Het |
Smg1 |
A |
T |
7: 117,802,287 (GRCm39) |
C270* |
probably null |
Het |
Sparcl1 |
C |
T |
5: 104,240,690 (GRCm39) |
E245K |
probably benign |
Het |
Taf2 |
T |
C |
15: 54,879,850 (GRCm39) |
H1162R |
probably damaging |
Het |
Tlr3 |
T |
C |
8: 45,851,010 (GRCm39) |
D105G |
probably benign |
Het |
Tmem62 |
T |
C |
2: 120,814,958 (GRCm39) |
|
probably null |
Het |
Ufd1 |
T |
G |
16: 18,642,003 (GRCm39) |
C151W |
probably damaging |
Het |
Upk1b |
T |
G |
16: 38,600,402 (GRCm39) |
M193L |
probably benign |
Het |
Usp15 |
A |
G |
10: 122,968,949 (GRCm39) |
M334T |
probably damaging |
Het |
Utp20 |
A |
G |
10: 88,645,631 (GRCm39) |
S541P |
probably benign |
Het |
Vmn1r61 |
A |
T |
7: 5,614,302 (GRCm39) |
L4* |
probably null |
Het |
Vmn2r96 |
G |
A |
17: 18,802,915 (GRCm39) |
G83D |
possibly damaging |
Het |
Zbtb8a |
T |
C |
4: 129,248,110 (GRCm39) |
D387G |
possibly damaging |
Het |
Zfp106 |
A |
T |
2: 120,365,656 (GRCm39) |
N250K |
probably damaging |
Het |
Zfp292 |
A |
G |
4: 34,811,043 (GRCm39) |
V667A |
probably benign |
Het |
|
Other mutations in Triobp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01634:Triobp
|
APN |
15 |
78,877,568 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01904:Triobp
|
APN |
15 |
78,851,564 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01957:Triobp
|
APN |
15 |
78,856,847 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02085:Triobp
|
APN |
15 |
78,858,497 (GRCm39) |
splice site |
probably benign |
|
IGL02260:Triobp
|
APN |
15 |
78,850,562 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02498:Triobp
|
APN |
15 |
78,845,243 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02551:Triobp
|
APN |
15 |
78,857,689 (GRCm39) |
missense |
probably benign |
|
IGL02740:Triobp
|
APN |
15 |
78,850,889 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02810:Triobp
|
APN |
15 |
78,886,403 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03063:Triobp
|
APN |
15 |
78,875,084 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Triobp
|
UTSW |
15 |
78,877,587 (GRCm39) |
unclassified |
probably benign |
|
FR4340:Triobp
|
UTSW |
15 |
78,877,590 (GRCm39) |
unclassified |
probably benign |
|
FR4342:Triobp
|
UTSW |
15 |
78,877,592 (GRCm39) |
unclassified |
probably benign |
|
FR4449:Triobp
|
UTSW |
15 |
78,877,589 (GRCm39) |
unclassified |
probably benign |
|
FR4548:Triobp
|
UTSW |
15 |
78,877,590 (GRCm39) |
unclassified |
probably benign |
|
FR4548:Triobp
|
UTSW |
15 |
78,877,587 (GRCm39) |
unclassified |
probably benign |
|
R0276:Triobp
|
UTSW |
15 |
78,857,876 (GRCm39) |
missense |
probably benign |
0.09 |
R0309:Triobp
|
UTSW |
15 |
78,860,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Triobp
|
UTSW |
15 |
78,852,401 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0464:Triobp
|
UTSW |
15 |
78,851,186 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0525:Triobp
|
UTSW |
15 |
78,858,098 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0665:Triobp
|
UTSW |
15 |
78,858,098 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0689:Triobp
|
UTSW |
15 |
78,844,188 (GRCm39) |
nonsense |
probably null |
|
R1149:Triobp
|
UTSW |
15 |
78,850,679 (GRCm39) |
missense |
probably benign |
0.00 |
R1149:Triobp
|
UTSW |
15 |
78,850,679 (GRCm39) |
missense |
probably benign |
0.00 |
R1151:Triobp
|
UTSW |
15 |
78,850,679 (GRCm39) |
missense |
probably benign |
0.00 |
R1152:Triobp
|
UTSW |
15 |
78,850,679 (GRCm39) |
missense |
probably benign |
0.00 |
R1510:Triobp
|
UTSW |
15 |
78,887,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R1519:Triobp
|
UTSW |
15 |
78,857,938 (GRCm39) |
missense |
probably benign |
0.00 |
R1642:Triobp
|
UTSW |
15 |
78,886,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R1732:Triobp
|
UTSW |
15 |
78,851,428 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1975:Triobp
|
UTSW |
15 |
78,850,908 (GRCm39) |
missense |
probably benign |
|
R2051:Triobp
|
UTSW |
15 |
78,888,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R2073:Triobp
|
UTSW |
15 |
78,858,095 (GRCm39) |
missense |
probably damaging |
0.99 |
R2260:Triobp
|
UTSW |
15 |
78,875,640 (GRCm39) |
critical splice donor site |
probably null |
|
R2351:Triobp
|
UTSW |
15 |
78,888,780 (GRCm39) |
missense |
probably benign |
0.09 |
R2902:Triobp
|
UTSW |
15 |
78,857,618 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3801:Triobp
|
UTSW |
15 |
78,857,900 (GRCm39) |
missense |
probably benign |
0.04 |
R3959:Triobp
|
UTSW |
15 |
78,886,589 (GRCm39) |
nonsense |
probably null |
|
R4003:Triobp
|
UTSW |
15 |
78,844,177 (GRCm39) |
unclassified |
probably benign |
|
R4084:Triobp
|
UTSW |
15 |
78,857,871 (GRCm39) |
missense |
probably benign |
0.19 |
R4482:Triobp
|
UTSW |
15 |
78,850,763 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4592:Triobp
|
UTSW |
15 |
78,851,295 (GRCm39) |
missense |
probably benign |
|
R4662:Triobp
|
UTSW |
15 |
78,877,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Triobp
|
UTSW |
15 |
78,851,313 (GRCm39) |
missense |
probably damaging |
0.99 |
R4733:Triobp
|
UTSW |
15 |
78,851,313 (GRCm39) |
missense |
probably damaging |
0.99 |
R4789:Triobp
|
UTSW |
15 |
78,875,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R4968:Triobp
|
UTSW |
15 |
78,850,816 (GRCm39) |
missense |
probably benign |
0.03 |
R4990:Triobp
|
UTSW |
15 |
78,851,205 (GRCm39) |
missense |
probably benign |
0.00 |
R5129:Triobp
|
UTSW |
15 |
78,845,296 (GRCm39) |
missense |
probably benign |
0.15 |
R5181:Triobp
|
UTSW |
15 |
78,851,954 (GRCm39) |
missense |
probably benign |
0.00 |
R5279:Triobp
|
UTSW |
15 |
78,878,591 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5584:Triobp
|
UTSW |
15 |
78,852,332 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5601:Triobp
|
UTSW |
15 |
78,857,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R5810:Triobp
|
UTSW |
15 |
78,852,467 (GRCm39) |
missense |
probably benign |
0.07 |
R5969:Triobp
|
UTSW |
15 |
78,851,740 (GRCm39) |
missense |
probably benign |
0.05 |
R6722:Triobp
|
UTSW |
15 |
78,885,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R6739:Triobp
|
UTSW |
15 |
78,850,566 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6810:Triobp
|
UTSW |
15 |
78,850,815 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7011:Triobp
|
UTSW |
15 |
78,862,923 (GRCm39) |
missense |
probably damaging |
0.98 |
R7015:Triobp
|
UTSW |
15 |
78,878,260 (GRCm39) |
missense |
probably damaging |
0.99 |
R7200:Triobp
|
UTSW |
15 |
78,851,042 (GRCm39) |
small deletion |
probably benign |
|
R7294:Triobp
|
UTSW |
15 |
78,858,176 (GRCm39) |
missense |
probably damaging |
0.99 |
R7688:Triobp
|
UTSW |
15 |
78,845,311 (GRCm39) |
splice site |
probably null |
|
R7805:Triobp
|
UTSW |
15 |
78,858,204 (GRCm39) |
missense |
probably benign |
0.37 |
R7972:Triobp
|
UTSW |
15 |
78,852,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7977:Triobp
|
UTSW |
15 |
78,885,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R7987:Triobp
|
UTSW |
15 |
78,885,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R7999:Triobp
|
UTSW |
15 |
78,844,144 (GRCm39) |
missense |
probably damaging |
0.99 |
R8344:Triobp
|
UTSW |
15 |
78,842,475 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8348:Triobp
|
UTSW |
15 |
78,878,326 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8446:Triobp
|
UTSW |
15 |
78,878,326 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8448:Triobp
|
UTSW |
15 |
78,878,326 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8469:Triobp
|
UTSW |
15 |
78,851,219 (GRCm39) |
missense |
probably benign |
0.00 |
R8491:Triobp
|
UTSW |
15 |
78,878,326 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8492:Triobp
|
UTSW |
15 |
78,878,326 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8493:Triobp
|
UTSW |
15 |
78,878,326 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9424:Triobp
|
UTSW |
15 |
78,844,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R9495:Triobp
|
UTSW |
15 |
78,877,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R9514:Triobp
|
UTSW |
15 |
78,877,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R9530:Triobp
|
UTSW |
15 |
78,886,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R9550:Triobp
|
UTSW |
15 |
78,858,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R9576:Triobp
|
UTSW |
15 |
78,844,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R9646:Triobp
|
UTSW |
15 |
78,887,934 (GRCm39) |
missense |
probably damaging |
1.00 |
RF001:Triobp
|
UTSW |
15 |
78,851,227 (GRCm39) |
small insertion |
probably benign |
|
RF005:Triobp
|
UTSW |
15 |
78,851,261 (GRCm39) |
small insertion |
probably benign |
|
RF007:Triobp
|
UTSW |
15 |
78,851,244 (GRCm39) |
small insertion |
probably benign |
|
RF022:Triobp
|
UTSW |
15 |
78,858,482 (GRCm39) |
missense |
probably benign |
0.05 |
RF028:Triobp
|
UTSW |
15 |
78,851,239 (GRCm39) |
small insertion |
probably benign |
|
RF032:Triobp
|
UTSW |
15 |
78,851,236 (GRCm39) |
small insertion |
probably benign |
|
RF035:Triobp
|
UTSW |
15 |
78,851,239 (GRCm39) |
small insertion |
probably benign |
|
RF039:Triobp
|
UTSW |
15 |
78,851,239 (GRCm39) |
small insertion |
probably benign |
|
RF039:Triobp
|
UTSW |
15 |
78,851,236 (GRCm39) |
small insertion |
probably benign |
|
RF040:Triobp
|
UTSW |
15 |
78,851,263 (GRCm39) |
small insertion |
probably benign |
|
RF049:Triobp
|
UTSW |
15 |
78,851,261 (GRCm39) |
small insertion |
probably benign |
|
RF051:Triobp
|
UTSW |
15 |
78,851,234 (GRCm39) |
small insertion |
probably benign |
|
RF058:Triobp
|
UTSW |
15 |
78,851,244 (GRCm39) |
small insertion |
probably benign |
|
X0026:Triobp
|
UTSW |
15 |
78,844,223 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1177:Triobp
|
UTSW |
15 |
78,886,381 (GRCm39) |
missense |
probably damaging |
1.00 |
|