Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730013G03Rik |
C |
T |
1: 192,515,845 (GRCm39) |
|
noncoding transcript |
Het |
Abca12 |
T |
A |
1: 71,327,856 (GRCm39) |
D1408V |
probably damaging |
Het |
Abca13 |
A |
T |
11: 9,243,877 (GRCm39) |
L1913F |
probably damaging |
Het |
Acad9 |
A |
G |
3: 36,127,752 (GRCm39) |
E118G |
probably damaging |
Het |
Adamts5 |
G |
A |
16: 85,665,531 (GRCm39) |
A590V |
probably damaging |
Het |
Ano6 |
A |
C |
15: 95,863,790 (GRCm39) |
Y791S |
probably benign |
Het |
Aox1 |
T |
C |
1: 58,346,603 (GRCm39) |
|
probably null |
Het |
Aox4 |
T |
A |
1: 58,261,051 (GRCm39) |
I128N |
probably damaging |
Het |
Atp2b3 |
A |
G |
X: 72,613,921 (GRCm39) |
M1142V |
probably benign |
Het |
AU041133 |
A |
G |
10: 81,987,223 (GRCm39) |
H292R |
probably damaging |
Het |
Bco2 |
A |
G |
9: 50,456,666 (GRCm39) |
M158T |
probably benign |
Het |
Bpnt1 |
T |
A |
1: 185,077,626 (GRCm39) |
|
probably benign |
Het |
Cadm1 |
A |
G |
9: 47,708,741 (GRCm39) |
D157G |
probably damaging |
Het |
Catsperg1 |
T |
C |
7: 28,895,357 (GRCm39) |
R499G |
possibly damaging |
Het |
Ccr7 |
T |
C |
11: 99,035,872 (GRCm39) |
E350G |
probably damaging |
Het |
Ceacam5 |
T |
A |
7: 17,486,076 (GRCm39) |
S524R |
probably benign |
Het |
Cep78 |
T |
C |
19: 15,936,943 (GRCm39) |
T588A |
probably benign |
Het |
Cfap65 |
T |
A |
1: 74,966,840 (GRCm39) |
E282D |
possibly damaging |
Het |
Drd2 |
A |
G |
9: 49,316,221 (GRCm39) |
K327R |
probably benign |
Het |
Erich5 |
C |
T |
15: 34,471,557 (GRCm39) |
P262L |
possibly damaging |
Het |
Ezh2 |
A |
C |
6: 47,510,748 (GRCm39) |
D578E |
probably damaging |
Het |
Fez1 |
A |
G |
9: 36,781,784 (GRCm39) |
N20S |
probably damaging |
Het |
Folr2 |
T |
G |
7: 101,492,906 (GRCm39) |
K39T |
probably damaging |
Het |
Gm10549 |
G |
T |
18: 33,597,530 (GRCm39) |
|
probably null |
Het |
Gm14393 |
C |
T |
2: 174,903,640 (GRCm39) |
C89Y |
probably benign |
Het |
Gm5329 |
T |
G |
7: 31,671,828 (GRCm39) |
|
noncoding transcript |
Het |
Gm7367 |
A |
G |
7: 59,805,517 (GRCm39) |
|
noncoding transcript |
Het |
Gpr162 |
A |
T |
6: 124,837,031 (GRCm39) |
W338R |
probably damaging |
Het |
Ift80 |
A |
T |
3: 68,898,141 (GRCm39) |
F65I |
possibly damaging |
Het |
Klra6 |
T |
G |
6: 129,995,885 (GRCm39) |
I158L |
probably benign |
Het |
Lpp |
T |
A |
16: 24,580,804 (GRCm39) |
Y173* |
probably null |
Het |
Lrp12 |
A |
G |
15: 39,735,976 (GRCm39) |
V671A |
probably benign |
Het |
Lrrc27 |
C |
T |
7: 138,803,609 (GRCm39) |
R178C |
probably damaging |
Het |
Lrrc49 |
G |
A |
9: 60,573,609 (GRCm39) |
T225M |
probably benign |
Het |
Megf8 |
T |
A |
7: 25,054,793 (GRCm39) |
S1915T |
probably benign |
Het |
Mmadhc |
T |
C |
2: 50,181,344 (GRCm39) |
T109A |
probably benign |
Het |
Mon2 |
T |
C |
10: 122,852,397 (GRCm39) |
E992G |
probably benign |
Het |
Msl3 |
A |
G |
X: 167,450,059 (GRCm39) |
I267T |
probably damaging |
Het |
Msl3 |
A |
T |
X: 167,445,430 (GRCm39) |
N430K |
probably damaging |
Het |
Nab2 |
G |
T |
10: 127,500,917 (GRCm39) |
Y25* |
probably null |
Het |
Or5ae2 |
C |
T |
7: 84,506,497 (GRCm39) |
H307Y |
probably benign |
Het |
Osgepl1 |
A |
G |
1: 53,354,167 (GRCm39) |
T44A |
probably damaging |
Het |
Pdpr |
A |
G |
8: 111,856,212 (GRCm39) |
|
probably benign |
Het |
Pfkp |
A |
G |
13: 6,669,261 (GRCm39) |
S241P |
probably damaging |
Het |
Phgdh |
A |
T |
3: 98,235,377 (GRCm39) |
S166T |
possibly damaging |
Het |
Plcl1 |
C |
T |
1: 55,790,494 (GRCm39) |
Q1055* |
probably null |
Het |
Plscr2 |
A |
G |
9: 92,169,790 (GRCm39) |
N80S |
probably benign |
Het |
Polr3k |
A |
T |
2: 181,510,035 (GRCm39) |
M80L |
probably benign |
Het |
Prex2 |
A |
G |
1: 11,171,383 (GRCm39) |
D304G |
probably damaging |
Het |
Prex2 |
A |
G |
1: 11,355,285 (GRCm39) |
T1529A |
probably damaging |
Het |
Rcvrn |
A |
T |
11: 67,586,514 (GRCm39) |
H91L |
possibly damaging |
Het |
Rin2 |
C |
T |
2: 145,702,366 (GRCm39) |
T354I |
probably benign |
Het |
Tbx18 |
T |
C |
9: 87,606,518 (GRCm39) |
Y209C |
probably damaging |
Het |
Themis3 |
T |
C |
17: 66,867,012 (GRCm39) |
N76S |
probably benign |
Het |
Trhde |
A |
T |
10: 114,623,975 (GRCm39) |
S310T |
possibly damaging |
Het |
Vmn1r213 |
G |
A |
13: 23,196,173 (GRCm39) |
C252Y |
possibly damaging |
Het |
Zfp523 |
T |
C |
17: 28,420,003 (GRCm39) |
V216A |
probably benign |
Het |
|
Other mutations in Notch3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00161:Notch3
|
APN |
17 |
32,377,088 (GRCm39) |
nonsense |
probably null |
|
IGL01065:Notch3
|
APN |
17 |
32,365,390 (GRCm39) |
nonsense |
probably null |
|
IGL01296:Notch3
|
APN |
17 |
32,385,731 (GRCm39) |
missense |
unknown |
|
IGL01322:Notch3
|
APN |
17 |
32,363,445 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01343:Notch3
|
APN |
17 |
32,362,410 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01358:Notch3
|
APN |
17 |
32,363,721 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01600:Notch3
|
APN |
17 |
32,363,472 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01622:Notch3
|
APN |
17 |
32,377,844 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01623:Notch3
|
APN |
17 |
32,377,844 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01971:Notch3
|
APN |
17 |
32,343,321 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02000:Notch3
|
APN |
17 |
32,341,716 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02072:Notch3
|
APN |
17 |
32,366,048 (GRCm39) |
nonsense |
probably null |
|
IGL02145:Notch3
|
APN |
17 |
32,373,715 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02256:Notch3
|
APN |
17 |
32,351,298 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02366:Notch3
|
APN |
17 |
32,363,179 (GRCm39) |
missense |
probably benign |
|
IGL02476:Notch3
|
APN |
17 |
32,377,612 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02502:Notch3
|
APN |
17 |
32,377,252 (GRCm39) |
nonsense |
probably null |
|
IGL02551:Notch3
|
APN |
17 |
32,373,705 (GRCm39) |
splice site |
probably benign |
|
divide
|
UTSW |
17 |
32,356,787 (GRCm39) |
splice site |
probably null |
|
impressed
|
UTSW |
17 |
32,385,652 (GRCm39) |
missense |
probably benign |
|
indented
|
UTSW |
17 |
32,366,937 (GRCm39) |
missense |
probably benign |
0.00 |
Lopressor
|
UTSW |
17 |
32,372,858 (GRCm39) |
missense |
probably damaging |
1.00 |
marginal
|
UTSW |
17 |
32,383,198 (GRCm39) |
missense |
probably benign |
|
PIT4486001:Notch3
|
UTSW |
17 |
32,373,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R0115:Notch3
|
UTSW |
17 |
32,352,436 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0201:Notch3
|
UTSW |
17 |
32,375,122 (GRCm39) |
splice site |
probably benign |
|
R0630:Notch3
|
UTSW |
17 |
32,366,446 (GRCm39) |
splice site |
probably benign |
|
R1167:Notch3
|
UTSW |
17 |
32,341,719 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1432:Notch3
|
UTSW |
17 |
32,383,198 (GRCm39) |
missense |
probably benign |
|
R1567:Notch3
|
UTSW |
17 |
32,377,554 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1623:Notch3
|
UTSW |
17 |
32,358,165 (GRCm39) |
missense |
probably benign |
0.00 |
R1663:Notch3
|
UTSW |
17 |
32,375,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R1668:Notch3
|
UTSW |
17 |
32,377,563 (GRCm39) |
missense |
probably damaging |
0.99 |
R1789:Notch3
|
UTSW |
17 |
32,377,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:Notch3
|
UTSW |
17 |
32,362,402 (GRCm39) |
missense |
probably benign |
0.08 |
R1837:Notch3
|
UTSW |
17 |
32,343,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R1896:Notch3
|
UTSW |
17 |
32,362,402 (GRCm39) |
missense |
probably benign |
0.08 |
R1937:Notch3
|
UTSW |
17 |
32,372,826 (GRCm39) |
missense |
probably benign |
0.03 |
R1954:Notch3
|
UTSW |
17 |
32,385,652 (GRCm39) |
missense |
probably benign |
|
R2014:Notch3
|
UTSW |
17 |
32,376,974 (GRCm39) |
missense |
probably benign |
0.00 |
R2058:Notch3
|
UTSW |
17 |
32,362,618 (GRCm39) |
missense |
probably benign |
|
R2068:Notch3
|
UTSW |
17 |
32,354,482 (GRCm39) |
missense |
probably benign |
0.00 |
R2097:Notch3
|
UTSW |
17 |
32,341,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R2112:Notch3
|
UTSW |
17 |
32,363,584 (GRCm39) |
missense |
probably benign |
0.19 |
R2156:Notch3
|
UTSW |
17 |
32,366,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R2211:Notch3
|
UTSW |
17 |
32,366,952 (GRCm39) |
missense |
probably benign |
0.00 |
R2324:Notch3
|
UTSW |
17 |
32,369,108 (GRCm39) |
splice site |
probably benign |
|
R2432:Notch3
|
UTSW |
17 |
32,372,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R3117:Notch3
|
UTSW |
17 |
32,377,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R3236:Notch3
|
UTSW |
17 |
32,377,435 (GRCm39) |
missense |
probably damaging |
0.96 |
R3409:Notch3
|
UTSW |
17 |
32,369,676 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3434:Notch3
|
UTSW |
17 |
32,377,592 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3435:Notch3
|
UTSW |
17 |
32,377,592 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3438:Notch3
|
UTSW |
17 |
32,372,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R3926:Notch3
|
UTSW |
17 |
32,372,531 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4087:Notch3
|
UTSW |
17 |
32,377,087 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4115:Notch3
|
UTSW |
17 |
32,377,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R4234:Notch3
|
UTSW |
17 |
32,360,315 (GRCm39) |
missense |
probably damaging |
0.97 |
R4242:Notch3
|
UTSW |
17 |
32,362,719 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4658:Notch3
|
UTSW |
17 |
32,373,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R4878:Notch3
|
UTSW |
17 |
32,366,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R4879:Notch3
|
UTSW |
17 |
32,366,937 (GRCm39) |
missense |
probably benign |
0.00 |
R4885:Notch3
|
UTSW |
17 |
32,360,351 (GRCm39) |
missense |
probably damaging |
0.98 |
R4924:Notch3
|
UTSW |
17 |
32,363,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R5084:Notch3
|
UTSW |
17 |
32,376,864 (GRCm39) |
critical splice donor site |
probably null |
|
R5086:Notch3
|
UTSW |
17 |
32,362,308 (GRCm39) |
missense |
probably benign |
0.13 |
R5343:Notch3
|
UTSW |
17 |
32,362,257 (GRCm39) |
missense |
probably benign |
0.03 |
R5389:Notch3
|
UTSW |
17 |
32,358,163 (GRCm39) |
missense |
probably benign |
|
R5503:Notch3
|
UTSW |
17 |
32,366,029 (GRCm39) |
missense |
probably benign |
0.00 |
R5698:Notch3
|
UTSW |
17 |
32,376,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R5824:Notch3
|
UTSW |
17 |
32,372,835 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5969:Notch3
|
UTSW |
17 |
32,372,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R6050:Notch3
|
UTSW |
17 |
32,362,501 (GRCm39) |
missense |
probably benign |
|
R6274:Notch3
|
UTSW |
17 |
32,366,264 (GRCm39) |
missense |
probably benign |
|
R6276:Notch3
|
UTSW |
17 |
32,373,723 (GRCm39) |
missense |
probably benign |
0.10 |
R6313:Notch3
|
UTSW |
17 |
32,370,128 (GRCm39) |
splice site |
probably null |
|
R6316:Notch3
|
UTSW |
17 |
32,356,787 (GRCm39) |
splice site |
probably null |
|
R6380:Notch3
|
UTSW |
17 |
32,363,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R6401:Notch3
|
UTSW |
17 |
32,377,597 (GRCm39) |
missense |
probably benign |
0.01 |
R6502:Notch3
|
UTSW |
17 |
32,377,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R6741:Notch3
|
UTSW |
17 |
32,362,458 (GRCm39) |
missense |
probably benign |
0.16 |
R7131:Notch3
|
UTSW |
17 |
32,363,191 (GRCm39) |
missense |
probably benign |
|
R7140:Notch3
|
UTSW |
17 |
32,375,351 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7162:Notch3
|
UTSW |
17 |
32,365,423 (GRCm39) |
missense |
probably damaging |
0.98 |
R7171:Notch3
|
UTSW |
17 |
32,377,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R7449:Notch3
|
UTSW |
17 |
32,376,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R7450:Notch3
|
UTSW |
17 |
32,360,365 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7554:Notch3
|
UTSW |
17 |
32,341,345 (GRCm39) |
missense |
probably benign |
0.03 |
R7575:Notch3
|
UTSW |
17 |
32,373,793 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7632:Notch3
|
UTSW |
17 |
32,377,480 (GRCm39) |
missense |
probably benign |
|
R7633:Notch3
|
UTSW |
17 |
32,377,596 (GRCm39) |
missense |
probably benign |
0.17 |
R7860:Notch3
|
UTSW |
17 |
32,341,747 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8052:Notch3
|
UTSW |
17 |
32,365,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R8250:Notch3
|
UTSW |
17 |
32,351,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R8296:Notch3
|
UTSW |
17 |
32,341,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R8306:Notch3
|
UTSW |
17 |
32,377,086 (GRCm39) |
missense |
probably damaging |
0.99 |
R8458:Notch3
|
UTSW |
17 |
32,375,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R8539:Notch3
|
UTSW |
17 |
32,375,329 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8865:Notch3
|
UTSW |
17 |
32,341,090 (GRCm39) |
missense |
probably benign |
0.01 |
R8925:Notch3
|
UTSW |
17 |
32,372,792 (GRCm39) |
missense |
probably benign |
0.14 |
R8927:Notch3
|
UTSW |
17 |
32,372,792 (GRCm39) |
missense |
probably benign |
0.14 |
R9062:Notch3
|
UTSW |
17 |
32,341,692 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9079:Notch3
|
UTSW |
17 |
32,383,033 (GRCm39) |
intron |
probably benign |
|
R9089:Notch3
|
UTSW |
17 |
32,370,521 (GRCm39) |
missense |
probably benign |
0.00 |
R9260:Notch3
|
UTSW |
17 |
32,362,216 (GRCm39) |
critical splice donor site |
probably null |
|
R9289:Notch3
|
UTSW |
17 |
32,377,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R9294:Notch3
|
UTSW |
17 |
32,362,665 (GRCm39) |
missense |
probably benign |
0.03 |
R9661:Notch3
|
UTSW |
17 |
32,373,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R9779:Notch3
|
UTSW |
17 |
32,372,757 (GRCm39) |
missense |
probably damaging |
1.00 |
T0975:Notch3
|
UTSW |
17 |
32,365,391 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Notch3
|
UTSW |
17 |
32,377,626 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Notch3
|
UTSW |
17 |
32,370,344 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Notch3
|
UTSW |
17 |
32,360,490 (GRCm39) |
missense |
probably benign |
0.12 |
Z1177:Notch3
|
UTSW |
17 |
32,385,668 (GRCm39) |
missense |
probably benign |
|
|