Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agtr2 |
A |
T |
X: 21,352,524 (GRCm39) |
M53L |
probably benign |
Het |
Apob |
T |
C |
12: 8,065,421 (GRCm39) |
V4097A |
probably benign |
Het |
Brip1 |
T |
C |
11: 86,039,227 (GRCm39) |
K436E |
possibly damaging |
Het |
Cavin2 |
A |
G |
1: 51,340,036 (GRCm39) |
K238E |
probably damaging |
Het |
Ccdc158 |
G |
A |
5: 92,798,626 (GRCm39) |
T358I |
probably damaging |
Het |
Cds1 |
A |
G |
5: 101,957,767 (GRCm39) |
I246M |
probably damaging |
Het |
Cep19 |
A |
G |
16: 31,925,898 (GRCm39) |
E102G |
probably damaging |
Het |
Clec4a1 |
T |
A |
6: 122,899,014 (GRCm39) |
C28S |
possibly damaging |
Het |
Csmd3 |
T |
A |
15: 47,574,360 (GRCm39) |
Y2082F |
possibly damaging |
Het |
Fbn1 |
T |
A |
2: 125,160,962 (GRCm39) |
T2193S |
possibly damaging |
Het |
Gm24124 |
G |
T |
19: 13,611,421 (GRCm39) |
|
probably benign |
Het |
Gpbp1l1 |
T |
A |
4: 116,444,710 (GRCm39) |
|
probably null |
Het |
Helq |
T |
C |
5: 100,912,948 (GRCm39) |
|
probably benign |
Het |
Hnrnpm |
C |
A |
17: 33,868,876 (GRCm39) |
R517L |
probably damaging |
Het |
Itga3 |
G |
A |
11: 94,956,712 (GRCm39) |
H122Y |
probably damaging |
Het |
Mettl18 |
T |
A |
1: 163,823,795 (GRCm39) |
S39T |
possibly damaging |
Het |
Ndst4 |
A |
T |
3: 125,355,102 (GRCm39) |
T337S |
probably benign |
Het |
Neb |
A |
G |
2: 52,160,329 (GRCm39) |
|
probably benign |
Het |
Nrbp1 |
T |
C |
5: 31,401,141 (GRCm39) |
S6P |
probably benign |
Het |
Oprk1 |
A |
G |
1: 5,669,128 (GRCm39) |
I191M |
probably damaging |
Het |
Or2a56 |
A |
T |
6: 42,933,370 (GRCm39) |
|
probably benign |
Het |
Or51k2 |
A |
G |
7: 103,596,204 (GRCm39) |
T144A |
probably benign |
Het |
Or52z13 |
A |
G |
7: 103,247,369 (GRCm39) |
N282S |
possibly damaging |
Het |
Psap |
T |
C |
10: 60,128,316 (GRCm39) |
V69A |
probably damaging |
Het |
Scn7a |
C |
T |
2: 66,514,475 (GRCm39) |
E1100K |
probably benign |
Het |
Tmem145 |
A |
G |
7: 25,014,155 (GRCm39) |
N423S |
possibly damaging |
Het |
Tpd52 |
A |
T |
3: 9,012,692 (GRCm39) |
|
probably null |
Het |
Trmt13 |
G |
A |
3: 116,383,884 (GRCm39) |
Q58* |
probably null |
Het |
Ttn |
T |
C |
2: 76,589,125 (GRCm39) |
E21346G |
probably damaging |
Het |
|
Other mutations in Cadps |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Cadps
|
APN |
14 |
12,715,374 (GRCm38) |
missense |
possibly damaging |
0.56 |
IGL01071:Cadps
|
APN |
14 |
12,509,091 (GRCm38) |
splice site |
probably null |
|
IGL01339:Cadps
|
APN |
14 |
12,486,543 (GRCm38) |
missense |
possibly damaging |
0.58 |
IGL01518:Cadps
|
APN |
14 |
12,522,352 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01560:Cadps
|
APN |
14 |
12,491,792 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01598:Cadps
|
APN |
14 |
12,522,202 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01603:Cadps
|
APN |
14 |
12,454,154 (GRCm38) |
splice site |
probably benign |
|
IGL01836:Cadps
|
APN |
14 |
12,522,311 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01839:Cadps
|
APN |
14 |
12,467,184 (GRCm38) |
splice site |
probably benign |
|
IGL01932:Cadps
|
APN |
14 |
12,373,609 (GRCm38) |
utr 3 prime |
probably benign |
|
IGL02172:Cadps
|
APN |
14 |
12,705,681 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02175:Cadps
|
APN |
14 |
12,467,092 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL02212:Cadps
|
APN |
14 |
12,522,345 (GRCm38) |
missense |
possibly damaging |
0.94 |
IGL02351:Cadps
|
APN |
14 |
12,597,380 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02358:Cadps
|
APN |
14 |
12,597,380 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02499:Cadps
|
APN |
14 |
12,822,725 (GRCm38) |
nonsense |
probably null |
|
IGL02505:Cadps
|
APN |
14 |
12,449,759 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02591:Cadps
|
APN |
14 |
12,473,465 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02592:Cadps
|
APN |
14 |
12,473,465 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02671:Cadps
|
APN |
14 |
12,491,824 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02956:Cadps
|
APN |
14 |
12,418,047 (GRCm38) |
splice site |
probably benign |
|
IGL03029:Cadps
|
APN |
14 |
12,376,675 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03216:Cadps
|
APN |
14 |
12,439,944 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03282:Cadps
|
APN |
14 |
12,465,856 (GRCm38) |
splice site |
probably benign |
|
turbo
|
UTSW |
14 |
12,491,800 (GRCm38) |
missense |
probably damaging |
1.00 |
R0241:Cadps
|
UTSW |
14 |
12,376,675 (GRCm38) |
missense |
probably damaging |
1.00 |
R0241:Cadps
|
UTSW |
14 |
12,376,675 (GRCm38) |
missense |
probably damaging |
1.00 |
R0420:Cadps
|
UTSW |
14 |
12,491,800 (GRCm38) |
missense |
probably damaging |
1.00 |
R1180:Cadps
|
UTSW |
14 |
12,457,836 (GRCm38) |
splice site |
probably benign |
|
R1398:Cadps
|
UTSW |
14 |
12,449,822 (GRCm38) |
missense |
probably damaging |
1.00 |
R1678:Cadps
|
UTSW |
14 |
12,517,802 (GRCm38) |
critical splice donor site |
probably null |
|
R1792:Cadps
|
UTSW |
14 |
12,449,802 (GRCm38) |
missense |
possibly damaging |
0.93 |
R1863:Cadps
|
UTSW |
14 |
12,505,796 (GRCm38) |
missense |
probably benign |
0.09 |
R1863:Cadps
|
UTSW |
14 |
12,449,802 (GRCm38) |
missense |
possibly damaging |
0.93 |
R1918:Cadps
|
UTSW |
14 |
12,546,372 (GRCm38) |
missense |
probably damaging |
0.99 |
R1920:Cadps
|
UTSW |
14 |
12,465,859 (GRCm38) |
missense |
possibly damaging |
0.64 |
R1921:Cadps
|
UTSW |
14 |
12,465,859 (GRCm38) |
missense |
possibly damaging |
0.64 |
R1922:Cadps
|
UTSW |
14 |
12,465,859 (GRCm38) |
missense |
possibly damaging |
0.64 |
R1925:Cadps
|
UTSW |
14 |
12,705,726 (GRCm38) |
missense |
probably damaging |
1.00 |
R1966:Cadps
|
UTSW |
14 |
12,822,450 (GRCm38) |
nonsense |
probably null |
|
R2013:Cadps
|
UTSW |
14 |
12,522,337 (GRCm38) |
missense |
probably damaging |
1.00 |
R2228:Cadps
|
UTSW |
14 |
12,465,935 (GRCm38) |
missense |
probably benign |
0.05 |
R2331:Cadps
|
UTSW |
14 |
12,603,692 (GRCm38) |
missense |
probably damaging |
1.00 |
R3436:Cadps
|
UTSW |
14 |
12,616,158 (GRCm38) |
splice site |
probably null |
|
R3853:Cadps
|
UTSW |
14 |
12,509,090 (GRCm38) |
splice site |
probably benign |
|
R3893:Cadps
|
UTSW |
14 |
12,488,883 (GRCm38) |
utr 3 prime |
probably benign |
|
R3916:Cadps
|
UTSW |
14 |
12,457,702 (GRCm38) |
missense |
probably benign |
0.00 |
R3917:Cadps
|
UTSW |
14 |
12,457,702 (GRCm38) |
missense |
probably benign |
0.00 |
R3953:Cadps
|
UTSW |
14 |
12,505,937 (GRCm38) |
missense |
probably damaging |
1.00 |
R3966:Cadps
|
UTSW |
14 |
12,522,161 (GRCm38) |
splice site |
probably null |
|
R4024:Cadps
|
UTSW |
14 |
12,705,539 (GRCm38) |
missense |
probably damaging |
1.00 |
R4079:Cadps
|
UTSW |
14 |
12,457,702 (GRCm38) |
missense |
probably benign |
0.00 |
R4230:Cadps
|
UTSW |
14 |
12,488,987 (GRCm38) |
missense |
probably damaging |
0.98 |
R4333:Cadps
|
UTSW |
14 |
12,467,031 (GRCm38) |
missense |
probably damaging |
1.00 |
R4410:Cadps
|
UTSW |
14 |
12,822,323 (GRCm38) |
missense |
probably damaging |
0.98 |
R4586:Cadps
|
UTSW |
14 |
12,505,808 (GRCm38) |
missense |
probably damaging |
1.00 |
R4685:Cadps
|
UTSW |
14 |
12,467,139 (GRCm38) |
missense |
possibly damaging |
0.77 |
R4698:Cadps
|
UTSW |
14 |
12,705,654 (GRCm38) |
missense |
possibly damaging |
0.90 |
R4855:Cadps
|
UTSW |
14 |
12,822,449 (GRCm38) |
missense |
unknown |
|
R4898:Cadps
|
UTSW |
14 |
12,411,588 (GRCm38) |
missense |
possibly damaging |
0.86 |
R4908:Cadps
|
UTSW |
14 |
12,536,386 (GRCm38) |
missense |
probably damaging |
1.00 |
R5208:Cadps
|
UTSW |
14 |
12,457,711 (GRCm38) |
missense |
possibly damaging |
0.68 |
R5297:Cadps
|
UTSW |
14 |
12,822,345 (GRCm38) |
missense |
probably damaging |
1.00 |
R5328:Cadps
|
UTSW |
14 |
12,457,790 (GRCm38) |
missense |
probably benign |
0.31 |
R5408:Cadps
|
UTSW |
14 |
12,705,759 (GRCm38) |
missense |
possibly damaging |
0.87 |
R5529:Cadps
|
UTSW |
14 |
12,454,285 (GRCm38) |
missense |
probably damaging |
1.00 |
R5567:Cadps
|
UTSW |
14 |
12,473,497 (GRCm38) |
missense |
possibly damaging |
0.49 |
R5570:Cadps
|
UTSW |
14 |
12,473,497 (GRCm38) |
missense |
possibly damaging |
0.49 |
R5727:Cadps
|
UTSW |
14 |
12,486,525 (GRCm38) |
nonsense |
probably null |
|
R5812:Cadps
|
UTSW |
14 |
12,376,685 (GRCm38) |
missense |
probably benign |
|
R6361:Cadps
|
UTSW |
14 |
12,491,778 (GRCm38) |
nonsense |
probably null |
|
R6767:Cadps
|
UTSW |
14 |
12,550,888 (GRCm38) |
missense |
probably damaging |
1.00 |
R6805:Cadps
|
UTSW |
14 |
12,467,103 (GRCm38) |
missense |
probably damaging |
0.99 |
R6861:Cadps
|
UTSW |
14 |
12,522,401 (GRCm38) |
nonsense |
probably null |
|
R6883:Cadps
|
UTSW |
14 |
12,465,883 (GRCm38) |
missense |
probably damaging |
0.96 |
R6887:Cadps
|
UTSW |
14 |
12,505,811 (GRCm38) |
missense |
probably damaging |
1.00 |
R6997:Cadps
|
UTSW |
14 |
12,505,793 (GRCm38) |
missense |
possibly damaging |
0.88 |
R7102:Cadps
|
UTSW |
14 |
12,603,738 (GRCm38) |
missense |
probably damaging |
1.00 |
R7120:Cadps
|
UTSW |
14 |
12,439,919 (GRCm38) |
missense |
probably damaging |
0.98 |
R7143:Cadps
|
UTSW |
14 |
12,491,838 (GRCm38) |
missense |
probably benign |
0.02 |
R7290:Cadps
|
UTSW |
14 |
12,616,099 (GRCm38) |
missense |
probably damaging |
1.00 |
R7614:Cadps
|
UTSW |
14 |
12,454,260 (GRCm38) |
missense |
probably damaging |
1.00 |
R7674:Cadps
|
UTSW |
14 |
12,411,581 (GRCm38) |
missense |
probably damaging |
0.99 |
R7715:Cadps
|
UTSW |
14 |
12,457,762 (GRCm38) |
missense |
probably benign |
0.01 |
R7801:Cadps
|
UTSW |
14 |
12,489,476 (GRCm38) |
critical splice donor site |
probably null |
|
R7814:Cadps
|
UTSW |
14 |
12,376,706 (GRCm38) |
missense |
probably damaging |
0.99 |
R7915:Cadps
|
UTSW |
14 |
12,705,544 (GRCm38) |
missense |
possibly damaging |
0.84 |
R8087:Cadps
|
UTSW |
14 |
12,536,380 (GRCm38) |
missense |
probably damaging |
1.00 |
R8109:Cadps
|
UTSW |
14 |
12,488,975 (GRCm38) |
missense |
probably benign |
0.00 |
R8485:Cadps
|
UTSW |
14 |
12,439,872 (GRCm38) |
missense |
probably damaging |
1.00 |
R9156:Cadps
|
UTSW |
14 |
12,705,676 (GRCm38) |
missense |
probably damaging |
1.00 |
R9158:Cadps
|
UTSW |
14 |
12,546,356 (GRCm38) |
missense |
probably benign |
0.10 |
R9312:Cadps
|
UTSW |
14 |
12,616,095 (GRCm38) |
missense |
probably damaging |
1.00 |
R9465:Cadps
|
UTSW |
14 |
12,489,002 (GRCm38) |
missense |
possibly damaging |
0.93 |
R9519:Cadps
|
UTSW |
14 |
12,546,290 (GRCm38) |
missense |
possibly damaging |
0.86 |
R9649:Cadps
|
UTSW |
14 |
12,597,418 (GRCm38) |
missense |
probably damaging |
0.99 |
R9662:Cadps
|
UTSW |
14 |
12,411,567 (GRCm38) |
missense |
probably benign |
0.02 |
R9674:Cadps
|
UTSW |
14 |
12,454,291 (GRCm38) |
missense |
probably damaging |
1.00 |
X0018:Cadps
|
UTSW |
14 |
12,373,690 (GRCm38) |
missense |
probably damaging |
1.00 |
X0028:Cadps
|
UTSW |
14 |
12,467,118 (GRCm38) |
missense |
possibly damaging |
0.93 |
Z1088:Cadps
|
UTSW |
14 |
12,467,113 (GRCm38) |
missense |
probably damaging |
0.96 |
Z1177:Cadps
|
UTSW |
14 |
12,465,880 (GRCm38) |
missense |
probably damaging |
0.99 |
|