Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447F04Rik |
A |
C |
X: 65,347,660 (GRCm39) |
V16G |
unknown |
Het |
4933427I04Rik |
A |
T |
4: 123,754,494 (GRCm39) |
E136V |
probably benign |
Het |
Aadac |
A |
G |
3: 59,943,320 (GRCm39) |
D75G |
probably damaging |
Het |
Arfgap1 |
T |
A |
2: 180,614,518 (GRCm39) |
S125T |
probably benign |
Het |
Atxn2 |
G |
T |
5: 121,949,042 (GRCm39) |
A813S |
probably damaging |
Het |
Ces1a |
G |
T |
8: 93,771,726 (GRCm39) |
P24T |
probably damaging |
Het |
Col4a4 |
T |
A |
1: 82,433,480 (GRCm39) |
M1488L |
unknown |
Het |
Fndc3c1 |
T |
C |
X: 105,475,029 (GRCm39) |
N941S |
probably damaging |
Het |
Fryl |
T |
C |
5: 73,244,305 (GRCm39) |
Y1172C |
possibly damaging |
Het |
Gm1527 |
T |
C |
3: 28,949,737 (GRCm39) |
|
probably benign |
Het |
Hsf2 |
T |
C |
10: 57,388,230 (GRCm39) |
L458P |
probably damaging |
Het |
Il2 |
T |
C |
3: 37,177,156 (GRCm39) |
T127A |
possibly damaging |
Het |
Inpp5e |
A |
G |
2: 26,287,946 (GRCm39) |
Y617H |
probably damaging |
Het |
Isoc2b |
G |
A |
7: 4,853,763 (GRCm39) |
S137F |
probably damaging |
Het |
Map2 |
C |
T |
1: 66,464,490 (GRCm39) |
P241S |
probably damaging |
Het |
Mfsd6 |
C |
A |
1: 52,748,481 (GRCm39) |
R128L |
probably damaging |
Het |
Mrnip |
A |
G |
11: 50,088,462 (GRCm39) |
T153A |
probably damaging |
Het |
Or4x6 |
A |
G |
2: 89,949,315 (GRCm39) |
F209S |
possibly damaging |
Het |
Or8d1 |
A |
T |
9: 38,767,095 (GRCm39) |
M246L |
probably benign |
Het |
Pi4ka |
T |
C |
16: 17,098,599 (GRCm39) |
N2022S |
probably benign |
Het |
Scrt2 |
C |
A |
2: 151,935,560 (GRCm39) |
R238S |
probably damaging |
Het |
St3gal6 |
T |
A |
16: 58,305,138 (GRCm39) |
D108V |
probably benign |
Het |
Tmem132b |
C |
T |
5: 125,855,855 (GRCm39) |
T529M |
probably damaging |
Het |
Trappc11 |
T |
C |
8: 47,954,904 (GRCm39) |
|
probably null |
Het |
Tspyl1 |
T |
A |
10: 34,159,195 (GRCm39) |
S307T |
possibly damaging |
Het |
Ush2a |
A |
G |
1: 188,131,982 (GRCm39) |
S735G |
probably benign |
Het |
Wnk2 |
T |
C |
13: 49,221,668 (GRCm39) |
M1186V |
possibly damaging |
Het |
|
Other mutations in Cadps |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00926:Cadps
|
APN |
14 |
12,491,795 (GRCm38) |
missense |
probably damaging |
1.00 |
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 |
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 |
|