Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930568D16Rik |
T |
A |
2: 35,254,801 (GRCm39) |
R27S |
probably benign |
Het |
4930596D02Rik |
C |
A |
14: 35,533,535 (GRCm39) |
V78L |
probably benign |
Het |
Abca3 |
T |
A |
17: 24,595,704 (GRCm39) |
C352* |
probably null |
Het |
Acat3 |
T |
A |
17: 13,144,207 (GRCm39) |
Y324F |
probably benign |
Het |
Adamts8 |
T |
C |
9: 30,862,650 (GRCm39) |
V285A |
probably damaging |
Het |
Anpep |
A |
G |
7: 79,484,929 (GRCm39) |
I652T |
probably damaging |
Het |
Arhgef6 |
T |
A |
X: 56,321,271 (GRCm39) |
Q320L |
probably damaging |
Het |
Armh1 |
A |
T |
4: 117,094,860 (GRCm39) |
I60K |
probably benign |
Het |
Atp11b |
T |
C |
3: 35,854,642 (GRCm39) |
V145A |
probably damaging |
Het |
Cacna1c |
T |
C |
6: 118,580,880 (GRCm39) |
T1674A |
probably benign |
Het |
Capn2 |
A |
T |
1: 182,301,519 (GRCm39) |
|
probably benign |
Het |
Cfd |
A |
G |
10: 79,726,776 (GRCm39) |
Y6C |
probably benign |
Het |
Csmd3 |
T |
A |
15: 47,864,870 (GRCm39) |
R786S |
possibly damaging |
Het |
Dna2 |
A |
T |
10: 62,792,815 (GRCm39) |
I277L |
probably damaging |
Het |
Gm5168 |
A |
T |
X: 25,999,005 (GRCm39) |
D50E |
probably damaging |
Het |
Grik4 |
T |
A |
9: 42,455,049 (GRCm39) |
|
probably benign |
Het |
Ift56 |
A |
G |
6: 38,402,067 (GRCm39) |
T520A |
probably benign |
Het |
Iqgap2 |
A |
G |
13: 95,811,913 (GRCm39) |
|
probably benign |
Het |
Klk10 |
A |
T |
7: 43,433,882 (GRCm39) |
|
probably benign |
Het |
Kng1 |
A |
G |
16: 22,892,187 (GRCm39) |
Y250C |
probably damaging |
Het |
Las1l |
A |
T |
X: 94,981,059 (GRCm39) |
M690K |
probably benign |
Het |
Mug1 |
T |
A |
6: 121,848,295 (GRCm39) |
M673K |
probably benign |
Het |
Myh9 |
T |
C |
15: 77,654,070 (GRCm39) |
H1245R |
probably benign |
Het |
Oprk1 |
C |
T |
1: 5,669,067 (GRCm39) |
T171I |
probably damaging |
Het |
Pgm5 |
A |
T |
19: 24,801,782 (GRCm39) |
S149T |
probably benign |
Het |
Pla2g4a |
T |
C |
1: 149,736,847 (GRCm39) |
N424S |
probably benign |
Het |
Plec |
A |
T |
15: 76,063,149 (GRCm39) |
L2334Q |
probably damaging |
Het |
Pus7l |
G |
A |
15: 94,438,059 (GRCm39) |
S262F |
probably damaging |
Het |
Rps24 |
C |
A |
14: 24,541,823 (GRCm39) |
D3E |
probably benign |
Het |
Rxfp1 |
T |
C |
3: 79,557,799 (GRCm39) |
N560D |
probably damaging |
Het |
Sema3c |
C |
T |
5: 17,926,923 (GRCm39) |
|
probably benign |
Het |
Slc47a2 |
A |
G |
11: 61,233,365 (GRCm39) |
F55S |
probably damaging |
Het |
Slco1a6 |
A |
G |
6: 142,047,309 (GRCm39) |
|
probably benign |
Het |
Taf4b |
A |
T |
18: 14,963,196 (GRCm39) |
E645D |
probably benign |
Het |
Tmem161a |
T |
A |
8: 70,631,624 (GRCm39) |
V158E |
probably damaging |
Het |
Trav13-2 |
A |
G |
14: 53,872,604 (GRCm39) |
S27G |
possibly damaging |
Het |
Trav13-2 |
G |
T |
14: 53,872,603 (GRCm39) |
Q26H |
probably damaging |
Het |
Trav13-2 |
A |
T |
14: 53,872,602 (GRCm39) |
Q26L |
possibly damaging |
Het |
Vmn2r108 |
T |
A |
17: 20,691,608 (GRCm39) |
H305L |
probably benign |
Het |
Zfp263 |
A |
G |
16: 3,562,482 (GRCm39) |
I82V |
probably damaging |
Het |
|
Other mutations in Cps1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00757:Cps1
|
APN |
1 |
67,191,539 (GRCm39) |
splice site |
probably benign |
|
IGL00897:Cps1
|
APN |
1 |
67,254,723 (GRCm39) |
missense |
probably benign |
0.08 |
IGL00928:Cps1
|
APN |
1 |
67,162,393 (GRCm39) |
missense |
probably benign |
|
IGL01063:Cps1
|
APN |
1 |
67,234,325 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01081:Cps1
|
APN |
1 |
67,245,983 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01361:Cps1
|
APN |
1 |
67,234,304 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01396:Cps1
|
APN |
1 |
67,196,945 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01516:Cps1
|
APN |
1 |
67,269,443 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01695:Cps1
|
APN |
1 |
67,236,194 (GRCm39) |
missense |
probably benign |
|
IGL02022:Cps1
|
APN |
1 |
67,212,031 (GRCm39) |
splice site |
probably benign |
|
IGL02032:Cps1
|
APN |
1 |
67,269,474 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02197:Cps1
|
APN |
1 |
67,196,923 (GRCm39) |
missense |
probably benign |
|
IGL02217:Cps1
|
APN |
1 |
67,213,541 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02555:Cps1
|
APN |
1 |
67,253,180 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02570:Cps1
|
APN |
1 |
67,187,862 (GRCm39) |
splice site |
probably benign |
|
IGL02633:Cps1
|
APN |
1 |
67,162,396 (GRCm39) |
missense |
probably benign |
|
IGL02711:Cps1
|
APN |
1 |
67,251,676 (GRCm39) |
splice site |
probably benign |
|
IGL02737:Cps1
|
APN |
1 |
67,187,933 (GRCm39) |
missense |
probably benign |
0.35 |
IGL03030:Cps1
|
APN |
1 |
67,182,080 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03255:Cps1
|
APN |
1 |
67,184,960 (GRCm39) |
nonsense |
probably null |
|
Madman
|
UTSW |
1 |
67,200,030 (GRCm39) |
missense |
probably damaging |
0.96 |
maniac
|
UTSW |
1 |
67,197,037 (GRCm39) |
critical splice donor site |
probably null |
|
R0109:Cps1
|
UTSW |
1 |
67,268,577 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0109:Cps1
|
UTSW |
1 |
67,268,577 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0140:Cps1
|
UTSW |
1 |
67,219,275 (GRCm39) |
missense |
probably benign |
|
R0318:Cps1
|
UTSW |
1 |
67,216,173 (GRCm39) |
missense |
probably damaging |
0.99 |
R0486:Cps1
|
UTSW |
1 |
67,204,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R0488:Cps1
|
UTSW |
1 |
67,187,967 (GRCm39) |
splice site |
probably benign |
|
R0492:Cps1
|
UTSW |
1 |
67,196,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R0521:Cps1
|
UTSW |
1 |
67,254,723 (GRCm39) |
missense |
probably benign |
0.02 |
R0534:Cps1
|
UTSW |
1 |
67,183,059 (GRCm39) |
missense |
probably benign |
0.06 |
R0565:Cps1
|
UTSW |
1 |
67,205,608 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0609:Cps1
|
UTSW |
1 |
67,211,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R0612:Cps1
|
UTSW |
1 |
67,178,929 (GRCm39) |
missense |
probably benign |
0.01 |
R1185:Cps1
|
UTSW |
1 |
67,234,358 (GRCm39) |
missense |
probably benign |
0.00 |
R1185:Cps1
|
UTSW |
1 |
67,234,358 (GRCm39) |
missense |
probably benign |
0.00 |
R1185:Cps1
|
UTSW |
1 |
67,234,358 (GRCm39) |
missense |
probably benign |
0.00 |
R1220:Cps1
|
UTSW |
1 |
67,243,862 (GRCm39) |
critical splice donor site |
probably null |
|
R1321:Cps1
|
UTSW |
1 |
67,182,178 (GRCm39) |
splice site |
probably benign |
|
R1343:Cps1
|
UTSW |
1 |
67,248,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R1373:Cps1
|
UTSW |
1 |
67,268,583 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1374:Cps1
|
UTSW |
1 |
67,269,440 (GRCm39) |
missense |
probably damaging |
0.97 |
R1481:Cps1
|
UTSW |
1 |
67,183,041 (GRCm39) |
missense |
probably damaging |
0.99 |
R1711:Cps1
|
UTSW |
1 |
67,207,533 (GRCm39) |
splice site |
probably null |
|
R1712:Cps1
|
UTSW |
1 |
67,269,440 (GRCm39) |
missense |
probably damaging |
0.97 |
R1774:Cps1
|
UTSW |
1 |
67,210,041 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1799:Cps1
|
UTSW |
1 |
67,248,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:Cps1
|
UTSW |
1 |
67,234,355 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2074:Cps1
|
UTSW |
1 |
67,243,797 (GRCm39) |
missense |
probably benign |
0.21 |
R2078:Cps1
|
UTSW |
1 |
67,234,424 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2078:Cps1
|
UTSW |
1 |
67,196,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Cps1
|
UTSW |
1 |
67,216,139 (GRCm39) |
missense |
probably benign |
0.01 |
R2112:Cps1
|
UTSW |
1 |
67,216,139 (GRCm39) |
missense |
probably benign |
0.01 |
R2146:Cps1
|
UTSW |
1 |
67,191,538 (GRCm39) |
splice site |
probably benign |
|
R2355:Cps1
|
UTSW |
1 |
67,195,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R2375:Cps1
|
UTSW |
1 |
67,257,019 (GRCm39) |
missense |
probably benign |
0.00 |
R2860:Cps1
|
UTSW |
1 |
67,205,534 (GRCm39) |
missense |
probably benign |
0.44 |
R2861:Cps1
|
UTSW |
1 |
67,205,534 (GRCm39) |
missense |
probably benign |
0.44 |
R2979:Cps1
|
UTSW |
1 |
67,243,863 (GRCm39) |
critical splice donor site |
probably null |
|
R3427:Cps1
|
UTSW |
1 |
67,213,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R3833:Cps1
|
UTSW |
1 |
67,178,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R3857:Cps1
|
UTSW |
1 |
67,207,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R3858:Cps1
|
UTSW |
1 |
67,207,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R3859:Cps1
|
UTSW |
1 |
67,207,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R3886:Cps1
|
UTSW |
1 |
67,204,659 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3887:Cps1
|
UTSW |
1 |
67,204,659 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3888:Cps1
|
UTSW |
1 |
67,204,659 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3889:Cps1
|
UTSW |
1 |
67,204,659 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4386:Cps1
|
UTSW |
1 |
67,210,154 (GRCm39) |
critical splice donor site |
probably null |
|
R4497:Cps1
|
UTSW |
1 |
67,244,358 (GRCm39) |
missense |
probably null |
1.00 |
R4671:Cps1
|
UTSW |
1 |
67,235,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R4774:Cps1
|
UTSW |
1 |
67,259,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R4799:Cps1
|
UTSW |
1 |
67,182,145 (GRCm39) |
missense |
probably damaging |
0.96 |
R4853:Cps1
|
UTSW |
1 |
67,195,361 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4884:Cps1
|
UTSW |
1 |
67,216,183 (GRCm39) |
missense |
probably benign |
0.11 |
R4900:Cps1
|
UTSW |
1 |
67,200,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R4906:Cps1
|
UTSW |
1 |
67,178,922 (GRCm39) |
missense |
probably benign |
0.10 |
R5091:Cps1
|
UTSW |
1 |
67,268,679 (GRCm39) |
critical splice donor site |
probably null |
|
R5102:Cps1
|
UTSW |
1 |
67,245,952 (GRCm39) |
missense |
probably benign |
0.00 |
R5215:Cps1
|
UTSW |
1 |
67,205,539 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5290:Cps1
|
UTSW |
1 |
67,211,868 (GRCm39) |
missense |
probably benign |
0.21 |
R5732:Cps1
|
UTSW |
1 |
67,196,923 (GRCm39) |
missense |
probably benign |
0.22 |
R5818:Cps1
|
UTSW |
1 |
67,205,647 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5878:Cps1
|
UTSW |
1 |
67,197,037 (GRCm39) |
critical splice donor site |
probably null |
|
R6002:Cps1
|
UTSW |
1 |
67,211,914 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6034:Cps1
|
UTSW |
1 |
67,196,872 (GRCm39) |
splice site |
probably null |
|
R6034:Cps1
|
UTSW |
1 |
67,196,872 (GRCm39) |
splice site |
probably null |
|
R6199:Cps1
|
UTSW |
1 |
67,201,774 (GRCm39) |
frame shift |
probably null |
|
R6310:Cps1
|
UTSW |
1 |
67,182,140 (GRCm39) |
missense |
probably benign |
0.00 |
R6554:Cps1
|
UTSW |
1 |
67,213,628 (GRCm39) |
nonsense |
probably null |
|
R6700:Cps1
|
UTSW |
1 |
67,268,682 (GRCm39) |
splice site |
probably null |
|
R6731:Cps1
|
UTSW |
1 |
67,200,030 (GRCm39) |
missense |
probably damaging |
0.96 |
R7052:Cps1
|
UTSW |
1 |
67,237,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:Cps1
|
UTSW |
1 |
67,210,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:Cps1
|
UTSW |
1 |
67,237,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R7323:Cps1
|
UTSW |
1 |
67,197,028 (GRCm39) |
missense |
probably benign |
0.03 |
R7339:Cps1
|
UTSW |
1 |
67,236,174 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7485:Cps1
|
UTSW |
1 |
67,179,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R7505:Cps1
|
UTSW |
1 |
67,219,240 (GRCm39) |
missense |
probably benign |
|
R7748:Cps1
|
UTSW |
1 |
67,178,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R7853:Cps1
|
UTSW |
1 |
67,213,640 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8097:Cps1
|
UTSW |
1 |
67,267,429 (GRCm39) |
missense |
probably benign |
0.08 |
R8357:Cps1
|
UTSW |
1 |
67,196,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R8435:Cps1
|
UTSW |
1 |
67,251,589 (GRCm39) |
missense |
probably benign |
0.07 |
R8457:Cps1
|
UTSW |
1 |
67,196,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Cps1
|
UTSW |
1 |
67,243,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R8805:Cps1
|
UTSW |
1 |
67,216,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R8811:Cps1
|
UTSW |
1 |
67,253,246 (GRCm39) |
missense |
probably benign |
0.03 |
R8819:Cps1
|
UTSW |
1 |
67,267,439 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8820:Cps1
|
UTSW |
1 |
67,267,439 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8854:Cps1
|
UTSW |
1 |
67,200,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R9138:Cps1
|
UTSW |
1 |
67,254,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R9185:Cps1
|
UTSW |
1 |
67,248,831 (GRCm39) |
missense |
probably benign |
0.08 |
R9273:Cps1
|
UTSW |
1 |
67,191,445 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9286:Cps1
|
UTSW |
1 |
67,198,030 (GRCm39) |
missense |
probably damaging |
0.99 |
R9308:Cps1
|
UTSW |
1 |
67,200,118 (GRCm39) |
critical splice donor site |
probably null |
|
R9326:Cps1
|
UTSW |
1 |
67,248,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R9449:Cps1
|
UTSW |
1 |
67,259,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R9454:Cps1
|
UTSW |
1 |
67,219,311 (GRCm39) |
missense |
probably damaging |
0.97 |
R9518:Cps1
|
UTSW |
1 |
67,259,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Cps1
|
UTSW |
1 |
67,198,048 (GRCm39) |
missense |
probably benign |
0.26 |
R9585:Cps1
|
UTSW |
1 |
67,195,341 (GRCm39) |
missense |
probably damaging |
0.99 |
R9618:Cps1
|
UTSW |
1 |
67,196,975 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9641:Cps1
|
UTSW |
1 |
67,234,342 (GRCm39) |
missense |
probably benign |
0.03 |
R9650:Cps1
|
UTSW |
1 |
67,254,636 (GRCm39) |
missense |
|
|
R9668:Cps1
|
UTSW |
1 |
67,213,649 (GRCm39) |
missense |
probably benign |
0.24 |
R9726:Cps1
|
UTSW |
1 |
67,195,395 (GRCm39) |
missense |
probably benign |
0.39 |
X0024:Cps1
|
UTSW |
1 |
67,162,406 (GRCm39) |
missense |
probably benign |
|
Z1176:Cps1
|
UTSW |
1 |
67,187,878 (GRCm39) |
frame shift |
probably null |
|
Z1176:Cps1
|
UTSW |
1 |
67,162,427 (GRCm39) |
missense |
possibly damaging |
0.54 |
|