Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833439L19Rik |
A |
G |
13: 54,701,057 (GRCm39) |
S174P |
probably damaging |
Het |
4931414P19Rik |
T |
C |
14: 54,823,168 (GRCm39) |
E343G |
probably damaging |
Het |
Abca14 |
T |
C |
7: 119,851,497 (GRCm39) |
V825A |
probably damaging |
Het |
Abca8b |
G |
T |
11: 109,827,210 (GRCm39) |
T1466K |
possibly damaging |
Het |
Adcy8 |
A |
G |
15: 64,678,553 (GRCm39) |
S467P |
probably damaging |
Het |
Agbl4 |
T |
C |
4: 110,976,237 (GRCm39) |
V198A |
possibly damaging |
Het |
Agpat4 |
A |
G |
17: 12,417,699 (GRCm39) |
K80R |
probably benign |
Het |
Akap8 |
T |
C |
17: 32,535,208 (GRCm39) |
T269A |
probably benign |
Het |
Ankhd1 |
A |
T |
18: 36,758,080 (GRCm39) |
I925F |
possibly damaging |
Het |
Aste1 |
A |
G |
9: 105,282,203 (GRCm39) |
Y57C |
probably damaging |
Het |
Axdnd1 |
A |
G |
1: 156,247,980 (GRCm39) |
S7P |
possibly damaging |
Het |
BC051019 |
T |
A |
7: 109,319,789 (GRCm39) |
R91S |
probably null |
Het |
Cavin2 |
C |
A |
1: 51,340,398 (GRCm39) |
N358K |
probably benign |
Het |
Cd2 |
T |
C |
3: 101,190,355 (GRCm39) |
N196S |
probably benign |
Het |
Clca3a1 |
C |
T |
3: 144,436,483 (GRCm39) |
V867I |
probably benign |
Het |
Col6a4 |
T |
A |
9: 105,952,262 (GRCm39) |
K545N |
probably damaging |
Het |
Cyp2c65 |
A |
T |
19: 39,076,009 (GRCm39) |
|
probably null |
Het |
Dcaf6 |
T |
C |
1: 165,157,572 (GRCm39) |
D856G |
possibly damaging |
Het |
Epcam |
T |
C |
17: 87,949,580 (GRCm39) |
I181T |
probably damaging |
Het |
Esrp2 |
A |
G |
8: 106,859,061 (GRCm39) |
S562P |
probably damaging |
Het |
Fcgbpl1 |
A |
C |
7: 27,856,383 (GRCm39) |
I2057L |
probably benign |
Het |
Ffar4 |
A |
G |
19: 38,085,627 (GRCm39) |
D18G |
probably benign |
Het |
Gen1 |
C |
T |
12: 11,296,347 (GRCm39) |
V337I |
probably damaging |
Het |
Gimap8 |
C |
T |
6: 48,633,581 (GRCm39) |
P467S |
possibly damaging |
Het |
Gnl3 |
T |
A |
14: 30,738,803 (GRCm39) |
H82L |
possibly damaging |
Het |
Grid2 |
T |
C |
6: 64,053,862 (GRCm39) |
S354P |
probably benign |
Het |
Ighmbp2 |
T |
A |
19: 3,315,084 (GRCm39) |
T779S |
possibly damaging |
Het |
Ints15 |
C |
T |
5: 143,293,443 (GRCm39) |
E345K |
possibly damaging |
Het |
Kif19a |
C |
A |
11: 114,673,923 (GRCm39) |
T348N |
probably damaging |
Het |
Lrrc15 |
T |
A |
16: 30,092,172 (GRCm39) |
N389I |
probably damaging |
Het |
Mrps26 |
A |
G |
2: 130,405,886 (GRCm39) |
Y63C |
probably damaging |
Het |
Myd88 |
C |
A |
9: 119,166,889 (GRCm39) |
V223F |
possibly damaging |
Het |
Nox4 |
T |
A |
7: 87,025,450 (GRCm39) |
W526R |
probably damaging |
Het |
Nrg2 |
A |
T |
18: 36,185,838 (GRCm39) |
N300K |
probably damaging |
Het |
Nsmf |
T |
C |
2: 24,950,464 (GRCm39) |
|
probably benign |
Het |
Patl2 |
A |
C |
2: 121,954,283 (GRCm39) |
H429Q |
probably benign |
Het |
Pcdhb12 |
A |
T |
18: 37,568,907 (GRCm39) |
K18* |
probably null |
Het |
Peg10 |
T |
A |
6: 4,754,511 (GRCm39) |
D97E |
probably benign |
Het |
Runx1t1 |
C |
T |
4: 13,846,830 (GRCm39) |
Q205* |
probably null |
Het |
Selenon |
T |
C |
4: 134,275,284 (GRCm39) |
K138R |
probably damaging |
Het |
Slc13a3 |
T |
C |
2: 165,262,000 (GRCm39) |
E369G |
probably benign |
Het |
Sorcs1 |
A |
G |
19: 50,248,190 (GRCm39) |
|
probably null |
Het |
Sptbn4 |
A |
T |
7: 27,068,816 (GRCm39) |
M499K |
probably damaging |
Het |
Sra1 |
A |
T |
18: 36,803,012 (GRCm39) |
|
probably benign |
Het |
Stra6 |
T |
C |
9: 58,048,429 (GRCm39) |
L174P |
probably damaging |
Het |
Syngr1 |
T |
C |
15: 80,000,086 (GRCm39) |
Y66H |
probably damaging |
Het |
Synpo |
G |
T |
18: 60,735,831 (GRCm39) |
S466* |
probably null |
Het |
Tenm3 |
T |
A |
8: 48,795,343 (GRCm39) |
M595L |
probably benign |
Het |
Tnks |
T |
C |
8: 35,308,963 (GRCm39) |
T1099A |
probably benign |
Het |
Tram1l1 |
G |
T |
3: 124,115,400 (GRCm39) |
V187F |
possibly damaging |
Het |
Trappc11 |
T |
C |
8: 47,965,639 (GRCm39) |
E529G |
probably benign |
Het |
Usp17la |
T |
C |
7: 104,510,139 (GRCm39) |
V248A |
probably damaging |
Het |
Virma |
T |
C |
4: 11,519,392 (GRCm39) |
Y880H |
probably benign |
Het |
Vmn1r214 |
C |
T |
13: 23,219,571 (GRCm39) |
T355I |
possibly damaging |
Het |
Vmn2r7 |
T |
C |
3: 64,598,205 (GRCm39) |
K784R |
possibly damaging |
Het |
Wrap53 |
C |
T |
11: 69,453,273 (GRCm39) |
W389* |
probably null |
Het |
Zfp748 |
A |
G |
13: 67,689,638 (GRCm39) |
S541P |
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 |
IGL02049:Cps1
|
APN |
1 |
67,183,113 (GRCm39) |
missense |
possibly damaging |
0.68 |
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 |
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 |
|