Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
Abr |
T |
C |
11: 76,355,087 (GRCm39) |
T244A |
probably damaging |
Het |
Adcy10 |
T |
A |
1: 165,375,782 (GRCm39) |
N803K |
probably benign |
Het |
Afm |
T |
C |
5: 90,699,326 (GRCm39) |
F590S |
probably damaging |
Het |
Agk |
T |
C |
6: 40,360,753 (GRCm39) |
|
probably null |
Het |
Agrn |
C |
T |
4: 156,270,007 (GRCm39) |
|
probably null |
Het |
Apon |
A |
G |
10: 128,090,951 (GRCm39) |
S210G |
probably benign |
Het |
Atad5 |
A |
G |
11: 79,986,098 (GRCm39) |
E395G |
probably damaging |
Het |
AU018091 |
A |
T |
7: 3,205,861 (GRCm39) |
L671H |
probably damaging |
Het |
Capn13 |
GCA |
G |
17: 73,658,501 (GRCm39) |
|
probably null |
Het |
Ccdc154 |
A |
T |
17: 25,389,941 (GRCm39) |
I524F |
probably damaging |
Het |
Clspn |
T |
A |
4: 126,460,348 (GRCm39) |
I525K |
probably damaging |
Het |
Cpne5 |
A |
T |
17: 29,380,172 (GRCm39) |
V448E |
probably benign |
Het |
Crybb2 |
T |
C |
5: 113,211,054 (GRCm39) |
E78G |
probably damaging |
Het |
Ctps1 |
G |
T |
4: 120,411,207 (GRCm39) |
L270I |
probably damaging |
Het |
Cyp19a1 |
T |
C |
9: 54,074,060 (GRCm39) |
D431G |
probably benign |
Het |
Cyp3a57 |
T |
G |
5: 145,302,489 (GRCm39) |
V95G |
probably damaging |
Het |
Ddx54 |
A |
G |
5: 120,761,694 (GRCm39) |
D490G |
probably benign |
Het |
Dnai2 |
A |
T |
11: 114,635,917 (GRCm39) |
I301F |
probably benign |
Het |
Dsg1b |
A |
G |
18: 20,541,793 (GRCm39) |
S767G |
probably benign |
Het |
Dsg1b |
A |
T |
18: 20,523,189 (GRCm39) |
|
probably null |
Het |
Ermap |
G |
A |
4: 119,044,451 (GRCm39) |
P115L |
probably damaging |
Het |
Esrra |
T |
G |
19: 6,897,440 (GRCm39) |
T106P |
probably damaging |
Het |
Exoc5 |
GTATT |
GT |
14: 49,289,826 (GRCm39) |
|
probably benign |
Het |
Flt1 |
C |
A |
5: 147,620,749 (GRCm39) |
A132S |
probably benign |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gnl3 |
T |
C |
14: 30,737,270 (GRCm39) |
K203E |
probably damaging |
Het |
H2ac13 |
A |
G |
13: 21,900,866 (GRCm39) |
E92G |
probably damaging |
Het |
Habp2 |
G |
A |
19: 56,299,623 (GRCm39) |
|
probably null |
Het |
Kcnh3 |
A |
C |
15: 99,139,970 (GRCm39) |
D952A |
possibly damaging |
Het |
Kif27 |
T |
C |
13: 58,459,072 (GRCm39) |
K920E |
probably benign |
Het |
Kmt2e |
C |
T |
5: 23,707,339 (GRCm39) |
P1634L |
probably damaging |
Het |
Lamc1 |
A |
T |
1: 153,104,846 (GRCm39) |
M1312K |
possibly damaging |
Het |
Myh14 |
T |
A |
7: 44,257,872 (GRCm39) |
Q1921L |
probably damaging |
Het |
Ncor2 |
A |
G |
5: 125,102,169 (GRCm39) |
V68A |
probably damaging |
Het |
Ncor2 |
A |
G |
5: 125,158,247 (GRCm39) |
F444L |
unknown |
Het |
Nedd9 |
A |
G |
13: 41,469,837 (GRCm39) |
Y439H |
probably benign |
Het |
Nsd1 |
T |
A |
13: 55,416,317 (GRCm39) |
H1454Q |
probably benign |
Het |
Or10v9 |
T |
A |
19: 11,832,645 (GRCm39) |
D224V |
probably benign |
Het |
Or51v8 |
G |
T |
7: 103,320,010 (GRCm39) |
T76K |
probably damaging |
Het |
Or5i1 |
T |
G |
2: 87,613,526 (GRCm39) |
F214C |
probably benign |
Het |
Or9m1b |
A |
G |
2: 87,836,448 (GRCm39) |
S216P |
probably damaging |
Het |
P4ha2 |
G |
A |
11: 54,010,996 (GRCm39) |
S337N |
probably benign |
Het |
Pck1 |
T |
A |
2: 172,996,507 (GRCm39) |
Y140* |
probably null |
Het |
Phldb2 |
T |
C |
16: 45,623,079 (GRCm39) |
M656V |
probably damaging |
Het |
Pif1 |
T |
C |
9: 65,500,858 (GRCm39) |
W559R |
probably damaging |
Het |
Pllp |
T |
C |
8: 95,406,022 (GRCm39) |
Y87C |
probably damaging |
Het |
Ppp1r3a |
T |
C |
6: 14,719,046 (GRCm39) |
N623D |
probably benign |
Het |
Prkcg |
C |
T |
7: 3,367,469 (GRCm39) |
R345C |
probably damaging |
Het |
Rgl1 |
T |
C |
1: 152,433,325 (GRCm39) |
I147V |
probably benign |
Het |
Sdk1 |
T |
A |
5: 142,132,018 (GRCm39) |
L1649Q |
probably damaging |
Het |
Sema3b |
C |
T |
9: 107,479,266 (GRCm39) |
|
probably null |
Het |
Sh3rf3 |
G |
A |
10: 58,919,341 (GRCm39) |
R486H |
probably damaging |
Het |
Shoc1 |
T |
C |
4: 59,072,345 (GRCm39) |
K624E |
possibly damaging |
Het |
Slain2 |
A |
G |
5: 73,105,941 (GRCm39) |
N192S |
probably benign |
Het |
Slc22a16 |
T |
A |
10: 40,450,047 (GRCm39) |
I161N |
probably damaging |
Het |
Strip1 |
T |
C |
3: 107,524,232 (GRCm39) |
K562E |
possibly damaging |
Het |
Sumf1 |
A |
G |
6: 108,162,456 (GRCm39) |
L21S |
probably benign |
Het |
Sytl3 |
T |
A |
17: 7,005,164 (GRCm39) |
S380T |
probably damaging |
Het |
Tgfb1i1 |
T |
A |
7: 127,847,840 (GRCm39) |
C74* |
probably null |
Het |
Tmprss15 |
T |
G |
16: 78,757,479 (GRCm39) |
I939L |
probably benign |
Het |
Tpsb2 |
GGCTGCTGCTGCTGCTG |
GGCTGCTGCTGCTG |
17: 25,585,536 (GRCm39) |
|
probably benign |
Het |
Vwde |
A |
T |
6: 13,215,639 (GRCm39) |
V139E |
probably damaging |
Het |
Wdr27 |
A |
G |
17: 15,137,475 (GRCm39) |
|
probably null |
Het |
Zkscan14 |
A |
G |
5: 145,132,001 (GRCm39) |
V510A |
probably benign |
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 |
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 |
|