Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,278,088 (GRCm39) |
C3089* |
probably null |
Het |
Abcc1 |
A |
G |
16: 14,290,850 (GRCm39) |
T1487A |
possibly damaging |
Het |
Agfg1 |
T |
A |
1: 82,860,132 (GRCm39) |
L333* |
probably null |
Het |
Agfg2 |
C |
A |
5: 137,652,130 (GRCm39) |
V410F |
possibly damaging |
Het |
Amotl2 |
T |
C |
9: 102,607,310 (GRCm39) |
V706A |
probably benign |
Het |
Apob |
A |
T |
12: 8,059,185 (GRCm39) |
T2556S |
probably benign |
Het |
Asb18 |
T |
A |
1: 89,920,755 (GRCm39) |
H174L |
possibly damaging |
Het |
Atp10a |
G |
A |
7: 58,308,275 (GRCm39) |
E25K |
unknown |
Het |
Aup1 |
T |
C |
6: 83,031,948 (GRCm39) |
L65P |
probably benign |
Het |
Blvra |
T |
C |
2: 126,928,769 (GRCm39) |
F86L |
probably damaging |
Het |
Cabp4 |
T |
C |
19: 4,189,398 (GRCm39) |
D53G |
probably benign |
Het |
Cd300c2 |
T |
A |
11: 114,889,122 (GRCm39) |
E153V |
probably benign |
Het |
Crxos |
A |
G |
7: 15,636,856 (GRCm39) |
E143G |
possibly damaging |
Het |
Csmd2 |
A |
G |
4: 128,439,920 (GRCm39) |
N3125D |
|
Het |
Dscam |
T |
A |
16: 96,621,089 (GRCm39) |
N540Y |
possibly damaging |
Het |
E2f8 |
G |
A |
7: 48,525,508 (GRCm39) |
R155W |
probably damaging |
Het |
Ext1 |
A |
T |
15: 53,207,885 (GRCm39) |
V292D |
probably damaging |
Het |
Extl3 |
T |
C |
14: 65,314,090 (GRCm39) |
E364G |
possibly damaging |
Het |
Fmn2 |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
1: 174,436,769 (GRCm39) |
|
probably benign |
Het |
Fsd1 |
A |
T |
17: 56,295,149 (GRCm39) |
D46V |
possibly damaging |
Het |
Gcnt2 |
T |
A |
13: 41,111,733 (GRCm39) |
L374H |
probably damaging |
Het |
Gm10309 |
G |
A |
17: 86,812,095 (GRCm39) |
|
probably benign |
Het |
Gm14410 |
A |
T |
2: 176,894,618 (GRCm39) |
|
probably null |
Het |
Gm5114 |
A |
T |
7: 39,057,404 (GRCm39) |
S738R |
probably benign |
Het |
Gtf3c2 |
C |
A |
5: 31,325,100 (GRCm39) |
G502W |
probably damaging |
Het |
Insc |
G |
A |
7: 114,368,058 (GRCm39) |
|
probably null |
Het |
Kcnt2 |
T |
C |
1: 140,498,216 (GRCm39) |
Y898H |
possibly damaging |
Het |
Kctd19 |
C |
A |
8: 106,118,664 (GRCm39) |
R299L |
probably benign |
Het |
Klf10 |
T |
C |
15: 38,297,446 (GRCm39) |
N198S |
probably benign |
Het |
L3mbtl1 |
A |
T |
2: 162,808,524 (GRCm39) |
D574V |
probably damaging |
Het |
Lamc1 |
G |
A |
1: 153,208,011 (GRCm39) |
A92V |
possibly damaging |
Het |
Lrrc63 |
T |
A |
14: 75,363,643 (GRCm39) |
T163S |
possibly damaging |
Het |
Mak |
T |
A |
13: 41,204,956 (GRCm39) |
K127N |
probably damaging |
Het |
Mdga2 |
G |
A |
12: 66,533,535 (GRCm39) |
Q945* |
probably null |
Het |
Mthfr |
T |
A |
4: 148,137,059 (GRCm39) |
I519N |
possibly damaging |
Het |
Mtmr2 |
C |
A |
9: 13,710,521 (GRCm39) |
H357N |
probably damaging |
Het |
Myh13 |
A |
T |
11: 67,217,990 (GRCm39) |
E21V |
possibly damaging |
Het |
Myh13 |
A |
C |
11: 67,258,537 (GRCm39) |
Q184P |
|
Het |
Nans |
T |
A |
4: 46,502,484 (GRCm39) |
L307Q |
probably damaging |
Het |
Ncan |
C |
A |
8: 70,554,691 (GRCm39) |
R1042L |
possibly damaging |
Het |
Nrg3 |
T |
C |
14: 38,733,956 (GRCm39) |
E310G |
probably damaging |
Het |
Obsl1 |
A |
C |
1: 75,474,828 (GRCm39) |
N857K |
probably benign |
Het |
Olfml2a |
T |
C |
2: 38,850,273 (GRCm39) |
V663A |
probably damaging |
Het |
Or14j10 |
T |
C |
17: 37,935,277 (GRCm39) |
D83G |
probably benign |
Het |
Or51v15-ps1 |
C |
A |
7: 103,278,354 (GRCm39) |
W271L |
unknown |
Het |
Or52e19b |
A |
G |
7: 103,032,969 (GRCm39) |
I80T |
probably damaging |
Het |
Or6d13 |
G |
T |
6: 116,517,999 (GRCm39) |
C195F |
probably damaging |
Het |
Or8i2 |
T |
C |
2: 86,852,898 (GRCm39) |
|
probably benign |
Het |
Pla2g4a |
T |
C |
1: 149,740,951 (GRCm39) |
M363V |
possibly damaging |
Het |
Pramel26 |
T |
C |
4: 143,538,269 (GRCm39) |
D234G |
probably benign |
Het |
Prickle1 |
A |
T |
15: 93,406,552 (GRCm39) |
V157D |
possibly damaging |
Het |
Pstk |
A |
G |
7: 130,975,362 (GRCm39) |
N105S |
probably benign |
Het |
Ptpn21 |
A |
G |
12: 98,703,622 (GRCm39) |
|
probably null |
Het |
Rnf2 |
T |
A |
1: 151,347,467 (GRCm39) |
E277D |
probably benign |
Het |
Rnpepl1 |
T |
C |
1: 92,846,694 (GRCm39) |
F532S |
probably benign |
Het |
Rtn1 |
C |
T |
12: 72,355,164 (GRCm39) |
A261T |
possibly damaging |
Het |
Ryr2 |
A |
G |
13: 11,609,762 (GRCm39) |
S4355P |
probably benign |
Het |
Sacs |
T |
G |
14: 61,448,627 (GRCm39) |
L3558V |
probably benign |
Het |
Senp6 |
T |
C |
9: 80,049,610 (GRCm39) |
V1047A |
probably damaging |
Het |
Slco2b1 |
A |
T |
7: 99,314,039 (GRCm39) |
C515S |
probably damaging |
Het |
Smgc |
T |
A |
15: 91,744,892 (GRCm39) |
V732E |
possibly damaging |
Het |
Sorcs1 |
T |
C |
19: 50,141,550 (GRCm39) |
M1105V |
possibly damaging |
Het |
Spats1 |
A |
G |
17: 45,768,087 (GRCm39) |
Y160H |
possibly damaging |
Het |
Tnfsf14 |
T |
A |
17: 57,497,848 (GRCm39) |
D128V |
|
Het |
Tns3 |
T |
C |
11: 8,480,894 (GRCm39) |
Q234R |
probably damaging |
Het |
Uxs1 |
A |
G |
1: 43,796,184 (GRCm39) |
V306A |
possibly damaging |
Het |
Vac14 |
T |
A |
8: 111,363,066 (GRCm39) |
V304D |
probably damaging |
Het |
Vangl1 |
A |
G |
3: 102,091,565 (GRCm39) |
F174L |
probably benign |
Het |
Vav1 |
A |
G |
17: 57,606,102 (GRCm39) |
E242G |
probably benign |
Het |
Vsir |
A |
G |
10: 60,204,701 (GRCm39) |
N305D |
probably benign |
Het |
Vwce |
T |
A |
19: 10,624,305 (GRCm39) |
C399S |
possibly damaging |
Het |
Wrn |
A |
T |
8: 33,819,209 (GRCm39) |
L248M |
probably damaging |
Het |
Zfp141 |
T |
A |
7: 42,125,678 (GRCm39) |
K265* |
probably null |
Het |
Zfp735 |
A |
T |
11: 73,602,002 (GRCm39) |
K315N |
possibly damaging |
Het |
|
Other mutations in Cyp2c67 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00955:Cyp2c67
|
APN |
19 |
39,631,829 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01025:Cyp2c67
|
APN |
19 |
39,628,376 (GRCm39) |
nonsense |
probably null |
|
IGL01363:Cyp2c67
|
APN |
19 |
39,628,411 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01819:Cyp2c67
|
APN |
19 |
39,604,165 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01902:Cyp2c67
|
APN |
19 |
39,637,470 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02172:Cyp2c67
|
APN |
19 |
39,637,446 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02351:Cyp2c67
|
APN |
19 |
39,605,861 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02355:Cyp2c67
|
APN |
19 |
39,605,826 (GRCm39) |
nonsense |
probably null |
|
IGL02355:Cyp2c67
|
APN |
19 |
39,631,849 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02358:Cyp2c67
|
APN |
19 |
39,605,861 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02362:Cyp2c67
|
APN |
19 |
39,605,826 (GRCm39) |
nonsense |
probably null |
|
IGL02362:Cyp2c67
|
APN |
19 |
39,631,849 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02388:Cyp2c67
|
APN |
19 |
39,631,799 (GRCm39) |
missense |
probably benign |
0.20 |
IGL03106:Cyp2c67
|
APN |
19 |
39,632,119 (GRCm39) |
missense |
probably benign |
0.27 |
IGL03219:Cyp2c67
|
APN |
19 |
39,631,738 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL03326:Cyp2c67
|
APN |
19 |
39,631,713 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03349:Cyp2c67
|
APN |
19 |
39,632,128 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03356:Cyp2c67
|
APN |
19 |
39,628,405 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03052:Cyp2c67
|
UTSW |
19 |
39,637,329 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0585:Cyp2c67
|
UTSW |
19 |
39,627,138 (GRCm39) |
missense |
possibly damaging |
0.59 |
R0975:Cyp2c67
|
UTSW |
19 |
39,597,622 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0976:Cyp2c67
|
UTSW |
19 |
39,631,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R1252:Cyp2c67
|
UTSW |
19 |
39,614,585 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1398:Cyp2c67
|
UTSW |
19 |
39,627,069 (GRCm39) |
missense |
probably damaging |
0.96 |
R1411:Cyp2c67
|
UTSW |
19 |
39,627,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R1505:Cyp2c67
|
UTSW |
19 |
39,637,408 (GRCm39) |
missense |
probably benign |
0.00 |
R1543:Cyp2c67
|
UTSW |
19 |
39,631,708 (GRCm39) |
splice site |
probably benign |
|
R1613:Cyp2c67
|
UTSW |
19 |
39,614,643 (GRCm39) |
missense |
probably benign |
0.00 |
R1618:Cyp2c67
|
UTSW |
19 |
39,631,708 (GRCm39) |
splice site |
probably benign |
|
R1667:Cyp2c67
|
UTSW |
19 |
39,632,034 (GRCm39) |
critical splice donor site |
probably null |
|
R1852:Cyp2c67
|
UTSW |
19 |
39,605,811 (GRCm39) |
missense |
probably benign |
0.01 |
R2005:Cyp2c67
|
UTSW |
19 |
39,631,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R2105:Cyp2c67
|
UTSW |
19 |
39,614,681 (GRCm39) |
missense |
probably benign |
0.24 |
R2181:Cyp2c67
|
UTSW |
19 |
39,597,541 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3817:Cyp2c67
|
UTSW |
19 |
39,627,127 (GRCm39) |
missense |
probably benign |
0.00 |
R4669:Cyp2c67
|
UTSW |
19 |
39,632,098 (GRCm39) |
missense |
probably benign |
0.00 |
R4689:Cyp2c67
|
UTSW |
19 |
39,627,032 (GRCm39) |
missense |
probably benign |
0.00 |
R4756:Cyp2c67
|
UTSW |
19 |
39,632,188 (GRCm39) |
missense |
probably benign |
0.03 |
R4823:Cyp2c67
|
UTSW |
19 |
39,604,168 (GRCm39) |
missense |
probably benign |
0.13 |
R5152:Cyp2c67
|
UTSW |
19 |
39,627,132 (GRCm39) |
missense |
probably benign |
0.00 |
R5345:Cyp2c67
|
UTSW |
19 |
39,614,676 (GRCm39) |
missense |
probably benign |
0.01 |
R5580:Cyp2c67
|
UTSW |
19 |
39,604,094 (GRCm39) |
missense |
probably damaging |
0.99 |
R5644:Cyp2c67
|
UTSW |
19 |
39,604,138 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6116:Cyp2c67
|
UTSW |
19 |
39,605,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R6516:Cyp2c67
|
UTSW |
19 |
39,605,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R6550:Cyp2c67
|
UTSW |
19 |
39,605,854 (GRCm39) |
nonsense |
probably null |
|
R6939:Cyp2c67
|
UTSW |
19 |
39,631,778 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6995:Cyp2c67
|
UTSW |
19 |
39,604,123 (GRCm39) |
missense |
probably damaging |
0.96 |
R7028:Cyp2c67
|
UTSW |
19 |
39,628,341 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7144:Cyp2c67
|
UTSW |
19 |
39,604,138 (GRCm39) |
missense |
probably benign |
0.00 |
R7242:Cyp2c67
|
UTSW |
19 |
39,605,783 (GRCm39) |
missense |
probably benign |
0.30 |
R7335:Cyp2c67
|
UTSW |
19 |
39,628,451 (GRCm39) |
nonsense |
probably null |
|
R7337:Cyp2c67
|
UTSW |
19 |
39,597,708 (GRCm39) |
splice site |
probably null |
|
R7642:Cyp2c67
|
UTSW |
19 |
39,604,084 (GRCm39) |
missense |
probably damaging |
0.97 |
R7870:Cyp2c67
|
UTSW |
19 |
39,597,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R8152:Cyp2c67
|
UTSW |
19 |
39,628,452 (GRCm39) |
missense |
probably benign |
0.21 |
R8367:Cyp2c67
|
UTSW |
19 |
39,627,118 (GRCm39) |
missense |
probably benign |
0.01 |
R8717:Cyp2c67
|
UTSW |
19 |
39,627,155 (GRCm39) |
missense |
probably benign |
0.05 |
R8728:Cyp2c67
|
UTSW |
19 |
39,614,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R9275:Cyp2c67
|
UTSW |
19 |
39,597,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R9278:Cyp2c67
|
UTSW |
19 |
39,597,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R9376:Cyp2c67
|
UTSW |
19 |
39,627,178 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cyp2c67
|
UTSW |
19 |
39,632,123 (GRCm39) |
missense |
possibly damaging |
0.89 |
|