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 |
Cyp2c67 |
T |
A |
19: 39,605,876 (GRCm39) |
Q340L |
probably null |
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 |
C |
11: 67,258,537 (GRCm39) |
Q184P |
|
Het |
Myh13 |
A |
T |
11: 67,217,990 (GRCm39) |
E21V |
possibly damaging |
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 |
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 Wrn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00659:Wrn
|
APN |
8 |
33,812,405 (GRCm39) |
splice site |
probably benign |
|
IGL00661:Wrn
|
APN |
8 |
33,809,173 (GRCm39) |
splice site |
probably benign |
|
IGL01472:Wrn
|
APN |
8 |
33,819,200 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01544:Wrn
|
APN |
8 |
33,814,554 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01599:Wrn
|
APN |
8 |
33,731,039 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01688:Wrn
|
APN |
8 |
33,800,730 (GRCm39) |
splice site |
probably benign |
|
IGL01916:Wrn
|
APN |
8 |
33,747,252 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01925:Wrn
|
APN |
8 |
33,809,208 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02068:Wrn
|
APN |
8 |
33,800,777 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02084:Wrn
|
APN |
8 |
33,775,207 (GRCm39) |
missense |
probably benign |
|
IGL02167:Wrn
|
APN |
8 |
33,807,583 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02230:Wrn
|
APN |
8 |
33,807,591 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02717:Wrn
|
APN |
8 |
33,833,601 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02982:Wrn
|
APN |
8 |
33,833,094 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03030:Wrn
|
APN |
8 |
33,738,989 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03088:Wrn
|
APN |
8 |
33,758,851 (GRCm39) |
splice site |
probably benign |
|
IGL03179:Wrn
|
APN |
8 |
33,800,734 (GRCm39) |
splice site |
probably null |
|
IGL03306:Wrn
|
APN |
8 |
33,826,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R0004:Wrn
|
UTSW |
8 |
33,807,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R0190:Wrn
|
UTSW |
8 |
33,731,011 (GRCm39) |
missense |
probably benign |
0.02 |
R0441:Wrn
|
UTSW |
8 |
33,758,778 (GRCm39) |
missense |
probably benign |
0.24 |
R0463:Wrn
|
UTSW |
8 |
33,770,843 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0538:Wrn
|
UTSW |
8 |
33,826,119 (GRCm39) |
missense |
probably damaging |
0.99 |
R0682:Wrn
|
UTSW |
8 |
33,757,848 (GRCm39) |
missense |
probably benign |
0.00 |
R0729:Wrn
|
UTSW |
8 |
33,738,946 (GRCm39) |
splice site |
probably null |
|
R0744:Wrn
|
UTSW |
8 |
33,785,034 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0836:Wrn
|
UTSW |
8 |
33,785,034 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1168:Wrn
|
UTSW |
8 |
33,806,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R1301:Wrn
|
UTSW |
8 |
33,782,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R1352:Wrn
|
UTSW |
8 |
33,784,944 (GRCm39) |
missense |
probably benign |
0.25 |
R1396:Wrn
|
UTSW |
8 |
33,758,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R1432:Wrn
|
UTSW |
8 |
33,809,169 (GRCm39) |
splice site |
probably benign |
|
R1523:Wrn
|
UTSW |
8 |
33,782,744 (GRCm39) |
missense |
probably benign |
0.23 |
R1625:Wrn
|
UTSW |
8 |
33,819,158 (GRCm39) |
missense |
probably benign |
0.01 |
R1664:Wrn
|
UTSW |
8 |
33,770,794 (GRCm39) |
splice site |
probably null |
|
R1773:Wrn
|
UTSW |
8 |
33,833,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R1864:Wrn
|
UTSW |
8 |
33,778,892 (GRCm39) |
missense |
probably damaging |
0.99 |
R1868:Wrn
|
UTSW |
8 |
33,747,249 (GRCm39) |
missense |
probably benign |
0.03 |
R2011:Wrn
|
UTSW |
8 |
33,726,432 (GRCm39) |
missense |
probably benign |
0.02 |
R2075:Wrn
|
UTSW |
8 |
33,812,357 (GRCm39) |
missense |
probably benign |
0.00 |
R2091:Wrn
|
UTSW |
8 |
33,757,853 (GRCm39) |
missense |
probably benign |
|
R2213:Wrn
|
UTSW |
8 |
33,747,043 (GRCm39) |
missense |
probably benign |
0.05 |
R2255:Wrn
|
UTSW |
8 |
33,819,230 (GRCm39) |
missense |
probably benign |
0.13 |
R2276:Wrn
|
UTSW |
8 |
33,814,584 (GRCm39) |
missense |
probably benign |
0.02 |
R3177:Wrn
|
UTSW |
8 |
33,807,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R3277:Wrn
|
UTSW |
8 |
33,807,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R3779:Wrn
|
UTSW |
8 |
33,731,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R3827:Wrn
|
UTSW |
8 |
33,814,548 (GRCm39) |
missense |
probably benign |
0.00 |
R4111:Wrn
|
UTSW |
8 |
33,842,183 (GRCm39) |
missense |
probably benign |
0.02 |
R4392:Wrn
|
UTSW |
8 |
33,741,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R4458:Wrn
|
UTSW |
8 |
33,785,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R4650:Wrn
|
UTSW |
8 |
33,745,537 (GRCm39) |
missense |
probably benign |
0.05 |
R4656:Wrn
|
UTSW |
8 |
33,826,019 (GRCm39) |
splice site |
probably null |
|
R4657:Wrn
|
UTSW |
8 |
33,826,019 (GRCm39) |
splice site |
probably null |
|
R4667:Wrn
|
UTSW |
8 |
33,814,366 (GRCm39) |
missense |
probably benign |
0.00 |
R4735:Wrn
|
UTSW |
8 |
33,775,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R4933:Wrn
|
UTSW |
8 |
33,812,371 (GRCm39) |
missense |
probably benign |
0.01 |
R5104:Wrn
|
UTSW |
8 |
33,757,895 (GRCm39) |
splice site |
probably null |
|
R5166:Wrn
|
UTSW |
8 |
33,842,100 (GRCm39) |
critical splice donor site |
probably null |
|
R5279:Wrn
|
UTSW |
8 |
33,731,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R5400:Wrn
|
UTSW |
8 |
33,784,945 (GRCm39) |
missense |
probably benign |
0.02 |
R5575:Wrn
|
UTSW |
8 |
33,826,158 (GRCm39) |
missense |
probably benign |
0.02 |
R5695:Wrn
|
UTSW |
8 |
33,814,346 (GRCm39) |
missense |
probably benign |
0.26 |
R5729:Wrn
|
UTSW |
8 |
33,758,806 (GRCm39) |
missense |
probably benign |
0.02 |
R6044:Wrn
|
UTSW |
8 |
33,726,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R6139:Wrn
|
UTSW |
8 |
33,843,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R6158:Wrn
|
UTSW |
8 |
33,809,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R6192:Wrn
|
UTSW |
8 |
33,774,682 (GRCm39) |
missense |
probably benign |
0.12 |
R6243:Wrn
|
UTSW |
8 |
33,774,682 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6354:Wrn
|
UTSW |
8 |
33,833,666 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6429:Wrn
|
UTSW |
8 |
33,833,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R6490:Wrn
|
UTSW |
8 |
33,809,248 (GRCm39) |
missense |
probably benign |
0.01 |
R6529:Wrn
|
UTSW |
8 |
33,826,004 (GRCm39) |
splice site |
probably null |
|
R6535:Wrn
|
UTSW |
8 |
33,826,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R7001:Wrn
|
UTSW |
8 |
33,842,157 (GRCm39) |
missense |
probably benign |
0.04 |
R7114:Wrn
|
UTSW |
8 |
33,775,149 (GRCm39) |
frame shift |
probably null |
|
R7198:Wrn
|
UTSW |
8 |
33,814,346 (GRCm39) |
missense |
probably benign |
0.00 |
R7200:Wrn
|
UTSW |
8 |
33,812,376 (GRCm39) |
missense |
probably benign |
0.00 |
R7227:Wrn
|
UTSW |
8 |
33,738,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R7299:Wrn
|
UTSW |
8 |
33,782,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R7374:Wrn
|
UTSW |
8 |
33,758,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R7402:Wrn
|
UTSW |
8 |
33,738,994 (GRCm39) |
missense |
probably benign |
0.00 |
R7404:Wrn
|
UTSW |
8 |
33,738,994 (GRCm39) |
missense |
probably benign |
0.00 |
R7405:Wrn
|
UTSW |
8 |
33,738,994 (GRCm39) |
missense |
probably benign |
0.00 |
R7464:Wrn
|
UTSW |
8 |
33,826,024 (GRCm39) |
critical splice donor site |
probably null |
|
R7609:Wrn
|
UTSW |
8 |
33,800,741 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7729:Wrn
|
UTSW |
8 |
33,814,454 (GRCm39) |
missense |
probably benign |
0.21 |
R7830:Wrn
|
UTSW |
8 |
33,759,082 (GRCm39) |
missense |
probably damaging |
0.97 |
R7998:Wrn
|
UTSW |
8 |
33,782,671 (GRCm39) |
missense |
probably benign |
0.10 |
R8239:Wrn
|
UTSW |
8 |
33,819,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8262:Wrn
|
UTSW |
8 |
33,814,274 (GRCm39) |
missense |
probably benign |
0.07 |
R8410:Wrn
|
UTSW |
8 |
33,759,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R8480:Wrn
|
UTSW |
8 |
33,778,796 (GRCm39) |
missense |
probably benign |
0.10 |
R8530:Wrn
|
UTSW |
8 |
33,770,852 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8540:Wrn
|
UTSW |
8 |
33,842,154 (GRCm39) |
missense |
probably damaging |
0.96 |
R8708:Wrn
|
UTSW |
8 |
33,782,671 (GRCm39) |
missense |
probably damaging |
0.96 |
R8783:Wrn
|
UTSW |
8 |
33,826,041 (GRCm39) |
missense |
probably null |
1.00 |
R8870:Wrn
|
UTSW |
8 |
33,819,220 (GRCm39) |
missense |
probably benign |
0.01 |
R8876:Wrn
|
UTSW |
8 |
33,814,422 (GRCm39) |
missense |
probably benign |
0.00 |
R9050:Wrn
|
UTSW |
8 |
33,833,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R9329:Wrn
|
UTSW |
8 |
33,731,006 (GRCm39) |
missense |
probably benign |
|
R9595:Wrn
|
UTSW |
8 |
33,758,961 (GRCm39) |
missense |
probably benign |
|
R9621:Wrn
|
UTSW |
8 |
33,814,301 (GRCm39) |
missense |
probably benign |
0.01 |
R9623:Wrn
|
UTSW |
8 |
33,774,644 (GRCm39) |
critical splice donor site |
probably null |
|
R9797:Wrn
|
UTSW |
8 |
33,758,950 (GRCm39) |
missense |
probably benign |
0.02 |
RF010:Wrn
|
UTSW |
8 |
33,778,793 (GRCm39) |
missense |
probably benign |
0.13 |
X0017:Wrn
|
UTSW |
8 |
33,770,810 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Wrn
|
UTSW |
8 |
33,824,237 (GRCm39) |
missense |
probably damaging |
0.98 |
|