Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930438A08Rik |
T |
G |
11: 58,184,210 (GRCm39) |
L299R |
unknown |
Het |
Abca9 |
T |
G |
11: 110,035,087 (GRCm39) |
R693S |
probably benign |
Het |
Adamts20 |
A |
T |
15: 94,227,795 (GRCm39) |
|
probably null |
Het |
Afg1l |
T |
A |
10: 42,302,493 (GRCm39) |
D169V |
probably damaging |
Het |
Agbl1 |
T |
A |
7: 76,369,890 (GRCm39) |
M663K |
probably benign |
Het |
Angpt2 |
T |
A |
8: 18,791,039 (GRCm39) |
I86F |
probably benign |
Het |
Ankrd2 |
G |
A |
19: 42,030,424 (GRCm39) |
E160K |
probably null |
Het |
As3mt |
G |
T |
19: 46,696,233 (GRCm39) |
V14F |
probably damaging |
Het |
Atp6v0a2 |
T |
C |
5: 124,791,171 (GRCm39) |
|
probably benign |
Het |
Atp6v0d1 |
T |
A |
8: 106,257,591 (GRCm39) |
I113F |
probably damaging |
Het |
Bank1 |
A |
G |
3: 135,799,123 (GRCm39) |
I406T |
probably damaging |
Het |
Bicdl1 |
A |
G |
5: 115,801,881 (GRCm39) |
V59A |
possibly damaging |
Het |
Brsk1 |
A |
G |
7: 4,713,453 (GRCm39) |
|
probably benign |
Het |
Cdh17 |
T |
A |
4: 11,810,473 (GRCm39) |
N721K |
probably damaging |
Het |
Cercam |
A |
G |
2: 29,771,699 (GRCm39) |
|
probably benign |
Het |
Clpb |
T |
A |
7: 101,434,656 (GRCm39) |
L484* |
probably null |
Het |
Creb3l1 |
T |
A |
2: 91,825,739 (GRCm39) |
M127L |
probably benign |
Het |
Cstdc1 |
A |
T |
2: 148,625,327 (GRCm39) |
H87L |
possibly damaging |
Het |
Ctla2b |
A |
C |
13: 61,043,874 (GRCm39) |
D122E |
probably damaging |
Het |
Cyb5rl |
C |
A |
4: 106,938,225 (GRCm39) |
Y12* |
probably null |
Het |
Dennd5a |
T |
C |
7: 109,507,588 (GRCm39) |
Y800C |
probably damaging |
Het |
Dmrt3 |
T |
G |
19: 25,600,411 (GRCm39) |
S419A |
probably benign |
Het |
Elapor1 |
A |
G |
3: 108,443,674 (GRCm39) |
W31R |
probably damaging |
Het |
Fbxo38 |
A |
G |
18: 62,655,543 (GRCm39) |
V381A |
possibly damaging |
Het |
Flg2 |
A |
T |
3: 93,110,498 (GRCm39) |
H842L |
unknown |
Het |
Fn1 |
A |
T |
1: 71,653,197 (GRCm39) |
|
probably null |
Het |
Fos |
A |
C |
12: 85,522,630 (GRCm39) |
T181P |
possibly damaging |
Het |
Fzd10 |
A |
G |
5: 128,679,669 (GRCm39) |
Y463C |
possibly damaging |
Het |
Gprc5b |
T |
C |
7: 118,582,856 (GRCm39) |
M338V |
probably benign |
Het |
Gsta4 |
T |
C |
9: 78,113,345 (GRCm39) |
|
probably benign |
Het |
Gstm2 |
T |
A |
3: 107,893,362 (GRCm39) |
T34S |
probably benign |
Het |
Haspin |
C |
T |
11: 73,027,451 (GRCm39) |
R546Q |
probably damaging |
Het |
Itgad |
G |
A |
7: 127,802,204 (GRCm39) |
R958H |
probably benign |
Het |
Kansl1l |
A |
T |
1: 66,774,884 (GRCm39) |
H647Q |
probably damaging |
Het |
Kif5c |
A |
C |
2: 49,634,455 (GRCm39) |
R762S |
probably benign |
Het |
Klf4 |
C |
A |
4: 55,530,758 (GRCm39) |
A68S |
possibly damaging |
Het |
Klf4 |
A |
G |
4: 55,530,811 (GRCm39) |
L50P |
probably damaging |
Het |
Kmt2c |
T |
C |
5: 25,504,802 (GRCm39) |
E3502G |
probably damaging |
Het |
Krt8 |
A |
G |
15: 101,909,022 (GRCm39) |
I202T |
possibly damaging |
Het |
Lmcd1 |
A |
T |
6: 112,287,649 (GRCm39) |
T112S |
probably damaging |
Het |
Lpxn |
T |
C |
19: 12,810,575 (GRCm39) |
C340R |
probably damaging |
Het |
Man2a2 |
C |
T |
7: 80,009,082 (GRCm39) |
V844M |
possibly damaging |
Het |
Map10 |
G |
A |
8: 126,397,809 (GRCm39) |
E401K |
probably benign |
Het |
Mark4 |
A |
T |
7: 19,185,509 (GRCm39) |
L75Q |
probably damaging |
Het |
Mlf2 |
T |
G |
6: 124,910,945 (GRCm39) |
M81R |
probably damaging |
Het |
Mup3 |
A |
G |
4: 62,005,079 (GRCm39) |
I67T |
probably damaging |
Het |
Mycbpap |
T |
C |
11: 94,404,769 (GRCm39) |
|
probably null |
Het |
Myt1l |
T |
C |
12: 29,970,476 (GRCm39) |
V1185A |
probably benign |
Het |
Ncoa7 |
C |
T |
10: 30,574,121 (GRCm39) |
|
probably null |
Het |
Nos1 |
C |
A |
5: 118,005,323 (GRCm39) |
N14K |
probably damaging |
Het |
Nova2 |
G |
T |
7: 18,684,494 (GRCm39) |
V116F |
unknown |
Het |
Obox3 |
G |
A |
7: 15,360,927 (GRCm39) |
|
probably benign |
Het |
Or10h1 |
A |
T |
17: 33,418,534 (GRCm39) |
T171S |
probably benign |
Het |
Or2t46 |
T |
A |
11: 58,472,653 (GRCm39) |
|
probably benign |
Het |
Or5v1 |
A |
G |
17: 37,809,539 (GRCm39) |
|
probably benign |
Het |
Or8b50 |
A |
T |
9: 38,518,597 (GRCm39) |
S279C |
probably damaging |
Het |
P2rx5 |
T |
A |
11: 73,056,446 (GRCm39) |
|
probably benign |
Het |
Parvb |
T |
A |
15: 84,193,044 (GRCm39) |
|
probably benign |
Het |
Popdc2 |
A |
T |
16: 38,194,184 (GRCm39) |
T202S |
probably damaging |
Het |
Ppm1j |
T |
A |
3: 104,692,725 (GRCm39) |
Y411* |
probably null |
Het |
Rapgefl1 |
C |
A |
11: 98,740,058 (GRCm39) |
L484M |
probably damaging |
Het |
Septin14 |
A |
G |
5: 129,774,797 (GRCm39) |
|
probably benign |
Het |
Slf1 |
A |
G |
13: 77,232,554 (GRCm39) |
C517R |
probably damaging |
Het |
Smyd3 |
A |
G |
1: 178,921,898 (GRCm39) |
|
probably null |
Het |
Snx9 |
A |
G |
17: 5,974,885 (GRCm39) |
T458A |
probably benign |
Het |
Srgap1 |
T |
C |
10: 121,661,598 (GRCm39) |
D514G |
possibly damaging |
Het |
Tbc1d14 |
A |
G |
5: 36,682,308 (GRCm39) |
S311P |
probably damaging |
Het |
Timd6 |
C |
A |
11: 46,475,244 (GRCm39) |
F146L |
probably benign |
Het |
Tmem150c |
T |
G |
5: 100,234,076 (GRCm39) |
K91N |
probably damaging |
Het |
Traf3 |
T |
A |
12: 111,228,277 (GRCm39) |
M471K |
probably damaging |
Het |
Tubd1 |
G |
T |
11: 86,443,825 (GRCm39) |
G178C |
probably damaging |
Het |
Vav2 |
T |
C |
2: 27,157,262 (GRCm39) |
K847E |
possibly damaging |
Het |
Vmn2r100 |
A |
T |
17: 19,742,301 (GRCm39) |
H225L |
probably benign |
Het |
Xpo7 |
T |
G |
14: 70,918,702 (GRCm39) |
S710R |
probably benign |
Het |
Zfp780b |
C |
T |
7: 27,662,417 (GRCm39) |
V713I |
possibly damaging |
Het |
Zkscan17 |
A |
T |
11: 59,378,592 (GRCm39) |
I197N |
probably 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 |
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 |
|
R7474:Wrn
|
UTSW |
8 |
33,819,209 (GRCm39) |
missense |
probably damaging |
0.96 |
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 |
|