Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
A |
G |
14: 32,382,309 (GRCm39) |
S1219P |
possibly damaging |
Het |
A2ml1 |
A |
G |
6: 128,538,489 (GRCm39) |
Y644H |
probably damaging |
Het |
Abca9 |
T |
G |
11: 110,007,902 (GRCm39) |
R1232S |
possibly damaging |
Het |
Acsf2 |
C |
T |
11: 94,463,975 (GRCm39) |
V70M |
probably benign |
Het |
Ampd1 |
A |
G |
3: 102,986,446 (GRCm39) |
I42V |
probably benign |
Het |
Arhgap10 |
A |
G |
8: 78,071,267 (GRCm39) |
|
probably null |
Het |
Atp1a4 |
A |
T |
1: 172,071,975 (GRCm39) |
L432Q |
probably damaging |
Het |
Bbs12 |
T |
A |
3: 37,374,598 (GRCm39) |
C349S |
possibly damaging |
Het |
Bnc2 |
A |
G |
4: 84,211,007 (GRCm39) |
V479A |
possibly damaging |
Het |
Cald1 |
A |
T |
6: 34,748,043 (GRCm39) |
K761* |
probably null |
Het |
Cd177 |
C |
T |
7: 24,451,688 (GRCm39) |
G443R |
probably null |
Het |
Cdc42bpb |
T |
C |
12: 111,292,410 (GRCm39) |
D375G |
probably damaging |
Het |
Chsy3 |
T |
C |
18: 59,309,268 (GRCm39) |
Y174H |
probably damaging |
Het |
Cmya5 |
T |
C |
13: 93,233,943 (GRCm39) |
M382V |
probably benign |
Het |
Col1a2 |
G |
A |
6: 4,531,926 (GRCm39) |
S782N |
unknown |
Het |
Crtac1 |
C |
T |
19: 42,297,629 (GRCm39) |
|
probably null |
Het |
Csmd3 |
T |
A |
15: 47,445,923 (GRCm39) |
D3683V |
probably damaging |
Het |
Ctrc |
A |
G |
4: 141,572,354 (GRCm39) |
L62P |
probably damaging |
Het |
Cyp3a57 |
A |
T |
5: 145,307,867 (GRCm39) |
K208* |
probably null |
Het |
Dnaaf2 |
A |
T |
12: 69,244,122 (GRCm39) |
L313Q |
probably damaging |
Het |
Dtl |
A |
G |
1: 191,278,680 (GRCm39) |
L394P |
probably benign |
Het |
Ehhadh |
T |
C |
16: 21,585,305 (GRCm39) |
E192G |
probably benign |
Het |
Fads2 |
T |
C |
19: 10,059,997 (GRCm39) |
I226V |
probably benign |
Het |
Fat2 |
T |
C |
11: 55,161,208 (GRCm39) |
E3174G |
probably damaging |
Het |
Galnt14 |
C |
T |
17: 73,881,826 (GRCm39) |
R91Q |
probably damaging |
Het |
Hdhd5 |
G |
T |
6: 120,487,252 (GRCm39) |
D368E |
probably benign |
Het |
Hk3 |
T |
A |
13: 55,158,617 (GRCm39) |
I528F |
probably damaging |
Het |
Il10ra |
A |
C |
9: 45,166,951 (GRCm39) |
S533R |
possibly damaging |
Het |
Itpr3 |
G |
T |
17: 27,305,950 (GRCm39) |
K169N |
probably benign |
Het |
Lrrc17 |
A |
G |
5: 21,780,264 (GRCm39) |
T413A |
probably benign |
Het |
Mcm2 |
C |
T |
6: 88,861,053 (GRCm39) |
D882N |
probably benign |
Het |
Met |
T |
C |
6: 17,562,197 (GRCm39) |
V1186A |
probably damaging |
Het |
Msh5 |
C |
T |
17: 35,248,628 (GRCm39) |
|
probably null |
Het |
Nav3 |
T |
C |
10: 109,600,648 (GRCm39) |
I1326M |
probably damaging |
Het |
Nek10 |
A |
G |
14: 14,850,896 (GRCm38) |
I314V |
probably benign |
Het |
Or10g1 |
A |
C |
14: 52,648,225 (GRCm39) |
F35V |
probably damaging |
Het |
Or8b53 |
T |
A |
9: 38,667,412 (GRCm39) |
Y143N |
probably benign |
Het |
Pim1 |
A |
G |
17: 29,712,720 (GRCm39) |
E211G |
probably damaging |
Het |
Plaat1 |
T |
A |
16: 29,039,189 (GRCm39) |
Y90N |
probably benign |
Het |
Ppp1r12b |
A |
T |
1: 134,704,144 (GRCm39) |
D903E |
probably benign |
Het |
Ptpn14 |
T |
C |
1: 189,583,229 (GRCm39) |
L692P |
probably benign |
Het |
Ptprt |
A |
G |
2: 161,977,138 (GRCm39) |
C387R |
probably damaging |
Het |
Qrfprl |
A |
G |
6: 65,418,369 (GRCm39) |
|
probably benign |
Het |
Scarb1 |
A |
G |
5: 125,381,341 (GRCm39) |
Y68H |
possibly damaging |
Het |
Shisa6 |
T |
A |
11: 66,108,800 (GRCm39) |
D359V |
probably damaging |
Het |
Shprh |
T |
C |
10: 11,063,817 (GRCm39) |
S1297P |
probably damaging |
Het |
Sik1 |
T |
C |
17: 32,069,125 (GRCm39) |
D250G |
probably damaging |
Het |
Slamf7 |
A |
G |
1: 171,466,635 (GRCm39) |
L190S |
probably damaging |
Het |
Slc22a3 |
G |
A |
17: 12,652,355 (GRCm39) |
P423L |
probably damaging |
Het |
Slc35e2 |
A |
T |
4: 155,697,137 (GRCm39) |
E217V |
probably damaging |
Het |
Spocd1 |
A |
T |
4: 129,850,254 (GRCm39) |
N760I |
probably damaging |
Het |
Tas2r136 |
G |
T |
6: 132,754,294 (GRCm39) |
P278T |
possibly damaging |
Het |
Tchhl1 |
A |
T |
3: 93,377,836 (GRCm39) |
Q180L |
probably benign |
Het |
Tmem151b |
T |
A |
17: 45,858,010 (GRCm39) |
T79S |
probably benign |
Het |
Trbv16 |
T |
A |
6: 41,128,936 (GRCm39) |
L40Q |
probably damaging |
Het |
Trmt1l |
T |
G |
1: 151,316,594 (GRCm39) |
I32S |
probably damaging |
Het |
Ubr4 |
A |
G |
4: 139,152,641 (GRCm39) |
T2011A |
probably damaging |
Het |
Urb1 |
C |
T |
16: 90,569,652 (GRCm39) |
W1358* |
probably null |
Het |
Usp31 |
T |
G |
7: 121,248,698 (GRCm39) |
H915P |
probably benign |
Het |
Vmn2r10 |
A |
T |
5: 109,151,377 (GRCm39) |
M79K |
possibly damaging |
Het |
Vmn2r14 |
A |
G |
5: 109,369,222 (GRCm39) |
I117T |
probably benign |
Het |
Vps13b |
A |
G |
15: 35,869,497 (GRCm39) |
H2667R |
possibly damaging |
Het |
Vwa5b1 |
G |
A |
4: 138,305,962 (GRCm39) |
T912M |
possibly damaging |
Het |
Zfp709 |
G |
A |
8: 72,643,363 (GRCm39) |
C264Y |
probably benign |
Het |
Zkscan5 |
A |
G |
5: 145,156,898 (GRCm39) |
I467V |
probably benign |
Het |
Zxdc |
A |
T |
6: 90,347,281 (GRCm39) |
D214V |
probably damaging |
Het |
|
Other mutations in Tomm70a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00849:Tomm70a
|
APN |
16 |
56,970,173 (GRCm39) |
splice site |
probably benign |
|
IGL01064:Tomm70a
|
APN |
16 |
56,972,975 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01597:Tomm70a
|
APN |
16 |
56,953,551 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02248:Tomm70a
|
APN |
16 |
56,958,465 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02560:Tomm70a
|
APN |
16 |
56,970,212 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03328:Tomm70a
|
APN |
16 |
56,965,150 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03335:Tomm70a
|
APN |
16 |
56,970,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R0164:Tomm70a
|
UTSW |
16 |
56,968,184 (GRCm39) |
missense |
probably damaging |
0.96 |
R0164:Tomm70a
|
UTSW |
16 |
56,968,184 (GRCm39) |
missense |
probably damaging |
0.96 |
R0196:Tomm70a
|
UTSW |
16 |
56,966,463 (GRCm39) |
missense |
probably benign |
0.03 |
R0417:Tomm70a
|
UTSW |
16 |
56,970,266 (GRCm39) |
missense |
probably benign |
0.28 |
R0763:Tomm70a
|
UTSW |
16 |
56,942,535 (GRCm39) |
missense |
probably benign |
0.30 |
R1099:Tomm70a
|
UTSW |
16 |
56,963,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R1680:Tomm70a
|
UTSW |
16 |
56,942,324 (GRCm39) |
missense |
unknown |
|
R2081:Tomm70a
|
UTSW |
16 |
56,961,121 (GRCm39) |
missense |
probably damaging |
0.99 |
R2127:Tomm70a
|
UTSW |
16 |
56,942,234 (GRCm39) |
missense |
unknown |
|
R3033:Tomm70a
|
UTSW |
16 |
56,942,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R4287:Tomm70a
|
UTSW |
16 |
56,960,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R5029:Tomm70a
|
UTSW |
16 |
56,942,514 (GRCm39) |
missense |
probably benign |
|
R5210:Tomm70a
|
UTSW |
16 |
56,953,614 (GRCm39) |
critical splice donor site |
probably null |
|
R5214:Tomm70a
|
UTSW |
16 |
56,942,300 (GRCm39) |
missense |
unknown |
|
R5586:Tomm70a
|
UTSW |
16 |
56,942,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R5744:Tomm70a
|
UTSW |
16 |
56,942,202 (GRCm39) |
start gained |
probably benign |
|
R6256:Tomm70a
|
UTSW |
16 |
56,973,055 (GRCm39) |
missense |
probably benign |
0.05 |
R6699:Tomm70a
|
UTSW |
16 |
56,963,165 (GRCm39) |
missense |
probably benign |
0.02 |
R6902:Tomm70a
|
UTSW |
16 |
56,958,444 (GRCm39) |
missense |
probably damaging |
0.96 |
R7106:Tomm70a
|
UTSW |
16 |
56,961,121 (GRCm39) |
missense |
probably damaging |
0.99 |
R7378:Tomm70a
|
UTSW |
16 |
56,966,407 (GRCm39) |
nonsense |
probably null |
|
R7817:Tomm70a
|
UTSW |
16 |
56,965,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R8002:Tomm70a
|
UTSW |
16 |
56,957,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R8214:Tomm70a
|
UTSW |
16 |
56,942,330 (GRCm39) |
missense |
unknown |
|
R8862:Tomm70a
|
UTSW |
16 |
56,942,546 (GRCm39) |
missense |
probably benign |
|
R9194:Tomm70a
|
UTSW |
16 |
56,973,070 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9223:Tomm70a
|
UTSW |
16 |
56,963,166 (GRCm39) |
missense |
probably benign |
0.00 |
R9242:Tomm70a
|
UTSW |
16 |
56,958,383 (GRCm39) |
splice site |
probably benign |
|
R9338:Tomm70a
|
UTSW |
16 |
56,942,399 (GRCm39) |
missense |
probably benign |
|
R9366:Tomm70a
|
UTSW |
16 |
56,970,259 (GRCm39) |
nonsense |
probably null |
|
R9649:Tomm70a
|
UTSW |
16 |
56,961,072 (GRCm39) |
missense |
possibly damaging |
0.93 |
|