Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
C |
A |
5: 114,378,721 (GRCm39) |
H2044Q |
possibly damaging |
Het |
Ankrd12 |
A |
T |
17: 66,293,244 (GRCm39) |
S730T |
probably benign |
Het |
Ano9 |
A |
T |
7: 140,682,382 (GRCm39) |
N655K |
probably benign |
Het |
Ap1ar |
A |
T |
3: 127,609,298 (GRCm39) |
Y108N |
probably damaging |
Het |
Asap3 |
A |
G |
4: 135,954,752 (GRCm39) |
I55V |
probably benign |
Het |
Camta1 |
T |
C |
4: 151,158,442 (GRCm39) |
|
probably null |
Het |
Ces2e |
C |
T |
8: 105,657,290 (GRCm39) |
|
probably benign |
Het |
Cflar |
T |
C |
1: 58,791,903 (GRCm39) |
I405T |
probably benign |
Het |
Cibar2 |
T |
A |
8: 120,896,461 (GRCm39) |
K174* |
probably null |
Het |
Cyp51 |
A |
G |
5: 4,133,247 (GRCm39) |
S464P |
probably damaging |
Het |
Ermard |
G |
A |
17: 15,271,826 (GRCm39) |
|
probably benign |
Het |
Glb1l2 |
T |
C |
9: 26,707,841 (GRCm39) |
T49A |
probably benign |
Het |
Gls |
A |
G |
1: 52,258,674 (GRCm39) |
V198A |
probably benign |
Het |
Heatr5b |
A |
T |
17: 79,115,855 (GRCm39) |
I867N |
probably damaging |
Het |
Ighv1-14 |
A |
T |
12: 114,610,334 (GRCm39) |
|
noncoding transcript |
Het |
Iqsec1 |
T |
C |
6: 90,641,051 (GRCm39) |
K1022E |
probably damaging |
Het |
Myo10 |
A |
G |
15: 25,726,574 (GRCm39) |
T299A |
probably benign |
Het |
Nr2e3 |
A |
T |
9: 59,856,291 (GRCm39) |
M82K |
probably benign |
Het |
Ntpcr |
A |
G |
8: 126,472,191 (GRCm39) |
|
probably benign |
Het |
Or1e26 |
A |
G |
11: 73,480,058 (GRCm39) |
C169R |
probably damaging |
Het |
Or4d10b |
T |
C |
19: 12,036,253 (GRCm39) |
T288A |
possibly damaging |
Het |
Or52s6 |
A |
G |
7: 103,092,159 (GRCm39) |
L57P |
probably damaging |
Het |
Or5p80 |
A |
G |
7: 108,229,739 (GRCm39) |
D180G |
probably damaging |
Het |
Or6c70 |
A |
T |
10: 129,710,091 (GRCm39) |
D178E |
probably benign |
Het |
Prkcb |
A |
G |
7: 122,189,390 (GRCm39) |
D506G |
probably damaging |
Het |
Rasgef1a |
A |
G |
6: 118,066,404 (GRCm39) |
I470V |
probably benign |
Het |
Rbm27 |
A |
G |
18: 42,452,978 (GRCm39) |
E514G |
possibly damaging |
Het |
Rgs22 |
G |
A |
15: 36,013,300 (GRCm39) |
A1048V |
probably benign |
Het |
Secisbp2l |
A |
G |
2: 125,617,498 (GRCm39) |
F60L |
possibly damaging |
Het |
Six4 |
T |
C |
12: 73,155,429 (GRCm39) |
S505G |
probably benign |
Het |
Skint1 |
T |
A |
4: 111,882,727 (GRCm39) |
V257E |
possibly damaging |
Het |
Smad9 |
A |
G |
3: 54,693,593 (GRCm39) |
N174S |
possibly damaging |
Het |
Smc2 |
A |
G |
4: 52,462,914 (GRCm39) |
N635D |
probably benign |
Het |
Stradb |
T |
A |
1: 59,028,937 (GRCm39) |
I135N |
probably damaging |
Het |
Syt12 |
T |
C |
19: 4,497,762 (GRCm39) |
T407A |
probably damaging |
Het |
Tmc8 |
T |
A |
11: 117,677,346 (GRCm39) |
I322N |
probably damaging |
Het |
Tnip1 |
A |
C |
11: 54,802,365 (GRCm39) |
*648G |
probably null |
Het |
Ttc3 |
T |
C |
16: 94,210,540 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Barx2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00481:Barx2
|
APN |
9 |
31,758,141 (GRCm39) |
missense |
unknown |
|
IGL03341:Barx2
|
APN |
9 |
31,770,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R1401:Barx2
|
UTSW |
9 |
31,770,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R1982:Barx2
|
UTSW |
9 |
31,824,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R2436:Barx2
|
UTSW |
9 |
31,824,383 (GRCm39) |
missense |
probably damaging |
0.99 |
R4543:Barx2
|
UTSW |
9 |
31,758,092 (GRCm39) |
missense |
unknown |
|
R4804:Barx2
|
UTSW |
9 |
31,758,108 (GRCm39) |
missense |
unknown |
|
R5399:Barx2
|
UTSW |
9 |
31,765,407 (GRCm39) |
critical splice donor site |
probably null |
|
R5436:Barx2
|
UTSW |
9 |
31,824,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R5700:Barx2
|
UTSW |
9 |
31,770,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R6036:Barx2
|
UTSW |
9 |
31,824,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R6036:Barx2
|
UTSW |
9 |
31,824,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R6042:Barx2
|
UTSW |
9 |
31,758,199 (GRCm39) |
missense |
probably benign |
0.35 |
R6533:Barx2
|
UTSW |
9 |
31,824,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R6618:Barx2
|
UTSW |
9 |
31,758,168 (GRCm39) |
missense |
probably benign |
0.01 |
R8242:Barx2
|
UTSW |
9 |
31,824,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R8307:Barx2
|
UTSW |
9 |
31,770,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R8507:Barx2
|
UTSW |
9 |
31,770,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R8722:Barx2
|
UTSW |
9 |
31,824,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R9089:Barx2
|
UTSW |
9 |
31,765,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R9470:Barx2
|
UTSW |
9 |
31,770,044 (GRCm39) |
nonsense |
probably null |
|
R9720:Barx2
|
UTSW |
9 |
31,765,407 (GRCm39) |
critical splice donor site |
probably null |
|
Z1088:Barx2
|
UTSW |
9 |
31,758,162 (GRCm39) |
missense |
possibly damaging |
0.59 |
|