Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahcyl2 |
A |
C |
6: 29,908,457 (GRCm39) |
N609T |
possibly damaging |
Het |
Ankzf1 |
G |
A |
1: 75,170,888 (GRCm39) |
C98Y |
probably damaging |
Het |
Atg101 |
T |
A |
15: 101,188,519 (GRCm39) |
M208K |
possibly damaging |
Het |
Baiap2l2 |
A |
G |
15: 79,143,930 (GRCm39) |
I388T |
probably benign |
Het |
Cabs1 |
C |
T |
5: 88,127,613 (GRCm39) |
T88I |
possibly damaging |
Het |
Chrnd |
T |
A |
1: 87,118,812 (GRCm39) |
D56E |
probably benign |
Het |
Col28a1 |
A |
T |
6: 8,162,247 (GRCm39) |
|
probably null |
Het |
Col4a1 |
G |
T |
8: 11,270,007 (GRCm39) |
P899Q |
probably damaging |
Het |
Cts3 |
C |
A |
13: 61,714,655 (GRCm39) |
A217S |
probably damaging |
Het |
Dab2 |
A |
G |
15: 6,465,941 (GRCm39) |
N495S |
possibly damaging |
Het |
Dnah2 |
T |
A |
11: 69,349,368 (GRCm39) |
I2423F |
probably damaging |
Het |
Dnah2 |
C |
T |
11: 69,349,746 (GRCm39) |
R2399Q |
probably benign |
Het |
Dock6 |
T |
C |
9: 21,733,041 (GRCm39) |
H1053R |
probably benign |
Het |
Eif1ad14 |
G |
A |
12: 87,886,521 (GRCm39) |
A36V |
probably damaging |
Het |
Fam184a |
G |
A |
10: 53,574,869 (GRCm39) |
L191F |
probably damaging |
Het |
Fbxl9 |
T |
C |
8: 106,049,925 (GRCm39) |
Y33C |
probably damaging |
Het |
Fip1l1 |
C |
T |
5: 74,752,608 (GRCm39) |
R472W |
probably damaging |
Het |
Gbp2 |
T |
C |
3: 142,338,018 (GRCm39) |
F378S |
probably damaging |
Het |
Ggt1 |
A |
T |
10: 75,420,799 (GRCm39) |
E388V |
probably damaging |
Het |
Gm14496 |
A |
G |
2: 181,638,050 (GRCm39) |
T375A |
probably benign |
Het |
Gm43302 |
A |
G |
5: 105,436,894 (GRCm39) |
S71P |
probably benign |
Het |
Gnrhr |
G |
T |
5: 86,330,216 (GRCm39) |
T268K |
probably damaging |
Het |
Htt |
T |
C |
5: 34,962,020 (GRCm39) |
V335A |
probably benign |
Het |
Klhl20 |
A |
T |
1: 160,933,037 (GRCm39) |
L257H |
probably damaging |
Het |
Med27 |
C |
A |
2: 29,414,376 (GRCm39) |
|
probably null |
Het |
Muc5ac |
T |
A |
7: 141,369,323 (GRCm39) |
C2433S |
possibly damaging |
Het |
Nasp |
A |
G |
4: 116,461,086 (GRCm39) |
|
probably null |
Het |
Nipal2 |
A |
C |
15: 34,600,172 (GRCm39) |
V215G |
probably damaging |
Het |
Or10al5 |
A |
T |
17: 38,063,038 (GRCm39) |
I98F |
probably damaging |
Het |
Or9i1b |
C |
T |
19: 13,897,104 (GRCm39) |
T240I |
probably damaging |
Het |
Pbrm1 |
A |
G |
14: 30,774,240 (GRCm39) |
I469V |
possibly damaging |
Het |
Phyhip |
A |
G |
14: 70,704,294 (GRCm39) |
H171R |
possibly damaging |
Het |
Pigs |
C |
T |
11: 78,219,326 (GRCm39) |
T9M |
probably benign |
Het |
Plek |
T |
C |
11: 16,935,539 (GRCm39) |
D256G |
probably damaging |
Het |
Prss50 |
T |
C |
9: 110,693,371 (GRCm39) |
V369A |
probably benign |
Het |
Psmc5 |
A |
G |
11: 106,152,088 (GRCm39) |
K82E |
possibly damaging |
Het |
Qrsl1 |
A |
T |
10: 43,758,189 (GRCm39) |
F301L |
probably benign |
Het |
Rasal1 |
T |
C |
5: 120,797,673 (GRCm39) |
L135P |
probably damaging |
Het |
Rbm47 |
A |
G |
5: 66,184,159 (GRCm39) |
V148A |
probably damaging |
Het |
Scyl1 |
T |
A |
19: 5,814,785 (GRCm39) |
D381V |
probably benign |
Het |
Selplg |
G |
T |
5: 113,957,162 (GRCm39) |
D381E |
probably benign |
Het |
Sh3rf2 |
C |
A |
18: 42,289,200 (GRCm39) |
Q674K |
probably damaging |
Het |
Sned1 |
A |
G |
1: 93,210,659 (GRCm39) |
T987A |
probably benign |
Het |
Sntb1 |
A |
G |
15: 55,539,698 (GRCm39) |
|
probably null |
Het |
Synj2 |
A |
T |
17: 6,036,327 (GRCm39) |
I14F |
probably damaging |
Het |
Taf2 |
A |
T |
15: 54,926,440 (GRCm39) |
M170K |
possibly damaging |
Het |
Tg |
A |
G |
15: 66,607,096 (GRCm39) |
E211G |
possibly damaging |
Het |
Thnsl1 |
G |
T |
2: 21,217,016 (GRCm39) |
E257* |
probably null |
Het |
Tlr4 |
A |
G |
4: 66,758,070 (GRCm39) |
R288G |
possibly damaging |
Het |
Trbc1 |
T |
C |
6: 41,515,385 (GRCm39) |
|
probably benign |
Het |
Trim37 |
G |
A |
11: 87,107,374 (GRCm39) |
|
probably null |
Het |
Txnrd3 |
T |
C |
6: 89,640,176 (GRCm39) |
|
probably null |
Het |
Tyk2 |
C |
A |
9: 21,021,800 (GRCm39) |
Q875H |
probably damaging |
Het |
Vmn2r55 |
A |
G |
7: 12,385,698 (GRCm39) |
Y761H |
probably damaging |
Het |
Zswim5 |
T |
C |
4: 116,836,876 (GRCm39) |
L720P |
probably damaging |
Het |
|
Other mutations in Oxct2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00552:Oxct2b
|
APN |
4 |
123,011,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R0504:Oxct2b
|
UTSW |
4 |
123,010,705 (GRCm39) |
small deletion |
probably benign |
|
R0504:Oxct2b
|
UTSW |
4 |
123,010,633 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0543:Oxct2b
|
UTSW |
4 |
123,010,782 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1167:Oxct2b
|
UTSW |
4 |
123,011,378 (GRCm39) |
missense |
probably damaging |
0.99 |
R1365:Oxct2b
|
UTSW |
4 |
123,011,162 (GRCm39) |
missense |
probably benign |
|
R1891:Oxct2b
|
UTSW |
4 |
123,010,938 (GRCm39) |
missense |
probably benign |
0.01 |
R2311:Oxct2b
|
UTSW |
4 |
123,011,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R2906:Oxct2b
|
UTSW |
4 |
123,010,823 (GRCm39) |
missense |
probably benign |
0.12 |
R4168:Oxct2b
|
UTSW |
4 |
123,011,478 (GRCm39) |
missense |
probably damaging |
0.96 |
R4657:Oxct2b
|
UTSW |
4 |
123,010,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R6221:Oxct2b
|
UTSW |
4 |
123,010,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R6271:Oxct2b
|
UTSW |
4 |
123,011,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R6357:Oxct2b
|
UTSW |
4 |
123,010,709 (GRCm39) |
missense |
probably benign |
0.00 |
R6389:Oxct2b
|
UTSW |
4 |
123,010,367 (GRCm39) |
missense |
probably benign |
0.21 |
R6996:Oxct2b
|
UTSW |
4 |
123,011,480 (GRCm39) |
missense |
probably benign |
0.05 |
R7210:Oxct2b
|
UTSW |
4 |
123,010,069 (GRCm39) |
start gained |
probably benign |
|
R7655:Oxct2b
|
UTSW |
4 |
123,011,550 (GRCm39) |
missense |
probably benign |
0.16 |
R7656:Oxct2b
|
UTSW |
4 |
123,011,550 (GRCm39) |
missense |
probably benign |
0.16 |
R7849:Oxct2b
|
UTSW |
4 |
123,010,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R7934:Oxct2b
|
UTSW |
4 |
123,010,447 (GRCm39) |
nonsense |
probably null |
|
R8094:Oxct2b
|
UTSW |
4 |
123,010,301 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8936:Oxct2b
|
UTSW |
4 |
123,010,838 (GRCm39) |
missense |
probably benign |
0.00 |
R8979:Oxct2b
|
UTSW |
4 |
123,011,169 (GRCm39) |
missense |
probably benign |
0.23 |
R9365:Oxct2b
|
UTSW |
4 |
123,010,589 (GRCm39) |
missense |
probably benign |
0.03 |
R9523:Oxct2b
|
UTSW |
4 |
123,011,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R9598:Oxct2b
|
UTSW |
4 |
123,010,413 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9612:Oxct2b
|
UTSW |
4 |
123,011,019 (GRCm39) |
missense |
probably damaging |
1.00 |
|