Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503L19Rik |
C |
T |
18: 70,600,401 (GRCm39) |
|
probably null |
Het |
Abca12 |
T |
C |
1: 71,325,634 (GRCm39) |
I1521M |
probably damaging |
Het |
Abcc3 |
A |
G |
11: 94,263,703 (GRCm39) |
S268P |
possibly damaging |
Het |
Adamts20 |
G |
C |
15: 94,249,626 (GRCm39) |
P464A |
probably damaging |
Het |
Apoa1 |
C |
A |
9: 46,141,280 (GRCm39) |
D125E |
probably benign |
Het |
Atp6v0a1 |
C |
A |
11: 100,909,414 (GRCm39) |
Q48K |
probably benign |
Het |
Bptf |
T |
C |
11: 107,002,170 (GRCm39) |
N314S |
probably damaging |
Het |
Cdh20 |
T |
C |
1: 109,988,785 (GRCm39) |
V229A |
probably damaging |
Het |
Cfap46 |
G |
A |
7: 139,246,229 (GRCm39) |
T378M |
|
Het |
Clca3b |
T |
A |
3: 144,543,575 (GRCm39) |
D418V |
probably damaging |
Het |
Dennd4c |
T |
A |
4: 86,754,625 (GRCm39) |
L1545* |
probably null |
Het |
Dnajc13 |
A |
G |
9: 104,115,728 (GRCm39) |
V27A |
probably benign |
Het |
Efcab3 |
A |
G |
11: 104,611,120 (GRCm39) |
K321E |
probably benign |
Het |
Eif2ak2 |
A |
T |
17: 79,183,632 (GRCm39) |
D72E |
probably benign |
Het |
Eif2ak4 |
T |
C |
2: 118,269,511 (GRCm39) |
I862T |
probably damaging |
Het |
Eif4g1 |
T |
C |
16: 20,502,863 (GRCm39) |
I1022T |
probably benign |
Het |
Enpp3 |
A |
T |
10: 24,649,802 (GRCm39) |
*875R |
probably null |
Het |
Fam98c |
A |
C |
7: 28,852,206 (GRCm39) |
W118G |
probably damaging |
Het |
Fbxo43 |
A |
T |
15: 36,152,282 (GRCm39) |
L509Q |
probably damaging |
Het |
Fbxw5 |
A |
G |
2: 25,393,870 (GRCm39) |
H366R |
probably damaging |
Het |
Flt1 |
G |
T |
5: 147,525,377 (GRCm39) |
N920K |
probably damaging |
Het |
Git1 |
T |
A |
11: 77,390,581 (GRCm39) |
F106I |
probably damaging |
Het |
Glipr1l2 |
A |
G |
10: 111,942,868 (GRCm39) |
E241G |
probably damaging |
Het |
Gm2381 |
A |
C |
7: 42,469,729 (GRCm39) |
C132G |
probably damaging |
Het |
Gm49383 |
A |
G |
12: 69,239,628 (GRCm39) |
I237T |
|
Het |
Gm7324 |
T |
A |
14: 43,952,282 (GRCm39) |
D308E |
probably benign |
Het |
Gpr17 |
A |
G |
18: 32,080,421 (GRCm39) |
L214P |
probably damaging |
Het |
Gtf3c1 |
A |
T |
7: 125,306,734 (GRCm39) |
L39Q |
probably damaging |
Het |
H2-Q6 |
C |
T |
17: 35,644,185 (GRCm39) |
R56C |
probably damaging |
Het |
Hcar2 |
T |
C |
5: 124,002,532 (GRCm39) |
T324A |
possibly damaging |
Het |
Ksr2 |
T |
C |
5: 117,885,425 (GRCm39) |
S750P |
probably damaging |
Het |
Lipi |
C |
A |
16: 75,357,689 (GRCm39) |
R292L |
probably benign |
Het |
Map4k3 |
C |
A |
17: 80,961,306 (GRCm39) |
M133I |
probably benign |
Het |
Marf1 |
A |
T |
16: 13,958,087 (GRCm39) |
L805Q |
probably damaging |
Het |
Mccc2 |
T |
A |
13: 100,090,754 (GRCm39) |
R460W |
probably damaging |
Het |
Mgam |
A |
G |
6: 40,721,311 (GRCm39) |
D312G |
possibly damaging |
Het |
Nadk2 |
A |
T |
15: 9,103,449 (GRCm39) |
K360* |
probably null |
Het |
Nalf1 |
T |
C |
8: 9,820,114 (GRCm39) |
D302G |
probably benign |
Het |
Nars2 |
A |
G |
7: 96,689,178 (GRCm39) |
I367V |
probably benign |
Het |
Nppb |
T |
C |
4: 148,070,951 (GRCm39) |
S109P |
possibly damaging |
Het |
Odf2 |
G |
A |
2: 29,779,813 (GRCm39) |
R15Q |
probably benign |
Het |
Or4f59 |
C |
A |
2: 111,872,823 (GRCm39) |
A185S |
probably damaging |
Het |
Or51l4 |
C |
T |
7: 103,404,028 (GRCm39) |
V255M |
probably damaging |
Het |
Or5ac25 |
A |
T |
16: 59,182,106 (GRCm39) |
H158Q |
probably damaging |
Het |
Osbpl1a |
A |
T |
18: 12,889,269 (GRCm39) |
I949N |
probably benign |
Het |
Pan3 |
T |
C |
5: 147,479,881 (GRCm39) |
F55L |
probably benign |
Het |
Patj |
A |
G |
4: 98,353,377 (GRCm39) |
D640G |
probably null |
Het |
Pdxk |
T |
C |
10: 78,287,403 (GRCm39) |
K53E |
probably benign |
Het |
Pja2 |
A |
G |
17: 64,599,868 (GRCm39) |
S539P |
probably damaging |
Het |
Plscr1 |
T |
A |
9: 92,148,535 (GRCm39) |
C158* |
probably null |
Het |
Prdm14 |
T |
C |
1: 13,189,145 (GRCm39) |
T400A |
probably benign |
Het |
Rag1 |
C |
T |
2: 101,473,229 (GRCm39) |
V638M |
possibly damaging |
Het |
Ros1 |
A |
G |
10: 51,967,069 (GRCm39) |
S1734P |
probably damaging |
Het |
S100a9 |
T |
C |
3: 90,600,081 (GRCm39) |
H105R |
unknown |
Het |
Shisa9 |
A |
T |
16: 12,062,520 (GRCm39) |
Q247L |
possibly damaging |
Het |
Slc14a1 |
C |
A |
18: 78,152,807 (GRCm39) |
A367S |
probably damaging |
Het |
Slc27a4 |
G |
A |
2: 29,701,301 (GRCm39) |
R364Q |
probably damaging |
Het |
Spag17 |
C |
T |
3: 99,934,932 (GRCm39) |
P713S |
possibly damaging |
Het |
Tbc1d4 |
T |
A |
14: 101,845,856 (GRCm39) |
H14L |
probably damaging |
Het |
Tmem144 |
T |
A |
3: 79,729,991 (GRCm39) |
Y253F |
probably damaging |
Het |
Tmem204 |
C |
T |
17: 25,299,322 (GRCm39) |
G66R |
possibly damaging |
Het |
Tnfrsf1b |
A |
T |
4: 144,942,424 (GRCm39) |
V453E |
probably damaging |
Het |
Tns1 |
G |
C |
1: 73,981,182 (GRCm39) |
Q1061E |
probably benign |
Het |
Tns1 |
G |
T |
1: 73,981,183 (GRCm39) |
N1060K |
probably benign |
Het |
Trav5-1 |
A |
G |
14: 52,860,428 (GRCm39) |
K78E |
probably benign |
Het |
Ttn |
C |
T |
2: 76,715,357 (GRCm39) |
E7912K |
unknown |
Het |
Usp17lc |
G |
A |
7: 103,067,389 (GRCm39) |
G228D |
possibly damaging |
Het |
Uvssa |
T |
C |
5: 33,568,333 (GRCm39) |
C574R |
probably damaging |
Het |
Veph1 |
G |
A |
3: 66,171,434 (GRCm39) |
Q3* |
probably null |
Het |
Vps13b |
T |
A |
15: 35,623,774 (GRCm39) |
D1230E |
probably benign |
Het |
Xkr9 |
T |
A |
1: 13,771,318 (GRCm39) |
I278N |
probably damaging |
Het |
Zbed4 |
C |
A |
15: 88,664,742 (GRCm39) |
A270E |
probably benign |
Het |
Zfp366 |
A |
T |
13: 99,365,435 (GRCm39) |
T199S |
probably benign |
Het |
|
Other mutations in F11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02008:F11
|
APN |
8 |
45,703,132 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02096:F11
|
APN |
8 |
45,699,791 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02363:F11
|
APN |
8 |
45,694,568 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02694:F11
|
APN |
8 |
45,705,196 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03374:F11
|
APN |
8 |
45,714,111 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0225:F11
|
UTSW |
8 |
45,702,114 (GRCm39) |
missense |
probably benign |
0.00 |
R0525:F11
|
UTSW |
8 |
45,706,086 (GRCm39) |
missense |
probably benign |
0.01 |
R0842:F11
|
UTSW |
8 |
45,705,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R0961:F11
|
UTSW |
8 |
45,694,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:F11
|
UTSW |
8 |
45,694,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R2044:F11
|
UTSW |
8 |
45,705,155 (GRCm39) |
missense |
probably benign |
0.03 |
R2113:F11
|
UTSW |
8 |
45,699,869 (GRCm39) |
missense |
probably benign |
0.00 |
R2273:F11
|
UTSW |
8 |
45,705,184 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2274:F11
|
UTSW |
8 |
45,705,184 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2275:F11
|
UTSW |
8 |
45,705,184 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2318:F11
|
UTSW |
8 |
45,701,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R2319:F11
|
UTSW |
8 |
45,701,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R2403:F11
|
UTSW |
8 |
45,701,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R2510:F11
|
UTSW |
8 |
45,701,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R2512:F11
|
UTSW |
8 |
45,714,098 (GRCm39) |
missense |
probably benign |
0.01 |
R2893:F11
|
UTSW |
8 |
45,701,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R2894:F11
|
UTSW |
8 |
45,701,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R2910:F11
|
UTSW |
8 |
45,694,486 (GRCm39) |
makesense |
probably null |
|
R3030:F11
|
UTSW |
8 |
45,701,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R3105:F11
|
UTSW |
8 |
45,698,754 (GRCm39) |
missense |
probably damaging |
0.97 |
R3721:F11
|
UTSW |
8 |
45,701,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R3726:F11
|
UTSW |
8 |
45,701,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R3906:F11
|
UTSW |
8 |
45,701,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R3909:F11
|
UTSW |
8 |
45,701,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R4465:F11
|
UTSW |
8 |
45,694,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R4467:F11
|
UTSW |
8 |
45,694,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R4710:F11
|
UTSW |
8 |
45,703,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R4824:F11
|
UTSW |
8 |
45,708,379 (GRCm39) |
missense |
probably damaging |
0.99 |
R4968:F11
|
UTSW |
8 |
45,698,770 (GRCm39) |
missense |
probably benign |
0.19 |
R5225:F11
|
UTSW |
8 |
45,708,341 (GRCm39) |
missense |
probably benign |
0.09 |
R5288:F11
|
UTSW |
8 |
45,699,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R5378:F11
|
UTSW |
8 |
45,705,180 (GRCm39) |
missense |
probably benign |
0.19 |
R6155:F11
|
UTSW |
8 |
45,705,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R6213:F11
|
UTSW |
8 |
45,694,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R6615:F11
|
UTSW |
8 |
45,701,811 (GRCm39) |
missense |
probably benign |
|
R6797:F11
|
UTSW |
8 |
45,706,092 (GRCm39) |
missense |
probably benign |
0.02 |
R7147:F11
|
UTSW |
8 |
45,703,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R7683:F11
|
UTSW |
8 |
45,702,545 (GRCm39) |
missense |
probably damaging |
0.97 |
R7688:F11
|
UTSW |
8 |
45,703,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R7720:F11
|
UTSW |
8 |
45,705,127 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8064:F11
|
UTSW |
8 |
45,698,810 (GRCm39) |
missense |
probably benign |
0.01 |
R8273:F11
|
UTSW |
8 |
45,701,644 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8848:F11
|
UTSW |
8 |
45,695,281 (GRCm39) |
nonsense |
probably null |
|
R8901:F11
|
UTSW |
8 |
45,701,851 (GRCm39) |
missense |
probably benign |
0.01 |
R9141:F11
|
UTSW |
8 |
45,703,092 (GRCm39) |
critical splice donor site |
probably null |
|
R9188:F11
|
UTSW |
8 |
45,698,736 (GRCm39) |
missense |
probably benign |
0.00 |
R9664:F11
|
UTSW |
8 |
45,694,566 (GRCm39) |
nonsense |
probably null |
|
U24488:F11
|
UTSW |
8 |
45,695,349 (GRCm39) |
missense |
probably benign |
0.04 |
Z1088:F11
|
UTSW |
8 |
45,698,809 (GRCm39) |
missense |
possibly damaging |
0.79 |
|