Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm5 |
A |
T |
4: 144,504,683 (GRCm39) |
I156N |
probably damaging |
Het |
Abca1 |
C |
A |
4: 53,042,381 (GRCm39) |
R1897L |
possibly damaging |
Het |
Ablim2 |
A |
G |
5: 36,015,170 (GRCm39) |
K461E |
probably damaging |
Het |
Acss3 |
A |
T |
10: 106,773,008 (GRCm39) |
Y659* |
probably null |
Het |
Actr8 |
T |
G |
14: 29,708,952 (GRCm39) |
L253R |
probably damaging |
Het |
Arid4b |
A |
G |
13: 14,362,281 (GRCm39) |
K915R |
probably damaging |
Het |
Cacna1c |
A |
T |
6: 118,631,333 (GRCm39) |
I1013N |
probably damaging |
Het |
Cep83 |
G |
A |
10: 94,625,600 (GRCm39) |
R670H |
probably benign |
Het |
Col19a1 |
T |
A |
1: 24,332,193 (GRCm39) |
D870V |
probably damaging |
Het |
Ddr2 |
A |
G |
1: 169,832,298 (GRCm39) |
V164A |
possibly damaging |
Het |
Dnaaf10 |
A |
G |
11: 17,162,031 (GRCm39) |
D23G |
possibly damaging |
Het |
Donson |
A |
T |
16: 91,476,814 (GRCm39) |
V549E |
probably damaging |
Het |
Egflam |
C |
T |
15: 7,254,144 (GRCm39) |
G824R |
probably damaging |
Het |
Extl3 |
A |
G |
14: 65,292,075 (GRCm39) |
F916S |
probably damaging |
Het |
Fam110c |
A |
G |
12: 31,124,406 (GRCm39) |
M123V |
unknown |
Het |
G3bp1 |
A |
T |
11: 55,388,813 (GRCm39) |
I342F |
probably damaging |
Het |
Golgb1 |
A |
G |
16: 36,720,870 (GRCm39) |
N409D |
probably benign |
Het |
Grin2b |
C |
T |
6: 135,713,304 (GRCm39) |
G859D |
probably damaging |
Het |
Hspb1 |
A |
T |
5: 135,918,186 (GRCm39) |
T178S |
probably benign |
Het |
Iigp1 |
A |
G |
18: 60,523,329 (GRCm39) |
Y149C |
probably damaging |
Het |
Il22 |
G |
T |
10: 118,045,366 (GRCm39) |
G159* |
probably null |
Het |
Jcad |
T |
C |
18: 4,675,790 (GRCm39) |
F1184S |
probably damaging |
Het |
Kcnj2 |
G |
T |
11: 110,963,057 (GRCm39) |
V150L |
probably damaging |
Het |
Kifc1 |
C |
T |
17: 34,105,639 (GRCm39) |
R56Q |
probably damaging |
Het |
Lce1h |
A |
G |
3: 92,671,027 (GRCm39) |
S42P |
unknown |
Het |
Lrp4 |
C |
A |
2: 91,327,418 (GRCm39) |
D1471E |
probably benign |
Het |
Lrrc3 |
C |
A |
10: 77,737,299 (GRCm39) |
V46L |
probably benign |
Het |
Mcf2l |
G |
A |
8: 12,976,646 (GRCm39) |
A2T |
possibly damaging |
Het |
Med12l |
G |
A |
3: 59,170,634 (GRCm39) |
C1673Y |
probably null |
Het |
Nckap1 |
T |
C |
2: 80,343,034 (GRCm39) |
E955G |
possibly damaging |
Het |
Ndufs3 |
T |
A |
2: 90,732,690 (GRCm39) |
|
probably null |
Het |
Nkx6-1 |
A |
G |
5: 101,809,698 (GRCm39) |
|
probably null |
Het |
Obscn |
C |
A |
11: 58,890,954 (GRCm39) |
E1713* |
probably null |
Het |
Or10ak12 |
G |
A |
4: 118,666,560 (GRCm39) |
T167I |
possibly damaging |
Het |
Or10g1b |
A |
G |
14: 52,627,582 (GRCm39) |
F216S |
probably damaging |
Het |
Or10n1 |
A |
G |
9: 39,524,916 (GRCm39) |
T18A |
probably benign |
Het |
Or2n1 |
T |
A |
17: 38,486,917 (GRCm39) |
|
probably null |
Het |
Or6n1 |
A |
G |
1: 173,917,541 (GRCm39) |
R312G |
probably benign |
Het |
Or7e165 |
A |
C |
9: 19,695,161 (GRCm39) |
H244P |
probably damaging |
Het |
Or8c15 |
A |
G |
9: 38,121,050 (GRCm39) |
T234A |
probably benign |
Het |
Osbpl5 |
A |
G |
7: 143,295,433 (GRCm39) |
F10L |
possibly damaging |
Het |
Plvap |
A |
C |
8: 71,964,095 (GRCm39) |
I89S |
probably damaging |
Het |
Ppp2r2a |
A |
G |
14: 67,259,772 (GRCm39) |
V308A |
possibly damaging |
Het |
Ppp2r5e |
T |
C |
12: 75,540,250 (GRCm39) |
S132G |
probably benign |
Het |
Pum3 |
G |
T |
19: 27,389,659 (GRCm39) |
Q398K |
probably benign |
Het |
Ralgapa2 |
T |
C |
2: 146,184,430 (GRCm39) |
T1526A |
probably benign |
Het |
Sh3tc2 |
T |
A |
18: 62,122,704 (GRCm39) |
Y488* |
probably null |
Het |
Spmip7 |
A |
T |
11: 11,440,244 (GRCm39) |
R8S |
possibly damaging |
Het |
Sqle |
A |
G |
15: 59,202,753 (GRCm39) |
Y537C |
probably benign |
Het |
Sult2a8 |
T |
G |
7: 14,159,439 (GRCm39) |
K60T |
probably damaging |
Het |
Tex15 |
T |
C |
8: 34,064,199 (GRCm39) |
S1210P |
possibly damaging |
Het |
Thumpd3 |
A |
G |
6: 113,043,825 (GRCm39) |
|
silent |
Het |
Timeless |
A |
G |
10: 128,077,604 (GRCm39) |
D228G |
probably damaging |
Het |
Trim31 |
A |
T |
17: 37,216,797 (GRCm39) |
|
probably null |
Het |
Ttc39c |
A |
T |
18: 12,828,428 (GRCm39) |
D196V |
possibly damaging |
Het |
Wbp4 |
C |
A |
14: 79,709,837 (GRCm39) |
V133L |
possibly damaging |
Het |
Zfp354c |
G |
T |
11: 50,706,597 (GRCm39) |
D159E |
probably benign |
Het |
Zfp940 |
C |
A |
7: 29,544,858 (GRCm39) |
D350Y |
probably benign |
Het |
|
Other mutations in C3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:C3
|
APN |
17 |
57,533,004 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00741:C3
|
APN |
17 |
57,527,206 (GRCm39) |
intron |
probably benign |
|
IGL01093:C3
|
APN |
17 |
57,530,949 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01309:C3
|
APN |
17 |
57,516,652 (GRCm39) |
intron |
probably benign |
|
IGL01312:C3
|
APN |
17 |
57,532,993 (GRCm39) |
unclassified |
probably benign |
|
IGL01344:C3
|
APN |
17 |
57,531,880 (GRCm39) |
missense |
probably benign |
|
IGL01514:C3
|
APN |
17 |
57,522,866 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01913:C3
|
APN |
17 |
57,520,767 (GRCm39) |
missense |
probably null |
0.01 |
IGL02165:C3
|
APN |
17 |
57,532,092 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02176:C3
|
APN |
17 |
57,533,337 (GRCm39) |
unclassified |
probably benign |
|
IGL02189:C3
|
APN |
17 |
57,527,113 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02378:C3
|
APN |
17 |
57,519,698 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02422:C3
|
APN |
17 |
57,533,823 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02715:C3
|
APN |
17 |
57,511,158 (GRCm39) |
intron |
probably benign |
|
IGL02737:C3
|
APN |
17 |
57,511,281 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03201:C3
|
APN |
17 |
57,529,249 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03210:C3
|
APN |
17 |
57,522,846 (GRCm39) |
nonsense |
probably null |
|
IGL03345:C3
|
APN |
17 |
57,526,585 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4431001:C3
|
UTSW |
17 |
57,513,242 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4494001:C3
|
UTSW |
17 |
57,516,263 (GRCm39) |
missense |
probably benign |
0.01 |
R0158:C3
|
UTSW |
17 |
57,531,851 (GRCm39) |
critical splice donor site |
probably null |
|
R0318:C3
|
UTSW |
17 |
57,531,709 (GRCm39) |
missense |
probably damaging |
0.99 |
R1132:C3
|
UTSW |
17 |
57,514,531 (GRCm39) |
critical splice donor site |
probably null |
|
R1765:C3
|
UTSW |
17 |
57,531,401 (GRCm39) |
splice site |
probably null |
|
R1793:C3
|
UTSW |
17 |
57,526,592 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1852:C3
|
UTSW |
17 |
57,529,823 (GRCm39) |
missense |
probably damaging |
0.98 |
R1908:C3
|
UTSW |
17 |
57,516,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:C3
|
UTSW |
17 |
57,527,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:C3
|
UTSW |
17 |
57,525,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R2026:C3
|
UTSW |
17 |
57,525,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:C3
|
UTSW |
17 |
57,530,974 (GRCm39) |
splice site |
probably null |
|
R2197:C3
|
UTSW |
17 |
57,526,623 (GRCm39) |
missense |
probably benign |
0.32 |
R2394:C3
|
UTSW |
17 |
57,529,303 (GRCm39) |
nonsense |
probably null |
|
R2998:C3
|
UTSW |
17 |
57,517,284 (GRCm39) |
missense |
probably benign |
0.00 |
R3727:C3
|
UTSW |
17 |
57,514,379 (GRCm39) |
missense |
possibly damaging |
0.50 |
R3767:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3768:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3769:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3770:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3784:C3
|
UTSW |
17 |
57,533,067 (GRCm39) |
missense |
probably damaging |
0.99 |
R3883:C3
|
UTSW |
17 |
57,524,173 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3884:C3
|
UTSW |
17 |
57,524,173 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3950:C3
|
UTSW |
17 |
57,532,286 (GRCm39) |
missense |
probably benign |
0.02 |
R3966:C3
|
UTSW |
17 |
57,525,664 (GRCm39) |
missense |
probably damaging |
0.99 |
R4077:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4078:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4079:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4168:C3
|
UTSW |
17 |
57,525,608 (GRCm39) |
missense |
probably benign |
0.00 |
R4208:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4695:C3
|
UTSW |
17 |
57,528,057 (GRCm39) |
missense |
probably benign |
|
R4909:C3
|
UTSW |
17 |
57,533,830 (GRCm39) |
critical splice donor site |
probably null |
|
R5011:C3
|
UTSW |
17 |
57,530,236 (GRCm39) |
missense |
probably benign |
0.06 |
R5094:C3
|
UTSW |
17 |
57,532,033 (GRCm39) |
critical splice donor site |
probably null |
|
R5141:C3
|
UTSW |
17 |
57,526,570 (GRCm39) |
missense |
probably damaging |
0.98 |
R5170:C3
|
UTSW |
17 |
57,530,938 (GRCm39) |
missense |
probably damaging |
0.96 |
R5339:C3
|
UTSW |
17 |
57,531,308 (GRCm39) |
missense |
probably damaging |
0.99 |
R5369:C3
|
UTSW |
17 |
57,528,159 (GRCm39) |
missense |
probably benign |
0.45 |
R5412:C3
|
UTSW |
17 |
57,527,187 (GRCm39) |
missense |
probably benign |
0.01 |
R5463:C3
|
UTSW |
17 |
57,518,720 (GRCm39) |
missense |
probably benign |
0.08 |
R5546:C3
|
UTSW |
17 |
57,529,976 (GRCm39) |
missense |
probably damaging |
0.99 |
R5572:C3
|
UTSW |
17 |
57,531,673 (GRCm39) |
missense |
probably damaging |
0.99 |
R5851:C3
|
UTSW |
17 |
57,518,612 (GRCm39) |
missense |
probably null |
0.14 |
R5863:C3
|
UTSW |
17 |
57,530,141 (GRCm39) |
missense |
probably benign |
0.06 |
R5888:C3
|
UTSW |
17 |
57,521,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R5940:C3
|
UTSW |
17 |
57,517,244 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6073:C3
|
UTSW |
17 |
57,513,223 (GRCm39) |
missense |
probably null |
|
R6091:C3
|
UTSW |
17 |
57,528,967 (GRCm39) |
nonsense |
probably null |
|
R6286:C3
|
UTSW |
17 |
57,531,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R6524:C3
|
UTSW |
17 |
57,524,264 (GRCm39) |
critical splice donor site |
probably null |
|
R6868:C3
|
UTSW |
17 |
57,511,029 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6896:C3
|
UTSW |
17 |
57,527,864 (GRCm39) |
splice site |
probably null |
|
R7007:C3
|
UTSW |
17 |
57,525,809 (GRCm39) |
missense |
probably benign |
0.00 |
R7022:C3
|
UTSW |
17 |
57,524,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R7099:C3
|
UTSW |
17 |
57,513,276 (GRCm39) |
missense |
probably benign |
0.28 |
R7117:C3
|
UTSW |
17 |
57,519,655 (GRCm39) |
missense |
probably benign |
0.01 |
R7347:C3
|
UTSW |
17 |
57,530,215 (GRCm39) |
missense |
probably benign |
0.09 |
R7366:C3
|
UTSW |
17 |
57,528,162 (GRCm39) |
missense |
probably benign |
0.00 |
R7423:C3
|
UTSW |
17 |
57,521,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R7425:C3
|
UTSW |
17 |
57,511,039 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7481:C3
|
UTSW |
17 |
57,527,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R7540:C3
|
UTSW |
17 |
57,513,220 (GRCm39) |
missense |
probably benign |
0.01 |
R7746:C3
|
UTSW |
17 |
57,525,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R7771:C3
|
UTSW |
17 |
57,522,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R7884:C3
|
UTSW |
17 |
57,533,264 (GRCm39) |
missense |
probably benign |
0.05 |
R8144:C3
|
UTSW |
17 |
57,533,276 (GRCm39) |
missense |
probably damaging |
0.98 |
R8279:C3
|
UTSW |
17 |
57,522,809 (GRCm39) |
missense |
probably benign |
0.28 |
R8284:C3
|
UTSW |
17 |
57,530,938 (GRCm39) |
missense |
probably benign |
0.39 |
R8328:C3
|
UTSW |
17 |
57,527,973 (GRCm39) |
missense |
probably benign |
0.00 |
R8353:C3
|
UTSW |
17 |
57,519,643 (GRCm39) |
missense |
probably benign |
0.00 |
R8396:C3
|
UTSW |
17 |
57,528,029 (GRCm39) |
missense |
probably benign |
|
R8429:C3
|
UTSW |
17 |
57,529,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R8453:C3
|
UTSW |
17 |
57,519,643 (GRCm39) |
missense |
probably benign |
0.00 |
R8557:C3
|
UTSW |
17 |
57,531,383 (GRCm39) |
missense |
probably benign |
0.00 |
R8738:C3
|
UTSW |
17 |
57,511,015 (GRCm39) |
makesense |
probably null |
|
R8794:C3
|
UTSW |
17 |
57,528,011 (GRCm39) |
missense |
probably benign |
|
R9130:C3
|
UTSW |
17 |
57,518,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R9296:C3
|
UTSW |
17 |
57,511,291 (GRCm39) |
missense |
probably benign |
|
R9432:C3
|
UTSW |
17 |
57,530,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R9451:C3
|
UTSW |
17 |
57,531,169 (GRCm39) |
missense |
probably benign |
0.03 |
R9542:C3
|
UTSW |
17 |
57,532,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R9615:C3
|
UTSW |
17 |
57,518,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R9624:C3
|
UTSW |
17 |
57,527,189 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:C3
|
UTSW |
17 |
57,533,171 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:C3
|
UTSW |
17 |
57,524,144 (GRCm39) |
missense |
probably benign |
0.07 |
|