Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2300002M23Rik |
T |
C |
17: 35,878,845 (GRCm39) |
V61A |
probably benign |
Het |
Arfgef1 |
G |
A |
1: 10,251,275 (GRCm39) |
|
probably benign |
Het |
Arhgef4 |
T |
A |
1: 34,850,804 (GRCm39) |
L594* |
probably null |
Het |
Cacna2d3 |
T |
C |
14: 29,015,066 (GRCm39) |
T375A |
possibly damaging |
Het |
Calb2 |
A |
C |
8: 110,875,160 (GRCm39) |
Y155D |
probably damaging |
Het |
Cfap91 |
A |
G |
16: 38,141,921 (GRCm39) |
|
probably benign |
Het |
Chsy3 |
A |
G |
18: 59,542,187 (GRCm39) |
S442G |
probably benign |
Het |
Cyp4f13 |
T |
C |
17: 33,151,395 (GRCm39) |
I173V |
probably benign |
Het |
Dapk1 |
A |
G |
13: 60,896,134 (GRCm39) |
T741A |
probably benign |
Het |
Dennd3 |
T |
C |
15: 73,428,252 (GRCm39) |
I866T |
probably damaging |
Het |
Dhrs2 |
A |
T |
14: 55,474,778 (GRCm39) |
I138F |
possibly damaging |
Het |
Dscaml1 |
C |
T |
9: 45,655,626 (GRCm39) |
|
probably benign |
Het |
Fsbp |
A |
G |
4: 11,584,147 (GRCm39) |
E282G |
probably damaging |
Het |
Hpgds |
A |
T |
6: 65,100,594 (GRCm39) |
L128Q |
probably damaging |
Het |
Hspa9 |
A |
G |
18: 35,087,266 (GRCm39) |
V13A |
unknown |
Het |
Itgb3 |
A |
G |
11: 104,553,269 (GRCm39) |
E709G |
probably damaging |
Het |
Jarid2 |
T |
C |
13: 45,027,877 (GRCm39) |
S148P |
probably damaging |
Het |
Kcna6 |
C |
T |
6: 126,716,167 (GRCm39) |
G241R |
probably benign |
Het |
Kdm5a |
T |
A |
6: 120,408,941 (GRCm39) |
N1541K |
probably benign |
Het |
Kel |
C |
A |
6: 41,664,516 (GRCm39) |
E640D |
probably damaging |
Het |
Lcp1 |
A |
T |
14: 75,461,566 (GRCm39) |
I520F |
probably benign |
Het |
Lgr4 |
A |
G |
2: 109,841,658 (GRCm39) |
I524V |
probably damaging |
Het |
Mup20 |
A |
C |
4: 61,970,141 (GRCm39) |
Y139D |
probably damaging |
Het |
Notch4 |
T |
C |
17: 34,784,362 (GRCm39) |
|
probably null |
Het |
Obox7 |
A |
G |
7: 14,399,293 (GRCm39) |
E173G |
probably benign |
Het |
Or10a49 |
T |
A |
7: 108,467,857 (GRCm39) |
Y168F |
probably benign |
Het |
Or2a25 |
T |
A |
6: 42,888,992 (GRCm39) |
C178* |
probably null |
Het |
Or5w22 |
A |
T |
2: 87,362,949 (GRCm39) |
T191S |
probably damaging |
Het |
Or8b40 |
C |
T |
9: 38,027,148 (GRCm39) |
Q19* |
probably null |
Het |
Or9i1 |
T |
A |
19: 13,839,170 (GRCm39) |
N4K |
probably benign |
Het |
Patl2 |
T |
G |
2: 121,955,814 (GRCm39) |
T241P |
possibly damaging |
Het |
Pip5k1c |
C |
A |
10: 81,153,155 (GRCm39) |
|
probably null |
Het |
Plekhg6 |
T |
C |
6: 125,354,342 (GRCm39) |
|
probably benign |
Het |
Pon1 |
C |
A |
6: 5,168,375 (GRCm39) |
G344V |
probably damaging |
Het |
Ppp1r21 |
G |
T |
17: 88,880,171 (GRCm39) |
K529N |
probably benign |
Het |
Prdm15 |
A |
G |
16: 97,623,142 (GRCm39) |
S203P |
probably benign |
Het |
Psmc2 |
T |
A |
5: 22,000,098 (GRCm39) |
|
probably null |
Het |
Ptn |
T |
C |
6: 36,692,653 (GRCm39) |
M166V |
unknown |
Het |
Ptpn13 |
A |
G |
5: 103,649,769 (GRCm39) |
N391D |
probably benign |
Het |
Rnf214 |
A |
G |
9: 45,780,841 (GRCm39) |
S383P |
probably damaging |
Het |
Rufy4 |
T |
A |
1: 74,173,348 (GRCm39) |
L438H |
probably damaging |
Het |
Scarf2 |
A |
G |
16: 17,621,608 (GRCm39) |
T353A |
probably damaging |
Het |
Serpinb9e |
A |
C |
13: 33,441,742 (GRCm39) |
I225L |
probably benign |
Het |
Slc25a40 |
T |
C |
5: 8,503,219 (GRCm39) |
V312A |
probably benign |
Het |
Tmc3 |
A |
G |
7: 83,271,827 (GRCm39) |
Y993C |
possibly damaging |
Het |
Trim56 |
A |
C |
5: 137,141,930 (GRCm39) |
C529G |
probably damaging |
Het |
Trim8 |
T |
C |
19: 46,503,917 (GRCm39) |
S490P |
probably damaging |
Het |
Trmt6 |
A |
T |
2: 132,652,357 (GRCm39) |
Y147* |
probably null |
Het |
Vmn2r109 |
T |
A |
17: 20,760,963 (GRCm39) |
H798L |
probably damaging |
Het |
Vps35 |
A |
G |
8: 86,013,018 (GRCm39) |
L153P |
probably damaging |
Het |
Wdr82 |
T |
C |
9: 106,060,880 (GRCm39) |
I131T |
probably damaging |
Het |
Zfp69 |
A |
T |
4: 120,788,660 (GRCm39) |
D218E |
probably benign |
Het |
|
Other mutations in Camkmt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00433:Camkmt
|
APN |
17 |
85,404,094 (GRCm39) |
splice site |
probably benign |
|
IGL00786:Camkmt
|
APN |
17 |
85,403,919 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00840:Camkmt
|
APN |
17 |
85,765,551 (GRCm39) |
nonsense |
probably null |
|
IGL02809:Camkmt
|
APN |
17 |
85,702,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R0465:Camkmt
|
UTSW |
17 |
85,738,950 (GRCm39) |
missense |
probably damaging |
0.99 |
R0537:Camkmt
|
UTSW |
17 |
85,702,087 (GRCm39) |
missense |
probably benign |
0.01 |
R1573:Camkmt
|
UTSW |
17 |
85,403,958 (GRCm39) |
missense |
probably damaging |
0.98 |
R2442:Camkmt
|
UTSW |
17 |
85,398,203 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2878:Camkmt
|
UTSW |
17 |
85,738,979 (GRCm39) |
splice site |
probably benign |
|
R5121:Camkmt
|
UTSW |
17 |
85,404,009 (GRCm39) |
missense |
probably benign |
0.00 |
R5174:Camkmt
|
UTSW |
17 |
85,759,665 (GRCm39) |
missense |
probably benign |
|
R6006:Camkmt
|
UTSW |
17 |
85,759,666 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6587:Camkmt
|
UTSW |
17 |
85,421,243 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6726:Camkmt
|
UTSW |
17 |
85,702,037 (GRCm39) |
missense |
probably damaging |
0.98 |
R7301:Camkmt
|
UTSW |
17 |
85,738,921 (GRCm39) |
missense |
probably benign |
0.10 |
R7523:Camkmt
|
UTSW |
17 |
85,699,056 (GRCm39) |
missense |
probably benign |
0.01 |
R7911:Camkmt
|
UTSW |
17 |
85,759,866 (GRCm39) |
splice site |
probably null |
|
R8341:Camkmt
|
UTSW |
17 |
85,747,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R8691:Camkmt
|
UTSW |
17 |
85,421,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R8710:Camkmt
|
UTSW |
17 |
85,421,277 (GRCm39) |
critical splice donor site |
probably benign |
|
R9049:Camkmt
|
UTSW |
17 |
85,709,912 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9119:Camkmt
|
UTSW |
17 |
85,403,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R9652:Camkmt
|
UTSW |
17 |
85,759,713 (GRCm39) |
missense |
probably benign |
0.04 |
|