Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2300003K06Rik |
A |
T |
11: 99,728,667 (GRCm39) |
C59S |
possibly damaging |
Het |
Abca5 |
A |
T |
11: 110,166,107 (GRCm39) |
N1556K |
possibly damaging |
Het |
Abcb10 |
G |
T |
8: 124,709,491 (GRCm39) |
A21E |
probably benign |
Het |
Ackr1 |
T |
C |
1: 173,160,052 (GRCm39) |
N156D |
probably benign |
Het |
Adamtsl3 |
A |
T |
7: 82,255,766 (GRCm39) |
S1593C |
probably benign |
Het |
Ank3 |
T |
A |
10: 69,786,772 (GRCm39) |
|
probably null |
Het |
Aqp4 |
A |
G |
18: 15,526,537 (GRCm39) |
S315P |
probably benign |
Het |
Atp7b |
T |
C |
8: 22,510,848 (GRCm39) |
I433V |
probably benign |
Het |
Bco1 |
G |
A |
8: 117,835,522 (GRCm39) |
|
probably null |
Het |
Cacna1g |
T |
A |
11: 94,306,762 (GRCm39) |
E1842V |
probably damaging |
Het |
Calhm3 |
T |
A |
19: 47,145,986 (GRCm39) |
Q73L |
probably damaging |
Het |
Car5a |
C |
T |
8: 122,671,408 (GRCm39) |
|
probably null |
Het |
Cdk11b |
T |
A |
4: 155,732,051 (GRCm39) |
|
probably benign |
Het |
Cdr2 |
A |
T |
7: 120,557,732 (GRCm39) |
H264Q |
possibly damaging |
Het |
Col9a2 |
C |
G |
4: 120,911,455 (GRCm39) |
R599G |
probably damaging |
Het |
D7Ertd443e |
A |
G |
7: 133,871,930 (GRCm39) |
S644P |
probably damaging |
Het |
Dnlz |
A |
T |
2: 26,241,483 (GRCm39) |
C82S |
probably damaging |
Het |
Egr4 |
A |
T |
6: 85,489,725 (GRCm39) |
F112I |
probably damaging |
Het |
Emilin1 |
C |
T |
5: 31,075,082 (GRCm39) |
P441L |
possibly damaging |
Het |
F11 |
T |
C |
8: 45,705,184 (GRCm39) |
D119G |
possibly damaging |
Het |
Fat4 |
T |
A |
3: 39,050,048 (GRCm39) |
V3970D |
possibly damaging |
Het |
Fbxw5 |
C |
A |
2: 25,394,773 (GRCm39) |
C222* |
probably null |
Het |
Fn1 |
C |
T |
1: 71,653,102 (GRCm39) |
G1296R |
probably null |
Het |
Ghr |
A |
G |
15: 3,349,507 (GRCm39) |
V557A |
probably benign |
Het |
Gm11568 |
A |
G |
11: 99,749,070 (GRCm39) |
S92G |
unknown |
Het |
Gpatch1 |
A |
T |
7: 34,988,103 (GRCm39) |
S678T |
probably benign |
Het |
Gpr155 |
A |
G |
2: 73,178,479 (GRCm39) |
|
probably null |
Het |
Gucy2f |
A |
T |
X: 140,899,269 (GRCm39) |
M697K |
probably benign |
Het |
Hecw1 |
T |
C |
13: 14,520,653 (GRCm39) |
T195A |
probably benign |
Het |
Hoxd1 |
A |
G |
2: 74,594,501 (GRCm39) |
K252R |
probably damaging |
Het |
Irf8 |
A |
G |
8: 121,480,266 (GRCm39) |
E168G |
probably damaging |
Het |
Kcnh1 |
T |
G |
1: 192,019,829 (GRCm39) |
V358G |
probably damaging |
Het |
Kifap3 |
T |
A |
1: 163,696,327 (GRCm39) |
V652D |
possibly damaging |
Het |
L3hypdh |
T |
C |
12: 72,131,632 (GRCm39) |
Y100C |
possibly damaging |
Het |
Map4k1 |
T |
A |
7: 28,701,382 (GRCm39) |
H729Q |
probably damaging |
Het |
Marchf1 |
T |
A |
8: 66,840,151 (GRCm39) |
N311K |
probably benign |
Het |
Mier2 |
T |
C |
10: 79,380,368 (GRCm39) |
I321V |
probably damaging |
Het |
Mta1 |
C |
T |
12: 113,091,770 (GRCm39) |
S291L |
probably damaging |
Het |
Myh2 |
A |
G |
11: 67,081,184 (GRCm39) |
K1267E |
possibly damaging |
Het |
Nbea |
A |
T |
3: 55,895,506 (GRCm39) |
|
probably null |
Het |
Nexmif |
T |
G |
X: 103,131,452 (GRCm39) |
E155A |
possibly damaging |
Het |
Nkpd1 |
A |
G |
7: 19,257,822 (GRCm39) |
I534V |
probably benign |
Het |
Nxph1 |
G |
T |
6: 9,247,746 (GRCm39) |
C239F |
probably damaging |
Het |
Odc1 |
A |
G |
12: 17,598,425 (GRCm39) |
I189V |
probably benign |
Het |
Or1n1 |
A |
T |
2: 36,750,113 (GRCm39) |
N82K |
probably damaging |
Het |
Or2t44 |
T |
C |
11: 58,677,492 (GRCm39) |
V144A |
probably benign |
Het |
Or5d41 |
A |
G |
2: 88,055,167 (GRCm39) |
F70L |
probably benign |
Het |
Or6c35 |
T |
C |
10: 129,169,326 (GRCm39) |
I192T |
probably benign |
Het |
Pcdhb15 |
T |
C |
18: 37,608,496 (GRCm39) |
L576P |
probably damaging |
Het |
Raph1 |
T |
C |
1: 60,537,659 (GRCm39) |
D499G |
probably damaging |
Het |
Rptor |
T |
A |
11: 119,647,148 (GRCm39) |
C246* |
probably null |
Het |
Rtl1 |
T |
C |
12: 109,561,101 (GRCm39) |
E246G |
unknown |
Het |
Setx |
GTGGCT |
GT |
2: 29,044,073 (GRCm39) |
1814 |
probably null |
Het |
Slc12a3 |
T |
A |
8: 95,059,915 (GRCm39) |
I187N |
possibly damaging |
Het |
Slc46a1 |
T |
G |
11: 78,357,249 (GRCm39) |
S101A |
probably benign |
Het |
Slc4a8 |
A |
G |
15: 100,705,283 (GRCm39) |
M830V |
probably benign |
Het |
Sned1 |
T |
A |
1: 93,209,364 (GRCm39) |
|
probably null |
Het |
St3gal6 |
T |
A |
16: 58,309,332 (GRCm39) |
E34D |
possibly damaging |
Het |
Tcstv3 |
C |
T |
13: 120,779,190 (GRCm39) |
Q30* |
probably null |
Het |
Tex16 |
T |
A |
X: 111,030,838 (GRCm39) |
D1112E |
probably damaging |
Het |
Tmcc3 |
G |
A |
10: 94,414,777 (GRCm39) |
V160I |
probably damaging |
Het |
Tmf1 |
T |
A |
6: 97,140,547 (GRCm39) |
L776F |
probably damaging |
Het |
Tsr1 |
A |
T |
11: 74,795,653 (GRCm39) |
|
probably null |
Het |
Tyrp1 |
A |
T |
4: 80,755,771 (GRCm39) |
E180V |
probably damaging |
Het |
Ubr3 |
T |
C |
2: 69,846,685 (GRCm39) |
V1636A |
probably benign |
Het |
Usp1 |
T |
C |
4: 98,818,079 (GRCm39) |
L139P |
probably damaging |
Het |
Vmn1r232 |
A |
G |
17: 21,134,465 (GRCm39) |
L45P |
probably benign |
Het |
Vmn1r49 |
G |
A |
6: 90,049,126 (GRCm39) |
T292I |
probably benign |
Het |
Wdr19 |
T |
A |
5: 65,398,334 (GRCm39) |
M853K |
possibly damaging |
Het |
Zkscan8 |
C |
T |
13: 21,705,966 (GRCm39) |
M265I |
probably benign |
Het |
|
Other mutations in Iqck |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01620:Iqck
|
APN |
7 |
118,476,901 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02810:Iqck
|
APN |
7 |
118,570,662 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03403:Iqck
|
APN |
7 |
118,475,494 (GRCm39) |
missense |
probably benign |
0.21 |
R0541:Iqck
|
UTSW |
7 |
118,514,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Iqck
|
UTSW |
7 |
118,498,880 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0829:Iqck
|
UTSW |
7 |
118,499,111 (GRCm39) |
critical splice donor site |
probably null |
|
R0898:Iqck
|
UTSW |
7 |
118,570,664 (GRCm39) |
missense |
probably damaging |
0.99 |
R2273:Iqck
|
UTSW |
7 |
118,498,880 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2275:Iqck
|
UTSW |
7 |
118,498,880 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2509:Iqck
|
UTSW |
7 |
118,475,505 (GRCm39) |
missense |
probably benign |
|
R4033:Iqck
|
UTSW |
7 |
118,540,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R6299:Iqck
|
UTSW |
7 |
118,475,485 (GRCm39) |
missense |
unknown |
|
R6520:Iqck
|
UTSW |
7 |
118,540,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R7095:Iqck
|
UTSW |
7 |
118,514,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R7823:Iqck
|
UTSW |
7 |
118,472,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R9038:Iqck
|
UTSW |
7 |
118,498,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R9218:Iqck
|
UTSW |
7 |
118,540,902 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Iqck
|
UTSW |
7 |
118,540,877 (GRCm39) |
missense |
probably benign |
0.19 |
|