Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
C |
T |
7: 45,629,449 (GRCm39) |
V1293M |
probably damaging |
Het |
Agt |
A |
G |
8: 125,290,537 (GRCm39) |
W257R |
possibly damaging |
Het |
Arhgef11 |
T |
A |
3: 87,620,406 (GRCm39) |
N457K |
probably benign |
Het |
Bcl3 |
G |
T |
7: 19,554,082 (GRCm39) |
H95Q |
probably benign |
Het |
C1d |
T |
A |
11: 17,213,662 (GRCm39) |
N64K |
probably damaging |
Het |
Casc3 |
C |
T |
11: 98,713,607 (GRCm39) |
R280C |
probably damaging |
Het |
Cdh8 |
A |
G |
8: 99,757,672 (GRCm39) |
V642A |
possibly damaging |
Het |
Cep290 |
A |
T |
10: 100,331,706 (GRCm39) |
I180F |
possibly damaging |
Het |
Copz2 |
A |
G |
11: 96,744,887 (GRCm39) |
E86G |
probably damaging |
Het |
Cplane1 |
A |
G |
15: 8,230,635 (GRCm39) |
I971V |
probably benign |
Het |
Cracdl |
A |
G |
1: 37,652,537 (GRCm39) |
V1090A |
probably benign |
Het |
Csf3r |
A |
T |
4: 125,923,712 (GRCm39) |
D74V |
possibly damaging |
Het |
Cyp11b1 |
T |
G |
15: 74,710,789 (GRCm39) |
E257A |
possibly damaging |
Het |
Dlg2 |
A |
G |
7: 92,024,875 (GRCm39) |
Q580R |
probably damaging |
Het |
Dnai2 |
A |
T |
11: 114,645,275 (GRCm39) |
K570M |
unknown |
Het |
Dock8 |
A |
G |
19: 25,133,281 (GRCm39) |
K1143E |
probably benign |
Het |
Dxo |
T |
C |
17: 35,058,099 (GRCm39) |
S394P |
probably benign |
Het |
Etl4 |
A |
G |
2: 20,810,977 (GRCm39) |
D1388G |
probably benign |
Het |
F13a1 |
C |
A |
13: 37,209,692 (GRCm39) |
R91L |
probably damaging |
Het |
Fam50b |
C |
T |
13: 34,930,856 (GRCm39) |
R111* |
probably null |
Het |
Fat2 |
T |
G |
11: 55,202,535 (GRCm39) |
N180H |
probably damaging |
Het |
Fitm2 |
A |
T |
2: 163,311,768 (GRCm39) |
H148Q |
probably benign |
Het |
Fjx1 |
A |
T |
2: 102,281,156 (GRCm39) |
S260T |
possibly damaging |
Het |
Fos |
T |
C |
12: 85,522,466 (GRCm39) |
L165P |
probably damaging |
Het |
Gm39115 |
C |
A |
7: 141,689,710 (GRCm39) |
C21F |
unknown |
Het |
Gucy1a1 |
C |
T |
3: 82,005,000 (GRCm39) |
C595Y |
probably damaging |
Het |
Hectd4 |
G |
T |
5: 121,467,172 (GRCm39) |
W2478L |
possibly damaging |
Het |
I830077J02Rik |
T |
A |
3: 105,836,060 (GRCm39) |
K9N |
probably damaging |
Het |
Ift70a1 |
T |
C |
2: 75,811,519 (GRCm39) |
D188G |
probably benign |
Het |
Ireb2 |
T |
C |
9: 54,811,265 (GRCm39) |
F723L |
possibly damaging |
Het |
Itpr1 |
G |
A |
6: 108,496,309 (GRCm39) |
V2580I |
probably damaging |
Het |
Kcnu1 |
G |
A |
8: 26,382,092 (GRCm39) |
G481R |
probably damaging |
Het |
Kdm3b |
G |
T |
18: 34,926,129 (GRCm39) |
A90S |
probably benign |
Het |
Klra8 |
A |
G |
6: 130,105,056 (GRCm39) |
V23A |
probably damaging |
Het |
Lig4 |
A |
G |
8: 10,023,777 (GRCm39) |
M1T |
probably null |
Het |
Lpin3 |
C |
T |
2: 160,737,273 (GRCm39) |
P107S |
probably damaging |
Het |
Lrp1b |
T |
A |
2: 41,265,867 (GRCm39) |
K1100* |
probably null |
Het |
Obscn |
G |
A |
11: 58,929,700 (GRCm39) |
H5172Y |
probably damaging |
Het |
Or10a3m |
T |
A |
7: 108,313,418 (GRCm39) |
M286K |
possibly damaging |
Het |
Or4p20 |
A |
G |
2: 88,253,745 (GRCm39) |
I208T |
probably benign |
Het |
Or5ae1 |
C |
T |
7: 84,565,787 (GRCm39) |
H267Y |
probably benign |
Het |
Or6z1 |
T |
A |
7: 6,504,734 (GRCm39) |
T170S |
probably damaging |
Het |
Or8c14-ps1 |
A |
T |
9: 38,101,498 (GRCm39) |
H159L |
possibly damaging |
Het |
Orc3 |
A |
G |
4: 34,593,173 (GRCm39) |
L298P |
probably damaging |
Het |
Otub1 |
A |
G |
19: 7,177,360 (GRCm39) |
F96L |
probably damaging |
Het |
Pcnx3 |
A |
G |
19: 5,736,670 (GRCm39) |
S156P |
probably benign |
Het |
Pde3b |
A |
G |
7: 114,126,129 (GRCm39) |
M788V |
probably damaging |
Het |
Pias4 |
A |
G |
10: 80,992,844 (GRCm39) |
|
probably null |
Het |
Polg |
A |
G |
7: 79,114,743 (GRCm39) |
C73R |
probably benign |
Het |
Ptbp2 |
T |
C |
3: 119,541,467 (GRCm39) |
Y190C |
probably damaging |
Het |
Rab33b |
T |
A |
3: 51,401,050 (GRCm39) |
F175I |
probably damaging |
Het |
Rfx1 |
A |
G |
8: 84,806,515 (GRCm39) |
T108A |
probably benign |
Het |
Ribc2 |
A |
G |
15: 85,019,461 (GRCm39) |
D81G |
probably benign |
Het |
Rnf213 |
T |
G |
11: 119,340,149 (GRCm39) |
M3460R |
|
Het |
Rsf1 |
T |
A |
7: 97,266,103 (GRCm39) |
S86T |
|
Het |
Rxfp2 |
C |
A |
5: 149,973,068 (GRCm39) |
T181N |
possibly damaging |
Het |
Samm50 |
G |
A |
15: 84,094,702 (GRCm39) |
E365K |
possibly damaging |
Het |
Shld2 |
A |
C |
14: 33,989,942 (GRCm39) |
N321K |
probably benign |
Het |
Slc22a18 |
T |
C |
7: 143,051,123 (GRCm39) |
V334A |
probably damaging |
Het |
Slc23a3 |
A |
T |
1: 75,110,085 (GRCm39) |
C97S |
probably benign |
Het |
Smchd1 |
T |
A |
17: 71,714,244 (GRCm39) |
H873L |
probably benign |
Het |
Snrpa1 |
G |
A |
7: 65,720,381 (GRCm39) |
G195R |
probably benign |
Het |
Sphkap |
T |
A |
1: 83,255,953 (GRCm39) |
I599F |
probably benign |
Het |
Stox1 |
A |
G |
10: 62,501,543 (GRCm39) |
V339A |
probably damaging |
Het |
Tlx1 |
A |
G |
19: 45,142,036 (GRCm39) |
E220G |
probably damaging |
Het |
Tmem71 |
C |
A |
15: 66,413,421 (GRCm39) |
|
probably null |
Het |
Tmprss3 |
T |
C |
17: 31,413,976 (GRCm39) |
D56G |
possibly damaging |
Het |
Trabd |
A |
G |
15: 88,970,107 (GRCm39) |
R368G |
probably benign |
Het |
Trf |
A |
G |
9: 103,094,675 (GRCm39) |
I461T |
probably damaging |
Het |
Trpm3 |
A |
G |
19: 22,676,226 (GRCm39) |
T133A |
possibly damaging |
Het |
Trpv3 |
G |
A |
11: 73,186,209 (GRCm39) |
V667I |
possibly damaging |
Het |
Vps13b |
T |
A |
15: 35,455,246 (GRCm39) |
N718K |
probably benign |
Het |
Zdbf2 |
T |
C |
1: 63,345,166 (GRCm39) |
S1182P |
possibly damaging |
Het |
Zfp13 |
T |
C |
17: 23,795,866 (GRCm39) |
D235G |
probably benign |
Het |
Zfp407 |
T |
C |
18: 84,227,987 (GRCm39) |
E1874G |
probably damaging |
Het |
Zfp503 |
T |
C |
14: 22,036,277 (GRCm39) |
K213R |
probably benign |
Het |
Zkscan2 |
A |
G |
7: 123,084,651 (GRCm39) |
V491A |
probably damaging |
Het |
|
Other mutations in Cd300c2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Cd300c2
|
APN |
11 |
114,892,375 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02695:Cd300c2
|
APN |
11 |
114,892,379 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03086:Cd300c2
|
APN |
11 |
114,891,649 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1933:Cd300c2
|
UTSW |
11 |
114,891,685 (GRCm39) |
missense |
probably benign |
0.22 |
R4707:Cd300c2
|
UTSW |
11 |
114,887,811 (GRCm39) |
missense |
probably benign |
0.03 |
R4866:Cd300c2
|
UTSW |
11 |
114,891,807 (GRCm39) |
nonsense |
probably null |
|
R4900:Cd300c2
|
UTSW |
11 |
114,891,807 (GRCm39) |
nonsense |
probably null |
|
R4906:Cd300c2
|
UTSW |
11 |
114,887,826 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4908:Cd300c2
|
UTSW |
11 |
114,887,772 (GRCm39) |
missense |
probably damaging |
0.97 |
R4946:Cd300c2
|
UTSW |
11 |
114,887,731 (GRCm39) |
missense |
probably benign |
0.04 |
R5568:Cd300c2
|
UTSW |
11 |
114,891,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R6870:Cd300c2
|
UTSW |
11 |
114,891,503 (GRCm39) |
missense |
probably damaging |
0.99 |
R7474:Cd300c2
|
UTSW |
11 |
114,889,122 (GRCm39) |
missense |
probably benign |
0.00 |
R7826:Cd300c2
|
UTSW |
11 |
114,891,644 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8210:Cd300c2
|
UTSW |
11 |
114,891,634 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8831:Cd300c2
|
UTSW |
11 |
114,891,844 (GRCm39) |
nonsense |
probably null |
|
R9405:Cd300c2
|
UTSW |
11 |
114,891,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R9762:Cd300c2
|
UTSW |
11 |
114,887,775 (GRCm39) |
missense |
probably damaging |
1.00 |
|