Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012B07Rik |
G |
T |
11: 109,684,980 (GRCm39) |
C172* |
probably null |
Het |
Aamp |
A |
G |
1: 74,320,386 (GRCm39) |
|
probably benign |
Het |
Abcb4 |
A |
G |
5: 8,986,783 (GRCm39) |
|
probably null |
Het |
Adam6b |
T |
A |
12: 113,453,256 (GRCm39) |
F24L |
possibly damaging |
Het |
Alms1 |
G |
A |
6: 85,597,870 (GRCm39) |
V1368I |
probably benign |
Het |
Angpt2 |
T |
A |
8: 18,749,139 (GRCm39) |
Q326L |
probably damaging |
Het |
Armc9 |
T |
A |
1: 86,116,661 (GRCm39) |
I327N |
possibly damaging |
Het |
Bace2 |
A |
G |
16: 97,237,856 (GRCm39) |
T436A |
probably benign |
Het |
Ccdc162 |
T |
A |
10: 41,532,324 (GRCm39) |
E450V |
possibly damaging |
Het |
Ccdc7b |
G |
T |
8: 129,811,708 (GRCm39) |
|
probably benign |
Het |
Cdh17 |
T |
C |
4: 11,814,628 (GRCm39) |
S728P |
probably damaging |
Het |
Chia1 |
T |
C |
3: 106,035,844 (GRCm39) |
L168P |
probably damaging |
Het |
Cnot1 |
A |
C |
8: 96,500,246 (GRCm39) |
L111V |
probably damaging |
Het |
Col14a1 |
A |
T |
15: 55,226,955 (GRCm39) |
N235I |
unknown |
Het |
Col2a1 |
A |
C |
15: 97,881,582 (GRCm39) |
L787R |
probably benign |
Het |
Cyp3a25 |
A |
T |
5: 145,939,841 (GRCm39) |
D55E |
probably benign |
Het |
Dennd6a |
A |
T |
14: 26,349,673 (GRCm39) |
|
probably benign |
Het |
Dnajc28 |
G |
A |
16: 91,413,755 (GRCm39) |
T187M |
probably damaging |
Het |
Etfbkmt |
T |
C |
6: 149,046,089 (GRCm39) |
|
probably benign |
Het |
Etfrf1 |
T |
C |
6: 145,161,098 (GRCm39) |
Y23H |
probably damaging |
Het |
Gemin4 |
T |
A |
11: 76,103,645 (GRCm39) |
E372V |
probably damaging |
Het |
Glyr1 |
T |
C |
16: 4,836,350 (GRCm39) |
K500E |
possibly damaging |
Het |
Gm10271 |
A |
T |
10: 116,803,943 (GRCm39) |
|
probably benign |
Het |
Gm20775 |
A |
T |
Y: 10,641,878 (GRCm39) |
|
noncoding transcript |
Het |
Gm5578 |
A |
G |
6: 112,583,466 (GRCm39) |
|
noncoding transcript |
Het |
Gxylt2 |
A |
G |
6: 100,760,167 (GRCm39) |
N234S |
probably damaging |
Het |
Kcna6 |
G |
C |
6: 126,716,737 (GRCm39) |
R51G |
probably damaging |
Het |
Klf17 |
A |
G |
4: 117,617,898 (GRCm39) |
V153A |
possibly damaging |
Het |
L3mbtl2 |
T |
C |
15: 81,566,170 (GRCm39) |
V331A |
possibly damaging |
Het |
Med1 |
A |
T |
11: 98,070,913 (GRCm39) |
V110E |
probably damaging |
Het |
Nsmaf |
A |
C |
4: 6,417,188 (GRCm39) |
Y535* |
probably null |
Het |
Pcdh10 |
G |
A |
3: 45,336,055 (GRCm39) |
V790M |
probably damaging |
Het |
Phlpp1 |
A |
G |
1: 106,292,068 (GRCm39) |
T976A |
probably damaging |
Het |
Prelid3a |
T |
C |
18: 67,605,967 (GRCm39) |
Y25H |
probably damaging |
Het |
Ptprk |
T |
A |
10: 28,351,284 (GRCm39) |
|
probably null |
Het |
Rbm5 |
A |
T |
9: 107,642,796 (GRCm39) |
D79E |
probably damaging |
Het |
Rhox3f |
G |
T |
X: 36,763,672 (GRCm39) |
E140* |
probably null |
Het |
Rnd3 |
T |
A |
2: 51,038,242 (GRCm39) |
T78S |
possibly damaging |
Het |
Scart2 |
G |
T |
7: 139,878,281 (GRCm39) |
G1003* |
probably null |
Het |
Sgca |
T |
C |
11: 94,863,396 (GRCm39) |
T27A |
possibly damaging |
Het |
Slc10a2 |
C |
T |
8: 5,155,135 (GRCm39) |
D17N |
probably benign |
Het |
Snap23 |
C |
T |
2: 120,414,856 (GRCm39) |
|
probably benign |
Het |
Sptb |
T |
A |
12: 76,644,553 (GRCm39) |
T2098S |
probably damaging |
Het |
Src |
T |
A |
2: 157,304,946 (GRCm39) |
L165H |
probably damaging |
Het |
Srr |
G |
T |
11: 74,803,898 (GRCm39) |
Q20K |
probably benign |
Het |
Stt3b |
A |
T |
9: 115,095,206 (GRCm39) |
F275Y |
probably damaging |
Het |
Sucnr1 |
C |
G |
3: 59,994,215 (GRCm39) |
R248G |
probably damaging |
Het |
Thsd7b |
A |
T |
1: 130,044,356 (GRCm39) |
D1112V |
probably benign |
Het |
Tmem80 |
A |
G |
7: 140,913,692 (GRCm39) |
|
probably benign |
Het |
Top2a |
C |
A |
11: 98,913,786 (GRCm39) |
K18N |
probably damaging |
Het |
Ttc24 |
T |
A |
3: 87,981,946 (GRCm39) |
D40V |
probably damaging |
Het |
Vmn2r129 |
G |
T |
4: 156,686,692 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Zfp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0684:Zfp3
|
UTSW |
11 |
70,662,395 (GRCm39) |
missense |
probably benign |
0.09 |
R1067:Zfp3
|
UTSW |
11 |
70,663,411 (GRCm39) |
missense |
probably damaging |
0.97 |
R1389:Zfp3
|
UTSW |
11 |
70,663,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R1940:Zfp3
|
UTSW |
11 |
70,662,202 (GRCm39) |
missense |
probably benign |
0.00 |
R1962:Zfp3
|
UTSW |
11 |
70,662,954 (GRCm39) |
nonsense |
probably null |
|
R4637:Zfp3
|
UTSW |
11 |
70,662,181 (GRCm39) |
missense |
probably benign |
0.21 |
R6006:Zfp3
|
UTSW |
11 |
70,662,590 (GRCm39) |
missense |
probably benign |
0.00 |
R6333:Zfp3
|
UTSW |
11 |
70,662,266 (GRCm39) |
missense |
probably benign |
0.00 |
R7213:Zfp3
|
UTSW |
11 |
70,663,351 (GRCm39) |
missense |
probably benign |
0.24 |
R7378:Zfp3
|
UTSW |
11 |
70,662,899 (GRCm39) |
missense |
probably benign |
0.11 |
R8434:Zfp3
|
UTSW |
11 |
70,663,384 (GRCm39) |
missense |
probably benign |
0.08 |
R9094:Zfp3
|
UTSW |
11 |
70,663,241 (GRCm39) |
missense |
probably benign |
0.31 |
R9095:Zfp3
|
UTSW |
11 |
70,662,405 (GRCm39) |
missense |
probably benign |
0.20 |
R9404:Zfp3
|
UTSW |
11 |
70,663,366 (GRCm39) |
missense |
probably damaging |
0.98 |
R9622:Zfp3
|
UTSW |
11 |
70,662,739 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1176:Zfp3
|
UTSW |
11 |
70,662,152 (GRCm39) |
missense |
probably benign |
|
Z1177:Zfp3
|
UTSW |
11 |
70,662,718 (GRCm39) |
missense |
probably damaging |
1.00 |
|