Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930011G23Rik |
A |
G |
5: 99,377,236 (GRCm39) |
S404P |
probably damaging |
Het |
A930011G23Rik |
G |
A |
5: 99,377,241 (GRCm39) |
P402L |
probably damaging |
Het |
Abcc9 |
A |
T |
6: 142,617,265 (GRCm39) |
|
probably null |
Het |
Abcg8 |
T |
C |
17: 84,990,693 (GRCm39) |
W12R |
probably benign |
Het |
Ablim1 |
A |
T |
19: 57,140,751 (GRCm39) |
C155* |
probably null |
Het |
Adam33 |
A |
G |
2: 130,895,157 (GRCm39) |
C658R |
probably damaging |
Het |
Adamts2 |
A |
G |
11: 50,664,135 (GRCm39) |
H357R |
possibly damaging |
Het |
Adamts2 |
G |
T |
11: 50,668,023 (GRCm39) |
K528N |
probably damaging |
Het |
Arhgef12 |
G |
A |
9: 42,893,339 (GRCm39) |
P955S |
probably benign |
Het |
Atp2b2 |
T |
A |
6: 113,770,815 (GRCm39) |
I365F |
probably damaging |
Het |
AW112010 |
T |
C |
19: 11,025,701 (GRCm39) |
|
noncoding transcript |
Het |
AY358078 |
T |
C |
14: 52,040,944 (GRCm39) |
S88P |
probably benign |
Het |
Cdc42bpg |
T |
C |
19: 6,372,823 (GRCm39) |
L1504S |
probably benign |
Het |
Cracdl |
T |
C |
1: 37,662,926 (GRCm39) |
T991A |
probably benign |
Het |
Dgkg |
T |
A |
16: 22,367,441 (GRCm39) |
H593L |
probably damaging |
Het |
Gm10463 |
T |
C |
5: 32,288,742 (GRCm39) |
|
probably benign |
Het |
Grm1 |
A |
T |
10: 10,595,723 (GRCm39) |
L635Q |
probably damaging |
Het |
Herc4 |
T |
C |
10: 63,109,244 (GRCm39) |
C160R |
probably benign |
Het |
Hs6st1 |
G |
A |
1: 36,142,821 (GRCm39) |
R252H |
probably damaging |
Het |
Litaf |
A |
G |
16: 10,784,423 (GRCm39) |
V29A |
possibly damaging |
Het |
Lmo7 |
G |
A |
14: 102,044,918 (GRCm39) |
V57I |
probably benign |
Het |
Loxl4 |
A |
T |
19: 42,593,412 (GRCm39) |
L253Q |
probably benign |
Het |
Mon2 |
C |
T |
10: 122,870,235 (GRCm39) |
V458I |
probably benign |
Het |
Ncstn |
G |
T |
1: 171,896,159 (GRCm39) |
F506L |
probably benign |
Het |
Nedd8 |
T |
A |
14: 55,901,273 (GRCm39) |
D21V |
probably damaging |
Het |
Oas1c |
T |
C |
5: 120,943,591 (GRCm39) |
T183A |
possibly damaging |
Het |
Pcsk5 |
A |
T |
19: 17,488,920 (GRCm39) |
Y967N |
probably damaging |
Het |
Phf2 |
A |
G |
13: 48,958,715 (GRCm39) |
S936P |
unknown |
Het |
Pkd1 |
T |
C |
17: 24,804,753 (GRCm39) |
I3159T |
possibly damaging |
Het |
Prrt3 |
C |
A |
6: 113,474,788 (GRCm39) |
V145F |
possibly damaging |
Het |
Prx |
T |
A |
7: 27,217,497 (GRCm39) |
V666E |
probably damaging |
Het |
Rapgef2 |
C |
T |
3: 78,974,060 (GRCm39) |
V1577M |
probably damaging |
Het |
Sesn3 |
T |
C |
9: 14,217,564 (GRCm39) |
|
probably benign |
Het |
Shoc2 |
T |
A |
19: 54,016,207 (GRCm39) |
L407* |
probably null |
Het |
Slc6a12 |
A |
G |
6: 121,338,029 (GRCm39) |
M435V |
probably benign |
Het |
Smarcc1 |
C |
T |
9: 110,020,002 (GRCm39) |
T623I |
probably damaging |
Het |
Snx14 |
A |
G |
9: 88,289,517 (GRCm39) |
L245S |
probably damaging |
Het |
Son |
T |
A |
16: 91,453,713 (GRCm39) |
M820K |
probably damaging |
Het |
Sorcs1 |
T |
C |
19: 50,666,606 (GRCm39) |
T101A |
probably benign |
Het |
Stoml2 |
C |
A |
4: 43,031,045 (GRCm39) |
V37L |
probably benign |
Het |
Syde2 |
T |
A |
3: 145,704,444 (GRCm39) |
H465Q |
probably benign |
Het |
Tmem164 |
T |
A |
X: 141,589,044 (GRCm39) |
V40D |
possibly damaging |
Het |
Trim37 |
A |
G |
11: 87,075,876 (GRCm39) |
E494G |
probably benign |
Het |
Triobp |
A |
G |
15: 78,845,243 (GRCm39) |
D195G |
probably benign |
Het |
Unc79 |
G |
A |
12: 103,137,837 (GRCm39) |
V2427M |
probably damaging |
Het |
Usp27x |
T |
C |
X: 7,239,780 (GRCm39) |
|
probably benign |
Het |
Vmn2r113 |
T |
A |
17: 23,177,349 (GRCm39) |
V711D |
probably damaging |
Het |
|
Other mutations in Zfp940 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01941:Zfp940
|
APN |
7 |
29,546,295 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02092:Zfp940
|
APN |
7 |
29,545,626 (GRCm39) |
missense |
probably benign |
|
R0503:Zfp940
|
UTSW |
7 |
29,545,445 (GRCm39) |
intron |
probably benign |
|
R0614:Zfp940
|
UTSW |
7 |
29,545,671 (GRCm39) |
missense |
probably benign |
0.03 |
R1604:Zfp940
|
UTSW |
7 |
29,545,500 (GRCm39) |
missense |
probably benign |
|
R1619:Zfp940
|
UTSW |
7 |
29,544,962 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1715:Zfp940
|
UTSW |
7 |
29,544,363 (GRCm39) |
missense |
probably damaging |
0.96 |
R1749:Zfp940
|
UTSW |
7 |
29,544,952 (GRCm39) |
nonsense |
probably null |
|
R1862:Zfp940
|
UTSW |
7 |
29,544,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R4017:Zfp940
|
UTSW |
7 |
29,545,359 (GRCm39) |
missense |
probably benign |
|
R4673:Zfp940
|
UTSW |
7 |
29,544,863 (GRCm39) |
missense |
probably benign |
0.00 |
R4761:Zfp940
|
UTSW |
7 |
29,545,578 (GRCm39) |
missense |
probably benign |
0.12 |
R4890:Zfp940
|
UTSW |
7 |
29,544,824 (GRCm39) |
missense |
probably benign |
0.01 |
R5027:Zfp940
|
UTSW |
7 |
29,550,381 (GRCm39) |
utr 5 prime |
probably benign |
|
R5285:Zfp940
|
UTSW |
7 |
29,545,025 (GRCm39) |
missense |
probably damaging |
0.99 |
R5340:Zfp940
|
UTSW |
7 |
29,544,266 (GRCm39) |
missense |
probably benign |
0.33 |
R5439:Zfp940
|
UTSW |
7 |
29,544,858 (GRCm39) |
missense |
probably benign |
0.02 |
R5983:Zfp940
|
UTSW |
7 |
29,544,477 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7873:Zfp940
|
UTSW |
7 |
29,535,042 (GRCm39) |
missense |
unknown |
|
R8035:Zfp940
|
UTSW |
7 |
29,544,948 (GRCm39) |
missense |
probably benign |
0.18 |
R8430:Zfp940
|
UTSW |
7 |
29,544,771 (GRCm39) |
missense |
probably benign |
0.32 |
R8469:Zfp940
|
UTSW |
7 |
29,544,572 (GRCm39) |
missense |
possibly damaging |
0.52 |
Z1186:Zfp940
|
UTSW |
7 |
29,545,404 (GRCm39) |
missense |
probably benign |
|
Z1186:Zfp940
|
UTSW |
7 |
29,545,361 (GRCm39) |
missense |
probably benign |
|
Z1186:Zfp940
|
UTSW |
7 |
29,535,031 (GRCm39) |
missense |
unknown |
|
|