Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg3 |
G |
T |
5: 105,121,962 (GRCm39) |
D138E |
probably benign |
Het |
Acvr2a |
T |
A |
2: 48,760,307 (GRCm39) |
I21K |
probably damaging |
Het |
Adam30 |
C |
G |
3: 98,070,194 (GRCm39) |
P676A |
probably benign |
Het |
Ankrd28 |
A |
C |
14: 31,470,627 (GRCm39) |
H145Q |
probably damaging |
Het |
Ap3m2 |
A |
G |
8: 23,289,774 (GRCm39) |
Y110H |
probably damaging |
Het |
Apoc4 |
A |
G |
7: 19,412,665 (GRCm39) |
S27P |
possibly damaging |
Het |
Bbs1 |
A |
C |
19: 4,941,070 (GRCm39) |
L548R |
possibly damaging |
Het |
Cfap99 |
A |
T |
5: 34,471,602 (GRCm39) |
D346V |
probably damaging |
Het |
Ckmt1 |
T |
A |
2: 121,189,870 (GRCm39) |
|
probably benign |
Het |
Col13a1 |
T |
C |
10: 61,703,612 (GRCm39) |
K436E |
possibly damaging |
Het |
Col15a1 |
G |
C |
4: 47,288,200 (GRCm39) |
|
probably benign |
Het |
Dbf4 |
A |
G |
5: 8,462,206 (GRCm39) |
V105A |
possibly damaging |
Het |
Disp2 |
T |
A |
2: 118,617,393 (GRCm39) |
V129E |
probably benign |
Het |
Dnah7b |
T |
C |
1: 46,181,194 (GRCm39) |
V1027A |
probably damaging |
Het |
Dst |
T |
A |
1: 34,231,818 (GRCm39) |
I3137N |
probably benign |
Het |
F5 |
A |
G |
1: 164,019,895 (GRCm39) |
D790G |
probably benign |
Het |
Fan1 |
A |
G |
7: 64,016,400 (GRCm39) |
S575P |
probably damaging |
Het |
Gemin5 |
C |
T |
11: 58,021,035 (GRCm39) |
A1051T |
probably benign |
Het |
Gsta4 |
A |
G |
9: 78,105,597 (GRCm39) |
Y9C |
probably damaging |
Het |
H2-M3 |
C |
A |
17: 37,583,172 (GRCm39) |
A211E |
probably damaging |
Het |
Ifna1 |
A |
T |
4: 88,768,453 (GRCm39) |
M44L |
probably benign |
Het |
Ildr2 |
A |
T |
1: 166,122,283 (GRCm39) |
D242V |
probably damaging |
Het |
Kif27 |
G |
T |
13: 58,492,543 (GRCm39) |
Q199K |
probably damaging |
Het |
Lmf1 |
T |
A |
17: 25,804,718 (GRCm39) |
L132H |
probably damaging |
Het |
Mbtd1 |
A |
G |
11: 93,803,241 (GRCm39) |
N173S |
probably benign |
Het |
Mettl25b |
A |
G |
3: 87,835,392 (GRCm39) |
|
probably benign |
Het |
Mgat4c |
A |
T |
10: 102,225,123 (GRCm39) |
N446Y |
probably benign |
Het |
Minar1 |
A |
G |
9: 89,485,394 (GRCm39) |
M1T |
probably null |
Het |
Mocs1 |
T |
A |
17: 49,756,801 (GRCm39) |
M261K |
probably damaging |
Het |
Nlrp10 |
A |
T |
7: 108,524,108 (GRCm39) |
F457L |
probably damaging |
Het |
Nlrp4e |
C |
T |
7: 23,061,270 (GRCm39) |
R954* |
probably null |
Het |
Or4s2 |
T |
C |
2: 88,473,348 (GRCm39) |
M79T |
probably benign |
Het |
Pigu |
T |
C |
2: 155,141,109 (GRCm39) |
I261M |
probably damaging |
Het |
Pkd1l3 |
T |
A |
8: 110,375,318 (GRCm39) |
I1576N |
probably damaging |
Het |
Plekhg6 |
A |
C |
6: 125,355,854 (GRCm39) |
|
probably benign |
Het |
Pmpca |
T |
C |
2: 26,283,365 (GRCm39) |
L388P |
probably damaging |
Het |
Polg |
A |
T |
7: 79,104,421 (GRCm39) |
I818N |
probably damaging |
Het |
Pramel46 |
A |
T |
5: 95,418,414 (GRCm39) |
V194D |
probably benign |
Het |
Radil |
A |
G |
5: 142,480,722 (GRCm39) |
Y578H |
probably damaging |
Het |
Retnlb |
A |
G |
16: 48,639,084 (GRCm39) |
D95G |
probably damaging |
Het |
Rufy2 |
A |
T |
10: 62,836,166 (GRCm39) |
Y365F |
possibly damaging |
Het |
Ssc5d |
A |
G |
7: 4,945,814 (GRCm39) |
T949A |
possibly damaging |
Het |
Svil |
C |
A |
18: 5,090,833 (GRCm39) |
R1312S |
possibly damaging |
Het |
Syne1 |
T |
C |
10: 5,063,994 (GRCm39) |
T7142A |
probably damaging |
Het |
Tert |
A |
T |
13: 73,785,294 (GRCm39) |
|
probably benign |
Het |
Tpbgl |
A |
T |
7: 99,274,776 (GRCm39) |
D360E |
probably damaging |
Het |
Traj13 |
G |
A |
14: 54,443,248 (GRCm39) |
V17I |
unknown |
Het |
Trim13 |
G |
A |
14: 61,842,046 (GRCm39) |
R21Q |
possibly damaging |
Het |
Wdr36 |
T |
C |
18: 32,981,382 (GRCm39) |
V357A |
possibly damaging |
Het |
Xdh |
G |
A |
17: 74,232,006 (GRCm39) |
R235C |
probably damaging |
Het |
Znfx1 |
C |
T |
2: 166,879,738 (GRCm39) |
C1546Y |
probably damaging |
Het |
Znfx1 |
T |
A |
2: 166,880,137 (GRCm39) |
E1413V |
probably benign |
Het |
Zscan4c |
A |
G |
7: 10,743,741 (GRCm39) |
M447V |
probably benign |
Het |
Zyx |
T |
A |
6: 42,334,818 (GRCm39) |
D541E |
probably damaging |
Het |
|
Other mutations in Zfp971 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01067:Zfp971
|
APN |
2 |
177,665,175 (GRCm39) |
critical splice donor site |
probably null |
|
R1108:Zfp971
|
UTSW |
2 |
177,675,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R1759:Zfp971
|
UTSW |
2 |
177,675,722 (GRCm39) |
missense |
probably damaging |
0.99 |
R2183:Zfp971
|
UTSW |
2 |
177,675,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2343:Zfp971
|
UTSW |
2 |
177,674,787 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4873:Zfp971
|
UTSW |
2 |
177,674,940 (GRCm39) |
missense |
probably benign |
0.24 |
R4875:Zfp971
|
UTSW |
2 |
177,674,940 (GRCm39) |
missense |
probably benign |
0.24 |
R5263:Zfp971
|
UTSW |
2 |
177,675,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R5396:Zfp971
|
UTSW |
2 |
177,675,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R6150:Zfp971
|
UTSW |
2 |
177,675,247 (GRCm39) |
missense |
probably benign |
0.26 |
R6693:Zfp971
|
UTSW |
2 |
177,675,224 (GRCm39) |
missense |
probably benign |
0.01 |
R6811:Zfp971
|
UTSW |
2 |
177,675,674 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7427:Zfp971
|
UTSW |
2 |
177,674,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R7428:Zfp971
|
UTSW |
2 |
177,674,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R7594:Zfp971
|
UTSW |
2 |
177,675,793 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7790:Zfp971
|
UTSW |
2 |
177,675,292 (GRCm39) |
missense |
probably damaging |
0.96 |
R7796:Zfp971
|
UTSW |
2 |
177,673,403 (GRCm39) |
missense |
probably benign |
0.00 |
R7934:Zfp971
|
UTSW |
2 |
177,675,173 (GRCm39) |
missense |
probably benign |
|
R7990:Zfp971
|
UTSW |
2 |
177,675,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R8671:Zfp971
|
UTSW |
2 |
177,675,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R9575:Zfp971
|
UTSW |
2 |
177,675,303 (GRCm39) |
missense |
probably damaging |
0.99 |
R9629:Zfp971
|
UTSW |
2 |
177,675,417 (GRCm39) |
missense |
probably damaging |
0.96 |
|