Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700067P10Rik |
G |
T |
17: 48,400,849 (GRCm39) |
E45* |
probably null |
Het |
Aadat |
A |
T |
8: 60,959,179 (GRCm39) |
|
probably benign |
Het |
Amigo3 |
A |
G |
9: 107,931,375 (GRCm39) |
H266R |
possibly damaging |
Het |
Amy2a1 |
A |
T |
3: 113,323,146 (GRCm39) |
M214K |
probably damaging |
Het |
Atp11b |
A |
T |
3: 35,874,066 (GRCm39) |
D685V |
probably benign |
Het |
Aunip |
T |
A |
4: 134,250,460 (GRCm39) |
M135K |
probably benign |
Het |
Brd10 |
T |
C |
19: 29,731,564 (GRCm39) |
T483A |
probably benign |
Het |
Card9 |
T |
C |
2: 26,247,950 (GRCm39) |
T134A |
probably benign |
Het |
Cd46 |
G |
A |
1: 194,764,949 (GRCm39) |
T216I |
probably benign |
Het |
Chit1 |
T |
C |
1: 134,079,005 (GRCm39) |
V360A |
unknown |
Het |
Crcp |
A |
G |
5: 130,071,077 (GRCm39) |
R59G |
probably benign |
Het |
Csmd1 |
T |
A |
8: 15,976,598 (GRCm39) |
E2873D |
probably benign |
Het |
Cyp8b1 |
T |
A |
9: 121,743,986 (GRCm39) |
M449L |
probably benign |
Het |
Dpp7 |
T |
C |
2: 25,246,133 (GRCm39) |
D40G |
probably benign |
Het |
Eif4g3 |
T |
A |
4: 137,853,823 (GRCm39) |
L463Q |
possibly damaging |
Het |
Fzd9 |
T |
C |
5: 135,278,524 (GRCm39) |
I454V |
probably benign |
Het |
Gbp11 |
T |
A |
5: 105,491,675 (GRCm39) |
I41F |
probably damaging |
Het |
Gkap1 |
G |
A |
13: 58,391,662 (GRCm39) |
T231I |
probably damaging |
Het |
Heatr5b |
A |
G |
17: 79,069,632 (GRCm39) |
L1705P |
probably damaging |
Het |
Herc3 |
T |
A |
6: 58,850,786 (GRCm39) |
F467I |
probably damaging |
Het |
Ifih1 |
T |
C |
2: 62,435,993 (GRCm39) |
E699G |
possibly damaging |
Het |
Ints5 |
T |
A |
19: 8,873,370 (GRCm39) |
L443Q |
probably damaging |
Het |
Itpr2 |
A |
T |
6: 146,276,016 (GRCm39) |
C764S |
probably damaging |
Het |
Kcnma1 |
A |
T |
14: 23,551,230 (GRCm39) |
I519N |
probably damaging |
Het |
Krtap4-1 |
C |
T |
11: 99,518,890 (GRCm39) |
C40Y |
unknown |
Het |
Mdn1 |
A |
G |
4: 32,768,793 (GRCm39) |
D5384G |
probably damaging |
Het |
Mpl |
T |
C |
4: 118,306,110 (GRCm39) |
Y310C |
probably damaging |
Het |
Mucl1 |
A |
G |
15: 103,784,063 (GRCm39) |
S48P |
possibly damaging |
Het |
Musk |
T |
G |
4: 58,286,051 (GRCm39) |
|
probably benign |
Het |
Nemp1 |
T |
C |
10: 127,512,988 (GRCm39) |
S8P |
probably benign |
Het |
Nisch |
A |
G |
14: 30,895,093 (GRCm39) |
C1068R |
probably damaging |
Het |
Npr3 |
T |
C |
15: 11,851,579 (GRCm39) |
N404D |
probably damaging |
Het |
Nwd1 |
C |
G |
8: 73,394,007 (GRCm39) |
H423Q |
probably damaging |
Het |
Or5a1 |
C |
T |
19: 12,097,921 (GRCm39) |
V52M |
probably benign |
Het |
Or6c66b |
T |
A |
10: 129,376,596 (GRCm39) |
N63K |
probably damaging |
Het |
Or8j3c |
T |
A |
2: 86,253,976 (GRCm39) |
M15L |
probably benign |
Het |
Pcdh9 |
T |
C |
14: 94,124,529 (GRCm39) |
N547S |
probably benign |
Het |
Pdha2 |
C |
A |
3: 140,917,124 (GRCm39) |
R128L |
probably damaging |
Het |
Pebp1 |
A |
G |
5: 117,421,336 (GRCm39) |
Y181H |
probably benign |
Het |
Peg3 |
T |
G |
7: 6,711,523 (GRCm39) |
D1233A |
possibly damaging |
Het |
Pepd |
C |
A |
7: 34,642,107 (GRCm39) |
T146N |
probably damaging |
Het |
Ptk2b |
A |
T |
14: 66,393,841 (GRCm39) |
D877E |
probably benign |
Het |
Rabgap1l |
A |
C |
1: 160,270,846 (GRCm39) |
M647R |
probably damaging |
Het |
Rp1 |
A |
G |
1: 4,419,007 (GRCm39) |
S702P |
possibly damaging |
Het |
Shb |
A |
T |
4: 45,489,161 (GRCm39) |
D238E |
probably damaging |
Het |
Slc36a1 |
T |
A |
11: 55,123,334 (GRCm39) |
V433D |
possibly damaging |
Het |
Spata31h1 |
A |
T |
10: 82,127,726 (GRCm39) |
N1761K |
probably benign |
Het |
Spen |
C |
T |
4: 141,197,681 (GRCm39) |
A3396T |
probably benign |
Het |
Tcerg1 |
A |
T |
18: 42,686,559 (GRCm39) |
K705N |
probably damaging |
Het |
Thbs1 |
C |
A |
2: 117,943,719 (GRCm39) |
N112K |
probably benign |
Het |
|
Other mutations in Zfp658 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00465:Zfp658
|
APN |
7 |
43,216,780 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00475:Zfp658
|
APN |
7 |
43,223,500 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01972:Zfp658
|
APN |
7 |
43,222,134 (GRCm39) |
nonsense |
probably null |
|
IGL03223:Zfp658
|
APN |
7 |
43,216,735 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0135:Zfp658
|
UTSW |
7 |
43,223,019 (GRCm39) |
nonsense |
probably null |
|
R1863:Zfp658
|
UTSW |
7 |
43,223,323 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1962:Zfp658
|
UTSW |
7 |
43,223,245 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2698:Zfp658
|
UTSW |
7 |
43,222,969 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3781:Zfp658
|
UTSW |
7 |
43,223,270 (GRCm39) |
missense |
probably benign |
|
R4791:Zfp658
|
UTSW |
7 |
43,223,890 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5392:Zfp658
|
UTSW |
7 |
43,222,355 (GRCm39) |
missense |
probably benign |
0.07 |
R6092:Zfp658
|
UTSW |
7 |
43,223,951 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6594:Zfp658
|
UTSW |
7 |
43,216,701 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7003:Zfp658
|
UTSW |
7 |
43,224,172 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7008:Zfp658
|
UTSW |
7 |
43,223,336 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7077:Zfp658
|
UTSW |
7 |
43,223,413 (GRCm39) |
missense |
probably benign |
0.32 |
R7689:Zfp658
|
UTSW |
7 |
43,224,102 (GRCm39) |
missense |
probably benign |
0.00 |
R7793:Zfp658
|
UTSW |
7 |
43,224,108 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7939:Zfp658
|
UTSW |
7 |
43,224,301 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8828:Zfp658
|
UTSW |
7 |
43,222,240 (GRCm39) |
missense |
probably benign |
|
R8995:Zfp658
|
UTSW |
7 |
43,222,798 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9021:Zfp658
|
UTSW |
7 |
43,223,381 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9259:Zfp658
|
UTSW |
7 |
43,224,280 (GRCm39) |
missense |
probably benign |
0.02 |
R9551:Zfp658
|
UTSW |
7 |
43,222,567 (GRCm39) |
missense |
probably benign |
0.00 |
R9552:Zfp658
|
UTSW |
7 |
43,222,567 (GRCm39) |
missense |
probably benign |
0.00 |
R9571:Zfp658
|
UTSW |
7 |
43,222,139 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1176:Zfp658
|
UTSW |
7 |
43,222,641 (GRCm39) |
missense |
possibly damaging |
0.72 |
|