Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
A |
G |
5: 77,024,148 (GRCm39) |
L168P |
probably damaging |
Het |
Atp6v0d1 |
A |
G |
8: 106,255,849 (GRCm39) |
L173P |
probably damaging |
Het |
Baiap2l2 |
A |
G |
15: 79,168,835 (GRCm39) |
F23L |
probably damaging |
Het |
Cd200l1 |
T |
A |
16: 45,264,366 (GRCm39) |
Y64F |
probably benign |
Het |
Cdh23 |
G |
C |
10: 60,485,893 (GRCm39) |
L41V |
probably benign |
Het |
Cep120 |
C |
A |
18: 53,836,277 (GRCm39) |
E803* |
probably null |
Het |
Clcn7 |
C |
T |
17: 25,376,188 (GRCm39) |
P560S |
probably damaging |
Het |
Cldn12 |
A |
T |
5: 5,557,707 (GRCm39) |
V240D |
probably damaging |
Het |
Clec1a |
C |
T |
6: 129,406,946 (GRCm39) |
E190K |
probably benign |
Het |
Cntnap5b |
A |
G |
1: 100,202,197 (GRCm39) |
E348G |
probably benign |
Het |
Crispld1 |
T |
A |
1: 17,832,365 (GRCm39) |
H450Q |
probably damaging |
Het |
Dsc2 |
A |
T |
18: 20,171,279 (GRCm39) |
N573K |
probably damaging |
Het |
Fam186a |
T |
A |
15: 99,838,082 (GRCm39) |
I2721F |
probably benign |
Het |
Fbxl13 |
A |
G |
5: 21,748,740 (GRCm39) |
F393S |
probably damaging |
Het |
Fut1 |
A |
T |
7: 45,268,963 (GRCm39) |
I306F |
probably damaging |
Het |
Gas2l3 |
T |
C |
10: 89,249,153 (GRCm39) |
D655G |
probably benign |
Het |
Gm57858 |
T |
A |
3: 36,104,766 (GRCm39) |
I32F |
possibly damaging |
Het |
Hmg20a |
T |
C |
9: 56,396,012 (GRCm39) |
V268A |
probably benign |
Het |
Il2rb |
T |
A |
15: 78,370,024 (GRCm39) |
Y205F |
probably damaging |
Het |
Ints4 |
A |
G |
7: 97,190,397 (GRCm39) |
*965W |
probably null |
Het |
Itsn2 |
T |
A |
12: 4,723,420 (GRCm39) |
C1118* |
probably null |
Het |
Jakmip1 |
T |
C |
5: 37,330,697 (GRCm39) |
L459P |
probably damaging |
Het |
Klhl8 |
T |
C |
5: 104,018,435 (GRCm39) |
T323A |
possibly damaging |
Het |
Mindy3 |
C |
A |
2: 12,400,989 (GRCm39) |
|
probably null |
Het |
Myo3a |
A |
G |
2: 22,250,369 (GRCm39) |
T79A |
probably benign |
Het |
Myom2 |
G |
A |
8: 15,167,741 (GRCm39) |
A1109T |
probably null |
Het |
Napa |
C |
T |
7: 15,843,034 (GRCm39) |
R53* |
probably null |
Het |
Nudt21 |
A |
C |
8: 94,755,508 (GRCm39) |
D133E |
probably benign |
Het |
Or2y3 |
T |
A |
17: 38,393,096 (GRCm39) |
I258F |
probably damaging |
Het |
Or4c115 |
T |
A |
2: 88,928,149 (GRCm39) |
M41L |
probably benign |
Het |
Or52b1 |
A |
T |
7: 104,978,913 (GRCm39) |
I162K |
probably damaging |
Het |
Or52s19 |
A |
G |
7: 103,007,789 (GRCm39) |
V204A |
possibly damaging |
Het |
Or56a41 |
A |
T |
7: 104,741,978 (GRCm39) |
M16K |
probably benign |
Het |
Or6c7 |
T |
C |
10: 129,323,331 (GRCm39) |
F151L |
probably damaging |
Het |
Pate13 |
G |
A |
9: 35,819,740 (GRCm39) |
M1I |
probably null |
Het |
Pira13 |
T |
C |
7: 3,828,124 (GRCm39) |
Y61C |
probably damaging |
Het |
Pla2g4e |
G |
T |
2: 120,004,851 (GRCm39) |
|
probably null |
Het |
Ptbp1 |
T |
C |
10: 79,695,111 (GRCm39) |
|
probably null |
Het |
Scfd2 |
A |
C |
5: 74,680,202 (GRCm39) |
V317G |
possibly damaging |
Het |
Slc45a1 |
T |
C |
4: 150,714,110 (GRCm39) |
M712V |
probably damaging |
Het |
Smg7 |
A |
T |
1: 152,717,334 (GRCm39) |
L919* |
probably null |
Het |
Sspo |
T |
A |
6: 48,440,811 (GRCm39) |
S1758T |
probably benign |
Het |
Tgfb2 |
A |
T |
1: 186,382,032 (GRCm39) |
M165K |
possibly damaging |
Het |
Tie1 |
C |
T |
4: 118,343,402 (GRCm39) |
V154M |
probably damaging |
Het |
Timm17a |
A |
G |
1: 135,238,816 (GRCm39) |
|
probably benign |
Het |
Tlr5 |
C |
T |
1: 182,801,076 (GRCm39) |
R127* |
probably null |
Het |
Ttc29 |
A |
C |
8: 79,003,545 (GRCm39) |
I254L |
possibly damaging |
Het |
Unc79 |
T |
C |
12: 103,079,174 (GRCm39) |
S1780P |
probably damaging |
Het |
Vmn2r106 |
A |
T |
17: 20,488,646 (GRCm39) |
Y584* |
probably null |
Het |
Zbtb24 |
A |
G |
10: 41,331,171 (GRCm39) |
E366G |
probably damaging |
Het |
|
Other mutations in Gm29106 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R4985:Gm29106
|
UTSW |
1 |
118,126,950 (GRCm39) |
missense |
probably benign |
0.02 |
R4991:Gm29106
|
UTSW |
1 |
118,106,121 (GRCm39) |
missense |
probably benign |
0.01 |
R6029:Gm29106
|
UTSW |
1 |
118,127,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R6922:Gm29106
|
UTSW |
1 |
118,127,524 (GRCm39) |
missense |
probably damaging |
0.98 |
R6954:Gm29106
|
UTSW |
1 |
118,128,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R7232:Gm29106
|
UTSW |
1 |
118,127,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R7337:Gm29106
|
UTSW |
1 |
118,104,642 (GRCm39) |
missense |
unknown |
|
R7457:Gm29106
|
UTSW |
1 |
118,126,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R7662:Gm29106
|
UTSW |
1 |
118,127,137 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7870:Gm29106
|
UTSW |
1 |
118,126,885 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7894:Gm29106
|
UTSW |
1 |
118,127,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R7986:Gm29106
|
UTSW |
1 |
118,128,000 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8099:Gm29106
|
UTSW |
1 |
118,126,521 (GRCm39) |
missense |
probably benign |
0.00 |
R8377:Gm29106
|
UTSW |
1 |
118,126,593 (GRCm39) |
missense |
probably damaging |
0.99 |
R8498:Gm29106
|
UTSW |
1 |
118,128,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R8553:Gm29106
|
UTSW |
1 |
118,128,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R8980:Gm29106
|
UTSW |
1 |
118,127,114 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9212:Gm29106
|
UTSW |
1 |
118,127,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R9451:Gm29106
|
UTSW |
1 |
118,127,644 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9746:Gm29106
|
UTSW |
1 |
118,127,254 (GRCm39) |
missense |
possibly damaging |
0.94 |
|