Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm2 |
T |
C |
4: 144,281,859 (GRCm39) |
Y311C |
probably damaging |
Het |
Abca1 |
A |
T |
4: 53,078,114 (GRCm39) |
I886N |
probably benign |
Het |
Adamts6 |
A |
G |
13: 104,433,694 (GRCm39) |
H41R |
probably benign |
Het |
Adck1 |
T |
C |
12: 88,425,975 (GRCm39) |
|
probably null |
Het |
Atat1 |
G |
T |
17: 36,208,706 (GRCm39) |
T398K |
probably benign |
Het |
Bahcc1 |
A |
G |
11: 120,167,031 (GRCm39) |
E1144G |
possibly damaging |
Het |
Cand2 |
G |
T |
6: 115,762,212 (GRCm39) |
E213* |
probably null |
Het |
Cep350 |
A |
G |
1: 155,791,375 (GRCm39) |
S1250P |
probably benign |
Het |
Cln3 |
A |
G |
7: 126,180,852 (GRCm39) |
L63P |
probably damaging |
Het |
Col4a4 |
A |
T |
1: 82,484,808 (GRCm39) |
C486* |
probably null |
Het |
Ctnnal1 |
A |
T |
4: 56,837,838 (GRCm39) |
M264K |
probably damaging |
Het |
Ddr2 |
T |
A |
1: 169,812,008 (GRCm39) |
D738V |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,104,887 (GRCm39) |
M1901V |
probably benign |
Het |
Dnhd1 |
A |
G |
7: 105,345,255 (GRCm39) |
T2200A |
probably benign |
Het |
Dolk |
A |
G |
2: 30,174,555 (GRCm39) |
Y497H |
probably benign |
Het |
Drd5 |
T |
C |
5: 38,478,195 (GRCm39) |
V396A |
probably benign |
Het |
Epsti1 |
A |
T |
14: 78,200,883 (GRCm39) |
|
probably null |
Het |
Erich3 |
A |
G |
3: 154,468,763 (GRCm39) |
T1072A |
unknown |
Het |
Ero1a |
A |
T |
14: 45,544,032 (GRCm39) |
N57K |
probably damaging |
Het |
Exph5 |
T |
C |
9: 53,278,514 (GRCm39) |
|
probably null |
Het |
Frmd5 |
C |
T |
2: 121,384,745 (GRCm39) |
|
probably null |
Het |
H2-Q7 |
A |
G |
17: 35,661,686 (GRCm39) |
T310A |
probably benign |
Het |
Hecw2 |
G |
T |
1: 53,965,215 (GRCm39) |
A537E |
probably benign |
Het |
Itga4 |
A |
T |
2: 79,131,333 (GRCm39) |
D567V |
probably damaging |
Het |
Kcnu1 |
A |
T |
8: 26,375,368 (GRCm39) |
N361Y |
probably damaging |
Het |
Keap1 |
A |
G |
9: 21,144,787 (GRCm39) |
S408P |
probably benign |
Het |
Mamdc4 |
T |
A |
2: 25,455,360 (GRCm39) |
I928F |
possibly damaging |
Het |
Mboat4 |
T |
C |
8: 34,591,028 (GRCm39) |
F155S |
probably benign |
Het |
Mtbp |
A |
G |
15: 55,440,742 (GRCm39) |
|
probably benign |
Het |
Nmi |
T |
G |
2: 51,842,492 (GRCm39) |
K200T |
probably benign |
Het |
Or2n1e |
G |
A |
17: 38,586,331 (GRCm39) |
C223Y |
probably benign |
Het |
Or8g19 |
G |
T |
9: 39,055,414 (GRCm39) |
R6L |
probably benign |
Het |
Pcdha7 |
G |
A |
18: 37,108,366 (GRCm39) |
V464M |
probably damaging |
Het |
Peg10 |
T |
A |
6: 4,756,796 (GRCm39) |
N457K |
unknown |
Het |
Plekha7 |
A |
T |
7: 115,736,519 (GRCm39) |
I944N |
possibly damaging |
Het |
Plpp1 |
T |
A |
13: 112,937,781 (GRCm39) |
D13E |
possibly damaging |
Het |
Pnpla6 |
G |
T |
8: 3,587,508 (GRCm39) |
V1070F |
probably damaging |
Het |
Riox1 |
T |
A |
12: 83,998,545 (GRCm39) |
Y360* |
probably null |
Het |
Sdhb |
A |
G |
4: 140,693,882 (GRCm39) |
D50G |
possibly damaging |
Het |
Slc35f2 |
T |
A |
9: 53,708,385 (GRCm39) |
V126D |
possibly damaging |
Het |
Slmap |
A |
G |
14: 26,148,575 (GRCm39) |
V612A |
probably benign |
Het |
Snap91 |
T |
A |
9: 86,721,702 (GRCm39) |
I46F |
probably damaging |
Het |
Sp110 |
G |
A |
1: 85,506,813 (GRCm39) |
R417C |
probably benign |
Het |
Tmc1 |
T |
A |
19: 20,776,542 (GRCm39) |
M606L |
probably damaging |
Het |
Trpm8 |
T |
A |
1: 88,271,043 (GRCm39) |
D444E |
probably benign |
Het |
Tsen54 |
A |
G |
11: 115,711,797 (GRCm39) |
T405A |
probably damaging |
Het |
Ttll5 |
T |
C |
12: 85,946,245 (GRCm39) |
W492R |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,728,123 (GRCm39) |
T5566S |
unknown |
Het |
Utp20 |
A |
T |
10: 88,654,457 (GRCm39) |
M210K |
probably damaging |
Het |
Zfand1 |
A |
G |
3: 10,411,009 (GRCm39) |
V115A |
probably damaging |
Het |
|
Other mutations in Taar7b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00330:Taar7b
|
APN |
10 |
23,876,740 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00771:Taar7b
|
APN |
10 |
23,876,096 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01662:Taar7b
|
APN |
10 |
23,875,874 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02186:Taar7b
|
APN |
10 |
23,875,879 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02399:Taar7b
|
APN |
10 |
23,876,050 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02514:Taar7b
|
APN |
10 |
23,876,882 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02601:Taar7b
|
APN |
10 |
23,876,204 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02717:Taar7b
|
APN |
10 |
23,876,258 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02724:Taar7b
|
APN |
10 |
23,876,581 (GRCm39) |
missense |
probably benign |
|
IGL02725:Taar7b
|
APN |
10 |
23,875,961 (GRCm39) |
missense |
probably benign |
0.03 |
R0103:Taar7b
|
UTSW |
10 |
23,876,192 (GRCm39) |
missense |
probably benign |
0.00 |
R2060:Taar7b
|
UTSW |
10 |
23,876,573 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4973:Taar7b
|
UTSW |
10 |
23,876,243 (GRCm39) |
missense |
probably benign |
0.08 |
R5055:Taar7b
|
UTSW |
10 |
23,876,845 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5068:Taar7b
|
UTSW |
10 |
23,876,359 (GRCm39) |
missense |
probably benign |
0.00 |
R5069:Taar7b
|
UTSW |
10 |
23,876,359 (GRCm39) |
missense |
probably benign |
0.00 |
R5070:Taar7b
|
UTSW |
10 |
23,876,359 (GRCm39) |
missense |
probably benign |
0.00 |
R5205:Taar7b
|
UTSW |
10 |
23,875,916 (GRCm39) |
missense |
probably benign |
0.05 |
R5994:Taar7b
|
UTSW |
10 |
23,876,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R6131:Taar7b
|
UTSW |
10 |
23,876,615 (GRCm39) |
missense |
probably benign |
0.20 |
R6302:Taar7b
|
UTSW |
10 |
23,876,158 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6332:Taar7b
|
UTSW |
10 |
23,875,849 (GRCm39) |
missense |
probably benign |
0.05 |
R6809:Taar7b
|
UTSW |
10 |
23,876,756 (GRCm39) |
missense |
probably benign |
0.03 |
R7126:Taar7b
|
UTSW |
10 |
23,875,960 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8962:Taar7b
|
UTSW |
10 |
23,876,359 (GRCm39) |
missense |
probably benign |
0.00 |
|