Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamdec1 |
T |
A |
14: 68,808,802 (GRCm39) |
H302L |
probably damaging |
Het |
Adamts12 |
T |
A |
15: 11,263,422 (GRCm39) |
C595S |
probably damaging |
Het |
Arid2 |
G |
A |
15: 96,268,154 (GRCm39) |
V756I |
probably damaging |
Het |
Asah1 |
A |
T |
8: 41,813,336 (GRCm39) |
W26R |
possibly damaging |
Het |
Brinp1 |
C |
T |
4: 68,822,973 (GRCm39) |
|
probably null |
Het |
Cers2 |
A |
G |
3: 95,228,663 (GRCm39) |
D162G |
probably damaging |
Het |
Clasp1 |
G |
T |
1: 118,429,053 (GRCm39) |
E106* |
probably null |
Het |
Col12a1 |
T |
C |
9: 79,588,719 (GRCm39) |
E1132G |
probably damaging |
Het |
Dhdds |
G |
T |
4: 133,710,182 (GRCm39) |
H196N |
probably benign |
Het |
Eps8 |
T |
C |
6: 137,504,379 (GRCm39) |
D118G |
probably damaging |
Het |
Fmo9 |
A |
G |
1: 166,505,220 (GRCm39) |
S7P |
probably damaging |
Het |
Gamt |
A |
G |
10: 80,094,272 (GRCm39) |
L197P |
probably damaging |
Het |
Grb7 |
A |
G |
11: 98,341,945 (GRCm39) |
I82V |
probably damaging |
Het |
Hectd2 |
T |
C |
19: 36,577,121 (GRCm39) |
|
probably null |
Het |
Ilk |
T |
C |
7: 105,389,542 (GRCm39) |
V83A |
probably damaging |
Het |
Kif21a |
T |
A |
15: 90,869,598 (GRCm39) |
I418F |
probably damaging |
Het |
Kndc1 |
A |
G |
7: 139,501,425 (GRCm39) |
I905V |
probably benign |
Het |
Lyl1 |
C |
T |
8: 85,429,300 (GRCm39) |
P3L |
possibly damaging |
Het |
Morc3 |
T |
C |
16: 93,667,971 (GRCm39) |
I710T |
probably damaging |
Het |
Nefm |
T |
C |
14: 68,357,728 (GRCm39) |
|
probably benign |
Het |
Or10d5 |
T |
C |
9: 39,862,040 (GRCm39) |
E9G |
probably damaging |
Het |
Or2f2 |
A |
G |
6: 42,767,599 (GRCm39) |
T209A |
probably benign |
Het |
Or8g23 |
C |
A |
9: 38,971,259 (GRCm39) |
R234S |
probably damaging |
Het |
Pard6g |
T |
G |
18: 80,123,068 (GRCm39) |
L34W |
probably damaging |
Het |
Patj |
C |
T |
4: 98,332,040 (GRCm39) |
S562L |
probably damaging |
Het |
Pcsk4 |
A |
G |
10: 80,164,883 (GRCm39) |
I61T |
probably damaging |
Het |
Pcsk7 |
T |
A |
9: 45,825,670 (GRCm39) |
H300Q |
probably damaging |
Het |
Pip5kl1 |
A |
G |
2: 32,470,033 (GRCm39) |
D288G |
probably damaging |
Het |
Plxnb2 |
T |
A |
15: 89,046,641 (GRCm39) |
|
probably benign |
Het |
Poldip2 |
T |
C |
11: 78,411,970 (GRCm39) |
|
probably benign |
Het |
Ralgapa2 |
T |
C |
2: 146,266,734 (GRCm39) |
Y614C |
probably damaging |
Het |
Rarres1 |
C |
A |
3: 67,403,145 (GRCm39) |
|
probably null |
Het |
Samd3 |
C |
T |
10: 26,147,606 (GRCm39) |
T427M |
probably damaging |
Het |
Skap1 |
A |
G |
11: 96,593,446 (GRCm39) |
I98V |
probably benign |
Het |
Skint11 |
T |
C |
4: 114,101,820 (GRCm39) |
S87P |
probably damaging |
Het |
Slc22a22 |
T |
G |
15: 57,126,670 (GRCm39) |
E133A |
probably damaging |
Het |
Slc23a2 |
T |
C |
2: 131,933,185 (GRCm39) |
Y91C |
probably damaging |
Het |
Slc6a20b |
T |
A |
9: 123,426,403 (GRCm39) |
E494V |
possibly damaging |
Het |
Slco1a4 |
A |
T |
6: 141,765,329 (GRCm39) |
D304E |
probably benign |
Het |
Slco1a4 |
A |
C |
6: 141,763,585 (GRCm39) |
M377R |
probably damaging |
Het |
Srpk2 |
T |
C |
5: 23,729,616 (GRCm39) |
|
probably null |
Het |
Supt3 |
T |
G |
17: 45,352,114 (GRCm39) |
C271W |
probably damaging |
Het |
Tmbim7 |
T |
C |
5: 3,729,158 (GRCm39) |
*225Q |
probably null |
Het |
Tpst1 |
T |
C |
5: 130,130,752 (GRCm39) |
I74T |
probably damaging |
Het |
Utp3 |
T |
C |
5: 88,703,179 (GRCm39) |
V236A |
possibly damaging |
Het |
Vmn2r55 |
A |
T |
7: 12,404,558 (GRCm39) |
F282I |
probably damaging |
Het |
Vwa5b1 |
A |
T |
4: 138,327,460 (GRCm39) |
I372N |
possibly damaging |
Het |
Wtip |
C |
T |
7: 33,824,958 (GRCm39) |
A209T |
probably damaging |
Het |
Zbbx |
T |
C |
3: 74,985,867 (GRCm39) |
D395G |
probably benign |
Het |
Zfp273 |
A |
T |
13: 67,973,769 (GRCm39) |
H299L |
probably damaging |
Het |
Zfp459 |
G |
A |
13: 67,556,796 (GRCm39) |
R96* |
probably null |
Het |
|
Other mutations in Taar7d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01719:Taar7d
|
APN |
10 |
23,903,865 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02070:Taar7d
|
APN |
10 |
23,904,152 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02280:Taar7d
|
APN |
10 |
23,904,006 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02525:Taar7d
|
APN |
10 |
23,903,994 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03339:Taar7d
|
APN |
10 |
23,903,204 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1509:Taar7d
|
UTSW |
10 |
23,904,102 (GRCm39) |
missense |
probably damaging |
0.99 |
R1826:Taar7d
|
UTSW |
10 |
23,903,474 (GRCm39) |
missense |
probably damaging |
0.99 |
R2016:Taar7d
|
UTSW |
10 |
23,903,642 (GRCm39) |
missense |
probably benign |
0.11 |
R2051:Taar7d
|
UTSW |
10 |
23,903,904 (GRCm39) |
missense |
probably benign |
0.00 |
R6075:Taar7d
|
UTSW |
10 |
23,903,558 (GRCm39) |
missense |
probably benign |
0.21 |
R6541:Taar7d
|
UTSW |
10 |
23,904,129 (GRCm39) |
missense |
probably benign |
0.01 |
R8165:Taar7d
|
UTSW |
10 |
23,903,495 (GRCm39) |
missense |
probably benign |
0.07 |
R9222:Taar7d
|
UTSW |
10 |
23,904,124 (GRCm39) |
missense |
probably benign |
0.08 |
R9456:Taar7d
|
UTSW |
10 |
23,903,287 (GRCm39) |
missense |
probably benign |
|
R9481:Taar7d
|
UTSW |
10 |
23,903,739 (GRCm39) |
missense |
probably benign |
0.00 |
X0067:Taar7d
|
UTSW |
10 |
23,903,906 (GRCm39) |
missense |
probably damaging |
1.00 |
|