Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alkal2 |
G |
T |
12: 30,934,850 (GRCm39) |
G23V |
probably damaging |
Het |
Atl2 |
C |
T |
17: 80,160,033 (GRCm39) |
W518* |
probably null |
Het |
Atp13a2 |
G |
A |
4: 140,730,046 (GRCm39) |
V646I |
probably benign |
Het |
Bcar1 |
A |
T |
8: 112,440,270 (GRCm39) |
F575I |
probably benign |
Het |
Bpifa6 |
T |
A |
2: 153,831,178 (GRCm39) |
L248* |
probably null |
Het |
Ccdc38 |
T |
C |
10: 93,399,111 (GRCm39) |
L193P |
probably damaging |
Het |
Ch25h |
A |
C |
19: 34,452,138 (GRCm39) |
I130S |
probably benign |
Het |
Chaf1a |
C |
A |
17: 56,351,109 (GRCm39) |
Q30K |
unknown |
Het |
Dab2ip |
T |
C |
2: 35,617,440 (GRCm39) |
L1106S |
probably damaging |
Het |
Dnah3 |
A |
G |
7: 119,550,375 (GRCm39) |
Y3315H |
probably benign |
Het |
Dnah7b |
G |
A |
1: 46,214,456 (GRCm39) |
V1074I |
possibly damaging |
Het |
Efemp1 |
A |
G |
11: 28,860,691 (GRCm39) |
Q200R |
probably benign |
Het |
Eif1ad3 |
A |
T |
12: 87,843,764 (GRCm39) |
D137V |
unknown |
Het |
Epx |
C |
T |
11: 87,763,557 (GRCm39) |
R221Q |
possibly damaging |
Het |
Exosc7 |
T |
C |
9: 122,956,942 (GRCm39) |
L109P |
probably damaging |
Het |
Fbxo22 |
T |
A |
9: 55,128,344 (GRCm39) |
F222I |
probably damaging |
Het |
Fcgbp |
A |
G |
7: 27,785,769 (GRCm39) |
D402G |
probably benign |
Het |
Foxr1 |
A |
G |
9: 44,347,351 (GRCm39) |
V62A |
probably damaging |
Het |
Gnptab |
T |
A |
10: 88,275,071 (GRCm39) |
Y1090N |
probably damaging |
Het |
Gpr20 |
A |
G |
15: 73,568,161 (GRCm39) |
F76S |
probably damaging |
Het |
Gpr33 |
A |
G |
12: 52,070,907 (GRCm39) |
V44A |
probably benign |
Het |
Grin3a |
G |
A |
4: 49,665,599 (GRCm39) |
T1012I |
probably benign |
Het |
Itga1 |
T |
A |
13: 115,103,120 (GRCm39) |
T1104S |
probably benign |
Het |
Kidins220 |
T |
A |
12: 25,054,110 (GRCm39) |
Y537N |
probably damaging |
Het |
Lama1 |
A |
G |
17: 68,057,515 (GRCm39) |
T530A |
|
Het |
Lysmd2 |
A |
T |
9: 75,533,040 (GRCm39) |
|
probably benign |
Het |
Mdk |
T |
C |
2: 91,761,178 (GRCm39) |
K128E |
unknown |
Het |
Mphosph8 |
AC |
A |
14: 56,916,062 (GRCm39) |
|
probably null |
Het |
Muc16 |
A |
C |
9: 18,436,443 (GRCm39) |
L7915W |
possibly damaging |
Het |
Muc4 |
A |
T |
16: 32,753,423 (GRCm38) |
T1100S |
probably benign |
Het |
Mxra7 |
T |
C |
11: 116,695,376 (GRCm39) |
Y176C |
probably damaging |
Het |
Myh15 |
C |
A |
16: 48,940,381 (GRCm39) |
T777N |
probably damaging |
Het |
Myo18b |
A |
G |
5: 113,023,045 (GRCm39) |
S116P |
unknown |
Het |
Noc3l |
A |
G |
19: 38,784,254 (GRCm39) |
L543P |
probably damaging |
Het |
Or5h24 |
C |
T |
16: 58,919,004 (GRCm39) |
G117D |
unknown |
Het |
Or7a39 |
C |
T |
10: 78,715,170 (GRCm39) |
P55S |
probably benign |
Het |
Or8c10 |
T |
A |
9: 38,279,346 (GRCm39) |
V168E |
probably damaging |
Het |
Pkm |
G |
T |
9: 59,575,902 (GRCm39) |
R106L |
probably benign |
Het |
Prkab2 |
G |
T |
3: 97,570,911 (GRCm39) |
V112F |
probably benign |
Het |
Prkaca |
A |
T |
8: 84,717,151 (GRCm39) |
N172Y |
probably damaging |
Het |
Prmt8 |
A |
G |
6: 127,666,813 (GRCm39) |
V387A |
probably benign |
Het |
Rad17 |
T |
C |
13: 100,761,074 (GRCm39) |
T485A |
probably benign |
Het |
Rita1 |
G |
T |
5: 120,747,716 (GRCm39) |
T194K |
possibly damaging |
Het |
Rogdi |
C |
A |
16: 4,831,313 (GRCm39) |
|
probably benign |
Het |
Senp5 |
T |
C |
16: 31,808,117 (GRCm39) |
D379G |
probably benign |
Het |
Slc4a4 |
A |
G |
5: 89,194,122 (GRCm39) |
K201E |
possibly damaging |
Het |
Slc9a4 |
C |
T |
1: 40,619,520 (GRCm39) |
|
probably benign |
Het |
Tmem175 |
T |
A |
5: 108,791,075 (GRCm39) |
S208R |
probably benign |
Het |
Tmem237 |
A |
T |
1: 59,147,237 (GRCm39) |
Y299N |
probably damaging |
Het |
Tnrc6a |
T |
A |
7: 122,769,936 (GRCm39) |
N575K |
possibly damaging |
Het |
Trak2 |
A |
T |
1: 58,960,306 (GRCm39) |
C232* |
probably null |
Het |
Ubr3 |
A |
G |
2: 69,775,478 (GRCm39) |
H589R |
probably damaging |
Het |
Vcp |
T |
C |
4: 42,988,728 (GRCm39) |
T249A |
possibly damaging |
Het |
Vmn1r208 |
G |
C |
13: 22,956,947 (GRCm39) |
I183M |
probably benign |
Het |
Vmn1r231 |
C |
T |
17: 21,110,289 (GRCm39) |
V209I |
probably benign |
Het |
Vmn1r80 |
T |
C |
7: 11,926,994 (GRCm39) |
F35L |
probably benign |
Het |
Vmn2r58 |
A |
T |
7: 41,521,952 (GRCm39) |
I48N |
probably benign |
Het |
Vstm2a |
T |
A |
11: 16,231,898 (GRCm39) |
V231E |
probably damaging |
Het |
Zfp108 |
A |
C |
7: 23,960,087 (GRCm39) |
Y226S |
possibly damaging |
Het |
Zfp445 |
A |
T |
9: 122,682,695 (GRCm39) |
N415K |
possibly damaging |
Het |
Zfp938 |
T |
G |
10: 82,061,422 (GRCm39) |
R399S |
possibly damaging |
Het |
Zmym4 |
G |
A |
4: 126,804,762 (GRCm39) |
H464Y |
probably benign |
Het |
|
Other mutations in Gm8267 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01345:Gm8267
|
APN |
14 |
44,962,412 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02031:Gm8267
|
APN |
14 |
44,955,374 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3619:Gm8267
|
UTSW |
14 |
44,961,513 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4715:Gm8267
|
UTSW |
14 |
44,955,292 (GRCm39) |
missense |
probably benign |
0.33 |
R6599:Gm8267
|
UTSW |
14 |
44,955,367 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7001:Gm8267
|
UTSW |
14 |
44,960,385 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7057:Gm8267
|
UTSW |
14 |
44,959,481 (GRCm39) |
missense |
probably damaging |
0.99 |
R7439:Gm8267
|
UTSW |
14 |
44,960,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R7441:Gm8267
|
UTSW |
14 |
44,960,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R8053:Gm8267
|
UTSW |
14 |
44,962,307 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8721:Gm8267
|
UTSW |
14 |
44,959,507 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9150:Gm8267
|
UTSW |
14 |
44,955,362 (GRCm39) |
missense |
probably benign |
0.18 |
R9464:Gm8267
|
UTSW |
14 |
44,960,346 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Gm8267
|
UTSW |
14 |
44,962,322 (GRCm39) |
missense |
probably benign |
0.28 |
|