Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921536K21Rik |
T |
A |
11: 3,839,784 (GRCm39) |
|
probably null |
Het |
Adora3 |
T |
C |
3: 105,815,039 (GRCm39) |
V263A |
probably benign |
Het |
Adprhl1 |
C |
T |
8: 13,298,682 (GRCm39) |
V83I |
probably damaging |
Het |
Arfgef1 |
A |
G |
1: 10,227,235 (GRCm39) |
V1368A |
possibly damaging |
Het |
Arid4a |
A |
T |
12: 71,108,363 (GRCm39) |
N56I |
possibly damaging |
Het |
Art3 |
A |
T |
5: 92,551,472 (GRCm39) |
Y277F |
probably damaging |
Het |
Atp2a1 |
A |
T |
7: 126,047,707 (GRCm39) |
|
probably null |
Het |
Banf1 |
T |
C |
19: 5,415,150 (GRCm39) |
K54E |
possibly damaging |
Het |
Bckdk |
A |
G |
7: 127,505,073 (GRCm39) |
Y151C |
probably damaging |
Het |
C1qtnf3 |
C |
A |
15: 10,958,130 (GRCm39) |
P58T |
possibly damaging |
Het |
Cadps2 |
T |
C |
6: 23,390,445 (GRCm39) |
R744G |
probably benign |
Het |
Cdc25b |
A |
G |
2: 131,031,029 (GRCm39) |
D118G |
probably damaging |
Het |
Cnot9 |
G |
A |
1: 74,566,151 (GRCm39) |
V181I |
probably damaging |
Het |
Cobl |
C |
T |
11: 12,204,488 (GRCm39) |
G738D |
probably benign |
Het |
Col18a1 |
T |
A |
10: 76,904,220 (GRCm39) |
|
probably null |
Het |
Crnkl1 |
A |
G |
2: 145,772,564 (GRCm39) |
V171A |
probably benign |
Het |
Dhx57 |
C |
T |
17: 80,580,507 (GRCm39) |
D482N |
possibly damaging |
Het |
Dpysl2 |
A |
T |
14: 67,066,425 (GRCm39) |
|
probably null |
Het |
Drd3 |
G |
T |
16: 43,582,758 (GRCm39) |
A52S |
probably benign |
Het |
Dst |
T |
C |
1: 34,220,469 (GRCm39) |
V2091A |
possibly damaging |
Het |
Evpl |
T |
C |
11: 116,112,261 (GRCm39) |
T1810A |
probably benign |
Het |
Fbxo2 |
T |
A |
4: 148,248,783 (GRCm39) |
W92R |
probably damaging |
Het |
Gas2l2 |
T |
A |
11: 83,320,103 (GRCm39) |
D51V |
possibly damaging |
Het |
Gm11232 |
A |
T |
4: 71,674,818 (GRCm39) |
V228E |
possibly damaging |
Het |
Gm14305 |
C |
T |
2: 176,412,764 (GRCm39) |
Q219* |
probably null |
Het |
Gpr137b |
T |
C |
13: 13,533,991 (GRCm39) |
Y355C |
|
Het |
Gpr39 |
G |
T |
1: 125,605,334 (GRCm39) |
M87I |
possibly damaging |
Het |
Heatr1 |
T |
C |
13: 12,432,522 (GRCm39) |
M1089T |
probably benign |
Het |
Ifi206 |
A |
T |
1: 173,308,640 (GRCm39) |
M452K |
|
Het |
Ints8 |
A |
T |
4: 11,227,190 (GRCm39) |
I561N |
probably damaging |
Het |
Itgb2 |
A |
T |
10: 77,396,946 (GRCm39) |
K660N |
probably benign |
Het |
Jun |
A |
C |
4: 94,939,081 (GRCm39) |
V143G |
probably benign |
Het |
Kalrn |
A |
G |
16: 33,851,952 (GRCm39) |
M2076T |
probably benign |
Het |
Krt10 |
G |
T |
11: 99,279,913 (GRCm39) |
S82R |
unknown |
Het |
Lipm |
T |
A |
19: 34,095,291 (GRCm39) |
H295Q |
probably damaging |
Het |
Mybpc2 |
A |
C |
7: 44,165,348 (GRCm39) |
|
probably null |
Het |
Nedd4 |
T |
C |
9: 72,584,608 (GRCm39) |
V103A |
possibly damaging |
Het |
Nol10 |
T |
C |
12: 17,398,586 (GRCm39) |
I11T |
probably damaging |
Het |
Nup210l |
A |
G |
3: 90,067,233 (GRCm39) |
S758G |
probably damaging |
Het |
Or13d1 |
T |
A |
4: 52,970,713 (GRCm39) |
C31S |
probably damaging |
Het |
Or52r1c |
T |
G |
7: 102,735,388 (GRCm39) |
I216S |
probably benign |
Het |
Or8d4 |
T |
C |
9: 40,038,661 (GRCm39) |
I199V |
probably benign |
Het |
Osbpl9 |
T |
C |
4: 108,923,384 (GRCm39) |
H425R |
probably damaging |
Het |
Parp1 |
G |
T |
1: 180,416,963 (GRCm39) |
R582S |
possibly damaging |
Het |
Piwil1 |
A |
T |
5: 128,816,527 (GRCm39) |
R36S |
probably benign |
Het |
Pjvk |
T |
C |
2: 76,487,877 (GRCm39) |
|
probably null |
Het |
Plekha6 |
G |
T |
1: 133,097,760 (GRCm39) |
E31D |
possibly damaging |
Het |
Polr1b |
C |
A |
2: 128,967,464 (GRCm39) |
F952L |
probably damaging |
Het |
Prm3 |
CTCTTCTTCTTCTTC |
CTCTTCTTCTTC |
16: 10,608,565 (GRCm39) |
|
probably benign |
Het |
Psmc6 |
T |
A |
14: 45,581,107 (GRCm39) |
I301N |
probably damaging |
Het |
Rfpl4 |
C |
A |
7: 5,118,543 (GRCm39) |
S9I |
probably benign |
Het |
Rnf14 |
G |
T |
18: 38,442,629 (GRCm39) |
C310F |
probably damaging |
Het |
Rnf17 |
T |
A |
14: 56,715,144 (GRCm39) |
F845L |
probably benign |
Het |
Robo2 |
T |
C |
16: 73,758,777 (GRCm39) |
I665V |
probably benign |
Het |
Rtl1 |
T |
A |
12: 109,559,619 (GRCm39) |
H740L |
probably damaging |
Het |
Ryr2 |
A |
G |
13: 11,765,897 (GRCm39) |
S1280P |
probably benign |
Het |
Slc12a8 |
G |
A |
16: 33,371,335 (GRCm39) |
R126H |
probably damaging |
Het |
Slc9a1 |
T |
C |
4: 133,139,276 (GRCm39) |
F165L |
probably damaging |
Het |
Snx19 |
T |
C |
9: 30,340,221 (GRCm39) |
I453T |
probably damaging |
Het |
Spag17 |
T |
C |
3: 99,987,434 (GRCm39) |
Y1575H |
probably damaging |
Het |
Spef2 |
T |
C |
15: 9,704,567 (GRCm39) |
I415M |
probably damaging |
Het |
Ssx2ip |
T |
G |
3: 146,138,885 (GRCm39) |
I459S |
probably damaging |
Het |
Stfa1 |
A |
G |
16: 36,097,363 (GRCm39) |
|
probably null |
Het |
Tmx3 |
T |
A |
18: 90,545,918 (GRCm39) |
|
probably null |
Het |
Unc93a |
A |
T |
17: 13,328,639 (GRCm39) |
F405I |
possibly damaging |
Het |
Vmn1r209 |
T |
A |
13: 22,990,664 (GRCm39) |
I9F |
possibly damaging |
Het |
Vmn2r93 |
A |
G |
17: 18,533,482 (GRCm39) |
D462G |
probably damaging |
Het |
Wdr90 |
T |
A |
17: 26,080,465 (GRCm39) |
|
probably benign |
Het |
Zfp551 |
T |
C |
7: 12,152,535 (GRCm39) |
D66G |
probably damaging |
Het |
Znrf4 |
A |
C |
17: 56,819,247 (GRCm39) |
V20G |
possibly damaging |
Het |
Zscan4d |
T |
C |
7: 10,896,770 (GRCm39) |
E200G |
probably benign |
Het |
Zup1 |
A |
T |
10: 33,797,698 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Tmem156 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00538:Tmem156
|
APN |
5 |
65,231,183 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01064:Tmem156
|
APN |
5 |
65,237,327 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01330:Tmem156
|
APN |
5 |
65,237,525 (GRCm39) |
missense |
probably benign |
0.17 |
IGL03336:Tmem156
|
APN |
5 |
65,233,107 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03383:Tmem156
|
APN |
5 |
65,233,040 (GRCm39) |
missense |
probably damaging |
0.98 |
R0526:Tmem156
|
UTSW |
5 |
65,233,161 (GRCm39) |
missense |
probably benign |
0.02 |
R2006:Tmem156
|
UTSW |
5 |
65,237,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R4721:Tmem156
|
UTSW |
5 |
65,248,870 (GRCm39) |
missense |
probably benign |
0.10 |
R4773:Tmem156
|
UTSW |
5 |
65,237,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R4810:Tmem156
|
UTSW |
5 |
65,248,790 (GRCm39) |
intron |
probably benign |
|
R4910:Tmem156
|
UTSW |
5 |
65,248,805 (GRCm39) |
intron |
probably benign |
|
R5148:Tmem156
|
UTSW |
5 |
65,231,111 (GRCm39) |
missense |
probably benign |
0.00 |
R5510:Tmem156
|
UTSW |
5 |
65,232,917 (GRCm39) |
missense |
probably benign |
0.02 |
R5809:Tmem156
|
UTSW |
5 |
65,232,950 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6033:Tmem156
|
UTSW |
5 |
65,232,964 (GRCm39) |
missense |
probably benign |
0.35 |
R6033:Tmem156
|
UTSW |
5 |
65,232,964 (GRCm39) |
missense |
probably benign |
0.35 |
R7731:Tmem156
|
UTSW |
5 |
65,232,905 (GRCm39) |
critical splice donor site |
probably null |
|
R7788:Tmem156
|
UTSW |
5 |
65,232,912 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7979:Tmem156
|
UTSW |
5 |
65,237,352 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8017:Tmem156
|
UTSW |
5 |
65,231,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R8132:Tmem156
|
UTSW |
5 |
65,233,098 (GRCm39) |
missense |
probably benign |
0.00 |
R8249:Tmem156
|
UTSW |
5 |
65,232,969 (GRCm39) |
nonsense |
probably null |
|
R8492:Tmem156
|
UTSW |
5 |
65,222,438 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9209:Tmem156
|
UTSW |
5 |
65,231,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R9287:Tmem156
|
UTSW |
5 |
65,231,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R9468:Tmem156
|
UTSW |
5 |
65,237,531 (GRCm39) |
missense |
probably damaging |
0.99 |
R9470:Tmem156
|
UTSW |
5 |
65,237,531 (GRCm39) |
missense |
probably damaging |
0.99 |
R9471:Tmem156
|
UTSW |
5 |
65,237,531 (GRCm39) |
missense |
probably damaging |
0.99 |
R9696:Tmem156
|
UTSW |
5 |
65,231,147 (GRCm39) |
missense |
possibly damaging |
0.83 |
RF020:Tmem156
|
UTSW |
5 |
65,248,890 (GRCm39) |
missense |
probably benign |
0.34 |
|