Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi3bp |
G |
A |
16: 56,440,867 (GRCm39) |
V701M |
unknown |
Het |
Adam2 |
G |
A |
14: 66,267,238 (GRCm39) |
P674S |
probably benign |
Het |
Adam24 |
T |
A |
8: 41,133,674 (GRCm39) |
Y381N |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,251,491 (GRCm39) |
S6209P |
probably damaging |
Het |
Aox4 |
A |
T |
1: 58,285,028 (GRCm39) |
K593N |
possibly damaging |
Het |
Aqp3 |
A |
G |
4: 41,093,640 (GRCm39) |
V258A |
possibly damaging |
Het |
Atg16l1 |
T |
A |
1: 87,707,906 (GRCm39) |
F390I |
possibly damaging |
Het |
B4galt6 |
T |
A |
18: 20,825,509 (GRCm39) |
Y239F |
possibly damaging |
Het |
Cmtr2 |
T |
C |
8: 110,948,977 (GRCm39) |
M429T |
probably benign |
Het |
Col5a2 |
C |
G |
1: 45,478,029 (GRCm39) |
|
probably null |
Het |
Dcc |
T |
C |
18: 71,815,249 (GRCm39) |
D375G |
possibly damaging |
Het |
Dnah14 |
T |
C |
1: 181,642,077 (GRCm39) |
Y31H |
|
Het |
Fam131a |
G |
A |
16: 20,520,243 (GRCm39) |
R232H |
possibly damaging |
Het |
Fam186a |
A |
G |
15: 99,839,879 (GRCm39) |
Y2122H |
probably damaging |
Het |
Focad |
A |
T |
4: 88,115,059 (GRCm39) |
I421F |
unknown |
Het |
Fscb |
T |
G |
12: 64,520,097 (GRCm39) |
E456D |
possibly damaging |
Het |
Furin |
C |
A |
7: 80,040,846 (GRCm39) |
S664I |
probably benign |
Het |
Ganc |
A |
G |
2: 120,290,381 (GRCm39) |
E906G |
probably benign |
Het |
Gdf5 |
C |
G |
2: 155,783,915 (GRCm39) |
D346H |
probably damaging |
Het |
Ifit1bl1 |
T |
C |
19: 34,571,908 (GRCm39) |
N183S |
probably benign |
Het |
Itpr1 |
T |
A |
6: 108,370,984 (GRCm39) |
F1084I |
probably damaging |
Het |
Katnal1 |
A |
T |
5: 148,831,021 (GRCm39) |
Y184* |
probably null |
Het |
Lrrc37a |
A |
G |
11: 103,391,633 (GRCm39) |
I1264T |
probably benign |
Het |
Map3k2 |
T |
A |
18: 32,342,805 (GRCm39) |
M234K |
probably damaging |
Het |
Mcm3ap |
T |
A |
10: 76,342,352 (GRCm39) |
V1615E |
probably damaging |
Het |
Mkrn2 |
A |
G |
6: 115,591,534 (GRCm39) |
|
probably null |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nradd |
T |
A |
9: 110,450,751 (GRCm39) |
Q142L |
possibly damaging |
Het |
Ophn1 |
G |
A |
X: 97,622,145 (GRCm39) |
T668M |
probably benign |
Het |
Or56b35 |
T |
C |
7: 104,963,781 (GRCm39) |
I190T |
probably benign |
Het |
Pdzd7 |
A |
G |
19: 45,028,622 (GRCm39) |
F174L |
probably damaging |
Het |
Pi4k2b |
C |
T |
5: 52,900,879 (GRCm39) |
T99I |
probably benign |
Het |
Pigv |
A |
T |
4: 133,391,973 (GRCm39) |
V399D |
probably damaging |
Het |
Pla2g4a |
C |
A |
1: 149,747,207 (GRCm39) |
L326F |
probably damaging |
Het |
Psmg1 |
T |
C |
16: 95,790,717 (GRCm39) |
I73M |
probably damaging |
Het |
Rcl1 |
T |
C |
19: 29,093,170 (GRCm39) |
S62P |
probably damaging |
Het |
Slc23a4 |
T |
A |
6: 34,955,861 (GRCm39) |
I58F |
probably damaging |
Het |
Slc36a2 |
G |
T |
11: 55,060,837 (GRCm39) |
T191K |
probably benign |
Het |
Sorbs2 |
T |
G |
8: 46,248,774 (GRCm39) |
V675G |
probably benign |
Het |
Tbc1d30 |
T |
C |
10: 121,142,128 (GRCm39) |
|
probably null |
Het |
Tbc1d4 |
A |
G |
14: 101,845,616 (GRCm39) |
V94A |
possibly damaging |
Het |
Tdrd5 |
T |
C |
1: 156,105,030 (GRCm39) |
Y532C |
probably benign |
Het |
Tll2 |
T |
A |
19: 41,074,772 (GRCm39) |
I931L |
probably benign |
Het |
Tlr3 |
T |
C |
8: 45,851,643 (GRCm39) |
N418S |
probably benign |
Het |
Tmco1 |
C |
T |
1: 167,136,132 (GRCm39) |
|
probably benign |
Het |
Tshr |
T |
A |
12: 91,474,518 (GRCm39) |
M164K |
possibly damaging |
Het |
Ttc21b |
A |
G |
2: 66,056,349 (GRCm39) |
V679A |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,730,861 (GRCm39) |
Y4951H |
unknown |
Het |
Usf1 |
T |
A |
1: 171,243,373 (GRCm39) |
V50D |
possibly damaging |
Het |
Utp6 |
A |
T |
11: 79,826,851 (GRCm39) |
M575K |
probably benign |
Het |
Vmn1r197 |
A |
T |
13: 22,512,608 (GRCm39) |
R176S |
possibly damaging |
Het |
Vmn2r104 |
A |
T |
17: 20,261,098 (GRCm39) |
F442I |
probably damaging |
Het |
Vmn2r94 |
A |
G |
17: 18,497,751 (GRCm39) |
F7S |
possibly damaging |
Het |
Vps41 |
G |
T |
13: 19,013,401 (GRCm39) |
E340* |
probably null |
Het |
|
Other mutations in Golga4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00711:Golga4
|
APN |
9 |
118,343,339 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00801:Golga4
|
APN |
9 |
118,367,994 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01395:Golga4
|
APN |
9 |
118,364,441 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01472:Golga4
|
APN |
9 |
118,361,642 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01519:Golga4
|
APN |
9 |
118,356,160 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01563:Golga4
|
APN |
9 |
118,356,074 (GRCm39) |
splice site |
probably benign |
|
IGL02593:Golga4
|
APN |
9 |
118,384,634 (GRCm39) |
unclassified |
probably benign |
|
IGL02803:Golga4
|
APN |
9 |
118,364,528 (GRCm39) |
missense |
probably benign |
|
IGL02939:Golga4
|
APN |
9 |
118,363,700 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Golga4
|
APN |
9 |
118,364,522 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03123:Golga4
|
APN |
9 |
118,365,953 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03334:Golga4
|
APN |
9 |
118,366,301 (GRCm39) |
splice site |
probably benign |
|
F5770:Golga4
|
UTSW |
9 |
118,385,143 (GRCm39) |
missense |
possibly damaging |
0.62 |
F6893:Golga4
|
UTSW |
9 |
118,382,525 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4382001:Golga4
|
UTSW |
9 |
118,382,521 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0179:Golga4
|
UTSW |
9 |
118,389,808 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0279:Golga4
|
UTSW |
9 |
118,398,061 (GRCm39) |
missense |
probably benign |
0.00 |
R0362:Golga4
|
UTSW |
9 |
118,384,853 (GRCm39) |
missense |
probably benign |
0.13 |
R0973:Golga4
|
UTSW |
9 |
118,366,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Golga4
|
UTSW |
9 |
118,366,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R0974:Golga4
|
UTSW |
9 |
118,366,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R1128:Golga4
|
UTSW |
9 |
118,377,852 (GRCm39) |
missense |
probably benign |
0.40 |
R1384:Golga4
|
UTSW |
9 |
118,394,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R1435:Golga4
|
UTSW |
9 |
118,364,508 (GRCm39) |
missense |
probably benign |
0.00 |
R1513:Golga4
|
UTSW |
9 |
118,384,800 (GRCm39) |
missense |
probably benign |
0.02 |
R1818:Golga4
|
UTSW |
9 |
118,402,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R2083:Golga4
|
UTSW |
9 |
118,361,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R2243:Golga4
|
UTSW |
9 |
118,385,972 (GRCm39) |
missense |
probably benign |
0.06 |
R2355:Golga4
|
UTSW |
9 |
118,389,810 (GRCm39) |
missense |
probably benign |
0.00 |
R2518:Golga4
|
UTSW |
9 |
118,385,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R2921:Golga4
|
UTSW |
9 |
118,388,411 (GRCm39) |
missense |
possibly damaging |
0.49 |
R2922:Golga4
|
UTSW |
9 |
118,388,411 (GRCm39) |
missense |
possibly damaging |
0.49 |
R2923:Golga4
|
UTSW |
9 |
118,388,411 (GRCm39) |
missense |
possibly damaging |
0.49 |
R3121:Golga4
|
UTSW |
9 |
118,386,448 (GRCm39) |
missense |
possibly damaging |
0.68 |
R3424:Golga4
|
UTSW |
9 |
118,363,715 (GRCm39) |
missense |
probably benign |
0.16 |
R3909:Golga4
|
UTSW |
9 |
118,387,804 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3913:Golga4
|
UTSW |
9 |
118,368,039 (GRCm39) |
missense |
probably damaging |
0.99 |
R4321:Golga4
|
UTSW |
9 |
118,385,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R4358:Golga4
|
UTSW |
9 |
118,380,946 (GRCm39) |
missense |
probably benign |
0.16 |
R4483:Golga4
|
UTSW |
9 |
118,343,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R4515:Golga4
|
UTSW |
9 |
118,388,076 (GRCm39) |
missense |
probably benign |
0.28 |
R4518:Golga4
|
UTSW |
9 |
118,388,076 (GRCm39) |
missense |
probably benign |
0.28 |
R4519:Golga4
|
UTSW |
9 |
118,388,076 (GRCm39) |
missense |
probably benign |
0.28 |
R4545:Golga4
|
UTSW |
9 |
118,385,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R4546:Golga4
|
UTSW |
9 |
118,385,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R4580:Golga4
|
UTSW |
9 |
118,386,327 (GRCm39) |
missense |
probably benign |
0.00 |
R4918:Golga4
|
UTSW |
9 |
118,387,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R5007:Golga4
|
UTSW |
9 |
118,387,368 (GRCm39) |
missense |
probably benign |
|
R5045:Golga4
|
UTSW |
9 |
118,394,724 (GRCm39) |
missense |
probably benign |
|
R5232:Golga4
|
UTSW |
9 |
118,335,626 (GRCm39) |
critical splice donor site |
probably null |
|
R5256:Golga4
|
UTSW |
9 |
118,385,569 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5502:Golga4
|
UTSW |
9 |
118,388,125 (GRCm39) |
nonsense |
probably null |
|
R5567:Golga4
|
UTSW |
9 |
118,387,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R5576:Golga4
|
UTSW |
9 |
118,382,602 (GRCm39) |
missense |
probably benign |
0.13 |
R5771:Golga4
|
UTSW |
9 |
118,387,351 (GRCm39) |
missense |
probably damaging |
0.96 |
R5807:Golga4
|
UTSW |
9 |
118,356,198 (GRCm39) |
missense |
probably damaging |
0.99 |
R5860:Golga4
|
UTSW |
9 |
118,387,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R6012:Golga4
|
UTSW |
9 |
118,388,764 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6285:Golga4
|
UTSW |
9 |
118,387,695 (GRCm39) |
nonsense |
probably null |
|
R6299:Golga4
|
UTSW |
9 |
118,386,438 (GRCm39) |
missense |
probably benign |
0.03 |
R6467:Golga4
|
UTSW |
9 |
118,365,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R6552:Golga4
|
UTSW |
9 |
118,343,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R6688:Golga4
|
UTSW |
9 |
118,343,278 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6965:Golga4
|
UTSW |
9 |
118,377,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R6987:Golga4
|
UTSW |
9 |
118,387,600 (GRCm39) |
missense |
probably benign |
|
R7212:Golga4
|
UTSW |
9 |
118,365,908 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7426:Golga4
|
UTSW |
9 |
118,388,563 (GRCm39) |
missense |
probably benign |
|
R7431:Golga4
|
UTSW |
9 |
118,388,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R7641:Golga4
|
UTSW |
9 |
118,386,643 (GRCm39) |
missense |
probably benign |
0.05 |
R7727:Golga4
|
UTSW |
9 |
118,377,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R7729:Golga4
|
UTSW |
9 |
118,385,131 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7811:Golga4
|
UTSW |
9 |
118,361,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R7849:Golga4
|
UTSW |
9 |
118,388,379 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7891:Golga4
|
UTSW |
9 |
118,385,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R7976:Golga4
|
UTSW |
9 |
118,365,836 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8275:Golga4
|
UTSW |
9 |
118,361,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R8378:Golga4
|
UTSW |
9 |
118,387,390 (GRCm39) |
missense |
probably benign |
0.03 |
R8514:Golga4
|
UTSW |
9 |
118,384,864 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8698:Golga4
|
UTSW |
9 |
118,385,029 (GRCm39) |
missense |
probably damaging |
0.97 |
R8856:Golga4
|
UTSW |
9 |
118,385,779 (GRCm39) |
missense |
probably damaging |
0.98 |
R9227:Golga4
|
UTSW |
9 |
118,385,941 (GRCm39) |
missense |
possibly damaging |
0.94 |
RF022:Golga4
|
UTSW |
9 |
118,387,057 (GRCm39) |
missense |
probably damaging |
1.00 |
V7583:Golga4
|
UTSW |
9 |
118,385,143 (GRCm39) |
missense |
possibly damaging |
0.62 |
|