Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr1c20 |
A |
C |
13: 4,557,843 (GRCm39) |
V201G |
probably damaging |
Het |
Atf7 |
A |
G |
15: 102,442,762 (GRCm39) |
V449A |
probably benign |
Het |
Ccr1 |
G |
A |
9: 123,764,437 (GRCm39) |
A31V |
probably benign |
Het |
Chrna6 |
A |
T |
8: 27,896,711 (GRCm39) |
S389T |
probably benign |
Het |
Clic6 |
C |
T |
16: 92,289,045 (GRCm39) |
|
probably benign |
Het |
Cmya5 |
G |
A |
13: 93,228,426 (GRCm39) |
R2221* |
probably null |
Het |
Coq8b |
G |
T |
7: 26,932,930 (GRCm39) |
C13F |
probably benign |
Het |
Cspg4 |
T |
A |
9: 56,795,913 (GRCm39) |
L1216Q |
possibly damaging |
Het |
Decr1 |
C |
A |
4: 15,930,979 (GRCm39) |
V118F |
probably damaging |
Het |
Dlec1 |
A |
T |
9: 118,957,146 (GRCm39) |
I796F |
probably damaging |
Het |
Dnajc11 |
T |
A |
4: 152,064,398 (GRCm39) |
D516E |
probably damaging |
Het |
Dock8 |
G |
A |
19: 25,165,722 (GRCm39) |
V1869M |
probably damaging |
Het |
Dst |
A |
G |
1: 34,227,819 (GRCm39) |
D1982G |
probably damaging |
Het |
Gnptab |
G |
A |
10: 88,250,457 (GRCm39) |
D190N |
probably benign |
Het |
Hecw2 |
T |
C |
1: 53,852,381 (GRCm39) |
*1579W |
probably null |
Het |
Ica1l |
A |
G |
1: 60,052,977 (GRCm39) |
|
probably null |
Het |
Ift122 |
T |
A |
6: 115,867,549 (GRCm39) |
L433Q |
probably damaging |
Het |
Iqgap1 |
T |
C |
7: 80,412,315 (GRCm39) |
|
probably null |
Het |
Klra13-ps |
T |
C |
6: 130,268,232 (GRCm39) |
|
noncoding transcript |
Het |
Mndal |
A |
T |
1: 173,703,230 (GRCm39) |
Y58* |
probably null |
Het |
Mvb12b |
G |
C |
2: 33,717,712 (GRCm39) |
P172R |
possibly damaging |
Het |
Ncapg |
T |
C |
5: 45,828,554 (GRCm39) |
F102L |
probably damaging |
Het |
Or1e30 |
T |
C |
11: 73,677,992 (GRCm39) |
V76A |
probably damaging |
Het |
Or5an11 |
T |
C |
19: 12,246,188 (GRCm39) |
V198A |
possibly damaging |
Het |
Or5b97 |
T |
A |
19: 12,878,632 (GRCm39) |
K171* |
probably null |
Het |
Pde8a |
A |
T |
7: 80,977,847 (GRCm39) |
R713S |
probably damaging |
Het |
Rbks |
T |
C |
5: 31,781,912 (GRCm39) |
N296S |
probably benign |
Het |
Sema3c |
G |
A |
5: 17,899,770 (GRCm39) |
V421I |
probably benign |
Het |
Tm9sf1 |
A |
G |
14: 55,875,565 (GRCm39) |
V393A |
possibly damaging |
Het |
Tubgcp2 |
G |
A |
7: 139,575,984 (GRCm39) |
P893L |
possibly damaging |
Het |
Uba52rt |
C |
T |
4: 3,973,244 (GRCm39) |
R106H |
probably benign |
Het |
Vnn3 |
G |
A |
10: 23,732,224 (GRCm39) |
R158H |
probably benign |
Het |
Zfa-ps |
G |
T |
10: 52,421,032 (GRCm39) |
|
noncoding transcript |
Het |
Zfp414 |
T |
C |
17: 33,850,622 (GRCm39) |
|
probably benign |
Het |
Zfp810 |
G |
A |
9: 22,190,041 (GRCm39) |
T289I |
probably damaging |
Het |
Zfp819 |
G |
T |
7: 43,267,209 (GRCm39) |
R488L |
probably damaging |
Het |
Zfp942 |
C |
T |
17: 22,147,285 (GRCm39) |
G448D |
probably benign |
Het |
Zscan12 |
A |
G |
13: 21,550,875 (GRCm39) |
K165E |
possibly damaging |
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 |
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 |
R9282:Golga4
|
UTSW |
9 |
118,385,893 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|