Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930111J21Rik1 |
A |
G |
11: 48,838,302 (GRCm39) |
F762L |
probably benign |
Het |
Angpt1 |
T |
A |
15: 42,359,808 (GRCm39) |
E208V |
possibly damaging |
Het |
Arhgef18 |
A |
T |
8: 3,438,023 (GRCm39) |
I286F |
probably benign |
Het |
Arhgef5 |
T |
C |
6: 43,250,934 (GRCm39) |
S562P |
possibly damaging |
Het |
Asb6 |
T |
C |
2: 30,714,496 (GRCm39) |
T205A |
probably benign |
Het |
B4galnt4 |
G |
A |
7: 140,647,354 (GRCm39) |
|
probably null |
Het |
Clca4a |
A |
T |
3: 144,659,627 (GRCm39) |
M743K |
probably benign |
Het |
Col14a1 |
T |
C |
15: 55,312,217 (GRCm39) |
|
probably benign |
Het |
Col27a1 |
A |
T |
4: 63,232,959 (GRCm39) |
Y359F |
probably damaging |
Het |
Dhcr7 |
T |
A |
7: 143,394,234 (GRCm39) |
V125D |
possibly damaging |
Het |
Ercc3 |
T |
C |
18: 32,373,890 (GRCm39) |
|
probably null |
Het |
Fnbp1l |
A |
G |
3: 122,351,598 (GRCm39) |
V315A |
probably benign |
Het |
Gm17174 |
T |
A |
14: 51,829,420 (GRCm39) |
R48* |
probably null |
Het |
Grin1 |
C |
T |
2: 25,188,405 (GRCm39) |
|
probably null |
Het |
Ifi203 |
T |
A |
1: 173,765,401 (GRCm39) |
K58* |
probably null |
Het |
Ighv2-9-1 |
A |
G |
12: 113,733,543 (GRCm39) |
S93P |
probably benign |
Het |
Il27ra |
A |
G |
8: 84,757,751 (GRCm39) |
V594A |
probably benign |
Het |
Krr1 |
T |
G |
10: 111,815,959 (GRCm39) |
S275R |
probably benign |
Het |
Lars1 |
T |
C |
18: 42,354,571 (GRCm39) |
D792G |
probably benign |
Het |
Myo1f |
G |
A |
17: 33,817,168 (GRCm39) |
R737H |
probably damaging |
Het |
Nebl |
T |
A |
2: 17,418,522 (GRCm39) |
H292L |
probably damaging |
Het |
Nell1 |
C |
A |
7: 49,712,359 (GRCm39) |
|
probably null |
Het |
Nktr |
T |
C |
9: 121,577,242 (GRCm39) |
F412L |
probably benign |
Het |
Nlrp3 |
T |
A |
11: 59,439,842 (GRCm39) |
I473N |
probably damaging |
Het |
Or1j10 |
T |
C |
2: 36,267,063 (GRCm39) |
Y92H |
possibly damaging |
Het |
Phf3 |
A |
G |
1: 30,844,810 (GRCm39) |
V1383A |
probably damaging |
Het |
Prss48 |
T |
C |
3: 85,904,625 (GRCm39) |
E191G |
probably damaging |
Het |
Psg25 |
T |
A |
7: 18,263,699 (GRCm39) |
L41F |
probably benign |
Het |
Sema3b |
A |
G |
9: 107,481,276 (GRCm39) |
L78P |
probably damaging |
Het |
Spen |
G |
T |
4: 141,197,280 (GRCm39) |
N3496K |
probably damaging |
Het |
Tbk1 |
A |
T |
10: 121,420,104 (GRCm39) |
H28Q |
possibly damaging |
Het |
Trpv3 |
T |
A |
11: 73,172,491 (GRCm39) |
|
probably benign |
Het |
Vmn1r218 |
T |
C |
13: 23,320,788 (GRCm39) |
L45P |
probably damaging |
Het |
Vmn2r35 |
T |
A |
7: 7,789,493 (GRCm39) |
Y748F |
probably damaging |
Het |
Vps18 |
C |
T |
2: 119,127,963 (GRCm39) |
R929W |
probably damaging |
Het |
Xpnpep1 |
T |
C |
19: 52,998,577 (GRCm39) |
K224E |
probably damaging |
Het |
Zbed5 |
T |
A |
5: 129,931,196 (GRCm39) |
F382I |
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 |
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 |
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 |
|