Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ano4 |
A |
G |
10: 88,870,961 (GRCm39) |
Y238H |
probably damaging |
Het |
Apol7a |
T |
C |
15: 77,274,055 (GRCm39) |
|
probably benign |
Het |
Cacna1d |
A |
T |
14: 29,773,699 (GRCm39) |
|
probably benign |
Het |
Col12a1 |
A |
G |
9: 79,541,023 (GRCm39) |
V2368A |
probably damaging |
Het |
Creb3l4 |
A |
G |
3: 90,150,138 (GRCm39) |
M1T |
probably null |
Het |
Dpys |
T |
C |
15: 39,710,045 (GRCm39) |
D128G |
probably damaging |
Het |
Ero1b |
A |
G |
13: 12,616,623 (GRCm39) |
|
probably null |
Het |
Fcgbpl1 |
T |
C |
7: 27,854,743 (GRCm39) |
C1790R |
probably damaging |
Het |
Fcgr4 |
A |
G |
1: 170,853,358 (GRCm39) |
S188G |
possibly damaging |
Het |
Fry |
A |
G |
5: 150,346,252 (GRCm39) |
D1587G |
probably benign |
Het |
Gm43638 |
T |
A |
5: 87,634,473 (GRCm39) |
R45* |
probably null |
Het |
Gm7647 |
T |
A |
5: 95,111,746 (GRCm39) |
C152S |
probably benign |
Het |
Iqub |
A |
T |
6: 24,501,005 (GRCm39) |
|
probably benign |
Het |
Irak3 |
A |
T |
10: 119,978,695 (GRCm39) |
Y493* |
probably null |
Het |
Jakmip1 |
G |
T |
5: 37,242,750 (GRCm39) |
E13* |
probably null |
Het |
Morc3 |
G |
A |
16: 93,659,534 (GRCm39) |
C446Y |
probably damaging |
Het |
Mroh2b |
G |
A |
15: 4,971,024 (GRCm39) |
D1010N |
probably damaging |
Het |
Or14c44 |
A |
G |
7: 86,061,998 (GRCm39) |
T184A |
probably damaging |
Het |
Or2y16 |
T |
A |
11: 49,335,201 (GRCm39) |
N174K |
probably damaging |
Het |
Or5m9 |
A |
T |
2: 85,876,996 (GRCm39) |
M57L |
possibly damaging |
Het |
Pkhd1 |
G |
A |
1: 20,593,482 (GRCm39) |
H1544Y |
possibly damaging |
Het |
Rps2-ps10 |
C |
T |
18: 61,392,896 (GRCm39) |
|
probably benign |
Het |
Smco1 |
T |
C |
16: 32,092,887 (GRCm39) |
V186A |
probably damaging |
Het |
Snx1 |
C |
T |
9: 66,001,713 (GRCm39) |
E314K |
possibly damaging |
Het |
Timd2 |
T |
C |
11: 46,567,170 (GRCm39) |
Y255C |
probably benign |
Het |
Tnc |
A |
T |
4: 63,935,571 (GRCm39) |
I455K |
probably benign |
Het |
Tsc22d1 |
A |
G |
14: 76,656,181 (GRCm39) |
I31V |
possibly damaging |
Het |
Tyk2 |
A |
G |
9: 21,031,996 (GRCm39) |
S360P |
probably benign |
Het |
Uroc1 |
G |
T |
6: 90,335,883 (GRCm39) |
|
probably benign |
Het |
Vmn1r122 |
A |
T |
7: 20,867,761 (GRCm39) |
V98E |
probably damaging |
Het |
|
Other mutations in Golga3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Golga3
|
APN |
5 |
110,368,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00594:Golga3
|
APN |
5 |
110,352,841 (GRCm39) |
missense |
probably benign |
0.37 |
IGL00672:Golga3
|
APN |
5 |
110,360,110 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00821:Golga3
|
APN |
5 |
110,352,799 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL01408:Golga3
|
APN |
5 |
110,365,675 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01651:Golga3
|
APN |
5 |
110,340,771 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02617:Golga3
|
APN |
5 |
110,336,612 (GRCm39) |
missense |
probably benign |
0.26 |
cles
|
UTSW |
5 |
110,336,573 (GRCm39) |
nonsense |
probably null |
|
tenta
|
UTSW |
5 |
110,365,996 (GRCm39) |
nonsense |
probably null |
|
PIT4544001:Golga3
|
UTSW |
5 |
110,336,556 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0058:Golga3
|
UTSW |
5 |
110,350,643 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0058:Golga3
|
UTSW |
5 |
110,350,643 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0591:Golga3
|
UTSW |
5 |
110,336,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R1219:Golga3
|
UTSW |
5 |
110,332,215 (GRCm39) |
nonsense |
probably null |
|
R1297:Golga3
|
UTSW |
5 |
110,352,709 (GRCm39) |
missense |
probably benign |
0.04 |
R1299:Golga3
|
UTSW |
5 |
110,352,709 (GRCm39) |
missense |
probably benign |
0.04 |
R1465:Golga3
|
UTSW |
5 |
110,357,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Golga3
|
UTSW |
5 |
110,357,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R1589:Golga3
|
UTSW |
5 |
110,329,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R1795:Golga3
|
UTSW |
5 |
110,355,493 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1992:Golga3
|
UTSW |
5 |
110,340,839 (GRCm39) |
missense |
probably damaging |
0.96 |
R2116:Golga3
|
UTSW |
5 |
110,335,261 (GRCm39) |
missense |
probably damaging |
0.97 |
R2130:Golga3
|
UTSW |
5 |
110,350,805 (GRCm39) |
critical splice donor site |
probably null |
|
R2153:Golga3
|
UTSW |
5 |
110,335,856 (GRCm39) |
splice site |
probably null |
|
R2158:Golga3
|
UTSW |
5 |
110,335,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R2357:Golga3
|
UTSW |
5 |
110,350,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R2397:Golga3
|
UTSW |
5 |
110,353,743 (GRCm39) |
splice site |
probably benign |
|
R2418:Golga3
|
UTSW |
5 |
110,349,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R2495:Golga3
|
UTSW |
5 |
110,355,462 (GRCm39) |
missense |
probably damaging |
0.99 |
R2763:Golga3
|
UTSW |
5 |
110,352,761 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3276:Golga3
|
UTSW |
5 |
110,349,864 (GRCm39) |
splice site |
probably benign |
|
R3614:Golga3
|
UTSW |
5 |
110,368,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R4520:Golga3
|
UTSW |
5 |
110,351,617 (GRCm39) |
nonsense |
probably null |
|
R5001:Golga3
|
UTSW |
5 |
110,353,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R5046:Golga3
|
UTSW |
5 |
110,340,806 (GRCm39) |
missense |
probably damaging |
0.99 |
R5157:Golga3
|
UTSW |
5 |
110,350,537 (GRCm39) |
missense |
probably benign |
0.00 |
R5191:Golga3
|
UTSW |
5 |
110,332,173 (GRCm39) |
intron |
probably benign |
|
R5376:Golga3
|
UTSW |
5 |
110,368,811 (GRCm39) |
critical splice donor site |
probably null |
|
R5399:Golga3
|
UTSW |
5 |
110,352,890 (GRCm39) |
missense |
probably damaging |
0.96 |
R5407:Golga3
|
UTSW |
5 |
110,349,856 (GRCm39) |
nonsense |
probably null |
|
R5884:Golga3
|
UTSW |
5 |
110,364,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R6087:Golga3
|
UTSW |
5 |
110,352,812 (GRCm39) |
missense |
probably damaging |
0.99 |
R6526:Golga3
|
UTSW |
5 |
110,352,761 (GRCm39) |
missense |
probably damaging |
0.98 |
R6651:Golga3
|
UTSW |
5 |
110,365,996 (GRCm39) |
nonsense |
probably null |
|
R7041:Golga3
|
UTSW |
5 |
110,356,450 (GRCm39) |
critical splice donor site |
probably null |
|
R7057:Golga3
|
UTSW |
5 |
110,336,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R7078:Golga3
|
UTSW |
5 |
110,340,953 (GRCm39) |
missense |
probably damaging |
0.99 |
R7114:Golga3
|
UTSW |
5 |
110,350,578 (GRCm39) |
missense |
probably benign |
0.01 |
R7190:Golga3
|
UTSW |
5 |
110,357,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R7405:Golga3
|
UTSW |
5 |
110,356,312 (GRCm39) |
missense |
probably damaging |
0.97 |
R7528:Golga3
|
UTSW |
5 |
110,360,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R7638:Golga3
|
UTSW |
5 |
110,353,694 (GRCm39) |
missense |
probably benign |
|
R7760:Golga3
|
UTSW |
5 |
110,353,716 (GRCm39) |
missense |
probably benign |
0.39 |
R8099:Golga3
|
UTSW |
5 |
110,336,573 (GRCm39) |
nonsense |
probably null |
|
R8144:Golga3
|
UTSW |
5 |
110,333,745 (GRCm39) |
missense |
probably damaging |
0.99 |
R8558:Golga3
|
UTSW |
5 |
110,356,421 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8708:Golga3
|
UTSW |
5 |
110,350,721 (GRCm39) |
missense |
probably benign |
0.05 |
R8887:Golga3
|
UTSW |
5 |
110,353,626 (GRCm39) |
intron |
probably benign |
|
R9039:Golga3
|
UTSW |
5 |
110,352,799 (GRCm39) |
missense |
probably benign |
0.00 |
R9045:Golga3
|
UTSW |
5 |
110,340,963 (GRCm39) |
missense |
probably benign |
0.00 |
R9057:Golga3
|
UTSW |
5 |
110,332,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R9100:Golga3
|
UTSW |
5 |
110,337,544 (GRCm39) |
missense |
probably benign |
0.31 |
R9112:Golga3
|
UTSW |
5 |
110,333,757 (GRCm39) |
missense |
probably benign |
0.08 |
R9198:Golga3
|
UTSW |
5 |
110,355,619 (GRCm39) |
missense |
probably benign |
0.11 |
R9755:Golga3
|
UTSW |
5 |
110,340,847 (GRCm39) |
missense |
probably benign |
0.42 |
|