Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A130010J15Rik |
A |
G |
1: 192,857,109 (GRCm39) |
T154A |
probably benign |
Het |
Acox1 |
A |
G |
11: 116,065,331 (GRCm39) |
|
probably benign |
Het |
Adgrg2 |
G |
A |
X: 159,268,773 (GRCm39) |
V677I |
probably benign |
Het |
Aifm1 |
T |
C |
X: 47,570,976 (GRCm39) |
T386A |
probably benign |
Het |
Aspm |
T |
C |
1: 139,415,160 (GRCm39) |
|
probably benign |
Het |
Fgfr2 |
A |
G |
7: 129,830,453 (GRCm39) |
V175A |
probably damaging |
Het |
Gm382 |
T |
C |
X: 125,970,775 (GRCm39) |
Y987H |
probably benign |
Het |
Hmgxb3 |
A |
G |
18: 61,290,811 (GRCm39) |
V354A |
probably benign |
Het |
Ifne |
T |
C |
4: 88,798,041 (GRCm39) |
N126D |
probably benign |
Het |
Igkv3-7 |
T |
C |
6: 70,584,807 (GRCm39) |
V49A |
possibly damaging |
Het |
Kbtbd8 |
A |
T |
6: 95,103,494 (GRCm39) |
Y381F |
probably damaging |
Het |
Klc1 |
C |
T |
12: 111,743,318 (GRCm39) |
T215M |
probably damaging |
Het |
Lrp2 |
A |
T |
2: 69,316,624 (GRCm39) |
V2119E |
probably benign |
Het |
Lrrc7 |
A |
G |
3: 157,892,647 (GRCm39) |
V322A |
probably benign |
Het |
Mageb5b |
C |
T |
X: 90,679,091 (GRCm39) |
Q348* |
probably null |
Het |
Ms4a14 |
A |
G |
19: 11,278,983 (GRCm39) |
S1192P |
possibly damaging |
Het |
Ndufaf6 |
T |
C |
4: 11,062,127 (GRCm39) |
Y168C |
probably damaging |
Het |
Plcg2 |
C |
T |
8: 118,282,810 (GRCm39) |
T97I |
possibly damaging |
Het |
Rasgrp4 |
T |
C |
7: 28,847,966 (GRCm39) |
|
probably benign |
Het |
Rgs22 |
T |
C |
15: 36,083,777 (GRCm39) |
H515R |
probably benign |
Het |
Rpn1 |
G |
T |
6: 88,072,611 (GRCm39) |
R318L |
probably damaging |
Het |
Shroom2 |
A |
T |
X: 151,396,512 (GRCm39) |
F1359Y |
probably damaging |
Het |
Tars3 |
T |
A |
7: 65,325,880 (GRCm39) |
|
probably null |
Het |
Tbc1d12 |
A |
G |
19: 38,884,487 (GRCm39) |
E346G |
possibly damaging |
Het |
Tbccd1 |
A |
G |
16: 22,641,294 (GRCm39) |
F361S |
possibly damaging |
Het |
Tenm1 |
G |
T |
X: 41,803,913 (GRCm39) |
P837T |
probably benign |
Het |
Tmem144 |
A |
G |
3: 79,746,474 (GRCm39) |
V27A |
probably benign |
Het |
Zfp616 |
T |
A |
11: 73,973,789 (GRCm39) |
N19K |
possibly damaging |
Het |
Zkscan7 |
T |
C |
9: 122,724,659 (GRCm39) |
Y543H |
possibly 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 |
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 |
IGL01015:Golga3
|
APN |
5 |
110,335,583 (GRCm39) |
missense |
probably benign |
0.04 |
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 |
|