Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Aff2 |
T |
A |
X: 68,907,543 (GRCm39) |
V1175E |
possibly damaging |
Het |
Agbl3 |
A |
G |
6: 34,800,022 (GRCm39) |
|
probably null |
Het |
Bcar3 |
C |
A |
3: 122,318,645 (GRCm39) |
Q678K |
probably benign |
Het |
Ccm2 |
G |
A |
11: 6,520,090 (GRCm39) |
V53I |
probably benign |
Het |
Cd3e |
G |
T |
9: 44,913,608 (GRCm39) |
C42* |
probably null |
Het |
Cd4 |
A |
T |
6: 124,844,633 (GRCm39) |
I384N |
probably benign |
Het |
Ceacam11 |
T |
A |
7: 17,707,379 (GRCm39) |
F54L |
probably benign |
Het |
Cfap46 |
A |
G |
7: 139,197,506 (GRCm39) |
S2122P |
probably damaging |
Het |
Clptm1 |
A |
G |
7: 19,369,271 (GRCm39) |
S461P |
probably damaging |
Het |
Dlat |
T |
C |
9: 50,549,331 (GRCm39) |
T518A |
possibly damaging |
Het |
Dnah17 |
T |
C |
11: 117,985,680 (GRCm39) |
T1466A |
probably benign |
Het |
Dnah9 |
G |
A |
11: 65,845,815 (GRCm39) |
T3023I |
probably benign |
Het |
Fam181a |
T |
G |
12: 103,282,348 (GRCm39) |
C84W |
possibly damaging |
Het |
Gask1a |
C |
T |
9: 121,793,935 (GRCm39) |
P30S |
possibly damaging |
Het |
H2-Q6 |
C |
A |
17: 35,644,676 (GRCm39) |
T155K |
probably damaging |
Het |
Hlx |
G |
T |
1: 184,464,184 (GRCm39) |
A52D |
probably damaging |
Het |
Inpp5b |
A |
G |
4: 124,674,279 (GRCm39) |
R329G |
probably benign |
Het |
Klrb1f |
A |
T |
6: 129,031,306 (GRCm39) |
I168L |
possibly damaging |
Het |
Lama4 |
A |
T |
10: 38,973,175 (GRCm39) |
I1581F |
probably damaging |
Het |
Lipn |
A |
G |
19: 34,046,138 (GRCm39) |
N37S |
probably benign |
Het |
Lyzl4 |
T |
C |
9: 121,413,233 (GRCm39) |
D65G |
probably benign |
Het |
Med29 |
A |
G |
7: 28,092,046 (GRCm39) |
|
probably benign |
Het |
Myrip |
C |
A |
9: 120,270,473 (GRCm39) |
D574E |
possibly damaging |
Het |
N4bp3 |
A |
T |
11: 51,536,761 (GRCm39) |
F104Y |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,270,810 (GRCm39) |
K892* |
probably null |
Het |
Nsd1 |
T |
A |
13: 55,460,701 (GRCm39) |
H2309Q |
possibly damaging |
Het |
Obscn |
T |
C |
11: 59,022,472 (GRCm39) |
R758G |
possibly damaging |
Het |
Optn |
T |
C |
2: 5,039,014 (GRCm39) |
S370G |
probably damaging |
Het |
Pbrm1 |
T |
C |
14: 30,754,432 (GRCm39) |
F151L |
probably damaging |
Het |
Plekhs1 |
A |
T |
19: 56,453,032 (GRCm39) |
|
probably null |
Het |
Rpn1 |
A |
G |
6: 88,080,396 (GRCm39) |
K565R |
probably benign |
Het |
Rrh |
T |
C |
3: 129,605,360 (GRCm39) |
Y110C |
probably damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Ryr1 |
C |
T |
7: 28,769,075 (GRCm39) |
|
probably null |
Het |
Scai |
C |
T |
2: 39,040,326 (GRCm39) |
|
probably benign |
Het |
Scap |
C |
G |
9: 110,208,650 (GRCm39) |
P564A |
probably damaging |
Het |
Setdb1 |
A |
G |
3: 95,246,065 (GRCm39) |
V619A |
probably damaging |
Het |
Slf2 |
A |
G |
19: 44,930,773 (GRCm39) |
I617V |
probably benign |
Het |
Sned1 |
G |
A |
1: 93,186,725 (GRCm39) |
R180Q |
probably benign |
Het |
Spata22 |
T |
A |
11: 73,236,713 (GRCm39) |
F340I |
probably damaging |
Het |
St8sia3 |
T |
C |
18: 64,402,886 (GRCm39) |
F175S |
probably damaging |
Het |
Supt20 |
T |
C |
3: 54,616,501 (GRCm39) |
S253P |
possibly damaging |
Het |
Syngap1 |
T |
A |
17: 27,176,067 (GRCm39) |
Y118* |
probably null |
Het |
Szt2 |
A |
C |
4: 118,240,231 (GRCm39) |
|
probably null |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Uba3 |
G |
T |
6: 97,163,201 (GRCm39) |
T319K |
probably damaging |
Het |
Vmn2r112 |
T |
A |
17: 22,822,096 (GRCm39) |
V258E |
probably damaging |
Het |
Zc3hav1 |
A |
G |
6: 38,296,650 (GRCm39) |
L751S |
probably damaging |
Het |
Zfp804b |
T |
C |
5: 6,819,239 (GRCm39) |
M1275V |
probably benign |
Het |
Zgrf1 |
A |
G |
3: 127,407,024 (GRCm39) |
D1597G |
probably damaging |
Het |
|
Other mutations in Slc41a3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00948:Slc41a3
|
APN |
6 |
90,622,696 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02583:Slc41a3
|
APN |
6 |
90,621,153 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4378001:Slc41a3
|
UTSW |
6 |
90,617,891 (GRCm39) |
missense |
probably benign |
0.36 |
R1076:Slc41a3
|
UTSW |
6 |
90,621,142 (GRCm39) |
missense |
probably benign |
|
R1529:Slc41a3
|
UTSW |
6 |
90,621,198 (GRCm39) |
missense |
probably damaging |
0.99 |
R1591:Slc41a3
|
UTSW |
6 |
90,610,677 (GRCm39) |
missense |
probably benign |
0.02 |
R1985:Slc41a3
|
UTSW |
6 |
90,619,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R2133:Slc41a3
|
UTSW |
6 |
90,603,363 (GRCm39) |
missense |
probably damaging |
0.99 |
R2308:Slc41a3
|
UTSW |
6 |
90,589,102 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2384:Slc41a3
|
UTSW |
6 |
90,603,393 (GRCm39) |
missense |
probably damaging |
0.98 |
R2697:Slc41a3
|
UTSW |
6 |
90,619,302 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4287:Slc41a3
|
UTSW |
6 |
90,617,904 (GRCm39) |
missense |
probably benign |
0.00 |
R4394:Slc41a3
|
UTSW |
6 |
90,612,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R5039:Slc41a3
|
UTSW |
6 |
90,603,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R5195:Slc41a3
|
UTSW |
6 |
90,610,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R5293:Slc41a3
|
UTSW |
6 |
90,603,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R5338:Slc41a3
|
UTSW |
6 |
90,589,153 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5608:Slc41a3
|
UTSW |
6 |
90,617,889 (GRCm39) |
missense |
probably benign |
0.06 |
R5681:Slc41a3
|
UTSW |
6 |
90,617,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R5783:Slc41a3
|
UTSW |
6 |
90,596,524 (GRCm39) |
missense |
probably benign |
0.06 |
R6648:Slc41a3
|
UTSW |
6 |
90,596,490 (GRCm39) |
missense |
probably damaging |
0.99 |
R7867:Slc41a3
|
UTSW |
6 |
90,617,909 (GRCm39) |
missense |
probably damaging |
0.96 |
R8733:Slc41a3
|
UTSW |
6 |
90,610,710 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8776:Slc41a3
|
UTSW |
6 |
90,621,165 (GRCm39) |
missense |
probably benign |
0.06 |
R8776-TAIL:Slc41a3
|
UTSW |
6 |
90,621,165 (GRCm39) |
missense |
probably benign |
0.06 |
R8905:Slc41a3
|
UTSW |
6 |
90,589,123 (GRCm39) |
missense |
probably benign |
0.11 |
R9365:Slc41a3
|
UTSW |
6 |
90,612,327 (GRCm39) |
missense |
probably benign |
0.05 |
R9747:Slc41a3
|
UTSW |
6 |
90,621,138 (GRCm39) |
missense |
probably benign |
0.37 |
X0025:Slc41a3
|
UTSW |
6 |
90,612,304 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Slc41a3
|
UTSW |
6 |
90,596,555 (GRCm39) |
nonsense |
probably null |
|
|