Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
A |
G |
6: 121,654,995 (GRCm39) |
R1440G |
probably benign |
Het |
Abca13 |
T |
A |
11: 9,278,168 (GRCm39) |
L3116Q |
probably damaging |
Het |
Adgb |
G |
A |
10: 10,287,593 (GRCm39) |
H55Y |
probably damaging |
Het |
AI182371 |
G |
T |
2: 34,974,717 (GRCm39) |
|
probably benign |
Het |
Ank3 |
T |
C |
10: 69,827,412 (GRCm39) |
|
probably benign |
Het |
Ccdc127 |
G |
T |
13: 74,501,042 (GRCm39) |
G20W |
probably damaging |
Het |
Ccdc149 |
G |
A |
5: 52,562,475 (GRCm39) |
Q184* |
probably null |
Het |
Cntrob |
G |
A |
11: 69,213,749 (GRCm39) |
P14S |
probably damaging |
Het |
Dnah11 |
T |
C |
12: 118,077,629 (GRCm39) |
E1288G |
possibly damaging |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Evpl |
T |
C |
11: 116,113,640 (GRCm39) |
D1350G |
possibly damaging |
Het |
Fasn |
T |
C |
11: 120,701,279 (GRCm39) |
T1990A |
probably damaging |
Het |
Itga2 |
T |
A |
13: 114,973,061 (GRCm39) |
N1166I |
possibly damaging |
Het |
Lmtk2 |
T |
A |
5: 144,085,175 (GRCm39) |
C216S |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 41,361,132 (GRCm39) |
D557G |
probably benign |
Het |
Lrrc32 |
T |
C |
7: 98,148,039 (GRCm39) |
V273A |
probably benign |
Het |
Nlrp4f |
C |
T |
13: 65,335,254 (GRCm39) |
|
probably null |
Het |
Ntng2 |
T |
G |
2: 29,090,940 (GRCm39) |
M360L |
probably benign |
Het |
Pik3c2b |
A |
G |
1: 133,003,559 (GRCm39) |
S504G |
probably benign |
Het |
Ppfia4 |
A |
C |
1: 134,256,909 (GRCm39) |
L104R |
probably damaging |
Het |
Raph1 |
A |
G |
1: 60,564,879 (GRCm39) |
S203P |
probably damaging |
Het |
Rbl1 |
G |
A |
2: 157,011,918 (GRCm39) |
T679I |
probably benign |
Het |
Rnase4 |
G |
T |
14: 51,342,486 (GRCm39) |
R70L |
probably benign |
Het |
Rnf146 |
A |
C |
10: 29,223,528 (GRCm39) |
D119E |
probably damaging |
Het |
Rrp1b |
A |
G |
17: 32,275,908 (GRCm39) |
H485R |
probably benign |
Het |
Rwdd4a |
T |
A |
8: 48,000,998 (GRCm39) |
|
probably null |
Het |
Scarf2 |
G |
A |
16: 17,624,351 (GRCm39) |
C552Y |
probably damaging |
Het |
Skic2 |
G |
A |
17: 35,064,166 (GRCm39) |
R507* |
probably null |
Het |
Sox10 |
T |
C |
15: 79,040,676 (GRCm39) |
N127S |
probably damaging |
Het |
Tars1 |
A |
T |
15: 11,394,427 (GRCm39) |
I70N |
probably damaging |
Het |
Thsd7a |
C |
T |
6: 12,408,815 (GRCm39) |
V736M |
probably damaging |
Het |
Timp3 |
G |
A |
10: 86,136,742 (GRCm39) |
V9M |
probably benign |
Het |
Tnfrsf1a |
A |
T |
6: 125,333,911 (GRCm39) |
N55Y |
probably damaging |
Het |
Trim43a |
G |
A |
9: 88,470,399 (GRCm39) |
V402I |
possibly damaging |
Het |
Tshz2 |
A |
G |
2: 169,725,677 (GRCm39) |
D91G |
probably damaging |
Het |
Ubac1 |
T |
C |
2: 25,895,418 (GRCm39) |
D345G |
possibly damaging |
Het |
Usp4 |
G |
A |
9: 108,251,438 (GRCm39) |
V538I |
possibly damaging |
Het |
Vmn2r19 |
A |
T |
6: 123,306,917 (GRCm39) |
Y475F |
possibly damaging |
Het |
Vmn2r87 |
A |
T |
10: 130,308,396 (GRCm39) |
V614E |
probably damaging |
Het |
Wfdc2 |
A |
T |
2: 164,404,706 (GRCm39) |
T21S |
probably benign |
Het |
Yod1 |
G |
A |
1: 130,645,275 (GRCm39) |
G19S |
probably damaging |
Het |
Zfp78 |
A |
G |
7: 6,381,277 (GRCm39) |
E109G |
probably damaging |
Het |
Zfp873 |
C |
A |
10: 81,894,256 (GRCm39) |
A19D |
probably damaging |
Het |
Zfp935 |
T |
A |
13: 62,602,293 (GRCm39) |
K302N |
probably damaging |
Het |
Zfpm2 |
G |
A |
15: 40,965,114 (GRCm39) |
S401N |
probably benign |
Het |
|
Other mutations in Speer4a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01783:Speer4a1
|
APN |
5 |
26,240,045 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01959:Speer4a1
|
APN |
5 |
26,240,902 (GRCm39) |
nonsense |
probably null |
|
IGL02294:Speer4a1
|
APN |
5 |
26,243,240 (GRCm39) |
missense |
probably benign |
0.21 |
FR4340:Speer4a1
|
UTSW |
5 |
26,241,746 (GRCm39) |
nonsense |
probably null |
|
FR4342:Speer4a1
|
UTSW |
5 |
26,241,746 (GRCm39) |
nonsense |
probably null |
|
FR4589:Speer4a1
|
UTSW |
5 |
26,241,746 (GRCm39) |
nonsense |
probably null |
|
R0137:Speer4a1
|
UTSW |
5 |
26,240,982 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1068:Speer4a1
|
UTSW |
5 |
26,241,024 (GRCm39) |
missense |
probably null |
0.84 |
R1209:Speer4a1
|
UTSW |
5 |
26,240,123 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3805:Speer4a1
|
UTSW |
5 |
26,240,082 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4525:Speer4a1
|
UTSW |
5 |
26,244,341 (GRCm39) |
critical splice donor site |
probably null |
|
R4851:Speer4a1
|
UTSW |
5 |
26,243,210 (GRCm39) |
missense |
probably damaging |
0.99 |
R5326:Speer4a1
|
UTSW |
5 |
26,241,736 (GRCm39) |
missense |
probably damaging |
0.99 |
R5542:Speer4a1
|
UTSW |
5 |
26,241,736 (GRCm39) |
missense |
probably damaging |
0.99 |
R6081:Speer4a1
|
UTSW |
5 |
26,239,960 (GRCm39) |
nonsense |
probably null |
|
R7521:Speer4a1
|
UTSW |
5 |
26,241,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R8669:Speer4a1
|
UTSW |
5 |
26,243,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R8782:Speer4a1
|
UTSW |
5 |
26,241,754 (GRCm39) |
missense |
probably benign |
0.39 |
R8830:Speer4a1
|
UTSW |
5 |
26,241,793 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1177:Speer4a1
|
UTSW |
5 |
26,240,036 (GRCm39) |
missense |
probably damaging |
1.00 |
|