Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aoc1l2 |
A |
T |
6: 48,909,452 (GRCm39) |
T566S |
probably benign |
Het |
Ap3b1 |
A |
G |
13: 94,585,003 (GRCm39) |
T405A |
probably benign |
Het |
Bicd2 |
G |
T |
13: 49,533,396 (GRCm39) |
V587L |
probably benign |
Het |
Bsn |
A |
T |
9: 107,993,192 (GRCm39) |
D853E |
probably damaging |
Het |
Cacna1i |
C |
A |
15: 80,246,440 (GRCm39) |
N611K |
probably damaging |
Het |
Capn11 |
A |
G |
17: 45,953,473 (GRCm39) |
L227P |
probably damaging |
Het |
Copb2 |
A |
G |
9: 98,452,426 (GRCm39) |
N70S |
probably benign |
Het |
Ddb1 |
T |
C |
19: 10,603,290 (GRCm39) |
V866A |
possibly damaging |
Het |
Dst |
A |
G |
1: 34,208,826 (GRCm39) |
|
probably benign |
Het |
Ero1b |
A |
G |
13: 12,596,551 (GRCm39) |
Y117C |
probably damaging |
Het |
Esyt1 |
T |
G |
10: 128,352,252 (GRCm39) |
R758S |
probably benign |
Het |
Gm20441 |
A |
G |
10: 75,607,326 (GRCm39) |
F55S |
probably damaging |
Het |
Gm20547 |
A |
T |
17: 35,078,492 (GRCm39) |
M362K |
probably damaging |
Het |
Gucy1b2 |
A |
G |
14: 62,653,393 (GRCm39) |
V334A |
probably benign |
Het |
Hnrnph3 |
A |
T |
10: 62,853,958 (GRCm39) |
F53L |
probably benign |
Het |
Kcnk18 |
C |
T |
19: 59,223,616 (GRCm39) |
P254S |
probably benign |
Het |
Lrfn5 |
T |
A |
12: 61,886,833 (GRCm39) |
L207Q |
probably damaging |
Het |
Lrp3 |
T |
C |
7: 34,902,052 (GRCm39) |
M589V |
possibly damaging |
Het |
Nlrp1b |
A |
G |
11: 71,052,665 (GRCm39) |
V918A |
probably benign |
Het |
Nsg2 |
A |
G |
11: 31,951,836 (GRCm39) |
T29A |
probably damaging |
Het |
Or51b4 |
T |
A |
7: 103,530,724 (GRCm39) |
H242L |
probably damaging |
Het |
Pank4 |
C |
T |
4: 155,059,172 (GRCm39) |
T435I |
probably damaging |
Het |
Prom1 |
C |
T |
5: 44,163,502 (GRCm39) |
|
probably null |
Het |
Prr14 |
G |
T |
7: 127,071,135 (GRCm39) |
L3F |
probably damaging |
Het |
Rfx7 |
A |
T |
9: 72,440,271 (GRCm39) |
|
probably benign |
Het |
Rhbdl3 |
A |
G |
11: 80,237,653 (GRCm39) |
N295S |
probably damaging |
Het |
Ripk3 |
A |
G |
14: 56,024,622 (GRCm39) |
|
probably benign |
Het |
Ror1 |
A |
T |
4: 100,269,092 (GRCm39) |
N310I |
possibly damaging |
Het |
Rpl23a |
T |
C |
11: 78,072,408 (GRCm39) |
Y74C |
possibly damaging |
Het |
Rtp3 |
A |
T |
9: 110,815,162 (GRCm39) |
|
probably benign |
Het |
Sbno1 |
A |
T |
5: 124,514,213 (GRCm39) |
N1326K |
probably damaging |
Het |
Sepsecs |
T |
C |
5: 52,818,018 (GRCm39) |
N253S |
probably damaging |
Het |
Setd2 |
A |
C |
9: 110,380,343 (GRCm39) |
E1386A |
possibly damaging |
Het |
Sf3b3 |
T |
C |
8: 111,537,596 (GRCm39) |
I1211V |
possibly damaging |
Het |
Sh3tc2 |
G |
A |
18: 62,107,549 (GRCm39) |
V187M |
possibly damaging |
Het |
Slc30a6 |
G |
T |
17: 74,716,373 (GRCm39) |
E136* |
probably null |
Het |
Sptan1 |
T |
A |
2: 29,881,045 (GRCm39) |
V438E |
probably damaging |
Het |
Stab2 |
A |
G |
10: 86,832,667 (GRCm39) |
|
probably null |
Het |
Sult2a1 |
T |
A |
7: 13,566,635 (GRCm39) |
|
probably benign |
Het |
Tmem198 |
A |
G |
1: 75,459,612 (GRCm39) |
D189G |
possibly damaging |
Het |
Tnfrsf8 |
C |
A |
4: 145,019,219 (GRCm39) |
L205F |
possibly damaging |
Het |
Vmn1r68 |
T |
A |
7: 10,262,074 (GRCm39) |
E8V |
probably damaging |
Het |
Wnk3 |
G |
A |
X: 150,059,924 (GRCm39) |
D742N |
probably damaging |
Het |
Xpc |
A |
T |
6: 91,468,297 (GRCm39) |
|
probably null |
Het |
Zfp120 |
A |
T |
2: 149,961,794 (GRCm39) |
D51E |
probably benign |
Het |
Zfp473 |
C |
T |
7: 44,382,522 (GRCm39) |
V603M |
probably benign |
Het |
|
Other mutations in Zfp113 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0217:Zfp113
|
UTSW |
5 |
138,148,953 (GRCm39) |
missense |
probably benign |
0.01 |
R0733:Zfp113
|
UTSW |
5 |
138,143,845 (GRCm39) |
missense |
probably benign |
0.18 |
R0764:Zfp113
|
UTSW |
5 |
138,143,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R0898:Zfp113
|
UTSW |
5 |
138,143,051 (GRCm39) |
missense |
probably benign |
0.01 |
R1591:Zfp113
|
UTSW |
5 |
138,149,459 (GRCm39) |
splice site |
probably benign |
|
R1623:Zfp113
|
UTSW |
5 |
138,143,930 (GRCm39) |
missense |
probably benign |
0.00 |
R2907:Zfp113
|
UTSW |
5 |
138,143,219 (GRCm39) |
missense |
probably benign |
0.13 |
R4840:Zfp113
|
UTSW |
5 |
138,143,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R4950:Zfp113
|
UTSW |
5 |
138,143,734 (GRCm39) |
missense |
probably benign |
|
R5216:Zfp113
|
UTSW |
5 |
138,148,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R6084:Zfp113
|
UTSW |
5 |
138,143,930 (GRCm39) |
missense |
probably benign |
0.00 |
R6766:Zfp113
|
UTSW |
5 |
138,143,608 (GRCm39) |
nonsense |
probably null |
|
R8190:Zfp113
|
UTSW |
5 |
138,143,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Zfp113
|
UTSW |
5 |
138,143,296 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8266:Zfp113
|
UTSW |
5 |
138,148,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R8933:Zfp113
|
UTSW |
5 |
138,143,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R9664:Zfp113
|
UTSW |
5 |
138,148,888 (GRCm39) |
nonsense |
probably null |
|
X0020:Zfp113
|
UTSW |
5 |
138,143,098 (GRCm39) |
missense |
probably damaging |
1.00 |
X0022:Zfp113
|
UTSW |
5 |
138,143,881 (GRCm39) |
missense |
possibly damaging |
0.71 |
X0027:Zfp113
|
UTSW |
5 |
138,143,975 (GRCm39) |
critical splice acceptor site |
probably null |
|
|