Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alpk2 |
T |
C |
18: 65,440,211 (GRCm39) |
D861G |
probably benign |
Het |
Anapc4 |
A |
G |
5: 53,005,970 (GRCm39) |
T326A |
probably damaging |
Het |
Atm |
T |
C |
9: 53,401,593 (GRCm39) |
I1425M |
probably damaging |
Het |
Bend5 |
T |
C |
4: 111,305,838 (GRCm39) |
L294P |
probably damaging |
Het |
Casp7 |
T |
A |
19: 56,425,177 (GRCm39) |
D193E |
probably benign |
Het |
Cdc16 |
T |
C |
8: 13,814,606 (GRCm39) |
V130A |
probably benign |
Het |
Chl1 |
T |
G |
6: 103,692,354 (GRCm39) |
Y331D |
probably damaging |
Het |
Cntn1 |
C |
A |
15: 92,237,458 (GRCm39) |
Y1017* |
probably null |
Het |
Cyb5d1 |
C |
A |
11: 69,284,610 (GRCm39) |
|
probably null |
Het |
Cyp2c38 |
A |
G |
19: 39,451,329 (GRCm39) |
|
probably null |
Het |
Dzip3 |
T |
C |
16: 48,750,037 (GRCm39) |
M827V |
probably benign |
Het |
Ehd1 |
T |
A |
19: 6,348,177 (GRCm39) |
M385K |
possibly damaging |
Het |
Eya3 |
C |
A |
4: 132,420,311 (GRCm39) |
Y52* |
probably null |
Het |
Itsn1 |
C |
T |
16: 91,603,089 (GRCm39) |
|
probably benign |
Het |
Ktn1 |
A |
T |
14: 47,952,178 (GRCm39) |
N983I |
probably damaging |
Het |
Lrrk2 |
T |
A |
15: 91,623,035 (GRCm39) |
N1068K |
probably damaging |
Het |
Mup6 |
T |
A |
4: 60,006,001 (GRCm39) |
N156K |
probably damaging |
Het |
Nedd9 |
T |
A |
13: 41,469,710 (GRCm39) |
H481L |
probably benign |
Het |
Obscn |
T |
C |
11: 59,024,588 (GRCm39) |
D484G |
probably damaging |
Het |
Ogdh |
T |
C |
11: 6,298,790 (GRCm39) |
V674A |
probably damaging |
Het |
Or4a27 |
T |
C |
2: 88,559,409 (GRCm39) |
D178G |
probably damaging |
Het |
Or4f54 |
G |
A |
2: 111,122,864 (GRCm39) |
D84N |
probably benign |
Het |
Or5b113 |
A |
G |
19: 13,342,063 (GRCm39) |
I24V |
probably benign |
Het |
Or5d38 |
T |
C |
2: 87,955,023 (GRCm39) |
Q102R |
probably damaging |
Het |
Or8g53 |
T |
C |
9: 39,683,293 (GRCm39) |
M268V |
probably benign |
Het |
Or8k32 |
T |
A |
2: 86,368,674 (GRCm39) |
D195V |
probably benign |
Het |
Osbpl6 |
A |
G |
2: 76,379,871 (GRCm39) |
T154A |
probably damaging |
Het |
P2rx1 |
T |
C |
11: 72,899,041 (GRCm39) |
V84A |
probably damaging |
Het |
Pcdh11x |
G |
A |
X: 119,310,611 (GRCm39) |
V685I |
possibly damaging |
Het |
Ppp4r3b |
T |
A |
11: 29,138,288 (GRCm39) |
V212E |
probably damaging |
Het |
Prune2 |
A |
G |
19: 17,101,243 (GRCm39) |
D2249G |
probably benign |
Het |
Slc5a8 |
T |
A |
10: 88,742,254 (GRCm39) |
S317T |
possibly damaging |
Het |
Ssc5d |
T |
A |
7: 4,940,111 (GRCm39) |
L822* |
probably null |
Het |
Swt1 |
A |
G |
1: 151,286,890 (GRCm39) |
S201P |
probably damaging |
Het |
Tet1 |
T |
A |
10: 62,715,553 (GRCm39) |
M81L |
probably benign |
Het |
Tex9 |
T |
A |
9: 72,395,349 (GRCm39) |
N39I |
probably damaging |
Het |
Ttc4 |
T |
C |
4: 106,520,360 (GRCm39) |
Y378C |
probably damaging |
Het |
Ubap2 |
T |
C |
4: 41,195,155 (GRCm39) |
N1131S |
probably damaging |
Het |
Ugt2b35 |
C |
T |
5: 87,156,165 (GRCm39) |
T419I |
probably damaging |
Het |
Ugt3a1 |
T |
G |
15: 9,367,354 (GRCm39) |
F366V |
probably damaging |
Het |
|
Other mutations in Zfp324 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01943:Zfp324
|
APN |
7 |
12,702,713 (GRCm39) |
splice site |
probably benign |
|
IGL02668:Zfp324
|
APN |
7 |
12,704,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R0883:Zfp324
|
UTSW |
7 |
12,704,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R0931:Zfp324
|
UTSW |
7 |
12,700,185 (GRCm39) |
missense |
probably benign |
0.05 |
R1164:Zfp324
|
UTSW |
7 |
12,705,551 (GRCm39) |
missense |
probably benign |
0.02 |
R1587:Zfp324
|
UTSW |
7 |
12,704,570 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1837:Zfp324
|
UTSW |
7 |
12,704,156 (GRCm39) |
missense |
probably benign |
0.15 |
R1982:Zfp324
|
UTSW |
7 |
12,705,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R2333:Zfp324
|
UTSW |
7 |
12,705,172 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3155:Zfp324
|
UTSW |
7 |
12,702,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R4050:Zfp324
|
UTSW |
7 |
12,704,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R4784:Zfp324
|
UTSW |
7 |
12,705,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Zfp324
|
UTSW |
7 |
12,703,300 (GRCm39) |
missense |
probably benign |
0.02 |
R5970:Zfp324
|
UTSW |
7 |
12,703,293 (GRCm39) |
missense |
probably benign |
0.28 |
R6767:Zfp324
|
UTSW |
7 |
12,704,527 (GRCm39) |
missense |
probably null |
0.13 |
R7007:Zfp324
|
UTSW |
7 |
12,705,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R7152:Zfp324
|
UTSW |
7 |
12,700,198 (GRCm39) |
missense |
probably benign |
0.07 |
R7164:Zfp324
|
UTSW |
7 |
12,702,810 (GRCm39) |
missense |
probably damaging |
0.97 |
R7233:Zfp324
|
UTSW |
7 |
12,704,524 (GRCm39) |
nonsense |
probably null |
|
R9039:Zfp324
|
UTSW |
7 |
12,705,455 (GRCm39) |
missense |
probably benign |
0.19 |
R9172:Zfp324
|
UTSW |
7 |
12,704,689 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Zfp324
|
UTSW |
7 |
12,705,316 (GRCm39) |
missense |
probably damaging |
1.00 |
|