Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg6 |
T |
A |
10: 14,302,521 (GRCm39) |
Y964F |
probably damaging |
Het |
Akap3 |
T |
A |
6: 126,842,521 (GRCm39) |
L380Q |
probably damaging |
Het |
Alpk1 |
A |
G |
3: 127,473,723 (GRCm39) |
I760T |
probably benign |
Het |
Aoc1l2 |
T |
A |
6: 48,910,412 (GRCm39) |
F701L |
probably damaging |
Het |
Arhgap20 |
G |
A |
9: 51,736,276 (GRCm39) |
|
probably benign |
Het |
Cacng3 |
T |
C |
7: 122,361,532 (GRCm39) |
F113S |
possibly damaging |
Het |
Ccdc158 |
G |
T |
5: 92,775,339 (GRCm39) |
N955K |
probably benign |
Het |
Ccdc63 |
T |
A |
5: 122,254,908 (GRCm39) |
M368L |
possibly damaging |
Het |
Cnot2 |
T |
C |
10: 116,363,851 (GRCm39) |
T18A |
probably damaging |
Het |
Ctnna2 |
A |
T |
6: 76,950,820 (GRCm39) |
D550E |
possibly damaging |
Het |
Cyp2c37 |
C |
T |
19: 40,000,176 (GRCm39) |
R433W |
probably damaging |
Het |
Dact2 |
A |
G |
17: 14,419,450 (GRCm39) |
S103P |
probably damaging |
Het |
Dek |
A |
G |
13: 47,255,077 (GRCm39) |
|
probably benign |
Het |
Dnah9 |
CAGTTGCTTAAA |
CA |
11: 65,986,066 (GRCm39) |
|
probably null |
Het |
Dock4 |
A |
G |
12: 40,671,250 (GRCm39) |
Y23C |
probably damaging |
Het |
Edar |
T |
A |
10: 58,439,001 (GRCm39) |
S344C |
probably damaging |
Het |
Epg5 |
T |
C |
18: 78,073,270 (GRCm39) |
V2431A |
probably benign |
Het |
Evc2 |
C |
T |
5: 37,562,068 (GRCm39) |
|
probably benign |
Het |
Idh3b |
A |
T |
2: 130,125,948 (GRCm39) |
D41E |
probably benign |
Het |
Igkv8-24 |
A |
T |
6: 70,193,956 (GRCm39) |
V84D |
probably damaging |
Het |
Iqca1l |
A |
T |
5: 24,749,164 (GRCm39) |
L778Q |
probably benign |
Het |
Mgam |
T |
C |
6: 40,660,989 (GRCm39) |
I1118T |
probably benign |
Het |
Mtmr3 |
A |
G |
11: 4,432,925 (GRCm39) |
V1116A |
probably damaging |
Het |
Myoc |
A |
G |
1: 162,466,936 (GRCm39) |
Y35C |
probably damaging |
Het |
Ncr1 |
A |
T |
7: 4,347,573 (GRCm39) |
D246V |
probably benign |
Het |
Nphp3 |
A |
G |
9: 103,880,236 (GRCm39) |
E86G |
probably damaging |
Het |
Or2l13b |
A |
T |
16: 19,349,076 (GRCm39) |
V198E |
probably damaging |
Het |
Or52e5 |
A |
T |
7: 104,719,064 (GRCm39) |
Y130F |
probably benign |
Het |
Or8h7 |
A |
C |
2: 86,720,676 (GRCm39) |
V281G |
probably damaging |
Het |
Pbld1 |
A |
T |
10: 62,912,193 (GRCm39) |
I275L |
probably benign |
Het |
Pde12 |
A |
G |
14: 26,386,786 (GRCm39) |
V574A |
possibly damaging |
Het |
Pdxk |
G |
T |
10: 78,280,872 (GRCm39) |
D189E |
probably benign |
Het |
Pkhd1 |
C |
A |
1: 20,444,960 (GRCm39) |
E2276* |
probably null |
Het |
Ppp1r10 |
A |
G |
17: 36,237,739 (GRCm39) |
N237S |
possibly damaging |
Het |
Rheb |
T |
A |
5: 25,012,067 (GRCm39) |
Y131F |
probably benign |
Het |
Rpgrip1l |
T |
C |
8: 92,031,613 (GRCm39) |
D88G |
probably damaging |
Het |
Scgb2b33 |
T |
C |
7: 32,812,239 (GRCm39) |
|
noncoding transcript |
Het |
Snx9 |
C |
A |
17: 5,974,896 (GRCm39) |
N461K |
possibly damaging |
Het |
Tbc1d2b |
C |
A |
9: 90,091,777 (GRCm39) |
V842F |
probably damaging |
Het |
Tgfbi |
G |
A |
13: 56,784,418 (GRCm39) |
E615K |
possibly damaging |
Het |
Tmem51 |
A |
G |
4: 141,759,346 (GRCm39) |
M134T |
probably damaging |
Het |
Tox4 |
A |
G |
14: 52,524,241 (GRCm39) |
D125G |
probably damaging |
Het |
Trappc3 |
A |
T |
4: 126,167,771 (GRCm39) |
N110I |
probably damaging |
Het |
Trim11 |
T |
A |
11: 58,881,419 (GRCm39) |
D437E |
probably damaging |
Het |
Ttc23l |
T |
C |
15: 10,537,682 (GRCm39) |
N196S |
probably benign |
Het |
Wnk1 |
C |
A |
6: 119,969,369 (GRCm39) |
G362V |
probably damaging |
Het |
Wwc1 |
A |
G |
11: 35,758,153 (GRCm39) |
F731S |
probably damaging |
Het |
Wwp1 |
A |
T |
4: 19,662,174 (GRCm39) |
D140E |
possibly damaging |
Het |
Zfp24 |
G |
A |
18: 24,151,095 (GRCm39) |
P17L |
possibly damaging |
Het |
Zfp853 |
C |
T |
5: 143,274,424 (GRCm39) |
V399M |
unknown |
Het |
Zfp868 |
T |
C |
8: 70,064,303 (GRCm39) |
H344R |
probably damaging |
Het |
|
Other mutations in Zfp354b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02029:Zfp354b
|
APN |
11 |
50,814,664 (GRCm39) |
missense |
probably benign |
|
R1299:Zfp354b
|
UTSW |
11 |
50,814,297 (GRCm39) |
missense |
probably benign |
0.04 |
R1353:Zfp354b
|
UTSW |
11 |
50,814,240 (GRCm39) |
missense |
probably damaging |
0.96 |
R1860:Zfp354b
|
UTSW |
11 |
50,814,369 (GRCm39) |
missense |
probably benign |
|
R2072:Zfp354b
|
UTSW |
11 |
50,813,279 (GRCm39) |
nonsense |
probably null |
|
R5221:Zfp354b
|
UTSW |
11 |
50,813,917 (GRCm39) |
missense |
probably benign |
0.00 |
R5231:Zfp354b
|
UTSW |
11 |
50,813,917 (GRCm39) |
missense |
probably benign |
0.00 |
R5258:Zfp354b
|
UTSW |
11 |
50,813,917 (GRCm39) |
missense |
probably benign |
0.00 |
R5775:Zfp354b
|
UTSW |
11 |
50,813,647 (GRCm39) |
missense |
probably benign |
0.00 |
R5929:Zfp354b
|
UTSW |
11 |
50,813,282 (GRCm39) |
missense |
probably damaging |
0.99 |
R6443:Zfp354b
|
UTSW |
11 |
50,813,581 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6748:Zfp354b
|
UTSW |
11 |
50,813,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R7439:Zfp354b
|
UTSW |
11 |
50,813,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R7706:Zfp354b
|
UTSW |
11 |
50,819,390 (GRCm39) |
critical splice donor site |
probably null |
|
R7819:Zfp354b
|
UTSW |
11 |
50,814,632 (GRCm39) |
nonsense |
probably null |
|
R7830:Zfp354b
|
UTSW |
11 |
50,814,136 (GRCm39) |
missense |
probably benign |
0.28 |
R8508:Zfp354b
|
UTSW |
11 |
50,814,297 (GRCm39) |
missense |
probably benign |
0.04 |
R9157:Zfp354b
|
UTSW |
11 |
50,813,887 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9170:Zfp354b
|
UTSW |
11 |
50,814,362 (GRCm39) |
missense |
probably benign |
|
R9303:Zfp354b
|
UTSW |
11 |
50,820,256 (GRCm39) |
missense |
probably damaging |
0.97 |
R9462:Zfp354b
|
UTSW |
11 |
50,814,523 (GRCm39) |
missense |
probably benign |
|
|