Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
T |
A |
11: 84,086,295 (GRCm39) |
D40E |
probably benign |
Het |
Acsf2 |
C |
T |
11: 94,452,224 (GRCm39) |
|
probably benign |
Het |
Adamts19 |
C |
T |
18: 59,181,917 (GRCm39) |
H1119Y |
possibly damaging |
Het |
Akap6 |
A |
G |
12: 52,983,937 (GRCm39) |
D827G |
probably damaging |
Het |
Ankrd33b |
T |
C |
15: 31,367,375 (GRCm39) |
D55G |
probably damaging |
Het |
Ano5 |
T |
A |
7: 51,229,316 (GRCm39) |
H569Q |
probably benign |
Het |
Aox1 |
A |
G |
1: 58,346,510 (GRCm39) |
D548G |
probably benign |
Het |
Baz2a |
A |
G |
10: 127,960,021 (GRCm39) |
D1433G |
possibly damaging |
Het |
BC031181 |
T |
G |
18: 75,141,767 (GRCm39) |
V8G |
probably damaging |
Het |
Bicdl2 |
A |
T |
17: 23,887,083 (GRCm39) |
M457L |
probably damaging |
Het |
C130074G19Rik |
T |
C |
1: 184,615,103 (GRCm39) |
D29G |
probably damaging |
Het |
Cd200r1 |
A |
T |
16: 44,586,390 (GRCm39) |
T7S |
probably benign |
Het |
Cdc37 |
A |
G |
9: 21,053,712 (GRCm39) |
|
probably benign |
Het |
Cmtr2 |
T |
C |
8: 110,949,267 (GRCm39) |
S526P |
probably damaging |
Het |
Cntn2 |
G |
T |
1: 132,451,430 (GRCm39) |
A433D |
probably damaging |
Het |
Cntnap5a |
T |
C |
1: 115,828,680 (GRCm39) |
S35P |
probably benign |
Het |
Csf3r |
A |
G |
4: 125,923,777 (GRCm39) |
T96A |
possibly damaging |
Het |
Ctbs |
A |
G |
3: 146,160,720 (GRCm39) |
N96D |
probably benign |
Het |
Dach1 |
A |
G |
14: 98,138,835 (GRCm39) |
L536P |
probably damaging |
Het |
Dcaf6 |
T |
C |
1: 165,179,589 (GRCm39) |
Q517R |
probably benign |
Het |
Dnah1 |
G |
T |
14: 31,014,994 (GRCm39) |
Q1733K |
probably damaging |
Het |
Dnah17 |
A |
T |
11: 117,985,841 (GRCm39) |
I1416N |
probably benign |
Het |
Dock11 |
G |
A |
X: 35,283,688 (GRCm39) |
R1102H |
probably damaging |
Het |
Dpp8 |
T |
C |
9: 64,971,096 (GRCm39) |
|
probably benign |
Het |
Emc1 |
G |
A |
4: 139,087,495 (GRCm39) |
|
probably null |
Het |
Emc8 |
A |
G |
8: 121,384,983 (GRCm39) |
L76P |
possibly damaging |
Het |
Emx2 |
T |
C |
19: 59,448,035 (GRCm39) |
Y130H |
possibly damaging |
Het |
Fbf1 |
C |
T |
11: 116,038,753 (GRCm39) |
R815Q |
probably damaging |
Het |
Foxb2 |
G |
A |
19: 16,849,878 (GRCm39) |
P376L |
probably damaging |
Het |
Gabrb1 |
C |
A |
5: 72,266,047 (GRCm39) |
L202I |
probably damaging |
Het |
Gabrb1 |
T |
A |
5: 72,266,048 (GRCm39) |
L202Q |
probably damaging |
Het |
Grin2c |
T |
A |
11: 115,144,676 (GRCm39) |
I617F |
probably damaging |
Het |
Gtf2h3 |
T |
A |
5: 124,728,933 (GRCm39) |
V164E |
probably damaging |
Het |
Gusb |
T |
C |
5: 130,029,731 (GRCm39) |
Q88R |
probably damaging |
Het |
Hormad2 |
T |
A |
11: 4,374,788 (GRCm39) |
K75N |
probably damaging |
Het |
Il33 |
A |
G |
19: 29,929,390 (GRCm39) |
T38A |
possibly damaging |
Het |
Ivns1abp |
A |
T |
1: 151,236,687 (GRCm39) |
Q416L |
possibly damaging |
Het |
Ivns1abp |
G |
C |
1: 151,236,688 (GRCm39) |
Q416H |
probably benign |
Het |
Kcnh5 |
T |
A |
12: 75,166,711 (GRCm39) |
H178L |
probably benign |
Het |
Kif21b |
A |
G |
1: 136,080,543 (GRCm39) |
N579S |
probably benign |
Het |
Kif26a |
G |
C |
12: 112,113,389 (GRCm39) |
R95P |
possibly damaging |
Het |
Kl |
A |
G |
5: 150,912,062 (GRCm39) |
I604V |
probably benign |
Het |
Klhl24 |
A |
G |
16: 19,941,686 (GRCm39) |
K545E |
probably damaging |
Het |
Mcm3ap |
A |
G |
10: 76,306,347 (GRCm39) |
I153M |
probably damaging |
Het |
Meis1 |
T |
G |
11: 18,831,682 (GRCm39) |
D452A |
probably damaging |
Het |
Msantd4 |
C |
T |
9: 4,384,138 (GRCm39) |
P153L |
probably benign |
Het |
Myot |
A |
G |
18: 44,475,422 (GRCm39) |
E181G |
probably damaging |
Het |
Nf1 |
T |
C |
11: 79,281,195 (GRCm39) |
F150S |
probably damaging |
Het |
Nyap2 |
T |
A |
1: 81,219,566 (GRCm39) |
S529R |
probably damaging |
Het |
Or10d3 |
T |
C |
9: 39,461,390 (GRCm39) |
Y259C |
probably damaging |
Het |
Or12e10 |
A |
T |
2: 87,640,988 (GRCm39) |
T275S |
probably benign |
Het |
Or2y1c |
A |
G |
11: 49,361,286 (GRCm39) |
I103V |
probably benign |
Het |
Or8b56 |
T |
A |
9: 38,739,660 (GRCm39) |
Y224* |
probably null |
Het |
Pcnt |
C |
T |
10: 76,240,496 (GRCm39) |
|
probably null |
Het |
Pik3c3 |
T |
C |
18: 30,455,289 (GRCm39) |
|
probably null |
Het |
Pkdcc |
A |
T |
17: 83,527,473 (GRCm39) |
Y217F |
possibly damaging |
Het |
Pnpla6 |
C |
A |
8: 3,585,459 (GRCm39) |
|
probably benign |
Het |
Polr3gl |
T |
C |
3: 96,488,190 (GRCm39) |
M26V |
probably benign |
Het |
Ppp1r13b |
T |
C |
12: 111,838,842 (GRCm39) |
N12S |
possibly damaging |
Het |
Ppp1r26 |
G |
A |
2: 28,341,528 (GRCm39) |
R386K |
probably benign |
Het |
Prdm10 |
A |
G |
9: 31,248,697 (GRCm39) |
E355G |
probably damaging |
Het |
Prex2 |
T |
C |
1: 11,131,554 (GRCm39) |
F41S |
possibly damaging |
Het |
Prkar1b |
G |
T |
5: 139,036,428 (GRCm39) |
Y231* |
probably null |
Het |
Prkdc |
A |
T |
16: 15,505,268 (GRCm39) |
I857L |
probably benign |
Het |
Psg21 |
A |
T |
7: 18,390,425 (GRCm39) |
N10K |
probably benign |
Het |
Rapgef3 |
A |
T |
15: 97,655,382 (GRCm39) |
V444E |
probably benign |
Het |
Rnf17 |
A |
T |
14: 56,705,243 (GRCm39) |
T716S |
probably benign |
Het |
Rps6ka1 |
C |
T |
4: 133,578,315 (GRCm39) |
R577H |
probably damaging |
Het |
Scn1a |
A |
C |
2: 66,161,629 (GRCm39) |
N306K |
possibly damaging |
Het |
Skint6 |
A |
G |
4: 113,095,329 (GRCm39) |
I110T |
probably damaging |
Het |
Ssu2 |
A |
G |
6: 112,364,959 (GRCm39) |
M1T |
probably null |
Het |
Stag3 |
A |
T |
5: 138,296,247 (GRCm39) |
T437S |
probably benign |
Het |
Tal2 |
A |
G |
4: 53,786,107 (GRCm39) |
Y96C |
probably benign |
Het |
Thoc3 |
A |
T |
13: 54,613,991 (GRCm39) |
|
probably null |
Het |
Tle1 |
T |
C |
4: 72,059,495 (GRCm39) |
D19G |
probably damaging |
Het |
Trpm4 |
A |
G |
7: 44,964,468 (GRCm39) |
I690T |
probably benign |
Het |
Trpm6 |
A |
T |
19: 18,853,295 (GRCm39) |
M1772L |
probably benign |
Het |
Unc5b |
G |
A |
10: 60,667,254 (GRCm39) |
|
probably benign |
Het |
Usf3 |
G |
T |
16: 44,041,561 (GRCm39) |
V2014F |
probably damaging |
Het |
Utp18 |
C |
T |
11: 93,776,390 (GRCm39) |
A32T |
probably benign |
Het |
Wdfy4 |
A |
G |
14: 32,682,765 (GRCm39) |
V2981A |
probably damaging |
Het |
Zfp608 |
A |
G |
18: 55,079,738 (GRCm39) |
V349A |
probably damaging |
Het |
Znfx1 |
A |
C |
2: 166,898,237 (GRCm39) |
I229S |
probably benign |
Het |
|
Other mutations in Cyp26b1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01713:Cyp26b1
|
APN |
6 |
84,551,283 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02530:Cyp26b1
|
APN |
6 |
84,551,294 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02624:Cyp26b1
|
APN |
6 |
84,561,321 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02676:Cyp26b1
|
APN |
6 |
84,553,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Cyp26b1
|
UTSW |
6 |
84,551,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R0127:Cyp26b1
|
UTSW |
6 |
84,554,190 (GRCm39) |
splice site |
probably benign |
|
R0268:Cyp26b1
|
UTSW |
6 |
84,551,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R0281:Cyp26b1
|
UTSW |
6 |
84,551,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R0575:Cyp26b1
|
UTSW |
6 |
84,552,288 (GRCm39) |
splice site |
probably benign |
|
R1167:Cyp26b1
|
UTSW |
6 |
84,561,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R1171:Cyp26b1
|
UTSW |
6 |
84,553,653 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1791:Cyp26b1
|
UTSW |
6 |
84,561,441 (GRCm39) |
missense |
probably benign |
0.05 |
R1799:Cyp26b1
|
UTSW |
6 |
84,561,254 (GRCm39) |
missense |
probably benign |
0.37 |
R2065:Cyp26b1
|
UTSW |
6 |
84,553,537 (GRCm39) |
missense |
probably benign |
0.00 |
R2103:Cyp26b1
|
UTSW |
6 |
84,552,032 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2900:Cyp26b1
|
UTSW |
6 |
84,553,623 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4510:Cyp26b1
|
UTSW |
6 |
84,551,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R4511:Cyp26b1
|
UTSW |
6 |
84,551,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R4934:Cyp26b1
|
UTSW |
6 |
84,553,954 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5585:Cyp26b1
|
UTSW |
6 |
84,554,171 (GRCm39) |
missense |
probably damaging |
0.99 |
R7229:Cyp26b1
|
UTSW |
6 |
84,554,132 (GRCm39) |
nonsense |
probably null |
|
R7497:Cyp26b1
|
UTSW |
6 |
84,553,964 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7672:Cyp26b1
|
UTSW |
6 |
84,561,351 (GRCm39) |
missense |
probably benign |
0.04 |
R8346:Cyp26b1
|
UTSW |
6 |
84,554,150 (GRCm39) |
missense |
probably benign |
0.21 |
R9020:Cyp26b1
|
UTSW |
6 |
84,552,056 (GRCm39) |
missense |
probably benign |
0.09 |
R9029:Cyp26b1
|
UTSW |
6 |
84,554,035 (GRCm39) |
missense |
probably benign |
0.20 |
R9042:Cyp26b1
|
UTSW |
6 |
84,553,590 (GRCm39) |
missense |
probably benign |
0.18 |
R9068:Cyp26b1
|
UTSW |
6 |
84,551,379 (GRCm39) |
missense |
probably damaging |
0.96 |
R9536:Cyp26b1
|
UTSW |
6 |
84,553,999 (GRCm39) |
missense |
probably benign |
0.02 |
R9779:Cyp26b1
|
UTSW |
6 |
84,552,113 (GRCm39) |
missense |
probably benign |
|
X0063:Cyp26b1
|
UTSW |
6 |
84,552,100 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Cyp26b1
|
UTSW |
6 |
84,554,096 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Cyp26b1
|
UTSW |
6 |
84,554,101 (GRCm39) |
missense |
probably damaging |
1.00 |
|