Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agfg1 |
T |
C |
1: 82,860,030 (GRCm39) |
F299S |
probably damaging |
Het |
Arhgap32 |
A |
T |
9: 32,157,220 (GRCm39) |
E72D |
probably benign |
Het |
Arid1a |
G |
T |
4: 133,408,391 (GRCm39) |
Q1654K |
unknown |
Het |
Atp6v1f |
A |
C |
6: 29,470,194 (GRCm39) |
H96P |
probably damaging |
Het |
Cast |
A |
G |
13: 74,887,960 (GRCm39) |
V161A |
probably damaging |
Het |
Ccdc186 |
A |
T |
19: 56,796,610 (GRCm39) |
C320S |
probably damaging |
Het |
Cgn |
T |
A |
3: 94,670,362 (GRCm39) |
K1031* |
probably null |
Het |
Cnot10 |
T |
C |
9: 114,460,894 (GRCm39) |
N92S |
probably benign |
Het |
Crat |
C |
T |
2: 30,294,577 (GRCm39) |
R497Q |
probably benign |
Het |
Cstf2t |
T |
C |
19: 31,060,593 (GRCm39) |
V43A |
possibly damaging |
Het |
D930020B18Rik |
T |
C |
10: 121,525,739 (GRCm39) |
L547P |
probably damaging |
Het |
Dennd1a |
G |
A |
2: 37,742,184 (GRCm39) |
|
probably null |
Het |
Dtnb |
T |
A |
12: 3,694,272 (GRCm39) |
|
probably null |
Het |
Entpd1 |
A |
G |
19: 40,727,309 (GRCm39) |
N486D |
possibly damaging |
Het |
Fes |
G |
A |
7: 80,028,410 (GRCm39) |
R736C |
probably damaging |
Het |
Galr1 |
T |
G |
18: 82,411,990 (GRCm39) |
Y292S |
probably damaging |
Het |
Gda |
T |
A |
19: 21,405,988 (GRCm39) |
D80V |
probably damaging |
Het |
Ghr |
A |
G |
15: 3,377,054 (GRCm39) |
C56R |
probably benign |
Het |
Golgb1 |
A |
G |
16: 36,718,909 (GRCm39) |
T313A |
probably damaging |
Het |
Gpaa1 |
A |
T |
15: 76,217,193 (GRCm39) |
D236V |
probably damaging |
Het |
Gsdmc |
A |
G |
15: 63,676,315 (GRCm39) |
S43P |
probably benign |
Het |
Gsdmd |
A |
G |
15: 75,738,202 (GRCm39) |
E295G |
probably damaging |
Het |
Htatip2 |
A |
G |
7: 49,409,534 (GRCm39) |
K96R |
probably benign |
Het |
Insm1 |
T |
A |
2: 146,064,711 (GRCm39) |
F176I |
probably benign |
Het |
Itih1 |
T |
C |
14: 30,665,117 (GRCm39) |
E36G |
probably benign |
Het |
Jak1 |
A |
G |
4: 101,032,379 (GRCm39) |
V409A |
probably damaging |
Het |
Knl1 |
A |
G |
2: 118,901,073 (GRCm39) |
I925V |
possibly damaging |
Het |
Lcmt2 |
A |
G |
2: 120,969,185 (GRCm39) |
S413P |
probably benign |
Het |
Lmo7 |
T |
C |
14: 102,118,389 (GRCm39) |
S205P |
probably damaging |
Het |
Lrch3 |
C |
A |
16: 32,807,113 (GRCm39) |
S462* |
probably null |
Het |
Lrrtm2 |
T |
C |
18: 35,346,688 (GRCm39) |
I205V |
possibly damaging |
Het |
Mark3 |
T |
G |
12: 111,600,223 (GRCm39) |
N479K |
probably damaging |
Het |
Mrpl19 |
C |
T |
6: 81,942,793 (GRCm39) |
G39D |
possibly damaging |
Het |
Msh4 |
A |
G |
3: 153,582,382 (GRCm39) |
Y497H |
probably benign |
Het |
Msl2 |
T |
A |
9: 100,979,316 (GRCm39) |
D563E |
probably benign |
Het |
Mta1 |
G |
A |
12: 113,095,088 (GRCm39) |
|
probably null |
Het |
Nalcn |
T |
A |
14: 123,529,272 (GRCm39) |
Q1401L |
probably benign |
Het |
Ncapg |
T |
C |
5: 45,853,135 (GRCm39) |
L867P |
probably benign |
Het |
Nkapl |
T |
C |
13: 21,652,013 (GRCm39) |
D200G |
unknown |
Het |
Nos1 |
A |
C |
5: 118,005,583 (GRCm39) |
E101A |
probably damaging |
Het |
Npat |
T |
C |
9: 53,481,216 (GRCm39) |
S1008P |
probably damaging |
Het |
Ntng1 |
A |
G |
3: 109,760,398 (GRCm39) |
I358T |
probably benign |
Het |
Or11h6 |
A |
G |
14: 50,879,852 (GRCm39) |
E32G |
probably benign |
Het |
Or13p4 |
C |
T |
4: 118,546,859 (GRCm39) |
M263I |
probably damaging |
Het |
Or4b1 |
T |
A |
2: 89,980,188 (GRCm39) |
H54L |
probably benign |
Het |
Or6c88 |
A |
G |
10: 129,406,493 (GRCm39) |
|
probably benign |
Het |
Pex1 |
A |
G |
5: 3,680,222 (GRCm39) |
D948G |
probably damaging |
Het |
Pkd1l2 |
A |
T |
8: 117,755,218 (GRCm39) |
I1660N |
possibly damaging |
Het |
Pkp2 |
T |
A |
16: 16,079,537 (GRCm39) |
Y540N |
possibly damaging |
Het |
Pkp4 |
T |
C |
2: 59,142,110 (GRCm39) |
L471P |
probably damaging |
Het |
Plekhm3 |
A |
T |
1: 64,977,143 (GRCm39) |
M109K |
probably benign |
Het |
Plekhn1 |
T |
C |
4: 156,318,418 (GRCm39) |
N68S |
probably benign |
Het |
Pramel7 |
T |
A |
2: 87,321,189 (GRCm39) |
D282V |
possibly damaging |
Het |
Pxdn |
T |
C |
12: 30,040,944 (GRCm39) |
Y407H |
probably benign |
Het |
Rab3ip |
T |
C |
10: 116,773,546 (GRCm39) |
D89G |
possibly damaging |
Het |
Rad17 |
G |
A |
13: 100,766,019 (GRCm39) |
Q370* |
probably null |
Het |
Robo4 |
T |
C |
9: 37,322,277 (GRCm39) |
C751R |
probably benign |
Het |
Sez6 |
A |
G |
11: 77,844,356 (GRCm39) |
T60A |
probably damaging |
Het |
Socs4 |
A |
G |
14: 47,527,296 (GRCm39) |
H77R |
probably benign |
Het |
Srrm3 |
T |
A |
5: 135,881,060 (GRCm39) |
M120K |
probably benign |
Het |
Steap4 |
A |
T |
5: 8,028,453 (GRCm39) |
I344F |
probably benign |
Het |
Stk36 |
T |
A |
1: 74,672,725 (GRCm39) |
F989Y |
probably damaging |
Het |
Toporsl |
A |
T |
4: 52,612,108 (GRCm39) |
Q667L |
probably benign |
Het |
Tspan17 |
T |
C |
13: 54,937,466 (GRCm39) |
F20S |
probably benign |
Het |
Tubgcp3 |
G |
A |
8: 12,711,359 (GRCm39) |
Q65* |
probably null |
Het |
Ush2a |
A |
T |
1: 188,465,726 (GRCm39) |
I2765F |
probably benign |
Het |
Vwa8 |
A |
C |
14: 79,219,674 (GRCm39) |
|
probably null |
Het |
Wdfy4 |
A |
G |
14: 32,800,264 (GRCm39) |
V1954A |
|
Het |
Xrn2 |
T |
A |
2: 146,884,017 (GRCm39) |
|
probably null |
Het |
Zfp687 |
C |
T |
3: 94,914,841 (GRCm39) |
R1220H |
probably damaging |
Het |
|
Other mutations in Or2d2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00981:Or2d2b
|
APN |
7 |
106,705,269 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00981:Or2d2b
|
APN |
7 |
106,705,268 (GRCm39) |
nonsense |
probably null |
|
IGL01642:Or2d2b
|
APN |
7 |
106,706,029 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL03174:Or2d2b
|
APN |
7 |
106,705,477 (GRCm39) |
missense |
probably benign |
0.05 |
R1724:Or2d2b
|
UTSW |
7 |
106,705,409 (GRCm39) |
missense |
probably benign |
0.00 |
R2029:Or2d2b
|
UTSW |
7 |
106,705,643 (GRCm39) |
missense |
probably benign |
|
R2860:Or2d2b
|
UTSW |
7 |
106,705,675 (GRCm39) |
missense |
probably benign |
0.10 |
R2861:Or2d2b
|
UTSW |
7 |
106,705,675 (GRCm39) |
missense |
probably benign |
0.10 |
R2862:Or2d2b
|
UTSW |
7 |
106,705,675 (GRCm39) |
missense |
probably benign |
0.10 |
R3807:Or2d2b
|
UTSW |
7 |
106,705,670 (GRCm39) |
missense |
probably benign |
0.01 |
R4797:Or2d2b
|
UTSW |
7 |
106,705,234 (GRCm39) |
missense |
probably benign |
0.26 |
R5008:Or2d2b
|
UTSW |
7 |
106,705,288 (GRCm39) |
missense |
probably damaging |
0.99 |
R5918:Or2d2b
|
UTSW |
7 |
106,705,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R6090:Or2d2b
|
UTSW |
7 |
106,705,456 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6174:Or2d2b
|
UTSW |
7 |
106,705,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R6253:Or2d2b
|
UTSW |
7 |
106,705,145 (GRCm39) |
missense |
probably benign |
0.00 |
R7483:Or2d2b
|
UTSW |
7 |
106,705,982 (GRCm39) |
missense |
probably benign |
0.00 |
R7750:Or2d2b
|
UTSW |
7 |
106,705,740 (GRCm39) |
nonsense |
probably null |
|
R8260:Or2d2b
|
UTSW |
7 |
106,706,062 (GRCm39) |
missense |
probably benign |
|
R8374:Or2d2b
|
UTSW |
7 |
106,706,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R8975:Or2d2b
|
UTSW |
7 |
106,705,664 (GRCm39) |
missense |
probably benign |
0.01 |
R9431:Or2d2b
|
UTSW |
7 |
106,705,336 (GRCm39) |
missense |
probably damaging |
1.00 |
|