Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
A |
G |
2: 69,154,320 (GRCm39) |
V82A |
probably benign |
Het |
Adam28 |
A |
G |
14: 68,848,443 (GRCm39) |
V671A |
probably benign |
Het |
Ak3 |
T |
A |
19: 29,025,118 (GRCm39) |
S38C |
probably damaging |
Het |
Arfgef1 |
A |
G |
1: 10,279,859 (GRCm39) |
V236A |
probably benign |
Het |
Arhgap10 |
T |
C |
8: 78,147,354 (GRCm39) |
N170S |
probably benign |
Het |
B020004C17Rik |
G |
T |
14: 57,254,645 (GRCm39) |
M156I |
possibly damaging |
Het |
Bicral |
T |
A |
17: 47,141,917 (GRCm39) |
M1L |
unknown |
Het |
Bop1 |
A |
G |
15: 76,338,076 (GRCm39) |
L598P |
probably damaging |
Het |
Cachd1 |
A |
T |
4: 100,828,085 (GRCm39) |
D611V |
probably damaging |
Het |
Cfap70 |
T |
A |
14: 20,489,787 (GRCm39) |
E246D |
probably benign |
Het |
Chl1 |
T |
A |
6: 103,692,245 (GRCm39) |
Y294* |
probably null |
Het |
Chrna2 |
T |
A |
14: 66,386,402 (GRCm39) |
Y183N |
probably damaging |
Het |
Dab2 |
A |
G |
15: 6,464,644 (GRCm39) |
|
probably null |
Het |
Dnajb6 |
T |
C |
5: 29,956,006 (GRCm39) |
F46L |
possibly damaging |
Het |
Exoc7 |
T |
C |
11: 116,187,588 (GRCm39) |
E275G |
probably benign |
Het |
Frem2 |
A |
G |
3: 53,559,491 (GRCm39) |
I1672T |
probably benign |
Het |
Gprc6a |
C |
A |
10: 51,497,197 (GRCm39) |
V449L |
probably benign |
Het |
H2-M10.4 |
A |
G |
17: 36,772,877 (GRCm39) |
V35A |
probably benign |
Het |
Hr |
A |
G |
14: 70,801,024 (GRCm39) |
T699A |
probably benign |
Het |
Iffo1 |
A |
G |
6: 125,137,552 (GRCm39) |
|
probably benign |
Het |
Iqgap1 |
G |
A |
7: 80,409,682 (GRCm39) |
H218Y |
probably damaging |
Het |
Itpr3 |
A |
C |
17: 27,304,105 (GRCm39) |
K109Q |
probably benign |
Het |
Itpr3 |
A |
G |
17: 27,310,546 (GRCm39) |
D443G |
probably damaging |
Het |
Katna1 |
T |
C |
10: 7,628,518 (GRCm39) |
M249T |
probably damaging |
Het |
Klk1b4 |
G |
A |
7: 43,861,017 (GRCm39) |
G220D |
probably damaging |
Het |
Krt24 |
A |
G |
11: 99,173,596 (GRCm39) |
C242R |
probably benign |
Het |
Madd |
G |
A |
2: 91,007,173 (GRCm39) |
T313I |
possibly damaging |
Het |
Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
Mical2 |
A |
G |
7: 112,006,885 (GRCm39) |
|
probably null |
Het |
Neil3 |
T |
C |
8: 54,076,699 (GRCm39) |
T79A |
probably damaging |
Het |
Nras |
A |
G |
3: 102,967,541 (GRCm39) |
I46V |
probably benign |
Het |
Or4a66 |
T |
C |
2: 88,530,792 (GRCm39) |
S294G |
probably benign |
Het |
Ppfia2 |
A |
G |
10: 106,666,490 (GRCm39) |
T399A |
possibly damaging |
Het |
Rarres1 |
A |
G |
3: 67,403,143 (GRCm39) |
V86A |
probably benign |
Het |
Rdh19 |
A |
T |
10: 127,685,944 (GRCm39) |
R19W |
possibly damaging |
Het |
Rock2 |
A |
G |
12: 17,022,737 (GRCm39) |
K1059E |
probably damaging |
Het |
Sft2d1rt |
T |
A |
11: 45,942,853 (GRCm39) |
K90M |
probably damaging |
Het |
Sparcl1 |
T |
C |
5: 104,240,647 (GRCm39) |
H259R |
probably benign |
Het |
Spata31d1c |
A |
G |
13: 65,182,974 (GRCm39) |
D172G |
possibly damaging |
Het |
Stab2 |
T |
C |
10: 86,699,320 (GRCm39) |
D515G |
possibly damaging |
Het |
Sycp2l |
A |
G |
13: 41,295,440 (GRCm39) |
I334M |
probably damaging |
Het |
Tas2r103 |
A |
G |
6: 133,013,280 (GRCm39) |
L262P |
probably benign |
Het |
Tasor |
T |
C |
14: 27,199,087 (GRCm39) |
L1335S |
possibly damaging |
Het |
Tcaf2 |
A |
G |
6: 42,619,481 (GRCm39) |
V182A |
probably damaging |
Het |
Tcof1 |
C |
T |
18: 60,964,605 (GRCm39) |
E674K |
possibly damaging |
Het |
Trp63 |
A |
G |
16: 25,639,490 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,575,738 (GRCm39) |
W25052R |
probably damaging |
Het |
Ubr1 |
T |
A |
2: 120,693,168 (GRCm39) |
N1746I |
probably benign |
Het |
Vax2 |
T |
C |
6: 83,714,529 (GRCm39) |
V148A |
probably damaging |
Het |
Vmn2r112 |
T |
A |
17: 22,822,096 (GRCm39) |
V258E |
probably damaging |
Het |
Vmn2r96 |
T |
A |
17: 18,817,941 (GRCm39) |
I698N |
probably damaging |
Het |
Wdr90 |
A |
G |
17: 26,078,252 (GRCm39) |
V372A |
probably benign |
Het |
Zfp335 |
C |
T |
2: 164,752,558 (GRCm39) |
G62D |
probably benign |
Het |
Zfp563 |
G |
A |
17: 33,324,701 (GRCm39) |
R432H |
probably benign |
Het |
Zhx1 |
T |
C |
15: 57,916,636 (GRCm39) |
T537A |
probably benign |
Het |
|
Other mutations in Or2w1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01689:Or2w1b
|
APN |
13 |
21,300,243 (GRCm39) |
missense |
probably damaging |
0.97 |
R0631:Or2w1b
|
UTSW |
13 |
21,300,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R0960:Or2w1b
|
UTSW |
13 |
21,300,435 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1499:Or2w1b
|
UTSW |
13 |
21,300,303 (GRCm39) |
missense |
probably benign |
0.32 |
R1549:Or2w1b
|
UTSW |
13 |
21,300,288 (GRCm39) |
missense |
probably benign |
0.01 |
R1698:Or2w1b
|
UTSW |
13 |
21,300,735 (GRCm39) |
missense |
probably benign |
0.11 |
R1711:Or2w1b
|
UTSW |
13 |
21,300,476 (GRCm39) |
missense |
probably benign |
0.01 |
R2404:Or2w1b
|
UTSW |
13 |
21,300,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R2471:Or2w1b
|
UTSW |
13 |
21,300,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R3844:Or2w1b
|
UTSW |
13 |
21,300,233 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3977:Or2w1b
|
UTSW |
13 |
21,300,031 (GRCm39) |
missense |
probably benign |
0.03 |
R4804:Or2w1b
|
UTSW |
13 |
21,300,175 (GRCm39) |
nonsense |
probably null |
|
R4914:Or2w1b
|
UTSW |
13 |
21,300,567 (GRCm39) |
missense |
probably benign |
0.12 |
R5210:Or2w1b
|
UTSW |
13 |
21,300,222 (GRCm39) |
missense |
probably damaging |
0.99 |
R5359:Or2w1b
|
UTSW |
13 |
21,300,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R5700:Or2w1b
|
UTSW |
13 |
21,300,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R6218:Or2w1b
|
UTSW |
13 |
21,300,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R6767:Or2w1b
|
UTSW |
13 |
21,300,227 (GRCm39) |
missense |
probably benign |
0.02 |
R7396:Or2w1b
|
UTSW |
13 |
21,300,477 (GRCm39) |
missense |
probably benign |
0.02 |
R7476:Or2w1b
|
UTSW |
13 |
21,300,191 (GRCm39) |
missense |
probably benign |
0.04 |
R7612:Or2w1b
|
UTSW |
13 |
21,300,217 (GRCm39) |
missense |
probably damaging |
0.99 |
R8257:Or2w1b
|
UTSW |
13 |
21,300,543 (GRCm39) |
missense |
probably benign |
0.11 |
R9388:Or2w1b
|
UTSW |
13 |
21,300,774 (GRCm39) |
missense |
probably damaging |
0.96 |
R9697:Or2w1b
|
UTSW |
13 |
21,299,892 (GRCm39) |
missense |
probably benign |
0.21 |
V8831:Or2w1b
|
UTSW |
13 |
21,300,173 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1176:Or2w1b
|
UTSW |
13 |
21,300,771 (GRCm39) |
missense |
probably damaging |
1.00 |
|