Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933411K16Rik |
C |
T |
19: 42,041,112 (GRCm39) |
A81V |
probably benign |
Het |
Abcc9 |
A |
T |
6: 142,634,853 (GRCm39) |
L137* |
probably null |
Het |
Akap10 |
A |
G |
11: 61,777,524 (GRCm39) |
|
probably null |
Het |
Alms1 |
T |
A |
6: 85,601,604 (GRCm39) |
Y1683N |
probably damaging |
Het |
Atl1 |
A |
G |
12: 69,978,408 (GRCm39) |
S127G |
probably damaging |
Het |
Cadm1 |
G |
A |
9: 47,710,708 (GRCm39) |
V204M |
probably damaging |
Het |
Cbr3 |
T |
A |
16: 93,487,438 (GRCm39) |
I207N |
probably damaging |
Het |
Ccdc148 |
A |
T |
2: 58,717,579 (GRCm39) |
Y475N |
probably damaging |
Het |
Ccdc33 |
A |
T |
9: 57,988,167 (GRCm39) |
S144T |
probably benign |
Het |
Ceacam5 |
C |
A |
7: 17,479,462 (GRCm39) |
A193E |
probably benign |
Het |
Chd2 |
T |
C |
7: 73,119,418 (GRCm39) |
D1042G |
probably benign |
Het |
Chmp5 |
A |
T |
4: 40,952,217 (GRCm39) |
|
probably null |
Het |
Clca3a1 |
T |
A |
3: 144,717,567 (GRCm39) |
N467I |
probably damaging |
Het |
D130040H23Rik |
T |
C |
8: 69,754,931 (GRCm39) |
V112A |
probably damaging |
Het |
Dbh |
A |
T |
2: 27,058,318 (GRCm39) |
D162V |
probably damaging |
Het |
Dnah12 |
G |
A |
14: 26,500,869 (GRCm39) |
|
probably null |
Het |
Dnm2 |
C |
T |
9: 21,385,862 (GRCm39) |
T295I |
probably benign |
Het |
Faiml |
A |
C |
9: 99,116,446 (GRCm39) |
D81E |
probably benign |
Het |
Fer1l4 |
T |
A |
2: 155,886,477 (GRCm39) |
Y720F |
probably benign |
Het |
Fn1 |
A |
C |
1: 71,639,697 (GRCm39) |
|
probably benign |
Het |
Ftsj3 |
T |
C |
11: 106,143,123 (GRCm39) |
E397G |
probably damaging |
Het |
Gm16506 |
T |
C |
14: 43,964,817 (GRCm39) |
K42E |
|
Het |
Gpr179 |
A |
G |
11: 97,225,556 (GRCm39) |
S2200P |
probably benign |
Het |
Gusb |
T |
C |
5: 130,028,884 (GRCm39) |
D202G |
probably benign |
Het |
Hspe1 |
A |
G |
1: 55,128,310 (GRCm39) |
E35G |
probably damaging |
Het |
Kptn |
T |
A |
7: 15,857,023 (GRCm39) |
H170Q |
probably damaging |
Het |
Lama3 |
G |
A |
18: 12,595,839 (GRCm39) |
A923T |
probably benign |
Het |
Lmo7 |
T |
A |
14: 102,124,471 (GRCm39) |
I432K |
probably damaging |
Het |
Maneal |
G |
A |
4: 124,750,905 (GRCm39) |
P284S |
probably benign |
Het |
Mrgbp |
A |
G |
2: 180,224,682 (GRCm39) |
T28A |
probably benign |
Het |
Myo1h |
T |
C |
5: 114,476,290 (GRCm39) |
V493A |
|
Het |
Naxd |
T |
C |
8: 11,556,745 (GRCm39) |
L122P |
probably damaging |
Het |
Neto2 |
T |
C |
8: 86,397,020 (GRCm39) |
|
probably null |
Het |
Obscn |
T |
A |
11: 58,904,078 (GRCm39) |
R7299* |
probably null |
Het |
Odf2l |
G |
A |
3: 144,845,581 (GRCm39) |
V363I |
possibly damaging |
Het |
Or2g25 |
T |
C |
17: 37,970,699 (GRCm39) |
H175R |
probably damaging |
Het |
Or2t35 |
A |
G |
14: 14,407,998 (GRCm38) |
T257A |
possibly damaging |
Het |
Or4c100 |
A |
T |
2: 88,356,170 (GRCm39) |
D81V |
probably damaging |
Het |
Or52a5b |
A |
T |
7: 103,416,940 (GRCm39) |
Y221* |
probably null |
Het |
Otud3 |
G |
A |
4: 138,624,067 (GRCm39) |
P325L |
probably benign |
Het |
Palb2 |
T |
C |
7: 121,724,057 (GRCm39) |
N564S |
probably benign |
Het |
Pcnt |
A |
G |
10: 76,263,761 (GRCm39) |
V401A |
possibly damaging |
Het |
Plcd4 |
G |
A |
1: 74,604,524 (GRCm39) |
E767K |
probably benign |
Het |
Ppp3ca |
T |
C |
3: 136,574,387 (GRCm39) |
F95S |
probably damaging |
Het |
Prkar2a |
A |
G |
9: 108,569,821 (GRCm39) |
T56A |
probably benign |
Het |
Psma2 |
T |
A |
13: 14,799,815 (GRCm39) |
D186E |
probably benign |
Het |
Psmd11 |
T |
A |
11: 80,329,099 (GRCm39) |
Y72* |
probably null |
Het |
Ror1 |
G |
A |
4: 100,160,142 (GRCm39) |
D53N |
probably benign |
Het |
Rubcn |
C |
T |
16: 32,656,839 (GRCm39) |
R527Q |
probably damaging |
Het |
Sgca |
G |
A |
11: 94,860,373 (GRCm39) |
P255S |
possibly damaging |
Het |
Skint11 |
A |
T |
4: 114,084,993 (GRCm39) |
R167S |
probably benign |
Het |
Slco5a1 |
A |
G |
1: 13,060,661 (GRCm39) |
V20A |
probably benign |
Het |
Snai2 |
T |
C |
16: 14,524,970 (GRCm39) |
S159P |
probably benign |
Het |
Taar2 |
T |
G |
10: 23,816,725 (GRCm39) |
S88R |
probably damaging |
Het |
Tacc3 |
T |
A |
5: 33,824,509 (GRCm39) |
N378K |
possibly damaging |
Het |
Tek |
A |
G |
4: 94,699,647 (GRCm39) |
K342E |
probably benign |
Het |
Tm9sf3 |
G |
T |
19: 41,233,944 (GRCm39) |
S198* |
probably null |
Het |
Tmbim4 |
T |
A |
10: 120,051,514 (GRCm39) |
F56I |
possibly damaging |
Het |
Tsen34 |
T |
A |
7: 3,697,986 (GRCm39) |
S85T |
probably benign |
Het |
Ttc27 |
C |
A |
17: 75,054,710 (GRCm39) |
Q339K |
probably benign |
Het |
Ubap2 |
G |
T |
4: 41,205,550 (GRCm39) |
P636T |
probably benign |
Het |
Ubr1 |
G |
A |
2: 120,705,979 (GRCm39) |
L1495F |
probably benign |
Het |
Vsig10 |
T |
C |
5: 117,481,967 (GRCm39) |
S386P |
probably damaging |
Het |
Wnk2 |
C |
A |
13: 49,300,653 (GRCm39) |
R19L |
probably benign |
Het |
Wsb2 |
T |
C |
5: 117,508,944 (GRCm39) |
L126P |
probably damaging |
Het |
Xylb |
A |
G |
9: 119,211,358 (GRCm39) |
I402V |
probably benign |
Het |
Yrdc |
A |
G |
4: 124,744,748 (GRCm39) |
S61G |
probably benign |
Het |
Zbtb3 |
A |
G |
19: 8,780,771 (GRCm39) |
D128G |
probably damaging |
Het |
Zfp423 |
C |
T |
8: 88,507,489 (GRCm39) |
G952R |
probably damaging |
Het |
Zfp646 |
A |
G |
7: 127,478,944 (GRCm39) |
T374A |
possibly damaging |
Het |
|
Other mutations in Or5b105 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01684:Or5b105
|
APN |
19 |
13,080,353 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02319:Or5b105
|
APN |
19 |
13,080,026 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02926:Or5b105
|
APN |
19 |
13,080,187 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL03107:Or5b105
|
APN |
19 |
13,080,401 (GRCm39) |
missense |
probably benign |
|
IGL03304:Or5b105
|
APN |
19 |
13,080,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R0046:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0049:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0099:Or5b105
|
UTSW |
19 |
13,080,504 (GRCm39) |
missense |
probably benign |
0.07 |
R0103:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0144:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0189:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0206:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0207:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0208:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0212:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0344:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0426:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0506:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0507:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0607:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0661:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0734:Or5b105
|
UTSW |
19 |
13,080,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1347:Or5b105
|
UTSW |
19 |
13,080,054 (GRCm39) |
missense |
probably benign |
0.03 |
R1347:Or5b105
|
UTSW |
19 |
13,080,054 (GRCm39) |
missense |
probably benign |
0.03 |
R1443:Or5b105
|
UTSW |
19 |
13,080,568 (GRCm39) |
nonsense |
probably null |
|
R1446:Or5b105
|
UTSW |
19 |
13,080,380 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1567:Or5b105
|
UTSW |
19 |
13,080,006 (GRCm39) |
missense |
probably benign |
0.00 |
R2190:Or5b105
|
UTSW |
19 |
13,079,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R2438:Or5b105
|
UTSW |
19 |
13,079,785 (GRCm39) |
missense |
probably benign |
0.00 |
R4020:Or5b105
|
UTSW |
19 |
13,079,790 (GRCm39) |
missense |
probably damaging |
0.99 |
R4406:Or5b105
|
UTSW |
19 |
13,079,958 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4631:Or5b105
|
UTSW |
19 |
13,080,636 (GRCm39) |
missense |
probably benign |
0.07 |
R4847:Or5b105
|
UTSW |
19 |
13,079,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R4979:Or5b105
|
UTSW |
19 |
13,080,053 (GRCm39) |
missense |
probably damaging |
0.97 |
R6086:Or5b105
|
UTSW |
19 |
13,079,745 (GRCm39) |
makesense |
probably null |
|
R6480:Or5b105
|
UTSW |
19 |
13,079,838 (GRCm39) |
missense |
probably benign |
0.34 |
R6484:Or5b105
|
UTSW |
19 |
13,080,431 (GRCm39) |
missense |
probably benign |
0.34 |
R6786:Or5b105
|
UTSW |
19 |
13,080,567 (GRCm39) |
missense |
probably benign |
0.09 |
R7547:Or5b105
|
UTSW |
19 |
13,080,407 (GRCm39) |
missense |
not run |
|
R7822:Or5b105
|
UTSW |
19 |
13,080,417 (GRCm39) |
missense |
probably benign |
0.00 |
R7949:Or5b105
|
UTSW |
19 |
13,080,610 (GRCm39) |
splice site |
probably null |
|
R8219:Or5b105
|
UTSW |
19 |
13,080,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R8441:Or5b105
|
UTSW |
19 |
13,080,020 (GRCm39) |
missense |
probably damaging |
0.98 |
R8458:Or5b105
|
UTSW |
19 |
13,079,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R9283:Or5b105
|
UTSW |
19 |
13,079,821 (GRCm39) |
missense |
probably damaging |
0.99 |
R9330:Or5b105
|
UTSW |
19 |
13,080,588 (GRCm39) |
missense |
probably benign |
0.10 |
R9592:Or5b105
|
UTSW |
19 |
13,079,906 (GRCm39) |
missense |
probably benign |
0.13 |
R9677:Or5b105
|
UTSW |
19 |
13,080,518 (GRCm39) |
missense |
probably damaging |
0.99 |
R9725:Or5b105
|
UTSW |
19 |
13,080,272 (GRCm39) |
missense |
possibly damaging |
0.74 |
X0024:Or5b105
|
UTSW |
19 |
13,080,573 (GRCm39) |
missense |
probably benign |
0.22 |
X0027:Or5b105
|
UTSW |
19 |
13,080,588 (GRCm39) |
missense |
probably benign |
0.10 |
|