Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrf4 |
T |
C |
17: 42,980,581 (GRCm39) |
N168S |
probably damaging |
Het |
Angptl3 |
A |
T |
4: 98,919,349 (GRCm39) |
R36S |
probably damaging |
Het |
Ap5z1 |
T |
C |
5: 142,460,214 (GRCm39) |
F514L |
probably benign |
Het |
Arhgef39 |
C |
A |
4: 43,497,578 (GRCm39) |
|
probably null |
Het |
Aste1 |
A |
G |
9: 105,275,043 (GRCm39) |
S11G |
probably damaging |
Het |
Cadm4 |
T |
C |
7: 24,198,986 (GRCm39) |
V87A |
probably benign |
Het |
Cd177 |
A |
G |
7: 24,451,777 (GRCm39) |
I413T |
probably benign |
Het |
Col5a2 |
A |
G |
1: 45,430,230 (GRCm39) |
|
probably null |
Het |
Dera |
C |
T |
6: 137,807,269 (GRCm39) |
A239V |
probably damaging |
Het |
Ecm1 |
T |
C |
3: 95,643,499 (GRCm39) |
E283G |
probably damaging |
Het |
Eml6 |
G |
T |
11: 29,709,066 (GRCm39) |
H24N |
probably benign |
Het |
Etl4 |
A |
G |
2: 20,811,240 (GRCm39) |
K1425E |
possibly damaging |
Het |
Fgd3 |
G |
A |
13: 49,450,225 (GRCm39) |
S8L |
possibly damaging |
Het |
Gli1 |
T |
C |
10: 127,172,369 (GRCm39) |
E228G |
probably benign |
Het |
Hivep3 |
A |
G |
4: 119,990,771 (GRCm39) |
|
probably benign |
Het |
Iqcc |
A |
G |
4: 129,512,818 (GRCm39) |
S11P |
probably damaging |
Het |
Itpkc |
G |
A |
7: 26,927,300 (GRCm39) |
Q205* |
probably null |
Het |
Jmjd1c |
T |
A |
10: 67,056,171 (GRCm39) |
S530R |
possibly damaging |
Het |
Kcnq1 |
A |
G |
7: 142,737,453 (GRCm39) |
H257R |
possibly damaging |
Het |
Kcnt2 |
G |
A |
1: 140,304,121 (GRCm39) |
V164I |
probably benign |
Het |
Lgr5 |
T |
C |
10: 115,288,763 (GRCm39) |
H603R |
possibly damaging |
Het |
Lrp2 |
T |
C |
2: 69,343,723 (GRCm39) |
|
probably null |
Het |
Lrrn2 |
A |
G |
1: 132,865,555 (GRCm39) |
M207V |
possibly damaging |
Het |
Miip |
A |
G |
4: 147,949,735 (GRCm39) |
|
probably benign |
Het |
Mrps35 |
T |
C |
6: 146,949,808 (GRCm39) |
|
probably benign |
Het |
Nuf2 |
A |
T |
1: 169,341,069 (GRCm39) |
M184K |
probably benign |
Het |
Or10q1 |
C |
A |
19: 13,727,165 (GRCm39) |
R232S |
probably benign |
Het |
Or2f2 |
A |
G |
6: 42,767,398 (GRCm39) |
T142A |
probably benign |
Het |
Or4a15 |
A |
T |
2: 89,193,172 (GRCm39) |
N200K |
probably damaging |
Het |
Or8g32 |
A |
T |
9: 39,305,830 (GRCm39) |
I248F |
probably damaging |
Het |
Os9 |
T |
C |
10: 126,956,861 (GRCm39) |
I42V |
possibly damaging |
Het |
Rapgef4 |
A |
C |
2: 72,010,405 (GRCm39) |
Q177P |
probably damaging |
Het |
Rhpn2 |
T |
C |
7: 35,070,536 (GRCm39) |
|
probably benign |
Het |
Scn5a |
T |
C |
9: 119,314,958 (GRCm39) |
R1916G |
probably damaging |
Het |
Serpine1 |
T |
A |
5: 137,095,889 (GRCm39) |
|
probably benign |
Het |
Snd1 |
C |
T |
6: 28,880,278 (GRCm39) |
P684L |
possibly damaging |
Het |
Tgds |
T |
C |
14: 118,350,534 (GRCm39) |
N340D |
probably benign |
Het |
Trpc4 |
A |
T |
3: 54,223,075 (GRCm39) |
Y706F |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,584,166 (GRCm39) |
D22314V |
probably damaging |
Het |
Utrn |
G |
A |
10: 12,519,163 (GRCm39) |
T2263I |
probably damaging |
Het |
Vmn1r11 |
A |
T |
6: 57,115,022 (GRCm39) |
T229S |
possibly damaging |
Het |
Zfp142 |
T |
G |
1: 74,609,022 (GRCm39) |
H1488P |
probably damaging |
Het |
Zfp219 |
A |
G |
14: 52,246,758 (GRCm39) |
L78P |
probably damaging |
Het |
Zfp629 |
T |
A |
7: 127,211,042 (GRCm39) |
T256S |
probably benign |
Het |
|
Other mutations in Or14j2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Or14j2
|
APN |
17 |
37,885,808 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01061:Or14j2
|
APN |
17 |
37,885,795 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL01293:Or14j2
|
APN |
17 |
37,886,308 (GRCm39) |
missense |
probably benign |
|
IGL01370:Or14j2
|
APN |
17 |
37,885,412 (GRCm39) |
splice site |
probably null |
|
IGL01535:Or14j2
|
APN |
17 |
37,885,679 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02536:Or14j2
|
APN |
17 |
37,885,817 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02640:Or14j2
|
APN |
17 |
37,885,912 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02652:Or14j2
|
APN |
17 |
37,885,836 (GRCm39) |
nonsense |
probably null |
|
IGL02963:Or14j2
|
APN |
17 |
37,885,745 (GRCm39) |
missense |
probably benign |
0.09 |
R0104:Or14j2
|
UTSW |
17 |
37,885,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Or14j2
|
UTSW |
17 |
37,886,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R2904:Or14j2
|
UTSW |
17 |
37,885,705 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5129:Or14j2
|
UTSW |
17 |
37,886,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R5197:Or14j2
|
UTSW |
17 |
37,886,111 (GRCm39) |
missense |
probably benign |
0.00 |
R5347:Or14j2
|
UTSW |
17 |
37,885,618 (GRCm39) |
missense |
probably damaging |
0.97 |
R6044:Or14j2
|
UTSW |
17 |
37,885,426 (GRCm39) |
missense |
probably damaging |
0.96 |
R7048:Or14j2
|
UTSW |
17 |
37,886,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R7064:Or14j2
|
UTSW |
17 |
37,885,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R8123:Or14j2
|
UTSW |
17 |
37,885,653 (GRCm39) |
missense |
probably benign |
0.05 |
R8205:Or14j2
|
UTSW |
17 |
37,885,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R8710:Or14j2
|
UTSW |
17 |
37,885,540 (GRCm39) |
missense |
probably benign |
0.00 |
R8989:Or14j2
|
UTSW |
17 |
37,885,542 (GRCm39) |
missense |
probably benign |
0.01 |
R9323:Or14j2
|
UTSW |
17 |
37,886,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R9439:Or14j2
|
UTSW |
17 |
37,885,825 (GRCm39) |
missense |
probably benign |
0.00 |
X0062:Or14j2
|
UTSW |
17 |
37,885,388 (GRCm39) |
missense |
probably benign |
0.01 |
|