Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl4 |
T |
A |
3: 151,203,511 (GRCm39) |
C124S |
probably damaging |
Het |
Aldh1a7 |
T |
C |
19: 20,704,368 (GRCm39) |
N42S |
probably damaging |
Het |
Arhgef1 |
T |
C |
7: 24,623,240 (GRCm39) |
L667P |
probably damaging |
Het |
C1qb |
C |
A |
4: 136,607,811 (GRCm39) |
R184L |
possibly damaging |
Het |
Cacna1s |
A |
G |
1: 136,002,914 (GRCm39) |
|
probably benign |
Het |
Cdk20 |
A |
G |
13: 64,585,734 (GRCm39) |
E244G |
probably benign |
Het |
Copg2 |
C |
A |
6: 30,840,469 (GRCm39) |
|
probably null |
Het |
Cyp2j6 |
A |
G |
4: 96,414,170 (GRCm39) |
I365T |
probably damaging |
Het |
Dhx29 |
A |
G |
13: 113,064,342 (GRCm39) |
K6E |
probably damaging |
Het |
Dpp10 |
T |
A |
1: 123,295,531 (GRCm39) |
T539S |
probably benign |
Het |
Ehbp1 |
A |
T |
11: 22,046,048 (GRCm39) |
I542K |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,493,593 (GRCm39) |
Y3913C |
probably damaging |
Het |
Flt4 |
C |
T |
11: 49,536,822 (GRCm39) |
T1264I |
probably benign |
Het |
Fmnl1 |
A |
G |
11: 103,070,364 (GRCm39) |
D51G |
probably damaging |
Het |
Gm17093 |
A |
G |
14: 44,755,807 (GRCm39) |
T25A |
unknown |
Het |
Gpatch2 |
A |
G |
1: 186,957,936 (GRCm39) |
E97G |
probably damaging |
Het |
Hcn1 |
T |
C |
13: 118,039,422 (GRCm39) |
L446P |
unknown |
Het |
Hpse2 |
A |
T |
19: 42,920,038 (GRCm39) |
L354I |
probably damaging |
Het |
Hspa4 |
A |
G |
11: 53,190,885 (GRCm39) |
|
probably null |
Het |
Krtap16-1 |
C |
T |
11: 99,877,129 (GRCm39) |
V92M |
probably damaging |
Het |
Med23 |
A |
T |
10: 24,773,239 (GRCm39) |
Q281L |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,039,873 (GRCm39) |
S963P |
probably benign |
Het |
Mical1 |
G |
A |
10: 41,362,660 (GRCm39) |
E932K |
possibly damaging |
Het |
Mycbp2 |
A |
G |
14: 103,479,643 (GRCm39) |
S1217P |
probably damaging |
Het |
Myocd |
C |
A |
11: 65,069,484 (GRCm39) |
L785F |
probably benign |
Het |
Nell2 |
T |
C |
15: 95,126,982 (GRCm39) |
T798A |
probably damaging |
Het |
Nfat5 |
T |
C |
8: 108,092,808 (GRCm39) |
|
probably benign |
Het |
Olfm5 |
T |
C |
7: 103,803,302 (GRCm39) |
|
probably null |
Het |
Or1e26 |
A |
G |
11: 73,480,081 (GRCm39) |
V161A |
probably benign |
Het |
P2ry1 |
A |
T |
3: 60,911,199 (GRCm39) |
N113Y |
possibly damaging |
Het |
Pan3 |
A |
G |
5: 147,466,933 (GRCm39) |
|
probably null |
Het |
Pappa |
A |
G |
4: 65,115,045 (GRCm39) |
R714G |
probably damaging |
Het |
Plcd1 |
A |
G |
9: 118,901,710 (GRCm39) |
F579L |
probably damaging |
Het |
Ptprb |
T |
C |
10: 116,155,238 (GRCm39) |
V664A |
probably benign |
Het |
Slc27a5 |
T |
A |
7: 12,731,487 (GRCm39) |
Q168L |
probably benign |
Het |
Spag8 |
T |
C |
4: 43,651,781 (GRCm39) |
E395G |
probably damaging |
Het |
Stfa2l1 |
T |
C |
16: 35,982,138 (GRCm39) |
Y70H |
probably damaging |
Het |
Taf2 |
T |
C |
15: 54,891,772 (GRCm39) |
N1017S |
probably benign |
Het |
Tnfrsf25 |
C |
A |
4: 152,203,779 (GRCm39) |
Q296K |
probably damaging |
Het |
Trpm3 |
T |
A |
19: 22,676,143 (GRCm39) |
I103N |
probably benign |
Het |
|
Other mutations in Cyp2d40 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01134:Cyp2d40
|
APN |
15 |
82,645,102 (GRCm39) |
missense |
unknown |
|
IGL01313:Cyp2d40
|
APN |
15 |
82,645,478 (GRCm39) |
missense |
unknown |
|
IGL01714:Cyp2d40
|
APN |
15 |
82,645,441 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02993:Cyp2d40
|
APN |
15 |
82,645,722 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03162:Cyp2d40
|
APN |
15 |
82,644,243 (GRCm39) |
missense |
unknown |
|
R0070:Cyp2d40
|
UTSW |
15 |
82,644,975 (GRCm39) |
missense |
unknown |
|
R0499:Cyp2d40
|
UTSW |
15 |
82,645,418 (GRCm39) |
missense |
probably benign |
0.11 |
R0885:Cyp2d40
|
UTSW |
15 |
82,645,116 (GRCm39) |
missense |
unknown |
|
R1587:Cyp2d40
|
UTSW |
15 |
82,645,334 (GRCm39) |
splice site |
probably null |
|
R1613:Cyp2d40
|
UTSW |
15 |
82,645,640 (GRCm39) |
missense |
unknown |
|
R4773:Cyp2d40
|
UTSW |
15 |
82,645,763 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5047:Cyp2d40
|
UTSW |
15 |
82,644,460 (GRCm39) |
missense |
unknown |
|
R5604:Cyp2d40
|
UTSW |
15 |
82,648,256 (GRCm39) |
missense |
probably damaging |
0.99 |
R6087:Cyp2d40
|
UTSW |
15 |
82,648,205 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6334:Cyp2d40
|
UTSW |
15 |
82,645,753 (GRCm39) |
missense |
probably benign |
0.03 |
R6841:Cyp2d40
|
UTSW |
15 |
82,645,687 (GRCm39) |
missense |
probably benign |
0.03 |
R7017:Cyp2d40
|
UTSW |
15 |
82,644,234 (GRCm39) |
missense |
unknown |
|
R7045:Cyp2d40
|
UTSW |
15 |
82,645,763 (GRCm39) |
missense |
probably benign |
0.01 |
R7565:Cyp2d40
|
UTSW |
15 |
82,644,975 (GRCm39) |
missense |
unknown |
|
R7934:Cyp2d40
|
UTSW |
15 |
82,648,212 (GRCm39) |
missense |
probably damaging |
0.99 |
R8896:Cyp2d40
|
UTSW |
15 |
82,644,454 (GRCm39) |
missense |
unknown |
|
R9378:Cyp2d40
|
UTSW |
15 |
82,645,802 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9522:Cyp2d40
|
UTSW |
15 |
82,648,274 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9558:Cyp2d40
|
UTSW |
15 |
82,645,667 (GRCm39) |
missense |
unknown |
|
|