Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110082I17Rik |
G |
A |
5: 139,349,770 (GRCm39) |
A93V |
probably benign |
Het |
Abca8b |
G |
A |
11: 109,865,865 (GRCm39) |
T296I |
possibly damaging |
Het |
Adamtsl1 |
A |
C |
4: 86,161,962 (GRCm39) |
Y365S |
probably damaging |
Het |
Ambp |
T |
A |
4: 63,067,677 (GRCm39) |
I178F |
probably damaging |
Het |
Ankle1 |
T |
C |
8: 71,858,899 (GRCm39) |
V44A |
possibly damaging |
Het |
Arhgef2 |
A |
G |
3: 88,537,221 (GRCm39) |
E37G |
probably damaging |
Het |
Atp2a2 |
A |
G |
5: 122,599,639 (GRCm39) |
I584T |
probably benign |
Het |
Ccdc171 |
T |
A |
4: 83,614,492 (GRCm39) |
L1031* |
probably null |
Het |
Cdh17 |
T |
A |
4: 11,799,754 (GRCm39) |
|
probably null |
Het |
Cdip1 |
T |
C |
16: 4,586,422 (GRCm39) |
T203A |
probably benign |
Het |
Ceacam1 |
C |
T |
7: 25,163,220 (GRCm39) |
V338I |
possibly damaging |
Het |
Cep78 |
G |
A |
19: 15,933,754 (GRCm39) |
T608I |
probably damaging |
Het |
Ces3a |
T |
A |
8: 105,775,345 (GRCm39) |
|
probably null |
Het |
Cfap210 |
G |
A |
2: 69,612,450 (GRCm39) |
Q97* |
probably null |
Het |
Chd7 |
A |
G |
4: 8,854,121 (GRCm39) |
T1898A |
probably benign |
Het |
Cpne6 |
T |
C |
14: 55,750,066 (GRCm39) |
C66R |
possibly damaging |
Het |
Creb1 |
G |
A |
1: 64,609,372 (GRCm39) |
A108T |
probably benign |
Het |
Ctnna3 |
A |
T |
10: 64,421,747 (GRCm39) |
I514F |
probably damaging |
Het |
Cyp2c55 |
T |
C |
19: 39,030,535 (GRCm39) |
F456L |
probably damaging |
Het |
Cyp2g1 |
A |
T |
7: 26,518,618 (GRCm39) |
T378S |
probably damaging |
Het |
Eif2b3 |
C |
A |
4: 116,923,675 (GRCm39) |
Q297K |
probably benign |
Het |
Fbll1 |
T |
C |
11: 35,689,048 (GRCm39) |
N72D |
unknown |
Het |
Fev |
C |
G |
1: 74,921,632 (GRCm39) |
R106P |
probably damaging |
Het |
Gal3st1 |
A |
G |
11: 3,948,405 (GRCm39) |
Y204C |
probably damaging |
Het |
Gm15130 |
A |
T |
2: 110,964,582 (GRCm39) |
L180Q |
|
Het |
Greb1l |
A |
T |
18: 10,474,371 (GRCm39) |
K229* |
probably null |
Het |
Haghl |
G |
T |
17: 26,002,519 (GRCm39) |
T214K |
probably damaging |
Het |
Hivep1 |
A |
G |
13: 42,308,174 (GRCm39) |
H138R |
probably benign |
Het |
Ighv1-53 |
G |
T |
12: 115,122,236 (GRCm39) |
Y46* |
probably null |
Het |
Igsf21 |
T |
C |
4: 139,761,755 (GRCm39) |
T308A |
possibly damaging |
Het |
Kcnb1 |
A |
G |
2: 166,946,536 (GRCm39) |
S771P |
probably benign |
Het |
Kndc1 |
T |
A |
7: 139,501,402 (GRCm39) |
M897K |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,367,727 (GRCm39) |
M2345V |
possibly damaging |
Het |
Mettl2 |
T |
C |
11: 105,019,773 (GRCm39) |
S137P |
probably benign |
Het |
Mrpl15 |
A |
G |
1: 4,844,725 (GRCm39) |
S189P |
probably benign |
Het |
Ndrg2 |
T |
C |
14: 52,143,661 (GRCm39) |
Q351R |
probably benign |
Het |
Nox4 |
A |
G |
7: 86,945,032 (GRCm39) |
N65S |
probably damaging |
Het |
Or1n1 |
A |
G |
2: 36,750,228 (GRCm39) |
I44T |
possibly damaging |
Het |
Or1p1b |
C |
T |
11: 74,131,326 (GRCm39) |
S312F |
probably benign |
Het |
Osbpl11 |
T |
A |
16: 33,056,752 (GRCm39) |
W729R |
probably damaging |
Het |
Oxct2b |
C |
A |
4: 123,010,447 (GRCm39) |
C122* |
probably null |
Het |
Pdcl3 |
A |
T |
1: 39,026,782 (GRCm39) |
|
probably benign |
Het |
Plcg1 |
A |
G |
2: 160,616,498 (GRCm39) |
H1294R |
possibly damaging |
Het |
Pnp2 |
C |
A |
14: 51,201,903 (GRCm39) |
S296R |
probably benign |
Het |
Ppp1r12c |
G |
A |
7: 4,488,416 (GRCm39) |
Q337* |
probably null |
Het |
Prr23a4 |
A |
G |
9: 98,785,880 (GRCm39) |
R182G |
possibly damaging |
Het |
Ranbp2 |
G |
A |
10: 58,312,297 (GRCm39) |
V1006I |
probably damaging |
Het |
Rxrg |
A |
G |
1: 167,454,927 (GRCm39) |
D170G |
probably damaging |
Het |
Sf3b3 |
T |
C |
8: 111,548,162 (GRCm39) |
T691A |
probably benign |
Het |
Slc1a4 |
A |
G |
11: 20,258,518 (GRCm39) |
I307T |
probably damaging |
Het |
Slc4a8 |
G |
A |
15: 100,685,173 (GRCm39) |
V235I |
probably damaging |
Het |
Srgap3 |
T |
A |
6: 112,708,450 (GRCm39) |
I750F |
probably damaging |
Het |
Trim30a |
A |
T |
7: 104,061,448 (GRCm39) |
L282Q |
probably damaging |
Het |
Tshr |
A |
G |
12: 91,478,702 (GRCm39) |
K183R |
possibly damaging |
Het |
Usp38 |
A |
T |
8: 81,711,077 (GRCm39) |
L986Q |
probably damaging |
Het |
Vmn1r257 |
T |
A |
7: 22,391,439 (GRCm39) |
T102S |
possibly damaging |
Het |
Vps18 |
A |
G |
2: 119,124,122 (GRCm39) |
T350A |
probably benign |
Het |
Zan |
T |
A |
5: 137,461,841 (GRCm39) |
T1113S |
unknown |
Het |
Zbtb37 |
A |
T |
1: 160,857,305 (GRCm39) |
S312R |
probably damaging |
Het |
Zeb1 |
A |
G |
18: 5,748,703 (GRCm39) |
N90S |
probably benign |
Het |
Zfp715 |
A |
T |
7: 42,949,308 (GRCm39) |
Y217* |
probably null |
Het |
Zfp9 |
T |
C |
6: 118,441,847 (GRCm39) |
T272A |
probably damaging |
Het |
Zfp943 |
T |
A |
17: 22,212,361 (GRCm39) |
H482Q |
probably damaging |
Het |
Zfp971 |
A |
T |
2: 177,675,173 (GRCm39) |
K257N |
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 |
IGL02324:Cyp2d40
|
APN |
15 |
82,645,149 (GRCm39) |
splice site |
probably benign |
|
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 |
|
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 |
|
|