Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
T |
11: 110,025,085 (GRCm39) |
M986K |
probably benign |
Het |
Adcyap1 |
A |
G |
17: 93,511,413 (GRCm39) |
K129R |
probably benign |
Het |
Anapc1 |
T |
C |
2: 128,526,528 (GRCm39) |
D90G |
probably damaging |
Het |
Ankrd17 |
G |
A |
5: 90,411,213 (GRCm39) |
H1361Y |
probably damaging |
Het |
Aqp4 |
T |
A |
18: 15,532,737 (GRCm39) |
I119F |
possibly damaging |
Het |
Bfsp1 |
T |
A |
2: 143,673,770 (GRCm39) |
I313F |
possibly damaging |
Het |
Cxcl9 |
A |
G |
5: 92,475,869 (GRCm39) |
V5A |
probably benign |
Het |
Cyfip1 |
G |
A |
7: 55,536,483 (GRCm39) |
V304M |
probably damaging |
Het |
Cyp2j12 |
A |
G |
4: 95,987,893 (GRCm39) |
V499A |
possibly damaging |
Het |
Cyth3 |
A |
G |
5: 143,683,509 (GRCm39) |
E136G |
probably benign |
Het |
Degs2 |
CTTAGTGAAT |
CT |
12: 108,658,460 (GRCm39) |
|
probably null |
Het |
Dnah7a |
A |
G |
1: 53,606,334 (GRCm39) |
S1229P |
probably benign |
Het |
Dop1a |
T |
A |
9: 86,424,818 (GRCm39) |
C2087* |
probably null |
Het |
Dop1b |
A |
T |
16: 93,560,829 (GRCm39) |
H889L |
probably damaging |
Het |
Elf1 |
A |
G |
14: 79,773,855 (GRCm39) |
E22G |
probably benign |
Het |
Gbgt1 |
T |
C |
2: 28,393,182 (GRCm39) |
V90A |
probably damaging |
Het |
Glis3 |
T |
C |
19: 28,294,773 (GRCm39) |
D675G |
possibly damaging |
Het |
Glt8d1 |
G |
T |
14: 30,723,788 (GRCm39) |
|
probably benign |
Het |
Gzf1 |
T |
A |
2: 148,525,815 (GRCm39) |
Y95* |
probably null |
Het |
Insig2 |
T |
C |
1: 121,240,049 (GRCm39) |
I84V |
probably benign |
Het |
Mapkapk2 |
A |
G |
1: 131,025,256 (GRCm39) |
S3P |
unknown |
Het |
Nell2 |
T |
C |
15: 95,196,819 (GRCm39) |
N499S |
probably benign |
Het |
Nlrp9b |
G |
A |
7: 19,758,398 (GRCm39) |
R545H |
possibly damaging |
Het |
Obox7 |
T |
A |
7: 14,399,350 (GRCm39) |
I192N |
probably benign |
Het |
Or10ad1 |
T |
C |
15: 98,106,026 (GRCm39) |
I80V |
probably damaging |
Het |
Or6c76b |
A |
T |
10: 129,692,899 (GRCm39) |
I171F |
possibly damaging |
Het |
Plec |
A |
T |
15: 76,060,583 (GRCm39) |
V3118E |
probably damaging |
Het |
Plk3 |
T |
C |
4: 116,986,527 (GRCm39) |
T571A |
probably damaging |
Het |
Ppa2 |
T |
C |
3: 133,082,351 (GRCm39) |
|
probably null |
Het |
Rabl6 |
A |
T |
2: 25,482,829 (GRCm39) |
H183Q |
probably damaging |
Het |
Rad51ap2 |
T |
A |
12: 11,507,238 (GRCm39) |
S387T |
possibly damaging |
Het |
Rbm33 |
A |
G |
5: 28,573,397 (GRCm39) |
|
probably null |
Het |
Robo4 |
T |
C |
9: 37,322,055 (GRCm39) |
S724P |
probably damaging |
Het |
Rtf2 |
T |
C |
2: 172,308,253 (GRCm39) |
|
probably null |
Het |
Sft2d1rt |
T |
C |
11: 45,942,887 (GRCm39) |
T79A |
possibly damaging |
Het |
Slc45a2 |
A |
T |
15: 11,027,835 (GRCm39) |
Q468L |
probably benign |
Het |
Slc6a15 |
A |
G |
10: 103,240,660 (GRCm39) |
I428V |
probably benign |
Het |
Sp140l2 |
C |
T |
1: 85,224,736 (GRCm39) |
M266I |
probably benign |
Het |
Taar7f |
C |
A |
10: 23,925,967 (GRCm39) |
A187E |
possibly damaging |
Het |
Tmt1a |
T |
C |
15: 100,202,957 (GRCm39) |
V77A |
possibly damaging |
Het |
Tob1 |
T |
A |
11: 94,104,598 (GRCm39) |
Y45N |
probably damaging |
Het |
Trappc10 |
A |
G |
10: 78,024,646 (GRCm39) |
V1161A |
possibly damaging |
Het |
Trbv13-2 |
T |
C |
6: 41,098,521 (GRCm39) |
V32A |
probably benign |
Het |
Trpm8 |
T |
A |
1: 88,254,176 (GRCm39) |
L133Q |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,538,512 (GRCm39) |
T34729A |
probably benign |
Het |
Uba6 |
G |
T |
5: 86,270,271 (GRCm39) |
|
probably null |
Het |
Unc13c |
T |
C |
9: 73,840,596 (GRCm39) |
D85G |
possibly damaging |
Het |
Vmn1r176 |
T |
C |
7: 23,534,394 (GRCm39) |
D253G |
possibly damaging |
Het |
Vmn2r34 |
T |
A |
7: 7,687,173 (GRCm39) |
I175F |
possibly damaging |
Het |
Vmn2r61 |
T |
A |
7: 41,916,032 (GRCm39) |
I215N |
probably damaging |
Het |
Vwa5a |
C |
A |
9: 38,634,799 (GRCm39) |
S202R |
probably damaging |
Het |
Zfp383 |
G |
A |
7: 29,614,483 (GRCm39) |
C246Y |
probably damaging |
Het |
Zfp40 |
T |
C |
17: 23,395,963 (GRCm39) |
D208G |
probably damaging |
Het |
Zfp992 |
C |
A |
4: 146,550,875 (GRCm39) |
L199I |
probably benign |
Het |
|
Other mutations in Cyp2d22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01305:Cyp2d22
|
APN |
15 |
82,255,869 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01750:Cyp2d22
|
APN |
15 |
82,258,570 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01801:Cyp2d22
|
APN |
15 |
82,257,046 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02449:Cyp2d22
|
APN |
15 |
82,257,442 (GRCm39) |
missense |
probably benign |
0.00 |
ANU22:Cyp2d22
|
UTSW |
15 |
82,255,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R0165:Cyp2d22
|
UTSW |
15 |
82,257,481 (GRCm39) |
missense |
probably benign |
0.06 |
R0294:Cyp2d22
|
UTSW |
15 |
82,258,646 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1381:Cyp2d22
|
UTSW |
15 |
82,256,709 (GRCm39) |
missense |
probably benign |
0.00 |
R1479:Cyp2d22
|
UTSW |
15 |
82,256,137 (GRCm39) |
missense |
probably damaging |
0.97 |
R1562:Cyp2d22
|
UTSW |
15 |
82,258,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R1968:Cyp2d22
|
UTSW |
15 |
82,257,373 (GRCm39) |
missense |
probably benign |
0.04 |
R1972:Cyp2d22
|
UTSW |
15 |
82,260,028 (GRCm39) |
missense |
probably benign |
0.11 |
R4492:Cyp2d22
|
UTSW |
15 |
82,258,571 (GRCm39) |
missense |
probably benign |
0.00 |
R4575:Cyp2d22
|
UTSW |
15 |
82,256,133 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4702:Cyp2d22
|
UTSW |
15 |
82,260,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R4703:Cyp2d22
|
UTSW |
15 |
82,260,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R5344:Cyp2d22
|
UTSW |
15 |
82,255,839 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5523:Cyp2d22
|
UTSW |
15 |
82,256,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R5888:Cyp2d22
|
UTSW |
15 |
82,258,014 (GRCm39) |
missense |
probably benign |
|
R6060:Cyp2d22
|
UTSW |
15 |
82,260,086 (GRCm39) |
missense |
probably benign |
0.00 |
R6108:Cyp2d22
|
UTSW |
15 |
82,256,106 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6146:Cyp2d22
|
UTSW |
15 |
82,258,036 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6279:Cyp2d22
|
UTSW |
15 |
82,258,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R6563:Cyp2d22
|
UTSW |
15 |
82,256,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R7597:Cyp2d22
|
UTSW |
15 |
82,260,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R7709:Cyp2d22
|
UTSW |
15 |
82,258,612 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8094:Cyp2d22
|
UTSW |
15 |
82,258,556 (GRCm39) |
missense |
probably benign |
0.19 |
R8302:Cyp2d22
|
UTSW |
15 |
82,256,021 (GRCm39) |
critical splice donor site |
probably null |
|
R8515:Cyp2d22
|
UTSW |
15 |
82,258,113 (GRCm39) |
missense |
probably benign |
0.27 |
R9245:Cyp2d22
|
UTSW |
15 |
82,256,748 (GRCm39) |
missense |
probably damaging |
0.97 |
R9323:Cyp2d22
|
UTSW |
15 |
82,258,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R9521:Cyp2d22
|
UTSW |
15 |
82,256,688 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1186:Cyp2d22
|
UTSW |
15 |
82,260,086 (GRCm39) |
missense |
probably benign |
0.00 |
Z1190:Cyp2d22
|
UTSW |
15 |
82,260,086 (GRCm39) |
missense |
probably benign |
0.00 |
|