Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
A |
14: 32,384,223 (GRCm39) |
R581* |
probably null |
Het |
Actn1 |
A |
T |
12: 80,215,741 (GRCm39) |
L799* |
probably null |
Het |
Adam12 |
A |
T |
7: 133,518,192 (GRCm39) |
N327K |
probably damaging |
Het |
Adamts9 |
A |
G |
6: 92,763,849 (GRCm39) |
V1314A |
probably damaging |
Het |
Agbl4 |
G |
T |
4: 110,976,216 (GRCm39) |
R191L |
probably damaging |
Het |
Ano6 |
T |
C |
15: 95,847,786 (GRCm39) |
I611T |
probably damaging |
Het |
Arhgef26 |
T |
A |
3: 62,330,953 (GRCm39) |
S556T |
possibly damaging |
Het |
AW209491 |
A |
G |
13: 14,812,041 (GRCm39) |
D298G |
probably benign |
Het |
Cc2d1a |
A |
G |
8: 84,861,258 (GRCm39) |
M763T |
probably benign |
Het |
Cep290 |
A |
G |
10: 100,336,127 (GRCm39) |
D388G |
probably benign |
Het |
Cept1 |
T |
C |
3: 106,440,706 (GRCm39) |
E151G |
probably damaging |
Het |
Chat |
T |
C |
14: 32,174,526 (GRCm39) |
K139E |
probably damaging |
Het |
Edc4 |
T |
A |
8: 106,614,146 (GRCm39) |
Y7* |
probably null |
Het |
Enpep |
T |
A |
3: 129,106,269 (GRCm39) |
Q319L |
probably benign |
Het |
F13a1 |
A |
G |
13: 37,082,054 (GRCm39) |
I550T |
probably benign |
Het |
Fbxw19 |
A |
G |
9: 109,324,038 (GRCm39) |
|
probably null |
Het |
Frem3 |
T |
G |
8: 81,341,170 (GRCm39) |
D1154E |
probably damaging |
Het |
Frmpd1 |
G |
T |
4: 45,284,383 (GRCm39) |
C1068F |
probably benign |
Het |
Fsip2 |
C |
A |
2: 82,820,814 (GRCm39) |
P5516T |
probably benign |
Het |
Hyou1 |
G |
A |
9: 44,296,206 (GRCm39) |
A429T |
probably damaging |
Het |
Lrp1b |
C |
T |
2: 41,000,790 (GRCm39) |
E2145K |
probably benign |
Het |
Map1b |
A |
T |
13: 99,563,776 (GRCm39) |
V2397D |
unknown |
Het |
Mcm3ap |
T |
C |
10: 76,320,483 (GRCm39) |
|
probably benign |
Het |
Mgst2 |
T |
G |
3: 51,571,933 (GRCm39) |
S20R |
possibly damaging |
Het |
Nr4a3 |
T |
A |
4: 48,070,987 (GRCm39) |
|
probably null |
Het |
Nup93 |
T |
A |
8: 95,036,339 (GRCm39) |
|
probably null |
Het |
Or1e1f |
T |
C |
11: 73,856,388 (GRCm39) |
|
probably benign |
Het |
Papola |
A |
T |
12: 105,795,381 (GRCm39) |
T611S |
probably benign |
Het |
Pik3ca |
C |
A |
3: 32,491,963 (GRCm39) |
|
probably null |
Het |
Pklr |
T |
C |
3: 89,050,036 (GRCm39) |
V337A |
probably benign |
Het |
Proc |
T |
C |
18: 32,256,326 (GRCm39) |
Y447C |
possibly damaging |
Het |
Pum1 |
T |
C |
4: 130,470,992 (GRCm39) |
|
probably benign |
Het |
Rimklb |
A |
T |
6: 122,441,077 (GRCm39) |
I32N |
probably damaging |
Het |
Rrm1 |
T |
A |
7: 102,114,951 (GRCm39) |
D644E |
possibly damaging |
Het |
Scgb2b7 |
A |
T |
7: 31,404,506 (GRCm39) |
C65S |
probably damaging |
Het |
Shbg |
A |
G |
11: 69,505,925 (GRCm39) |
S361P |
probably damaging |
Het |
Trmt9b |
A |
C |
8: 36,972,823 (GRCm39) |
D91A |
probably damaging |
Het |
Zfp647 |
T |
A |
15: 76,795,568 (GRCm39) |
H364L |
probably damaging |
Het |
Zfp715 |
A |
T |
7: 42,949,160 (GRCm39) |
S267T |
probably benign |
Het |
|
Other mutations in Prl7b1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00473:Prl7b1
|
APN |
13 |
27,788,573 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01350:Prl7b1
|
APN |
13 |
27,786,804 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01602:Prl7b1
|
APN |
13 |
27,786,027 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL01605:Prl7b1
|
APN |
13 |
27,786,027 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03106:Prl7b1
|
APN |
13 |
27,790,918 (GRCm39) |
missense |
probably benign |
0.17 |
fleshy
|
UTSW |
13 |
27,786,878 (GRCm39) |
splice site |
probably null |
|
G1Funyon:Prl7b1
|
UTSW |
13 |
27,786,755 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1169:Prl7b1
|
UTSW |
13 |
27,790,887 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1423:Prl7b1
|
UTSW |
13 |
27,786,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R1846:Prl7b1
|
UTSW |
13 |
27,786,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R2294:Prl7b1
|
UTSW |
13 |
27,786,854 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6049:Prl7b1
|
UTSW |
13 |
27,790,161 (GRCm39) |
missense |
probably benign |
0.03 |
R6065:Prl7b1
|
UTSW |
13 |
27,788,529 (GRCm39) |
missense |
probably benign |
0.01 |
R6324:Prl7b1
|
UTSW |
13 |
27,786,878 (GRCm39) |
splice site |
probably null |
|
R6870:Prl7b1
|
UTSW |
13 |
27,788,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R7473:Prl7b1
|
UTSW |
13 |
27,785,996 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7742:Prl7b1
|
UTSW |
13 |
27,791,031 (GRCm39) |
missense |
probably benign |
0.07 |
R8301:Prl7b1
|
UTSW |
13 |
27,786,755 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9131:Prl7b1
|
UTSW |
13 |
27,790,968 (GRCm39) |
missense |
probably benign |
0.00 |
|