Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd13d |
A |
G |
19: 4,331,097 (GRCm39) |
S64P |
probably damaging |
Het |
Armh4 |
T |
C |
14: 49,988,896 (GRCm39) |
E691G |
probably damaging |
Het |
Bag4 |
T |
C |
8: 26,258,302 (GRCm39) |
S342G |
probably damaging |
Het |
Bbs1 |
G |
A |
19: 4,944,291 (GRCm39) |
T446I |
probably benign |
Het |
Bmyc |
A |
G |
2: 25,597,236 (GRCm39) |
D100G |
probably damaging |
Het |
Btbd7 |
T |
C |
12: 102,751,734 (GRCm39) |
D1010G |
possibly damaging |
Het |
Celsr3 |
A |
T |
9: 108,704,104 (GRCm39) |
T196S |
probably benign |
Het |
Crtam |
C |
A |
9: 40,884,918 (GRCm39) |
R161L |
probably benign |
Het |
Cyp11b2 |
C |
A |
15: 74,724,979 (GRCm39) |
G290V |
probably damaging |
Het |
Edc4 |
C |
T |
8: 106,617,843 (GRCm39) |
|
probably benign |
Het |
Exd1 |
A |
T |
2: 119,370,494 (GRCm39) |
|
probably benign |
Het |
Fam120a |
G |
T |
13: 49,039,219 (GRCm39) |
A979E |
possibly damaging |
Het |
Fbxo16 |
T |
C |
14: 65,524,623 (GRCm39) |
|
probably benign |
Het |
Fbxo44 |
C |
G |
4: 148,240,726 (GRCm39) |
R220S |
probably damaging |
Het |
Gabrb2 |
A |
G |
11: 42,420,298 (GRCm39) |
N173S |
probably damaging |
Het |
Gm13741 |
A |
T |
2: 87,486,674 (GRCm39) |
I197K |
possibly damaging |
Het |
Helb |
T |
A |
10: 119,944,871 (GRCm39) |
I222F |
probably damaging |
Het |
Hesx1 |
A |
T |
14: 26,723,876 (GRCm39) |
Q153L |
probably null |
Het |
Isca1 |
T |
C |
13: 59,910,593 (GRCm39) |
N33S |
probably benign |
Het |
Itsn2 |
T |
C |
12: 4,723,572 (GRCm39) |
V1142A |
probably damaging |
Het |
Lama5 |
T |
G |
2: 179,837,434 (GRCm39) |
T984P |
probably damaging |
Het |
Lima1 |
T |
A |
15: 99,717,626 (GRCm39) |
K127* |
probably null |
Het |
Lmbrd1 |
T |
A |
1: 24,785,959 (GRCm39) |
V418D |
probably damaging |
Het |
Mertk |
T |
C |
2: 128,620,883 (GRCm39) |
V575A |
probably damaging |
Het |
Mrps28 |
T |
C |
3: 8,965,184 (GRCm39) |
H85R |
probably benign |
Het |
Mrtfb |
T |
C |
16: 13,230,105 (GRCm39) |
V930A |
possibly damaging |
Het |
Naip2 |
G |
A |
13: 100,291,386 (GRCm39) |
T1184M |
probably benign |
Het |
Naip2 |
C |
T |
13: 100,298,368 (GRCm39) |
G556D |
probably benign |
Het |
Naip2 |
TCCC |
TCC |
13: 100,291,355 (GRCm39) |
|
probably benign |
Het |
Naip2 |
G |
A |
13: 100,291,380 (GRCm39) |
S1186F |
possibly damaging |
Het |
Nhlrc3 |
A |
T |
3: 53,369,836 (GRCm39) |
L45H |
probably damaging |
Het |
Or52e5 |
T |
G |
7: 104,719,226 (GRCm39) |
M184R |
probably damaging |
Het |
Or52u1 |
C |
T |
7: 104,237,682 (GRCm39) |
R224* |
probably null |
Het |
Or8s16 |
T |
C |
15: 98,211,324 (GRCm39) |
T36A |
probably damaging |
Het |
Parp14 |
G |
A |
16: 35,677,130 (GRCm39) |
A946V |
probably benign |
Het |
Pcdhb15 |
A |
T |
18: 37,606,975 (GRCm39) |
D69V |
probably damaging |
Het |
Pitpnm1 |
G |
A |
19: 4,162,392 (GRCm39) |
R1074H |
probably damaging |
Het |
Plb1 |
A |
G |
5: 32,450,601 (GRCm39) |
N381D |
probably benign |
Het |
Poc1b |
T |
C |
10: 98,988,725 (GRCm39) |
S247P |
probably damaging |
Het |
Riok1 |
T |
C |
13: 38,233,090 (GRCm39) |
M241T |
probably damaging |
Het |
Tigit |
T |
C |
16: 43,469,395 (GRCm39) |
E232G |
probably benign |
Het |
Tpst2 |
T |
A |
5: 112,455,488 (GRCm39) |
L9Q |
probably benign |
Het |
Ttbk1 |
T |
C |
17: 46,757,080 (GRCm39) |
|
probably benign |
Het |
Vmn1r3 |
A |
T |
4: 3,185,231 (GRCm39) |
N25K |
probably damaging |
Het |
Vmn2r121 |
T |
A |
X: 123,039,602 (GRCm39) |
H522L |
possibly damaging |
Het |
Vmn2r15 |
T |
C |
5: 109,441,093 (GRCm39) |
Y255C |
probably damaging |
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 |
IGL03401:Prl7b1
|
APN |
13 |
27,785,964 (GRCm39) |
missense |
probably benign |
0.02 |
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 |
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 |
|