Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930111J21Rik2 |
G |
A |
11: 48,910,700 (GRCm39) |
H578Y |
probably damaging |
Het |
Atp11b |
A |
G |
3: 35,909,289 (GRCm39) |
D1161G |
probably damaging |
Het |
Atp8b1 |
G |
C |
18: 64,664,453 (GRCm39) |
I1238M |
probably benign |
Het |
AY358078 |
T |
A |
14: 52,059,617 (GRCm39) |
V318D |
unknown |
Het |
Boc |
T |
A |
16: 44,341,558 (GRCm39) |
I16F |
probably benign |
Het |
Brinp3 |
A |
T |
1: 146,577,537 (GRCm39) |
T191S |
probably benign |
Het |
Cald1 |
T |
A |
6: 34,739,255 (GRCm39) |
N419K |
probably damaging |
Het |
Cecr2 |
G |
A |
6: 120,732,521 (GRCm39) |
G471D |
probably damaging |
Het |
Cftr |
T |
A |
6: 18,255,364 (GRCm39) |
|
probably null |
Het |
Cyp2c38 |
T |
A |
19: 39,449,156 (GRCm39) |
T66S |
probably damaging |
Het |
Fbxo11 |
A |
T |
17: 88,323,136 (GRCm39) |
D83E |
probably benign |
Het |
Fshr |
T |
A |
17: 89,293,257 (GRCm39) |
M474L |
possibly damaging |
Het |
Hhla1 |
T |
A |
15: 65,813,663 (GRCm39) |
E223V |
probably damaging |
Het |
Hnrnpa1 |
G |
C |
15: 103,148,955 (GRCm39) |
E5D |
possibly damaging |
Het |
Htr2a |
T |
A |
14: 74,943,143 (GRCm39) |
V241E |
probably damaging |
Het |
Ier5 |
T |
C |
1: 154,974,491 (GRCm39) |
E229G |
possibly damaging |
Het |
Inka2 |
C |
A |
3: 105,623,748 (GRCm39) |
Q22K |
probably damaging |
Het |
Krt87 |
A |
T |
15: 101,331,910 (GRCm39) |
M276K |
possibly damaging |
Het |
Mast1 |
G |
C |
8: 85,655,597 (GRCm39) |
Y182* |
probably null |
Het |
Mia3 |
T |
A |
1: 183,139,998 (GRCm39) |
D239V |
probably damaging |
Het |
Mmut |
T |
A |
17: 41,258,002 (GRCm39) |
D389E |
probably damaging |
Het |
Mpp7 |
A |
G |
18: 7,355,016 (GRCm39) |
|
probably null |
Het |
Mycbp2 |
A |
G |
14: 103,520,101 (GRCm39) |
C739R |
probably null |
Het |
Or13e8 |
C |
G |
4: 43,696,636 (GRCm39) |
C179S |
probably damaging |
Het |
Or5k14 |
A |
G |
16: 58,692,847 (GRCm39) |
L222P |
probably damaging |
Het |
Or8k21 |
A |
G |
2: 86,144,784 (GRCm39) |
I282T |
probably benign |
Het |
Or9e1 |
A |
T |
11: 58,732,317 (GRCm39) |
R126* |
probably null |
Het |
Palld |
A |
T |
8: 61,991,822 (GRCm39) |
I510N |
probably damaging |
Het |
Pappa |
A |
G |
4: 65,074,589 (GRCm39) |
E381G |
probably damaging |
Het |
Phldb1 |
G |
A |
9: 44,623,200 (GRCm39) |
T618I |
probably damaging |
Het |
Pkd1 |
A |
G |
17: 24,810,361 (GRCm39) |
E3631G |
possibly damaging |
Het |
Pkhd1 |
C |
T |
1: 20,188,031 (GRCm39) |
V3426I |
probably benign |
Het |
Plk4 |
A |
G |
3: 40,767,940 (GRCm39) |
T828A |
probably benign |
Het |
Psmb5 |
C |
T |
14: 54,854,221 (GRCm39) |
A86T |
possibly damaging |
Het |
Rasal2 |
A |
G |
1: 156,984,951 (GRCm39) |
V907A |
probably damaging |
Het |
Rxra |
C |
T |
2: 27,627,353 (GRCm39) |
T24M |
probably benign |
Het |
Senp1 |
A |
G |
15: 97,974,498 (GRCm39) |
S105P |
probably benign |
Het |
Sh3rf1 |
A |
G |
8: 61,816,201 (GRCm39) |
D486G |
probably damaging |
Het |
Slc49a4 |
G |
A |
16: 35,555,986 (GRCm39) |
A158V |
probably benign |
Het |
Slfn5 |
A |
C |
11: 82,851,490 (GRCm39) |
N596H |
probably benign |
Het |
Tanc2 |
T |
A |
11: 105,689,526 (GRCm39) |
D229E |
probably benign |
Het |
Taok2 |
T |
C |
7: 126,479,455 (GRCm39) |
K57E |
probably damaging |
Het |
Thsd7a |
C |
T |
6: 12,343,212 (GRCm39) |
C1135Y |
probably damaging |
Het |
V1ra8 |
T |
C |
6: 90,180,508 (GRCm39) |
L237P |
probably benign |
Het |
Vcpip1 |
G |
A |
1: 9,818,065 (GRCm39) |
T106M |
probably damaging |
Het |
Vmn1r215 |
T |
G |
13: 23,259,981 (GRCm39) |
I7S |
possibly damaging |
Het |
Vmn1r233 |
T |
A |
17: 21,214,279 (GRCm39) |
M224L |
probably benign |
Het |
Xpot |
A |
T |
10: 121,440,454 (GRCm39) |
D592E |
probably damaging |
Het |
|
Other mutations in B020004C17Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02063:B020004C17Rik
|
APN |
14 |
57,253,480 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03396:B020004C17Rik
|
APN |
14 |
57,253,993 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0664:B020004C17Rik
|
UTSW |
14 |
57,254,225 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3977:B020004C17Rik
|
UTSW |
14 |
57,254,645 (GRCm39) |
missense |
possibly damaging |
0.78 |
R3978:B020004C17Rik
|
UTSW |
14 |
57,254,645 (GRCm39) |
missense |
possibly damaging |
0.78 |
R3979:B020004C17Rik
|
UTSW |
14 |
57,254,645 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4415:B020004C17Rik
|
UTSW |
14 |
57,254,874 (GRCm39) |
makesense |
probably null |
|
R5290:B020004C17Rik
|
UTSW |
14 |
57,254,036 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5479:B020004C17Rik
|
UTSW |
14 |
57,253,999 (GRCm39) |
missense |
probably benign |
0.36 |
R5655:B020004C17Rik
|
UTSW |
14 |
57,252,689 (GRCm39) |
start gained |
probably benign |
|
R5736:B020004C17Rik
|
UTSW |
14 |
57,254,823 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7368:B020004C17Rik
|
UTSW |
14 |
57,254,773 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7759:B020004C17Rik
|
UTSW |
14 |
57,254,242 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9299:B020004C17Rik
|
UTSW |
14 |
57,254,230 (GRCm39) |
missense |
probably damaging |
0.96 |
R9410:B020004C17Rik
|
UTSW |
14 |
57,254,273 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1177:B020004C17Rik
|
UTSW |
14 |
57,252,717 (GRCm39) |
nonsense |
probably null |
|
|