Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
A |
6: 121,636,353 (GRCm39) |
W741R |
probably damaging |
Het |
Abcb8 |
C |
T |
5: 24,605,137 (GRCm39) |
R108C |
possibly damaging |
Het |
Acan |
A |
G |
7: 78,761,068 (GRCm39) |
T1927A |
probably damaging |
Het |
Agbl4 |
A |
G |
4: 110,812,869 (GRCm39) |
|
probably null |
Het |
Bltp1 |
T |
C |
3: 36,985,265 (GRCm39) |
F865S |
probably benign |
Het |
Ccr8 |
T |
A |
9: 119,923,529 (GRCm39) |
C215S |
probably damaging |
Het |
Cd209b |
T |
C |
8: 3,968,688 (GRCm39) |
T314A |
probably benign |
Het |
Cd244a |
T |
G |
1: 171,409,208 (GRCm39) |
|
probably null |
Het |
Cdh23 |
T |
C |
10: 60,249,356 (GRCm39) |
E849G |
possibly damaging |
Het |
Cep57 |
A |
G |
9: 13,721,175 (GRCm39) |
V268A |
probably damaging |
Het |
Clip4 |
T |
C |
17: 72,163,305 (GRCm39) |
S626P |
probably damaging |
Het |
Col19a1 |
C |
T |
1: 24,367,152 (GRCm39) |
G477R |
probably damaging |
Het |
Col4a4 |
T |
C |
1: 82,433,449 (GRCm39) |
D1498G |
unknown |
Het |
Coro6 |
T |
C |
11: 77,357,322 (GRCm39) |
V177A |
probably benign |
Het |
Crip3 |
T |
C |
17: 46,742,210 (GRCm39) |
S202P |
possibly damaging |
Het |
Cxcr2 |
T |
C |
1: 74,197,619 (GRCm39) |
C38R |
probably damaging |
Het |
Cyp4f13 |
C |
T |
17: 33,148,447 (GRCm39) |
G327R |
possibly damaging |
Het |
Dab2 |
C |
T |
15: 6,464,792 (GRCm39) |
Q415* |
probably null |
Het |
Dennd5b |
A |
G |
6: 148,969,593 (GRCm39) |
F287L |
probably benign |
Het |
Dlg4 |
G |
A |
11: 69,908,057 (GRCm39) |
R6K |
probably benign |
Het |
Edc4 |
A |
G |
8: 106,614,033 (GRCm39) |
K429E |
probably damaging |
Het |
Fam107b |
T |
A |
2: 3,780,667 (GRCm39) |
|
probably null |
Het |
Flt4 |
A |
T |
11: 49,541,897 (GRCm39) |
D1360V |
probably damaging |
Het |
Gm1043 |
A |
T |
5: 37,317,168 (GRCm39) |
|
probably benign |
Het |
Gm4894 |
A |
T |
9: 49,189,970 (GRCm39) |
I82L |
unknown |
Het |
Gm7247 |
C |
T |
14: 51,601,805 (GRCm39) |
S26F |
probably benign |
Het |
Gpr176 |
A |
C |
2: 118,114,385 (GRCm39) |
|
probably null |
Het |
Gtse1 |
T |
C |
15: 85,748,381 (GRCm39) |
L262P |
probably benign |
Het |
Il4ra |
T |
C |
7: 125,166,393 (GRCm39) |
W46R |
probably damaging |
Het |
Itga11 |
A |
G |
9: 62,662,955 (GRCm39) |
Y557C |
probably benign |
Het |
Kcnab2 |
A |
C |
4: 152,519,287 (GRCm39) |
|
probably null |
Het |
Kcnh7 |
G |
A |
2: 63,014,441 (GRCm39) |
|
probably benign |
Het |
Ly9 |
T |
A |
1: 171,429,396 (GRCm39) |
Q230L |
probably damaging |
Het |
Map2 |
C |
A |
1: 66,454,043 (GRCm39) |
H978N |
possibly damaging |
Het |
Map2k6 |
A |
G |
11: 110,388,732 (GRCm39) |
I225V |
possibly damaging |
Het |
Map3k13 |
A |
G |
16: 21,723,995 (GRCm39) |
N326D |
possibly damaging |
Het |
Mdga2 |
A |
G |
12: 66,844,537 (GRCm39) |
F85L |
probably benign |
Het |
Mmp13 |
C |
T |
9: 7,274,269 (GRCm39) |
P192L |
probably damaging |
Het |
Mrpl37 |
T |
C |
4: 106,923,704 (GRCm39) |
T97A |
probably benign |
Het |
Mycbpap |
C |
T |
11: 94,404,420 (GRCm39) |
G121D |
probably benign |
Het |
Nabp1 |
A |
G |
1: 51,510,544 (GRCm39) |
S153P |
probably benign |
Het |
Nsun3 |
A |
T |
16: 62,590,049 (GRCm39) |
F222I |
probably benign |
Het |
Or4q3 |
A |
G |
14: 50,582,969 (GRCm39) |
V310A |
possibly damaging |
Het |
Pcdhga4 |
A |
T |
18: 37,818,991 (GRCm39) |
D180V |
probably benign |
Het |
Pex6 |
C |
A |
17: 47,025,384 (GRCm39) |
|
probably null |
Het |
Phrf1 |
C |
A |
7: 140,839,015 (GRCm39) |
|
probably benign |
Het |
Ppp1r36 |
A |
G |
12: 76,485,936 (GRCm39) |
T365A |
possibly damaging |
Het |
Ranbp10 |
A |
G |
8: 106,499,672 (GRCm39) |
M519T |
probably benign |
Het |
Rfx4 |
G |
A |
10: 84,675,881 (GRCm39) |
W32* |
probably null |
Het |
Ryr1 |
T |
C |
7: 28,723,666 (GRCm39) |
N4131S |
probably benign |
Het |
Slc27a6 |
A |
G |
18: 58,745,306 (GRCm39) |
E580G |
possibly damaging |
Het |
Slc7a14 |
T |
C |
3: 31,263,385 (GRCm39) |
D719G |
probably benign |
Het |
Slfn9 |
A |
G |
11: 82,878,310 (GRCm39) |
I273T |
possibly damaging |
Het |
Spice1 |
A |
G |
16: 44,205,037 (GRCm39) |
E781G |
probably benign |
Het |
Sspo |
C |
T |
6: 48,471,110 (GRCm39) |
P4686S |
possibly damaging |
Het |
Stab1 |
G |
T |
14: 30,861,508 (GRCm39) |
R2500S |
probably benign |
Het |
Stox2 |
A |
T |
8: 47,656,182 (GRCm39) |
M98K |
possibly damaging |
Het |
Tacc2 |
T |
C |
7: 130,225,213 (GRCm39) |
S633P |
probably damaging |
Het |
Tex51 |
G |
T |
18: 32,595,545 (GRCm39) |
|
probably benign |
Het |
Tm9sf4 |
T |
C |
2: 153,037,491 (GRCm39) |
|
probably null |
Het |
Togaram2 |
T |
A |
17: 72,011,778 (GRCm39) |
F486I |
probably damaging |
Het |
Trappc12 |
A |
G |
12: 28,797,113 (GRCm39) |
S140P |
possibly damaging |
Het |
Ttc29 |
A |
T |
8: 79,003,525 (GRCm39) |
N247I |
probably damaging |
Het |
Uso1 |
A |
T |
5: 92,340,589 (GRCm39) |
E668D |
probably benign |
Het |
Vmn2r69 |
A |
T |
7: 85,061,117 (GRCm39) |
|
probably null |
Het |
Xirp2 |
T |
A |
2: 67,341,994 (GRCm39) |
L1412I |
possibly damaging |
Het |
Xrcc5 |
T |
A |
1: 72,349,617 (GRCm39) |
D15E |
probably damaging |
Het |
Zfp661 |
T |
C |
2: 127,418,968 (GRCm39) |
K391E |
probably damaging |
Het |
Zfp729b |
A |
G |
13: 67,741,977 (GRCm39) |
I106T |
probably benign |
Het |
Zfyve9 |
A |
C |
4: 108,576,557 (GRCm39) |
S175A |
probably benign |
Het |
|
Other mutations in 1700093K21Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01348:1700093K21Rik
|
APN |
11 |
23,467,213 (GRCm39) |
missense |
probably null |
1.00 |
IGL02897:1700093K21Rik
|
APN |
11 |
23,467,308 (GRCm39) |
missense |
probably benign |
0.00 |
R1155:1700093K21Rik
|
UTSW |
11 |
23,467,270 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1677:1700093K21Rik
|
UTSW |
11 |
23,467,357 (GRCm39) |
missense |
probably benign |
0.16 |
R3983:1700093K21Rik
|
UTSW |
11 |
23,467,220 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5485:1700093K21Rik
|
UTSW |
11 |
23,467,378 (GRCm39) |
missense |
probably benign |
0.05 |
R5589:1700093K21Rik
|
UTSW |
11 |
23,468,066 (GRCm39) |
missense |
probably benign |
0.25 |
R5678:1700093K21Rik
|
UTSW |
11 |
23,466,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R5783:1700093K21Rik
|
UTSW |
11 |
23,468,787 (GRCm39) |
missense |
probably damaging |
0.99 |
R6072:1700093K21Rik
|
UTSW |
11 |
23,467,357 (GRCm39) |
missense |
probably benign |
0.16 |
R6520:1700093K21Rik
|
UTSW |
11 |
23,467,285 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6930:1700093K21Rik
|
UTSW |
11 |
23,466,563 (GRCm39) |
missense |
probably benign |
0.03 |
R7432:1700093K21Rik
|
UTSW |
11 |
23,468,839 (GRCm39) |
missense |
probably benign |
0.07 |
R7558:1700093K21Rik
|
UTSW |
11 |
23,466,285 (GRCm39) |
splice site |
probably null |
|
R8077:1700093K21Rik
|
UTSW |
11 |
23,467,237 (GRCm39) |
missense |
probably benign |
|
R9688:1700093K21Rik
|
UTSW |
11 |
23,469,067 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:1700093K21Rik
|
UTSW |
11 |
23,468,144 (GRCm39) |
critical splice acceptor site |
probably null |
|
|