Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm4 |
G |
A |
7: 119,293,889 (GRCm39) |
V87M |
possibly damaging |
Het |
Adamts3 |
T |
C |
5: 90,009,288 (GRCm39) |
N125S |
probably benign |
Het |
Arhgef4 |
A |
G |
1: 34,760,885 (GRCm39) |
E47G |
unknown |
Het |
C1ra |
A |
G |
6: 124,496,374 (GRCm39) |
M367V |
probably benign |
Het |
Ces2b |
T |
C |
8: 105,559,385 (GRCm39) |
W84R |
probably damaging |
Het |
Clca3a1 |
T |
C |
3: 144,436,579 (GRCm39) |
T835A |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,232,865 (GRCm39) |
E741G |
probably damaging |
Het |
Cspg4b |
C |
T |
13: 113,456,140 (GRCm39) |
R729C |
|
Het |
D330020A13Rik |
T |
C |
6: 120,271,819 (GRCm39) |
L165P |
unknown |
Het |
Dtnbp1 |
A |
T |
13: 45,075,765 (GRCm39) |
L326* |
probably null |
Het |
Ecpas |
T |
C |
4: 58,828,593 (GRCm39) |
I947V |
probably benign |
Het |
Fat4 |
A |
T |
3: 39,003,588 (GRCm39) |
|
probably null |
Het |
Fbxl9 |
A |
T |
8: 106,042,165 (GRCm39) |
I221N |
possibly damaging |
Het |
Fuom |
T |
A |
7: 139,679,492 (GRCm39) |
I143F |
unknown |
Het |
Gm14444 |
A |
T |
2: 174,858,524 (GRCm39) |
M33L |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,540,643 (GRCm39) |
T2889A |
probably benign |
Het |
Kif5b |
G |
A |
18: 6,212,517 (GRCm39) |
T769M |
probably benign |
Het |
Kif9 |
G |
A |
9: 110,343,682 (GRCm39) |
R567H |
not run |
Het |
Kmt2c |
A |
T |
5: 25,504,814 (GRCm39) |
M3498K |
probably benign |
Het |
Ly6e |
T |
A |
15: 74,829,700 (GRCm39) |
L15* |
probably null |
Het |
Malt1 |
G |
A |
18: 65,597,187 (GRCm39) |
|
probably null |
Het |
Msantd5 |
G |
A |
11: 51,125,613 (GRCm39) |
E179K |
possibly damaging |
Het |
Mylk |
G |
C |
16: 34,699,894 (GRCm39) |
S419T |
probably benign |
Het |
Oacyl |
T |
C |
18: 65,870,918 (GRCm39) |
L373P |
probably benign |
Het |
Or10d1 |
A |
C |
9: 39,483,845 (GRCm39) |
S237A |
possibly damaging |
Het |
Or4b1d |
T |
C |
2: 89,968,836 (GRCm39) |
I216V |
probably benign |
Het |
Or5b116 |
T |
A |
19: 13,422,662 (GRCm39) |
C95* |
probably null |
Het |
Or5b21 |
C |
T |
19: 12,839,843 (GRCm39) |
R235* |
probably null |
Het |
Pcdh20 |
A |
T |
14: 88,704,867 (GRCm39) |
L811* |
probably null |
Het |
Pgrmc2 |
A |
T |
3: 41,037,415 (GRCm39) |
D5E |
probably damaging |
Het |
Pign |
A |
C |
1: 105,585,401 (GRCm39) |
F49L |
probably benign |
Het |
Pip5k1b |
T |
C |
19: 24,337,457 (GRCm39) |
D277G |
probably benign |
Het |
Ppm1m |
A |
G |
9: 106,075,895 (GRCm39) |
V11A |
probably benign |
Het |
Prl7a1 |
A |
T |
13: 27,817,661 (GRCm39) |
V201E |
not run |
Het |
Samhd1 |
A |
G |
2: 156,958,415 (GRCm39) |
S269P |
probably damaging |
Het |
Sik2 |
A |
G |
9: 50,920,132 (GRCm39) |
V15A |
probably damaging |
Het |
Slc4a7 |
G |
A |
14: 14,773,348 (GRCm38) |
E773K |
probably benign |
Het |
Sntg1 |
T |
C |
1: 8,853,024 (GRCm39) |
D42G |
probably damaging |
Het |
Speg |
A |
T |
1: 75,403,810 (GRCm39) |
N2664Y |
probably damaging |
Het |
Tcstv1b |
G |
T |
13: 120,634,695 (GRCm39) |
|
probably benign |
Het |
Treh |
A |
G |
9: 44,596,015 (GRCm39) |
Y435C |
probably damaging |
Het |
Trim59 |
A |
G |
3: 68,945,140 (GRCm39) |
S67P |
probably benign |
Het |
Trim68 |
A |
T |
7: 102,328,004 (GRCm39) |
C309S |
unknown |
Het |
Tubb4a |
G |
T |
17: 57,387,880 (GRCm39) |
S382* |
probably null |
Het |
Vmn2r15 |
A |
T |
5: 109,434,217 (GRCm39) |
I829N |
probably damaging |
Het |
Vmn2r68 |
T |
C |
7: 84,883,722 (GRCm39) |
T128A |
probably benign |
Het |
Vmn2r70 |
T |
A |
7: 85,208,588 (GRCm39) |
I630L |
possibly damaging |
Het |
Zc3hav1 |
A |
G |
6: 38,306,156 (GRCm39) |
I632T |
probably benign |
Het |
Zfp558 |
A |
G |
9: 18,379,993 (GRCm39) |
S13P |
possibly damaging |
Het |
|
Other mutations in A630010A05Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0709:A630010A05Rik
|
UTSW |
16 |
14,436,358 (GRCm39) |
missense |
probably damaging |
0.99 |
R1444:A630010A05Rik
|
UTSW |
16 |
14,427,558 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1467:A630010A05Rik
|
UTSW |
16 |
14,436,447 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1467:A630010A05Rik
|
UTSW |
16 |
14,436,447 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3731:A630010A05Rik
|
UTSW |
16 |
14,427,485 (GRCm39) |
splice site |
probably null |
|
R4423:A630010A05Rik
|
UTSW |
16 |
14,436,577 (GRCm39) |
missense |
probably benign |
0.00 |
R4475:A630010A05Rik
|
UTSW |
16 |
14,407,227 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5352:A630010A05Rik
|
UTSW |
16 |
14,436,565 (GRCm39) |
nonsense |
probably null |
|
R5354:A630010A05Rik
|
UTSW |
16 |
14,436,535 (GRCm39) |
missense |
probably benign |
0.00 |
R5449:A630010A05Rik
|
UTSW |
16 |
14,436,537 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6868:A630010A05Rik
|
UTSW |
16 |
14,436,559 (GRCm39) |
missense |
probably damaging |
0.97 |
R8021:A630010A05Rik
|
UTSW |
16 |
14,407,110 (GRCm39) |
missense |
|
|
R8114:A630010A05Rik
|
UTSW |
16 |
14,407,091 (GRCm39) |
nonsense |
probably null |
|
R8849:A630010A05Rik
|
UTSW |
16 |
14,439,376 (GRCm39) |
critical splice donor site |
probably null |
|
R9640:A630010A05Rik
|
UTSW |
16 |
14,436,589 (GRCm39) |
missense |
|
|
|