Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
C |
11: 109,867,320 (GRCm39) |
E246G |
probably damaging |
Het |
B3galt5 |
T |
A |
16: 96,117,091 (GRCm39) |
D241E |
probably damaging |
Het |
Camta1 |
A |
G |
4: 151,229,507 (GRCm39) |
F442L |
possibly damaging |
Het |
Cntnap5b |
A |
T |
1: 100,359,504 (GRCm39) |
E709V |
probably benign |
Het |
Ctnnal1 |
T |
C |
4: 56,835,243 (GRCm39) |
I345V |
probably damaging |
Het |
Evpl |
T |
C |
11: 116,124,270 (GRCm39) |
N183S |
probably damaging |
Het |
Fam90a1b |
T |
C |
X: 93,400,365 (GRCm39) |
D155G |
probably benign |
Het |
Fsip2 |
G |
A |
2: 82,807,863 (GRCm39) |
S1394N |
probably benign |
Het |
Gcnt2 |
A |
T |
13: 41,041,339 (GRCm39) |
Q166L |
probably benign |
Het |
Gpatch1 |
T |
C |
7: 35,007,763 (GRCm39) |
D99G |
probably null |
Het |
Grin2b |
A |
T |
6: 136,021,263 (GRCm39) |
W13R |
probably null |
Het |
Hbb-bh1 |
C |
T |
7: 103,491,024 (GRCm39) |
V127M |
probably benign |
Het |
Hc |
C |
T |
2: 34,929,250 (GRCm39) |
M282I |
probably benign |
Het |
Hirip3 |
A |
G |
7: 126,461,876 (GRCm39) |
E57G |
probably damaging |
Het |
Inpp5j |
C |
T |
11: 3,445,932 (GRCm39) |
|
probably null |
Het |
Krt84 |
A |
T |
15: 101,437,179 (GRCm39) |
V328E |
probably damaging |
Het |
Lrriq1 |
C |
A |
10: 103,053,977 (GRCm39) |
E247* |
probably null |
Het |
Myh13 |
A |
G |
11: 67,238,769 (GRCm39) |
E704G |
possibly damaging |
Het |
Myo16 |
T |
A |
8: 10,420,908 (GRCm39) |
N249K |
probably damaging |
Het |
Nobox |
C |
A |
6: 43,281,057 (GRCm39) |
K472N |
probably damaging |
Het |
Or1j1 |
T |
A |
2: 36,702,415 (GRCm39) |
T230S |
probably benign |
Het |
Orc4 |
A |
T |
2: 48,807,236 (GRCm39) |
S232T |
probably benign |
Het |
Pign |
A |
T |
1: 105,580,903 (GRCm39) |
Y159N |
probably damaging |
Het |
Rere |
T |
A |
4: 150,700,012 (GRCm39) |
V1032E |
possibly damaging |
Het |
Ror2 |
T |
C |
13: 53,272,999 (GRCm39) |
Q210R |
probably benign |
Het |
Sh3tc2 |
G |
A |
18: 62,123,954 (GRCm39) |
R905Q |
probably benign |
Het |
Ttn |
A |
G |
2: 76,785,327 (GRCm39) |
S683P |
possibly damaging |
Het |
|
Other mutations in Mmrn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02529:Mmrn2
|
APN |
14 |
34,120,570 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02590:Mmrn2
|
APN |
14 |
34,121,224 (GRCm39) |
nonsense |
probably null |
|
P0037:Mmrn2
|
UTSW |
14 |
34,125,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R0323:Mmrn2
|
UTSW |
14 |
34,119,991 (GRCm39) |
missense |
probably damaging |
0.97 |
R0499:Mmrn2
|
UTSW |
14 |
34,119,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R1073:Mmrn2
|
UTSW |
14 |
34,118,251 (GRCm39) |
critical splice donor site |
probably null |
|
R1422:Mmrn2
|
UTSW |
14 |
34,118,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R1455:Mmrn2
|
UTSW |
14 |
34,121,089 (GRCm39) |
missense |
probably benign |
0.00 |
R1584:Mmrn2
|
UTSW |
14 |
34,097,642 (GRCm39) |
missense |
probably benign |
0.19 |
R1702:Mmrn2
|
UTSW |
14 |
34,119,871 (GRCm39) |
missense |
probably benign |
0.34 |
R1919:Mmrn2
|
UTSW |
14 |
34,119,600 (GRCm39) |
missense |
probably benign |
0.10 |
R1961:Mmrn2
|
UTSW |
14 |
34,120,432 (GRCm39) |
splice site |
probably null |
|
R2267:Mmrn2
|
UTSW |
14 |
34,121,449 (GRCm39) |
missense |
probably benign |
0.41 |
R2268:Mmrn2
|
UTSW |
14 |
34,121,449 (GRCm39) |
missense |
probably benign |
0.41 |
R2516:Mmrn2
|
UTSW |
14 |
34,120,759 (GRCm39) |
missense |
probably benign |
0.12 |
R2571:Mmrn2
|
UTSW |
14 |
34,124,896 (GRCm39) |
missense |
probably damaging |
0.99 |
R2696:Mmrn2
|
UTSW |
14 |
34,120,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R2892:Mmrn2
|
UTSW |
14 |
34,118,587 (GRCm39) |
missense |
probably benign |
0.01 |
R2919:Mmrn2
|
UTSW |
14 |
34,124,879 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3611:Mmrn2
|
UTSW |
14 |
34,120,632 (GRCm39) |
missense |
probably benign |
0.00 |
R3898:Mmrn2
|
UTSW |
14 |
34,121,517 (GRCm39) |
splice site |
probably null |
|
R3899:Mmrn2
|
UTSW |
14 |
34,121,517 (GRCm39) |
splice site |
probably null |
|
R3900:Mmrn2
|
UTSW |
14 |
34,121,517 (GRCm39) |
splice site |
probably null |
|
R4363:Mmrn2
|
UTSW |
14 |
34,119,934 (GRCm39) |
missense |
probably damaging |
0.99 |
R4392:Mmrn2
|
UTSW |
14 |
34,119,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R4510:Mmrn2
|
UTSW |
14 |
34,125,016 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4511:Mmrn2
|
UTSW |
14 |
34,125,016 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4993:Mmrn2
|
UTSW |
14 |
34,118,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R5026:Mmrn2
|
UTSW |
14 |
34,121,158 (GRCm39) |
missense |
probably benign |
0.07 |
R5263:Mmrn2
|
UTSW |
14 |
34,121,541 (GRCm39) |
missense |
probably benign |
|
R5478:Mmrn2
|
UTSW |
14 |
34,118,539 (GRCm39) |
missense |
probably benign |
0.11 |
R5606:Mmrn2
|
UTSW |
14 |
34,119,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R6059:Mmrn2
|
UTSW |
14 |
34,119,548 (GRCm39) |
nonsense |
probably null |
|
R6279:Mmrn2
|
UTSW |
14 |
34,119,614 (GRCm39) |
missense |
probably benign |
|
R6300:Mmrn2
|
UTSW |
14 |
34,119,614 (GRCm39) |
missense |
probably benign |
|
R6938:Mmrn2
|
UTSW |
14 |
34,120,671 (GRCm39) |
missense |
probably benign |
0.22 |
R7491:Mmrn2
|
UTSW |
14 |
34,121,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R7607:Mmrn2
|
UTSW |
14 |
34,120,897 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7979:Mmrn2
|
UTSW |
14 |
34,118,138 (GRCm39) |
nonsense |
probably null |
|
R7999:Mmrn2
|
UTSW |
14 |
34,119,879 (GRCm39) |
missense |
probably benign |
0.30 |
R8113:Mmrn2
|
UTSW |
14 |
34,119,593 (GRCm39) |
missense |
probably benign |
0.39 |
R9063:Mmrn2
|
UTSW |
14 |
34,120,567 (GRCm39) |
missense |
probably benign |
0.04 |
R9092:Mmrn2
|
UTSW |
14 |
34,118,587 (GRCm39) |
missense |
probably benign |
0.00 |
R9180:Mmrn2
|
UTSW |
14 |
34,121,158 (GRCm39) |
missense |
probably benign |
0.07 |
R9327:Mmrn2
|
UTSW |
14 |
34,097,473 (GRCm39) |
unclassified |
probably benign |
|
R9476:Mmrn2
|
UTSW |
14 |
34,120,407 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9510:Mmrn2
|
UTSW |
14 |
34,120,407 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9606:Mmrn2
|
UTSW |
14 |
34,119,654 (GRCm39) |
missense |
possibly damaging |
0.58 |
X0064:Mmrn2
|
UTSW |
14 |
34,121,109 (GRCm39) |
missense |
probably benign |
|
|