Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921539E11Rik |
T |
A |
4: 103,123,579 (GRCm39) |
I98F |
probably benign |
Het |
4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
A630010A05Rik |
A |
G |
16: 14,436,537 (GRCm39) |
K197E |
possibly damaging |
Het |
Agrn |
A |
G |
4: 156,251,737 (GRCm39) |
|
probably null |
Het |
Atad5 |
A |
G |
11: 80,014,934 (GRCm39) |
I1337V |
probably damaging |
Het |
Cd44 |
T |
C |
2: 102,662,891 (GRCm39) |
T550A |
probably damaging |
Het |
Cdk5rap2 |
A |
C |
4: 70,194,888 (GRCm39) |
L952V |
probably benign |
Het |
Cep104 |
T |
A |
4: 154,069,762 (GRCm39) |
|
probably null |
Het |
Cfl1 |
A |
G |
19: 5,543,521 (GRCm39) |
*167W |
probably null |
Het |
Col22a1 |
T |
C |
15: 71,693,798 (GRCm39) |
D734G |
unknown |
Het |
Cry1 |
G |
A |
10: 84,968,999 (GRCm39) |
L581F |
probably benign |
Het |
Dmpk |
A |
G |
7: 18,824,916 (GRCm39) |
D406G |
probably benign |
Het |
Faah |
T |
C |
4: 115,856,692 (GRCm39) |
|
probably null |
Het |
Fchsd2 |
T |
C |
7: 100,926,731 (GRCm39) |
F607S |
probably damaging |
Het |
Fga |
CAAAG |
CAAAGAAAG |
3: 82,938,169 (GRCm39) |
|
probably null |
Het |
Hdac5 |
G |
A |
11: 102,086,923 (GRCm39) |
Q46* |
probably null |
Het |
Hltf |
A |
G |
3: 20,123,247 (GRCm39) |
T212A |
possibly damaging |
Het |
Ilvbl |
G |
A |
10: 78,412,862 (GRCm39) |
|
probably null |
Het |
Ldhc |
T |
C |
7: 46,519,082 (GRCm39) |
S102P |
possibly damaging |
Het |
Med12l |
T |
C |
3: 59,167,127 (GRCm39) |
V1529A |
probably damaging |
Het |
Nlrp9a |
A |
G |
7: 26,257,254 (GRCm39) |
I202V |
probably benign |
Het |
Pdc |
A |
C |
1: 150,209,190 (GRCm39) |
L224F |
probably damaging |
Het |
Pgr |
T |
C |
9: 8,956,344 (GRCm39) |
V764A |
possibly damaging |
Het |
Plxna1 |
T |
C |
6: 89,300,590 (GRCm39) |
D1578G |
probably damaging |
Het |
Prpf40a |
G |
T |
2: 53,046,938 (GRCm39) |
T266N |
possibly damaging |
Het |
Ptrh1 |
A |
G |
2: 32,666,358 (GRCm39) |
S37G |
probably damaging |
Het |
Rgs9 |
T |
C |
11: 109,116,570 (GRCm39) |
D411G |
probably benign |
Het |
Riok3 |
A |
T |
18: 12,288,303 (GRCm39) |
E493D |
probably damaging |
Het |
Rnf213 |
T |
C |
11: 119,305,902 (GRCm39) |
M570T |
probably benign |
Het |
Scamp2 |
A |
G |
9: 57,488,154 (GRCm39) |
D187G |
probably damaging |
Het |
Scn1a |
T |
A |
2: 66,151,346 (GRCm39) |
I819F |
probably damaging |
Het |
Slc7a5 |
C |
A |
8: 122,613,087 (GRCm39) |
W330C |
probably damaging |
Het |
Syn3 |
A |
T |
10: 86,187,434 (GRCm39) |
F230Y |
probably damaging |
Het |
Tmem8b |
G |
A |
4: 43,673,992 (GRCm39) |
V208I |
probably benign |
Het |
Tro |
T |
C |
X: 149,428,966 (GRCm39) |
|
probably benign |
Het |
Ubr1 |
T |
A |
2: 120,793,981 (GRCm39) |
M68L |
probably benign |
Het |
Vmn1r120 |
A |
C |
7: 20,787,074 (GRCm39) |
H212Q |
possibly damaging |
Het |
Vmn1r46 |
T |
C |
6: 89,953,343 (GRCm39) |
V64A |
probably benign |
Het |
Vmn2r114 |
ATTT |
ATT |
17: 23,509,906 (GRCm39) |
|
probably null |
Het |
Wee1 |
TCCCC |
TCCC |
7: 109,723,776 (GRCm39) |
|
probably null |
Het |
Zfp384 |
T |
C |
6: 125,001,101 (GRCm39) |
S58P |
probably damaging |
Het |
|
Other mutations in Nscme3l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02983:Nscme3l
|
APN |
19 |
5,553,209 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL03285:Nscme3l
|
APN |
19 |
5,553,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R4445:Nscme3l
|
UTSW |
19 |
5,553,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R4804:Nscme3l
|
UTSW |
19 |
5,553,028 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5542:Nscme3l
|
UTSW |
19 |
5,553,463 (GRCm39) |
missense |
probably damaging |
0.99 |
R6435:Nscme3l
|
UTSW |
19 |
5,553,446 (GRCm39) |
missense |
probably benign |
0.06 |
R6476:Nscme3l
|
UTSW |
19 |
5,553,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R6764:Nscme3l
|
UTSW |
19 |
5,552,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R7102:Nscme3l
|
UTSW |
19 |
5,553,623 (GRCm39) |
missense |
probably benign |
0.00 |
R7232:Nscme3l
|
UTSW |
19 |
5,553,659 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7541:Nscme3l
|
UTSW |
19 |
5,553,439 (GRCm39) |
missense |
probably benign |
0.40 |
R7640:Nscme3l
|
UTSW |
19 |
5,553,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R9459:Nscme3l
|
UTSW |
19 |
5,553,757 (GRCm39) |
missense |
probably benign |
|
|