Other mutations in this stock |
Total: 25 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agpat3 |
A |
T |
10: 78,109,516 (GRCm39) |
|
probably benign |
Het |
Arhgap35 |
T |
C |
7: 16,298,340 (GRCm39) |
T242A |
probably benign |
Het |
Asb15 |
C |
A |
6: 24,558,649 (GRCm39) |
R55S |
probably benign |
Het |
Brca2 |
C |
T |
5: 150,484,003 (GRCm39) |
R2941W |
probably benign |
Het |
Chrng |
T |
C |
1: 87,134,469 (GRCm39) |
V135A |
probably damaging |
Het |
Corin |
G |
T |
5: 72,462,231 (GRCm39) |
H859Q |
probably damaging |
Het |
Cul7 |
A |
G |
17: 46,963,434 (GRCm39) |
E208G |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,172,603 (GRCm39) |
N285S |
possibly damaging |
Het |
Ell2 |
T |
A |
13: 75,904,409 (GRCm39) |
I166N |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,821,657 (GRCm39) |
R5797G |
possibly damaging |
Het |
Galntl6 |
T |
C |
8: 59,364,451 (GRCm39) |
I20V |
possibly damaging |
Het |
Glra2 |
A |
G |
X: 164,072,633 (GRCm39) |
F78L |
possibly damaging |
Het |
Gm12258 |
A |
G |
11: 58,746,896 (GRCm39) |
D51G |
probably benign |
Het |
Gsta2 |
T |
A |
9: 78,238,525 (GRCm39) |
K185* |
probably null |
Het |
Hmgcr |
C |
T |
13: 96,795,786 (GRCm39) |
D294N |
probably benign |
Het |
Myo10 |
T |
A |
15: 25,776,466 (GRCm39) |
L63H |
probably damaging |
Het |
P2ry10b |
T |
C |
X: 106,215,243 (GRCm39) |
V201A |
probably benign |
Het |
Psmb2 |
A |
G |
4: 126,571,642 (GRCm39) |
|
probably null |
Het |
Samd4 |
T |
A |
14: 47,290,355 (GRCm39) |
L154H |
probably damaging |
Het |
Sult2a4 |
A |
T |
7: 13,718,870 (GRCm39) |
D124E |
probably damaging |
Het |
Trav9-1 |
A |
T |
14: 53,725,815 (GRCm39) |
Y43F |
probably damaging |
Het |
Trpv2 |
A |
G |
11: 62,483,681 (GRCm39) |
N506S |
probably damaging |
Het |
Ube3c |
T |
C |
5: 29,824,227 (GRCm39) |
S474P |
probably damaging |
Het |
Wdr87-ps |
A |
G |
7: 29,235,227 (GRCm39) |
|
noncoding transcript |
Het |
Zfp942 |
A |
T |
17: 22,148,042 (GRCm39) |
C196S |
probably benign |
Het |
|
Other mutations in Iglv2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01376:Iglv2
|
APN |
16 |
19,079,315 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3831:Iglv2
|
UTSW |
16 |
19,079,593 (GRCm39) |
start codon destroyed |
probably null |
0.53 |
R3832:Iglv2
|
UTSW |
16 |
19,079,593 (GRCm39) |
start codon destroyed |
probably null |
0.53 |
R3833:Iglv2
|
UTSW |
16 |
19,079,593 (GRCm39) |
start codon destroyed |
probably null |
0.53 |
R7195:Iglv2
|
UTSW |
16 |
19,079,260 (GRCm39) |
missense |
not run |
|
R9149:Iglv2
|
UTSW |
16 |
19,079,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R9762:Iglv2
|
UTSW |
16 |
19,079,548 (GRCm39) |
critical splice donor site |
probably benign |
|
|