Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310002L09Rik |
A |
T |
4: 73,861,290 (GRCm39) |
D103E |
probably benign |
Het |
Abcc3 |
A |
T |
11: 94,266,381 (GRCm39) |
S70T |
possibly damaging |
Het |
Atp6v0a1 |
A |
G |
11: 100,920,009 (GRCm39) |
Y214C |
possibly damaging |
Het |
Azi2 |
A |
G |
9: 117,878,963 (GRCm39) |
|
probably null |
Het |
Cacnb2 |
T |
A |
2: 14,990,826 (GRCm39) |
V636E |
possibly damaging |
Het |
Cd8a |
A |
C |
6: 71,351,546 (GRCm39) |
T169P |
probably damaging |
Het |
Cfap44 |
G |
A |
16: 44,224,495 (GRCm39) |
V68I |
probably benign |
Het |
Cspg4b |
C |
A |
13: 113,454,912 (GRCm39) |
S319R |
probably damaging |
Het |
Dnaaf10 |
G |
A |
11: 17,172,309 (GRCm39) |
V133M |
probably damaging |
Het |
Eea1 |
G |
T |
10: 95,873,340 (GRCm39) |
C1134F |
probably benign |
Het |
Ehmt2 |
T |
G |
17: 35,131,748 (GRCm39) |
F1192V |
probably damaging |
Het |
Emc1 |
T |
C |
4: 139,092,661 (GRCm39) |
F531L |
probably damaging |
Het |
Eme1 |
G |
A |
11: 94,541,303 (GRCm39) |
T173I |
probably benign |
Het |
Gli2 |
A |
T |
1: 118,772,146 (GRCm39) |
C520S |
probably damaging |
Het |
Gm43302 |
T |
C |
5: 105,428,004 (GRCm39) |
K186E |
probably benign |
Het |
Gpr108 |
A |
T |
17: 57,543,990 (GRCm39) |
N405K |
probably damaging |
Het |
Hmgcl |
C |
A |
4: 135,682,953 (GRCm39) |
T135N |
probably benign |
Het |
Hydin |
G |
A |
8: 111,259,488 (GRCm39) |
D2487N |
possibly damaging |
Het |
Igfl3 |
G |
T |
7: 17,913,725 (GRCm39) |
R25L |
probably benign |
Het |
Igsf10 |
A |
C |
3: 59,239,354 (GRCm39) |
S276A |
probably benign |
Het |
Kctd1 |
A |
G |
18: 15,107,045 (GRCm39) |
S211P |
probably damaging |
Het |
Kctd7 |
A |
T |
5: 130,181,342 (GRCm39) |
Q255L |
probably benign |
Het |
Lrig1 |
A |
G |
6: 94,602,044 (GRCm39) |
Y270H |
probably benign |
Het |
Muc5ac |
C |
T |
7: 141,363,481 (GRCm39) |
|
probably benign |
Het |
Myh15 |
A |
G |
16: 48,973,474 (GRCm39) |
N1248S |
possibly damaging |
Het |
Nod1 |
A |
G |
6: 54,921,094 (GRCm39) |
F408S |
probably benign |
Het |
Nrp1 |
T |
C |
8: 129,219,538 (GRCm39) |
F652S |
probably damaging |
Het |
Opa1 |
G |
T |
16: 29,439,686 (GRCm39) |
R792L |
probably benign |
Het |
Or10ak14 |
G |
A |
4: 118,611,504 (GRCm39) |
T79I |
probably damaging |
Het |
Or51t4 |
A |
T |
7: 102,597,975 (GRCm39) |
H91L |
possibly damaging |
Het |
Or5p63 |
A |
T |
7: 107,811,125 (GRCm39) |
F204I |
probably benign |
Het |
Or6c74 |
T |
C |
10: 129,870,401 (GRCm39) |
M302T |
probably benign |
Het |
Pcdha6 |
G |
T |
18: 37,101,396 (GRCm39) |
L196F |
probably damaging |
Het |
Pdia2 |
A |
T |
17: 26,415,944 (GRCm39) |
Y347* |
probably null |
Het |
Pdpr |
G |
T |
8: 111,851,245 (GRCm39) |
|
probably null |
Het |
Pigt |
T |
A |
2: 164,349,251 (GRCm39) |
L518Q |
probably damaging |
Het |
Ppfibp2 |
A |
C |
7: 107,337,188 (GRCm39) |
D591A |
possibly damaging |
Het |
Prrg2 |
G |
A |
7: 44,709,413 (GRCm39) |
T97M |
possibly damaging |
Het |
Qars1 |
A |
G |
9: 108,390,382 (GRCm39) |
T428A |
probably damaging |
Het |
Rai1 |
T |
C |
11: 60,076,541 (GRCm39) |
F202L |
probably damaging |
Het |
Rars1 |
A |
T |
11: 35,699,313 (GRCm39) |
M660K |
probably damaging |
Het |
Rsf1 |
GCGGCGGCG |
GCGGCGGCGTCGGCGGCG |
7: 97,229,132 (GRCm39) |
|
probably benign |
Het |
Slc16a6 |
A |
C |
11: 109,345,866 (GRCm39) |
F382V |
probably damaging |
Het |
Slc30a7 |
T |
C |
3: 115,747,802 (GRCm39) |
T330A |
probably damaging |
Het |
Smc1b |
A |
T |
15: 84,951,960 (GRCm39) |
L1157Q |
probably damaging |
Het |
Snx4 |
G |
T |
16: 33,071,840 (GRCm39) |
A4S |
possibly damaging |
Het |
Sv2b |
A |
C |
7: 74,775,515 (GRCm39) |
|
probably null |
Het |
Syt9 |
A |
T |
7: 107,024,493 (GRCm39) |
I129L |
probably damaging |
Het |
Ttbk2 |
T |
C |
2: 120,603,834 (GRCm39) |
E198G |
probably damaging |
Het |
Ubr3 |
A |
T |
2: 69,774,644 (GRCm39) |
D488V |
possibly damaging |
Het |
Ush2a |
T |
A |
1: 188,530,068 (GRCm39) |
C3286S |
probably damaging |
Het |
Vill |
A |
G |
9: 118,894,950 (GRCm39) |
D56G |
possibly damaging |
Het |
Vmn1r41 |
A |
T |
6: 89,724,352 (GRCm39) |
I298F |
probably damaging |
Het |
Vmn2r2 |
A |
T |
3: 64,024,688 (GRCm39) |
V631D |
probably damaging |
Het |
Vmn2r53 |
A |
G |
7: 12,335,069 (GRCm39) |
V197A |
probably benign |
Het |
Wasf1 |
A |
T |
10: 40,796,365 (GRCm39) |
I32F |
probably damaging |
Het |
Wasf2 |
G |
T |
4: 132,922,041 (GRCm39) |
A387S |
unknown |
Het |
Zbtb14 |
G |
A |
17: 69,694,674 (GRCm39) |
C124Y |
probably damaging |
Het |
Zfp462 |
G |
T |
4: 55,007,671 (GRCm39) |
A37S |
probably damaging |
Het |
Zfp532 |
A |
G |
18: 65,820,061 (GRCm39) |
E882G |
possibly damaging |
Het |
|
Other mutations in Vmn2r32 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02140:Vmn2r32
|
APN |
7 |
7,479,696 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02333:Vmn2r32
|
APN |
7 |
7,467,143 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02406:Vmn2r32
|
APN |
7 |
7,479,709 (GRCm39) |
missense |
probably benign |
|
IGL02428:Vmn2r32
|
APN |
7 |
7,477,283 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02484:Vmn2r32
|
APN |
7 |
7,467,116 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03277:Vmn2r32
|
APN |
7 |
7,477,251 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03366:Vmn2r32
|
APN |
7 |
7,467,029 (GRCm39) |
missense |
probably damaging |
0.99 |
R1055:Vmn2r32
|
UTSW |
7 |
7,477,326 (GRCm39) |
nonsense |
probably null |
|
R1695:Vmn2r32
|
UTSW |
7 |
7,466,991 (GRCm39) |
missense |
probably benign |
0.01 |
R2172:Vmn2r32
|
UTSW |
7 |
7,477,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R2262:Vmn2r32
|
UTSW |
7 |
7,477,618 (GRCm39) |
missense |
probably benign |
|
R3150:Vmn2r32
|
UTSW |
7 |
7,475,554 (GRCm39) |
missense |
probably benign |
|
R4362:Vmn2r32
|
UTSW |
7 |
7,482,857 (GRCm39) |
nonsense |
probably null |
|
R4432:Vmn2r32
|
UTSW |
7 |
7,482,918 (GRCm39) |
missense |
probably damaging |
0.98 |
R4851:Vmn2r32
|
UTSW |
7 |
7,482,953 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4949:Vmn2r32
|
UTSW |
7 |
7,467,083 (GRCm39) |
missense |
probably benign |
0.22 |
R5990:Vmn2r32
|
UTSW |
7 |
7,482,809 (GRCm39) |
missense |
probably damaging |
0.97 |
R6083:Vmn2r32
|
UTSW |
7 |
7,467,209 (GRCm39) |
missense |
probably benign |
0.15 |
R6084:Vmn2r32
|
UTSW |
7 |
7,467,209 (GRCm39) |
missense |
probably benign |
0.15 |
R6116:Vmn2r32
|
UTSW |
7 |
7,467,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R6263:Vmn2r32
|
UTSW |
7 |
7,479,691 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7286:Vmn2r32
|
UTSW |
7 |
7,482,807 (GRCm39) |
missense |
probably benign |
0.21 |
R7390:Vmn2r32
|
UTSW |
7 |
7,482,851 (GRCm39) |
missense |
probably benign |
0.00 |
R7412:Vmn2r32
|
UTSW |
7 |
7,477,212 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7508:Vmn2r32
|
UTSW |
7 |
7,470,373 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8812:Vmn2r32
|
UTSW |
7 |
7,477,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R8968:Vmn2r32
|
UTSW |
7 |
7,477,204 (GRCm39) |
missense |
probably benign |
0.00 |
R9331:Vmn2r32
|
UTSW |
7 |
7,467,402 (GRCm39) |
nonsense |
probably null |
|
R9358:Vmn2r32
|
UTSW |
7 |
7,477,197 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Vmn2r32
|
UTSW |
7 |
7,477,160 (GRCm39) |
missense |
probably damaging |
0.98 |
|