Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
Aacs |
T |
C |
5: 125,588,984 (GRCm39) |
Y421H |
probably damaging |
Het |
Abca13 |
A |
G |
11: 9,251,298 (GRCm39) |
K2890R |
possibly damaging |
Het |
Aff4 |
T |
A |
11: 53,299,299 (GRCm39) |
|
probably null |
Het |
Brd10 |
A |
G |
19: 29,731,518 (GRCm39) |
V498A |
probably benign |
Het |
Cntn4 |
A |
T |
6: 106,650,911 (GRCm39) |
Q698L |
possibly damaging |
Het |
D5Ertd579e |
G |
T |
5: 36,772,601 (GRCm39) |
S598Y |
probably damaging |
Het |
Dmrt1 |
A |
G |
19: 25,487,164 (GRCm39) |
M157V |
probably benign |
Het |
Dnah2 |
C |
T |
11: 69,349,746 (GRCm39) |
R2399Q |
probably benign |
Het |
Gm10521 |
T |
A |
1: 171,724,067 (GRCm39) |
M126K |
unknown |
Het |
Hs2st1 |
A |
G |
3: 144,262,709 (GRCm39) |
|
probably benign |
Het |
Lats2 |
T |
C |
14: 57,937,010 (GRCm39) |
D113G |
probably benign |
Het |
Myo15a |
A |
C |
11: 60,368,503 (GRCm39) |
D421A |
probably damaging |
Het |
Or5k15 |
T |
A |
16: 58,710,107 (GRCm39) |
I159F |
probably benign |
Het |
Or5k17 |
A |
T |
16: 58,746,393 (GRCm39) |
D180E |
possibly damaging |
Het |
Or6z6 |
T |
C |
7: 6,491,570 (GRCm39) |
Y94C |
probably benign |
Het |
Pappa2 |
T |
A |
1: 158,784,308 (GRCm39) |
D234V |
probably benign |
Het |
Parl |
G |
T |
16: 20,098,824 (GRCm39) |
T311K |
possibly damaging |
Het |
Pias3 |
G |
A |
3: 96,612,319 (GRCm39) |
R557H |
probably damaging |
Het |
Pskh1 |
C |
T |
8: 106,656,511 (GRCm39) |
R396C |
probably damaging |
Het |
Rc3h2 |
T |
C |
2: 37,289,642 (GRCm39) |
D390G |
possibly damaging |
Het |
Ryr2 |
G |
T |
13: 11,720,542 (GRCm39) |
P2702Q |
probably damaging |
Het |
Senp6 |
C |
A |
9: 80,051,125 (GRCm39) |
A961D |
probably damaging |
Het |
Slc27a3 |
A |
G |
3: 90,294,146 (GRCm39) |
S503P |
probably benign |
Het |
Slc39a12 |
T |
C |
2: 14,394,193 (GRCm39) |
V21A |
possibly damaging |
Het |
Sox7 |
A |
G |
14: 64,185,945 (GRCm39) |
Y327C |
probably damaging |
Het |
Spdl1 |
A |
T |
11: 34,713,037 (GRCm39) |
F288I |
possibly damaging |
Het |
Ssbp2 |
T |
A |
13: 91,812,244 (GRCm39) |
M127K |
probably damaging |
Het |
Sspo |
A |
C |
6: 48,475,327 (GRCm39) |
S5032R |
possibly damaging |
Het |
Sycp1 |
A |
T |
3: 102,726,206 (GRCm39) |
W973R |
probably damaging |
Het |
Tm4sf5 |
C |
T |
11: 70,401,174 (GRCm39) |
T130I |
probably benign |
Het |
Top2a |
T |
A |
11: 98,907,306 (GRCm39) |
K175* |
probably null |
Het |
Trim30d |
T |
A |
7: 104,121,347 (GRCm39) |
Y316F |
probably damaging |
Het |
Zfp715 |
T |
C |
7: 42,949,378 (GRCm39) |
Y194C |
probably damaging |
Het |
|
Other mutations in Vmn1r124 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02102:Vmn1r124
|
APN |
7 |
20,994,467 (GRCm39) |
missense |
probably benign |
0.00 |
FR4976:Vmn1r124
|
UTSW |
7 |
20,993,861 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0062:Vmn1r124
|
UTSW |
7 |
20,993,743 (GRCm39) |
missense |
probably benign |
0.35 |
R0671:Vmn1r124
|
UTSW |
7 |
20,994,436 (GRCm39) |
missense |
probably damaging |
0.96 |
R1305:Vmn1r124
|
UTSW |
7 |
20,994,188 (GRCm39) |
missense |
probably benign |
0.01 |
R3954:Vmn1r124
|
UTSW |
7 |
20,994,448 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4628:Vmn1r124
|
UTSW |
7 |
20,994,302 (GRCm39) |
nonsense |
probably null |
|
R4830:Vmn1r124
|
UTSW |
7 |
20,993,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R5119:Vmn1r124
|
UTSW |
7 |
20,994,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R5381:Vmn1r124
|
UTSW |
7 |
20,994,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R6276:Vmn1r124
|
UTSW |
7 |
20,994,104 (GRCm39) |
missense |
probably benign |
0.03 |
R6987:Vmn1r124
|
UTSW |
7 |
20,993,743 (GRCm39) |
missense |
probably benign |
0.35 |
R7151:Vmn1r124
|
UTSW |
7 |
20,994,184 (GRCm39) |
missense |
probably benign |
0.04 |
R7152:Vmn1r124
|
UTSW |
7 |
20,994,184 (GRCm39) |
missense |
probably benign |
0.04 |
R9635:Vmn1r124
|
UTSW |
7 |
20,993,720 (GRCm39) |
missense |
probably benign |
0.23 |
X0065:Vmn1r124
|
UTSW |
7 |
20,994,255 (GRCm39) |
missense |
probably benign |
0.19 |
|