Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acta1 |
A |
G |
8: 124,618,864 (GRCm39) |
S340P |
probably benign |
Het |
Anpep |
T |
C |
7: 79,486,139 (GRCm39) |
T528A |
probably benign |
Het |
Apob |
T |
A |
12: 8,065,074 (GRCm39) |
D4014E |
probably benign |
Het |
Atp23 |
A |
G |
10: 126,735,451 (GRCm39) |
C78R |
probably damaging |
Het |
Atp8b3 |
A |
G |
10: 80,356,007 (GRCm39) |
F1235S |
probably benign |
Het |
B3gnt3 |
T |
C |
8: 72,145,582 (GRCm39) |
D262G |
probably benign |
Het |
Bltp1 |
A |
T |
3: 37,012,863 (GRCm39) |
I1848F |
probably damaging |
Het |
Brca1 |
G |
A |
11: 101,416,127 (GRCm39) |
A669V |
possibly damaging |
Het |
Caprin2 |
A |
T |
6: 148,770,820 (GRCm39) |
S391R |
probably benign |
Het |
Cdh15 |
G |
A |
8: 123,583,326 (GRCm39) |
R43Q |
possibly damaging |
Het |
Celsr1 |
A |
T |
15: 85,917,156 (GRCm39) |
N272K |
probably damaging |
Het |
Cryzl2 |
T |
G |
1: 157,298,357 (GRCm39) |
S249A |
probably benign |
Het |
Dsg1b |
A |
T |
18: 20,542,279 (GRCm39) |
T929S |
possibly damaging |
Het |
Dusp16 |
G |
T |
6: 134,695,277 (GRCm39) |
T518N |
probably benign |
Het |
Eno2 |
A |
T |
6: 124,743,261 (GRCm39) |
H158Q |
probably damaging |
Het |
Ep400 |
T |
C |
5: 110,867,450 (GRCm39) |
D954G |
unknown |
Het |
Erg28 |
T |
C |
12: 85,866,254 (GRCm39) |
T75A |
possibly damaging |
Het |
Fam135b |
T |
A |
15: 71,350,881 (GRCm39) |
T332S |
probably damaging |
Het |
Fam221b |
A |
G |
4: 43,660,683 (GRCm39) |
F357L |
probably damaging |
Het |
Fcgr2b |
C |
T |
1: 170,790,957 (GRCm39) |
G279R |
probably damaging |
Het |
Fryl |
A |
T |
5: 73,230,121 (GRCm39) |
L1679M |
probably damaging |
Het |
Galm |
T |
A |
17: 80,435,146 (GRCm39) |
M1K |
probably null |
Het |
Gsg1 |
A |
T |
6: 135,221,348 (GRCm39) |
I17N |
possibly damaging |
Het |
Hif3a |
A |
T |
7: 16,785,909 (GRCm39) |
I129N |
probably damaging |
Het |
Ighv1-11 |
A |
T |
12: 114,576,051 (GRCm39) |
W55R |
probably damaging |
Het |
Ighv1-20 |
C |
A |
12: 114,687,497 (GRCm39) |
K82N |
probably benign |
Het |
Igsf21 |
C |
T |
4: 139,764,832 (GRCm39) |
E148K |
probably benign |
Het |
Il22b |
C |
A |
10: 118,130,768 (GRCm39) |
E43* |
probably null |
Het |
Klhdc7b |
A |
T |
15: 89,271,523 (GRCm39) |
R802W |
probably damaging |
Het |
Krt8 |
T |
C |
15: 101,912,374 (GRCm39) |
I101V |
probably damaging |
Het |
Lrrc7 |
A |
G |
3: 157,876,380 (GRCm39) |
L570P |
probably damaging |
Het |
Map4k1 |
C |
G |
7: 28,693,646 (GRCm39) |
N412K |
probably benign |
Het |
Metrnl |
A |
T |
11: 121,605,564 (GRCm39) |
I118F |
possibly damaging |
Het |
Mmp12 |
T |
A |
9: 7,350,106 (GRCm39) |
D202E |
probably damaging |
Het |
Mpp2 |
A |
T |
11: 101,955,269 (GRCm39) |
S119T |
probably benign |
Het |
Ncoa6 |
T |
C |
2: 155,248,688 (GRCm39) |
T1539A |
probably benign |
Het |
Nlrc5 |
A |
G |
8: 95,206,154 (GRCm39) |
T715A |
possibly damaging |
Het |
Nsd1 |
T |
A |
13: 55,454,792 (GRCm39) |
N1963K |
probably damaging |
Het |
Nsd3 |
T |
C |
8: 26,149,834 (GRCm39) |
Y340H |
probably damaging |
Het |
Nwd1 |
T |
A |
8: 73,419,745 (GRCm39) |
S977T |
probably damaging |
Het |
Or5d39 |
T |
A |
2: 87,979,961 (GRCm39) |
Y134F |
probably damaging |
Het |
Or7d10 |
G |
T |
9: 19,832,337 (GRCm39) |
M277I |
probably benign |
Het |
Pcdh8 |
T |
C |
14: 80,008,197 (GRCm39) |
E122G |
probably damaging |
Het |
Pcmtd2 |
A |
C |
2: 181,496,991 (GRCm39) |
T323P |
probably benign |
Het |
Pign |
C |
A |
1: 105,519,447 (GRCm39) |
G492C |
probably damaging |
Het |
Plppr3 |
A |
G |
10: 79,702,337 (GRCm39) |
V245A |
possibly damaging |
Het |
Prl7a2 |
C |
T |
13: 27,844,983 (GRCm39) |
W134* |
probably null |
Het |
Prom1 |
A |
T |
5: 44,164,389 (GRCm39) |
N722K |
probably benign |
Het |
Rasal2 |
A |
T |
1: 156,988,860 (GRCm39) |
N663K |
probably damaging |
Het |
Rgl1 |
G |
T |
1: 152,428,172 (GRCm39) |
H315Q |
probably benign |
Het |
Smpdl3a |
C |
A |
10: 57,677,097 (GRCm39) |
A65E |
probably damaging |
Het |
Spdye4b |
G |
A |
5: 143,188,142 (GRCm39) |
D212N |
probably damaging |
Het |
Tafa3 |
T |
A |
3: 104,679,505 (GRCm39) |
K126N |
probably damaging |
Het |
Tanc1 |
G |
T |
2: 59,529,691 (GRCm39) |
|
probably null |
Het |
Trio |
A |
G |
15: 27,856,250 (GRCm39) |
V706A |
probably benign |
Het |
Tshz1 |
T |
A |
18: 84,033,805 (GRCm39) |
Q201L |
probably damaging |
Het |
Ubqln1 |
C |
T |
13: 58,331,131 (GRCm39) |
M365I |
probably benign |
Het |
Usp42 |
A |
T |
5: 143,705,331 (GRCm39) |
Y383N |
probably damaging |
Het |
Vmn2r49 |
A |
T |
7: 9,710,274 (GRCm39) |
S819R |
probably damaging |
Het |
|
Other mutations in Vmn1r189 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03084:Vmn1r189
|
APN |
13 |
22,286,008 (GRCm39) |
nonsense |
probably null |
|
R0437:Vmn1r189
|
UTSW |
13 |
22,286,231 (GRCm39) |
missense |
probably damaging |
0.99 |
R1199:Vmn1r189
|
UTSW |
13 |
22,286,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R1795:Vmn1r189
|
UTSW |
13 |
22,286,324 (GRCm39) |
missense |
probably benign |
0.03 |
R2251:Vmn1r189
|
UTSW |
13 |
22,286,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R3751:Vmn1r189
|
UTSW |
13 |
22,286,382 (GRCm39) |
missense |
probably benign |
0.00 |
R3824:Vmn1r189
|
UTSW |
13 |
22,286,382 (GRCm39) |
missense |
probably benign |
0.02 |
R3825:Vmn1r189
|
UTSW |
13 |
22,286,382 (GRCm39) |
missense |
probably benign |
0.02 |
R3856:Vmn1r189
|
UTSW |
13 |
22,286,439 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4688:Vmn1r189
|
UTSW |
13 |
22,286,289 (GRCm39) |
missense |
probably damaging |
0.99 |
R5665:Vmn1r189
|
UTSW |
13 |
22,286,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R6149:Vmn1r189
|
UTSW |
13 |
22,286,054 (GRCm39) |
missense |
probably benign |
0.33 |
R6431:Vmn1r189
|
UTSW |
13 |
22,286,525 (GRCm39) |
missense |
probably damaging |
0.98 |
R6660:Vmn1r189
|
UTSW |
13 |
22,286,066 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6974:Vmn1r189
|
UTSW |
13 |
22,286,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R7051:Vmn1r189
|
UTSW |
13 |
22,286,285 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7269:Vmn1r189
|
UTSW |
13 |
22,286,737 (GRCm39) |
missense |
probably benign |
0.00 |
R7330:Vmn1r189
|
UTSW |
13 |
22,286,711 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7611:Vmn1r189
|
UTSW |
13 |
22,286,322 (GRCm39) |
missense |
probably benign |
0.02 |
R7894:Vmn1r189
|
UTSW |
13 |
22,285,906 (GRCm39) |
nonsense |
probably null |
|
R8214:Vmn1r189
|
UTSW |
13 |
22,286,301 (GRCm39) |
missense |
probably benign |
0.01 |
R8925:Vmn1r189
|
UTSW |
13 |
22,286,811 (GRCm39) |
missense |
probably benign |
0.01 |
R8927:Vmn1r189
|
UTSW |
13 |
22,286,811 (GRCm39) |
missense |
probably benign |
0.01 |
R9329:Vmn1r189
|
UTSW |
13 |
22,286,430 (GRCm39) |
missense |
probably benign |
0.03 |
R9562:Vmn1r189
|
UTSW |
13 |
22,286,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Vmn1r189
|
UTSW |
13 |
22,286,426 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Vmn1r189
|
UTSW |
13 |
22,286,053 (GRCm39) |
missense |
probably benign |
0.00 |
|