Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
G |
T |
7: 120,540,602 (GRCm38) |
A1496S |
probably damaging |
Het |
Abra |
A |
T |
15: 41,869,187 (GRCm38) |
V161E |
probably damaging |
Het |
Adcy4 |
G |
A |
14: 55,770,047 (GRCm38) |
T942I |
possibly damaging |
Het |
Atrip |
A |
G |
9: 109,065,419 (GRCm38) |
V480A |
probably damaging |
Het |
Azin1 |
A |
T |
15: 38,491,565 (GRCm38) |
D382E |
probably benign |
Het |
BC034090 |
G |
T |
1: 155,225,153 (GRCm38) |
A455E |
probably benign |
Het |
Clstn1 |
A |
G |
4: 149,627,359 (GRCm38) |
Y121C |
probably damaging |
Het |
Cpq |
T |
A |
15: 33,302,508 (GRCm38) |
N268K |
probably damaging |
Het |
Cpsf7 |
A |
G |
19: 10,531,988 (GRCm38) |
S88G |
probably damaging |
Het |
Csgalnact1 |
C |
A |
8: 68,401,492 (GRCm38) |
G219V |
probably damaging |
Het |
Cyp2j11 |
G |
A |
4: 96,348,539 (GRCm38) |
A10V |
possibly damaging |
Het |
Dock4 |
T |
C |
12: 40,777,207 (GRCm38) |
V983A |
probably benign |
Het |
Dspp |
G |
T |
5: 104,177,366 (GRCm38) |
E532* |
probably null |
Het |
Ercc4 |
G |
T |
16: 13,123,536 (GRCm38) |
D243Y |
probably damaging |
Het |
Fars2 |
C |
A |
13: 36,410,162 (GRCm38) |
D383E |
probably benign |
Het |
Fip1l1 |
A |
G |
5: 74,564,544 (GRCm38) |
T280A |
probably benign |
Het |
Gcgr |
T |
G |
11: 120,537,184 (GRCm38) |
N292K |
probably damaging |
Het |
Gtpbp4 |
T |
A |
13: 8,991,750 (GRCm38) |
K85M |
possibly damaging |
Het |
Jhy |
A |
G |
9: 40,910,989 (GRCm38) |
Y618H |
probably damaging |
Het |
Mbd4 |
A |
T |
6: 115,849,025 (GRCm38) |
I314N |
possibly damaging |
Het |
Mbtd1 |
C |
T |
11: 93,908,858 (GRCm38) |
T70M |
probably damaging |
Het |
Mki67 |
T |
C |
7: 135,698,793 (GRCm38) |
H1504R |
probably benign |
Het |
Mks1 |
T |
C |
11: 87,862,785 (GRCm38) |
V515A |
probably benign |
Het |
Msantd2 |
G |
T |
9: 37,523,459 (GRCm38) |
V332L |
probably damaging |
Het |
Myrip |
A |
T |
9: 120,467,532 (GRCm38) |
T836S |
probably benign |
Het |
Nbea |
T |
C |
3: 56,086,266 (GRCm38) |
I238V |
probably benign |
Het |
Plekhh1 |
T |
C |
12: 79,069,009 (GRCm38) |
|
probably benign |
Het |
Prkdc |
A |
G |
16: 15,670,535 (GRCm38) |
N507S |
probably benign |
Het |
Prss12 |
G |
A |
3: 123,505,474 (GRCm38) |
V632I |
possibly damaging |
Het |
Puf60 |
A |
G |
15: 76,074,609 (GRCm38) |
S121P |
probably damaging |
Het |
Raet1e |
G |
A |
10: 22,180,636 (GRCm38) |
C37Y |
probably damaging |
Het |
Ralgps2 |
G |
T |
1: 156,828,268 (GRCm38) |
A362E |
possibly damaging |
Het |
Scn1a |
A |
G |
2: 66,326,036 (GRCm38) |
S510P |
possibly damaging |
Het |
Skap2 |
A |
C |
6: 51,874,473 (GRCm38) |
|
probably null |
Het |
Slc4a10 |
G |
A |
2: 62,190,769 (GRCm38) |
V54M |
probably benign |
Het |
Spata17 |
A |
G |
1: 187,117,261 (GRCm38) |
|
probably null |
Het |
Stoml3 |
T |
A |
3: 53,503,250 (GRCm38) |
N128K |
probably damaging |
Het |
Tatdn2 |
T |
A |
6: 113,704,213 (GRCm38) |
S402R |
probably benign |
Het |
Tmprss11f |
A |
G |
5: 86,533,666 (GRCm38) |
W243R |
probably damaging |
Het |
Vmn2r86 |
T |
A |
10: 130,448,639 (GRCm38) |
T528S |
possibly damaging |
Het |
Zfhx3 |
C |
T |
8: 108,955,742 (GRCm38) |
A3271V |
unknown |
Het |
Zkscan3 |
T |
C |
13: 21,388,178 (GRCm38) |
N428S |
possibly damaging |
Het |
Zxdc |
A |
G |
6: 90,398,836 (GRCm38) |
S765G |
probably benign |
Het |
|
Other mutations in Vmn2r32 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02140:Vmn2r32
|
APN |
7 |
7,476,697 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL02333:Vmn2r32
|
APN |
7 |
7,464,144 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02428:Vmn2r32
|
APN |
7 |
7,474,284 (GRCm38) |
missense |
probably benign |
0.02 |
IGL02484:Vmn2r32
|
APN |
7 |
7,464,117 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03277:Vmn2r32
|
APN |
7 |
7,474,252 (GRCm38) |
missense |
probably benign |
0.23 |
IGL03366:Vmn2r32
|
APN |
7 |
7,464,030 (GRCm38) |
missense |
probably damaging |
0.99 |
R1055:Vmn2r32
|
UTSW |
7 |
7,474,327 (GRCm38) |
nonsense |
probably null |
|
R1695:Vmn2r32
|
UTSW |
7 |
7,463,992 (GRCm38) |
missense |
probably benign |
0.01 |
R2172:Vmn2r32
|
UTSW |
7 |
7,474,615 (GRCm38) |
missense |
probably damaging |
0.99 |
R2262:Vmn2r32
|
UTSW |
7 |
7,474,619 (GRCm38) |
missense |
probably benign |
|
R3150:Vmn2r32
|
UTSW |
7 |
7,472,555 (GRCm38) |
missense |
probably benign |
|
R4362:Vmn2r32
|
UTSW |
7 |
7,479,858 (GRCm38) |
nonsense |
probably null |
|
R4432:Vmn2r32
|
UTSW |
7 |
7,479,919 (GRCm38) |
missense |
probably damaging |
0.98 |
R4851:Vmn2r32
|
UTSW |
7 |
7,479,954 (GRCm38) |
missense |
possibly damaging |
0.59 |
R4949:Vmn2r32
|
UTSW |
7 |
7,464,084 (GRCm38) |
missense |
probably benign |
0.22 |
R5990:Vmn2r32
|
UTSW |
7 |
7,479,810 (GRCm38) |
missense |
probably damaging |
0.97 |
R6083:Vmn2r32
|
UTSW |
7 |
7,464,210 (GRCm38) |
missense |
probably benign |
0.15 |
R6084:Vmn2r32
|
UTSW |
7 |
7,464,210 (GRCm38) |
missense |
probably benign |
0.15 |
R6116:Vmn2r32
|
UTSW |
7 |
7,464,093 (GRCm38) |
missense |
probably damaging |
1.00 |
R6263:Vmn2r32
|
UTSW |
7 |
7,476,692 (GRCm38) |
missense |
possibly damaging |
0.90 |
R6889:Vmn2r32
|
UTSW |
7 |
7,472,574 (GRCm38) |
missense |
possibly damaging |
0.82 |
R7286:Vmn2r32
|
UTSW |
7 |
7,479,808 (GRCm38) |
missense |
probably benign |
0.21 |
R7390:Vmn2r32
|
UTSW |
7 |
7,479,852 (GRCm38) |
missense |
probably benign |
0.00 |
R7412:Vmn2r32
|
UTSW |
7 |
7,474,213 (GRCm38) |
missense |
possibly damaging |
0.53 |
R7508:Vmn2r32
|
UTSW |
7 |
7,467,374 (GRCm38) |
missense |
possibly damaging |
0.87 |
R8812:Vmn2r32
|
UTSW |
7 |
7,474,670 (GRCm38) |
missense |
probably damaging |
1.00 |
R8968:Vmn2r32
|
UTSW |
7 |
7,474,205 (GRCm38) |
missense |
probably benign |
0.00 |
R9331:Vmn2r32
|
UTSW |
7 |
7,464,403 (GRCm38) |
nonsense |
probably null |
|
R9358:Vmn2r32
|
UTSW |
7 |
7,474,198 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Vmn2r32
|
UTSW |
7 |
7,474,161 (GRCm38) |
missense |
probably damaging |
0.98 |
|