Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr1 |
A |
G |
2: 58,367,823 (GRCm39) |
S113P |
probably benign |
Het |
Arhgdib |
A |
T |
6: 136,901,166 (GRCm39) |
W188R |
probably damaging |
Het |
Bcr |
T |
A |
10: 75,001,878 (GRCm39) |
N927K |
possibly damaging |
Het |
Cd209c |
A |
G |
8: 3,990,324 (GRCm39) |
Y165H |
probably damaging |
Het |
Cnnm2 |
A |
G |
19: 46,750,515 (GRCm39) |
K102E |
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,606,623 (GRCm39) |
E600G |
probably damaging |
Het |
Ddx4 |
A |
T |
13: 112,758,720 (GRCm39) |
H280Q |
probably benign |
Het |
Eya4 |
T |
C |
10: 22,992,498 (GRCm39) |
Y462C |
probably damaging |
Het |
Fibcd1 |
T |
A |
2: 31,728,576 (GRCm39) |
I94F |
probably damaging |
Het |
Gm4846 |
C |
A |
1: 166,322,195 (GRCm39) |
G124V |
probably damaging |
Het |
Gm5624 |
A |
G |
14: 44,797,469 (GRCm39) |
I108T |
possibly damaging |
Het |
Gpr179 |
A |
T |
11: 97,242,691 (GRCm39) |
M51K |
probably benign |
Het |
Hck |
A |
G |
2: 152,976,054 (GRCm39) |
I198V |
probably damaging |
Het |
Kcnd2 |
T |
A |
6: 21,216,924 (GRCm39) |
C209* |
probably null |
Het |
Klhl1 |
T |
A |
14: 96,438,778 (GRCm39) |
I507F |
possibly damaging |
Het |
Knl1 |
A |
T |
2: 118,908,450 (GRCm39) |
K1693N |
possibly damaging |
Het |
Mcam |
T |
C |
9: 44,051,714 (GRCm39) |
V490A |
possibly damaging |
Het |
Mrgprx1 |
A |
T |
7: 47,671,740 (GRCm39) |
D2E |
probably damaging |
Het |
Myof |
C |
A |
19: 37,909,929 (GRCm39) |
R1512L |
probably benign |
Het |
Nrp2 |
C |
T |
1: 62,810,996 (GRCm39) |
T679I |
probably benign |
Het |
Nwd2 |
C |
A |
5: 63,962,020 (GRCm39) |
L535I |
probably benign |
Het |
Nwd2 |
T |
A |
5: 63,962,021 (GRCm39) |
L535H |
probably damaging |
Het |
Or4f14b |
T |
A |
2: 111,775,285 (GRCm39) |
N172I |
probably damaging |
Het |
Or52j3 |
A |
T |
7: 102,836,221 (GRCm39) |
I138F |
probably damaging |
Het |
Or5b94 |
T |
C |
19: 12,652,033 (GRCm39) |
S155P |
probably damaging |
Het |
Phkb |
A |
G |
8: 86,602,275 (GRCm39) |
*41W |
probably null |
Het |
Prl5a1 |
T |
A |
13: 28,329,403 (GRCm39) |
N27K |
probably benign |
Het |
Rims1 |
T |
C |
1: 22,358,708 (GRCm39) |
T1292A |
probably damaging |
Het |
Rnf38 |
G |
A |
4: 44,133,745 (GRCm39) |
A376V |
probably damaging |
Het |
Slc34a2 |
T |
C |
5: 53,216,580 (GRCm39) |
V117A |
possibly damaging |
Het |
Slfn8 |
A |
T |
11: 82,894,517 (GRCm39) |
F707L |
probably damaging |
Het |
Snx16 |
G |
A |
3: 10,503,235 (GRCm39) |
P4L |
probably damaging |
Het |
Snx6 |
T |
C |
12: 54,801,130 (GRCm39) |
D289G |
probably damaging |
Het |
St8sia3 |
G |
T |
18: 64,402,750 (GRCm39) |
V130F |
probably damaging |
Het |
U2surp |
A |
G |
9: 95,363,704 (GRCm39) |
|
probably null |
Het |
Ubqln3 |
A |
G |
7: 103,791,272 (GRCm39) |
F273L |
probably benign |
Het |
Vmn2r101 |
A |
T |
17: 19,832,507 (GRCm39) |
R834S |
possibly damaging |
Het |
Vmn2r18 |
G |
T |
5: 151,508,102 (GRCm39) |
H341N |
probably damaging |
Het |
Vrk3 |
A |
G |
7: 44,403,244 (GRCm39) |
I2V |
probably benign |
Het |
Zglp1 |
A |
G |
9: 20,977,534 (GRCm39) |
S94P |
probably benign |
Het |
|
Other mutations in Mtg1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01739:Mtg1
|
APN |
7 |
139,730,149 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02105:Mtg1
|
APN |
7 |
139,730,119 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02458:Mtg1
|
APN |
7 |
139,730,085 (GRCm39) |
missense |
probably benign |
0.01 |
R0666:Mtg1
|
UTSW |
7 |
139,724,257 (GRCm39) |
missense |
probably benign |
|
R0893:Mtg1
|
UTSW |
7 |
139,729,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R3707:Mtg1
|
UTSW |
7 |
139,729,717 (GRCm39) |
missense |
probably damaging |
0.99 |
R4993:Mtg1
|
UTSW |
7 |
139,720,196 (GRCm39) |
missense |
probably null |
1.00 |
R5810:Mtg1
|
UTSW |
7 |
139,725,898 (GRCm39) |
splice site |
probably null |
|
R5886:Mtg1
|
UTSW |
7 |
139,729,778 (GRCm39) |
splice site |
probably null |
|
R5960:Mtg1
|
UTSW |
7 |
139,726,906 (GRCm39) |
unclassified |
probably benign |
|
R7069:Mtg1
|
UTSW |
7 |
139,723,657 (GRCm39) |
missense |
probably benign |
0.00 |
R7110:Mtg1
|
UTSW |
7 |
139,726,779 (GRCm39) |
missense |
probably benign |
0.02 |
R7492:Mtg1
|
UTSW |
7 |
139,724,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R7790:Mtg1
|
UTSW |
7 |
139,729,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R7917:Mtg1
|
UTSW |
7 |
139,727,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R8155:Mtg1
|
UTSW |
7 |
139,724,622 (GRCm39) |
missense |
probably benign |
0.07 |
R8444:Mtg1
|
UTSW |
7 |
139,718,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R8713:Mtg1
|
UTSW |
7 |
139,720,136 (GRCm39) |
missense |
probably benign |
0.12 |
R8713:Mtg1
|
UTSW |
7 |
139,717,688 (GRCm39) |
critical splice donor site |
probably null |
|
R9424:Mtg1
|
UTSW |
7 |
139,727,212 (GRCm39) |
nonsense |
probably null |
|
|