Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aamp |
C |
A |
1: 74,320,595 (GRCm39) |
|
probably benign |
Het |
Adamts19 |
T |
A |
18: 59,140,397 (GRCm39) |
|
probably benign |
Het |
Afg3l1 |
T |
A |
8: 124,214,128 (GRCm39) |
F190I |
probably benign |
Het |
Alms1 |
T |
A |
6: 85,618,353 (GRCm39) |
S2800T |
possibly damaging |
Het |
Alox5 |
A |
T |
6: 116,392,478 (GRCm39) |
W348R |
probably damaging |
Het |
Atp13a5 |
G |
A |
16: 29,085,766 (GRCm39) |
Q823* |
probably null |
Het |
Atp6v1b2 |
T |
C |
8: 69,541,586 (GRCm39) |
|
probably null |
Het |
Chuk |
T |
C |
19: 44,076,462 (GRCm39) |
I416M |
possibly damaging |
Het |
Cimip2b |
G |
A |
4: 43,428,158 (GRCm39) |
R100W |
possibly damaging |
Het |
Dmbt1 |
A |
T |
7: 130,701,020 (GRCm39) |
Q1066L |
possibly damaging |
Het |
Dnah5 |
A |
G |
15: 28,421,766 (GRCm39) |
T3873A |
probably damaging |
Het |
Endog |
C |
T |
2: 30,062,912 (GRCm39) |
T184M |
probably damaging |
Het |
Fcgbp |
T |
C |
7: 27,800,966 (GRCm39) |
|
probably benign |
Het |
Flii |
A |
G |
11: 60,606,659 (GRCm39) |
I1061T |
probably benign |
Het |
Hdac2 |
T |
A |
10: 36,873,067 (GRCm39) |
N308K |
probably damaging |
Het |
Hoxa2 |
T |
G |
6: 52,140,497 (GRCm39) |
Y163S |
probably damaging |
Het |
Hsd3b7 |
T |
C |
7: 127,402,144 (GRCm39) |
L263P |
probably damaging |
Het |
Klf17 |
T |
C |
4: 117,618,235 (GRCm39) |
T41A |
probably benign |
Het |
Lrrfip1 |
T |
C |
1: 90,996,343 (GRCm39) |
M42T |
probably damaging |
Het |
Mapk8ip1 |
C |
T |
2: 92,215,533 (GRCm39) |
V614I |
probably benign |
Het |
Mocs1 |
T |
G |
17: 49,742,292 (GRCm39) |
|
probably null |
Het |
Moxd1 |
T |
C |
10: 24,158,453 (GRCm39) |
|
probably benign |
Het |
Mterf1a |
T |
C |
5: 3,941,610 (GRCm39) |
E86G |
probably damaging |
Het |
Muc4 |
A |
G |
16: 32,574,613 (GRCm39) |
D1021G |
probably benign |
Het |
Nomo1 |
T |
C |
7: 45,694,760 (GRCm39) |
S212P |
possibly damaging |
Het |
Or5b116 |
A |
G |
19: 13,422,988 (GRCm39) |
D204G |
probably benign |
Het |
Or8c15 |
T |
A |
9: 38,120,534 (GRCm39) |
Y60N |
probably damaging |
Het |
Phf21a |
A |
C |
2: 92,178,374 (GRCm39) |
T385P |
probably damaging |
Het |
Piwil4 |
A |
T |
9: 14,626,327 (GRCm39) |
|
probably benign |
Het |
Pknox1 |
T |
C |
17: 31,818,619 (GRCm39) |
|
probably null |
Het |
Prr14l |
T |
C |
5: 32,988,410 (GRCm39) |
I362V |
probably benign |
Het |
Sergef |
C |
T |
7: 46,284,844 (GRCm39) |
|
probably null |
Het |
Sez6l |
T |
C |
5: 112,572,511 (GRCm39) |
D948G |
probably damaging |
Het |
Skor1 |
A |
T |
9: 63,053,723 (GRCm39) |
L54Q |
probably damaging |
Het |
Sntn |
C |
T |
14: 13,679,086 (GRCm38) |
Q87* |
probably null |
Het |
Syde2 |
A |
G |
3: 145,720,096 (GRCm39) |
K772E |
possibly damaging |
Het |
Taf2 |
T |
A |
15: 54,934,845 (GRCm39) |
|
probably null |
Het |
Tbc1d13 |
T |
A |
2: 30,030,523 (GRCm39) |
Y113N |
probably damaging |
Het |
Tmem154 |
T |
C |
3: 84,591,722 (GRCm39) |
F91L |
probably benign |
Het |
Tmem63a |
A |
G |
1: 180,794,062 (GRCm39) |
D533G |
possibly damaging |
Het |
Tmprss15 |
A |
T |
16: 78,782,882 (GRCm39) |
N712K |
possibly damaging |
Het |
Trip12 |
A |
T |
1: 84,708,262 (GRCm39) |
D603E |
probably damaging |
Het |
Trmt11 |
T |
C |
10: 30,442,445 (GRCm39) |
D246G |
probably damaging |
Het |
Wdr54 |
T |
C |
6: 83,132,755 (GRCm39) |
H33R |
probably benign |
Het |
Zfp207 |
A |
G |
11: 80,279,828 (GRCm39) |
D111G |
probably benign |
Het |
|
Other mutations in Vmn1r174 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00950:Vmn1r174
|
APN |
7 |
23,453,911 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01484:Vmn1r174
|
APN |
7 |
23,453,749 (GRCm39) |
nonsense |
probably null |
|
IGL02014:Vmn1r174
|
APN |
7 |
23,453,583 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02190:Vmn1r174
|
APN |
7 |
23,454,252 (GRCm39) |
missense |
unknown |
|
IGL03265:Vmn1r174
|
APN |
7 |
23,453,898 (GRCm39) |
nonsense |
probably null |
|
IGL03335:Vmn1r174
|
APN |
7 |
23,453,937 (GRCm39) |
missense |
probably benign |
0.41 |
R0529:Vmn1r174
|
UTSW |
7 |
23,453,622 (GRCm39) |
missense |
probably benign |
0.00 |
R1489:Vmn1r174
|
UTSW |
7 |
23,453,981 (GRCm39) |
nonsense |
probably null |
|
R1645:Vmn1r174
|
UTSW |
7 |
23,453,777 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1691:Vmn1r174
|
UTSW |
7 |
23,453,337 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R1753:Vmn1r174
|
UTSW |
7 |
23,453,622 (GRCm39) |
missense |
probably benign |
0.00 |
R1939:Vmn1r174
|
UTSW |
7 |
23,453,532 (GRCm39) |
missense |
probably damaging |
0.99 |
R1988:Vmn1r174
|
UTSW |
7 |
23,454,050 (GRCm39) |
missense |
probably damaging |
0.98 |
R2299:Vmn1r174
|
UTSW |
7 |
23,453,429 (GRCm39) |
missense |
probably benign |
0.08 |
R4429:Vmn1r174
|
UTSW |
7 |
23,453,565 (GRCm39) |
missense |
probably benign |
0.02 |
R4516:Vmn1r174
|
UTSW |
7 |
23,453,768 (GRCm39) |
missense |
probably benign |
0.01 |
R4589:Vmn1r174
|
UTSW |
7 |
23,454,204 (GRCm39) |
nonsense |
probably null |
|
R5175:Vmn1r174
|
UTSW |
7 |
23,454,153 (GRCm39) |
missense |
probably benign |
0.03 |
R5392:Vmn1r174
|
UTSW |
7 |
23,454,227 (GRCm39) |
missense |
unknown |
|
R5503:Vmn1r174
|
UTSW |
7 |
23,453,562 (GRCm39) |
missense |
probably benign |
0.03 |
R5568:Vmn1r174
|
UTSW |
7 |
23,453,919 (GRCm39) |
missense |
probably damaging |
0.96 |
R6705:Vmn1r174
|
UTSW |
7 |
23,453,851 (GRCm39) |
missense |
probably benign |
0.25 |
R8168:Vmn1r174
|
UTSW |
7 |
23,454,096 (GRCm39) |
missense |
probably damaging |
0.99 |
R8190:Vmn1r174
|
UTSW |
7 |
23,453,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R8523:Vmn1r174
|
UTSW |
7 |
23,454,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R8555:Vmn1r174
|
UTSW |
7 |
23,453,970 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8913:Vmn1r174
|
UTSW |
7 |
23,453,375 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8979:Vmn1r174
|
UTSW |
7 |
23,453,892 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8990:Vmn1r174
|
UTSW |
7 |
23,453,956 (GRCm39) |
missense |
possibly damaging |
0.71 |
X0011:Vmn1r174
|
UTSW |
7 |
23,453,906 (GRCm39) |
missense |
probably benign |
0.03 |
|