Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
T |
A |
6: 23,109,437 (GRCm39) |
E344D |
probably benign |
Het |
Acoxl |
G |
A |
2: 127,917,855 (GRCm39) |
|
probably null |
Het |
Adora1 |
A |
T |
1: 134,131,224 (GRCm39) |
L149Q |
possibly damaging |
Het |
Aebp1 |
C |
A |
11: 5,818,501 (GRCm39) |
D115E |
possibly damaging |
Het |
Ank3 |
A |
G |
10: 69,822,938 (GRCm39) |
I1819V |
probably benign |
Het |
Ankrd44 |
T |
C |
1: 54,706,539 (GRCm39) |
H454R |
probably damaging |
Het |
Ap4e1 |
C |
T |
2: 126,906,842 (GRCm39) |
A1034V |
possibly damaging |
Het |
B3galt2 |
T |
A |
1: 143,522,849 (GRCm39) |
F328L |
probably benign |
Het |
Bbip1 |
G |
A |
19: 53,919,786 (GRCm39) |
|
probably benign |
Het |
Brsk1 |
G |
A |
7: 4,711,865 (GRCm39) |
E572K |
possibly damaging |
Het |
Clca3a1 |
G |
T |
3: 144,442,897 (GRCm39) |
P716T |
possibly damaging |
Het |
Clpx |
T |
C |
9: 65,228,132 (GRCm39) |
V380A |
probably damaging |
Het |
Epha3 |
T |
A |
16: 63,418,620 (GRCm39) |
Q608H |
probably damaging |
Het |
Gprc6a |
G |
T |
10: 51,491,089 (GRCm39) |
P712T |
probably damaging |
Het |
Itpr1 |
C |
A |
6: 108,519,023 (GRCm39) |
Q2720K |
probably damaging |
Het |
Kdm5b |
A |
G |
1: 134,548,735 (GRCm39) |
E1080G |
probably benign |
Het |
Macf1 |
G |
A |
4: 123,295,567 (GRCm39) |
R3163* |
probably null |
Het |
Map4k5 |
T |
C |
12: 69,888,755 (GRCm39) |
D292G |
probably benign |
Het |
Mau2 |
A |
T |
8: 70,481,373 (GRCm39) |
C217S |
probably benign |
Het |
Mtf1 |
T |
C |
4: 124,714,220 (GRCm39) |
F210L |
probably damaging |
Het |
Mtif2 |
G |
A |
11: 29,486,889 (GRCm39) |
V300M |
probably damaging |
Het |
Mtmr2 |
T |
C |
9: 13,694,905 (GRCm39) |
|
probably benign |
Het |
Mybpc3 |
C |
A |
2: 90,955,573 (GRCm39) |
|
probably null |
Het |
Ncmap |
T |
C |
4: 135,107,430 (GRCm39) |
|
probably null |
Het |
Nek9 |
A |
G |
12: 85,355,751 (GRCm39) |
F672S |
probably damaging |
Het |
Nuak1 |
A |
T |
10: 84,245,542 (GRCm39) |
I101N |
probably damaging |
Het |
Or8s16 |
T |
C |
15: 98,211,311 (GRCm39) |
N40S |
probably damaging |
Het |
Pcdh7 |
T |
A |
5: 58,286,515 (GRCm39) |
M1197K |
probably damaging |
Het |
Pcdhb17 |
A |
C |
18: 37,618,939 (GRCm39) |
Q243P |
probably benign |
Het |
Pcf11 |
T |
G |
7: 92,310,699 (GRCm39) |
K221Q |
probably damaging |
Het |
Pkhd1 |
C |
T |
1: 20,604,769 (GRCm39) |
R1182H |
probably benign |
Het |
Ptprz1 |
C |
A |
6: 23,001,900 (GRCm39) |
P1330Q |
probably benign |
Het |
Rbm33 |
T |
G |
5: 28,542,050 (GRCm39) |
|
probably null |
Het |
Rhobtb1 |
A |
G |
10: 69,084,615 (GRCm39) |
D2G |
probably damaging |
Het |
Rngtt |
T |
A |
4: 33,325,110 (GRCm39) |
C110* |
probably null |
Het |
Setx |
T |
A |
2: 29,038,430 (GRCm39) |
N1638K |
probably benign |
Het |
Slc24a3 |
A |
T |
2: 145,446,437 (GRCm39) |
M282L |
probably benign |
Het |
Slc7a1 |
A |
T |
5: 148,270,798 (GRCm39) |
V556D |
possibly damaging |
Het |
Sppl2c |
A |
T |
11: 104,077,407 (GRCm39) |
D69V |
possibly damaging |
Het |
Srpk3 |
C |
T |
X: 72,818,555 (GRCm39) |
R82* |
probably null |
Het |
Tas2r120 |
A |
T |
6: 132,634,110 (GRCm39) |
N64I |
probably damaging |
Het |
Tcf25 |
G |
T |
8: 124,100,678 (GRCm39) |
A23S |
probably damaging |
Het |
Tigd2 |
A |
T |
6: 59,188,138 (GRCm39) |
K335I |
probably damaging |
Het |
Tlr6 |
A |
G |
5: 65,112,647 (GRCm39) |
S87P |
probably benign |
Het |
Tmem135 |
T |
A |
7: 88,797,200 (GRCm39) |
Y352F |
probably damaging |
Het |
Tob2 |
T |
C |
15: 81,735,918 (GRCm39) |
Y17C |
probably damaging |
Het |
Tymp |
GC |
GCC |
15: 89,258,567 (GRCm39) |
|
probably null |
Het |
Zfp946 |
T |
C |
17: 22,673,447 (GRCm39) |
V67A |
probably benign |
Het |
Zswim4 |
G |
T |
8: 84,946,561 (GRCm39) |
N698K |
probably benign |
Het |
Zzz3 |
A |
G |
3: 152,133,182 (GRCm39) |
Q80R |
probably damaging |
Het |
|
Other mutations in Vmn1r179 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02211:Vmn1r179
|
APN |
7 |
23,628,630 (GRCm39) |
missense |
probably benign |
0.00 |
R0029:Vmn1r179
|
UTSW |
7 |
23,628,630 (GRCm39) |
missense |
probably benign |
0.00 |
R0029:Vmn1r179
|
UTSW |
7 |
23,628,630 (GRCm39) |
missense |
probably benign |
0.00 |
R0058:Vmn1r179
|
UTSW |
7 |
23,628,592 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0470:Vmn1r179
|
UTSW |
7 |
23,627,818 (GRCm39) |
missense |
probably benign |
0.00 |
R1451:Vmn1r179
|
UTSW |
7 |
23,628,275 (GRCm39) |
nonsense |
probably null |
|
R4923:Vmn1r179
|
UTSW |
7 |
23,628,491 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4953:Vmn1r179
|
UTSW |
7 |
23,628,515 (GRCm39) |
missense |
probably damaging |
0.99 |
R5304:Vmn1r179
|
UTSW |
7 |
23,628,100 (GRCm39) |
missense |
probably benign |
0.02 |
R5434:Vmn1r179
|
UTSW |
7 |
23,628,387 (GRCm39) |
missense |
probably benign |
0.21 |
R6341:Vmn1r179
|
UTSW |
7 |
23,628,491 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6451:Vmn1r179
|
UTSW |
7 |
23,628,076 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6501:Vmn1r179
|
UTSW |
7 |
23,628,342 (GRCm39) |
missense |
probably benign |
0.25 |
R7107:Vmn1r179
|
UTSW |
7 |
23,627,819 (GRCm39) |
nonsense |
probably null |
|
R7480:Vmn1r179
|
UTSW |
7 |
23,628,558 (GRCm39) |
nonsense |
probably null |
|
R8185:Vmn1r179
|
UTSW |
7 |
23,628,163 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8245:Vmn1r179
|
UTSW |
7 |
23,628,396 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8255:Vmn1r179
|
UTSW |
7 |
23,628,436 (GRCm39) |
missense |
probably benign |
0.21 |
R8413:Vmn1r179
|
UTSW |
7 |
23,628,277 (GRCm39) |
missense |
probably benign |
0.20 |
R9031:Vmn1r179
|
UTSW |
7 |
23,628,234 (GRCm39) |
missense |
probably benign |
0.01 |
R9522:Vmn1r179
|
UTSW |
7 |
23,628,202 (GRCm39) |
missense |
probably damaging |
0.97 |
X0061:Vmn1r179
|
UTSW |
7 |
23,627,819 (GRCm39) |
nonsense |
probably null |
|
Z1088:Vmn1r179
|
UTSW |
7 |
23,627,907 (GRCm39) |
missense |
probably benign |
0.10 |
|