Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Calm3 |
A |
T |
7: 16,917,079 (GRCm38) |
Y139* |
probably null |
Het |
Ccdc27 |
T |
C |
4: 154,028,066 (GRCm38) |
N584S |
probably benign |
Het |
Cdh24 |
C |
G |
14: 54,639,507 (GRCm38) |
G13A |
probably damaging |
Het |
Chd8 |
T |
C |
14: 52,215,220 (GRCm38) |
K1281E |
probably damaging |
Het |
Clasp1 |
G |
T |
1: 118,482,086 (GRCm38) |
G4C |
probably benign |
Het |
Cul9 |
G |
T |
17: 46,500,839 (GRCm38) |
P2488T |
probably damaging |
Het |
Daam2 |
A |
G |
17: 49,482,945 (GRCm38) |
V428A |
probably damaging |
Het |
Dcaf8 |
A |
G |
1: 172,188,968 (GRCm38) |
S441G |
probably damaging |
Het |
Dchs2 |
A |
G |
3: 83,348,274 (GRCm38) |
T2426A |
probably benign |
Het |
Dpys |
A |
G |
15: 39,826,883 (GRCm38) |
V358A |
probably damaging |
Het |
Efhd1 |
A |
G |
1: 87,289,497 (GRCm38) |
D112G |
probably damaging |
Het |
Exoc1 |
T |
C |
5: 76,566,953 (GRCm38) |
S120P |
unknown |
Het |
Fyco1 |
A |
G |
9: 123,797,719 (GRCm38) |
L1309S |
probably damaging |
Het |
Gm14403 |
A |
G |
2: 177,509,321 (GRCm38) |
N111S |
possibly damaging |
Het |
Gm5901 |
A |
G |
7: 105,377,348 (GRCm38) |
T108A |
probably benign |
Het |
Idh2 |
TCCCAGG |
T |
7: 80,098,331 (GRCm38) |
|
probably benign |
Het |
Itgb5 |
T |
G |
16: 33,885,094 (GRCm38) |
D251E |
probably damaging |
Het |
Kcnk15 |
T |
C |
2: 163,858,717 (GRCm38) |
V292A |
probably benign |
Het |
Kdm2a |
A |
T |
19: 4,319,141 (GRCm38) |
Y1149N |
probably damaging |
Het |
Kdm3a |
T |
C |
6: 71,595,545 (GRCm38) |
T1011A |
possibly damaging |
Het |
Krt35 |
A |
T |
11: 100,095,672 (GRCm38) |
|
probably null |
Het |
Lipn |
T |
A |
19: 34,071,780 (GRCm38) |
D115E |
possibly damaging |
Het |
Lpin3 |
T |
G |
2: 160,896,752 (GRCm38) |
L208R |
probably damaging |
Het |
Ltf |
C |
A |
9: 111,025,980 (GRCm38) |
Q354K |
probably benign |
Het |
Marf1 |
C |
A |
16: 14,111,702 (GRCm38) |
C1680F |
possibly damaging |
Het |
Mtss1l |
T |
A |
8: 110,730,024 (GRCm38) |
V242E |
probably damaging |
Het |
Myo7b |
T |
C |
18: 31,998,712 (GRCm38) |
Y477C |
probably damaging |
Het |
Nbn |
T |
A |
4: 15,981,350 (GRCm38) |
S481T |
probably benign |
Het |
Ncoa2 |
A |
G |
1: 13,186,838 (GRCm38) |
Y146H |
probably damaging |
Het |
Ntng1 |
A |
T |
3: 109,935,180 (GRCm38) |
C92* |
probably null |
Het |
Olfr1049 |
T |
A |
2: 86,255,076 (GRCm38) |
N206Y |
probably damaging |
Het |
Olfr1077-ps1 |
T |
C |
2: 86,526,127 (GRCm38) |
I17V |
probably benign |
Het |
Olfr133 |
G |
A |
17: 38,149,494 (GRCm38) |
G302D |
probably benign |
Het |
Olfr286 |
C |
T |
15: 98,227,202 (GRCm38) |
V150I |
probably benign |
Het |
Os9 |
A |
T |
10: 127,099,678 (GRCm38) |
S308T |
probably benign |
Het |
Otx2 |
T |
A |
14: 48,658,735 (GRCm38) |
T289S |
probably benign |
Het |
Palm2 |
C |
T |
4: 57,648,042 (GRCm38) |
A60V |
probably benign |
Het |
Pigg |
A |
G |
5: 108,336,512 (GRCm38) |
T675A |
possibly damaging |
Het |
Pink1 |
C |
T |
4: 138,315,601 (GRCm38) |
E461K |
probably damaging |
Het |
Pip5k1a |
A |
G |
3: 95,060,498 (GRCm38) |
S543P |
possibly damaging |
Het |
Prkaa1 |
A |
G |
15: 5,177,130 (GRCm38) |
T454A |
probably benign |
Het |
Ptk2 |
G |
A |
15: 73,221,809 (GRCm38) |
P854S |
possibly damaging |
Het |
Rab31 |
C |
T |
17: 65,698,017 (GRCm38) |
V83I |
possibly damaging |
Het |
Rabggtb |
G |
T |
3: 153,910,349 (GRCm38) |
D117E |
probably benign |
Het |
Rbl1 |
T |
C |
2: 157,152,900 (GRCm38) |
H951R |
probably benign |
Het |
Sapcd2 |
A |
G |
2: 25,376,079 (GRCm38) |
S314G |
probably benign |
Het |
Sept4 |
T |
C |
11: 87,584,438 (GRCm38) |
L164P |
probably damaging |
Het |
Shroom1 |
A |
G |
11: 53,465,933 (GRCm38) |
E541G |
probably damaging |
Het |
Slc26a7 |
C |
A |
4: 14,565,460 (GRCm38) |
G208* |
probably null |
Het |
Smco2 |
A |
G |
6: 146,871,213 (GRCm38) |
I304M |
probably damaging |
Het |
Spg7 |
T |
C |
8: 123,091,752 (GRCm38) |
|
probably null |
Het |
Spocd1 |
T |
C |
4: 129,953,898 (GRCm38) |
F552L |
|
Het |
St6galnac2 |
T |
C |
11: 116,677,635 (GRCm38) |
D334G |
probably damaging |
Het |
Sub1 |
A |
G |
15: 11,986,486 (GRCm38) |
S92P |
probably benign |
Het |
Syne2 |
T |
C |
12: 75,942,351 (GRCm38) |
F1829L |
probably benign |
Het |
Tdrd1 |
T |
C |
19: 56,851,401 (GRCm38) |
V631A |
probably benign |
Het |
Tdrd9 |
T |
C |
12: 111,992,470 (GRCm38) |
S113P |
probably benign |
Het |
Tgfbrap1 |
A |
C |
1: 43,071,565 (GRCm38) |
V260G |
probably damaging |
Het |
Tyw3 |
G |
C |
3: 154,593,789 (GRCm38) |
S94R |
probably benign |
Het |
Urb2 |
T |
C |
8: 124,030,599 (GRCm38) |
V1015A |
probably benign |
Het |
Usp5 |
A |
G |
6: 124,829,394 (GRCm38) |
M1T |
probably null |
Het |
Utrn |
T |
C |
10: 12,684,516 (GRCm38) |
D1343G |
possibly damaging |
Het |
Vmn2r56 |
T |
C |
7: 12,715,327 (GRCm38) |
Y328C |
probably damaging |
Het |
Wdr63 |
C |
A |
3: 146,040,827 (GRCm38) |
K881N |
possibly damaging |
Het |
Zc3h8 |
T |
C |
2: 128,935,321 (GRCm38) |
T133A |
possibly damaging |
Het |
|
Other mutations in Vmn2r99 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00503:Vmn2r99
|
APN |
17 |
19,378,854 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01113:Vmn2r99
|
APN |
17 |
19,394,256 (GRCm38) |
missense |
probably benign |
0.20 |
IGL01138:Vmn2r99
|
APN |
17 |
19,382,623 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL01646:Vmn2r99
|
APN |
17 |
19,393,658 (GRCm38) |
splice site |
probably benign |
|
IGL01769:Vmn2r99
|
APN |
17 |
19,380,115 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02112:Vmn2r99
|
APN |
17 |
19,380,232 (GRCm38) |
missense |
probably null |
0.99 |
IGL02891:Vmn2r99
|
APN |
17 |
19,378,690 (GRCm38) |
nonsense |
probably null |
|
IGL03132:Vmn2r99
|
APN |
17 |
19,378,223 (GRCm38) |
nonsense |
probably null |
|
FR4548:Vmn2r99
|
UTSW |
17 |
19,394,285 (GRCm38) |
missense |
probably damaging |
0.97 |
FR4976:Vmn2r99
|
UTSW |
17 |
19,394,285 (GRCm38) |
missense |
probably damaging |
0.97 |
PIT4382001:Vmn2r99
|
UTSW |
17 |
19,394,343 (GRCm38) |
missense |
probably damaging |
1.00 |
R0196:Vmn2r99
|
UTSW |
17 |
19,394,573 (GRCm38) |
missense |
probably benign |
0.00 |
R0720:Vmn2r99
|
UTSW |
17 |
19,379,043 (GRCm38) |
missense |
probably benign |
0.00 |
R1501:Vmn2r99
|
UTSW |
17 |
19,362,259 (GRCm38) |
missense |
possibly damaging |
0.93 |
R1519:Vmn2r99
|
UTSW |
17 |
19,380,060 (GRCm38) |
missense |
probably benign |
0.00 |
R1670:Vmn2r99
|
UTSW |
17 |
19,362,252 (GRCm38) |
missense |
probably benign |
0.37 |
R1682:Vmn2r99
|
UTSW |
17 |
19,377,945 (GRCm38) |
missense |
probably damaging |
0.97 |
R1873:Vmn2r99
|
UTSW |
17 |
19,362,153 (GRCm38) |
missense |
probably benign |
0.25 |
R1967:Vmn2r99
|
UTSW |
17 |
19,378,815 (GRCm38) |
missense |
probably benign |
0.01 |
R2101:Vmn2r99
|
UTSW |
17 |
19,377,991 (GRCm38) |
missense |
probably damaging |
1.00 |
R2474:Vmn2r99
|
UTSW |
17 |
19,378,629 (GRCm38) |
missense |
probably benign |
0.04 |
R2519:Vmn2r99
|
UTSW |
17 |
19,378,708 (GRCm38) |
missense |
probably damaging |
0.99 |
R3911:Vmn2r99
|
UTSW |
17 |
19,394,373 (GRCm38) |
missense |
possibly damaging |
0.92 |
R3947:Vmn2r99
|
UTSW |
17 |
19,378,990 (GRCm38) |
missense |
probably benign |
0.40 |
R3949:Vmn2r99
|
UTSW |
17 |
19,378,990 (GRCm38) |
missense |
probably benign |
0.40 |
R4016:Vmn2r99
|
UTSW |
17 |
19,378,570 (GRCm38) |
missense |
possibly damaging |
0.86 |
R4413:Vmn2r99
|
UTSW |
17 |
19,379,260 (GRCm38) |
missense |
probably damaging |
1.00 |
R4594:Vmn2r99
|
UTSW |
17 |
19,393,662 (GRCm38) |
missense |
probably damaging |
1.00 |
R4999:Vmn2r99
|
UTSW |
17 |
19,362,135 (GRCm38) |
start codon destroyed |
probably null |
0.96 |
R5206:Vmn2r99
|
UTSW |
17 |
19,378,606 (GRCm38) |
missense |
probably benign |
0.40 |
R5362:Vmn2r99
|
UTSW |
17 |
19,379,339 (GRCm38) |
missense |
probably benign |
0.00 |
R5377:Vmn2r99
|
UTSW |
17 |
19,379,269 (GRCm38) |
missense |
probably damaging |
1.00 |
R5455:Vmn2r99
|
UTSW |
17 |
19,394,146 (GRCm38) |
nonsense |
probably null |
|
R6021:Vmn2r99
|
UTSW |
17 |
19,377,948 (GRCm38) |
missense |
probably damaging |
1.00 |
R6059:Vmn2r99
|
UTSW |
17 |
19,378,980 (GRCm38) |
missense |
probably benign |
0.00 |
R6214:Vmn2r99
|
UTSW |
17 |
19,382,558 (GRCm38) |
missense |
probably benign |
0.19 |
R6215:Vmn2r99
|
UTSW |
17 |
19,382,558 (GRCm38) |
missense |
probably benign |
0.19 |
R6313:Vmn2r99
|
UTSW |
17 |
19,382,605 (GRCm38) |
missense |
probably damaging |
1.00 |
R6646:Vmn2r99
|
UTSW |
17 |
19,380,031 (GRCm38) |
missense |
probably damaging |
1.00 |
R6810:Vmn2r99
|
UTSW |
17 |
19,380,034 (GRCm38) |
missense |
probably benign |
0.20 |
R6885:Vmn2r99
|
UTSW |
17 |
19,380,195 (GRCm38) |
missense |
possibly damaging |
0.52 |
R6991:Vmn2r99
|
UTSW |
17 |
19,378,110 (GRCm38) |
missense |
probably benign |
0.03 |
R7060:Vmn2r99
|
UTSW |
17 |
19,394,564 (GRCm38) |
nonsense |
probably null |
|
R7094:Vmn2r99
|
UTSW |
17 |
19,379,311 (GRCm38) |
missense |
probably benign |
0.00 |
R7449:Vmn2r99
|
UTSW |
17 |
19,379,145 (GRCm38) |
missense |
probably benign |
0.01 |
R7789:Vmn2r99
|
UTSW |
17 |
19,393,817 (GRCm38) |
missense |
possibly damaging |
0.91 |
R8039:Vmn2r99
|
UTSW |
17 |
19,380,040 (GRCm38) |
missense |
probably benign |
0.00 |
R8493:Vmn2r99
|
UTSW |
17 |
19,393,758 (GRCm38) |
missense |
probably benign |
0.15 |
R8511:Vmn2r99
|
UTSW |
17 |
19,394,181 (GRCm38) |
missense |
probably damaging |
1.00 |
R8715:Vmn2r99
|
UTSW |
17 |
19,393,660 (GRCm38) |
critical splice acceptor site |
probably benign |
|
R9462:Vmn2r99
|
UTSW |
17 |
19,378,126 (GRCm38) |
nonsense |
probably null |
|
R9681:Vmn2r99
|
UTSW |
17 |
19,378,627 (GRCm38) |
missense |
probably damaging |
1.00 |
R9737:Vmn2r99
|
UTSW |
17 |
19,362,301 (GRCm38) |
missense |
probably benign |
|
Z1088:Vmn2r99
|
UTSW |
17 |
19,379,301 (GRCm38) |
missense |
probably benign |
0.18 |
|