Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930504O13Rik |
C |
A |
11: 58,447,478 |
M29I |
probably benign |
Het |
A530084C06Rik |
G |
T |
13: 31,558,995 |
R92S |
unknown |
Het |
Acaca |
A |
G |
11: 84,372,639 |
I2029V |
probably benign |
Het |
Anks1b |
A |
C |
10: 90,948,584 |
D1138A |
probably damaging |
Het |
Atr |
T |
A |
9: 95,947,118 |
V2508E |
probably damaging |
Het |
C4b |
C |
T |
17: 34,729,399 |
|
probably null |
Het |
C530008M17Rik |
A |
G |
5: 76,857,520 |
E576G |
unknown |
Het |
Cd46 |
A |
T |
1: 195,083,619 |
M146K |
probably null |
Het |
Chp1 |
A |
G |
2: 119,560,745 |
I28V |
probably benign |
Het |
Chrnb1 |
T |
A |
11: 69,792,873 |
R216W |
probably damaging |
Het |
Clmn |
G |
A |
12: 104,782,112 |
T392M |
probably benign |
Het |
Dcxr |
A |
C |
11: 120,726,453 |
L88R |
probably benign |
Het |
Dedd |
C |
T |
1: 171,338,910 |
P138L |
probably benign |
Het |
Degs1 |
A |
G |
1: 182,279,698 |
S35P |
probably damaging |
Het |
Ehmt1 |
T |
C |
2: 24,815,780 |
D851G |
possibly damaging |
Het |
Fam117b |
A |
G |
1: 59,981,534 |
D521G |
probably damaging |
Het |
Fam26d |
G |
A |
10: 34,043,908 |
T121M |
possibly damaging |
Het |
Gm14085 |
A |
T |
2: 122,486,680 |
R7S |
probably null |
Het |
Gm21731 |
G |
A |
13: 120,240,840 |
W57* |
probably null |
Het |
Gm6882 |
A |
G |
7: 21,427,652 |
V97A |
probably damaging |
Het |
Hgs |
A |
T |
11: 120,474,302 |
Q172L |
probably damaging |
Het |
Hormad2 |
T |
C |
11: 4,346,662 |
Q274R |
probably benign |
Het |
Igkv8-19 |
C |
T |
6: 70,341,399 |
|
probably benign |
Het |
Ikbkb |
T |
C |
8: 22,671,741 |
N377S |
probably benign |
Het |
Intu |
G |
A |
3: 40,654,253 |
G232S |
probably damaging |
Het |
Mov10 |
A |
G |
3: 104,797,065 |
S806P |
possibly damaging |
Het |
Mrgprb1 |
A |
G |
7: 48,447,583 |
F194L |
probably benign |
Het |
Notch3 |
A |
T |
17: 32,158,622 |
I160K |
probably benign |
Het |
Nup155 |
C |
G |
15: 8,109,453 |
S3W |
probably damaging |
Het |
Olfr1287 |
A |
G |
2: 111,449,622 |
I161V |
probably benign |
Het |
Olfr284 |
A |
G |
15: 98,340,086 |
I301T |
probably damaging |
Het |
Plxdc1 |
A |
T |
11: 97,956,151 |
F147L |
possibly damaging |
Het |
Ppfia1 |
T |
C |
7: 144,552,436 |
D33G |
possibly damaging |
Het |
Prdm11 |
G |
A |
2: 92,980,654 |
A200V |
probably damaging |
Het |
Qrich2 |
A |
T |
11: 116,456,629 |
I1123K |
unknown |
Het |
Rgs1 |
A |
G |
1: 144,248,477 |
|
probably null |
Het |
Skint7 |
T |
A |
4: 111,984,140 |
V259E |
probably benign |
Het |
Slc25a3 |
A |
T |
10: 91,118,042 |
|
probably null |
Het |
Slco1a6 |
A |
T |
6: 142,145,755 |
I73N |
probably damaging |
Het |
Sltm |
C |
G |
9: 70,586,673 |
P802R |
possibly damaging |
Het |
Smc4 |
CTA |
CTATA |
3: 69,018,067 |
|
probably benign |
Het |
Spock2 |
G |
A |
10: 60,126,180 |
D206N |
probably damaging |
Het |
Stard3nl |
T |
G |
13: 19,367,838 |
R185S |
probably damaging |
Het |
Supt16 |
A |
G |
14: 52,197,099 |
Y18H |
probably benign |
Het |
Synpo |
G |
A |
18: 60,603,428 |
T482I |
probably damaging |
Het |
Tmc6 |
G |
T |
11: 117,769,220 |
T694K |
probably benign |
Het |
Trim59 |
T |
A |
3: 69,037,926 |
H27L |
probably damaging |
Het |
Trpv2 |
G |
A |
11: 62,591,006 |
|
probably null |
Het |
Tyw5 |
A |
T |
1: 57,393,485 |
D117E |
probably benign |
Het |
Usp17la |
T |
C |
7: 104,861,147 |
Y320H |
probably damaging |
Het |
Usp31 |
T |
C |
7: 121,658,962 |
D694G |
probably damaging |
Het |
Vmn2r57 |
C |
T |
7: 41,425,089 |
V517M |
possibly damaging |
Het |
Yipf1 |
A |
G |
4: 107,318,996 |
N29S |
probably benign |
Het |
Zfp954 |
A |
T |
7: 7,115,824 |
F240L |
possibly damaging |
Het |
|
Other mutations in Vmn1r159 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
ANU23:Vmn1r159
|
UTSW |
7 |
22,843,163 (GRCm38) |
missense |
probably damaging |
0.99 |
R1183:Vmn1r159
|
UTSW |
7 |
22,843,594 (GRCm38) |
missense |
probably null |
0.80 |
R1522:Vmn1r159
|
UTSW |
7 |
22,843,268 (GRCm38) |
missense |
probably damaging |
0.98 |
R1700:Vmn1r159
|
UTSW |
7 |
22,842,965 (GRCm38) |
missense |
probably damaging |
1.00 |
R2570:Vmn1r159
|
UTSW |
7 |
22,842,882 (GRCm38) |
missense |
probably benign |
0.07 |
R3620:Vmn1r159
|
UTSW |
7 |
22,842,833 (GRCm38) |
missense |
possibly damaging |
0.89 |
R4939:Vmn1r159
|
UTSW |
7 |
22,842,891 (GRCm38) |
missense |
probably damaging |
1.00 |
R4985:Vmn1r159
|
UTSW |
7 |
22,843,534 (GRCm38) |
missense |
probably damaging |
1.00 |
R6161:Vmn1r159
|
UTSW |
7 |
22,843,187 (GRCm38) |
missense |
possibly damaging |
0.63 |
R6365:Vmn1r159
|
UTSW |
7 |
22,843,401 (GRCm38) |
missense |
probably damaging |
1.00 |
R7033:Vmn1r159
|
UTSW |
7 |
22,842,864 (GRCm38) |
missense |
probably damaging |
1.00 |
R7817:Vmn1r159
|
UTSW |
7 |
22,843,062 (GRCm38) |
missense |
possibly damaging |
0.47 |
R7846:Vmn1r159
|
UTSW |
7 |
22,843,271 (GRCm38) |
missense |
probably benign |
0.01 |
R8008:Vmn1r159
|
UTSW |
7 |
22,843,240 (GRCm38) |
missense |
possibly damaging |
0.56 |
R8019:Vmn1r159
|
UTSW |
7 |
22,842,823 (GRCm38) |
missense |
probably benign |
0.01 |
R8222:Vmn1r159
|
UTSW |
7 |
22,843,183 (GRCm38) |
nonsense |
probably null |
|
R8291:Vmn1r159
|
UTSW |
7 |
22,842,830 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8817:Vmn1r159
|
UTSW |
7 |
22,843,134 (GRCm38) |
missense |
probably benign |
0.04 |
R9170:Vmn1r159
|
UTSW |
7 |
22,843,340 (GRCm38) |
missense |
probably damaging |
1.00 |
R9242:Vmn1r159
|
UTSW |
7 |
22,843,487 (GRCm38) |
missense |
probably benign |
0.00 |
R9467:Vmn1r159
|
UTSW |
7 |
22,842,716 (GRCm38) |
missense |
possibly damaging |
0.90 |
R9525:Vmn1r159
|
UTSW |
7 |
22,842,992 (GRCm38) |
missense |
probably damaging |
0.96 |
R9601:Vmn1r159
|
UTSW |
7 |
22,843,191 (GRCm38) |
missense |
probably damaging |
1.00 |
R9699:Vmn1r159
|
UTSW |
7 |
22,843,250 (GRCm38) |
missense |
probably damaging |
0.98 |
|