Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg3 |
A |
T |
8: 95,766,221 (GRCm39) |
M351L |
possibly damaging |
Het |
Alk |
T |
C |
17: 72,228,891 (GRCm39) |
K725E |
possibly damaging |
Het |
Castor1 |
A |
C |
11: 4,171,850 (GRCm39) |
E309A |
probably damaging |
Het |
Dspp |
T |
A |
5: 104,323,233 (GRCm39) |
H125Q |
possibly damaging |
Het |
Elmo2 |
A |
T |
2: 165,138,907 (GRCm39) |
|
probably benign |
Het |
Erg |
A |
G |
16: 95,190,912 (GRCm39) |
|
probably benign |
Het |
Fam20c |
A |
G |
5: 138,794,910 (GRCm39) |
E513G |
possibly damaging |
Het |
Gm9839 |
G |
T |
1: 32,559,917 (GRCm39) |
T55N |
possibly damaging |
Het |
Gpd2 |
A |
T |
2: 57,228,879 (GRCm39) |
M228L |
probably damaging |
Het |
Hp |
A |
T |
8: 110,302,033 (GRCm39) |
M305K |
probably benign |
Het |
Ifng |
T |
A |
10: 118,281,174 (GRCm39) |
|
probably benign |
Het |
Igkv9-123 |
T |
C |
6: 67,931,449 (GRCm39) |
D39G |
possibly damaging |
Het |
Melk |
T |
A |
4: 44,347,262 (GRCm39) |
F431I |
probably benign |
Het |
Or10ak12 |
A |
G |
4: 118,666,653 (GRCm39) |
V136A |
probably damaging |
Het |
Or12j5 |
A |
T |
7: 140,084,097 (GRCm39) |
S92T |
probably damaging |
Het |
Or4p19 |
A |
G |
2: 88,242,135 (GRCm39) |
M289T |
probably damaging |
Het |
Or51k1 |
A |
C |
7: 103,661,321 (GRCm39) |
L196W |
probably damaging |
Het |
Or8g27 |
G |
A |
9: 39,129,412 (GRCm39) |
G253D |
probably damaging |
Het |
Pappa |
T |
C |
4: 65,107,553 (GRCm39) |
Y655H |
probably damaging |
Het |
Prss58 |
A |
T |
6: 40,872,399 (GRCm39) |
I208N |
probably damaging |
Het |
Ryr2 |
T |
A |
13: 11,718,430 (GRCm39) |
I2720F |
probably damaging |
Het |
Slc13a1 |
G |
T |
6: 24,104,076 (GRCm39) |
T322K |
probably damaging |
Het |
Spag17 |
T |
C |
3: 99,970,691 (GRCm39) |
F1292L |
probably benign |
Het |
Tbx5 |
A |
G |
5: 120,021,091 (GRCm39) |
T366A |
probably benign |
Het |
Tmeff2 |
G |
A |
1: 50,969,705 (GRCm39) |
|
probably benign |
Het |
Tmem101 |
C |
A |
11: 102,045,378 (GRCm39) |
|
probably null |
Het |
Tpp2 |
C |
A |
1: 44,000,048 (GRCm39) |
P389T |
probably damaging |
Het |
Tyk2 |
A |
G |
9: 21,020,159 (GRCm39) |
Y1000H |
probably damaging |
Het |
Ush2a |
C |
A |
1: 188,410,574 (GRCm39) |
N2407K |
probably damaging |
Het |
Vmn1r94 |
C |
T |
7: 19,901,561 (GRCm39) |
V248I |
probably damaging |
Het |
Vmn2r12 |
T |
A |
5: 109,234,125 (GRCm39) |
I696F |
probably damaging |
Het |
Vmn2r83 |
A |
G |
10: 79,313,662 (GRCm39) |
E90G |
probably damaging |
Het |
Wee2 |
A |
G |
6: 40,440,187 (GRCm39) |
E445G |
probably benign |
Het |
Zfp518b |
T |
C |
5: 38,830,131 (GRCm39) |
T625A |
probably benign |
Het |
|
Other mutations in Washc5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00861:Washc5
|
APN |
15 |
59,209,125 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01305:Washc5
|
APN |
15 |
59,227,688 (GRCm39) |
nonsense |
probably null |
|
IGL01707:Washc5
|
APN |
15 |
59,213,864 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01921:Washc5
|
APN |
15 |
59,213,958 (GRCm39) |
splice site |
probably null |
|
IGL02056:Washc5
|
APN |
15 |
59,222,185 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02145:Washc5
|
APN |
15 |
59,241,060 (GRCm39) |
missense |
probably benign |
|
IGL02430:Washc5
|
APN |
15 |
59,238,140 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02450:Washc5
|
APN |
15 |
59,204,166 (GRCm39) |
nonsense |
probably null |
|
IGL03238:Washc5
|
APN |
15 |
59,218,691 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03351:Washc5
|
APN |
15 |
59,235,199 (GRCm39) |
splice site |
probably benign |
|
ANU22:Washc5
|
UTSW |
15 |
59,227,688 (GRCm39) |
nonsense |
probably null |
|
R0004:Washc5
|
UTSW |
15 |
59,239,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R0004:Washc5
|
UTSW |
15 |
59,239,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R0100:Washc5
|
UTSW |
15 |
59,215,947 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0100:Washc5
|
UTSW |
15 |
59,215,947 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0179:Washc5
|
UTSW |
15 |
59,224,379 (GRCm39) |
missense |
probably benign |
0.01 |
R0265:Washc5
|
UTSW |
15 |
59,210,809 (GRCm39) |
missense |
probably benign |
0.43 |
R0315:Washc5
|
UTSW |
15 |
59,213,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R0545:Washc5
|
UTSW |
15 |
59,213,942 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0611:Washc5
|
UTSW |
15 |
59,213,007 (GRCm39) |
missense |
probably damaging |
0.99 |
R0636:Washc5
|
UTSW |
15 |
59,231,258 (GRCm39) |
missense |
probably benign |
0.01 |
R1006:Washc5
|
UTSW |
15 |
59,241,036 (GRCm39) |
missense |
probably benign |
0.06 |
R1006:Washc5
|
UTSW |
15 |
59,241,035 (GRCm39) |
missense |
probably benign |
0.21 |
R1237:Washc5
|
UTSW |
15 |
59,210,757 (GRCm39) |
splice site |
probably benign |
|
R1835:Washc5
|
UTSW |
15 |
59,231,189 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1888:Washc5
|
UTSW |
15 |
59,231,174 (GRCm39) |
missense |
probably damaging |
0.99 |
R1888:Washc5
|
UTSW |
15 |
59,231,174 (GRCm39) |
missense |
probably damaging |
0.99 |
R2005:Washc5
|
UTSW |
15 |
59,213,004 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2006:Washc5
|
UTSW |
15 |
59,213,004 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2060:Washc5
|
UTSW |
15 |
59,222,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R2134:Washc5
|
UTSW |
15 |
59,241,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R2139:Washc5
|
UTSW |
15 |
59,221,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R2177:Washc5
|
UTSW |
15 |
59,235,118 (GRCm39) |
nonsense |
probably null |
|
R2975:Washc5
|
UTSW |
15 |
59,217,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Washc5
|
UTSW |
15 |
59,211,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R4824:Washc5
|
UTSW |
15 |
59,205,485 (GRCm39) |
nonsense |
probably null |
|
R4843:Washc5
|
UTSW |
15 |
59,222,220 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4991:Washc5
|
UTSW |
15 |
59,215,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R4996:Washc5
|
UTSW |
15 |
59,205,484 (GRCm39) |
missense |
probably benign |
|
R5103:Washc5
|
UTSW |
15 |
59,222,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R5312:Washc5
|
UTSW |
15 |
59,217,377 (GRCm39) |
splice site |
probably null |
|
R5591:Washc5
|
UTSW |
15 |
59,241,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R6073:Washc5
|
UTSW |
15 |
59,207,019 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6123:Washc5
|
UTSW |
15 |
59,206,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R6156:Washc5
|
UTSW |
15 |
59,217,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R6292:Washc5
|
UTSW |
15 |
59,227,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R6297:Washc5
|
UTSW |
15 |
59,215,895 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6374:Washc5
|
UTSW |
15 |
59,209,044 (GRCm39) |
missense |
probably benign |
0.14 |
R6659:Washc5
|
UTSW |
15 |
59,212,739 (GRCm39) |
critical splice donor site |
probably null |
|
R6880:Washc5
|
UTSW |
15 |
59,222,021 (GRCm39) |
missense |
probably benign |
0.00 |
R7146:Washc5
|
UTSW |
15 |
59,224,350 (GRCm39) |
nonsense |
probably null |
|
R7330:Washc5
|
UTSW |
15 |
59,205,516 (GRCm39) |
missense |
probably benign |
0.02 |
R7430:Washc5
|
UTSW |
15 |
59,241,762 (GRCm39) |
nonsense |
probably null |
|
R7490:Washc5
|
UTSW |
15 |
59,209,053 (GRCm39) |
missense |
probably benign |
0.18 |
R7532:Washc5
|
UTSW |
15 |
59,239,260 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7560:Washc5
|
UTSW |
15 |
59,238,041 (GRCm39) |
missense |
probably damaging |
0.97 |
R7803:Washc5
|
UTSW |
15 |
59,240,308 (GRCm39) |
missense |
probably damaging |
0.98 |
R8242:Washc5
|
UTSW |
15 |
59,215,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R8841:Washc5
|
UTSW |
15 |
59,206,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R9022:Washc5
|
UTSW |
15 |
59,233,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R9022:Washc5
|
UTSW |
15 |
59,217,233 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9123:Washc5
|
UTSW |
15 |
59,209,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R9125:Washc5
|
UTSW |
15 |
59,209,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R9310:Washc5
|
UTSW |
15 |
59,218,067 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9423:Washc5
|
UTSW |
15 |
59,227,735 (GRCm39) |
missense |
probably benign |
|
R9556:Washc5
|
UTSW |
15 |
59,218,716 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9569:Washc5
|
UTSW |
15 |
59,215,980 (GRCm39) |
missense |
probably benign |
|
R9668:Washc5
|
UTSW |
15 |
59,218,062 (GRCm39) |
critical splice donor site |
probably null |
|
R9691:Washc5
|
UTSW |
15 |
59,218,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R9718:Washc5
|
UTSW |
15 |
59,217,192 (GRCm39) |
missense |
probably benign |
0.19 |
|