Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
A |
T |
5: 8,996,071 (GRCm39) |
|
probably null |
Het |
Acss1 |
A |
T |
2: 150,463,450 (GRCm39) |
V618E |
probably damaging |
Het |
Adgrg6 |
T |
C |
10: 14,310,084 (GRCm39) |
N774D |
probably damaging |
Het |
Atp9a |
A |
G |
2: 168,532,932 (GRCm39) |
V134A |
probably damaging |
Het |
Csmd3 |
T |
A |
15: 47,492,635 (GRCm39) |
T3169S |
probably benign |
Het |
D030068K23Rik |
T |
A |
8: 109,978,009 (GRCm39) |
Q52L |
unknown |
Het |
Dnah5 |
T |
C |
15: 28,311,480 (GRCm39) |
S1820P |
possibly damaging |
Het |
Fem1c |
A |
C |
18: 46,639,343 (GRCm39) |
S220A |
probably benign |
Het |
Gm10305 |
G |
A |
4: 99,161,414 (GRCm39) |
D108N |
unknown |
Het |
Gtdc1 |
A |
G |
2: 44,481,891 (GRCm39) |
|
probably null |
Het |
Il2ra |
T |
C |
2: 11,685,207 (GRCm39) |
V181A |
possibly damaging |
Het |
Lrrn1 |
T |
C |
6: 107,544,454 (GRCm39) |
I84T |
probably damaging |
Het |
Map3k1 |
T |
A |
13: 111,894,723 (GRCm39) |
|
probably null |
Het |
Mical1 |
T |
G |
10: 41,356,325 (GRCm39) |
Y293D |
probably damaging |
Het |
Mpzl1 |
T |
C |
1: 165,421,161 (GRCm39) |
D266G |
probably damaging |
Het |
Or55b4 |
C |
A |
7: 102,134,254 (GRCm39) |
M24I |
probably benign |
Het |
Pabpc4l |
A |
T |
3: 46,401,581 (GRCm39) |
V21D |
probably damaging |
Het |
Prdm10 |
T |
C |
9: 31,258,149 (GRCm39) |
C525R |
probably damaging |
Het |
Ptprj |
C |
A |
2: 90,271,139 (GRCm39) |
|
probably benign |
Het |
Rgs3 |
T |
C |
4: 62,537,981 (GRCm39) |
F4S |
probably damaging |
Het |
Ryr3 |
G |
A |
2: 112,603,073 (GRCm39) |
T2457I |
probably damaging |
Het |
Scn3a |
A |
G |
2: 65,291,775 (GRCm39) |
I1657T |
probably damaging |
Het |
Sema6a |
A |
G |
18: 47,381,884 (GRCm39) |
S888P |
probably damaging |
Het |
Slc37a1 |
T |
A |
17: 31,538,122 (GRCm39) |
Y148* |
probably null |
Het |
Tex10 |
T |
C |
4: 48,469,906 (GRCm39) |
N53S |
possibly damaging |
Het |
Vmn2r100 |
A |
G |
17: 19,751,495 (GRCm39) |
S513G |
possibly damaging |
Het |
|
Other mutations in Tyr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01568:Tyr
|
APN |
7 |
87,087,156 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02963:Tyr
|
APN |
7 |
87,133,205 (GRCm39) |
missense |
probably benign |
|
IGL03356:Tyr
|
APN |
7 |
87,141,922 (GRCm39) |
missense |
possibly damaging |
0.71 |
ghost
|
UTSW |
7 |
87,121,703 (GRCm39) |
missense |
probably damaging |
1.00 |
pale
|
UTSW |
7 |
87,087,175 (GRCm39) |
missense |
probably damaging |
1.00 |
pale_rider
|
UTSW |
7 |
87,087,231 (GRCm39) |
missense |
probably damaging |
1.00 |
rufus
|
UTSW |
7 |
87,141,914 (GRCm39) |
missense |
probably damaging |
1.00 |
shocked
|
UTSW |
7 |
87,142,330 (GRCm39) |
missense |
probably damaging |
1.00 |
siamese
|
UTSW |
7 |
87,087,252 (GRCm39) |
missense |
probably damaging |
0.99 |
Venusaur
|
UTSW |
7 |
87,141,914 (GRCm39) |
missense |
probably damaging |
1.00 |
waffle
|
UTSW |
7 |
87,142,429 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0322:Tyr
|
UTSW |
7 |
87,142,125 (GRCm39) |
missense |
probably benign |
0.35 |
R0479:Tyr
|
UTSW |
7 |
87,142,429 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1544:Tyr
|
UTSW |
7 |
87,141,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R1546:Tyr
|
UTSW |
7 |
87,087,200 (GRCm39) |
missense |
probably benign |
0.02 |
R1606:Tyr
|
UTSW |
7 |
87,087,179 (GRCm39) |
missense |
probably benign |
0.01 |
R1666:Tyr
|
UTSW |
7 |
87,142,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R2064:Tyr
|
UTSW |
7 |
87,142,051 (GRCm39) |
missense |
probably benign |
0.13 |
R2213:Tyr
|
UTSW |
7 |
87,142,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R2420:Tyr
|
UTSW |
7 |
87,078,397 (GRCm39) |
missense |
probably benign |
0.17 |
R4013:Tyr
|
UTSW |
7 |
87,087,148 (GRCm39) |
missense |
probably benign |
0.00 |
R4014:Tyr
|
UTSW |
7 |
87,087,148 (GRCm39) |
missense |
probably benign |
0.00 |
R4015:Tyr
|
UTSW |
7 |
87,087,148 (GRCm39) |
missense |
probably benign |
0.00 |
R4016:Tyr
|
UTSW |
7 |
87,087,148 (GRCm39) |
missense |
probably benign |
0.00 |
R4202:Tyr
|
UTSW |
7 |
87,078,276 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4205:Tyr
|
UTSW |
7 |
87,078,276 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4206:Tyr
|
UTSW |
7 |
87,078,276 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4361:Tyr
|
UTSW |
7 |
87,078,284 (GRCm39) |
missense |
probably benign |
0.01 |
R4738:Tyr
|
UTSW |
7 |
87,141,855 (GRCm39) |
missense |
probably null |
1.00 |
R5306:Tyr
|
UTSW |
7 |
87,087,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R5378:Tyr
|
UTSW |
7 |
87,121,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R5395:Tyr
|
UTSW |
7 |
87,121,698 (GRCm39) |
missense |
probably damaging |
0.98 |
R5782:Tyr
|
UTSW |
7 |
87,142,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R7007:Tyr
|
UTSW |
7 |
87,142,548 (GRCm39) |
missense |
probably benign |
0.04 |
R7609:Tyr
|
UTSW |
7 |
87,133,092 (GRCm39) |
missense |
probably benign |
0.06 |
R7767:Tyr
|
UTSW |
7 |
87,142,218 (GRCm39) |
missense |
probably benign |
0.37 |
R7794:Tyr
|
UTSW |
7 |
87,133,028 (GRCm39) |
critical splice donor site |
probably null |
|
R8158:Tyr
|
UTSW |
7 |
87,121,724 (GRCm39) |
missense |
probably damaging |
0.99 |
R8383:Tyr
|
UTSW |
7 |
87,133,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R8403:Tyr
|
UTSW |
7 |
87,087,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R8544:Tyr
|
UTSW |
7 |
87,142,000 (GRCm39) |
missense |
probably benign |
0.05 |
R8822:Tyr
|
UTSW |
7 |
87,142,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R8837:Tyr
|
UTSW |
7 |
87,087,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R9492:Tyr
|
UTSW |
7 |
87,121,705 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9492:Tyr
|
UTSW |
7 |
87,121,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R9748:Tyr
|
UTSW |
7 |
87,142,072 (GRCm39) |
missense |
possibly damaging |
0.89 |
|