Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Brip1 |
T |
A |
11: 85,952,830 (GRCm39) |
T984S |
possibly damaging |
Het |
Cdh17 |
T |
C |
4: 11,795,670 (GRCm39) |
Y417H |
probably damaging |
Het |
Chd7 |
T |
A |
4: 8,833,834 (GRCm39) |
I1196N |
probably damaging |
Het |
Cyp3a57 |
T |
C |
5: 145,323,854 (GRCm39) |
F447S |
probably damaging |
Het |
Dock8 |
C |
T |
19: 25,067,252 (GRCm39) |
|
probably benign |
Het |
Eif1ad5 |
A |
T |
12: 87,940,530 (GRCm39) |
|
noncoding transcript |
Het |
Fam163b |
A |
G |
2: 27,002,688 (GRCm39) |
F103S |
probably damaging |
Het |
G0s2 |
A |
G |
1: 192,954,964 (GRCm39) |
L40P |
probably damaging |
Het |
Gucy1b1 |
C |
T |
3: 81,942,660 (GRCm39) |
R494Q |
probably benign |
Het |
Hsd17b1 |
T |
C |
11: 100,969,755 (GRCm39) |
V89A |
probably damaging |
Het |
Iqcg |
T |
C |
16: 32,837,348 (GRCm39) |
|
probably benign |
Het |
Lmo7 |
T |
C |
14: 102,148,192 (GRCm39) |
|
probably benign |
Het |
Mmp17 |
A |
G |
5: 129,679,008 (GRCm39) |
D331G |
probably benign |
Het |
Mnx1 |
T |
C |
5: 29,682,591 (GRCm39) |
D228G |
unknown |
Het |
Msh2 |
T |
C |
17: 88,003,917 (GRCm39) |
|
probably benign |
Het |
Pabpc1 |
A |
G |
15: 36,599,550 (GRCm39) |
Y382H |
probably benign |
Het |
Prl7b1 |
A |
G |
13: 27,786,027 (GRCm39) |
S214P |
possibly damaging |
Het |
Rbpj-ps3 |
T |
C |
6: 46,507,025 (GRCm39) |
|
probably benign |
Het |
Sgsm1 |
A |
T |
5: 113,433,531 (GRCm39) |
M162K |
possibly damaging |
Het |
Skint2 |
A |
G |
4: 112,483,191 (GRCm39) |
T199A |
probably benign |
Het |
Stim1 |
A |
G |
7: 102,035,322 (GRCm39) |
D100G |
possibly damaging |
Het |
Taar5 |
C |
T |
10: 23,846,962 (GRCm39) |
T120I |
probably benign |
Het |
Trhde |
A |
G |
10: 114,623,848 (GRCm39) |
V352A |
probably benign |
Het |
Ubap2 |
T |
A |
4: 41,227,237 (GRCm39) |
D160V |
probably damaging |
Het |
Vmn2r18 |
A |
G |
5: 151,510,106 (GRCm39) |
V89A |
possibly damaging |
Het |
Wbp1l |
A |
G |
19: 46,642,839 (GRCm39) |
D264G |
possibly damaging |
Het |
|
Other mutations in Ptk2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00861:Ptk2
|
APN |
15 |
73,134,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00913:Ptk2
|
APN |
15 |
73,167,238 (GRCm39) |
splice site |
probably benign |
|
IGL01631:Ptk2
|
APN |
15 |
73,088,220 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01952:Ptk2
|
APN |
15 |
73,101,780 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01957:Ptk2
|
APN |
15 |
73,114,322 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02441:Ptk2
|
APN |
15 |
73,192,675 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02471:Ptk2
|
APN |
15 |
73,170,036 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02621:Ptk2
|
APN |
15 |
73,077,994 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03198:Ptk2
|
APN |
15 |
73,108,065 (GRCm39) |
missense |
probably damaging |
1.00 |
Shooter
|
UTSW |
15 |
73,176,293 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0239:Ptk2
|
UTSW |
15 |
73,215,132 (GRCm39) |
splice site |
probably null |
|
R0239:Ptk2
|
UTSW |
15 |
73,215,132 (GRCm39) |
splice site |
probably null |
|
R1254:Ptk2
|
UTSW |
15 |
73,101,819 (GRCm39) |
missense |
probably benign |
0.01 |
R1291:Ptk2
|
UTSW |
15 |
73,082,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R1307:Ptk2
|
UTSW |
15 |
73,163,895 (GRCm39) |
missense |
probably benign |
0.01 |
R1608:Ptk2
|
UTSW |
15 |
73,134,424 (GRCm39) |
missense |
probably damaging |
0.98 |
R1690:Ptk2
|
UTSW |
15 |
73,134,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1724:Ptk2
|
UTSW |
15 |
73,114,255 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1725:Ptk2
|
UTSW |
15 |
73,114,255 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1740:Ptk2
|
UTSW |
15 |
73,114,255 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1741:Ptk2
|
UTSW |
15 |
73,114,255 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1840:Ptk2
|
UTSW |
15 |
73,082,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1956:Ptk2
|
UTSW |
15 |
73,087,832 (GRCm39) |
missense |
possibly damaging |
0.49 |
R2022:Ptk2
|
UTSW |
15 |
73,114,255 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2092:Ptk2
|
UTSW |
15 |
73,108,040 (GRCm39) |
nonsense |
probably null |
|
R2114:Ptk2
|
UTSW |
15 |
73,114,255 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2115:Ptk2
|
UTSW |
15 |
73,114,255 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2336:Ptk2
|
UTSW |
15 |
73,137,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R2571:Ptk2
|
UTSW |
15 |
73,103,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R4232:Ptk2
|
UTSW |
15 |
73,181,698 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4245:Ptk2
|
UTSW |
15 |
73,103,825 (GRCm39) |
missense |
probably benign |
0.00 |
R4594:Ptk2
|
UTSW |
15 |
73,078,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R4688:Ptk2
|
UTSW |
15 |
73,078,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R4834:Ptk2
|
UTSW |
15 |
73,087,945 (GRCm39) |
splice site |
probably null |
|
R4847:Ptk2
|
UTSW |
15 |
73,103,805 (GRCm39) |
missense |
probably benign |
|
R5558:Ptk2
|
UTSW |
15 |
73,176,294 (GRCm39) |
missense |
probably damaging |
0.97 |
R5682:Ptk2
|
UTSW |
15 |
73,134,413 (GRCm39) |
nonsense |
probably null |
|
R5858:Ptk2
|
UTSW |
15 |
73,192,944 (GRCm39) |
missense |
probably benign |
0.12 |
R5951:Ptk2
|
UTSW |
15 |
73,175,682 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6014:Ptk2
|
UTSW |
15 |
73,176,293 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6027:Ptk2
|
UTSW |
15 |
73,101,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R6082:Ptk2
|
UTSW |
15 |
73,148,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R7025:Ptk2
|
UTSW |
15 |
73,093,658 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7031:Ptk2
|
UTSW |
15 |
73,093,658 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7032:Ptk2
|
UTSW |
15 |
73,093,658 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7077:Ptk2
|
UTSW |
15 |
73,093,658 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7078:Ptk2
|
UTSW |
15 |
73,093,658 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7079:Ptk2
|
UTSW |
15 |
73,093,658 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7090:Ptk2
|
UTSW |
15 |
73,093,658 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7091:Ptk2
|
UTSW |
15 |
73,093,658 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7092:Ptk2
|
UTSW |
15 |
73,093,658 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7136:Ptk2
|
UTSW |
15 |
73,093,658 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7137:Ptk2
|
UTSW |
15 |
73,093,658 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7798:Ptk2
|
UTSW |
15 |
73,167,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R8057:Ptk2
|
UTSW |
15 |
73,170,048 (GRCm39) |
frame shift |
probably null |
|
R8235:Ptk2
|
UTSW |
15 |
73,215,140 (GRCm39) |
missense |
probably benign |
0.00 |
R9106:Ptk2
|
UTSW |
15 |
73,131,457 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9160:Ptk2
|
UTSW |
15 |
73,087,933 (GRCm39) |
missense |
probably benign |
0.01 |
R9301:Ptk2
|
UTSW |
15 |
73,146,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R9448:Ptk2
|
UTSW |
15 |
73,215,041 (GRCm39) |
missense |
possibly damaging |
0.78 |
|