Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5830473C10Rik |
T |
C |
5: 90,571,765 |
V240A |
possibly damaging |
Het |
9230104M06Rik |
T |
C |
12: 113,000,175 |
D61G |
probably benign |
Het |
Ascc2 |
G |
A |
11: 4,640,481 |
|
probably null |
Het |
Atrn |
C |
T |
2: 130,970,144 |
Q670* |
probably null |
Het |
Atrn |
G |
T |
2: 130,947,734 |
|
probably benign |
Het |
Calr |
A |
C |
8: 84,844,488 |
W236G |
probably damaging |
Het |
Camk2g |
T |
A |
14: 20,766,016 |
|
probably null |
Het |
Cd101 |
G |
T |
3: 101,020,399 |
T122K |
probably damaging |
Het |
Col4a3bp |
T |
A |
13: 96,629,135 |
N469K |
possibly damaging |
Het |
Cryl1 |
T |
C |
14: 57,303,724 |
T168A |
probably benign |
Het |
Diaph3 |
A |
G |
14: 86,918,825 |
I684T |
probably damaging |
Het |
Ednrb |
A |
T |
14: 103,823,059 |
M266K |
possibly damaging |
Het |
Eif4h |
T |
C |
5: 134,639,292 |
D3G |
probably damaging |
Het |
Eny2 |
C |
T |
15: 44,429,635 |
R28C |
possibly damaging |
Het |
Epsti1 |
A |
G |
14: 77,939,923 |
E181G |
probably damaging |
Het |
Ezh2 |
A |
G |
6: 47,533,764 |
F598S |
probably damaging |
Het |
Fat3 |
G |
T |
9: 16,006,711 |
T1472K |
possibly damaging |
Het |
Gabra4 |
T |
A |
5: 71,638,147 |
I262F |
probably benign |
Het |
Gm15448 |
A |
G |
7: 3,822,625 |
I415T |
probably damaging |
Het |
Gpat4 |
A |
T |
8: 23,180,870 |
Y109N |
probably damaging |
Het |
Gpsm1 |
C |
T |
2: 26,339,675 |
T36I |
probably damaging |
Het |
Hikeshi |
C |
T |
7: 89,935,889 |
V36I |
possibly damaging |
Het |
Hip1 |
T |
C |
5: 135,444,751 |
M238V |
probably benign |
Het |
Hnrnpll |
A |
T |
17: 80,061,991 |
M1K |
probably null |
Het |
Irx2 |
G |
A |
13: 72,631,310 |
D238N |
probably damaging |
Het |
Kcnip4 |
T |
A |
5: 48,409,785 |
|
probably benign |
Het |
Lair1 |
G |
A |
7: 4,028,901 |
T69I |
possibly damaging |
Het |
Lamc1 |
A |
G |
1: 153,249,853 |
I558T |
possibly damaging |
Het |
Map4k5 |
C |
T |
12: 69,815,806 |
E639K |
probably benign |
Het |
Mc4r |
A |
G |
18: 66,859,662 |
S127P |
probably damaging |
Het |
Mmp23 |
A |
G |
4: 155,651,532 |
M221T |
possibly damaging |
Het |
Mre11a |
T |
C |
9: 14,826,591 |
S587P |
possibly damaging |
Het |
Myh9 |
A |
T |
15: 77,807,986 |
Y124* |
probably null |
Het |
Nek9 |
C |
A |
12: 85,305,507 |
A861S |
probably benign |
Het |
Nup155 |
T |
A |
15: 8,134,076 |
Y576N |
probably damaging |
Het |
Olfr1128 |
C |
T |
2: 87,544,657 |
V296M |
probably damaging |
Het |
Pcca |
A |
T |
14: 122,534,388 |
T8S |
probably benign |
Het |
Pcdh15 |
A |
G |
10: 74,631,068 |
D1573G |
probably benign |
Het |
Pdpr |
T |
A |
8: 111,118,090 |
V373E |
probably benign |
Het |
Pdzph1 |
A |
T |
17: 58,932,483 |
L950Q |
possibly damaging |
Het |
Psg22 |
A |
T |
7: 18,723,019 |
T237S |
possibly damaging |
Het |
Rdh13 |
A |
G |
7: 4,427,704 |
Y252H |
probably damaging |
Het |
Sema3d |
T |
C |
5: 12,563,145 |
|
probably benign |
Het |
Slc35b2 |
G |
A |
17: 45,566,567 |
V207I |
probably benign |
Het |
Sparcl1 |
T |
G |
5: 104,092,880 |
E226A |
possibly damaging |
Het |
Srms |
C |
A |
2: 181,209,509 |
A155S |
possibly damaging |
Het |
Tas2r107 |
A |
T |
6: 131,659,954 |
I44N |
probably damaging |
Het |
Tmem236 |
C |
T |
2: 14,219,321 |
T307M |
probably damaging |
Het |
Ush2a |
C |
T |
1: 188,946,958 |
P4788S |
probably damaging |
Het |
Vmn1r170 |
A |
T |
7: 23,606,291 |
L39F |
probably benign |
Het |
Vmn2r90 |
T |
A |
17: 17,726,860 |
*121R |
probably null |
Het |
|
Other mutations in Prss35 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01548:Prss35
|
APN |
9 |
86,755,274 (GRCm38) |
missense |
probably benign |
0.00 |
R0346:Prss35
|
UTSW |
9 |
86,755,351 (GRCm38) |
missense |
probably benign |
0.04 |
R0403:Prss35
|
UTSW |
9 |
86,756,037 (GRCm38) |
missense |
probably damaging |
1.00 |
R1664:Prss35
|
UTSW |
9 |
86,755,647 (GRCm38) |
missense |
probably benign |
0.29 |
R2016:Prss35
|
UTSW |
9 |
86,755,512 (GRCm38) |
missense |
probably benign |
0.37 |
R2017:Prss35
|
UTSW |
9 |
86,755,512 (GRCm38) |
missense |
probably benign |
0.37 |
R2325:Prss35
|
UTSW |
9 |
86,756,304 (GRCm38) |
missense |
probably damaging |
1.00 |
R2429:Prss35
|
UTSW |
9 |
86,755,345 (GRCm38) |
missense |
probably benign |
|
R2965:Prss35
|
UTSW |
9 |
86,755,582 (GRCm38) |
missense |
probably damaging |
1.00 |
R2966:Prss35
|
UTSW |
9 |
86,755,582 (GRCm38) |
missense |
probably damaging |
1.00 |
R3961:Prss35
|
UTSW |
9 |
86,755,749 (GRCm38) |
missense |
probably benign |
0.02 |
R4792:Prss35
|
UTSW |
9 |
86,755,669 (GRCm38) |
missense |
probably damaging |
1.00 |
R4902:Prss35
|
UTSW |
9 |
86,756,122 (GRCm38) |
missense |
probably damaging |
1.00 |
R6169:Prss35
|
UTSW |
9 |
86,755,438 (GRCm38) |
missense |
probably benign |
0.00 |
R6446:Prss35
|
UTSW |
9 |
86,755,653 (GRCm38) |
missense |
probably damaging |
0.99 |
R6753:Prss35
|
UTSW |
9 |
86,756,100 (GRCm38) |
missense |
probably damaging |
1.00 |
R7008:Prss35
|
UTSW |
9 |
86,756,308 (GRCm38) |
missense |
probably benign |
0.01 |
R7387:Prss35
|
UTSW |
9 |
86,755,921 (GRCm38) |
missense |
probably damaging |
1.00 |
R7523:Prss35
|
UTSW |
9 |
86,755,374 (GRCm38) |
missense |
probably damaging |
1.00 |
R7587:Prss35
|
UTSW |
9 |
86,755,374 (GRCm38) |
missense |
probably damaging |
1.00 |
R7652:Prss35
|
UTSW |
9 |
86,755,970 (GRCm38) |
missense |
probably benign |
|
R8013:Prss35
|
UTSW |
9 |
86,755,425 (GRCm38) |
missense |
probably damaging |
1.00 |
R8194:Prss35
|
UTSW |
9 |
86,755,613 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8871:Prss35
|
UTSW |
9 |
86,755,191 (GRCm38) |
missense |
possibly damaging |
0.84 |
R9444:Prss35
|
UTSW |
9 |
86,756,104 (GRCm38) |
missense |
probably damaging |
1.00 |
R9462:Prss35
|
UTSW |
9 |
86,756,339 (GRCm38) |
missense |
|
|
R9695:Prss35
|
UTSW |
9 |
86,755,708 (GRCm38) |
missense |
probably damaging |
1.00 |
|