Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg6 |
A |
G |
10: 14,296,428 (GRCm39) |
F991L |
probably damaging |
Het |
Ahnak |
A |
G |
19: 8,990,164 (GRCm39) |
D3816G |
unknown |
Het |
Arhgdig |
T |
C |
17: 26,418,608 (GRCm39) |
T153A |
probably damaging |
Het |
Ash2l |
T |
C |
8: 26,329,792 (GRCm39) |
D122G |
probably damaging |
Het |
Bora |
A |
G |
14: 99,310,162 (GRCm39) |
K497R |
probably benign |
Het |
Btbd9 |
T |
C |
17: 30,736,177 (GRCm39) |
H312R |
probably damaging |
Het |
Cbr2 |
T |
C |
11: 120,620,609 (GRCm39) |
D225G |
probably benign |
Het |
Cemip |
C |
A |
7: 83,652,616 (GRCm39) |
|
probably benign |
Het |
Cfap70 |
G |
A |
14: 20,486,854 (GRCm39) |
T275M |
probably benign |
Het |
Clca4b |
T |
C |
3: 144,622,421 (GRCm39) |
D548G |
possibly damaging |
Het |
Ctsf |
T |
G |
19: 4,906,567 (GRCm39) |
F165V |
probably damaging |
Het |
Cyp3a44 |
T |
A |
5: 145,738,135 (GRCm39) |
I57L |
probably benign |
Het |
Dbx2 |
C |
T |
15: 95,552,199 (GRCm39) |
G149S |
probably benign |
Het |
Dennd2a |
A |
G |
6: 39,457,207 (GRCm39) |
V745A |
possibly damaging |
Het |
Dock10 |
A |
T |
1: 80,564,085 (GRCm39) |
S509R |
possibly damaging |
Het |
Enpp3 |
T |
C |
10: 24,660,752 (GRCm39) |
Y630C |
probably damaging |
Het |
Eomes |
C |
T |
9: 118,307,574 (GRCm39) |
|
probably benign |
Het |
Fchsd1 |
A |
T |
18: 38,097,212 (GRCm39) |
V385E |
probably damaging |
Het |
Flg |
A |
T |
3: 93,193,984 (GRCm39) |
H34L |
unknown |
Het |
Frs3 |
G |
T |
17: 48,010,463 (GRCm39) |
E32D |
possibly damaging |
Het |
Gm14443 |
C |
T |
2: 175,012,035 (GRCm39) |
C137Y |
probably benign |
Het |
H3c13 |
C |
A |
3: 96,176,309 (GRCm39) |
Y100* |
probably null |
Het |
Havcr1 |
T |
A |
11: 46,643,402 (GRCm39) |
C107* |
probably null |
Het |
Hectd4 |
C |
T |
5: 121,448,692 (GRCm39) |
R347W |
probably damaging |
Het |
Hspbp1 |
A |
G |
7: 4,684,841 (GRCm39) |
|
probably null |
Het |
Irs1 |
C |
T |
1: 82,266,443 (GRCm39) |
R591H |
possibly damaging |
Het |
Kif5b |
A |
G |
18: 6,241,040 (GRCm39) |
V23A |
probably benign |
Het |
Myo1e |
A |
T |
9: 70,242,501 (GRCm39) |
I339F |
possibly damaging |
Het |
Nkx2-5 |
T |
C |
17: 27,058,150 (GRCm39) |
Y268C |
probably damaging |
Het |
Or7g12 |
T |
C |
9: 18,899,952 (GRCm39) |
S223P |
probably damaging |
Het |
Polrmt |
T |
C |
10: 79,574,623 (GRCm39) |
M857V |
probably damaging |
Het |
Prkd3 |
T |
A |
17: 79,315,691 (GRCm39) |
M1L |
not run |
Het |
Psmc3 |
T |
A |
2: 90,887,007 (GRCm39) |
V202E |
possibly damaging |
Het |
Rab3d |
G |
A |
9: 21,826,229 (GRCm39) |
R93C |
probably damaging |
Het |
Rasgrf2 |
A |
C |
13: 92,167,300 (GRCm39) |
Y258D |
probably damaging |
Het |
Rassf8 |
G |
A |
6: 145,761,669 (GRCm39) |
|
probably null |
Het |
Rcbtb1 |
A |
C |
14: 59,459,016 (GRCm39) |
S199R |
probably benign |
Het |
Rif1 |
T |
G |
2: 51,964,288 (GRCm39) |
V45G |
probably damaging |
Het |
Riok3 |
G |
A |
18: 12,269,776 (GRCm39) |
G69E |
probably benign |
Het |
Scn1a |
A |
G |
2: 66,158,786 (GRCm39) |
L378P |
probably damaging |
Het |
Sil1 |
A |
T |
18: 35,481,719 (GRCm39) |
N113K |
probably benign |
Het |
Slc35c2 |
C |
T |
2: 165,119,462 (GRCm39) |
D293N |
probably damaging |
Het |
Slc37a3 |
A |
T |
6: 39,324,325 (GRCm39) |
S308T |
possibly damaging |
Het |
Smarca5 |
A |
T |
8: 81,463,388 (GRCm39) |
V60E |
probably benign |
Het |
Smok3c |
T |
A |
5: 138,063,341 (GRCm39) |
V276D |
probably damaging |
Het |
Snx29 |
G |
A |
16: 11,231,221 (GRCm39) |
|
probably null |
Het |
Spata24 |
T |
C |
18: 35,795,093 (GRCm39) |
E30G |
probably damaging |
Het |
Stard13 |
T |
A |
5: 150,975,838 (GRCm39) |
I777F |
probably damaging |
Het |
Synpo2 |
A |
G |
3: 123,029,635 (GRCm39) |
C8R |
probably benign |
Het |
Tmem104 |
T |
C |
11: 115,134,307 (GRCm39) |
V281A |
probably damaging |
Het |
Tmprss11a |
C |
T |
5: 86,567,879 (GRCm39) |
G283R |
probably damaging |
Het |
Trpc2 |
G |
A |
7: 101,738,388 (GRCm39) |
V457M |
probably benign |
Het |
Usp53 |
A |
T |
3: 122,728,000 (GRCm39) |
S861T |
possibly damaging |
Het |
Uty |
G |
T |
Y: 1,154,210 (GRCm39) |
S738* |
probably null |
Het |
Wdr17 |
C |
T |
8: 55,113,806 (GRCm39) |
|
probably null |
Het |
Wdr7 |
A |
T |
18: 64,037,157 (GRCm39) |
S1194C |
probably damaging |
Het |
Zyx |
A |
C |
6: 42,333,505 (GRCm39) |
D477A |
probably damaging |
Het |
|
Other mutations in Prss3b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01120:Prss3b
|
APN |
6 |
41,008,607 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01625:Prss3b
|
APN |
6 |
41,009,882 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02159:Prss3b
|
APN |
6 |
41,009,891 (GRCm39) |
missense |
probably benign |
0.34 |
IGL03161:Prss3b
|
APN |
6 |
41,011,240 (GRCm39) |
missense |
probably damaging |
0.96 |
R0419:Prss3b
|
UTSW |
6 |
41,011,281 (GRCm39) |
missense |
probably benign |
0.05 |
R1715:Prss3b
|
UTSW |
6 |
41,009,870 (GRCm39) |
splice site |
probably null |
|
R2057:Prss3b
|
UTSW |
6 |
41,009,315 (GRCm39) |
missense |
probably benign |
0.06 |
R2059:Prss3b
|
UTSW |
6 |
41,009,315 (GRCm39) |
missense |
probably benign |
0.06 |
R2136:Prss3b
|
UTSW |
6 |
41,012,396 (GRCm39) |
missense |
probably benign |
0.28 |
R2446:Prss3b
|
UTSW |
6 |
41,008,582 (GRCm39) |
missense |
probably benign |
0.15 |
R4862:Prss3b
|
UTSW |
6 |
41,009,345 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5068:Prss3b
|
UTSW |
6 |
41,009,370 (GRCm39) |
missense |
probably benign |
0.35 |
R5369:Prss3b
|
UTSW |
6 |
41,009,940 (GRCm39) |
missense |
probably benign |
0.00 |
R6392:Prss3b
|
UTSW |
6 |
41,009,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R7010:Prss3b
|
UTSW |
6 |
41,009,247 (GRCm39) |
missense |
probably benign |
0.42 |
R7567:Prss3b
|
UTSW |
6 |
41,010,127 (GRCm39) |
missense |
probably benign |
0.04 |
R7727:Prss3b
|
UTSW |
6 |
41,010,127 (GRCm39) |
missense |
probably benign |
0.04 |
R8373:Prss3b
|
UTSW |
6 |
41,008,622 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8529:Prss3b
|
UTSW |
6 |
41,009,369 (GRCm39) |
missense |
probably benign |
0.00 |
R8883:Prss3b
|
UTSW |
6 |
41,009,305 (GRCm39) |
nonsense |
probably null |
|
R8916:Prss3b
|
UTSW |
6 |
41,010,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R9066:Prss3b
|
UTSW |
6 |
41,008,640 (GRCm39) |
missense |
probably benign |
0.41 |
R9095:Prss3b
|
UTSW |
6 |
41,010,038 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9180:Prss3b
|
UTSW |
6 |
41,008,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R9389:Prss3b
|
UTSW |
6 |
41,010,079 (GRCm39) |
missense |
probably benign |
0.02 |
|