Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018F24Rik |
T |
A |
5: 144,979,957 (GRCm39) |
H37Q |
possibly damaging |
Het |
Akr1c19 |
T |
A |
13: 4,283,816 (GRCm39) |
I16N |
probably damaging |
Het |
Arpc1b |
T |
C |
5: 145,058,555 (GRCm39) |
|
probably null |
Het |
Bzw1 |
A |
G |
1: 58,440,599 (GRCm39) |
T191A |
probably benign |
Het |
Cacna1h |
G |
A |
17: 25,604,686 (GRCm39) |
T1209I |
possibly damaging |
Het |
Cacna1h |
T |
C |
17: 25,602,459 (GRCm39) |
D1523G |
probably damaging |
Het |
Cdc20b |
T |
C |
13: 113,196,319 (GRCm39) |
L148P |
possibly damaging |
Het |
Cubn |
A |
G |
2: 13,311,085 (GRCm39) |
F3147L |
possibly damaging |
Het |
Dagla |
A |
G |
19: 10,228,566 (GRCm39) |
|
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,935,471 (GRCm39) |
N1983D |
probably damaging |
Het |
Fbxw10 |
G |
A |
11: 62,750,853 (GRCm39) |
D479N |
probably damaging |
Het |
Fer |
A |
T |
17: 64,344,621 (GRCm39) |
Q630L |
probably damaging |
Het |
Gbp5 |
A |
G |
3: 142,208,789 (GRCm39) |
N111D |
probably damaging |
Het |
Gm8127 |
T |
G |
14: 43,148,520 (GRCm39) |
|
probably benign |
Het |
Heatr1 |
T |
A |
13: 12,428,409 (GRCm39) |
N814K |
probably damaging |
Het |
Iba57 |
G |
A |
11: 59,049,775 (GRCm39) |
R191W |
probably damaging |
Het |
Itgae |
C |
A |
11: 73,010,263 (GRCm39) |
F584L |
probably benign |
Het |
Kdm5b |
A |
G |
1: 134,545,706 (GRCm39) |
K956E |
possibly damaging |
Het |
Muc4 |
C |
T |
16: 32,575,918 (GRCm39) |
|
probably benign |
Het |
Mybpc2 |
T |
C |
7: 44,166,337 (GRCm39) |
K218E |
possibly damaging |
Het |
Pcdh10 |
T |
C |
3: 45,333,832 (GRCm39) |
S49P |
probably damaging |
Het |
Rai14 |
T |
C |
15: 10,572,460 (GRCm39) |
D889G |
probably benign |
Het |
Rbpjl |
A |
G |
2: 164,249,705 (GRCm39) |
K102R |
possibly damaging |
Het |
Retreg2 |
A |
G |
1: 75,121,359 (GRCm39) |
|
probably benign |
Het |
Rfc4 |
A |
T |
16: 22,934,573 (GRCm39) |
L149Q |
probably damaging |
Het |
Rft1 |
T |
A |
14: 30,398,853 (GRCm39) |
D274E |
possibly damaging |
Het |
Rlf |
A |
T |
4: 121,045,457 (GRCm39) |
S143R |
possibly damaging |
Het |
Rptn |
T |
A |
3: 93,305,201 (GRCm39) |
S845T |
probably benign |
Het |
Slamf8 |
C |
A |
1: 172,410,049 (GRCm39) |
D267Y |
probably damaging |
Het |
Smoc2 |
C |
T |
17: 14,545,876 (GRCm39) |
S55L |
probably damaging |
Het |
Sptan1 |
C |
T |
2: 29,916,126 (GRCm39) |
A2038V |
probably damaging |
Het |
Stx17 |
C |
A |
4: 48,181,526 (GRCm39) |
P210T |
probably damaging |
Het |
Tbc1d5 |
A |
G |
17: 51,224,601 (GRCm39) |
Y317H |
probably benign |
Het |
Tenm4 |
C |
A |
7: 96,534,565 (GRCm39) |
T1737N |
probably damaging |
Het |
Tesk2 |
T |
C |
4: 116,628,998 (GRCm39) |
F116L |
possibly damaging |
Het |
Tln2 |
T |
C |
9: 67,277,905 (GRCm39) |
S370G |
probably damaging |
Het |
Tm6sf2 |
G |
T |
8: 70,528,733 (GRCm39) |
G162C |
probably null |
Het |
Togaram2 |
A |
C |
17: 72,021,693 (GRCm39) |
E718D |
probably benign |
Het |
Ttn |
A |
C |
2: 76,578,327 (GRCm39) |
F15862V |
probably damaging |
Het |
Uba6 |
T |
A |
5: 86,268,388 (GRCm39) |
R916* |
probably null |
Het |
Umodl1 |
A |
G |
17: 31,215,229 (GRCm39) |
M1018V |
probably benign |
Het |
Wdr26 |
G |
A |
1: 181,019,381 (GRCm39) |
T332I |
possibly damaging |
Het |
Xdh |
A |
T |
17: 74,223,781 (GRCm39) |
|
probably null |
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 |
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 |
R7962:Prss3b
|
UTSW |
6 |
41,012,387 (GRCm39) |
missense |
probably benign |
0.01 |
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 |
|