Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
T |
A |
9: 44,192,909 (GRCm39) |
I146F |
probably damaging |
Het |
Adcy8 |
G |
T |
15: 64,792,874 (GRCm39) |
D27E |
probably benign |
Het |
Ahnak |
A |
G |
19: 8,986,113 (GRCm39) |
I2466V |
probably benign |
Het |
BC005624 |
T |
A |
2: 30,871,817 (GRCm39) |
E19V |
possibly damaging |
Het |
Bnc2 |
A |
T |
4: 84,211,608 (GRCm39) |
F279I |
probably damaging |
Het |
Bub1 |
A |
T |
2: 127,659,353 (GRCm39) |
L335M |
probably benign |
Het |
Cdkn1c |
G |
A |
7: 143,014,324 (GRCm39) |
H41Y |
possibly damaging |
Het |
Celsr1 |
G |
A |
15: 85,914,415 (GRCm39) |
P1186L |
probably damaging |
Het |
Cnot2 |
A |
G |
10: 116,353,236 (GRCm39) |
L75S |
probably benign |
Het |
Cntn6 |
A |
T |
6: 104,749,580 (GRCm39) |
E338D |
possibly damaging |
Het |
Cracd |
GCGCGAGGCCGAGAGGCAGGAGGAGGAAGCAAGACAACGCGAGGCCGAGAGGCAGG |
GCGCGAGGCCGAGAGGCAGG |
5: 77,004,801 (GRCm39) |
|
probably benign |
Het |
Dlg2 |
G |
T |
7: 91,617,441 (GRCm39) |
M289I |
probably benign |
Het |
Dzip1l |
A |
T |
9: 99,519,875 (GRCm39) |
D134V |
possibly damaging |
Het |
Fam171b |
A |
G |
2: 83,683,801 (GRCm39) |
Y106C |
probably damaging |
Het |
Fgd3 |
T |
C |
13: 49,420,081 (GRCm39) |
K599E |
possibly damaging |
Het |
Gabrr2 |
A |
T |
4: 33,084,375 (GRCm39) |
I154F |
probably damaging |
Het |
Gjd2 |
T |
A |
2: 113,842,053 (GRCm39) |
E141D |
probably benign |
Het |
Gmds |
T |
C |
13: 32,003,906 (GRCm39) |
N371S |
probably benign |
Het |
Gp2 |
C |
T |
7: 119,053,554 (GRCm39) |
A136T |
probably damaging |
Het |
Gstm2 |
A |
G |
3: 107,893,672 (GRCm39) |
|
probably null |
Het |
Hnmt |
T |
C |
2: 23,938,836 (GRCm39) |
M1V |
probably null |
Het |
Hydin |
T |
C |
8: 111,237,553 (GRCm39) |
V1942A |
probably benign |
Het |
Krt87 |
C |
A |
15: 101,332,506 (GRCm39) |
A236S |
probably benign |
Het |
Lama3 |
A |
T |
18: 12,582,896 (GRCm39) |
H654L |
probably damaging |
Het |
Lrp2 |
G |
A |
2: 69,322,250 (GRCm39) |
T1893M |
probably damaging |
Het |
Lyg1 |
A |
T |
1: 37,988,922 (GRCm39) |
Y99* |
probably null |
Het |
Mdga1 |
T |
C |
17: 30,068,703 (GRCm39) |
D208G |
probably damaging |
Het |
Mgarp |
T |
C |
3: 51,296,348 (GRCm39) |
E218G |
probably damaging |
Het |
Mif4gd |
T |
A |
11: 115,499,324 (GRCm39) |
D186V |
probably benign |
Het |
Mlec |
T |
C |
5: 115,288,283 (GRCm39) |
Y191C |
probably damaging |
Het |
Mtus1 |
C |
A |
8: 41,536,271 (GRCm39) |
V482L |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,570,435 (GRCm39) |
T695S |
unknown |
Het |
Muc4 |
A |
T |
16: 32,574,201 (GRCm39) |
M760L |
probably benign |
Het |
Mybl2 |
A |
T |
2: 162,916,638 (GRCm39) |
S430C |
probably damaging |
Het |
Nepn |
A |
G |
10: 52,276,896 (GRCm39) |
N211D |
probably benign |
Het |
Nuggc |
A |
G |
14: 65,851,011 (GRCm39) |
T294A |
probably damaging |
Het |
Or51k2 |
G |
A |
7: 103,595,834 (GRCm39) |
|
probably null |
Het |
Or5w16 |
A |
T |
2: 87,577,437 (GRCm39) |
E299V |
probably benign |
Het |
Pcca |
A |
G |
14: 122,922,526 (GRCm39) |
|
probably null |
Het |
Pcdhb13 |
T |
G |
18: 37,576,287 (GRCm39) |
S222A |
possibly damaging |
Het |
Peg10 |
C |
CTCA |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Plppr3 |
A |
T |
10: 79,703,397 (GRCm39) |
V29E |
probably damaging |
Het |
Plxna2 |
C |
T |
1: 194,326,354 (GRCm39) |
P96L |
probably damaging |
Het |
Pop4 |
A |
T |
7: 37,962,599 (GRCm39) |
*222R |
probably null |
Het |
Prss2 |
T |
A |
6: 41,498,739 (GRCm39) |
M1K |
probably null |
Het |
Recql5 |
G |
A |
11: 115,787,619 (GRCm39) |
Q512* |
probably null |
Het |
Rnf148 |
A |
G |
6: 23,654,801 (GRCm39) |
I65T |
probably benign |
Het |
Scgb1b19 |
G |
A |
7: 32,987,082 (GRCm39) |
A78T |
probably benign |
Het |
Sftpd |
A |
G |
14: 40,897,583 (GRCm39) |
|
probably null |
Het |
Shank1 |
A |
G |
7: 44,003,605 (GRCm39) |
R1766G |
possibly damaging |
Het |
Slc35e2 |
T |
C |
4: 155,694,615 (GRCm39) |
L54P |
probably damaging |
Het |
Smg6 |
A |
G |
11: 74,820,886 (GRCm39) |
K386E |
probably benign |
Het |
Sorcs1 |
A |
G |
19: 50,248,248 (GRCm39) |
S393P |
probably damaging |
Het |
Spen |
A |
G |
4: 141,249,590 (GRCm39) |
V66A |
unknown |
Het |
Tpm1 |
G |
T |
9: 66,955,512 (GRCm39) |
A45E |
probably benign |
Het |
Trmt2a |
T |
C |
16: 18,069,039 (GRCm39) |
Y294H |
probably damaging |
Het |
Txnl4b |
T |
C |
8: 110,299,430 (GRCm39) |
V130A |
possibly damaging |
Het |
Vmn2r14 |
C |
A |
5: 109,369,340 (GRCm39) |
V78L |
probably benign |
Het |
Vmn2r27 |
A |
G |
6: 124,169,168 (GRCm39) |
V654A |
probably damaging |
Het |
Wee2 |
G |
T |
6: 40,420,914 (GRCm39) |
M1I |
probably null |
Het |
Xpnpep3 |
A |
G |
15: 81,332,672 (GRCm39) |
K403R |
probably benign |
Het |
Zranb1 |
A |
G |
7: 132,551,810 (GRCm39) |
T154A |
possibly damaging |
Het |
|
Other mutations in Prss3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0535:Prss3
|
UTSW |
6 |
41,351,903 (GRCm39) |
missense |
probably benign |
0.26 |
R1583:Prss3
|
UTSW |
6 |
41,354,561 (GRCm39) |
start gained |
probably benign |
|
R4324:Prss3
|
UTSW |
6 |
41,350,779 (GRCm39) |
missense |
probably benign |
0.00 |
R4859:Prss3
|
UTSW |
6 |
41,350,857 (GRCm39) |
missense |
probably damaging |
0.96 |
R5004:Prss3
|
UTSW |
6 |
41,350,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R5361:Prss3
|
UTSW |
6 |
41,350,780 (GRCm39) |
missense |
probably benign |
0.00 |
R5929:Prss3
|
UTSW |
6 |
41,353,738 (GRCm39) |
splice site |
probably null |
|
R6026:Prss3
|
UTSW |
6 |
41,354,488 (GRCm39) |
splice site |
probably null |
|
R6179:Prss3
|
UTSW |
6 |
41,352,060 (GRCm39) |
missense |
probably benign |
0.11 |
R7510:Prss3
|
UTSW |
6 |
41,352,044 (GRCm39) |
nonsense |
probably null |
|
R7514:Prss3
|
UTSW |
6 |
41,350,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R8323:Prss3
|
UTSW |
6 |
41,351,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R8734:Prss3
|
UTSW |
6 |
41,350,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R8885:Prss3
|
UTSW |
6 |
41,354,512 (GRCm39) |
missense |
probably damaging |
0.99 |
R8972:Prss3
|
UTSW |
6 |
41,353,872 (GRCm39) |
missense |
probably damaging |
1.00 |
|