Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts2 |
A |
G |
11: 50,628,181 (GRCm39) |
T294A |
probably damaging |
Het |
Adamtsl2 |
G |
A |
2: 26,997,473 (GRCm39) |
V893I |
probably damaging |
Het |
Amph |
T |
A |
13: 19,333,908 (GRCm39) |
D656E |
probably benign |
Het |
Aoah |
T |
C |
13: 21,207,485 (GRCm39) |
F568S |
probably damaging |
Het |
Atr |
G |
A |
9: 95,747,425 (GRCm39) |
G236S |
probably damaging |
Het |
Brd3 |
T |
A |
2: 27,340,406 (GRCm39) |
Q601L |
probably damaging |
Het |
Ccar2 |
T |
C |
14: 70,379,426 (GRCm39) |
E524G |
probably damaging |
Het |
Cog2 |
T |
C |
8: 125,267,853 (GRCm39) |
|
probably null |
Het |
Csnka2ip |
C |
A |
16: 64,299,120 (GRCm39) |
V415F |
unknown |
Het |
Dmp1 |
A |
T |
5: 104,359,729 (GRCm39) |
D135V |
probably damaging |
Het |
Dtna |
T |
C |
18: 23,786,436 (GRCm39) |
|
probably null |
Het |
Endou |
A |
G |
15: 97,616,810 (GRCm39) |
S238P |
probably damaging |
Het |
Ep400 |
T |
A |
5: 110,881,651 (GRCm39) |
E779D |
unknown |
Het |
Fcgbp |
A |
G |
7: 27,784,387 (GRCm39) |
E149G |
probably benign |
Het |
G6pc1 |
C |
A |
11: 101,265,413 (GRCm39) |
|
probably null |
Het |
Gmeb1 |
T |
C |
4: 131,962,179 (GRCm39) |
H160R |
probably damaging |
Het |
Gramd1b |
T |
C |
9: 40,312,902 (GRCm39) |
Y22C |
unknown |
Het |
Hcrtr2 |
C |
T |
9: 76,161,793 (GRCm39) |
G199D |
probably benign |
Het |
Hoxb2 |
T |
C |
11: 96,244,447 (GRCm39) |
F353L |
possibly damaging |
Het |
Itpr2 |
C |
A |
6: 146,226,572 (GRCm39) |
V1391F |
probably damaging |
Het |
Jakmip2 |
T |
A |
18: 43,673,648 (GRCm39) |
|
probably null |
Het |
Kcnmb4 |
T |
C |
10: 116,309,164 (GRCm39) |
Y88C |
possibly damaging |
Het |
Kif1a |
T |
C |
1: 93,005,507 (GRCm39) |
Y89C |
probably damaging |
Het |
Kif23 |
T |
A |
9: 61,827,174 (GRCm39) |
K892N |
probably damaging |
Het |
Lama3 |
T |
A |
18: 12,664,936 (GRCm39) |
S646T |
probably benign |
Het |
Lig3 |
T |
A |
11: 82,688,138 (GRCm39) |
M709K |
probably benign |
Het |
Mindy3 |
C |
A |
2: 12,405,885 (GRCm39) |
A137S |
possibly damaging |
Het |
Mis18bp1 |
T |
C |
12: 65,196,057 (GRCm39) |
E569G |
possibly damaging |
Het |
Misp |
T |
A |
10: 79,662,999 (GRCm39) |
L472Q |
probably damaging |
Het |
Mrps5 |
A |
T |
2: 127,443,330 (GRCm39) |
T303S |
probably damaging |
Het |
Msh3 |
T |
G |
13: 92,411,308 (GRCm39) |
I630L |
probably benign |
Het |
Muc21 |
C |
A |
17: 35,932,432 (GRCm39) |
A585S |
unknown |
Het |
Myo16 |
A |
G |
8: 10,619,673 (GRCm39) |
Y1408C |
unknown |
Het |
N4bp2 |
T |
C |
5: 65,964,189 (GRCm39) |
V746A |
probably benign |
Het |
Oga |
G |
A |
19: 45,771,605 (GRCm39) |
|
probably benign |
Het |
Or4c120 |
A |
G |
2: 89,000,827 (GRCm39) |
I243T |
possibly damaging |
Het |
Or4d11 |
A |
G |
19: 12,013,752 (GRCm39) |
M118T |
probably damaging |
Het |
Or5p56 |
A |
G |
7: 107,589,805 (GRCm39) |
T78A |
possibly damaging |
Het |
Ostf1 |
C |
T |
19: 18,573,715 (GRCm39) |
M44I |
probably null |
Het |
Pik3c2b |
T |
G |
1: 133,033,712 (GRCm39) |
L1572R |
probably damaging |
Het |
Pilra |
T |
C |
5: 137,829,488 (GRCm39) |
D192G |
possibly damaging |
Het |
Pkhd1l1 |
A |
G |
15: 44,437,027 (GRCm39) |
I3462V |
probably benign |
Het |
Plekhh1 |
A |
G |
12: 79,113,429 (GRCm39) |
D619G |
probably benign |
Het |
Pramel31 |
C |
T |
4: 144,090,297 (GRCm39) |
R446C |
probably benign |
Het |
Rb1 |
T |
C |
14: 73,500,084 (GRCm39) |
D521G |
probably damaging |
Het |
Rnf17 |
T |
G |
14: 56,708,763 (GRCm39) |
F728V |
possibly damaging |
Het |
Slc16a4 |
T |
C |
3: 107,218,787 (GRCm39) |
S463P |
probably damaging |
Het |
Slc4a1 |
A |
T |
11: 102,244,693 (GRCm39) |
I634K |
probably damaging |
Het |
Slc4a1ap |
T |
C |
5: 31,701,201 (GRCm39) |
V634A |
probably benign |
Het |
Spam1 |
A |
G |
6: 24,800,583 (GRCm39) |
M441V |
probably benign |
Het |
Teddm3 |
A |
C |
16: 20,971,729 (GRCm39) |
L280* |
probably null |
Het |
Tmem231 |
T |
C |
8: 112,645,517 (GRCm39) |
|
probably null |
Het |
Tom1l1 |
T |
C |
11: 90,561,907 (GRCm39) |
|
probably null |
Het |
Topors |
C |
T |
4: 40,261,706 (GRCm39) |
G526D |
probably benign |
Het |
Trpm6 |
A |
T |
19: 18,790,911 (GRCm39) |
I649F |
possibly damaging |
Het |
Ttc16 |
T |
A |
2: 32,664,440 (GRCm39) |
M66L |
probably benign |
Het |
Tubgcp6 |
A |
G |
15: 88,985,232 (GRCm39) |
F1619L |
probably damaging |
Het |
Vps13d |
G |
T |
4: 144,842,062 (GRCm39) |
A2619E |
|
Het |
Vps8 |
G |
A |
16: 21,345,191 (GRCm39) |
R838H |
probably damaging |
Het |
Vwde |
T |
A |
6: 13,215,799 (GRCm39) |
M86L |
probably benign |
Het |
Zfp64 |
A |
T |
2: 168,768,357 (GRCm39) |
D418E |
probably benign |
Het |
Zfp952 |
C |
T |
17: 33,222,606 (GRCm39) |
P362S |
possibly damaging |
Het |
Zglp1 |
T |
C |
9: 20,977,368 (GRCm39) |
E149G |
probably benign |
Het |
|
Other mutations in Ptprb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01295:Ptprb
|
APN |
10 |
116,198,553 (GRCm39) |
missense |
probably benign |
0.15 |
IGL01354:Ptprb
|
APN |
10 |
116,179,796 (GRCm39) |
missense |
probably benign |
0.24 |
IGL01404:Ptprb
|
APN |
10 |
116,175,341 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01410:Ptprb
|
APN |
10 |
116,138,179 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL01412:Ptprb
|
APN |
10 |
116,179,820 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01731:Ptprb
|
APN |
10 |
116,208,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02003:Ptprb
|
APN |
10 |
116,203,410 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02110:Ptprb
|
APN |
10 |
116,167,108 (GRCm39) |
splice site |
probably benign |
|
IGL02178:Ptprb
|
APN |
10 |
116,158,437 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02304:Ptprb
|
APN |
10 |
116,167,164 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02324:Ptprb
|
APN |
10 |
116,155,238 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02388:Ptprb
|
APN |
10 |
116,203,426 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02640:Ptprb
|
APN |
10 |
116,174,569 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02698:Ptprb
|
APN |
10 |
116,199,185 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02876:Ptprb
|
APN |
10 |
116,184,116 (GRCm39) |
splice site |
probably benign |
|
IGL02879:Ptprb
|
APN |
10 |
116,163,873 (GRCm39) |
missense |
probably benign |
|
IGL02982:Ptprb
|
APN |
10 |
116,158,533 (GRCm39) |
missense |
probably benign |
0.20 |
IGL03146:Ptprb
|
APN |
10 |
116,164,032 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03351:Ptprb
|
APN |
10 |
116,175,487 (GRCm39) |
missense |
probably benign |
0.03 |
R0306:Ptprb
|
UTSW |
10 |
116,179,893 (GRCm39) |
missense |
probably benign |
0.04 |
R0385:Ptprb
|
UTSW |
10 |
116,186,083 (GRCm39) |
missense |
probably benign |
0.00 |
R0600:Ptprb
|
UTSW |
10 |
116,204,712 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0613:Ptprb
|
UTSW |
10 |
116,138,283 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0613:Ptprb
|
UTSW |
10 |
116,138,230 (GRCm39) |
missense |
possibly damaging |
0.59 |
R0850:Ptprb
|
UTSW |
10 |
116,175,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R0850:Ptprb
|
UTSW |
10 |
116,138,030 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1331:Ptprb
|
UTSW |
10 |
116,203,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R1413:Ptprb
|
UTSW |
10 |
116,175,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R1418:Ptprb
|
UTSW |
10 |
116,155,375 (GRCm39) |
missense |
probably benign |
0.00 |
R1545:Ptprb
|
UTSW |
10 |
116,216,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R1562:Ptprb
|
UTSW |
10 |
116,175,372 (GRCm39) |
missense |
probably benign |
0.00 |
R1752:Ptprb
|
UTSW |
10 |
116,176,895 (GRCm39) |
missense |
probably benign |
0.44 |
R1837:Ptprb
|
UTSW |
10 |
116,177,531 (GRCm39) |
missense |
probably benign |
0.00 |
R1940:Ptprb
|
UTSW |
10 |
116,155,515 (GRCm39) |
splice site |
probably benign |
|
R1958:Ptprb
|
UTSW |
10 |
116,177,441 (GRCm39) |
missense |
probably benign |
0.10 |
R2029:Ptprb
|
UTSW |
10 |
116,182,958 (GRCm39) |
missense |
probably benign |
0.37 |
R2031:Ptprb
|
UTSW |
10 |
116,153,448 (GRCm39) |
missense |
probably benign |
|
R2101:Ptprb
|
UTSW |
10 |
116,150,943 (GRCm39) |
splice site |
probably benign |
|
R2209:Ptprb
|
UTSW |
10 |
116,205,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R3016:Ptprb
|
UTSW |
10 |
116,193,200 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3076:Ptprb
|
UTSW |
10 |
116,179,931 (GRCm39) |
missense |
probably damaging |
0.99 |
R3821:Ptprb
|
UTSW |
10 |
116,185,979 (GRCm39) |
missense |
probably benign |
0.11 |
R3824:Ptprb
|
UTSW |
10 |
116,186,694 (GRCm39) |
missense |
probably benign |
0.05 |
R3825:Ptprb
|
UTSW |
10 |
116,186,694 (GRCm39) |
missense |
probably benign |
0.05 |
R3841:Ptprb
|
UTSW |
10 |
116,182,887 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3953:Ptprb
|
UTSW |
10 |
116,177,399 (GRCm39) |
missense |
probably benign |
0.00 |
R4125:Ptprb
|
UTSW |
10 |
116,189,754 (GRCm39) |
missense |
probably benign |
0.12 |
R4227:Ptprb
|
UTSW |
10 |
116,138,130 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4385:Ptprb
|
UTSW |
10 |
116,182,772 (GRCm39) |
missense |
probably benign |
|
R4731:Ptprb
|
UTSW |
10 |
116,155,238 (GRCm39) |
missense |
probably benign |
0.03 |
R5009:Ptprb
|
UTSW |
10 |
116,184,032 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5104:Ptprb
|
UTSW |
10 |
116,158,364 (GRCm39) |
missense |
probably benign |
0.17 |
R5114:Ptprb
|
UTSW |
10 |
116,184,088 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5145:Ptprb
|
UTSW |
10 |
116,179,820 (GRCm39) |
missense |
probably benign |
0.27 |
R5214:Ptprb
|
UTSW |
10 |
116,205,229 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5382:Ptprb
|
UTSW |
10 |
116,189,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R5553:Ptprb
|
UTSW |
10 |
116,186,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R5585:Ptprb
|
UTSW |
10 |
116,216,759 (GRCm39) |
missense |
probably damaging |
0.98 |
R5586:Ptprb
|
UTSW |
10 |
116,189,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R5808:Ptprb
|
UTSW |
10 |
116,175,392 (GRCm39) |
missense |
probably benign |
0.00 |
R5875:Ptprb
|
UTSW |
10 |
116,184,071 (GRCm39) |
missense |
probably benign |
0.00 |
R6051:Ptprb
|
UTSW |
10 |
116,176,995 (GRCm39) |
nonsense |
probably null |
|
R6383:Ptprb
|
UTSW |
10 |
116,182,912 (GRCm39) |
nonsense |
probably null |
|
R6511:Ptprb
|
UTSW |
10 |
116,182,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R6817:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R6826:Ptprb
|
UTSW |
10 |
116,153,277 (GRCm39) |
missense |
probably benign |
0.26 |
R6958:Ptprb
|
UTSW |
10 |
116,113,153 (GRCm39) |
missense |
probably benign |
0.32 |
R7129:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R7181:Ptprb
|
UTSW |
10 |
116,204,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R7215:Ptprb
|
UTSW |
10 |
116,174,681 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7289:Ptprb
|
UTSW |
10 |
116,164,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R7315:Ptprb
|
UTSW |
10 |
116,198,284 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7319:Ptprb
|
UTSW |
10 |
116,177,309 (GRCm39) |
missense |
probably benign |
0.01 |
R7381:Ptprb
|
UTSW |
10 |
116,177,038 (GRCm39) |
missense |
probably benign |
|
R7412:Ptprb
|
UTSW |
10 |
116,177,043 (GRCm39) |
missense |
probably benign |
|
R7483:Ptprb
|
UTSW |
10 |
116,119,334 (GRCm39) |
missense |
probably benign |
0.01 |
R7495:Ptprb
|
UTSW |
10 |
116,177,353 (GRCm39) |
missense |
probably benign |
0.12 |
R7508:Ptprb
|
UTSW |
10 |
116,189,896 (GRCm39) |
nonsense |
probably null |
|
R7571:Ptprb
|
UTSW |
10 |
116,175,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R7586:Ptprb
|
UTSW |
10 |
116,179,779 (GRCm39) |
missense |
probably damaging |
0.97 |
R7623:Ptprb
|
UTSW |
10 |
116,205,214 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7694:Ptprb
|
UTSW |
10 |
116,208,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R7744:Ptprb
|
UTSW |
10 |
116,113,389 (GRCm39) |
missense |
probably benign |
0.10 |
R7752:Ptprb
|
UTSW |
10 |
116,205,333 (GRCm39) |
missense |
probably benign |
0.37 |
R7826:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R7833:Ptprb
|
UTSW |
10 |
116,151,156 (GRCm39) |
missense |
probably benign |
0.01 |
R7834:Ptprb
|
UTSW |
10 |
116,175,329 (GRCm39) |
missense |
probably benign |
0.00 |
R7846:Ptprb
|
UTSW |
10 |
116,119,453 (GRCm39) |
missense |
probably benign |
0.17 |
R7896:Ptprb
|
UTSW |
10 |
116,205,362 (GRCm39) |
splice site |
probably null |
|
R7901:Ptprb
|
UTSW |
10 |
116,205,333 (GRCm39) |
missense |
probably benign |
0.37 |
R7912:Ptprb
|
UTSW |
10 |
116,158,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7941:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R8147:Ptprb
|
UTSW |
10 |
116,153,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R8202:Ptprb
|
UTSW |
10 |
116,189,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R8339:Ptprb
|
UTSW |
10 |
116,119,356 (GRCm39) |
missense |
probably benign |
0.14 |
R8400:Ptprb
|
UTSW |
10 |
116,119,477 (GRCm39) |
small deletion |
probably benign |
|
R8504:Ptprb
|
UTSW |
10 |
116,176,936 (GRCm39) |
missense |
probably benign |
0.27 |
R8679:Ptprb
|
UTSW |
10 |
116,203,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8786:Ptprb
|
UTSW |
10 |
116,155,306 (GRCm39) |
missense |
probably benign |
0.40 |
R8914:Ptprb
|
UTSW |
10 |
116,158,567 (GRCm39) |
nonsense |
probably null |
|
R8980:Ptprb
|
UTSW |
10 |
116,119,526 (GRCm39) |
missense |
probably benign |
0.07 |
R8982:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R9256:Ptprb
|
UTSW |
10 |
116,219,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R9288:Ptprb
|
UTSW |
10 |
116,155,353 (GRCm39) |
missense |
probably benign |
0.03 |
R9369:Ptprb
|
UTSW |
10 |
116,151,057 (GRCm39) |
missense |
probably benign |
0.00 |
R9448:Ptprb
|
UTSW |
10 |
116,149,819 (GRCm39) |
nonsense |
probably null |
|
R9467:Ptprb
|
UTSW |
10 |
116,158,390 (GRCm39) |
missense |
probably benign |
0.00 |
R9468:Ptprb
|
UTSW |
10 |
116,113,274 (GRCm39) |
missense |
probably benign |
0.00 |
R9481:Ptprb
|
UTSW |
10 |
116,155,353 (GRCm39) |
missense |
probably benign |
0.03 |
R9486:Ptprb
|
UTSW |
10 |
116,155,494 (GRCm39) |
nonsense |
probably null |
|
R9513:Ptprb
|
UTSW |
10 |
116,138,142 (GRCm39) |
missense |
probably benign |
0.00 |
R9529:Ptprb
|
UTSW |
10 |
116,174,519 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9535:Ptprb
|
UTSW |
10 |
116,158,431 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9614:Ptprb
|
UTSW |
10 |
116,203,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R9686:Ptprb
|
UTSW |
10 |
116,204,694 (GRCm39) |
missense |
probably damaging |
1.00 |
RF041:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
X0020:Ptprb
|
UTSW |
10 |
116,138,085 (GRCm39) |
missense |
possibly damaging |
0.62 |
Z1176:Ptprb
|
UTSW |
10 |
116,138,061 (GRCm39) |
frame shift |
probably null |
|
Z1177:Ptprb
|
UTSW |
10 |
116,198,547 (GRCm39) |
critical splice acceptor site |
probably null |
|
|