Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
A |
T |
6: 23,092,561 (GRCm39) |
Y146* |
probably null |
Het |
Adcy2 |
A |
G |
13: 68,944,722 (GRCm39) |
L220P |
probably damaging |
Het |
Agl |
T |
C |
3: 116,574,914 (GRCm39) |
Y660C |
probably damaging |
Het |
Ak1 |
A |
G |
2: 32,519,622 (GRCm39) |
T17A |
probably benign |
Het |
Amph |
G |
A |
13: 19,326,198 (GRCm39) |
V643M |
probably damaging |
Het |
Ankrd11 |
A |
T |
8: 123,629,161 (GRCm39) |
|
probably null |
Het |
Ap5b1 |
T |
C |
19: 5,620,502 (GRCm39) |
S641P |
possibly damaging |
Het |
Apoc4 |
A |
G |
7: 19,415,304 (GRCm39) |
M1T |
probably null |
Het |
Arhgap5 |
T |
C |
12: 52,564,817 (GRCm39) |
V596A |
probably benign |
Het |
Ascc3 |
A |
G |
10: 50,493,838 (GRCm39) |
E91G |
probably damaging |
Het |
Bach2 |
T |
A |
4: 32,580,055 (GRCm39) |
V637E |
probably benign |
Het |
Bicd2 |
T |
G |
13: 49,532,881 (GRCm39) |
L489R |
possibly damaging |
Het |
Bltp1 |
C |
T |
3: 36,949,527 (GRCm39) |
T2I |
possibly damaging |
Het |
Boc |
A |
T |
16: 44,322,007 (GRCm39) |
|
probably null |
Het |
Cbln2 |
T |
A |
18: 86,734,791 (GRCm39) |
V188D |
probably damaging |
Het |
Ccl11 |
A |
C |
11: 81,953,123 (GRCm39) |
T94P |
probably damaging |
Het |
Cd109 |
A |
T |
9: 78,611,044 (GRCm39) |
H1220L |
probably benign |
Het |
Cd226 |
A |
G |
18: 89,265,435 (GRCm39) |
I125V |
probably benign |
Het |
Cep135 |
T |
A |
5: 76,780,176 (GRCm39) |
|
probably null |
Het |
Cgnl1 |
T |
G |
9: 71,537,821 (GRCm39) |
E1233A |
probably damaging |
Het |
Ckap5 |
T |
A |
2: 91,437,891 (GRCm39) |
D1597E |
possibly damaging |
Het |
Clptm1 |
A |
G |
7: 19,380,762 (GRCm39) |
I63T |
possibly damaging |
Het |
Cpsf7 |
C |
T |
19: 10,518,073 (GRCm39) |
P428S |
probably damaging |
Het |
Cuedc1 |
C |
T |
11: 88,068,216 (GRCm39) |
P155S |
probably damaging |
Het |
Dgkb |
T |
C |
12: 38,134,228 (GRCm39) |
Y45H |
probably damaging |
Het |
Dglucy |
T |
C |
12: 100,823,181 (GRCm39) |
F459L |
probably damaging |
Het |
Dmp1 |
T |
A |
5: 104,359,790 (GRCm39) |
D155E |
possibly damaging |
Het |
Dnah1 |
T |
A |
14: 31,023,813 (GRCm39) |
I960F |
possibly damaging |
Het |
Drosha |
G |
T |
15: 12,915,467 (GRCm39) |
M795I |
probably damaging |
Het |
Dsg1b |
A |
G |
18: 20,529,532 (GRCm39) |
T326A |
probably damaging |
Het |
Dusp16 |
T |
G |
6: 134,695,802 (GRCm39) |
N343T |
probably benign |
Het |
Faim2 |
T |
C |
15: 99,398,127 (GRCm39) |
S274G |
possibly damaging |
Het |
Fhip2a |
G |
T |
19: 57,370,324 (GRCm39) |
V523L |
probably benign |
Het |
Fndc1 |
T |
C |
17: 8,023,761 (GRCm39) |
R65G |
probably damaging |
Het |
Fnip2 |
A |
T |
3: 79,419,632 (GRCm39) |
|
probably benign |
Het |
Grm3 |
T |
C |
5: 9,639,793 (GRCm39) |
Y84C |
possibly damaging |
Het |
Herc2 |
T |
C |
7: 55,787,607 (GRCm39) |
F1755L |
probably damaging |
Het |
Hivep1 |
C |
T |
13: 42,313,625 (GRCm39) |
T1955I |
possibly damaging |
Het |
Ift20 |
T |
C |
11: 78,431,797 (GRCm39) |
I97T |
probably damaging |
Het |
Il36rn |
T |
C |
2: 24,171,376 (GRCm39) |
C155R |
probably damaging |
Het |
Lca5l |
T |
A |
16: 95,963,849 (GRCm39) |
K358N |
probably damaging |
Het |
Lca5l |
T |
C |
16: 95,977,218 (GRCm39) |
N196S |
possibly damaging |
Het |
Maf1 |
G |
A |
15: 76,237,563 (GRCm39) |
D175N |
probably damaging |
Het |
Mical3 |
T |
C |
6: 120,928,283 (GRCm39) |
K996E |
probably damaging |
Het |
Midn |
A |
G |
10: 79,990,983 (GRCm39) |
N331S |
probably benign |
Het |
Mki67 |
T |
A |
7: 135,300,238 (GRCm39) |
K1599* |
probably null |
Het |
Mlx |
A |
G |
11: 100,979,805 (GRCm39) |
Q162R |
possibly damaging |
Het |
Nalf1 |
A |
G |
8: 9,820,607 (GRCm39) |
S138P |
probably benign |
Het |
Ngp |
T |
C |
9: 110,249,929 (GRCm39) |
C76R |
probably damaging |
Het |
Nin |
C |
T |
12: 70,072,251 (GRCm39) |
G1210D |
probably benign |
Het |
Nlgn1 |
A |
G |
3: 25,488,034 (GRCm39) |
I738T |
probably benign |
Het |
Nop53 |
A |
C |
7: 15,672,153 (GRCm39) |
F465C |
probably damaging |
Het |
Npas3 |
A |
G |
12: 54,114,680 (GRCm39) |
D503G |
possibly damaging |
Het |
Npbwr1 |
T |
A |
1: 5,986,570 (GRCm39) |
S315C |
probably damaging |
Het |
Nup42 |
G |
T |
5: 24,386,989 (GRCm39) |
G260* |
probably null |
Het |
Ogdh |
G |
C |
11: 6,284,626 (GRCm39) |
R200P |
possibly damaging |
Het |
Or4b13 |
T |
A |
2: 90,083,036 (GRCm39) |
I99L |
probably benign |
Het |
Or52n20 |
A |
G |
7: 104,320,808 (GRCm39) |
T300A |
possibly damaging |
Het |
Or5m13b |
T |
G |
2: 85,753,939 (GRCm39) |
|
probably null |
Het |
Or6ae1 |
C |
T |
7: 139,742,729 (GRCm39) |
V45I |
probably damaging |
Het |
Or7g16 |
G |
A |
9: 18,726,801 (GRCm39) |
S263L |
probably benign |
Het |
Or7g33 |
A |
T |
9: 19,448,688 (GRCm39) |
C179* |
probably null |
Het |
Ovgp1 |
T |
A |
3: 105,894,309 (GRCm39) |
|
probably benign |
Het |
Papln |
T |
A |
12: 83,819,992 (GRCm39) |
C150S |
probably damaging |
Het |
Pde1c |
A |
T |
6: 56,135,996 (GRCm39) |
L316Q |
probably damaging |
Het |
Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
Piezo2 |
G |
T |
18: 63,277,997 (GRCm39) |
D302E |
probably damaging |
Het |
Plin1 |
A |
G |
7: 79,375,378 (GRCm39) |
|
probably benign |
Het |
Plxnc1 |
A |
G |
10: 94,688,484 (GRCm39) |
I698T |
probably damaging |
Het |
Ppp1r12c |
G |
T |
7: 4,485,974 (GRCm39) |
C572* |
probably null |
Het |
Ptgis |
T |
C |
2: 167,056,769 (GRCm39) |
M273V |
possibly damaging |
Het |
Samd14 |
C |
A |
11: 94,914,110 (GRCm39) |
T283K |
probably damaging |
Het |
Scnn1g |
A |
T |
7: 121,337,411 (GRCm39) |
K91* |
probably null |
Het |
Slc24a4 |
A |
G |
12: 102,180,166 (GRCm39) |
Q95R |
probably damaging |
Het |
Slfn9 |
T |
G |
11: 82,879,027 (GRCm39) |
D34A |
probably benign |
Het |
Smarca4 |
A |
T |
9: 21,588,776 (GRCm39) |
I1193F |
probably damaging |
Het |
Spata31e5 |
A |
G |
1: 28,816,260 (GRCm39) |
W591R |
probably damaging |
Het |
Sphkap |
T |
C |
1: 83,255,632 (GRCm39) |
M706V |
probably benign |
Het |
Stard9 |
C |
A |
2: 120,504,117 (GRCm39) |
S221R |
probably damaging |
Het |
Stxbp1 |
T |
C |
2: 32,688,201 (GRCm39) |
D488G |
probably damaging |
Het |
Sugp2 |
C |
T |
8: 70,695,306 (GRCm39) |
|
probably null |
Het |
Tekt5 |
T |
C |
16: 10,213,070 (GRCm39) |
I72V |
probably benign |
Het |
Themis |
T |
A |
10: 28,658,720 (GRCm39) |
N582K |
probably benign |
Het |
Tmed11 |
C |
A |
5: 108,934,000 (GRCm39) |
M65I |
possibly damaging |
Het |
Top3a |
G |
T |
11: 60,633,315 (GRCm39) |
P927Q |
probably damaging |
Het |
Trpa1 |
A |
T |
1: 14,976,207 (GRCm39) |
N165K |
possibly damaging |
Het |
Tsfm |
A |
G |
10: 126,866,663 (GRCm39) |
S2P |
probably damaging |
Het |
Wdr47 |
C |
A |
3: 108,534,758 (GRCm39) |
S559* |
probably null |
Het |
Wnt2b |
T |
C |
3: 104,860,331 (GRCm39) |
Y192C |
probably damaging |
Het |
Zfp280b |
A |
G |
10: 75,874,370 (GRCm39) |
D83G |
probably benign |
Het |
Zfp345 |
T |
C |
2: 150,314,038 (GRCm39) |
T500A |
possibly damaging |
Het |
Zfp78 |
T |
A |
7: 6,382,074 (GRCm39) |
C343S |
probably damaging |
Het |
|
Other mutations in Pirb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01295:Pirb
|
APN |
7 |
3,720,405 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01744:Pirb
|
APN |
7 |
3,720,175 (GRCm39) |
nonsense |
probably null |
|
IGL01755:Pirb
|
APN |
7 |
3,720,169 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02580:Pirb
|
APN |
7 |
3,717,205 (GRCm39) |
splice site |
probably null |
|
IGL02941:Pirb
|
APN |
7 |
3,720,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R0394:Pirb
|
UTSW |
7 |
3,722,247 (GRCm39) |
missense |
probably benign |
0.08 |
R0680:Pirb
|
UTSW |
7 |
3,720,360 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0787:Pirb
|
UTSW |
7 |
3,720,637 (GRCm39) |
missense |
probably benign |
|
R0790:Pirb
|
UTSW |
7 |
3,720,637 (GRCm39) |
missense |
probably benign |
|
R0832:Pirb
|
UTSW |
7 |
3,720,637 (GRCm39) |
missense |
probably benign |
|
R1124:Pirb
|
UTSW |
7 |
3,722,731 (GRCm39) |
missense |
probably benign |
0.02 |
R1178:Pirb
|
UTSW |
7 |
3,720,637 (GRCm39) |
missense |
probably benign |
|
R1180:Pirb
|
UTSW |
7 |
3,720,637 (GRCm39) |
missense |
probably benign |
|
R1181:Pirb
|
UTSW |
7 |
3,720,637 (GRCm39) |
missense |
probably benign |
|
R1281:Pirb
|
UTSW |
7 |
3,720,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R1343:Pirb
|
UTSW |
7 |
3,720,637 (GRCm39) |
missense |
probably benign |
|
R1579:Pirb
|
UTSW |
7 |
3,720,637 (GRCm39) |
missense |
probably benign |
|
R1699:Pirb
|
UTSW |
7 |
3,720,637 (GRCm39) |
missense |
probably benign |
|
R1768:Pirb
|
UTSW |
7 |
3,720,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R1909:Pirb
|
UTSW |
7 |
3,717,587 (GRCm39) |
missense |
probably benign |
0.33 |
R1965:Pirb
|
UTSW |
7 |
3,720,637 (GRCm39) |
missense |
probably benign |
|
R1966:Pirb
|
UTSW |
7 |
3,720,637 (GRCm39) |
missense |
probably benign |
|
R2305:Pirb
|
UTSW |
7 |
3,715,990 (GRCm39) |
missense |
probably benign |
0.00 |
R2931:Pirb
|
UTSW |
7 |
3,720,205 (GRCm39) |
missense |
probably benign |
0.08 |
R3858:Pirb
|
UTSW |
7 |
3,720,662 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3928:Pirb
|
UTSW |
7 |
3,720,637 (GRCm39) |
missense |
probably benign |
|
R3938:Pirb
|
UTSW |
7 |
3,720,637 (GRCm39) |
missense |
probably benign |
|
R4119:Pirb
|
UTSW |
7 |
3,720,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R4174:Pirb
|
UTSW |
7 |
3,719,031 (GRCm39) |
critical splice donor site |
probably null |
|
R4248:Pirb
|
UTSW |
7 |
3,722,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R4827:Pirb
|
UTSW |
7 |
3,720,602 (GRCm39) |
missense |
probably benign |
|
R4828:Pirb
|
UTSW |
7 |
3,720,602 (GRCm39) |
missense |
probably benign |
|
R4829:Pirb
|
UTSW |
7 |
3,720,602 (GRCm39) |
missense |
probably benign |
|
R4830:Pirb
|
UTSW |
7 |
3,720,602 (GRCm39) |
missense |
probably benign |
|
R4870:Pirb
|
UTSW |
7 |
3,715,661 (GRCm39) |
missense |
probably benign |
0.00 |
R4909:Pirb
|
UTSW |
7 |
3,722,361 (GRCm39) |
nonsense |
probably null |
|
R5146:Pirb
|
UTSW |
7 |
3,715,620 (GRCm39) |
utr 3 prime |
probably benign |
|
R5244:Pirb
|
UTSW |
7 |
3,719,062 (GRCm39) |
missense |
probably benign |
0.32 |
R5323:Pirb
|
UTSW |
7 |
3,719,598 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5921:Pirb
|
UTSW |
7 |
3,719,693 (GRCm39) |
nonsense |
probably null |
|
R6316:Pirb
|
UTSW |
7 |
3,720,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R6502:Pirb
|
UTSW |
7 |
3,720,392 (GRCm39) |
missense |
probably benign |
0.00 |
R6811:Pirb
|
UTSW |
7 |
3,722,641 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7216:Pirb
|
UTSW |
7 |
3,719,273 (GRCm39) |
missense |
probably benign |
0.00 |
R7275:Pirb
|
UTSW |
7 |
3,719,177 (GRCm39) |
missense |
probably benign |
0.00 |
R7327:Pirb
|
UTSW |
7 |
3,720,187 (GRCm39) |
nonsense |
probably null |
|
R7582:Pirb
|
UTSW |
7 |
3,716,817 (GRCm39) |
critical splice donor site |
probably null |
|
R7717:Pirb
|
UTSW |
7 |
3,720,800 (GRCm39) |
missense |
not run |
|
R7717:Pirb
|
UTSW |
7 |
3,720,782 (GRCm39) |
missense |
not run |
|
R7807:Pirb
|
UTSW |
7 |
3,722,864 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7844:Pirb
|
UTSW |
7 |
3,722,410 (GRCm39) |
nonsense |
probably null |
|
R7947:Pirb
|
UTSW |
7 |
3,722,857 (GRCm39) |
missense |
probably damaging |
0.96 |
R8206:Pirb
|
UTSW |
7 |
3,715,905 (GRCm39) |
critical splice donor site |
probably null |
|
R8397:Pirb
|
UTSW |
7 |
3,719,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774:Pirb
|
UTSW |
7 |
3,720,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774-TAIL:Pirb
|
UTSW |
7 |
3,720,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R9033:Pirb
|
UTSW |
7 |
3,720,584 (GRCm39) |
missense |
probably benign |
|
R9275:Pirb
|
UTSW |
7 |
3,719,859 (GRCm39) |
missense |
probably benign |
|
R9452:Pirb
|
UTSW |
7 |
3,720,617 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9595:Pirb
|
UTSW |
7 |
3,722,406 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9605:Pirb
|
UTSW |
7 |
3,720,617 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9607:Pirb
|
UTSW |
7 |
3,720,617 (GRCm39) |
missense |
possibly damaging |
0.68 |
X0025:Pirb
|
UTSW |
7 |
3,720,267 (GRCm39) |
missense |
probably benign |
0.00 |
|