Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd3 |
T |
C |
3: 121,570,642 (GRCm39) |
|
probably benign |
Het |
Cdk12 |
T |
A |
11: 98,136,214 (GRCm39) |
L1156Q |
unknown |
Het |
Ctsl |
T |
C |
13: 64,515,982 (GRCm39) |
Y66C |
probably damaging |
Het |
Esd |
C |
T |
14: 74,973,467 (GRCm39) |
H21Y |
probably damaging |
Het |
Fcrlb |
A |
C |
1: 170,736,393 (GRCm39) |
Y128D |
possibly damaging |
Het |
Gm17027 |
A |
T |
14: 41,981,267 (GRCm39) |
N196K |
unknown |
Het |
Gm4553 |
T |
C |
7: 141,718,964 (GRCm39) |
S155G |
unknown |
Het |
Hpcal1 |
A |
G |
12: 17,841,146 (GRCm39) |
S175G |
probably benign |
Het |
Itgam |
A |
T |
7: 127,684,833 (GRCm39) |
D401V |
probably damaging |
Het |
Kank1 |
A |
G |
19: 25,389,122 (GRCm39) |
T932A |
probably benign |
Het |
Lmod1 |
A |
G |
1: 135,292,216 (GRCm39) |
K357R |
probably benign |
Het |
Muc4 |
A |
G |
16: 32,599,186 (GRCm39) |
I3271V |
probably benign |
Het |
Nlrc5 |
A |
G |
8: 95,248,107 (GRCm39) |
K1692E |
probably damaging |
Het |
Ocln |
A |
G |
13: 100,671,521 (GRCm39) |
W279R |
probably damaging |
Het |
Or4p20 |
T |
C |
2: 88,254,130 (GRCm39) |
I80V |
probably benign |
Het |
Pcsk1 |
A |
G |
13: 75,280,206 (GRCm39) |
K677R |
probably benign |
Het |
Pitrm1 |
T |
A |
13: 6,618,702 (GRCm39) |
L586Q |
probably damaging |
Het |
Plppr3 |
G |
A |
10: 79,702,503 (GRCm39) |
S217L |
probably damaging |
Het |
Pramel12 |
T |
A |
4: 143,143,237 (GRCm39) |
M1K |
probably null |
Het |
Pramel13 |
A |
G |
4: 144,121,310 (GRCm39) |
L238P |
possibly damaging |
Het |
Sema6b |
C |
T |
17: 56,437,048 (GRCm39) |
D204N |
probably damaging |
Het |
Slc12a5 |
A |
G |
2: 164,839,041 (GRCm39) |
N1063S |
probably damaging |
Het |
Tg |
T |
C |
15: 66,565,273 (GRCm39) |
V1205A |
probably benign |
Het |
Tmem260 |
T |
C |
14: 48,724,336 (GRCm39) |
F205L |
probably benign |
Het |
Trappc11 |
A |
T |
8: 47,956,337 (GRCm39) |
|
probably benign |
Het |
Tsen34 |
A |
G |
7: 3,703,530 (GRCm39) |
*296W |
probably null |
Het |
Ubr2 |
A |
G |
17: 47,296,986 (GRCm39) |
|
probably benign |
Het |
Vmn2r23 |
T |
A |
6: 123,706,684 (GRCm39) |
W505R |
possibly damaging |
Het |
Wbp11 |
A |
G |
6: 136,798,668 (GRCm39) |
|
probably benign |
Het |
Znfx1 |
A |
T |
2: 166,878,649 (GRCm39) |
M1909K |
possibly damaging |
Het |
|
Other mutations in Pnldc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01599:Pnldc1
|
APN |
17 |
13,125,415 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02109:Pnldc1
|
APN |
17 |
13,124,425 (GRCm39) |
missense |
probably benign |
0.01 |
R0022:Pnldc1
|
UTSW |
17 |
13,109,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R0423:Pnldc1
|
UTSW |
17 |
13,108,963 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1921:Pnldc1
|
UTSW |
17 |
13,107,815 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1978:Pnldc1
|
UTSW |
17 |
13,125,392 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2403:Pnldc1
|
UTSW |
17 |
13,118,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R4027:Pnldc1
|
UTSW |
17 |
13,109,666 (GRCm39) |
missense |
probably benign |
0.01 |
R4574:Pnldc1
|
UTSW |
17 |
13,111,669 (GRCm39) |
missense |
probably benign |
0.01 |
R5148:Pnldc1
|
UTSW |
17 |
13,111,676 (GRCm39) |
missense |
probably benign |
0.00 |
R5381:Pnldc1
|
UTSW |
17 |
13,109,283 (GRCm39) |
missense |
probably benign |
0.07 |
R5973:Pnldc1
|
UTSW |
17 |
13,113,260 (GRCm39) |
missense |
probably benign |
0.07 |
R6073:Pnldc1
|
UTSW |
17 |
13,109,250 (GRCm39) |
missense |
probably null |
0.05 |
R6368:Pnldc1
|
UTSW |
17 |
13,124,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R6551:Pnldc1
|
UTSW |
17 |
13,124,456 (GRCm39) |
missense |
probably damaging |
0.98 |
R7909:Pnldc1
|
UTSW |
17 |
13,122,098 (GRCm39) |
missense |
probably benign |
0.04 |
R8088:Pnldc1
|
UTSW |
17 |
13,116,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R8724:Pnldc1
|
UTSW |
17 |
13,111,703 (GRCm39) |
missense |
probably damaging |
0.96 |
R8728:Pnldc1
|
UTSW |
17 |
13,116,165 (GRCm39) |
missense |
probably damaging |
1.00 |
|