Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930009A15Rik |
A |
C |
10: 115,406,104 (GRCm39) |
|
probably benign |
Het |
Arhgap29 |
T |
A |
3: 121,782,200 (GRCm39) |
S71T |
possibly damaging |
Het |
BC048507 |
T |
C |
13: 68,011,817 (GRCm39) |
Y65H |
probably damaging |
Het |
C3 |
T |
C |
17: 57,518,720 (GRCm39) |
E1221G |
probably benign |
Het |
Calb1 |
G |
T |
4: 15,885,656 (GRCm39) |
V76L |
probably benign |
Het |
Crybg1 |
T |
A |
10: 43,879,689 (GRCm39) |
K500* |
probably null |
Het |
Csmd1 |
G |
A |
8: 16,034,860 (GRCm39) |
T2437I |
probably benign |
Het |
Cyp27b1 |
G |
A |
10: 126,887,966 (GRCm39) |
V493I |
possibly damaging |
Het |
Cyp3a44 |
T |
A |
5: 145,740,554 (GRCm39) |
T29S |
probably benign |
Het |
Dclk3 |
T |
C |
9: 111,298,328 (GRCm39) |
V624A |
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,069,140 (GRCm39) |
I2464V |
probably benign |
Het |
Dock6 |
A |
T |
9: 21,721,254 (GRCm39) |
|
probably null |
Het |
Erap1 |
C |
T |
13: 74,794,533 (GRCm39) |
T64I |
probably damaging |
Het |
Erbb3 |
A |
T |
10: 128,405,948 (GRCm39) |
Y1156* |
probably null |
Het |
Fam168a |
G |
A |
7: 100,484,602 (GRCm39) |
A231T |
probably benign |
Het |
Farp1 |
C |
T |
14: 121,472,489 (GRCm39) |
P208L |
probably damaging |
Het |
Fbxo30 |
T |
C |
10: 11,166,813 (GRCm39) |
Y512H |
probably damaging |
Het |
Gcnt2 |
A |
T |
13: 41,071,650 (GRCm39) |
I98F |
possibly damaging |
Het |
Got1 |
G |
A |
19: 43,493,036 (GRCm39) |
T295I |
probably benign |
Het |
Herc2 |
A |
G |
7: 55,844,010 (GRCm39) |
E3538G |
probably damaging |
Het |
Kcnmb4 |
A |
T |
10: 116,309,410 (GRCm39) |
V6E |
probably benign |
Het |
Kmt2d |
G |
A |
15: 98,749,990 (GRCm39) |
|
probably benign |
Het |
Letmd1 |
C |
T |
15: 100,367,009 (GRCm39) |
A2V |
probably damaging |
Het |
Lynx1 |
G |
T |
15: 74,623,462 (GRCm39) |
Y28* |
probably null |
Het |
Mast1 |
T |
C |
8: 85,652,136 (GRCm39) |
E304G |
probably damaging |
Het |
Nipa1 |
G |
A |
7: 55,629,205 (GRCm39) |
Q303* |
probably null |
Het |
Nomo1 |
G |
A |
7: 45,712,426 (GRCm39) |
R657H |
possibly damaging |
Het |
Or51b4 |
C |
T |
7: 103,530,541 (GRCm39) |
R303H |
probably benign |
Het |
Pcdha7 |
T |
A |
18: 37,108,628 (GRCm39) |
L551Q |
probably damaging |
Het |
Pik3r4 |
T |
C |
9: 105,525,930 (GRCm39) |
Y267H |
probably damaging |
Het |
Prph |
G |
A |
15: 98,953,281 (GRCm39) |
G65D |
probably benign |
Het |
Pskh1 |
T |
C |
8: 106,639,464 (GRCm39) |
L48P |
probably benign |
Het |
Ptdss1 |
C |
A |
13: 67,093,365 (GRCm39) |
N68K |
probably damaging |
Het |
Rexo5 |
G |
A |
7: 119,433,526 (GRCm39) |
G495R |
probably damaging |
Het |
Ryr1 |
C |
A |
7: 28,723,448 (GRCm39) |
A4204S |
possibly damaging |
Het |
Serpinb9 |
G |
A |
13: 33,199,659 (GRCm39) |
S318N |
probably damaging |
Het |
Slc22a8 |
G |
A |
19: 8,586,638 (GRCm39) |
R383H |
probably benign |
Het |
Trim26 |
A |
G |
17: 37,162,016 (GRCm39) |
H145R |
probably damaging |
Het |
Trps1 |
A |
T |
15: 50,695,286 (GRCm39) |
Y286* |
probably null |
Het |
Vmn1r181 |
A |
G |
7: 23,683,787 (GRCm39) |
N84S |
probably benign |
Het |
Wdfy4 |
G |
T |
14: 32,873,689 (GRCm39) |
Q207K |
probably benign |
Het |
Whrn |
G |
A |
4: 63,351,053 (GRCm39) |
T427I |
probably benign |
Het |
|
Other mutations in Pnliprp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00495:Pnliprp1
|
APN |
19 |
58,723,162 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02367:Pnliprp1
|
APN |
19 |
58,726,601 (GRCm39) |
missense |
probably benign |
|
R0463:Pnliprp1
|
UTSW |
19 |
58,726,628 (GRCm39) |
nonsense |
probably null |
|
R0573:Pnliprp1
|
UTSW |
19 |
58,723,314 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0591:Pnliprp1
|
UTSW |
19 |
58,723,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R0608:Pnliprp1
|
UTSW |
19 |
58,726,628 (GRCm39) |
nonsense |
probably null |
|
R1169:Pnliprp1
|
UTSW |
19 |
58,723,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R1575:Pnliprp1
|
UTSW |
19 |
58,728,901 (GRCm39) |
missense |
probably benign |
0.07 |
R1723:Pnliprp1
|
UTSW |
19 |
58,720,574 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1879:Pnliprp1
|
UTSW |
19 |
58,732,516 (GRCm39) |
missense |
probably benign |
0.07 |
R1955:Pnliprp1
|
UTSW |
19 |
58,723,404 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2090:Pnliprp1
|
UTSW |
19 |
58,728,901 (GRCm39) |
missense |
probably benign |
0.03 |
R2092:Pnliprp1
|
UTSW |
19 |
58,729,616 (GRCm39) |
missense |
probably benign |
0.02 |
R2342:Pnliprp1
|
UTSW |
19 |
58,729,691 (GRCm39) |
splice site |
probably benign |
|
R2421:Pnliprp1
|
UTSW |
19 |
58,732,517 (GRCm39) |
missense |
probably benign |
0.21 |
R4716:Pnliprp1
|
UTSW |
19 |
58,728,901 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5478:Pnliprp1
|
UTSW |
19 |
58,723,423 (GRCm39) |
splice site |
probably null |
|
R6155:Pnliprp1
|
UTSW |
19 |
58,718,565 (GRCm39) |
critical splice donor site |
probably null |
|
R6284:Pnliprp1
|
UTSW |
19 |
58,723,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R7107:Pnliprp1
|
UTSW |
19 |
58,717,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R7454:Pnliprp1
|
UTSW |
19 |
58,729,532 (GRCm39) |
missense |
probably benign |
0.29 |
R7470:Pnliprp1
|
UTSW |
19 |
58,720,457 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7574:Pnliprp1
|
UTSW |
19 |
58,726,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R7601:Pnliprp1
|
UTSW |
19 |
58,720,526 (GRCm39) |
missense |
probably damaging |
0.99 |
R8782:Pnliprp1
|
UTSW |
19 |
58,719,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R9081:Pnliprp1
|
UTSW |
19 |
58,723,406 (GRCm39) |
missense |
probably benign |
|
R9445:Pnliprp1
|
UTSW |
19 |
58,720,628 (GRCm39) |
intron |
probably benign |
|
R9466:Pnliprp1
|
UTSW |
19 |
58,723,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|