Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arap2 |
T |
C |
5: 62,828,297 (GRCm39) |
D958G |
possibly damaging |
Het |
Bag4 |
T |
C |
8: 26,261,259 (GRCm39) |
T161A |
probably benign |
Het |
Bora |
A |
T |
14: 99,299,730 (GRCm39) |
Q234L |
possibly damaging |
Het |
Cacna2d2 |
T |
C |
9: 107,374,720 (GRCm39) |
|
probably null |
Het |
Cass4 |
G |
T |
2: 172,268,832 (GRCm39) |
A307S |
probably benign |
Het |
Cbln4 |
A |
T |
2: 171,884,016 (GRCm39) |
V68E |
probably damaging |
Het |
Cc2d2a |
T |
A |
5: 43,826,015 (GRCm39) |
N2K |
probably benign |
Het |
Ccnf |
T |
A |
17: 24,450,811 (GRCm39) |
D389V |
probably damaging |
Het |
Cdipt |
T |
C |
7: 126,578,773 (GRCm39) |
S161P |
probably benign |
Het |
Ceacam19 |
T |
C |
7: 19,616,812 (GRCm39) |
I161V |
probably benign |
Het |
Cfap65 |
A |
G |
1: 74,959,564 (GRCm39) |
I862T |
probably damaging |
Het |
Cfi |
T |
A |
3: 129,652,019 (GRCm39) |
L230Q |
probably benign |
Het |
Chac2 |
G |
A |
11: 30,936,159 (GRCm39) |
R30W |
probably damaging |
Het |
Cmc2 |
G |
A |
8: 117,616,566 (GRCm39) |
|
probably benign |
Het |
Col1a2 |
A |
T |
6: 4,505,840 (GRCm39) |
M1L |
probably benign |
Het |
Cox8a |
C |
A |
19: 7,194,783 (GRCm39) |
R32L |
possibly damaging |
Het |
Cubn |
T |
A |
2: 13,435,708 (GRCm39) |
N1083Y |
probably damaging |
Het |
D630003M21Rik |
T |
C |
2: 158,059,504 (GRCm39) |
D132G |
probably damaging |
Het |
Dedd2 |
G |
A |
7: 24,910,715 (GRCm39) |
P154S |
probably benign |
Het |
Dnaaf3 |
T |
C |
7: 4,527,212 (GRCm39) |
D358G |
probably benign |
Het |
Dysf |
T |
A |
6: 83,996,586 (GRCm39) |
F29L |
probably damaging |
Het |
Dysf |
T |
C |
6: 84,089,101 (GRCm39) |
L888P |
probably damaging |
Het |
Ebf4 |
A |
G |
2: 130,151,643 (GRCm39) |
D277G |
probably damaging |
Het |
Ecm2 |
T |
A |
13: 49,668,570 (GRCm39) |
L91* |
probably null |
Het |
Foxs1 |
T |
C |
2: 152,774,762 (GRCm39) |
D97G |
possibly damaging |
Het |
Frs2 |
A |
C |
10: 116,912,714 (GRCm39) |
|
probably null |
Het |
Grp |
A |
T |
18: 66,013,008 (GRCm39) |
D58V |
probably damaging |
Het |
Hif1a |
T |
G |
12: 73,988,616 (GRCm39) |
F537C |
probably damaging |
Het |
Icam4 |
G |
A |
9: 20,940,835 (GRCm39) |
S29N |
probably benign |
Het |
Itfg1 |
T |
C |
8: 86,452,799 (GRCm39) |
E523G |
probably benign |
Het |
Jph2 |
T |
C |
2: 163,217,600 (GRCm39) |
K359E |
probably damaging |
Het |
Katnip |
G |
A |
7: 125,414,037 (GRCm39) |
G394R |
probably benign |
Het |
Kcnq2 |
A |
T |
2: 180,729,449 (GRCm39) |
V490E |
possibly damaging |
Het |
Klhl18 |
C |
T |
9: 110,257,795 (GRCm39) |
M548I |
possibly damaging |
Het |
Lpin3 |
A |
G |
2: 160,737,721 (GRCm39) |
Y197C |
probably benign |
Het |
Lrp1 |
T |
C |
10: 127,396,422 (GRCm39) |
N2381D |
probably benign |
Het |
Man1a |
A |
T |
10: 53,795,307 (GRCm39) |
W649R |
probably damaging |
Het |
Map4 |
T |
C |
9: 109,893,360 (GRCm39) |
L542P |
probably damaging |
Het |
Mboat2 |
A |
T |
12: 24,928,284 (GRCm39) |
H52L |
probably damaging |
Het |
Mok |
C |
G |
12: 110,781,380 (GRCm39) |
S91T |
probably benign |
Het |
Mtmr11 |
G |
T |
3: 96,075,400 (GRCm39) |
R360L |
probably damaging |
Het |
Myt1l |
G |
A |
12: 29,882,331 (GRCm39) |
G509R |
unknown |
Het |
Ncoa4-ps |
A |
G |
12: 119,225,386 (GRCm39) |
|
noncoding transcript |
Het |
Or1j13 |
A |
G |
2: 36,369,524 (GRCm39) |
V206A |
probably benign |
Het |
Or4g7 |
A |
T |
2: 111,309,734 (GRCm39) |
N202Y |
probably damaging |
Het |
Or52z1 |
C |
T |
7: 103,437,162 (GRCm39) |
M107I |
probably benign |
Het |
Or55b4 |
T |
C |
7: 102,133,596 (GRCm39) |
T244A |
probably damaging |
Het |
Or7d11 |
A |
T |
9: 19,966,179 (GRCm39) |
H75Q |
possibly damaging |
Het |
Or7g21 |
A |
G |
9: 19,032,623 (GRCm39) |
D121G |
probably damaging |
Het |
Padi3 |
G |
T |
4: 140,523,154 (GRCm39) |
T292N |
probably damaging |
Het |
Pard6g |
A |
C |
18: 80,160,420 (GRCm39) |
T178P |
possibly damaging |
Het |
Plxdc1 |
G |
A |
11: 97,819,289 (GRCm39) |
T398I |
probably damaging |
Het |
Prickle2 |
A |
T |
6: 92,393,829 (GRCm39) |
C225* |
probably null |
Het |
Prmt2 |
G |
A |
10: 76,046,278 (GRCm39) |
T317I |
probably benign |
Het |
Psg22 |
T |
G |
7: 18,453,705 (GRCm39) |
N172K |
probably benign |
Het |
Ptpn9 |
C |
T |
9: 56,940,447 (GRCm39) |
R196* |
probably null |
Het |
Rap1b |
C |
T |
10: 117,660,516 (GRCm39) |
V14I |
probably damaging |
Het |
Rapgef4 |
T |
A |
2: 72,026,622 (GRCm39) |
|
probably null |
Het |
Rlf |
A |
T |
4: 121,006,412 (GRCm39) |
M856K |
possibly damaging |
Het |
Rnf149 |
A |
G |
1: 39,616,255 (GRCm39) |
L34P |
probably benign |
Het |
Rock1 |
T |
C |
18: 10,101,007 (GRCm39) |
E636G |
probably benign |
Het |
Rsad2 |
A |
T |
12: 26,504,122 (GRCm39) |
Y136N |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,738,838 (GRCm39) |
H563R |
probably damaging |
Het |
Slc18b1 |
A |
G |
10: 23,680,110 (GRCm39) |
M102V |
probably benign |
Het |
Slc34a2 |
T |
A |
5: 53,224,989 (GRCm39) |
C377S |
possibly damaging |
Het |
Slco1c1 |
T |
C |
6: 141,492,496 (GRCm39) |
V293A |
probably benign |
Het |
Spidr |
A |
T |
16: 15,957,888 (GRCm39) |
S80T |
possibly damaging |
Het |
Syne1 |
C |
T |
10: 5,298,994 (GRCm39) |
E1031K |
probably damaging |
Het |
Synj2 |
G |
A |
17: 6,067,889 (GRCm39) |
V121I |
probably damaging |
Het |
Synj2 |
A |
T |
17: 6,088,373 (GRCm39) |
T1430S |
probably damaging |
Het |
Tecpr2 |
G |
T |
12: 110,895,543 (GRCm39) |
K343N |
probably damaging |
Het |
Tmem132d |
T |
A |
5: 127,861,164 (GRCm39) |
I986F |
probably benign |
Het |
Trib1 |
G |
A |
15: 59,526,324 (GRCm39) |
R298H |
probably damaging |
Het |
Ttll10 |
T |
A |
4: 156,129,814 (GRCm39) |
D283V |
probably benign |
Het |
Ttn |
T |
A |
2: 76,645,123 (GRCm39) |
K673* |
probably null |
Het |
Ubqlnl |
T |
A |
7: 103,797,905 (GRCm39) |
M531L |
probably benign |
Het |
Vmn2r120 |
A |
T |
17: 57,832,721 (GRCm39) |
W153R |
probably benign |
Het |
Vmn2r2 |
A |
C |
3: 64,024,467 (GRCm39) |
S705A |
probably benign |
Het |
Vmn2r32 |
T |
A |
7: 7,467,209 (GRCm39) |
D773V |
probably benign |
Het |
Vmn2r54 |
T |
A |
7: 12,366,205 (GRCm39) |
Q243L |
probably damaging |
Het |
Wdr24 |
C |
A |
17: 26,043,504 (GRCm39) |
R109S |
probably damaging |
Het |
Zfp113 |
T |
C |
5: 138,143,930 (GRCm39) |
M107V |
probably benign |
Het |
Zfp426 |
G |
T |
9: 20,381,923 (GRCm39) |
Q341K |
possibly damaging |
Het |
Zfp616 |
A |
T |
11: 73,974,672 (GRCm39) |
K314* |
probably null |
Het |
|
Other mutations in Pkd1l2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01338:Pkd1l2
|
APN |
8 |
117,786,259 (GRCm39) |
nonsense |
probably null |
|
IGL01353:Pkd1l2
|
APN |
8 |
117,784,182 (GRCm39) |
missense |
probably benign |
0.24 |
IGL01362:Pkd1l2
|
APN |
8 |
117,748,595 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01486:Pkd1l2
|
APN |
8 |
117,786,331 (GRCm39) |
missense |
probably benign |
|
IGL01672:Pkd1l2
|
APN |
8 |
117,807,471 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01696:Pkd1l2
|
APN |
8 |
117,783,126 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01819:Pkd1l2
|
APN |
8 |
117,724,913 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01833:Pkd1l2
|
APN |
8 |
117,787,264 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01981:Pkd1l2
|
APN |
8 |
117,743,655 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02066:Pkd1l2
|
APN |
8 |
117,736,303 (GRCm39) |
splice site |
probably benign |
|
IGL02381:Pkd1l2
|
APN |
8 |
117,762,539 (GRCm39) |
splice site |
probably benign |
|
IGL02416:Pkd1l2
|
APN |
8 |
117,767,574 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02736:Pkd1l2
|
APN |
8 |
117,767,405 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02828:Pkd1l2
|
APN |
8 |
117,756,298 (GRCm39) |
missense |
probably benign |
|
IGL02861:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02862:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02883:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02884:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02894:Pkd1l2
|
APN |
8 |
117,740,630 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02900:Pkd1l2
|
APN |
8 |
117,750,830 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02901:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02929:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02941:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02957:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02969:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03028:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03059:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03065:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03066:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03083:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03084:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03124:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03162:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03165:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03335:Pkd1l2
|
APN |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03357:Pkd1l2
|
APN |
8 |
117,722,548 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02835:Pkd1l2
|
UTSW |
8 |
117,792,484 (GRCm39) |
missense |
probably benign |
0.07 |
PIT4453001:Pkd1l2
|
UTSW |
8 |
117,748,761 (GRCm39) |
missense |
probably benign |
0.00 |
R0127:Pkd1l2
|
UTSW |
8 |
117,776,787 (GRCm39) |
splice site |
probably benign |
|
R0309:Pkd1l2
|
UTSW |
8 |
117,724,315 (GRCm39) |
missense |
probably damaging |
0.99 |
R0365:Pkd1l2
|
UTSW |
8 |
117,748,589 (GRCm39) |
missense |
probably benign |
0.02 |
R0526:Pkd1l2
|
UTSW |
8 |
117,808,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R0571:Pkd1l2
|
UTSW |
8 |
117,808,957 (GRCm39) |
missense |
probably benign |
0.01 |
R0716:Pkd1l2
|
UTSW |
8 |
117,777,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R0787:Pkd1l2
|
UTSW |
8 |
117,802,916 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0893:Pkd1l2
|
UTSW |
8 |
117,771,231 (GRCm39) |
missense |
probably damaging |
0.99 |
R1256:Pkd1l2
|
UTSW |
8 |
117,746,282 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1391:Pkd1l2
|
UTSW |
8 |
117,781,673 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1474:Pkd1l2
|
UTSW |
8 |
117,792,236 (GRCm39) |
splice site |
probably benign |
|
R1491:Pkd1l2
|
UTSW |
8 |
117,755,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R1520:Pkd1l2
|
UTSW |
8 |
117,772,898 (GRCm39) |
missense |
probably benign |
0.00 |
R1521:Pkd1l2
|
UTSW |
8 |
117,792,239 (GRCm39) |
splice site |
probably null |
|
R1544:Pkd1l2
|
UTSW |
8 |
117,764,974 (GRCm39) |
frame shift |
probably null |
|
R1558:Pkd1l2
|
UTSW |
8 |
117,808,991 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1673:Pkd1l2
|
UTSW |
8 |
117,767,514 (GRCm39) |
missense |
probably benign |
0.00 |
R1691:Pkd1l2
|
UTSW |
8 |
117,783,158 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1754:Pkd1l2
|
UTSW |
8 |
117,757,458 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1857:Pkd1l2
|
UTSW |
8 |
117,767,408 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1939:Pkd1l2
|
UTSW |
8 |
117,772,921 (GRCm39) |
nonsense |
probably null |
|
R1955:Pkd1l2
|
UTSW |
8 |
117,770,100 (GRCm39) |
missense |
probably benign |
|
R1957:Pkd1l2
|
UTSW |
8 |
117,757,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Pkd1l2
|
UTSW |
8 |
117,769,970 (GRCm39) |
critical splice donor site |
probably null |
|
R2024:Pkd1l2
|
UTSW |
8 |
117,746,272 (GRCm39) |
missense |
probably benign |
|
R2046:Pkd1l2
|
UTSW |
8 |
117,726,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R2102:Pkd1l2
|
UTSW |
8 |
117,808,208 (GRCm39) |
missense |
probably damaging |
0.98 |
R2116:Pkd1l2
|
UTSW |
8 |
117,757,461 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2148:Pkd1l2
|
UTSW |
8 |
117,783,064 (GRCm39) |
missense |
probably damaging |
0.98 |
R2251:Pkd1l2
|
UTSW |
8 |
117,784,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R2252:Pkd1l2
|
UTSW |
8 |
117,784,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R2366:Pkd1l2
|
UTSW |
8 |
117,770,056 (GRCm39) |
missense |
probably benign |
0.01 |
R2566:Pkd1l2
|
UTSW |
8 |
117,746,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Pkd1l2
|
UTSW |
8 |
117,764,903 (GRCm39) |
missense |
probably benign |
0.10 |
R2872:Pkd1l2
|
UTSW |
8 |
117,764,903 (GRCm39) |
missense |
probably benign |
0.10 |
R2985:Pkd1l2
|
UTSW |
8 |
117,792,290 (GRCm39) |
missense |
probably benign |
0.00 |
R3055:Pkd1l2
|
UTSW |
8 |
117,795,054 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3436:Pkd1l2
|
UTSW |
8 |
117,767,478 (GRCm39) |
missense |
probably benign |
0.01 |
R4732:Pkd1l2
|
UTSW |
8 |
117,722,581 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4733:Pkd1l2
|
UTSW |
8 |
117,722,581 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4763:Pkd1l2
|
UTSW |
8 |
117,746,168 (GRCm39) |
missense |
probably damaging |
0.96 |
R4789:Pkd1l2
|
UTSW |
8 |
117,738,314 (GRCm39) |
missense |
probably damaging |
0.99 |
R4921:Pkd1l2
|
UTSW |
8 |
117,781,624 (GRCm39) |
missense |
probably benign |
0.03 |
R4921:Pkd1l2
|
UTSW |
8 |
117,799,288 (GRCm39) |
missense |
probably damaging |
0.97 |
R4999:Pkd1l2
|
UTSW |
8 |
117,774,113 (GRCm39) |
splice site |
probably null |
|
R5057:Pkd1l2
|
UTSW |
8 |
117,781,747 (GRCm39) |
missense |
probably benign |
0.21 |
R5209:Pkd1l2
|
UTSW |
8 |
117,783,181 (GRCm39) |
missense |
probably benign |
0.23 |
R5241:Pkd1l2
|
UTSW |
8 |
117,761,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R5480:Pkd1l2
|
UTSW |
8 |
117,757,388 (GRCm39) |
missense |
probably damaging |
0.99 |
R5501:Pkd1l2
|
UTSW |
8 |
117,792,569 (GRCm39) |
missense |
probably damaging |
0.98 |
R5533:Pkd1l2
|
UTSW |
8 |
117,794,855 (GRCm39) |
missense |
probably benign |
0.03 |
R5582:Pkd1l2
|
UTSW |
8 |
117,767,522 (GRCm39) |
nonsense |
probably null |
|
R5610:Pkd1l2
|
UTSW |
8 |
117,769,059 (GRCm39) |
missense |
probably benign |
0.04 |
R5770:Pkd1l2
|
UTSW |
8 |
117,781,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R5854:Pkd1l2
|
UTSW |
8 |
117,792,485 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5867:Pkd1l2
|
UTSW |
8 |
117,781,750 (GRCm39) |
missense |
probably damaging |
0.96 |
R5881:Pkd1l2
|
UTSW |
8 |
117,724,321 (GRCm39) |
missense |
probably damaging |
0.99 |
R5906:Pkd1l2
|
UTSW |
8 |
117,756,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R5909:Pkd1l2
|
UTSW |
8 |
117,750,795 (GRCm39) |
missense |
probably benign |
0.00 |
R6030:Pkd1l2
|
UTSW |
8 |
117,769,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R6030:Pkd1l2
|
UTSW |
8 |
117,769,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R6122:Pkd1l2
|
UTSW |
8 |
117,809,107 (GRCm39) |
missense |
probably benign |
0.02 |
R6216:Pkd1l2
|
UTSW |
8 |
117,808,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R6406:Pkd1l2
|
UTSW |
8 |
117,762,586 (GRCm39) |
missense |
probably damaging |
0.99 |
R6417:Pkd1l2
|
UTSW |
8 |
117,740,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R6420:Pkd1l2
|
UTSW |
8 |
117,740,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R6601:Pkd1l2
|
UTSW |
8 |
117,767,405 (GRCm39) |
missense |
probably benign |
0.00 |
R6743:Pkd1l2
|
UTSW |
8 |
117,757,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R7053:Pkd1l2
|
UTSW |
8 |
117,740,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R7144:Pkd1l2
|
UTSW |
8 |
117,802,870 (GRCm39) |
nonsense |
probably null |
|
R7148:Pkd1l2
|
UTSW |
8 |
117,807,525 (GRCm39) |
missense |
probably benign |
0.00 |
R7169:Pkd1l2
|
UTSW |
8 |
117,767,574 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7217:Pkd1l2
|
UTSW |
8 |
117,722,536 (GRCm39) |
missense |
probably benign |
0.24 |
R7310:Pkd1l2
|
UTSW |
8 |
117,750,773 (GRCm39) |
missense |
probably benign |
|
R7382:Pkd1l2
|
UTSW |
8 |
117,781,610 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7397:Pkd1l2
|
UTSW |
8 |
117,762,641 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7408:Pkd1l2
|
UTSW |
8 |
117,755,218 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7437:Pkd1l2
|
UTSW |
8 |
117,757,421 (GRCm39) |
missense |
probably damaging |
0.96 |
R7492:Pkd1l2
|
UTSW |
8 |
117,794,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R7496:Pkd1l2
|
UTSW |
8 |
117,787,333 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7519:Pkd1l2
|
UTSW |
8 |
117,792,268 (GRCm39) |
missense |
probably benign |
|
R7590:Pkd1l2
|
UTSW |
8 |
117,807,525 (GRCm39) |
missense |
probably benign |
0.00 |
R7623:Pkd1l2
|
UTSW |
8 |
117,756,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R7768:Pkd1l2
|
UTSW |
8 |
117,781,599 (GRCm39) |
critical splice donor site |
probably null |
|
R7897:Pkd1l2
|
UTSW |
8 |
117,724,827 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7982:Pkd1l2
|
UTSW |
8 |
117,777,926 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8024:Pkd1l2
|
UTSW |
8 |
117,802,921 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8140:Pkd1l2
|
UTSW |
8 |
117,774,236 (GRCm39) |
missense |
probably benign |
|
R8145:Pkd1l2
|
UTSW |
8 |
117,781,742 (GRCm39) |
missense |
probably benign |
|
R8228:Pkd1l2
|
UTSW |
8 |
117,792,514 (GRCm39) |
missense |
probably damaging |
0.97 |
R8252:Pkd1l2
|
UTSW |
8 |
117,767,472 (GRCm39) |
missense |
probably benign |
0.29 |
R8500:Pkd1l2
|
UTSW |
8 |
117,774,302 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8732:Pkd1l2
|
UTSW |
8 |
117,792,311 (GRCm39) |
missense |
probably benign |
0.28 |
R8809:Pkd1l2
|
UTSW |
8 |
117,726,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R8896:Pkd1l2
|
UTSW |
8 |
117,740,615 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8961:Pkd1l2
|
UTSW |
8 |
117,726,717 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8985:Pkd1l2
|
UTSW |
8 |
117,764,849 (GRCm39) |
missense |
probably benign |
0.01 |
R9008:Pkd1l2
|
UTSW |
8 |
117,769,037 (GRCm39) |
missense |
probably benign |
0.32 |
R9091:Pkd1l2
|
UTSW |
8 |
117,759,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R9138:Pkd1l2
|
UTSW |
8 |
117,781,748 (GRCm39) |
missense |
probably benign |
0.43 |
R9160:Pkd1l2
|
UTSW |
8 |
117,767,408 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9249:Pkd1l2
|
UTSW |
8 |
117,746,159 (GRCm39) |
missense |
probably damaging |
0.99 |
R9270:Pkd1l2
|
UTSW |
8 |
117,759,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R9735:Pkd1l2
|
UTSW |
8 |
117,772,820 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Pkd1l2
|
UTSW |
8 |
117,781,653 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Pkd1l2
|
UTSW |
8 |
117,757,430 (GRCm39) |
missense |
probably damaging |
1.00 |
|