Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
C |
T |
13: 81,545,570 (GRCm39) |
V5572I |
probably benign |
Het |
Agap1 |
C |
T |
1: 89,770,818 (GRCm39) |
T656I |
probably damaging |
Het |
Als2cl |
C |
T |
9: 110,716,432 (GRCm39) |
R247W |
probably damaging |
Het |
Ankfy1 |
A |
T |
11: 72,603,071 (GRCm39) |
R33S |
probably benign |
Het |
Ano5 |
T |
C |
7: 51,235,079 (GRCm39) |
F671L |
probably damaging |
Het |
Arhgap26 |
A |
G |
18: 39,283,145 (GRCm39) |
M361V |
probably damaging |
Het |
Bckdk |
A |
G |
7: 127,505,145 (GRCm39) |
E175G |
probably damaging |
Het |
Bptf |
G |
T |
11: 106,964,022 (GRCm39) |
T1724K |
probably damaging |
Het |
Btn2a2 |
T |
A |
13: 23,670,398 (GRCm39) |
I112F |
probably damaging |
Het |
Cln8 |
T |
A |
8: 14,946,621 (GRCm39) |
W212R |
probably damaging |
Het |
Cnbd1 |
T |
C |
4: 18,886,119 (GRCm39) |
E300G |
probably benign |
Het |
Cnksr3 |
T |
C |
10: 7,092,993 (GRCm39) |
I173V |
probably benign |
Het |
Cntn2 |
T |
A |
1: 132,451,170 (GRCm39) |
D484V |
probably damaging |
Het |
Cyp4a14 |
C |
A |
4: 115,348,607 (GRCm39) |
G319V |
probably damaging |
Het |
Cyp4f37 |
G |
A |
17: 32,848,957 (GRCm39) |
R275Q |
possibly damaging |
Het |
Def8 |
C |
T |
8: 124,186,809 (GRCm39) |
|
probably benign |
Het |
Dnaaf4 |
T |
C |
9: 72,879,280 (GRCm39) |
V356A |
probably damaging |
Het |
Dnah10 |
T |
C |
5: 124,868,855 (GRCm39) |
|
probably null |
Het |
Dock6 |
A |
G |
9: 21,735,712 (GRCm39) |
V1012A |
probably benign |
Het |
Dus3l |
T |
A |
17: 57,076,579 (GRCm39) |
N586K |
probably damaging |
Het |
Dyrk2 |
T |
A |
10: 118,696,173 (GRCm39) |
I362F |
probably damaging |
Het |
Eeig2 |
A |
T |
3: 108,887,468 (GRCm39) |
S265R |
probably benign |
Het |
Erc2 |
T |
A |
14: 27,498,815 (GRCm39) |
D230E |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,497,073 (GRCm39) |
H4186R |
probably benign |
Het |
Fbxo44 |
A |
G |
4: 148,241,052 (GRCm39) |
F179S |
probably damaging |
Het |
Fech |
A |
G |
18: 64,611,720 (GRCm39) |
|
probably null |
Het |
Fer1l5 |
T |
A |
1: 36,424,254 (GRCm39) |
C289* |
probably null |
Het |
Fhl5 |
T |
A |
4: 25,214,756 (GRCm39) |
D7V |
probably benign |
Het |
Flvcr1 |
G |
T |
1: 190,741,748 (GRCm39) |
T514K |
probably damaging |
Het |
Fmo1 |
A |
T |
1: 162,667,185 (GRCm39) |
|
probably null |
Het |
Gabra6 |
G |
A |
11: 42,198,268 (GRCm39) |
T384M |
probably benign |
Het |
Gli3 |
A |
G |
13: 15,723,210 (GRCm39) |
Y117C |
probably damaging |
Het |
Gnao1 |
A |
G |
8: 94,622,873 (GRCm39) |
D59G |
probably benign |
Het |
Gria2 |
T |
C |
3: 80,614,556 (GRCm39) |
I495V |
possibly damaging |
Het |
Hnf1b |
C |
A |
11: 83,754,811 (GRCm39) |
H161Q |
probably benign |
Het |
Itga8 |
T |
A |
2: 12,235,019 (GRCm39) |
D413V |
possibly damaging |
Het |
Itpr3 |
A |
T |
17: 27,329,895 (GRCm39) |
Q1563L |
possibly damaging |
Het |
Kctd16 |
A |
G |
18: 40,663,882 (GRCm39) |
N337S |
probably benign |
Het |
Klra4 |
C |
T |
6: 130,030,016 (GRCm39) |
V190M |
possibly damaging |
Het |
Krtap4-9 |
T |
A |
11: 99,676,462 (GRCm39) |
|
probably benign |
Het |
L3mbtl1 |
GGCCG |
GG |
2: 162,809,256 (GRCm39) |
|
probably benign |
Het |
Mchr1 |
T |
C |
15: 81,122,044 (GRCm39) |
F265L |
probably damaging |
Het |
Megf8 |
T |
A |
7: 25,025,866 (GRCm39) |
Y83* |
probably null |
Het |
Mettl18 |
A |
G |
1: 163,824,746 (GRCm39) |
M356V |
probably null |
Het |
Mrm1 |
G |
A |
11: 84,710,018 (GRCm39) |
R61W |
probably damaging |
Het |
Muc4 |
A |
T |
16: 32,570,523 (GRCm39) |
T528S |
probably benign |
Het |
Myef2 |
A |
T |
2: 124,937,651 (GRCm39) |
L530* |
probably null |
Het |
Nhlrc4 |
T |
C |
17: 26,162,693 (GRCm39) |
E18G |
probably benign |
Het |
Nisch |
C |
T |
14: 30,895,102 (GRCm39) |
V1065I |
probably benign |
Het |
Nlgn2 |
C |
T |
11: 69,724,975 (GRCm39) |
R97H |
probably damaging |
Het |
Nos2 |
T |
C |
11: 78,828,741 (GRCm39) |
L321S |
probably damaging |
Het |
Oaz3 |
T |
C |
3: 94,343,717 (GRCm39) |
M49V |
possibly damaging |
Het |
Olfm5 |
A |
G |
7: 103,803,362 (GRCm39) |
V367A |
probably damaging |
Het |
Omd |
C |
T |
13: 49,743,112 (GRCm39) |
P54L |
possibly damaging |
Het |
Or10ak12 |
C |
T |
4: 118,666,575 (GRCm39) |
R162H |
probably benign |
Het |
Or11g26 |
C |
A |
14: 50,753,249 (GRCm39) |
A196D |
probably benign |
Het |
Or2g7 |
C |
A |
17: 38,378,641 (GRCm39) |
A193D |
probably benign |
Het |
Or51f23 |
A |
T |
7: 102,453,481 (GRCm39) |
R265S |
probably damaging |
Het |
Or7d10 |
A |
G |
9: 19,832,206 (GRCm39) |
K234E |
probably damaging |
Het |
Pard3b |
T |
A |
1: 61,807,289 (GRCm39) |
|
probably benign |
Het |
Pcdhb18 |
A |
C |
18: 37,624,988 (GRCm39) |
I773L |
possibly damaging |
Het |
Pde11a |
T |
C |
2: 75,970,175 (GRCm39) |
|
probably null |
Het |
Pfkfb4 |
A |
C |
9: 108,859,462 (GRCm39) |
|
probably benign |
Het |
Phb2 |
T |
G |
6: 124,692,612 (GRCm39) |
I260S |
probably damaging |
Het |
Pla2g6 |
T |
C |
15: 79,187,728 (GRCm39) |
|
probably benign |
Het |
Pou4f2 |
G |
A |
8: 79,163,020 (GRCm39) |
S5F |
unknown |
Het |
Ppp1r9a |
A |
T |
6: 5,157,002 (GRCm39) |
|
probably null |
Het |
Pramel5 |
A |
G |
4: 143,999,553 (GRCm39) |
I178T |
probably benign |
Het |
Prom2 |
C |
T |
2: 127,372,053 (GRCm39) |
W745* |
probably null |
Het |
Pros1 |
T |
A |
16: 62,748,424 (GRCm39) |
N632K |
probably damaging |
Het |
Rab4b |
A |
G |
7: 26,873,927 (GRCm39) |
I117T |
probably benign |
Het |
Rbm25 |
T |
A |
12: 83,724,640 (GRCm39) |
H796Q |
possibly damaging |
Het |
Rnf151 |
A |
T |
17: 24,937,004 (GRCm39) |
|
probably null |
Het |
Rps6ka1 |
A |
T |
4: 133,598,882 (GRCm39) |
L97I |
probably damaging |
Het |
Scart1 |
C |
T |
7: 139,810,359 (GRCm39) |
P984S |
probably benign |
Het |
Semp2l2a |
T |
A |
8: 13,887,263 (GRCm39) |
D276V |
probably benign |
Het |
Sergef |
T |
A |
7: 46,092,888 (GRCm39) |
T374S |
probably benign |
Het |
Sh3rf3 |
G |
T |
10: 58,966,808 (GRCm39) |
G717C |
probably damaging |
Het |
Slc29a4 |
C |
T |
5: 142,707,157 (GRCm39) |
T500I |
possibly damaging |
Het |
Smc1b |
T |
A |
15: 84,970,322 (GRCm39) |
D977V |
probably damaging |
Het |
Spata31d1d |
C |
T |
13: 59,874,829 (GRCm39) |
C902Y |
probably benign |
Het |
St14 |
A |
T |
9: 31,015,056 (GRCm39) |
V314D |
probably damaging |
Het |
Stat3 |
A |
T |
11: 100,784,496 (GRCm39) |
I602N |
possibly damaging |
Het |
Stx4a |
T |
A |
7: 127,445,661 (GRCm39) |
I189N |
probably damaging |
Het |
Tacc1 |
A |
G |
8: 25,672,215 (GRCm39) |
S338P |
probably benign |
Het |
Tcirg1 |
T |
A |
19: 3,952,424 (GRCm39) |
T315S |
possibly damaging |
Het |
Tenm4 |
A |
T |
7: 96,503,926 (GRCm39) |
N1295I |
probably damaging |
Het |
Tm7sf3 |
T |
C |
6: 146,505,409 (GRCm39) |
K516E |
possibly damaging |
Het |
Tmem198b |
T |
C |
10: 128,637,323 (GRCm39) |
E272G |
possibly damaging |
Het |
Tnip3 |
A |
G |
6: 65,582,937 (GRCm39) |
Q237R |
probably damaging |
Het |
Trim15 |
C |
T |
17: 37,173,252 (GRCm39) |
|
probably null |
Het |
Trim30a |
T |
A |
7: 104,070,657 (GRCm39) |
N252I |
possibly damaging |
Het |
Ttc39a |
A |
G |
4: 109,288,075 (GRCm39) |
E227G |
probably benign |
Het |
Ttll13 |
A |
G |
7: 79,902,914 (GRCm39) |
E194G |
probably damaging |
Het |
Upf1 |
G |
A |
8: 70,796,912 (GRCm39) |
T107I |
probably benign |
Het |
Vac14 |
A |
G |
8: 111,436,981 (GRCm39) |
I565V |
probably damaging |
Het |
Zcchc14 |
A |
T |
8: 122,338,097 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Pkd1l1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00093:Pkd1l1
|
APN |
11 |
8,911,971 (GRCm39) |
missense |
unknown |
|
IGL00156:Pkd1l1
|
APN |
11 |
8,900,515 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00161:Pkd1l1
|
APN |
11 |
8,879,353 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00489:Pkd1l1
|
APN |
11 |
8,784,773 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00495:Pkd1l1
|
APN |
11 |
8,818,493 (GRCm39) |
missense |
probably benign |
0.34 |
IGL00983:Pkd1l1
|
APN |
11 |
8,794,585 (GRCm39) |
missense |
probably benign |
|
IGL01071:Pkd1l1
|
APN |
11 |
8,798,921 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01093:Pkd1l1
|
APN |
11 |
8,851,345 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01295:Pkd1l1
|
APN |
11 |
8,883,685 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01311:Pkd1l1
|
APN |
11 |
8,851,174 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01412:Pkd1l1
|
APN |
11 |
8,900,409 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01978:Pkd1l1
|
APN |
11 |
8,911,336 (GRCm39) |
missense |
unknown |
|
IGL01999:Pkd1l1
|
APN |
11 |
8,786,291 (GRCm39) |
missense |
probably benign |
|
IGL02080:Pkd1l1
|
APN |
11 |
8,911,345 (GRCm39) |
missense |
unknown |
|
IGL02106:Pkd1l1
|
APN |
11 |
8,783,800 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02216:Pkd1l1
|
APN |
11 |
8,784,897 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02305:Pkd1l1
|
APN |
11 |
8,852,467 (GRCm39) |
missense |
probably benign |
|
IGL02337:Pkd1l1
|
APN |
11 |
8,892,079 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02576:Pkd1l1
|
APN |
11 |
8,794,560 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02704:Pkd1l1
|
APN |
11 |
8,784,910 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02814:Pkd1l1
|
APN |
11 |
8,852,582 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02904:Pkd1l1
|
APN |
11 |
8,818,450 (GRCm39) |
splice site |
probably benign |
|
IGL02972:Pkd1l1
|
APN |
11 |
8,813,908 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03091:Pkd1l1
|
APN |
11 |
8,805,564 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03113:Pkd1l1
|
APN |
11 |
8,784,793 (GRCm39) |
missense |
probably benign |
0.20 |
IGL03210:Pkd1l1
|
APN |
11 |
8,915,127 (GRCm39) |
missense |
unknown |
|
PIT4581001:Pkd1l1
|
UTSW |
11 |
8,866,298 (GRCm39) |
frame shift |
probably null |
|
R0020:Pkd1l1
|
UTSW |
11 |
8,825,765 (GRCm39) |
splice site |
probably benign |
|
R0020:Pkd1l1
|
UTSW |
11 |
8,825,765 (GRCm39) |
splice site |
probably benign |
|
R0496:Pkd1l1
|
UTSW |
11 |
8,879,430 (GRCm39) |
missense |
probably damaging |
0.96 |
R0547:Pkd1l1
|
UTSW |
11 |
8,786,448 (GRCm39) |
splice site |
probably benign |
|
R0582:Pkd1l1
|
UTSW |
11 |
8,881,699 (GRCm39) |
splice site |
probably benign |
|
R0761:Pkd1l1
|
UTSW |
11 |
8,804,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R0969:Pkd1l1
|
UTSW |
11 |
8,886,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R1348:Pkd1l1
|
UTSW |
11 |
8,784,806 (GRCm39) |
missense |
probably benign |
0.18 |
R1366:Pkd1l1
|
UTSW |
11 |
8,891,038 (GRCm39) |
splice site |
probably benign |
|
R1401:Pkd1l1
|
UTSW |
11 |
8,804,487 (GRCm39) |
nonsense |
probably null |
|
R1444:Pkd1l1
|
UTSW |
11 |
8,804,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R1445:Pkd1l1
|
UTSW |
11 |
8,820,313 (GRCm39) |
missense |
probably benign |
0.00 |
R1463:Pkd1l1
|
UTSW |
11 |
8,866,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R1496:Pkd1l1
|
UTSW |
11 |
8,891,077 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1542:Pkd1l1
|
UTSW |
11 |
8,824,179 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1543:Pkd1l1
|
UTSW |
11 |
8,851,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R1619:Pkd1l1
|
UTSW |
11 |
8,900,413 (GRCm39) |
missense |
probably damaging |
0.98 |
R1875:Pkd1l1
|
UTSW |
11 |
8,794,670 (GRCm39) |
splice site |
probably benign |
|
R1929:Pkd1l1
|
UTSW |
11 |
8,786,197 (GRCm39) |
splice site |
probably benign |
|
R1958:Pkd1l1
|
UTSW |
11 |
8,824,161 (GRCm39) |
missense |
probably benign |
0.01 |
R2223:Pkd1l1
|
UTSW |
11 |
8,900,422 (GRCm39) |
missense |
probably benign |
|
R2223:Pkd1l1
|
UTSW |
11 |
8,839,063 (GRCm39) |
missense |
probably benign |
0.18 |
R2264:Pkd1l1
|
UTSW |
11 |
8,829,112 (GRCm39) |
missense |
probably damaging |
0.97 |
R2349:Pkd1l1
|
UTSW |
11 |
8,776,819 (GRCm39) |
splice site |
probably null |
|
R2431:Pkd1l1
|
UTSW |
11 |
8,897,197 (GRCm39) |
missense |
probably damaging |
0.99 |
R2483:Pkd1l1
|
UTSW |
11 |
8,912,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R2517:Pkd1l1
|
UTSW |
11 |
8,908,900 (GRCm39) |
missense |
unknown |
|
R2888:Pkd1l1
|
UTSW |
11 |
8,897,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R2965:Pkd1l1
|
UTSW |
11 |
8,824,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R3123:Pkd1l1
|
UTSW |
11 |
8,923,021 (GRCm39) |
missense |
unknown |
|
R3153:Pkd1l1
|
UTSW |
11 |
8,817,207 (GRCm39) |
missense |
probably benign |
0.01 |
R3840:Pkd1l1
|
UTSW |
11 |
8,839,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R3855:Pkd1l1
|
UTSW |
11 |
8,915,047 (GRCm39) |
critical splice donor site |
probably null |
|
R3880:Pkd1l1
|
UTSW |
11 |
8,911,983 (GRCm39) |
missense |
unknown |
|
R3970:Pkd1l1
|
UTSW |
11 |
8,824,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R4195:Pkd1l1
|
UTSW |
11 |
8,859,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R4196:Pkd1l1
|
UTSW |
11 |
8,859,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R4246:Pkd1l1
|
UTSW |
11 |
8,815,543 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4247:Pkd1l1
|
UTSW |
11 |
8,815,543 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4249:Pkd1l1
|
UTSW |
11 |
8,815,543 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4250:Pkd1l1
|
UTSW |
11 |
8,815,543 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4593:Pkd1l1
|
UTSW |
11 |
8,851,253 (GRCm39) |
missense |
probably damaging |
0.97 |
R4609:Pkd1l1
|
UTSW |
11 |
8,908,964 (GRCm39) |
missense |
unknown |
|
R4797:Pkd1l1
|
UTSW |
11 |
8,911,340 (GRCm39) |
missense |
unknown |
|
R4910:Pkd1l1
|
UTSW |
11 |
8,879,360 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4940:Pkd1l1
|
UTSW |
11 |
8,794,585 (GRCm39) |
missense |
probably benign |
|
R5084:Pkd1l1
|
UTSW |
11 |
8,892,004 (GRCm39) |
missense |
probably benign |
0.05 |
R5147:Pkd1l1
|
UTSW |
11 |
8,799,003 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5360:Pkd1l1
|
UTSW |
11 |
8,829,204 (GRCm39) |
missense |
probably benign |
|
R5483:Pkd1l1
|
UTSW |
11 |
8,851,141 (GRCm39) |
critical splice donor site |
probably null |
|
R5604:Pkd1l1
|
UTSW |
11 |
8,783,877 (GRCm39) |
missense |
probably damaging |
0.98 |
R5642:Pkd1l1
|
UTSW |
11 |
8,829,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R5652:Pkd1l1
|
UTSW |
11 |
8,859,889 (GRCm39) |
missense |
probably benign |
0.03 |
R5751:Pkd1l1
|
UTSW |
11 |
8,817,204 (GRCm39) |
missense |
possibly damaging |
0.45 |
R5761:Pkd1l1
|
UTSW |
11 |
8,866,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R5800:Pkd1l1
|
UTSW |
11 |
8,811,302 (GRCm39) |
missense |
probably benign |
|
R5874:Pkd1l1
|
UTSW |
11 |
8,858,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R5897:Pkd1l1
|
UTSW |
11 |
8,829,176 (GRCm39) |
missense |
probably benign |
0.03 |
R5913:Pkd1l1
|
UTSW |
11 |
8,813,849 (GRCm39) |
missense |
probably benign |
0.00 |
R6000:Pkd1l1
|
UTSW |
11 |
8,900,427 (GRCm39) |
missense |
probably benign |
0.00 |
R6005:Pkd1l1
|
UTSW |
11 |
8,807,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R6013:Pkd1l1
|
UTSW |
11 |
8,819,452 (GRCm39) |
splice site |
probably null |
|
R6027:Pkd1l1
|
UTSW |
11 |
8,866,272 (GRCm39) |
nonsense |
probably null |
|
R6028:Pkd1l1
|
UTSW |
11 |
8,786,267 (GRCm39) |
missense |
probably benign |
0.06 |
R6129:Pkd1l1
|
UTSW |
11 |
8,818,543 (GRCm39) |
missense |
probably benign |
0.00 |
R6182:Pkd1l1
|
UTSW |
11 |
8,815,555 (GRCm39) |
missense |
probably benign |
0.36 |
R6226:Pkd1l1
|
UTSW |
11 |
8,851,287 (GRCm39) |
missense |
probably benign |
0.00 |
R6257:Pkd1l1
|
UTSW |
11 |
8,892,195 (GRCm39) |
missense |
probably benign |
0.22 |
R6340:Pkd1l1
|
UTSW |
11 |
8,794,649 (GRCm39) |
missense |
probably benign |
0.09 |
R6478:Pkd1l1
|
UTSW |
11 |
8,813,911 (GRCm39) |
missense |
probably benign |
0.00 |
R6558:Pkd1l1
|
UTSW |
11 |
8,839,052 (GRCm39) |
missense |
probably benign |
0.00 |
R6750:Pkd1l1
|
UTSW |
11 |
8,923,217 (GRCm39) |
missense |
unknown |
|
R6987:Pkd1l1
|
UTSW |
11 |
8,852,575 (GRCm39) |
missense |
probably benign |
0.01 |
R6996:Pkd1l1
|
UTSW |
11 |
8,799,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R7139:Pkd1l1
|
UTSW |
11 |
8,840,737 (GRCm39) |
missense |
|
|
R7224:Pkd1l1
|
UTSW |
11 |
8,895,241 (GRCm39) |
missense |
|
|
R7244:Pkd1l1
|
UTSW |
11 |
8,821,771 (GRCm39) |
missense |
|
|
R7265:Pkd1l1
|
UTSW |
11 |
8,879,402 (GRCm39) |
missense |
|
|
R7358:Pkd1l1
|
UTSW |
11 |
8,895,202 (GRCm39) |
missense |
|
|
R7387:Pkd1l1
|
UTSW |
11 |
8,851,203 (GRCm39) |
missense |
|
|
R7414:Pkd1l1
|
UTSW |
11 |
8,866,267 (GRCm39) |
missense |
|
|
R7459:Pkd1l1
|
UTSW |
11 |
8,852,428 (GRCm39) |
missense |
|
|
R7478:Pkd1l1
|
UTSW |
11 |
8,879,441 (GRCm39) |
missense |
|
|
R7485:Pkd1l1
|
UTSW |
11 |
8,915,148 (GRCm39) |
missense |
|
|
R7490:Pkd1l1
|
UTSW |
11 |
8,866,265 (GRCm39) |
missense |
|
|
R7644:Pkd1l1
|
UTSW |
11 |
8,825,758 (GRCm39) |
missense |
|
|
R7647:Pkd1l1
|
UTSW |
11 |
8,897,296 (GRCm39) |
missense |
|
|
R7676:Pkd1l1
|
UTSW |
11 |
8,912,708 (GRCm39) |
missense |
|
|
R7687:Pkd1l1
|
UTSW |
11 |
8,804,390 (GRCm39) |
missense |
|
|
R7699:Pkd1l1
|
UTSW |
11 |
8,915,142 (GRCm39) |
missense |
|
|
R7922:Pkd1l1
|
UTSW |
11 |
8,859,857 (GRCm39) |
missense |
|
|
R7922:Pkd1l1
|
UTSW |
11 |
8,799,013 (GRCm39) |
missense |
|
|
R7980:Pkd1l1
|
UTSW |
11 |
8,804,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R7993:Pkd1l1
|
UTSW |
11 |
8,895,262 (GRCm39) |
missense |
|
|
R8052:Pkd1l1
|
UTSW |
11 |
8,897,315 (GRCm39) |
missense |
|
|
R8125:Pkd1l1
|
UTSW |
11 |
8,897,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R8420:Pkd1l1
|
UTSW |
11 |
8,820,277 (GRCm39) |
nonsense |
probably null |
|
R8675:Pkd1l1
|
UTSW |
11 |
8,798,916 (GRCm39) |
critical splice donor site |
probably null |
|
R8683:Pkd1l1
|
UTSW |
11 |
8,821,805 (GRCm39) |
missense |
|
|
R8709:Pkd1l1
|
UTSW |
11 |
8,805,567 (GRCm39) |
missense |
|
|
R8711:Pkd1l1
|
UTSW |
11 |
8,815,550 (GRCm39) |
missense |
|
|
R8725:Pkd1l1
|
UTSW |
11 |
8,911,482 (GRCm39) |
missense |
|
|
R8733:Pkd1l1
|
UTSW |
11 |
8,883,657 (GRCm39) |
missense |
|
|
R8822:Pkd1l1
|
UTSW |
11 |
8,806,312 (GRCm39) |
missense |
|
|
R8871:Pkd1l1
|
UTSW |
11 |
8,900,503 (GRCm39) |
missense |
|
|
R9009:Pkd1l1
|
UTSW |
11 |
8,881,552 (GRCm39) |
missense |
|
|
R9099:Pkd1l1
|
UTSW |
11 |
8,922,986 (GRCm39) |
missense |
|
|
R9119:Pkd1l1
|
UTSW |
11 |
8,829,107 (GRCm39) |
missense |
|
|
R9150:Pkd1l1
|
UTSW |
11 |
8,786,256 (GRCm39) |
missense |
|
|
R9314:Pkd1l1
|
UTSW |
11 |
8,829,153 (GRCm39) |
missense |
|
|
R9341:Pkd1l1
|
UTSW |
11 |
8,911,305 (GRCm39) |
missense |
|
|
R9341:Pkd1l1
|
UTSW |
11 |
8,786,399 (GRCm39) |
missense |
|
|
R9343:Pkd1l1
|
UTSW |
11 |
8,911,305 (GRCm39) |
missense |
|
|
R9343:Pkd1l1
|
UTSW |
11 |
8,786,399 (GRCm39) |
missense |
|
|
R9392:Pkd1l1
|
UTSW |
11 |
8,794,567 (GRCm39) |
missense |
|
|
R9424:Pkd1l1
|
UTSW |
11 |
8,820,091 (GRCm39) |
missense |
|
|
R9496:Pkd1l1
|
UTSW |
11 |
8,783,773 (GRCm39) |
critical splice donor site |
probably null |
|
R9504:Pkd1l1
|
UTSW |
11 |
8,815,631 (GRCm39) |
missense |
|
|
R9563:Pkd1l1
|
UTSW |
11 |
8,815,502 (GRCm39) |
missense |
|
|
R9570:Pkd1l1
|
UTSW |
11 |
8,840,697 (GRCm39) |
missense |
|
|
R9585:Pkd1l1
|
UTSW |
11 |
8,804,390 (GRCm39) |
missense |
|
|
R9618:Pkd1l1
|
UTSW |
11 |
8,911,420 (GRCm39) |
missense |
|
|
R9709:Pkd1l1
|
UTSW |
11 |
8,799,016 (GRCm39) |
missense |
probably damaging |
0.98 |
R9741:Pkd1l1
|
UTSW |
11 |
8,897,224 (GRCm39) |
missense |
|
|
R9801:Pkd1l1
|
UTSW |
11 |
8,908,964 (GRCm39) |
nonsense |
probably null |
|
X0024:Pkd1l1
|
UTSW |
11 |
8,900,413 (GRCm39) |
missense |
probably benign |
0.01 |
X0063:Pkd1l1
|
UTSW |
11 |
8,879,430 (GRCm39) |
missense |
probably damaging |
0.96 |
X0065:Pkd1l1
|
UTSW |
11 |
8,859,921 (GRCm39) |
missense |
probably benign |
0.10 |
Z1176:Pkd1l1
|
UTSW |
11 |
8,776,801 (GRCm39) |
missense |
|
|
Z1177:Pkd1l1
|
UTSW |
11 |
8,895,208 (GRCm39) |
missense |
|
|
|