Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadac |
C |
T |
3: 59,943,275 (GRCm39) |
T60M |
probably benign |
Het |
Actn4 |
C |
T |
7: 28,661,509 (GRCm39) |
A34T |
probably benign |
Het |
Acvrl1 |
A |
G |
15: 101,041,245 (GRCm39) |
M466V |
probably benign |
Het |
Adamts7 |
T |
C |
9: 90,067,868 (GRCm39) |
Y453H |
probably damaging |
Het |
Amfr |
G |
A |
8: 94,711,484 (GRCm39) |
P351S |
probably damaging |
Het |
Ankrd26 |
G |
A |
6: 118,516,688 (GRCm39) |
T492M |
probably benign |
Het |
Anxa6 |
A |
G |
11: 54,876,993 (GRCm39) |
F547L |
probably damaging |
Het |
Ap5m1 |
T |
G |
14: 49,318,384 (GRCm39) |
Y394D |
unknown |
Het |
Atic |
G |
A |
1: 71,610,014 (GRCm39) |
V342I |
probably benign |
Het |
Atl1 |
C |
A |
12: 70,002,127 (GRCm39) |
T362N |
probably benign |
Het |
Atp10a |
A |
T |
7: 58,447,219 (GRCm39) |
M654L |
probably benign |
Het |
B3gnt5 |
A |
T |
16: 19,588,503 (GRCm39) |
M241L |
probably benign |
Het |
Bbs7 |
A |
G |
3: 36,659,877 (GRCm39) |
V186A |
possibly damaging |
Het |
Brme1 |
A |
G |
8: 84,898,842 (GRCm39) |
T577A |
probably benign |
Het |
C8b |
T |
C |
4: 104,637,795 (GRCm39) |
L89P |
probably damaging |
Het |
Capn7 |
G |
T |
14: 31,092,678 (GRCm39) |
E742* |
probably null |
Het |
Ccdc162 |
G |
A |
10: 41,437,187 (GRCm39) |
R1741C |
probably damaging |
Het |
Cdhr17 |
T |
C |
5: 17,041,592 (GRCm39) |
V615A |
possibly damaging |
Het |
Chsy3 |
T |
A |
18: 59,542,047 (GRCm39) |
L395H |
probably damaging |
Het |
Cnot9 |
A |
G |
1: 74,556,388 (GRCm39) |
T62A |
probably benign |
Het |
Cyfip1 |
AGTGT |
AGT |
7: 55,577,937 (GRCm39) |
|
probably null |
Het |
Cyp2d12 |
T |
A |
15: 82,441,849 (GRCm39) |
|
probably null |
Het |
Dnah7a |
A |
G |
1: 53,436,420 (GRCm39) |
V3974A |
probably benign |
Het |
Dync1h1 |
G |
A |
12: 110,584,196 (GRCm39) |
G533D |
possibly damaging |
Het |
Eddm13 |
T |
G |
7: 6,271,801 (GRCm39) |
M77R |
probably benign |
Het |
Elfn1 |
A |
G |
5: 139,958,228 (GRCm39) |
S411G |
probably benign |
Het |
Enpp3 |
T |
C |
10: 24,652,782 (GRCm39) |
D725G |
possibly damaging |
Het |
Fmnl1 |
T |
C |
11: 103,073,595 (GRCm39) |
|
probably null |
Het |
Fndc8 |
T |
C |
11: 82,783,151 (GRCm39) |
M44T |
probably benign |
Het |
Gcgr |
A |
T |
11: 120,425,538 (GRCm39) |
|
probably benign |
Het |
Ggt1 |
T |
A |
10: 75,410,110 (GRCm39) |
V14D |
possibly damaging |
Het |
Gigyf2 |
A |
G |
1: 87,331,447 (GRCm39) |
I198M |
unknown |
Het |
Gm40460 |
GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG |
GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG |
7: 141,794,171 (GRCm39) |
|
probably benign |
Het |
Gm6034 |
T |
A |
17: 36,367,331 (GRCm39) |
S59T |
unknown |
Het |
Gm6408 |
G |
A |
5: 146,421,180 (GRCm39) |
V270I |
probably benign |
Het |
Gpr20 |
A |
T |
15: 73,567,981 (GRCm39) |
I136N |
probably damaging |
Het |
Ide |
T |
C |
19: 37,268,160 (GRCm39) |
E565G |
|
Het |
Igsf9 |
T |
C |
1: 172,322,349 (GRCm39) |
S515P |
probably damaging |
Het |
Kbtbd12 |
G |
A |
6: 88,590,965 (GRCm39) |
R416* |
probably null |
Het |
Kcnd3 |
A |
T |
3: 105,576,400 (GRCm39) |
I615F |
probably damaging |
Het |
Kcnk7 |
A |
T |
19: 5,756,805 (GRCm39) |
M265L |
probably benign |
Het |
Klhdc1 |
G |
A |
12: 69,309,923 (GRCm39) |
S275N |
probably damaging |
Het |
Ldc1 |
C |
G |
4: 130,112,992 (GRCm39) |
A135P |
probably damaging |
Het |
Lrba |
A |
C |
3: 86,302,553 (GRCm39) |
N1871T |
probably damaging |
Het |
Lrrk1 |
A |
G |
7: 65,982,134 (GRCm39) |
V169A |
probably damaging |
Het |
Magi1 |
A |
G |
6: 93,660,070 (GRCm39) |
I1175T |
probably benign |
Het |
Man1a2 |
T |
C |
3: 100,489,369 (GRCm39) |
T537A |
possibly damaging |
Het |
Mrpl17 |
T |
C |
7: 105,459,209 (GRCm39) |
N129S |
probably damaging |
Het |
Mup5 |
G |
A |
4: 61,750,622 (GRCm39) |
R174C |
probably damaging |
Het |
Ndufaf1 |
G |
A |
2: 119,488,877 (GRCm39) |
R216C |
probably damaging |
Het |
Neb |
T |
C |
2: 52,224,671 (GRCm39) |
|
probably null |
Het |
Olfml3 |
T |
C |
3: 103,643,176 (GRCm39) |
K402E |
probably damaging |
Het |
Or52m2 |
A |
T |
7: 102,263,974 (GRCm39) |
M74K |
probably damaging |
Het |
Or5a1 |
T |
C |
19: 12,097,912 (GRCm39) |
T55A |
probably benign |
Het |
Or8b12b |
G |
A |
9: 37,684,711 (GRCm39) |
G252D |
possibly damaging |
Het |
Osbpl8 |
C |
T |
10: 111,110,872 (GRCm39) |
P458L |
possibly damaging |
Het |
Pcdh20 |
T |
C |
14: 88,706,511 (GRCm39) |
E263G |
possibly damaging |
Het |
Plxdc1 |
T |
C |
11: 97,823,153 (GRCm39) |
T363A |
possibly damaging |
Het |
Pole3 |
T |
C |
4: 62,442,287 (GRCm39) |
D111G |
unknown |
Het |
R3hdm2 |
T |
A |
10: 127,294,022 (GRCm39) |
L172Q |
probably damaging |
Het |
Rbm33 |
T |
C |
5: 28,599,322 (GRCm39) |
V90A |
|
Het |
Rcbtb1 |
C |
G |
14: 59,465,828 (GRCm39) |
I390M |
probably damaging |
Het |
Romo1 |
G |
A |
2: 155,986,295 (GRCm39) |
|
probably benign |
Het |
Sars1 |
A |
G |
3: 108,335,519 (GRCm39) |
Y410H |
probably damaging |
Het |
Sesn2 |
T |
C |
4: 132,224,724 (GRCm39) |
T327A |
probably benign |
Het |
Slc30a5 |
A |
G |
13: 100,945,762 (GRCm39) |
V530A |
probably damaging |
Het |
Slc30a9 |
G |
A |
5: 67,473,044 (GRCm39) |
E43K |
probably benign |
Het |
Slc38a2 |
A |
C |
15: 96,589,240 (GRCm39) |
L418W |
probably damaging |
Het |
Snx14 |
T |
C |
9: 88,276,614 (GRCm39) |
E557G |
possibly damaging |
Het |
Spata33 |
T |
A |
8: 123,948,737 (GRCm39) |
I123K |
probably damaging |
Het |
Tdrd3 |
A |
T |
14: 87,714,839 (GRCm39) |
H170L |
probably damaging |
Het |
Trpm1 |
A |
G |
7: 63,868,854 (GRCm39) |
|
probably null |
Het |
Tsr3 |
A |
T |
17: 25,461,569 (GRCm39) |
E302D |
probably benign |
Het |
Ttll11 |
A |
G |
2: 35,792,685 (GRCm39) |
I386T |
probably damaging |
Het |
Usp2 |
C |
T |
9: 43,987,266 (GRCm39) |
T188M |
possibly damaging |
Het |
Usp44 |
A |
G |
10: 93,681,855 (GRCm39) |
I102V |
probably benign |
Het |
Wasf1 |
A |
G |
10: 40,802,546 (GRCm39) |
N67S |
probably benign |
Het |
Zfp445 |
T |
C |
9: 122,681,208 (GRCm39) |
N911S |
probably benign |
Het |
Zfp467 |
A |
G |
6: 48,421,903 (GRCm39) |
|
probably null |
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 |
R5930:Pkd1l1
|
UTSW |
11 |
8,908,969 (GRCm39) |
missense |
unknown |
|
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 |
|
|
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 |
8,799,013 (GRCm39) |
missense |
|
|
R7922:Pkd1l1
|
UTSW |
11 |
8,859,857 (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 |
|
|
|