Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy10 |
A |
T |
1: 165,337,866 (GRCm39) |
E160V |
probably damaging |
Het |
Amdhd2 |
T |
C |
17: 24,376,860 (GRCm39) |
|
probably null |
Het |
Angel1 |
A |
C |
12: 86,749,093 (GRCm39) |
L656V |
probably damaging |
Het |
Ankrd12 |
G |
A |
17: 66,293,681 (GRCm39) |
S584L |
possibly damaging |
Het |
Apbb2 |
T |
A |
5: 66,464,958 (GRCm39) |
N679Y |
probably benign |
Het |
Arid3c |
T |
A |
4: 41,724,744 (GRCm39) |
I364F |
probably damaging |
Het |
Bcan |
T |
A |
3: 87,900,401 (GRCm39) |
S611C |
probably damaging |
Het |
Bnip3 |
T |
G |
7: 138,496,359 (GRCm39) |
|
silent |
Het |
Btc |
T |
C |
5: 91,510,260 (GRCm39) |
Y111C |
probably damaging |
Het |
Carnmt1 |
T |
C |
19: 18,680,734 (GRCm39) |
L336P |
probably damaging |
Het |
Ccdc83 |
C |
T |
7: 89,873,285 (GRCm39) |
V357I |
probably damaging |
Het |
Cd2bp2 |
T |
C |
7: 126,793,050 (GRCm39) |
D324G |
probably benign |
Het |
Cdc20b |
A |
G |
13: 113,208,451 (GRCm39) |
T216A |
probably benign |
Het |
Cdk17 |
T |
C |
10: 93,064,540 (GRCm39) |
Y270H |
probably damaging |
Het |
Cenpv |
T |
C |
11: 62,416,059 (GRCm39) |
E230G |
probably benign |
Het |
Chst11 |
T |
C |
10: 83,027,004 (GRCm39) |
Y144H |
probably damaging |
Het |
Cracr2a |
T |
A |
6: 127,584,261 (GRCm39) |
F107I |
probably damaging |
Het |
Cyfip1 |
G |
T |
7: 55,549,705 (GRCm39) |
R624L |
probably null |
Het |
Cyp27b1 |
T |
A |
10: 126,884,181 (GRCm39) |
V11D |
probably damaging |
Het |
Ddc |
T |
C |
11: 11,785,764 (GRCm39) |
N308D |
probably damaging |
Het |
Des |
T |
G |
1: 75,340,137 (GRCm39) |
M348R |
probably damaging |
Het |
Dis3l |
T |
A |
9: 64,238,165 (GRCm39) |
D109V |
probably damaging |
Het |
Dnah3 |
T |
A |
7: 119,574,352 (GRCm39) |
I2136F |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,867,224 (GRCm39) |
S2785G |
probably benign |
Het |
Dop1a |
T |
G |
9: 86,376,471 (GRCm39) |
V235G |
probably damaging |
Het |
Dtx3l |
A |
T |
16: 35,754,059 (GRCm39) |
D182E |
possibly damaging |
Het |
Efcab6 |
A |
G |
15: 83,777,163 (GRCm39) |
|
probably benign |
Het |
Elac2 |
T |
A |
11: 64,870,015 (GRCm39) |
S27T |
probably benign |
Het |
Emsy |
T |
G |
7: 98,275,830 (GRCm39) |
K352N |
probably damaging |
Het |
Erbb4 |
T |
C |
1: 68,238,047 (GRCm39) |
N814S |
probably damaging |
Het |
Fgd6 |
T |
C |
10: 93,880,868 (GRCm39) |
V574A |
probably benign |
Het |
Filip1 |
T |
C |
9: 79,727,212 (GRCm39) |
E469G |
probably damaging |
Het |
Fmo1 |
A |
T |
1: 162,661,424 (GRCm39) |
D286E |
probably damaging |
Het |
Fmo4 |
A |
T |
1: 162,626,616 (GRCm39) |
I310N |
possibly damaging |
Het |
Focad |
A |
G |
4: 88,260,449 (GRCm39) |
N902D |
unknown |
Het |
Focad |
A |
G |
4: 88,315,416 (GRCm39) |
S1525G |
probably benign |
Het |
Fras1 |
T |
C |
5: 96,815,296 (GRCm39) |
W1338R |
probably benign |
Het |
Fry |
A |
G |
5: 150,324,389 (GRCm39) |
I1151V |
probably null |
Het |
Garin5b |
T |
A |
7: 4,761,186 (GRCm39) |
T509S |
probably benign |
Het |
Gm10076 |
T |
G |
14: 105,919,304 (GRCm39) |
|
noncoding transcript |
Het |
Gm5698 |
T |
G |
1: 31,017,042 (GRCm39) |
D3A |
probably damaging |
Het |
Gngt2 |
C |
T |
11: 95,735,972 (GRCm39) |
|
probably benign |
Het |
Gsdma |
T |
C |
11: 98,562,193 (GRCm39) |
|
probably null |
Het |
Gtf2h3 |
A |
T |
5: 124,740,262 (GRCm39) |
|
probably benign |
Het |
Hkdc1 |
T |
C |
10: 62,253,677 (GRCm39) |
T35A |
probably benign |
Het |
Irs1 |
T |
C |
1: 82,266,180 (GRCm39) |
S679G |
probably benign |
Het |
Itpr1 |
T |
A |
6: 108,470,716 (GRCm39) |
C2214S |
probably damaging |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
Kcnk16 |
A |
G |
14: 20,315,347 (GRCm39) |
V72A |
probably damaging |
Het |
Lipa |
T |
A |
19: 34,488,290 (GRCm39) |
R119* |
probably null |
Het |
Matr3 |
T |
A |
18: 35,721,378 (GRCm39) |
|
probably benign |
Het |
Med13l |
T |
G |
5: 118,866,898 (GRCm39) |
F651V |
probably benign |
Het |
Mfsd11 |
T |
C |
11: 116,764,740 (GRCm39) |
V388A |
probably benign |
Het |
Mki67 |
C |
T |
7: 135,299,794 (GRCm39) |
V1747I |
possibly damaging |
Het |
Mms22l |
T |
C |
4: 24,535,936 (GRCm39) |
|
probably benign |
Het |
Msh5 |
A |
G |
17: 35,263,366 (GRCm39) |
I154T |
probably benign |
Het |
Myo5b |
G |
T |
18: 74,866,996 (GRCm39) |
L1382F |
probably damaging |
Het |
Ncbp2 |
T |
C |
16: 31,775,769 (GRCm39) |
Y138H |
probably damaging |
Het |
Ndufv1 |
C |
A |
19: 4,058,347 (GRCm39) |
R359L |
probably benign |
Het |
Ntrk3 |
A |
C |
7: 78,166,471 (GRCm39) |
|
probably null |
Het |
Or1e1c |
T |
A |
11: 73,266,427 (GRCm39) |
V287E |
probably damaging |
Het |
Or4a15 |
A |
G |
2: 89,193,353 (GRCm39) |
V140A |
probably benign |
Het |
Or8b12i |
T |
A |
9: 20,082,705 (GRCm39) |
H54L |
possibly damaging |
Het |
P4ha1 |
A |
G |
10: 59,206,859 (GRCm39) |
E523G |
probably damaging |
Het |
Per3 |
T |
A |
4: 151,103,342 (GRCm39) |
Y530F |
probably damaging |
Het |
Pes1 |
C |
A |
11: 3,919,524 (GRCm39) |
L66I |
probably damaging |
Het |
Pigr |
G |
A |
1: 130,774,399 (GRCm39) |
|
probably benign |
Het |
Plch1 |
T |
A |
3: 63,651,956 (GRCm39) |
K378N |
probably damaging |
Het |
Plxnb1 |
T |
C |
9: 108,931,776 (GRCm39) |
|
probably null |
Het |
Pramel22 |
G |
A |
4: 143,380,712 (GRCm39) |
T437I |
probably damaging |
Het |
Prkdc |
A |
G |
16: 15,472,681 (GRCm39) |
|
probably null |
Het |
Prrc1 |
G |
T |
18: 57,514,718 (GRCm39) |
D312Y |
probably damaging |
Het |
Psma5-ps |
A |
G |
10: 85,149,595 (GRCm39) |
|
noncoding transcript |
Het |
Rab3gap2 |
T |
A |
1: 185,015,739 (GRCm39) |
|
probably null |
Het |
Rgs3 |
A |
G |
4: 62,620,384 (GRCm39) |
I537V |
probably damaging |
Het |
Rhobtb2 |
T |
G |
14: 70,033,893 (GRCm39) |
D444A |
probably damaging |
Het |
Rnf40 |
T |
C |
7: 127,190,956 (GRCm39) |
S314P |
probably damaging |
Het |
Rngtt |
T |
A |
4: 33,500,302 (GRCm39) |
C565* |
probably null |
Het |
Samd3 |
A |
G |
10: 26,139,884 (GRCm39) |
|
probably benign |
Het |
Sec61a2 |
A |
G |
2: 5,878,547 (GRCm39) |
|
probably benign |
Het |
Serpina3m |
G |
A |
12: 104,355,581 (GRCm39) |
A83T |
probably damaging |
Het |
Serpinb13 |
A |
T |
1: 106,926,756 (GRCm39) |
I251L |
possibly damaging |
Het |
Sez6 |
C |
T |
11: 77,863,758 (GRCm39) |
T439I |
probably damaging |
Het |
Shc1 |
G |
A |
3: 89,330,849 (GRCm39) |
G91S |
probably damaging |
Het |
Slc26a2 |
A |
G |
18: 61,331,650 (GRCm39) |
C594R |
possibly damaging |
Het |
Specc1l |
C |
T |
10: 75,081,438 (GRCm39) |
S278F |
probably damaging |
Het |
Spg11 |
C |
T |
2: 121,890,688 (GRCm39) |
V2044M |
probably damaging |
Het |
Stx18 |
T |
A |
5: 38,285,383 (GRCm39) |
|
probably null |
Het |
Suclg2 |
T |
C |
6: 95,566,075 (GRCm39) |
|
probably benign |
Het |
Tlr4 |
A |
T |
4: 66,757,681 (GRCm39) |
H158L |
probably damaging |
Het |
Tmem131 |
A |
G |
1: 36,851,352 (GRCm39) |
V966A |
possibly damaging |
Het |
Tram1l1 |
T |
A |
3: 124,115,635 (GRCm39) |
I265N |
probably damaging |
Het |
Trim58 |
T |
A |
11: 58,531,493 (GRCm39) |
F67Y |
possibly damaging |
Het |
Ttc19 |
A |
G |
11: 62,172,650 (GRCm39) |
Q74R |
probably benign |
Het |
Usp7 |
T |
C |
16: 8,516,333 (GRCm39) |
S649G |
probably benign |
Het |
Vmn2r16 |
A |
G |
5: 109,487,124 (GRCm39) |
Y115C |
possibly damaging |
Het |
Zfp444 |
T |
C |
7: 6,192,554 (GRCm39) |
C191R |
probably damaging |
Het |
Zfp451 |
A |
G |
1: 33,821,274 (GRCm39) |
F151L |
probably damaging |
Het |
Zfp451 |
G |
A |
1: 33,822,937 (GRCm39) |
P99S |
probably benign |
Het |
Zfp729b |
A |
T |
13: 67,740,352 (GRCm39) |
C648S |
probably damaging |
Het |
Zfp799 |
A |
G |
17: 33,040,777 (GRCm39) |
Y58H |
probably damaging |
Het |
Zfp804b |
A |
G |
5: 6,819,748 (GRCm39) |
V1069A |
probably benign |
Het |
Zfp938 |
C |
T |
10: 82,061,381 (GRCm39) |
G413D |
probably damaging |
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 |
|
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 |
|
|
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 |
|
|
|