Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700008P02Rik |
C |
T |
3: 6,682,310 (GRCm39) |
|
probably null |
Het |
Aanat |
A |
T |
11: 116,486,950 (GRCm39) |
|
probably null |
Het |
Abca17 |
A |
T |
17: 24,506,820 (GRCm39) |
V1178E |
possibly damaging |
Het |
Abcf3 |
T |
A |
16: 20,369,311 (GRCm39) |
|
probably null |
Het |
Alk |
A |
G |
17: 72,207,732 (GRCm39) |
M1001T |
probably benign |
Het |
Arhgap23 |
C |
A |
11: 97,391,818 (GRCm39) |
S1445Y |
probably damaging |
Het |
Atp10a |
T |
C |
7: 58,447,538 (GRCm39) |
I760T |
probably benign |
Het |
Cadm1 |
C |
T |
9: 47,768,572 (GRCm39) |
|
probably benign |
Het |
Car10 |
A |
T |
11: 93,076,105 (GRCm39) |
|
probably benign |
Het |
Casq2 |
G |
T |
3: 102,052,945 (GRCm39) |
|
probably null |
Het |
Cemip2 |
G |
A |
19: 21,809,403 (GRCm39) |
V928I |
possibly damaging |
Het |
Clec4f |
T |
C |
6: 83,632,070 (GRCm39) |
I55V |
probably benign |
Het |
Cngb1 |
T |
C |
8: 96,010,949 (GRCm39) |
|
probably benign |
Het |
Csn1s2b |
A |
G |
5: 87,972,098 (GRCm39) |
|
probably null |
Het |
Cyp2c39 |
A |
C |
19: 39,501,969 (GRCm39) |
R119S |
probably benign |
Het |
Cyp4f16 |
C |
T |
17: 32,765,652 (GRCm39) |
A345V |
probably null |
Het |
Ddx43 |
T |
C |
9: 78,321,567 (GRCm39) |
L412S |
probably damaging |
Het |
Dnajb12 |
G |
A |
10: 59,730,163 (GRCm39) |
|
probably null |
Het |
Ephx2 |
A |
G |
14: 66,347,691 (GRCm39) |
S56P |
probably benign |
Het |
Fam83h |
A |
G |
15: 75,875,849 (GRCm39) |
F496S |
probably damaging |
Het |
Gcnt4 |
T |
C |
13: 97,083,786 (GRCm39) |
S361P |
possibly damaging |
Het |
H2-T23 |
G |
T |
17: 36,341,474 (GRCm39) |
H332Q |
probably benign |
Het |
Hrob |
T |
C |
11: 102,145,859 (GRCm39) |
V45A |
probably benign |
Het |
Ift57 |
G |
T |
16: 49,519,667 (GRCm39) |
|
probably null |
Het |
Il1rl2 |
A |
G |
1: 40,391,017 (GRCm39) |
H320R |
possibly damaging |
Het |
Kansl1 |
A |
G |
11: 104,241,465 (GRCm39) |
V618A |
probably benign |
Het |
Kctd3 |
T |
C |
1: 188,728,665 (GRCm39) |
E157G |
probably benign |
Het |
Magohb |
T |
A |
6: 131,270,037 (GRCm39) |
D31V |
possibly damaging |
Het |
Mdn1 |
C |
A |
4: 32,715,713 (GRCm39) |
F1993L |
probably damaging |
Het |
Med29 |
C |
A |
7: 28,086,418 (GRCm39) |
C130F |
probably benign |
Het |
Mtmr7 |
G |
A |
8: 41,034,570 (GRCm39) |
R251C |
probably damaging |
Het |
Ncor1 |
T |
C |
11: 62,211,903 (GRCm39) |
I49V |
probably benign |
Het |
Nfkb1 |
G |
T |
3: 135,332,445 (GRCm39) |
T109K |
possibly damaging |
Het |
Pkp1 |
T |
A |
1: 135,811,648 (GRCm39) |
T408S |
probably damaging |
Het |
Plec |
A |
T |
15: 76,073,510 (GRCm39) |
D501E |
possibly damaging |
Het |
Prcp |
A |
C |
7: 92,576,976 (GRCm39) |
Y335S |
possibly damaging |
Het |
Reg2 |
T |
A |
6: 78,384,952 (GRCm39) |
Y165N |
possibly damaging |
Het |
Rnf7 |
T |
C |
9: 96,353,787 (GRCm39) |
*114W |
probably null |
Het |
Scg3 |
T |
C |
9: 75,584,090 (GRCm39) |
D137G |
probably damaging |
Het |
Serpinb7 |
T |
C |
1: 107,377,919 (GRCm39) |
V204A |
probably benign |
Het |
Sez6 |
C |
T |
11: 77,864,623 (GRCm39) |
H528Y |
probably damaging |
Het |
Sf3b1 |
A |
T |
1: 55,039,457 (GRCm39) |
S723T |
probably damaging |
Het |
Shtn1 |
T |
C |
19: 58,963,533 (GRCm39) |
D594G |
probably damaging |
Het |
Sptbn4 |
A |
G |
7: 27,063,904 (GRCm39) |
L2174P |
probably damaging |
Het |
Stk25 |
A |
G |
1: 93,553,181 (GRCm39) |
|
probably null |
Het |
Tep1 |
A |
T |
14: 51,098,505 (GRCm39) |
F429I |
probably damaging |
Het |
Thada |
T |
A |
17: 84,580,228 (GRCm39) |
I1409F |
probably benign |
Het |
Usp25 |
G |
A |
16: 76,873,909 (GRCm39) |
G495E |
probably benign |
Het |
Washc2 |
A |
G |
6: 116,231,114 (GRCm39) |
S844G |
probably damaging |
Het |
Xirp2 |
A |
T |
2: 67,341,287 (GRCm39) |
H1176L |
possibly damaging |
Het |
Ypel1 |
T |
C |
16: 16,918,129 (GRCm39) |
N96D |
probably damaging |
Het |
Zfand6 |
C |
A |
7: 84,281,900 (GRCm39) |
V110L |
probably benign |
Het |
Zfp30 |
A |
G |
7: 29,488,846 (GRCm39) |
R8G |
possibly 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 |
|
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 |
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 |
|
|
|