Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp2c2 |
T |
C |
8: 119,749,126 (GRCm38) |
V586A |
probably benign |
Het |
Atp8a2 |
T |
A |
14: 59,791,183 (GRCm38) |
H945L |
probably benign |
Het |
Bfar |
G |
T |
16: 13,688,846 (GRCm38) |
V187F |
probably damaging |
Het |
C130026I21Rik |
A |
G |
1: 85,254,186 (GRCm38) |
|
probably benign |
Het |
Capn2 |
A |
T |
1: 182,517,137 (GRCm38) |
I73N |
probably damaging |
Het |
Cfc1 |
C |
A |
1: 34,536,473 (GRCm38) |
A76E |
possibly damaging |
Het |
Chl1 |
T |
C |
6: 103,690,242 (GRCm38) |
F398L |
probably benign |
Het |
Cyp2u1 |
A |
G |
3: 131,302,701 (GRCm38) |
S143P |
probably damaging |
Het |
Dlgap4 |
T |
A |
2: 156,749,136 (GRCm38) |
Y57* |
probably null |
Het |
Epha4 |
T |
A |
1: 77,374,926 (GRCm38) |
R897S |
probably benign |
Het |
Fscn2 |
A |
T |
11: 120,366,685 (GRCm38) |
T291S |
probably damaging |
Het |
Gga1 |
G |
A |
15: 78,888,470 (GRCm38) |
S267N |
probably damaging |
Het |
Gigyf2 |
A |
G |
1: 87,449,128 (GRCm38) |
T1287A |
probably damaging |
Het |
Gm10037 |
T |
C |
13: 67,842,990 (GRCm38) |
|
probably benign |
Het |
Gm10845 |
C |
A |
14: 79,863,229 (GRCm38) |
|
noncoding transcript |
Het |
Gm11559 |
T |
A |
11: 99,865,056 (GRCm38) |
L177Q |
unknown |
Het |
Itga9 |
A |
G |
9: 118,843,502 (GRCm38) |
T195A |
probably benign |
Het |
Lama1 |
A |
G |
17: 67,767,033 (GRCm38) |
T935A |
probably benign |
Het |
Lrrn1 |
G |
A |
6: 107,568,366 (GRCm38) |
C375Y |
probably damaging |
Het |
Maip1 |
T |
C |
1: 57,409,985 (GRCm38) |
|
probably null |
Het |
Mecom |
A |
T |
3: 29,987,088 (GRCm38) |
I119N |
probably damaging |
Het |
Mrpl2 |
G |
A |
17: 46,647,499 (GRCm38) |
R69H |
probably benign |
Het |
Muc16 |
A |
G |
9: 18,510,477 (GRCm38) |
V8246A |
possibly damaging |
Het |
Myh3 |
C |
T |
11: 67,088,736 (GRCm38) |
|
probably benign |
Het |
Myocd |
A |
G |
11: 65,196,394 (GRCm38) |
S236P |
probably benign |
Het |
Myot |
A |
T |
18: 44,337,058 (GRCm38) |
Q34L |
possibly damaging |
Het |
Nlrp5 |
A |
G |
7: 23,418,639 (GRCm38) |
D596G |
probably damaging |
Het |
Npas2 |
T |
C |
1: 39,333,912 (GRCm38) |
S415P |
possibly damaging |
Het |
Obox2 |
A |
G |
7: 15,397,041 (GRCm38) |
E66G |
probably benign |
Het |
Olfr1312 |
G |
T |
2: 112,042,246 (GRCm38) |
T262K |
probably benign |
Het |
Pcdh9 |
G |
A |
14: 93,888,305 (GRCm38) |
P143L |
probably damaging |
Het |
Phactr1 |
G |
T |
13: 43,094,897 (GRCm38) |
V356L |
probably damaging |
Het |
Pparg |
A |
T |
6: 115,473,281 (GRCm38) |
I414L |
probably benign |
Het |
Rapgef6 |
A |
T |
11: 54,626,594 (GRCm38) |
I371L |
possibly damaging |
Het |
Rc3h1 |
T |
C |
1: 160,954,973 (GRCm38) |
V674A |
probably benign |
Het |
Rps6ka4 |
T |
C |
19: 6,838,149 (GRCm38) |
Y159C |
probably damaging |
Het |
Sf3b6 |
T |
C |
12: 4,826,808 (GRCm38) |
I67T |
possibly damaging |
Het |
Spata17 |
T |
C |
1: 187,183,215 (GRCm38) |
|
probably benign |
Het |
Ston1 |
A |
G |
17: 88,635,816 (GRCm38) |
T217A |
probably benign |
Het |
Tank |
A |
G |
2: 61,650,098 (GRCm38) |
D326G |
possibly damaging |
Het |
Tbc1d9 |
T |
A |
8: 83,249,595 (GRCm38) |
N594K |
probably damaging |
Het |
Tfpi2 |
T |
A |
6: 3,965,507 (GRCm38) |
T102S |
probably benign |
Het |
Ulk4 |
T |
G |
9: 121,204,805 (GRCm38) |
E589D |
possibly damaging |
Het |
Usp40 |
A |
T |
1: 87,994,225 (GRCm38) |
H305Q |
probably damaging |
Het |
Vmn1r170 |
A |
G |
7: 23,606,329 (GRCm38) |
K52R |
probably benign |
Het |
Vmn1r194 |
A |
G |
13: 22,244,963 (GRCm38) |
D250G |
probably damaging |
Het |
Wdr6 |
A |
T |
9: 108,574,655 (GRCm38) |
D676E |
possibly damaging |
Het |
Xirp2 |
T |
A |
2: 67,510,835 (GRCm38) |
V1140E |
probably damaging |
Het |
|
Other mutations in Lrrk1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01365:Lrrk1
|
APN |
7 |
66,287,701 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01511:Lrrk1
|
APN |
7 |
66,265,450 (GRCm38) |
missense |
possibly damaging |
0.48 |
IGL02337:Lrrk1
|
APN |
7 |
66,279,416 (GRCm38) |
missense |
possibly damaging |
0.92 |
IGL02636:Lrrk1
|
APN |
7 |
66,308,659 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02679:Lrrk1
|
APN |
7 |
66,274,872 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02711:Lrrk1
|
APN |
7 |
66,330,767 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02742:Lrrk1
|
APN |
7 |
66,308,691 (GRCm38) |
missense |
probably benign |
0.12 |
IGL02878:Lrrk1
|
APN |
7 |
66,262,563 (GRCm38) |
missense |
probably benign |
|
IGL03135:Lrrk1
|
APN |
7 |
66,262,890 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03191:Lrrk1
|
APN |
7 |
66,259,959 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL03198:Lrrk1
|
APN |
7 |
66,306,894 (GRCm38) |
missense |
probably damaging |
1.00 |
combustion
|
UTSW |
7 |
66,262,665 (GRCm38) |
missense |
possibly damaging |
0.94 |
fluorine
|
UTSW |
7 |
66,302,710 (GRCm38) |
missense |
possibly damaging |
0.89 |
halide
|
UTSW |
7 |
66,265,474 (GRCm38) |
missense |
possibly damaging |
0.82 |
Heiland
|
UTSW |
7 |
66,262,733 (GRCm38) |
missense |
probably damaging |
0.96 |
liebster
|
UTSW |
7 |
66,294,981 (GRCm38) |
missense |
probably damaging |
1.00 |
magi
|
UTSW |
7 |
66,281,648 (GRCm38) |
missense |
probably damaging |
1.00 |
oxidation
|
UTSW |
7 |
66,279,372 (GRCm38) |
missense |
probably benign |
0.00 |
phlogiston
|
UTSW |
7 |
66,278,520 (GRCm38) |
splice site |
probably benign |
|
Savior
|
UTSW |
7 |
66,262,487 (GRCm38) |
missense |
probably damaging |
1.00 |
wenig
|
UTSW |
7 |
66,273,001 (GRCm38) |
missense |
probably damaging |
1.00 |
R0105:Lrrk1
|
UTSW |
7 |
66,292,341 (GRCm38) |
missense |
probably damaging |
1.00 |
R0105:Lrrk1
|
UTSW |
7 |
66,292,341 (GRCm38) |
missense |
probably damaging |
1.00 |
R0276:Lrrk1
|
UTSW |
7 |
66,296,263 (GRCm38) |
splice site |
probably benign |
|
R0505:Lrrk1
|
UTSW |
7 |
66,290,908 (GRCm38) |
splice site |
probably null |
|
R0609:Lrrk1
|
UTSW |
7 |
66,266,615 (GRCm38) |
splice site |
probably null |
|
R0650:Lrrk1
|
UTSW |
7 |
66,292,336 (GRCm38) |
missense |
probably damaging |
1.00 |
R0676:Lrrk1
|
UTSW |
7 |
66,294,981 (GRCm38) |
missense |
probably damaging |
1.00 |
R1157:Lrrk1
|
UTSW |
7 |
66,262,283 (GRCm38) |
missense |
probably benign |
0.00 |
R1435:Lrrk1
|
UTSW |
7 |
66,273,028 (GRCm38) |
missense |
probably damaging |
1.00 |
R1468:Lrrk1
|
UTSW |
7 |
66,259,974 (GRCm38) |
missense |
probably damaging |
1.00 |
R1468:Lrrk1
|
UTSW |
7 |
66,259,974 (GRCm38) |
missense |
probably damaging |
1.00 |
R1498:Lrrk1
|
UTSW |
7 |
66,302,671 (GRCm38) |
nonsense |
probably null |
|
R1884:Lrrk1
|
UTSW |
7 |
66,262,437 (GRCm38) |
missense |
probably benign |
|
R1891:Lrrk1
|
UTSW |
7 |
66,279,300 (GRCm38) |
missense |
probably damaging |
1.00 |
R1989:Lrrk1
|
UTSW |
7 |
66,281,684 (GRCm38) |
missense |
probably damaging |
1.00 |
R2107:Lrrk1
|
UTSW |
7 |
66,279,282 (GRCm38) |
missense |
probably damaging |
1.00 |
R2140:Lrrk1
|
UTSW |
7 |
66,330,750 (GRCm38) |
missense |
probably damaging |
1.00 |
R2144:Lrrk1
|
UTSW |
7 |
66,296,163 (GRCm38) |
missense |
probably damaging |
0.98 |
R2147:Lrrk1
|
UTSW |
7 |
66,285,411 (GRCm38) |
splice site |
probably null |
|
R3176:Lrrk1
|
UTSW |
7 |
66,305,521 (GRCm38) |
missense |
possibly damaging |
0.69 |
R3276:Lrrk1
|
UTSW |
7 |
66,305,521 (GRCm38) |
missense |
possibly damaging |
0.69 |
R3886:Lrrk1
|
UTSW |
7 |
66,292,364 (GRCm38) |
missense |
probably damaging |
1.00 |
R3893:Lrrk1
|
UTSW |
7 |
66,278,520 (GRCm38) |
splice site |
probably benign |
|
R3906:Lrrk1
|
UTSW |
7 |
66,294,903 (GRCm38) |
missense |
possibly damaging |
0.84 |
R4259:Lrrk1
|
UTSW |
7 |
66,330,764 (GRCm38) |
missense |
probably damaging |
1.00 |
R4649:Lrrk1
|
UTSW |
7 |
66,273,053 (GRCm38) |
missense |
probably benign |
0.12 |
R4653:Lrrk1
|
UTSW |
7 |
66,273,053 (GRCm38) |
missense |
probably benign |
0.12 |
R4672:Lrrk1
|
UTSW |
7 |
66,279,372 (GRCm38) |
missense |
probably benign |
0.00 |
R4693:Lrrk1
|
UTSW |
7 |
66,262,487 (GRCm38) |
missense |
probably damaging |
1.00 |
R4729:Lrrk1
|
UTSW |
7 |
66,262,293 (GRCm38) |
missense |
probably benign |
|
R4737:Lrrk1
|
UTSW |
7 |
66,306,873 (GRCm38) |
missense |
probably benign |
0.09 |
R4795:Lrrk1
|
UTSW |
7 |
66,262,665 (GRCm38) |
missense |
possibly damaging |
0.94 |
R4911:Lrrk1
|
UTSW |
7 |
66,295,454 (GRCm38) |
missense |
probably damaging |
0.97 |
R5002:Lrrk1
|
UTSW |
7 |
66,332,363 (GRCm38) |
missense |
probably damaging |
1.00 |
R5254:Lrrk1
|
UTSW |
7 |
66,307,107 (GRCm38) |
missense |
probably benign |
0.00 |
R5407:Lrrk1
|
UTSW |
7 |
66,270,797 (GRCm38) |
missense |
probably benign |
0.20 |
R5482:Lrrk1
|
UTSW |
7 |
66,330,670 (GRCm38) |
missense |
probably benign |
|
R5600:Lrrk1
|
UTSW |
7 |
66,307,215 (GRCm38) |
missense |
probably benign |
0.31 |
R5615:Lrrk1
|
UTSW |
7 |
66,287,615 (GRCm38) |
missense |
probably damaging |
1.00 |
R6041:Lrrk1
|
UTSW |
7 |
66,262,133 (GRCm38) |
missense |
probably benign |
|
R6211:Lrrk1
|
UTSW |
7 |
66,302,710 (GRCm38) |
missense |
possibly damaging |
0.89 |
R6271:Lrrk1
|
UTSW |
7 |
66,307,103 (GRCm38) |
critical splice donor site |
probably null |
|
R6276:Lrrk1
|
UTSW |
7 |
66,306,839 (GRCm38) |
splice site |
probably null |
|
R6447:Lrrk1
|
UTSW |
7 |
66,302,728 (GRCm38) |
missense |
probably benign |
0.19 |
R6478:Lrrk1
|
UTSW |
7 |
66,262,733 (GRCm38) |
missense |
probably damaging |
0.96 |
R6615:Lrrk1
|
UTSW |
7 |
66,281,648 (GRCm38) |
missense |
probably damaging |
1.00 |
R6745:Lrrk1
|
UTSW |
7 |
66,273,001 (GRCm38) |
missense |
probably damaging |
1.00 |
R6836:Lrrk1
|
UTSW |
7 |
66,342,779 (GRCm38) |
missense |
probably benign |
0.05 |
R6995:Lrrk1
|
UTSW |
7 |
66,292,342 (GRCm38) |
missense |
probably damaging |
1.00 |
R7107:Lrrk1
|
UTSW |
7 |
66,287,443 (GRCm38) |
missense |
possibly damaging |
0.94 |
R7137:Lrrk1
|
UTSW |
7 |
66,285,279 (GRCm38) |
missense |
probably benign |
0.06 |
R7203:Lrrk1
|
UTSW |
7 |
66,270,825 (GRCm38) |
missense |
probably damaging |
1.00 |
R7224:Lrrk1
|
UTSW |
7 |
66,332,386 (GRCm38) |
missense |
probably damaging |
0.99 |
R7239:Lrrk1
|
UTSW |
7 |
66,262,155 (GRCm38) |
missense |
probably benign |
|
R7440:Lrrk1
|
UTSW |
7 |
66,290,854 (GRCm38) |
missense |
probably damaging |
1.00 |
R7515:Lrrk1
|
UTSW |
7 |
66,262,562 (GRCm38) |
missense |
probably benign |
|
R7593:Lrrk1
|
UTSW |
7 |
66,308,691 (GRCm38) |
missense |
probably benign |
0.12 |
R7728:Lrrk1
|
UTSW |
7 |
66,262,715 (GRCm38) |
missense |
probably benign |
0.00 |
R7984:Lrrk1
|
UTSW |
7 |
66,300,729 (GRCm38) |
splice site |
probably null |
|
R7993:Lrrk1
|
UTSW |
7 |
66,262,454 (GRCm38) |
missense |
probably benign |
0.00 |
R8009:Lrrk1
|
UTSW |
7 |
66,265,474 (GRCm38) |
missense |
possibly damaging |
0.82 |
R8037:Lrrk1
|
UTSW |
7 |
66,285,341 (GRCm38) |
missense |
probably benign |
|
R8101:Lrrk1
|
UTSW |
7 |
66,342,782 (GRCm38) |
missense |
probably benign |
|
R8116:Lrrk1
|
UTSW |
7 |
66,262,623 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8126:Lrrk1
|
UTSW |
7 |
66,292,315 (GRCm38) |
missense |
probably damaging |
1.00 |
R8278:Lrrk1
|
UTSW |
7 |
66,278,684 (GRCm38) |
missense |
probably benign |
0.37 |
R8559:Lrrk1
|
UTSW |
7 |
66,282,327 (GRCm38) |
missense |
possibly damaging |
0.48 |
R8669:Lrrk1
|
UTSW |
7 |
66,262,596 (GRCm38) |
missense |
probably benign |
0.20 |
R8690:Lrrk1
|
UTSW |
7 |
66,302,729 (GRCm38) |
missense |
probably benign |
0.02 |
R8955:Lrrk1
|
UTSW |
7 |
66,269,825 (GRCm38) |
missense |
probably benign |
0.09 |
R9135:Lrrk1
|
UTSW |
7 |
66,278,609 (GRCm38) |
missense |
probably damaging |
1.00 |
R9380:Lrrk1
|
UTSW |
7 |
66,278,583 (GRCm38) |
missense |
probably damaging |
1.00 |
R9625:Lrrk1
|
UTSW |
7 |
66,259,918 (GRCm38) |
makesense |
probably null |
|
R9721:Lrrk1
|
UTSW |
7 |
66,274,875 (GRCm38) |
missense |
probably damaging |
1.00 |
RF018:Lrrk1
|
UTSW |
7 |
66,381,502 (GRCm38) |
missense |
possibly damaging |
0.83 |
|