Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
A |
T |
10: 79,844,889 (GRCm39) |
H1537L |
probably damaging |
Het |
Actg2 |
T |
A |
6: 83,500,169 (GRCm39) |
N116I |
probably damaging |
Het |
Actn1 |
G |
A |
12: 80,219,796 (GRCm39) |
H692Y |
probably damaging |
Het |
Adamts6 |
C |
T |
13: 104,449,285 (GRCm39) |
P36S |
probably benign |
Het |
Agr3 |
G |
A |
12: 35,997,858 (GRCm39) |
|
probably null |
Het |
Ank3 |
T |
C |
10: 69,715,805 (GRCm39) |
V500A |
probably damaging |
Het |
BC051019 |
T |
A |
7: 109,317,269 (GRCm39) |
D141V |
probably damaging |
Het |
Bco1 |
T |
C |
8: 117,835,454 (GRCm39) |
F135S |
probably damaging |
Het |
Cacna1c |
C |
T |
6: 118,589,586 (GRCm39) |
R1446H |
probably damaging |
Het |
Ccdc42 |
A |
G |
11: 68,485,115 (GRCm39) |
K210E |
probably damaging |
Het |
Cckar |
A |
T |
5: 53,857,409 (GRCm39) |
W263R |
probably damaging |
Het |
Cela2a |
A |
G |
4: 141,553,252 (GRCm39) |
|
probably null |
Het |
Cep97 |
A |
T |
16: 55,748,159 (GRCm39) |
N90K |
probably damaging |
Het |
Ces2g |
A |
T |
8: 105,693,984 (GRCm39) |
Q440L |
probably damaging |
Het |
Chchd6 |
G |
T |
6: 89,396,736 (GRCm39) |
T225K |
possibly damaging |
Het |
Chd1l |
C |
T |
3: 97,490,047 (GRCm39) |
E503K |
probably benign |
Het |
Chrna5 |
A |
G |
9: 54,911,649 (GRCm39) |
T46A |
probably benign |
Het |
Col16a1 |
G |
A |
4: 129,992,733 (GRCm39) |
G1531S |
probably damaging |
Het |
Col19a1 |
A |
T |
1: 24,573,172 (GRCm39) |
V200E |
unknown |
Het |
Csf2rb |
A |
G |
15: 78,219,411 (GRCm39) |
D2G |
probably damaging |
Het |
Csmd3 |
G |
A |
15: 47,813,346 (GRCm39) |
S1062L |
probably damaging |
Het |
Cul5 |
G |
T |
9: 53,569,893 (GRCm39) |
Q113K |
probably benign |
Het |
Dmwd |
TAGCCTGGGAA |
TAGCCTGGGAAGCCTGGGAA |
7: 18,814,959 (GRCm39) |
|
probably benign |
Het |
Dse |
T |
C |
10: 34,029,230 (GRCm39) |
D620G |
probably damaging |
Het |
Dsg1c |
A |
G |
18: 20,397,899 (GRCm39) |
N33S |
probably benign |
Het |
Epc2 |
G |
A |
2: 49,439,990 (GRCm39) |
V803I |
probably damaging |
Het |
Erap1 |
T |
A |
13: 74,819,500 (GRCm39) |
H171Q |
probably damaging |
Het |
Esrrb |
T |
C |
12: 86,561,274 (GRCm39) |
V336A |
possibly damaging |
Het |
Fech |
A |
T |
18: 64,595,189 (GRCm39) |
W300R |
probably damaging |
Het |
Fgd4 |
T |
C |
16: 16,241,920 (GRCm39) |
I635V |
possibly damaging |
Het |
Galc |
A |
T |
12: 98,200,563 (GRCm39) |
N282K |
probably benign |
Het |
Gpat2 |
A |
G |
2: 127,270,637 (GRCm39) |
Y95C |
probably benign |
Het |
Grm2 |
T |
A |
9: 106,524,670 (GRCm39) |
I682F |
probably damaging |
Het |
Hdac10 |
G |
T |
15: 89,010,878 (GRCm39) |
A241D |
probably damaging |
Het |
Helz |
T |
A |
11: 107,527,105 (GRCm39) |
C182* |
probably null |
Het |
Ift140 |
A |
G |
17: 25,307,839 (GRCm39) |
Y978C |
probably damaging |
Het |
Intu |
T |
A |
3: 40,652,061 (GRCm39) |
C839* |
probably null |
Het |
Jmjd1c |
T |
C |
10: 67,055,654 (GRCm39) |
V358A |
probably benign |
Het |
Kif26b |
A |
G |
1: 178,744,043 (GRCm39) |
S1380G |
probably benign |
Het |
Lrp1b |
A |
G |
2: 40,587,601 (GRCm39) |
S116P |
unknown |
Het |
Lrrc2 |
T |
A |
9: 110,790,041 (GRCm39) |
S99R |
probably benign |
Het |
Mrpl48 |
G |
A |
7: 100,195,482 (GRCm39) |
|
probably benign |
Het |
Mup9 |
A |
G |
4: 60,377,878 (GRCm39) |
|
probably benign |
Het |
Nap1l1 |
G |
A |
10: 111,329,240 (GRCm39) |
V285I |
possibly damaging |
Het |
Nepro |
A |
G |
16: 44,547,391 (GRCm39) |
D36G |
probably benign |
Het |
Nkain4 |
A |
G |
2: 180,577,794 (GRCm39) |
F187L |
probably damaging |
Het |
Nobox |
A |
T |
6: 43,284,401 (GRCm39) |
C82S |
possibly damaging |
Het |
Ntn4 |
C |
A |
10: 93,480,596 (GRCm39) |
Q70K |
probably damaging |
Het |
Or13j1 |
A |
G |
4: 43,706,292 (GRCm39) |
I92T |
probably damaging |
Het |
Or1e26 |
A |
T |
11: 73,480,118 (GRCm39) |
W149R |
probably damaging |
Het |
Or4k37 |
A |
G |
2: 111,159,306 (GRCm39) |
I181V |
probably benign |
Het |
Or51a43 |
T |
C |
7: 103,717,738 (GRCm39) |
R167G |
probably damaging |
Het |
Or5b122 |
T |
A |
19: 13,562,978 (GRCm39) |
F103L |
probably benign |
Het |
Or9r3 |
A |
G |
10: 129,948,548 (GRCm39) |
I37T |
possibly damaging |
Het |
Pappa |
A |
G |
4: 65,094,466 (GRCm39) |
E497G |
probably damaging |
Het |
Pard3 |
C |
A |
8: 128,106,983 (GRCm39) |
T569K |
probably benign |
Het |
Parp14 |
G |
A |
16: 35,677,130 (GRCm39) |
A946V |
probably benign |
Het |
Pcdh10 |
A |
G |
3: 45,334,747 (GRCm39) |
N354D |
possibly damaging |
Het |
Pdgfc |
T |
C |
3: 81,082,194 (GRCm39) |
V129A |
probably benign |
Het |
Pdia3 |
G |
A |
2: 121,262,858 (GRCm39) |
G275S |
probably damaging |
Het |
Phf20l1 |
A |
T |
15: 66,487,108 (GRCm39) |
H407L |
possibly damaging |
Het |
Phip |
A |
T |
9: 82,753,502 (GRCm39) |
D1747E |
probably benign |
Het |
Pkd1l1 |
A |
G |
11: 8,900,413 (GRCm39) |
S43P |
probably damaging |
Het |
Rapsn |
A |
G |
2: 90,873,504 (GRCm39) |
D270G |
possibly damaging |
Het |
Rims2 |
A |
C |
15: 39,370,382 (GRCm39) |
S939R |
probably damaging |
Het |
Ripor3 |
T |
C |
2: 167,822,765 (GRCm39) |
D932G |
probably damaging |
Het |
Rtp2 |
A |
T |
16: 23,749,421 (GRCm39) |
W30R |
probably damaging |
Het |
Scgb2b27 |
A |
T |
7: 33,711,557 (GRCm39) |
D97E |
probably benign |
Het |
Slc25a46 |
T |
C |
18: 31,716,542 (GRCm39) |
N320S |
probably benign |
Het |
Slc9b1 |
A |
G |
3: 135,060,765 (GRCm39) |
|
probably null |
Het |
Socs4 |
T |
A |
14: 47,527,740 (GRCm39) |
M225K |
possibly damaging |
Het |
Spata31d1a |
A |
T |
13: 59,850,247 (GRCm39) |
L627* |
probably null |
Het |
Srcin1 |
A |
G |
11: 97,416,307 (GRCm39) |
L975P |
probably damaging |
Het |
Stard3 |
T |
A |
11: 98,267,435 (GRCm39) |
|
probably null |
Het |
Susd2 |
G |
T |
10: 75,473,878 (GRCm39) |
S572R |
possibly damaging |
Het |
Tll1 |
C |
A |
8: 64,509,307 (GRCm39) |
A568S |
probably benign |
Het |
Tmem132a |
C |
G |
19: 10,839,062 (GRCm39) |
G460A |
probably damaging |
Het |
Trim62 |
A |
G |
4: 128,803,281 (GRCm39) |
K444E |
probably damaging |
Het |
Trpm3 |
A |
G |
19: 22,689,271 (GRCm39) |
T67A |
probably damaging |
Het |
Ttc6 |
T |
C |
12: 57,784,454 (GRCm39) |
M1841T |
possibly damaging |
Het |
Ulk2 |
A |
T |
11: 61,672,572 (GRCm39) |
V922D |
probably damaging |
Het |
Vmn2r38 |
C |
A |
7: 9,078,532 (GRCm39) |
V617L |
probably damaging |
Het |
Xkr6 |
G |
A |
14: 64,056,766 (GRCm39) |
V226M |
probably benign |
Het |
Zfp940 |
G |
A |
7: 29,544,962 (GRCm39) |
A315V |
possibly damaging |
Het |
Zfr |
C |
A |
15: 12,150,473 (GRCm39) |
T480K |
possibly damaging |
Het |
|
Other mutations in Plekhg2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00815:Plekhg2
|
APN |
7 |
28,060,294 (GRCm39) |
nonsense |
probably null |
|
IGL00933:Plekhg2
|
APN |
7 |
28,060,114 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02037:Plekhg2
|
APN |
7 |
28,068,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02103:Plekhg2
|
APN |
7 |
28,059,501 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02598:Plekhg2
|
APN |
7 |
28,059,900 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02892:Plekhg2
|
APN |
7 |
28,062,342 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03249:Plekhg2
|
APN |
7 |
28,067,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R0561:Plekhg2
|
UTSW |
7 |
28,069,908 (GRCm39) |
missense |
probably benign |
|
R1134:Plekhg2
|
UTSW |
7 |
28,061,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R2225:Plekhg2
|
UTSW |
7 |
28,059,760 (GRCm39) |
missense |
probably benign |
0.02 |
R4043:Plekhg2
|
UTSW |
7 |
28,064,144 (GRCm39) |
unclassified |
probably benign |
|
R4117:Plekhg2
|
UTSW |
7 |
28,060,313 (GRCm39) |
missense |
probably benign |
0.02 |
R4296:Plekhg2
|
UTSW |
7 |
28,070,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R4956:Plekhg2
|
UTSW |
7 |
28,067,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R5376:Plekhg2
|
UTSW |
7 |
28,062,094 (GRCm39) |
missense |
probably damaging |
0.99 |
R5378:Plekhg2
|
UTSW |
7 |
28,062,094 (GRCm39) |
missense |
probably damaging |
0.99 |
R5523:Plekhg2
|
UTSW |
7 |
28,069,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R5545:Plekhg2
|
UTSW |
7 |
28,061,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R5667:Plekhg2
|
UTSW |
7 |
28,067,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R5913:Plekhg2
|
UTSW |
7 |
28,064,027 (GRCm39) |
missense |
probably damaging |
0.99 |
R6017:Plekhg2
|
UTSW |
7 |
28,062,309 (GRCm39) |
missense |
probably damaging |
0.97 |
R6088:Plekhg2
|
UTSW |
7 |
28,060,438 (GRCm39) |
missense |
probably benign |
0.01 |
R6912:Plekhg2
|
UTSW |
7 |
28,059,684 (GRCm39) |
missense |
probably benign |
0.39 |
R7258:Plekhg2
|
UTSW |
7 |
28,064,203 (GRCm39) |
missense |
probably benign |
0.00 |
R7530:Plekhg2
|
UTSW |
7 |
28,061,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R8054:Plekhg2
|
UTSW |
7 |
28,064,741 (GRCm39) |
missense |
probably damaging |
0.96 |
R8217:Plekhg2
|
UTSW |
7 |
28,067,717 (GRCm39) |
missense |
probably null |
1.00 |
R8441:Plekhg2
|
UTSW |
7 |
28,060,291 (GRCm39) |
missense |
probably benign |
0.34 |
R8855:Plekhg2
|
UTSW |
7 |
28,069,526 (GRCm39) |
missense |
probably benign |
0.25 |
R8877:Plekhg2
|
UTSW |
7 |
28,060,278 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9234:Plekhg2
|
UTSW |
7 |
28,064,215 (GRCm39) |
missense |
probably benign |
0.21 |
R9464:Plekhg2
|
UTSW |
7 |
28,062,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R9561:Plekhg2
|
UTSW |
7 |
28,064,249 (GRCm39) |
missense |
probably damaging |
0.96 |
R9593:Plekhg2
|
UTSW |
7 |
28,059,710 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9773:Plekhg2
|
UTSW |
7 |
28,069,743 (GRCm39) |
missense |
probably damaging |
0.96 |
RF051:Plekhg2
|
UTSW |
7 |
28,061,777 (GRCm39) |
frame shift |
probably null |
|
Z1186:Plekhg2
|
UTSW |
7 |
28,070,727 (GRCm39) |
intron |
probably benign |
|
Z1186:Plekhg2
|
UTSW |
7 |
28,062,360 (GRCm39) |
missense |
possibly damaging |
0.77 |
|