Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A130010J15Rik |
T |
A |
1: 192,857,089 (GRCm39) |
V147E |
possibly damaging |
Het |
Abtb3 |
A |
G |
10: 85,467,240 (GRCm39) |
T732A |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,621,072 (GRCm39) |
M3893K |
probably benign |
Het |
Aox3 |
T |
C |
1: 58,157,840 (GRCm39) |
S66P |
probably damaging |
Het |
Apeh |
G |
A |
9: 107,969,878 (GRCm39) |
H186Y |
probably damaging |
Het |
Bloc1s5 |
A |
G |
13: 38,787,961 (GRCm39) |
V141A |
probably benign |
Het |
Bltp1 |
A |
G |
3: 36,928,431 (GRCm39) |
N61S |
probably damaging |
Het |
Col28a1 |
T |
C |
6: 7,999,468 (GRCm39) |
Y1083C |
probably damaging |
Het |
Crb1 |
A |
G |
1: 139,170,864 (GRCm39) |
V842A |
probably benign |
Het |
Dapk1 |
A |
G |
13: 60,899,103 (GRCm39) |
S858G |
probably benign |
Het |
Dlgap2 |
G |
T |
8: 14,229,619 (GRCm39) |
|
probably benign |
Het |
Dpysl4 |
A |
G |
7: 138,673,576 (GRCm39) |
D199G |
probably benign |
Het |
Eml6 |
C |
T |
11: 29,753,161 (GRCm39) |
V917I |
probably benign |
Het |
Fut9 |
T |
A |
4: 25,620,647 (GRCm39) |
T56S |
probably benign |
Het |
Gtdc1 |
G |
C |
2: 44,465,563 (GRCm39) |
S214* |
probably null |
Het |
Gtdc1 |
A |
G |
2: 44,715,396 (GRCm39) |
F49S |
probably damaging |
Het |
Hoxd9 |
A |
G |
2: 74,529,590 (GRCm39) |
Y282C |
probably damaging |
Het |
Hrc |
A |
G |
7: 44,985,803 (GRCm39) |
E318G |
probably benign |
Het |
Ikzf2 |
T |
C |
1: 69,609,661 (GRCm39) |
T195A |
probably damaging |
Het |
Krt36 |
A |
T |
11: 99,996,335 (GRCm39) |
S30T |
probably benign |
Het |
Lrp1 |
A |
G |
10: 127,390,925 (GRCm39) |
F2991L |
probably benign |
Het |
Mapk1 |
A |
T |
16: 16,853,326 (GRCm39) |
M49L |
probably benign |
Het |
Mroh2a |
G |
T |
1: 88,162,938 (GRCm39) |
Q360H |
probably benign |
Het |
Mrpl48 |
A |
G |
7: 100,195,574 (GRCm39) |
|
probably benign |
Het |
Ncln |
A |
G |
10: 81,323,512 (GRCm39) |
|
probably null |
Het |
Nol4 |
T |
A |
18: 23,053,882 (GRCm39) |
Q96L |
probably damaging |
Het |
Or2y1e |
G |
T |
11: 49,218,687 (GRCm39) |
V150L |
probably benign |
Het |
Or5g25 |
G |
A |
2: 85,478,317 (GRCm39) |
A116V |
probably damaging |
Het |
Padi2 |
A |
G |
4: 140,674,077 (GRCm39) |
|
probably null |
Het |
Pak5 |
T |
G |
2: 135,939,501 (GRCm39) |
I545L |
possibly damaging |
Het |
Paqr5 |
T |
A |
9: 61,876,064 (GRCm39) |
R157W |
probably null |
Het |
Pard3b |
G |
A |
1: 62,200,340 (GRCm39) |
R293H |
probably damaging |
Het |
Phf11d |
C |
A |
14: 59,593,844 (GRCm39) |
C110F |
probably damaging |
Het |
Pkn2 |
G |
A |
3: 142,504,765 (GRCm39) |
P804S |
probably damaging |
Het |
Pnpla6 |
G |
A |
8: 3,584,611 (GRCm39) |
C743Y |
possibly damaging |
Het |
Pramel14 |
A |
G |
4: 143,719,651 (GRCm39) |
V238A |
probably benign |
Het |
Pramel58 |
C |
A |
5: 94,831,277 (GRCm39) |
Q95K |
probably benign |
Het |
Psip1 |
A |
G |
4: 83,386,879 (GRCm39) |
M164T |
probably benign |
Het |
Rgs22 |
C |
G |
15: 36,048,910 (GRCm39) |
S914T |
probably damaging |
Het |
Rufy4 |
G |
A |
1: 74,172,206 (GRCm39) |
V310I |
probably benign |
Het |
Ryr2 |
G |
A |
13: 11,741,816 (GRCm39) |
L2122F |
probably damaging |
Het |
Sgcb |
T |
G |
5: 73,798,036 (GRCm39) |
N142T |
probably benign |
Het |
Slc27a6 |
A |
G |
18: 58,738,126 (GRCm39) |
E394G |
probably benign |
Het |
Slc29a2 |
T |
C |
19: 5,079,271 (GRCm39) |
V298A |
probably damaging |
Het |
Slf2 |
C |
A |
19: 44,931,907 (GRCm39) |
T654N |
probably damaging |
Het |
Spata4 |
A |
C |
8: 55,055,368 (GRCm39) |
K123Q |
possibly damaging |
Het |
Taar7b |
T |
C |
10: 23,876,756 (GRCm39) |
V307A |
probably benign |
Het |
Tenm4 |
G |
A |
7: 96,202,703 (GRCm39) |
R106H |
probably benign |
Het |
Ttn |
T |
C |
2: 76,693,983 (GRCm39) |
E295G |
possibly damaging |
Het |
Ubqln4 |
A |
T |
3: 88,462,679 (GRCm39) |
Q48L |
possibly damaging |
Het |
Ugt1a10 |
T |
A |
1: 87,983,647 (GRCm39) |
D148E |
probably damaging |
Het |
Vmn2r85 |
T |
A |
10: 130,261,795 (GRCm39) |
N181Y |
probably benign |
Het |
Wdfy3 |
C |
T |
5: 102,071,813 (GRCm39) |
V1026I |
possibly damaging |
Het |
|
Other mutations in Lrrc34 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02502:Lrrc34
|
APN |
3 |
30,699,394 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02738:Lrrc34
|
APN |
3 |
30,685,441 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02985:Lrrc34
|
APN |
3 |
30,690,444 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02999:Lrrc34
|
APN |
3 |
30,688,782 (GRCm39) |
missense |
probably damaging |
0.99 |
R0367:Lrrc34
|
UTSW |
3 |
30,684,142 (GRCm39) |
missense |
probably benign |
0.08 |
R0761:Lrrc34
|
UTSW |
3 |
30,685,425 (GRCm39) |
splice site |
probably null |
|
R1426:Lrrc34
|
UTSW |
3 |
30,697,728 (GRCm39) |
unclassified |
probably benign |
|
R1980:Lrrc34
|
UTSW |
3 |
30,696,890 (GRCm39) |
missense |
probably benign |
0.33 |
R2215:Lrrc34
|
UTSW |
3 |
30,697,678 (GRCm39) |
missense |
probably benign |
0.03 |
R2414:Lrrc34
|
UTSW |
3 |
30,688,711 (GRCm39) |
missense |
probably benign |
0.00 |
R4379:Lrrc34
|
UTSW |
3 |
30,685,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R5214:Lrrc34
|
UTSW |
3 |
30,690,397 (GRCm39) |
nonsense |
probably null |
|
R5418:Lrrc34
|
UTSW |
3 |
30,696,923 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5662:Lrrc34
|
UTSW |
3 |
30,685,473 (GRCm39) |
missense |
probably benign |
0.03 |
R6736:Lrrc34
|
UTSW |
3 |
30,679,008 (GRCm39) |
missense |
probably benign |
0.03 |
R6941:Lrrc34
|
UTSW |
3 |
30,678,969 (GRCm39) |
missense |
probably benign |
0.01 |
R7017:Lrrc34
|
UTSW |
3 |
30,699,465 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7080:Lrrc34
|
UTSW |
3 |
30,688,705 (GRCm39) |
missense |
probably damaging |
0.96 |
R7139:Lrrc34
|
UTSW |
3 |
30,679,036 (GRCm39) |
missense |
probably benign |
0.22 |
R7191:Lrrc34
|
UTSW |
3 |
30,679,027 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7398:Lrrc34
|
UTSW |
3 |
30,697,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R7662:Lrrc34
|
UTSW |
3 |
30,697,452 (GRCm39) |
missense |
probably benign |
0.16 |
R7707:Lrrc34
|
UTSW |
3 |
30,679,041 (GRCm39) |
missense |
probably benign |
0.00 |
R7945:Lrrc34
|
UTSW |
3 |
30,696,886 (GRCm39) |
critical splice donor site |
probably null |
|
R8799:Lrrc34
|
UTSW |
3 |
30,678,979 (GRCm39) |
missense |
probably benign |
0.06 |
R9764:Lrrc34
|
UTSW |
3 |
30,697,467 (GRCm39) |
missense |
probably damaging |
1.00 |
|