Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adad2 |
T |
C |
8: 120,342,708 (GRCm39) |
V418A |
probably benign |
Het |
Adamts16 |
T |
C |
13: 70,901,345 (GRCm39) |
T911A |
probably benign |
Het |
Adgra1 |
T |
C |
7: 139,427,619 (GRCm39) |
F62S |
possibly damaging |
Het |
Adgra3 |
A |
G |
5: 50,159,272 (GRCm39) |
V326A |
probably damaging |
Het |
Adgrg6 |
A |
G |
10: 14,316,114 (GRCm39) |
F569S |
probably benign |
Het |
Alcam |
T |
C |
16: 52,130,261 (GRCm39) |
T30A |
probably null |
Het |
Arnt2 |
G |
A |
7: 83,924,655 (GRCm39) |
R391W |
probably damaging |
Het |
Ascc3 |
T |
C |
10: 50,576,196 (GRCm39) |
V817A |
probably damaging |
Het |
Atp13a4 |
G |
T |
16: 29,232,567 (GRCm39) |
T923K |
probably damaging |
Het |
Atp5po |
C |
T |
16: 91,725,794 (GRCm39) |
R64H |
probably damaging |
Het |
Ccdc185 |
T |
G |
1: 182,576,313 (GRCm39) |
Q125H |
possibly damaging |
Het |
Ccdc88a |
T |
A |
11: 29,436,006 (GRCm39) |
C10S |
probably damaging |
Het |
Cct2 |
T |
C |
10: 116,897,968 (GRCm39) |
N73S |
probably benign |
Het |
Clock |
G |
A |
5: 76,377,401 (GRCm39) |
Q633* |
probably null |
Het |
Col6a2 |
T |
C |
10: 76,439,193 (GRCm39) |
I826V |
probably benign |
Het |
Cpsf1 |
G |
T |
15: 76,485,981 (GRCm39) |
Y396* |
probably null |
Het |
Dnah1 |
A |
T |
14: 30,991,774 (GRCm39) |
M3076K |
possibly damaging |
Het |
Dxo |
A |
G |
17: 35,057,825 (GRCm39) |
N177D |
probably damaging |
Het |
Fbxw28 |
A |
T |
9: 109,167,472 (GRCm39) |
V95E |
possibly damaging |
Het |
Galnt6 |
T |
C |
15: 100,597,018 (GRCm39) |
N383D |
probably damaging |
Het |
Gpat2 |
G |
A |
2: 127,270,211 (GRCm39) |
V75M |
probably damaging |
Het |
Grik5 |
T |
C |
7: 24,762,397 (GRCm39) |
D198G |
probably benign |
Het |
Gsdmc4 |
A |
G |
15: 63,763,895 (GRCm39) |
S401P |
probably benign |
Het |
Gspt1 |
A |
T |
16: 11,047,109 (GRCm39) |
D435E |
probably damaging |
Het |
Hsf2 |
T |
C |
10: 57,381,378 (GRCm39) |
S266P |
probably damaging |
Het |
Jade2 |
T |
C |
11: 51,708,050 (GRCm39) |
D721G |
probably benign |
Het |
Klhl7 |
G |
T |
5: 24,343,319 (GRCm39) |
V212L |
probably damaging |
Het |
Klra17 |
T |
A |
6: 129,851,809 (GRCm39) |
N21I |
probably damaging |
Het |
L3mbtl3 |
T |
C |
10: 26,215,197 (GRCm39) |
N196S |
unknown |
Het |
Lama3 |
G |
C |
18: 12,546,915 (GRCm39) |
|
probably null |
Het |
Mcm5 |
T |
C |
8: 75,848,272 (GRCm39) |
M507T |
possibly damaging |
Het |
Mycbp2 |
T |
C |
14: 103,372,553 (GRCm39) |
R814G |
probably damaging |
Het |
Nlrp4b |
A |
G |
7: 10,449,456 (GRCm39) |
E186G |
probably damaging |
Het |
Nlrp4c |
A |
G |
7: 6,095,569 (GRCm39) |
K816E |
possibly damaging |
Het |
Nod1 |
G |
T |
6: 54,921,902 (GRCm39) |
R139S |
probably benign |
Het |
Nudcd1 |
T |
C |
15: 44,284,207 (GRCm39) |
M60V |
probably benign |
Het |
Or5b101 |
G |
C |
19: 13,005,411 (GRCm39) |
A94G |
probably benign |
Het |
Or5p63 |
G |
A |
7: 107,811,490 (GRCm39) |
P82L |
possibly damaging |
Het |
Or5p69 |
A |
T |
7: 107,967,551 (GRCm39) |
I285F |
possibly damaging |
Het |
Or8g28 |
G |
T |
9: 39,169,897 (GRCm39) |
Q24K |
possibly damaging |
Het |
Ovol2 |
A |
G |
2: 144,159,796 (GRCm39) |
S82P |
probably benign |
Het |
Ppl |
T |
C |
16: 4,925,381 (GRCm39) |
E86G |
possibly damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Ripk4 |
T |
C |
16: 97,545,157 (GRCm39) |
T497A |
probably benign |
Het |
Scml4 |
A |
G |
10: 42,833,667 (GRCm39) |
Y327C |
probably damaging |
Het |
Serpina3n |
A |
G |
12: 104,377,536 (GRCm39) |
E263G |
possibly damaging |
Het |
Six4 |
A |
G |
12: 73,159,657 (GRCm39) |
F101S |
probably damaging |
Het |
Sltm |
T |
G |
9: 70,493,240 (GRCm39) |
L728V |
probably damaging |
Het |
Sptb |
T |
G |
12: 76,657,589 (GRCm39) |
K1311Q |
possibly damaging |
Het |
Sycp1 |
T |
C |
3: 102,748,357 (GRCm39) |
K812E |
possibly damaging |
Het |
Tenm4 |
T |
C |
7: 96,501,737 (GRCm39) |
Y1314H |
probably damaging |
Het |
Tmem67 |
A |
T |
4: 12,073,952 (GRCm39) |
M288K |
probably benign |
Het |
Ttn |
A |
C |
2: 76,772,749 (GRCm39) |
N2415K |
possibly damaging |
Het |
Vmn2r65 |
T |
C |
7: 84,595,896 (GRCm39) |
I263V |
probably benign |
Het |
Vmn2r89 |
A |
T |
14: 51,693,628 (GRCm39) |
E326V |
probably damaging |
Het |
Wdr81 |
A |
G |
11: 75,343,758 (GRCm39) |
I503T |
probably damaging |
Het |
|
Other mutations in Toporsl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00870:Toporsl
|
APN |
4 |
52,610,172 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01611:Toporsl
|
APN |
4 |
52,610,794 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02638:Toporsl
|
APN |
4 |
52,611,624 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02642:Toporsl
|
APN |
4 |
52,611,114 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03410:Toporsl
|
APN |
4 |
52,611,134 (GRCm39) |
missense |
probably benign |
0.07 |
torsion
|
UTSW |
4 |
52,610,489 (GRCm39) |
missense |
probably damaging |
1.00 |
wound
|
UTSW |
4 |
52,612,140 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03134:Toporsl
|
UTSW |
4 |
52,610,281 (GRCm39) |
missense |
probably damaging |
0.97 |
R0548:Toporsl
|
UTSW |
4 |
52,612,140 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1444:Toporsl
|
UTSW |
4 |
52,610,254 (GRCm39) |
missense |
probably benign |
0.01 |
R2165:Toporsl
|
UTSW |
4 |
52,612,072 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2295:Toporsl
|
UTSW |
4 |
52,610,176 (GRCm39) |
missense |
probably damaging |
0.99 |
R3905:Toporsl
|
UTSW |
4 |
52,611,750 (GRCm39) |
nonsense |
probably null |
|
R4719:Toporsl
|
UTSW |
4 |
52,611,996 (GRCm39) |
missense |
probably benign |
0.21 |
R4782:Toporsl
|
UTSW |
4 |
52,610,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R5642:Toporsl
|
UTSW |
4 |
52,611,515 (GRCm39) |
nonsense |
probably null |
|
R5724:Toporsl
|
UTSW |
4 |
52,611,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R5728:Toporsl
|
UTSW |
4 |
52,611,469 (GRCm39) |
missense |
probably benign |
|
R6433:Toporsl
|
UTSW |
4 |
52,611,548 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7023:Toporsl
|
UTSW |
4 |
52,611,211 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7292:Toporsl
|
UTSW |
4 |
52,611,630 (GRCm39) |
missense |
probably benign |
0.14 |
R7294:Toporsl
|
UTSW |
4 |
52,611,903 (GRCm39) |
missense |
probably benign |
0.03 |
R7408:Toporsl
|
UTSW |
4 |
52,612,108 (GRCm39) |
missense |
probably benign |
0.12 |
R7673:Toporsl
|
UTSW |
4 |
52,610,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R7974:Toporsl
|
UTSW |
4 |
52,611,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R8156:Toporsl
|
UTSW |
4 |
52,609,975 (GRCm39) |
start gained |
probably benign |
|
R8186:Toporsl
|
UTSW |
4 |
52,610,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R8744:Toporsl
|
UTSW |
4 |
52,611,967 (GRCm39) |
missense |
probably benign |
0.01 |
R9117:Toporsl
|
UTSW |
4 |
52,609,943 (GRCm39) |
start gained |
probably benign |
|
R9451:Toporsl
|
UTSW |
4 |
52,611,663 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9512:Toporsl
|
UTSW |
4 |
52,610,382 (GRCm39) |
missense |
probably benign |
0.28 |
X0065:Toporsl
|
UTSW |
4 |
52,610,539 (GRCm39) |
missense |
probably damaging |
0.99 |
|