Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
A |
G |
2: 25,336,116 (GRCm39) |
E2162G |
probably benign |
Het |
Ackr4 |
A |
G |
9: 103,976,761 (GRCm39) |
V62A |
probably damaging |
Het |
Atox1 |
T |
A |
11: 55,341,365 (GRCm39) |
K57* |
probably null |
Het |
Atp6v1e1 |
G |
A |
6: 120,799,350 (GRCm39) |
|
probably benign |
Het |
Bmpr2 |
T |
C |
1: 59,906,842 (GRCm39) |
V645A |
probably benign |
Het |
Brwd1 |
T |
C |
16: 95,810,730 (GRCm39) |
T1602A |
probably benign |
Het |
Cdc42bpg |
T |
C |
19: 6,365,219 (GRCm39) |
V692A |
probably damaging |
Het |
Cdca2 |
T |
C |
14: 67,935,551 (GRCm39) |
D388G |
probably damaging |
Het |
Celsr1 |
G |
A |
15: 85,816,652 (GRCm39) |
R1764C |
possibly damaging |
Het |
Copz2 |
G |
T |
11: 96,747,538 (GRCm39) |
V174L |
probably benign |
Het |
Dnaaf1 |
T |
C |
8: 120,309,335 (GRCm39) |
L141P |
probably damaging |
Het |
Fam170a |
T |
A |
18: 50,413,740 (GRCm39) |
|
probably null |
Het |
Fshr |
A |
T |
17: 89,404,539 (GRCm39) |
|
probably null |
Het |
Gbx1 |
C |
T |
5: 24,731,298 (GRCm39) |
A173T |
probably benign |
Het |
Gm3604 |
G |
A |
13: 62,518,109 (GRCm39) |
A83V |
probably damaging |
Het |
Gpr19 |
A |
T |
6: 134,847,419 (GRCm39) |
V88D |
probably damaging |
Het |
Hnrnpd |
C |
T |
5: 100,124,392 (GRCm39) |
|
probably null |
Het |
Homez |
T |
C |
14: 55,095,112 (GRCm39) |
S199G |
probably benign |
Het |
Kit |
T |
C |
5: 75,767,941 (GRCm39) |
I108T |
probably damaging |
Het |
Lrrc34 |
A |
C |
3: 30,688,705 (GRCm39) |
Y199D |
probably damaging |
Het |
Mapk12 |
T |
C |
15: 89,017,350 (GRCm39) |
D208G |
probably damaging |
Het |
Mon1a |
A |
G |
9: 107,778,985 (GRCm39) |
D403G |
probably damaging |
Het |
Myo1d |
C |
T |
11: 80,565,460 (GRCm39) |
E426K |
probably damaging |
Het |
Nol11 |
G |
A |
11: 107,070,878 (GRCm39) |
T307I |
probably damaging |
Het |
Or10d5 |
A |
G |
9: 39,861,444 (GRCm39) |
C208R |
probably damaging |
Het |
Or52b4 |
A |
T |
7: 102,184,172 (GRCm39) |
I73F |
possibly damaging |
Het |
Or5aq1b |
A |
G |
2: 86,902,083 (GRCm39) |
Y132H |
probably damaging |
Het |
Or6d15 |
A |
T |
6: 116,559,314 (GRCm39) |
F198I |
probably damaging |
Het |
Or8k28 |
A |
T |
2: 86,285,835 (GRCm39) |
L260* |
probably null |
Het |
Pcdhb16 |
C |
T |
18: 37,611,516 (GRCm39) |
Q159* |
probably null |
Het |
Phf19 |
G |
A |
2: 34,788,724 (GRCm39) |
|
probably null |
Het |
Qrfpr |
C |
T |
3: 36,234,198 (GRCm39) |
R381H |
probably benign |
Het |
Rad51ap2 |
A |
G |
12: 11,506,366 (GRCm39) |
D96G |
probably benign |
Het |
Ranbp1 |
T |
C |
16: 18,063,097 (GRCm39) |
D93G |
possibly damaging |
Het |
Reep1 |
A |
G |
6: 71,757,749 (GRCm39) |
D116G |
possibly damaging |
Het |
Rps6kb1 |
T |
C |
11: 86,397,666 (GRCm39) |
D393G |
probably damaging |
Het |
Slc2a12 |
T |
C |
10: 22,541,216 (GRCm39) |
V357A |
probably benign |
Het |
Spryd3 |
T |
C |
15: 102,026,627 (GRCm39) |
D348G |
probably benign |
Het |
Syne2 |
G |
A |
12: 76,099,501 (GRCm39) |
A569T |
probably benign |
Het |
Tcstv5 |
T |
C |
13: 120,411,270 (GRCm39) |
D112G |
probably benign |
Het |
Thoc6 |
C |
T |
17: 23,892,503 (GRCm39) |
R6Q |
probably null |
Het |
Tyw3 |
G |
C |
3: 154,299,426 (GRCm39) |
S94R |
probably benign |
Het |
Unc13b |
C |
T |
4: 43,171,926 (GRCm39) |
T918I |
unknown |
Het |
Unc80 |
A |
T |
1: 66,685,680 (GRCm39) |
H2268L |
possibly damaging |
Het |
Urod |
C |
T |
4: 116,849,838 (GRCm39) |
A187T |
probably damaging |
Het |
Usp46 |
G |
T |
5: 74,177,344 (GRCm39) |
N205K |
probably benign |
Het |
Wapl |
T |
C |
14: 34,414,313 (GRCm39) |
F392L |
probably benign |
Het |
Zim1 |
T |
C |
7: 6,680,305 (GRCm39) |
T453A |
possibly damaging |
Het |
|
Other mutations in Rinl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02370:Rinl
|
APN |
7 |
28,494,397 (GRCm39) |
splice site |
probably null |
|
IGL03126:Rinl
|
APN |
7 |
28,495,075 (GRCm39) |
splice site |
probably benign |
|
IGL03345:Rinl
|
APN |
7 |
28,496,222 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1453:Rinl
|
UTSW |
7 |
28,496,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R1648:Rinl
|
UTSW |
7 |
28,497,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R1722:Rinl
|
UTSW |
7 |
28,491,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R2127:Rinl
|
UTSW |
7 |
28,496,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R2290:Rinl
|
UTSW |
7 |
28,491,696 (GRCm39) |
missense |
probably benign |
0.00 |
R2472:Rinl
|
UTSW |
7 |
28,489,803 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2883:Rinl
|
UTSW |
7 |
28,497,083 (GRCm39) |
frame shift |
probably null |
|
R4062:Rinl
|
UTSW |
7 |
28,490,140 (GRCm39) |
missense |
probably benign |
|
R6180:Rinl
|
UTSW |
7 |
28,496,365 (GRCm39) |
missense |
probably benign |
0.02 |
R8112:Rinl
|
UTSW |
7 |
28,490,014 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8893:Rinl
|
UTSW |
7 |
28,491,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R9145:Rinl
|
UTSW |
7 |
28,495,089 (GRCm39) |
missense |
|
|
R9168:Rinl
|
UTSW |
7 |
28,490,084 (GRCm39) |
missense |
possibly damaging |
0.82 |
RF044:Rinl
|
UTSW |
7 |
28,496,988 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Rinl
|
UTSW |
7 |
28,489,830 (GRCm39) |
missense |
probably benign |
|
X0066:Rinl
|
UTSW |
7 |
28,491,768 (GRCm39) |
splice site |
probably null |
|
|