Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
A |
G |
13: 119,617,563 (GRCm39) |
N562S |
probably benign |
Het |
Abi1 |
A |
G |
2: 22,843,479 (GRCm39) |
V316A |
probably benign |
Het |
Acsm1 |
A |
T |
7: 119,232,403 (GRCm39) |
Q100L |
possibly damaging |
Het |
Akr1c21 |
T |
C |
13: 4,627,457 (GRCm39) |
Y184H |
possibly damaging |
Het |
Anks3 |
T |
C |
16: 4,775,891 (GRCm39) |
T104A |
probably damaging |
Het |
Bcl2l2 |
A |
G |
14: 55,122,224 (GRCm39) |
Y129C |
probably damaging |
Het |
Cenpf |
T |
A |
1: 189,391,207 (GRCm39) |
K875I |
probably damaging |
Het |
Cntnap1 |
T |
C |
11: 101,067,127 (GRCm39) |
V15A |
probably benign |
Het |
Dnaaf9 |
A |
T |
2: 130,633,915 (GRCm39) |
|
probably null |
Het |
Elmo3 |
C |
A |
8: 106,033,013 (GRCm39) |
R66S |
probably damaging |
Het |
Elp1 |
A |
G |
4: 56,779,717 (GRCm39) |
S565P |
probably benign |
Het |
Epn1 |
C |
A |
7: 5,098,684 (GRCm39) |
A370E |
probably benign |
Het |
Esrrg |
T |
C |
1: 187,730,184 (GRCm39) |
|
probably benign |
Het |
Fgd5 |
T |
G |
6: 92,042,145 (GRCm39) |
L1034R |
probably damaging |
Het |
Fpgs |
A |
G |
2: 32,573,135 (GRCm39) |
V567A |
possibly damaging |
Het |
Fut2 |
C |
T |
7: 45,300,193 (GRCm39) |
G193E |
possibly damaging |
Het |
H3c3 |
T |
C |
13: 23,929,425 (GRCm39) |
K19R |
possibly damaging |
Het |
Hsd17b14 |
T |
C |
7: 45,205,503 (GRCm39) |
F38S |
possibly damaging |
Het |
Larp1 |
T |
C |
11: 57,941,703 (GRCm39) |
V712A |
possibly damaging |
Het |
Mep1b |
T |
C |
18: 21,221,617 (GRCm39) |
F189S |
probably damaging |
Het |
Mill1 |
T |
C |
7: 17,989,832 (GRCm39) |
V38A |
probably benign |
Het |
Niban2 |
C |
T |
2: 32,766,398 (GRCm39) |
R13W |
possibly damaging |
Het |
Npy4r |
T |
C |
14: 33,868,290 (GRCm39) |
I333V |
probably benign |
Het |
Numa1 |
G |
T |
7: 101,649,874 (GRCm39) |
E1202* |
probably null |
Het |
Or3a1b |
C |
T |
11: 74,012,610 (GRCm39) |
A165V |
probably benign |
Het |
Or6k6 |
A |
G |
1: 173,945,276 (GRCm39) |
I102T |
probably benign |
Het |
Oxr1 |
A |
T |
15: 41,683,645 (GRCm39) |
Q356L |
possibly damaging |
Het |
Prdx2 |
T |
C |
8: 85,698,198 (GRCm39) |
F130L |
probably damaging |
Het |
Rasa1 |
A |
T |
13: 85,404,515 (GRCm39) |
S248R |
possibly damaging |
Het |
Rgs19 |
A |
G |
2: 181,333,114 (GRCm39) |
S49P |
probably benign |
Het |
Serpinb11 |
T |
C |
1: 107,307,654 (GRCm39) |
F362L |
probably damaging |
Het |
Slamf8 |
T |
C |
1: 172,411,736 (GRCm39) |
H253R |
possibly damaging |
Het |
Tet3 |
C |
A |
6: 83,353,769 (GRCm39) |
R829L |
probably damaging |
Het |
Trappc8 |
A |
G |
18: 20,996,652 (GRCm39) |
L420P |
probably damaging |
Het |
Ube2u |
A |
T |
4: 100,407,199 (GRCm39) |
*353Y |
probably null |
Het |
Wbp1l |
A |
C |
19: 46,632,838 (GRCm39) |
D46A |
probably damaging |
Het |
Zbtb21 |
A |
G |
16: 97,752,945 (GRCm39) |
V474A |
probably 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 |
|
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 |
R7080:Rinl
|
UTSW |
7 |
28,496,101 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|
|