Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
A |
G |
12: 71,236,356 (GRCm39) |
T1236A |
possibly damaging |
Het |
9930111J21Rik1 |
A |
T |
11: 48,838,829 (GRCm39) |
M586K |
probably damaging |
Het |
Adamts4 |
T |
C |
1: 171,080,314 (GRCm39) |
V289A |
possibly damaging |
Het |
Ankrd44 |
A |
T |
1: 54,762,257 (GRCm39) |
D522E |
probably benign |
Het |
Asb14 |
A |
G |
14: 26,637,067 (GRCm39) |
Y603C |
probably damaging |
Het |
Bcl7b |
A |
G |
5: 135,197,308 (GRCm39) |
|
probably benign |
Het |
Cd5 |
T |
C |
19: 10,700,469 (GRCm39) |
K345R |
possibly damaging |
Het |
Celsr3 |
T |
C |
9: 108,708,988 (GRCm39) |
F1278S |
probably damaging |
Het |
Cndp1 |
T |
A |
18: 84,650,049 (GRCm39) |
T215S |
possibly damaging |
Het |
Crygb |
T |
G |
1: 65,119,709 (GRCm39) |
R90S |
probably damaging |
Het |
Dlg4 |
T |
A |
11: 69,933,078 (GRCm39) |
F555I |
possibly damaging |
Het |
Dnah3 |
C |
T |
7: 119,551,728 (GRCm39) |
V2864M |
probably damaging |
Het |
Dnttip2 |
A |
G |
3: 122,070,351 (GRCm39) |
E522G |
probably damaging |
Het |
Ercc4 |
G |
C |
16: 12,948,001 (GRCm39) |
R406P |
probably benign |
Het |
Foxp1 |
G |
A |
6: 98,922,543 (GRCm39) |
P430S |
unknown |
Het |
Galnt1 |
A |
G |
18: 24,400,628 (GRCm39) |
T245A |
probably benign |
Het |
Jcad |
C |
A |
18: 4,649,402 (GRCm39) |
A91E |
possibly damaging |
Het |
Kat6a |
G |
A |
8: 23,352,275 (GRCm39) |
V20I |
probably damaging |
Het |
Kcnb2 |
A |
G |
1: 15,781,777 (GRCm39) |
N883S |
probably damaging |
Het |
Lrch3 |
A |
T |
16: 32,775,750 (GRCm39) |
R205S |
probably damaging |
Het |
Lrr1 |
A |
G |
12: 69,215,825 (GRCm39) |
T66A |
probably benign |
Het |
Lrrc37a |
T |
A |
11: 103,351,635 (GRCm39) |
I2569F |
unknown |
Het |
Maip1 |
A |
T |
1: 57,449,102 (GRCm39) |
Q161L |
probably damaging |
Het |
Neb |
T |
C |
2: 52,047,923 (GRCm39) |
E6699G |
probably benign |
Het |
Nup205 |
A |
G |
6: 35,202,182 (GRCm39) |
R1305G |
probably damaging |
Het |
Or1e19 |
T |
A |
11: 73,316,794 (GRCm39) |
N5I |
probably damaging |
Het |
Or5ac21 |
A |
T |
16: 59,124,418 (GRCm39) |
R301* |
probably null |
Het |
Pate1 |
G |
A |
9: 35,596,418 (GRCm39) |
R116W |
probably damaging |
Het |
Pcsk5 |
T |
G |
19: 17,410,809 (GRCm39) |
E1861A |
probably benign |
Het |
Peg10 |
C |
CTCA |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Per1 |
A |
T |
11: 68,999,953 (GRCm39) |
D1215V |
possibly damaging |
Het |
Phactr2 |
A |
G |
10: 13,129,570 (GRCm39) |
S233P |
probably damaging |
Het |
Pramel28 |
A |
G |
4: 143,692,212 (GRCm39) |
V263A |
probably benign |
Het |
Rgsl1 |
T |
A |
1: 153,701,435 (GRCm39) |
N340Y |
possibly damaging |
Het |
Rhot1 |
C |
T |
11: 80,114,786 (GRCm39) |
P65S |
probably damaging |
Het |
Scrn2 |
T |
C |
11: 96,921,869 (GRCm39) |
L113P |
probably damaging |
Het |
Sema6a |
T |
C |
18: 47,381,958 (GRCm39) |
K863R |
probably benign |
Het |
Slc15a1 |
A |
G |
14: 121,715,528 (GRCm39) |
V337A |
possibly damaging |
Het |
Slc25a1 |
T |
C |
16: 17,743,720 (GRCm39) |
D298G |
probably benign |
Het |
Slc25a22 |
G |
A |
7: 141,011,737 (GRCm39) |
P168S |
probably benign |
Het |
Slc29a4 |
A |
T |
5: 142,691,109 (GRCm39) |
|
probably null |
Het |
Slc35d1 |
T |
C |
4: 103,047,007 (GRCm39) |
T264A |
|
Het |
Spice1 |
T |
C |
16: 44,205,060 (GRCm39) |
S789P |
probably damaging |
Het |
Sprr2b |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
3: 92,224,826 (GRCm39) |
|
probably benign |
Het |
Tectb |
T |
C |
19: 55,178,099 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
A |
2: 76,544,810 (GRCm39) |
Y32764F |
probably damaging |
Het |
Utrn |
T |
G |
10: 12,545,887 (GRCm39) |
S1684R |
possibly damaging |
Het |
Zic1 |
G |
T |
9: 91,246,847 (GRCm39) |
A75E |
probably damaging |
Het |
Zswim4 |
A |
G |
8: 84,939,014 (GRCm39) |
V956A |
possibly damaging |
Het |
|
Other mutations in Gnl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01977:Gnl2
|
APN |
4 |
124,941,405 (GRCm39) |
splice site |
probably null |
|
IGL02536:Gnl2
|
APN |
4 |
124,946,401 (GRCm39) |
nonsense |
probably null |
|
IGL03358:Gnl2
|
APN |
4 |
124,946,387 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4283001:Gnl2
|
UTSW |
4 |
124,940,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R0377:Gnl2
|
UTSW |
4 |
124,940,175 (GRCm39) |
splice site |
probably benign |
|
R0419:Gnl2
|
UTSW |
4 |
124,947,320 (GRCm39) |
missense |
probably benign |
0.00 |
R0975:Gnl2
|
UTSW |
4 |
124,942,171 (GRCm39) |
missense |
probably damaging |
0.99 |
R1529:Gnl2
|
UTSW |
4 |
124,940,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R1550:Gnl2
|
UTSW |
4 |
124,938,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R1942:Gnl2
|
UTSW |
4 |
124,923,957 (GRCm39) |
missense |
probably benign |
0.01 |
R2095:Gnl2
|
UTSW |
4 |
124,928,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Gnl2
|
UTSW |
4 |
124,947,278 (GRCm39) |
missense |
probably benign |
0.01 |
R3712:Gnl2
|
UTSW |
4 |
124,940,067 (GRCm39) |
missense |
probably damaging |
0.98 |
R3781:Gnl2
|
UTSW |
4 |
124,931,399 (GRCm39) |
missense |
probably damaging |
0.99 |
R4656:Gnl2
|
UTSW |
4 |
124,934,790 (GRCm39) |
nonsense |
probably null |
|
R4676:Gnl2
|
UTSW |
4 |
124,947,266 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4710:Gnl2
|
UTSW |
4 |
124,947,252 (GRCm39) |
missense |
probably benign |
0.01 |
R4734:Gnl2
|
UTSW |
4 |
124,934,811 (GRCm39) |
missense |
probably benign |
|
R4916:Gnl2
|
UTSW |
4 |
124,937,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R5106:Gnl2
|
UTSW |
4 |
124,947,329 (GRCm39) |
critical splice donor site |
probably null |
|
R5310:Gnl2
|
UTSW |
4 |
124,946,633 (GRCm39) |
missense |
probably benign |
0.00 |
R5506:Gnl2
|
UTSW |
4 |
124,949,158 (GRCm39) |
utr 3 prime |
probably benign |
|
R5967:Gnl2
|
UTSW |
4 |
124,934,823 (GRCm39) |
missense |
probably benign |
0.00 |
R6184:Gnl2
|
UTSW |
4 |
124,948,022 (GRCm39) |
critical splice donor site |
probably null |
|
R6395:Gnl2
|
UTSW |
4 |
124,940,058 (GRCm39) |
missense |
probably damaging |
0.99 |
R6432:Gnl2
|
UTSW |
4 |
124,946,353 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6672:Gnl2
|
UTSW |
4 |
124,942,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7657:Gnl2
|
UTSW |
4 |
124,923,951 (GRCm39) |
missense |
probably benign |
0.00 |
R8387:Gnl2
|
UTSW |
4 |
124,949,127 (GRCm39) |
makesense |
probably null |
|
R9083:Gnl2
|
UTSW |
4 |
124,941,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R9276:Gnl2
|
UTSW |
4 |
124,947,250 (GRCm39) |
missense |
possibly damaging |
0.83 |
RF003:Gnl2
|
UTSW |
4 |
124,937,518 (GRCm39) |
critical splice donor site |
probably null |
|
|