Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akip1 |
C |
T |
7: 109,306,716 (GRCm39) |
Q138* |
probably null |
Het |
Cdc5l |
A |
G |
17: 45,730,698 (GRCm39) |
I196T |
probably damaging |
Het |
Dnah7b |
G |
T |
1: 46,266,106 (GRCm39) |
R2225L |
probably damaging |
Het |
Gfra2 |
C |
A |
14: 71,133,521 (GRCm39) |
T117K |
possibly damaging |
Het |
Gle1 |
T |
C |
2: 29,828,538 (GRCm39) |
I120T |
probably benign |
Het |
Guf1 |
T |
A |
5: 69,715,572 (GRCm39) |
N52K |
possibly damaging |
Het |
Helq |
T |
C |
5: 100,919,713 (GRCm39) |
K813E |
probably benign |
Het |
Ighv7-4 |
A |
T |
12: 114,186,635 (GRCm39) |
F46I |
probably damaging |
Het |
Il6st |
G |
A |
13: 112,631,861 (GRCm39) |
D467N |
probably benign |
Het |
Jak1 |
C |
A |
4: 101,016,329 (GRCm39) |
V812L |
probably benign |
Het |
Kank4 |
G |
T |
4: 98,667,358 (GRCm39) |
T363K |
probably damaging |
Het |
Lcat |
C |
A |
8: 106,669,059 (GRCm39) |
W72L |
possibly damaging |
Het |
Map2 |
T |
C |
1: 66,452,759 (GRCm39) |
S392P |
possibly damaging |
Het |
Mtmr2 |
T |
C |
9: 13,711,358 (GRCm39) |
F456L |
probably damaging |
Het |
Myh8 |
A |
T |
11: 67,183,247 (GRCm39) |
R709W |
probably damaging |
Het |
Nop14 |
T |
C |
5: 34,807,951 (GRCm39) |
N337S |
probably damaging |
Het |
Or4c58 |
T |
G |
2: 89,675,122 (GRCm39) |
D65A |
probably damaging |
Het |
Oxsm |
A |
T |
14: 16,242,079 (GRCm38) |
V230E |
probably damaging |
Het |
Paox |
G |
A |
7: 139,713,941 (GRCm39) |
G234R |
probably damaging |
Het |
Polq |
C |
T |
16: 36,881,120 (GRCm39) |
H1095Y |
probably benign |
Het |
Rad51c |
T |
C |
11: 87,293,572 (GRCm39) |
T77A |
probably damaging |
Het |
Ryr3 |
C |
A |
2: 112,624,815 (GRCm39) |
V2202F |
probably damaging |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Snx27 |
T |
C |
3: 94,410,794 (GRCm39) |
H452R |
probably benign |
Het |
Son |
C |
T |
16: 91,456,250 (GRCm39) |
H1666Y |
probably damaging |
Het |
Spata25 |
C |
A |
2: 164,669,408 (GRCm39) |
W201L |
possibly damaging |
Het |
Spint2 |
A |
G |
7: 28,963,097 (GRCm39) |
V67A |
probably damaging |
Het |
Srgap1 |
T |
C |
10: 121,691,268 (GRCm39) |
Y322C |
probably benign |
Het |
Synm |
T |
C |
7: 67,385,109 (GRCm39) |
Y409C |
probably damaging |
Het |
Tex11 |
C |
A |
X: 99,977,021 (GRCm39) |
A487S |
possibly damaging |
Het |
Tpm1 |
T |
C |
9: 66,930,649 (GRCm39) |
N283D |
probably benign |
Het |
Trpv6 |
T |
C |
6: 41,602,432 (GRCm39) |
D318G |
probably damaging |
Het |
Ube2j2 |
A |
G |
4: 156,033,543 (GRCm39) |
D39G |
probably damaging |
Het |
Ubr1 |
C |
T |
2: 120,777,103 (GRCm39) |
|
probably null |
Het |
Vwa5a |
T |
C |
9: 38,635,166 (GRCm39) |
F224L |
probably damaging |
Het |
Zfp445 |
T |
A |
9: 122,681,002 (GRCm39) |
M980L |
probably benign |
Het |
|
Other mutations in Npbwr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02282:Npbwr1
|
APN |
1 |
5,987,184 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0140:Npbwr1
|
UTSW |
1 |
5,986,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R0585:Npbwr1
|
UTSW |
1 |
5,986,677 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0827:Npbwr1
|
UTSW |
1 |
5,987,008 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1472:Npbwr1
|
UTSW |
1 |
5,986,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R1646:Npbwr1
|
UTSW |
1 |
5,987,473 (GRCm39) |
missense |
probably benign |
0.01 |
R2001:Npbwr1
|
UTSW |
1 |
5,987,394 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2004:Npbwr1
|
UTSW |
1 |
5,986,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R2005:Npbwr1
|
UTSW |
1 |
5,986,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R2006:Npbwr1
|
UTSW |
1 |
5,986,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R2259:Npbwr1
|
UTSW |
1 |
5,986,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R5614:Npbwr1
|
UTSW |
1 |
5,987,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R6379:Npbwr1
|
UTSW |
1 |
5,987,438 (GRCm39) |
missense |
probably benign |
0.03 |
R7022:Npbwr1
|
UTSW |
1 |
5,987,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R7462:Npbwr1
|
UTSW |
1 |
5,987,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R7678:Npbwr1
|
UTSW |
1 |
5,986,927 (GRCm39) |
missense |
probably benign |
0.03 |
R8441:Npbwr1
|
UTSW |
1 |
5,987,397 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8547:Npbwr1
|
UTSW |
1 |
5,987,446 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8694:Npbwr1
|
UTSW |
1 |
5,986,617 (GRCm39) |
missense |
probably damaging |
1.00 |
|