Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aaas |
A |
T |
15: 102,248,385 (GRCm39) |
V277D |
probably damaging |
Het |
Akap9 |
T |
A |
5: 4,010,218 (GRCm39) |
V325D |
probably benign |
Het |
Ambra1 |
A |
G |
2: 91,741,757 (GRCm39) |
|
probably null |
Het |
Ano9 |
A |
G |
7: 140,690,352 (GRCm39) |
L94P |
probably damaging |
Het |
Atad3a |
G |
T |
4: 155,830,535 (GRCm39) |
T521K |
probably damaging |
Het |
Bckdk |
A |
G |
7: 127,504,948 (GRCm39) |
K126E |
possibly damaging |
Het |
Bdp1 |
A |
T |
13: 100,220,713 (GRCm39) |
|
probably benign |
Het |
Btbd17 |
T |
C |
11: 114,686,599 (GRCm39) |
T26A |
probably benign |
Het |
Cadps2 |
G |
A |
6: 23,587,461 (GRCm39) |
S314L |
probably benign |
Het |
Ccl8 |
A |
T |
11: 82,007,435 (GRCm39) |
Q90L |
probably damaging |
Het |
Chit1 |
T |
C |
1: 134,078,257 (GRCm39) |
V355A |
probably damaging |
Het |
Col17a1 |
A |
G |
19: 47,656,978 (GRCm39) |
I555T |
possibly damaging |
Het |
Dmwd |
T |
A |
7: 18,815,159 (GRCm39) |
|
probably null |
Het |
Dtna |
T |
C |
18: 23,758,144 (GRCm39) |
I483T |
probably damaging |
Het |
Eloc |
T |
A |
1: 16,713,502 (GRCm39) |
|
probably benign |
Het |
Emc7 |
T |
A |
2: 112,295,119 (GRCm39) |
L177H |
probably damaging |
Het |
Emsy |
T |
A |
7: 98,275,831 (GRCm39) |
K352I |
probably damaging |
Het |
Ermn |
T |
C |
2: 57,942,502 (GRCm39) |
E76G |
probably benign |
Het |
Flot1 |
A |
T |
17: 36,140,763 (GRCm39) |
E203V |
possibly damaging |
Het |
Hsd11b2 |
A |
G |
8: 106,249,529 (GRCm39) |
K266R |
probably benign |
Het |
Iqck |
A |
T |
7: 118,476,901 (GRCm39) |
K154M |
probably damaging |
Het |
Itgb5 |
T |
A |
16: 33,740,168 (GRCm39) |
V426E |
probably damaging |
Het |
Kash5 |
T |
C |
7: 44,839,384 (GRCm39) |
D359G |
probably damaging |
Het |
Kif13a |
T |
C |
13: 47,018,296 (GRCm39) |
K53R |
probably benign |
Het |
Klhl2 |
A |
T |
8: 65,232,772 (GRCm39) |
H168Q |
probably damaging |
Het |
Lpcat2b |
T |
C |
5: 107,581,759 (GRCm39) |
Y363H |
probably damaging |
Het |
Lrp6 |
A |
T |
6: 134,488,225 (GRCm39) |
N290K |
probably damaging |
Het |
Map2k3 |
T |
C |
11: 60,840,873 (GRCm39) |
F301L |
possibly damaging |
Het |
Mns1 |
A |
G |
9: 72,364,195 (GRCm39) |
|
probably benign |
Het |
Or1j17 |
T |
A |
2: 36,578,550 (GRCm39) |
C179S |
probably damaging |
Het |
Or52h7 |
T |
A |
7: 104,214,220 (GRCm39) |
V264D |
probably damaging |
Het |
Pask |
A |
T |
1: 93,237,844 (GRCm39) |
H1374Q |
possibly damaging |
Het |
Pik3r1 |
G |
A |
13: 101,822,728 (GRCm39) |
A658V |
probably damaging |
Het |
Ppp2r2a |
A |
T |
14: 67,307,726 (GRCm39) |
F14I |
probably damaging |
Het |
Ptprc |
C |
T |
1: 137,996,148 (GRCm39) |
E904K |
possibly damaging |
Het |
Rab11fip4 |
G |
T |
11: 79,582,705 (GRCm39) |
D591Y |
possibly damaging |
Het |
Rab3gap2 |
A |
G |
1: 184,936,523 (GRCm39) |
T29A |
probably benign |
Het |
Rgs19 |
A |
G |
2: 181,331,381 (GRCm39) |
V84A |
possibly damaging |
Het |
Shisa6 |
T |
G |
11: 66,108,705 (GRCm39) |
M391L |
probably benign |
Het |
Sipa1l1 |
G |
A |
12: 82,469,263 (GRCm39) |
G1254D |
probably damaging |
Het |
Slfn8 |
A |
T |
11: 82,895,059 (GRCm39) |
Y358* |
probably null |
Het |
Taf3 |
G |
T |
2: 9,957,472 (GRCm39) |
R232S |
probably benign |
Het |
Terb2 |
T |
A |
2: 122,035,338 (GRCm39) |
H186Q |
possibly damaging |
Het |
Trav13n-4 |
T |
C |
14: 53,601,473 (GRCm39) |
S81P |
probably damaging |
Het |
Trim30d |
G |
T |
7: 104,121,333 (GRCm39) |
P321T |
possibly damaging |
Het |
Tyrp1 |
G |
T |
4: 80,763,039 (GRCm39) |
G309* |
probably null |
Het |
Vps13d |
C |
A |
4: 144,821,437 (GRCm39) |
G2979V |
possibly damaging |
Het |
|
Other mutations in Nos1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Nos1
|
APN |
5 |
118,048,165 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01155:Nos1
|
APN |
5 |
118,083,991 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01462:Nos1
|
APN |
5 |
118,005,774 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01464:Nos1
|
APN |
5 |
118,081,257 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01621:Nos1
|
APN |
5 |
118,083,949 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01796:Nos1
|
APN |
5 |
118,076,339 (GRCm39) |
nonsense |
probably null |
|
IGL02003:Nos1
|
APN |
5 |
118,043,530 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02274:Nos1
|
APN |
5 |
118,035,845 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02885:Nos1
|
APN |
5 |
118,033,855 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02947:Nos1
|
APN |
5 |
118,081,382 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03088:Nos1
|
APN |
5 |
118,005,323 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03166:Nos1
|
APN |
5 |
118,052,517 (GRCm39) |
splice site |
probably benign |
|
Crumple
|
UTSW |
5 |
118,033,925 (GRCm39) |
missense |
possibly damaging |
0.95 |
penurious
|
UTSW |
5 |
118,033,967 (GRCm39) |
missense |
probably damaging |
0.97 |
spendthrift
|
UTSW |
5 |
118,091,848 (GRCm39) |
splice site |
probably benign |
|
squanderer
|
UTSW |
5 |
118,048,303 (GRCm39) |
missense |
probably damaging |
0.97 |
R0007:Nos1
|
UTSW |
5 |
118,048,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Nos1
|
UTSW |
5 |
118,031,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R0080:Nos1
|
UTSW |
5 |
118,031,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R0212:Nos1
|
UTSW |
5 |
118,048,277 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0240:Nos1
|
UTSW |
5 |
118,005,948 (GRCm39) |
missense |
probably benign |
|
R0240:Nos1
|
UTSW |
5 |
118,005,948 (GRCm39) |
missense |
probably benign |
|
R0454:Nos1
|
UTSW |
5 |
118,081,385 (GRCm39) |
missense |
probably benign |
0.00 |
R0494:Nos1
|
UTSW |
5 |
118,043,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R0882:Nos1
|
UTSW |
5 |
118,085,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R1099:Nos1
|
UTSW |
5 |
118,061,460 (GRCm39) |
missense |
probably damaging |
0.96 |
R1243:Nos1
|
UTSW |
5 |
118,043,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R1387:Nos1
|
UTSW |
5 |
118,091,848 (GRCm39) |
splice site |
probably benign |
|
R1432:Nos1
|
UTSW |
5 |
118,087,684 (GRCm39) |
splice site |
probably benign |
|
R1698:Nos1
|
UTSW |
5 |
118,005,297 (GRCm39) |
missense |
probably benign |
0.01 |
R1710:Nos1
|
UTSW |
5 |
118,033,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R1859:Nos1
|
UTSW |
5 |
118,043,527 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1973:Nos1
|
UTSW |
5 |
118,074,491 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2084:Nos1
|
UTSW |
5 |
118,081,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R2112:Nos1
|
UTSW |
5 |
118,074,636 (GRCm39) |
missense |
probably benign |
0.00 |
R4689:Nos1
|
UTSW |
5 |
118,017,450 (GRCm39) |
missense |
probably benign |
0.04 |
R4769:Nos1
|
UTSW |
5 |
118,081,310 (GRCm39) |
nonsense |
probably null |
|
R4893:Nos1
|
UTSW |
5 |
118,090,942 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4916:Nos1
|
UTSW |
5 |
118,085,635 (GRCm39) |
critical splice donor site |
probably null |
|
R4956:Nos1
|
UTSW |
5 |
118,085,575 (GRCm39) |
missense |
probably benign |
|
R4971:Nos1
|
UTSW |
5 |
118,081,899 (GRCm39) |
missense |
probably benign |
0.05 |
R4987:Nos1
|
UTSW |
5 |
118,064,598 (GRCm39) |
critical splice donor site |
probably null |
|
R5015:Nos1
|
UTSW |
5 |
118,005,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R5031:Nos1
|
UTSW |
5 |
118,017,378 (GRCm39) |
missense |
probably benign |
|
R5137:Nos1
|
UTSW |
5 |
118,043,378 (GRCm39) |
missense |
probably benign |
0.29 |
R5481:Nos1
|
UTSW |
5 |
118,005,819 (GRCm39) |
missense |
probably benign |
0.06 |
R5541:Nos1
|
UTSW |
5 |
118,043,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Nos1
|
UTSW |
5 |
118,061,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R5866:Nos1
|
UTSW |
5 |
118,033,967 (GRCm39) |
missense |
probably damaging |
0.97 |
R5934:Nos1
|
UTSW |
5 |
118,074,510 (GRCm39) |
missense |
probably damaging |
0.99 |
R6158:Nos1
|
UTSW |
5 |
118,005,639 (GRCm39) |
missense |
probably benign |
0.05 |
R6225:Nos1
|
UTSW |
5 |
118,050,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R6261:Nos1
|
UTSW |
5 |
118,074,635 (GRCm39) |
missense |
probably benign |
|
R6388:Nos1
|
UTSW |
5 |
118,052,501 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6987:Nos1
|
UTSW |
5 |
118,033,850 (GRCm39) |
missense |
probably benign |
0.05 |
R7104:Nos1
|
UTSW |
5 |
118,085,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R7136:Nos1
|
UTSW |
5 |
118,033,925 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7276:Nos1
|
UTSW |
5 |
118,048,303 (GRCm39) |
missense |
probably damaging |
0.97 |
R7299:Nos1
|
UTSW |
5 |
118,005,970 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7301:Nos1
|
UTSW |
5 |
118,005,970 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7402:Nos1
|
UTSW |
5 |
118,087,880 (GRCm39) |
missense |
probably benign |
0.34 |
R7408:Nos1
|
UTSW |
5 |
118,005,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R7618:Nos1
|
UTSW |
5 |
118,042,009 (GRCm39) |
missense |
probably benign |
0.01 |
R7689:Nos1
|
UTSW |
5 |
118,035,792 (GRCm39) |
missense |
probably damaging |
0.98 |
R7964:Nos1
|
UTSW |
5 |
118,038,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Nos1
|
UTSW |
5 |
118,017,405 (GRCm39) |
missense |
probably benign |
0.05 |
R9147:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9148:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9149:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9246:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9248:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9249:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9254:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9255:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9256:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9283:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9320:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9321:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9326:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9327:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9331:Nos1
|
UTSW |
5 |
118,038,589 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9379:Nos1
|
UTSW |
5 |
118,017,402 (GRCm39) |
missense |
probably benign |
0.44 |
R9432:Nos1
|
UTSW |
5 |
118,034,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R9470:Nos1
|
UTSW |
5 |
118,064,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R9581:Nos1
|
UTSW |
5 |
118,043,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R9623:Nos1
|
UTSW |
5 |
118,087,849 (GRCm39) |
missense |
probably benign |
0.00 |
X0025:Nos1
|
UTSW |
5 |
118,081,890 (GRCm39) |
missense |
probably benign |
0.00 |
X0026:Nos1
|
UTSW |
5 |
118,081,217 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Nos1
|
UTSW |
5 |
118,061,343 (GRCm39) |
missense |
probably damaging |
0.99 |
|