Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgef10 |
A |
G |
8: 14,997,205 (GRCm39) |
D48G |
probably damaging |
Het |
Asnsd1 |
T |
C |
1: 53,386,734 (GRCm39) |
I298V |
probably benign |
Het |
Cacna2d3 |
G |
T |
14: 28,678,827 (GRCm39) |
|
probably null |
Het |
Cbs |
T |
C |
17: 31,844,922 (GRCm39) |
|
probably null |
Het |
Ccm2 |
C |
A |
11: 6,540,808 (GRCm39) |
T216K |
probably damaging |
Het |
Galc |
C |
T |
12: 98,220,473 (GRCm39) |
W131* |
probably null |
Het |
Gemin5 |
T |
C |
11: 58,047,621 (GRCm39) |
R318G |
possibly damaging |
Het |
Gsta3 |
T |
G |
1: 21,320,012 (GRCm39) |
V6G |
possibly damaging |
Het |
Hdlbp |
A |
T |
1: 93,336,229 (GRCm39) |
|
probably null |
Het |
Igkv13-55-1 |
T |
G |
6: 69,577,132 (GRCm39) |
|
noncoding transcript |
Het |
Il17rd |
A |
G |
14: 26,821,867 (GRCm39) |
Y387C |
probably damaging |
Het |
Katnip |
A |
G |
7: 125,369,742 (GRCm39) |
|
probably null |
Het |
Kmt2e |
C |
T |
5: 23,705,758 (GRCm39) |
T1344I |
probably benign |
Het |
L3mbtl4 |
A |
C |
17: 69,071,579 (GRCm39) |
H502P |
probably benign |
Het |
Lrig1 |
A |
T |
6: 94,640,919 (GRCm39) |
N95K |
possibly damaging |
Het |
Neurl2 |
G |
T |
2: 164,675,012 (GRCm39) |
R117S |
probably damaging |
Het |
Noxa1 |
A |
T |
2: 24,975,767 (GRCm39) |
V435E |
probably benign |
Het |
Parp9 |
C |
T |
16: 35,768,317 (GRCm39) |
R166W |
probably damaging |
Het |
Pdzd2 |
A |
G |
15: 12,445,735 (GRCm39) |
I158T |
probably damaging |
Het |
Pip5k1c |
T |
C |
10: 81,142,218 (GRCm39) |
Y143H |
probably damaging |
Het |
Qrfpr |
A |
G |
3: 36,276,285 (GRCm39) |
V35A |
probably damaging |
Het |
Rab3gap1 |
T |
G |
1: 127,866,817 (GRCm39) |
S881A |
probably benign |
Het |
Rita1 |
C |
T |
5: 120,747,858 (GRCm39) |
A147T |
probably damaging |
Het |
Scai |
G |
A |
2: 38,992,329 (GRCm39) |
|
probably benign |
Het |
Skic2 |
T |
A |
17: 35,064,839 (GRCm39) |
I418F |
probably damaging |
Het |
Tenm4 |
A |
C |
7: 96,503,941 (GRCm39) |
H1300P |
probably damaging |
Het |
Tmppe |
A |
G |
9: 114,234,499 (GRCm39) |
H266R |
probably benign |
Het |
Wdr11 |
A |
T |
7: 129,232,896 (GRCm39) |
|
probably null |
Het |
Xirp2 |
A |
G |
2: 67,338,995 (GRCm39) |
E412G |
probably benign |
Het |
Zan |
A |
G |
5: 137,419,429 (GRCm39) |
V2910A |
unknown |
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 |
IGL01620:Nos1
|
APN |
5 |
118,043,374 (GRCm39) |
critical splice acceptor site |
probably null |
|
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 |
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 |
|