Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Capn9 |
A |
T |
8: 125,335,922 (GRCm39) |
|
probably benign |
Het |
Cchcr1 |
A |
C |
17: 35,841,699 (GRCm39) |
K761Q |
probably benign |
Het |
Cfap20dc |
T |
C |
14: 8,516,507 (GRCm38) |
N347S |
probably benign |
Het |
Csk |
G |
T |
9: 57,538,672 (GRCm39) |
|
probably benign |
Het |
Cyp2j7 |
T |
C |
4: 96,118,366 (GRCm39) |
K76E |
probably benign |
Het |
Dpep1 |
G |
A |
8: 123,920,888 (GRCm39) |
A23T |
possibly damaging |
Het |
Dpp8 |
T |
A |
9: 64,949,549 (GRCm39) |
M98K |
possibly damaging |
Het |
Eno2 |
T |
C |
6: 124,738,626 (GRCm39) |
Y364C |
probably damaging |
Het |
Gfra1 |
A |
G |
19: 58,441,683 (GRCm39) |
S83P |
probably benign |
Het |
Gramd1b |
T |
C |
9: 40,218,127 (GRCm39) |
E563G |
probably damaging |
Het |
Kcns2 |
G |
T |
15: 34,838,961 (GRCm39) |
W108L |
probably damaging |
Het |
Mroh4 |
T |
C |
15: 74,480,086 (GRCm39) |
|
probably benign |
Het |
Obscn |
A |
T |
11: 59,015,446 (GRCm39) |
S1009T |
probably benign |
Het |
Or2y11 |
A |
G |
11: 49,443,506 (GRCm39) |
R311G |
probably benign |
Het |
Or5b119 |
A |
G |
19: 13,456,699 (GRCm39) |
Y288H |
probably damaging |
Het |
Or7g32 |
T |
C |
9: 19,388,805 (GRCm39) |
H244R |
probably damaging |
Het |
Or8b41 |
A |
G |
9: 38,054,707 (GRCm39) |
K92R |
probably benign |
Het |
Plcb2 |
G |
A |
2: 118,547,500 (GRCm39) |
|
probably benign |
Het |
Rpl13a-ps1 |
T |
A |
19: 50,019,111 (GRCm39) |
I22F |
possibly damaging |
Het |
Skil |
A |
G |
3: 31,171,673 (GRCm39) |
E599G |
probably damaging |
Het |
Snx19 |
A |
G |
9: 30,343,556 (GRCm39) |
N572S |
possibly damaging |
Het |
Spata31 |
T |
C |
13: 65,068,463 (GRCm39) |
S204P |
probably benign |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Tenm3 |
A |
T |
8: 48,729,938 (GRCm39) |
V1356E |
probably benign |
Het |
Trpc3 |
T |
A |
3: 36,704,377 (GRCm39) |
I527F |
probably benign |
Het |
Vmn2r69 |
A |
G |
7: 85,059,416 (GRCm39) |
W498R |
probably damaging |
Het |
Vwde |
T |
A |
6: 13,205,759 (GRCm39) |
I263L |
probably damaging |
Het |
Vwf |
G |
T |
6: 125,619,893 (GRCm39) |
V1524L |
possibly damaging |
Het |
Wdr55 |
A |
G |
18: 36,896,435 (GRCm39) |
E375G |
probably benign |
Het |
|
Other mutations in Dspp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00973:Dspp
|
APN |
5 |
104,324,758 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01096:Dspp
|
APN |
5 |
104,323,233 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01317:Dspp
|
APN |
5 |
104,321,914 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02365:Dspp
|
APN |
5 |
104,323,927 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02387:Dspp
|
APN |
5 |
104,323,490 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02406:Dspp
|
APN |
5 |
104,325,232 (GRCm39) |
nonsense |
probably null |
|
IGL02445:Dspp
|
APN |
5 |
104,324,963 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02481:Dspp
|
APN |
5 |
104,323,514 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02536:Dspp
|
APN |
5 |
104,323,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02572:Dspp
|
APN |
5 |
104,324,935 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02677:Dspp
|
APN |
5 |
104,323,843 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02709:Dspp
|
APN |
5 |
104,325,116 (GRCm39) |
missense |
unknown |
|
IGL02740:Dspp
|
APN |
5 |
104,325,104 (GRCm39) |
nonsense |
probably null |
|
IGL03274:Dspp
|
APN |
5 |
104,322,814 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03293:Dspp
|
APN |
5 |
104,325,427 (GRCm39) |
missense |
unknown |
|
FR4449:Dspp
|
UTSW |
5 |
104,326,254 (GRCm39) |
small deletion |
probably benign |
|
R0018:Dspp
|
UTSW |
5 |
104,326,096 (GRCm39) |
missense |
unknown |
|
R0125:Dspp
|
UTSW |
5 |
104,325,905 (GRCm39) |
missense |
unknown |
|
R0503:Dspp
|
UTSW |
5 |
104,325,122 (GRCm39) |
missense |
unknown |
|
R1709:Dspp
|
UTSW |
5 |
104,323,590 (GRCm39) |
missense |
probably damaging |
0.98 |
R1851:Dspp
|
UTSW |
5 |
104,321,951 (GRCm39) |
critical splice donor site |
probably null |
|
R2001:Dspp
|
UTSW |
5 |
104,326,425 (GRCm39) |
missense |
unknown |
|
R2002:Dspp
|
UTSW |
5 |
104,326,425 (GRCm39) |
missense |
unknown |
|
R2198:Dspp
|
UTSW |
5 |
104,323,567 (GRCm39) |
missense |
probably benign |
0.37 |
R2279:Dspp
|
UTSW |
5 |
104,326,250 (GRCm39) |
missense |
unknown |
|
R4026:Dspp
|
UTSW |
5 |
104,325,563 (GRCm39) |
missense |
unknown |
|
R4066:Dspp
|
UTSW |
5 |
104,325,060 (GRCm39) |
missense |
unknown |
|
R4632:Dspp
|
UTSW |
5 |
104,325,272 (GRCm39) |
missense |
unknown |
|
R4693:Dspp
|
UTSW |
5 |
104,325,928 (GRCm39) |
missense |
unknown |
|
R4841:Dspp
|
UTSW |
5 |
104,325,053 (GRCm39) |
missense |
unknown |
|
R4841:Dspp
|
UTSW |
5 |
104,325,052 (GRCm39) |
missense |
unknown |
|
R4917:Dspp
|
UTSW |
5 |
104,325,789 (GRCm39) |
missense |
unknown |
|
R5008:Dspp
|
UTSW |
5 |
104,323,439 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5015:Dspp
|
UTSW |
5 |
104,324,926 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5214:Dspp
|
UTSW |
5 |
104,326,364 (GRCm39) |
missense |
unknown |
|
R5359:Dspp
|
UTSW |
5 |
104,323,752 (GRCm39) |
missense |
probably damaging |
0.98 |
R5538:Dspp
|
UTSW |
5 |
104,323,096 (GRCm39) |
nonsense |
probably null |
|
R5703:Dspp
|
UTSW |
5 |
104,324,917 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5887:Dspp
|
UTSW |
5 |
104,323,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R5902:Dspp
|
UTSW |
5 |
104,325,977 (GRCm39) |
missense |
unknown |
|
R5992:Dspp
|
UTSW |
5 |
104,326,317 (GRCm39) |
missense |
unknown |
|
R6019:Dspp
|
UTSW |
5 |
104,325,905 (GRCm39) |
missense |
unknown |
|
R6191:Dspp
|
UTSW |
5 |
104,325,214 (GRCm39) |
missense |
unknown |
|
R6362:Dspp
|
UTSW |
5 |
104,323,900 (GRCm39) |
missense |
probably benign |
0.19 |
R6736:Dspp
|
UTSW |
5 |
104,326,041 (GRCm39) |
missense |
unknown |
|
R6805:Dspp
|
UTSW |
5 |
104,323,716 (GRCm39) |
missense |
probably benign |
0.03 |
R7064:Dspp
|
UTSW |
5 |
104,324,804 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7178:Dspp
|
UTSW |
5 |
104,321,932 (GRCm39) |
missense |
probably benign |
0.02 |
R7243:Dspp
|
UTSW |
5 |
104,326,227 (GRCm39) |
small deletion |
probably benign |
|
R7390:Dspp
|
UTSW |
5 |
104,323,552 (GRCm39) |
missense |
probably damaging |
0.98 |
R7454:Dspp
|
UTSW |
5 |
104,323,476 (GRCm39) |
missense |
probably benign |
0.01 |
R7585:Dspp
|
UTSW |
5 |
104,323,391 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7662:Dspp
|
UTSW |
5 |
104,325,736 (GRCm39) |
missense |
unknown |
|
R7739:Dspp
|
UTSW |
5 |
104,326,012 (GRCm39) |
missense |
unknown |
|
R7755:Dspp
|
UTSW |
5 |
104,326,227 (GRCm39) |
small deletion |
probably benign |
|
R7805:Dspp
|
UTSW |
5 |
104,323,259 (GRCm39) |
missense |
probably damaging |
0.99 |
R7869:Dspp
|
UTSW |
5 |
104,323,531 (GRCm39) |
missense |
probably damaging |
0.99 |
R7945:Dspp
|
UTSW |
5 |
104,326,227 (GRCm39) |
small deletion |
probably benign |
|
R7978:Dspp
|
UTSW |
5 |
104,326,227 (GRCm39) |
small deletion |
probably benign |
|
R8088:Dspp
|
UTSW |
5 |
104,325,122 (GRCm39) |
missense |
unknown |
|
R8254:Dspp
|
UTSW |
5 |
104,323,194 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8257:Dspp
|
UTSW |
5 |
104,324,867 (GRCm39) |
missense |
probably benign |
0.01 |
R8439:Dspp
|
UTSW |
5 |
104,325,162 (GRCm39) |
missense |
unknown |
|
R8486:Dspp
|
UTSW |
5 |
104,321,883 (GRCm39) |
start gained |
probably benign |
|
R8722:Dspp
|
UTSW |
5 |
104,326,433 (GRCm39) |
missense |
unknown |
|
R8969:Dspp
|
UTSW |
5 |
104,325,640 (GRCm39) |
missense |
unknown |
|
R9254:Dspp
|
UTSW |
5 |
104,322,760 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9379:Dspp
|
UTSW |
5 |
104,322,760 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9509:Dspp
|
UTSW |
5 |
104,325,657 (GRCm39) |
missense |
unknown |
|
R9647:Dspp
|
UTSW |
5 |
104,323,636 (GRCm39) |
missense |
possibly damaging |
0.89 |
RF007:Dspp
|
UTSW |
5 |
104,326,227 (GRCm39) |
small deletion |
probably benign |
|
RF044:Dspp
|
UTSW |
5 |
104,326,290 (GRCm39) |
small insertion |
probably benign |
|
|