Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
A |
T |
6: 23,094,318 (GRCm39) |
|
probably benign |
Het |
Ano3 |
A |
T |
2: 110,527,363 (GRCm39) |
|
probably benign |
Het |
Arpp21 |
T |
C |
9: 112,005,268 (GRCm39) |
Y193C |
probably damaging |
Het |
Atm |
G |
A |
9: 53,364,740 (GRCm39) |
|
probably benign |
Het |
Ceacam13 |
C |
T |
7: 17,744,988 (GRCm39) |
|
probably benign |
Het |
Cenpi |
T |
A |
X: 133,250,017 (GRCm39) |
C599S |
possibly damaging |
Het |
Clec7a |
A |
C |
6: 129,442,441 (GRCm39) |
D195E |
possibly damaging |
Het |
Cnksr1 |
T |
C |
4: 133,962,417 (GRCm39) |
|
probably null |
Het |
Cntn1 |
A |
G |
15: 92,143,891 (GRCm39) |
T285A |
probably benign |
Het |
Dusp4 |
G |
T |
8: 35,285,726 (GRCm39) |
G329V |
probably damaging |
Het |
Esyt1 |
A |
T |
10: 128,355,040 (GRCm39) |
S496T |
probably damaging |
Het |
Evpl |
T |
C |
11: 116,112,648 (GRCm39) |
T1681A |
probably damaging |
Het |
Fam131b |
A |
C |
6: 42,297,926 (GRCm39) |
|
probably benign |
Het |
Fam162b |
T |
C |
10: 51,463,392 (GRCm39) |
M92V |
probably damaging |
Het |
Fbxw2 |
T |
C |
2: 34,695,723 (GRCm39) |
*455W |
probably null |
Het |
Gm12886 |
A |
G |
4: 121,280,234 (GRCm39) |
L14P |
unknown |
Het |
Gpc4 |
A |
T |
X: 51,163,178 (GRCm39) |
V235E |
probably damaging |
Het |
Gss |
A |
G |
2: 155,419,541 (GRCm39) |
L170P |
probably damaging |
Het |
Hbs1l |
C |
T |
10: 21,217,610 (GRCm39) |
|
probably benign |
Het |
Hhatl |
T |
C |
9: 121,618,857 (GRCm39) |
M92V |
probably benign |
Het |
Hhla1 |
A |
T |
15: 65,814,542 (GRCm39) |
L194H |
probably damaging |
Het |
Hivep2 |
C |
A |
10: 14,004,757 (GRCm39) |
R452S |
probably benign |
Het |
Homer2 |
C |
A |
7: 81,299,393 (GRCm39) |
W24L |
probably damaging |
Het |
Lhcgr |
A |
T |
17: 89,050,050 (GRCm39) |
L492H |
probably damaging |
Het |
Lrba |
C |
A |
3: 86,217,691 (GRCm39) |
|
probably null |
Het |
Lrp2 |
G |
T |
2: 69,318,181 (GRCm39) |
P2090Q |
probably damaging |
Het |
Lyl1 |
C |
T |
8: 85,429,300 (GRCm39) |
P3L |
possibly damaging |
Het |
Madd |
T |
A |
2: 90,973,172 (GRCm39) |
M1497L |
probably benign |
Het |
Naprt |
C |
T |
15: 75,764,206 (GRCm39) |
R336Q |
probably damaging |
Het |
Nars1 |
A |
G |
18: 64,638,266 (GRCm39) |
C266R |
possibly damaging |
Het |
Or10v1 |
T |
A |
19: 11,874,145 (GRCm39) |
Y253* |
probably null |
Het |
Or5k8 |
T |
A |
16: 58,644,451 (GRCm39) |
Q207L |
probably benign |
Het |
Pard3 |
A |
T |
8: 128,032,975 (GRCm39) |
T190S |
probably benign |
Het |
Pstpip2 |
A |
G |
18: 77,942,507 (GRCm39) |
N86S |
probably benign |
Het |
Ptgfrn |
T |
C |
3: 100,980,135 (GRCm39) |
T402A |
probably benign |
Het |
Rnf130 |
T |
C |
11: 49,943,598 (GRCm39) |
|
probably benign |
Het |
Ropn1l |
T |
C |
15: 31,451,325 (GRCm39) |
D53G |
possibly damaging |
Het |
Rps6ka2 |
G |
A |
17: 7,521,849 (GRCm39) |
|
probably null |
Het |
Rtn2 |
T |
C |
7: 19,027,036 (GRCm39) |
S17P |
probably damaging |
Het |
Shank2 |
T |
C |
7: 143,963,373 (GRCm39) |
V327A |
probably benign |
Het |
Slc22a16 |
T |
G |
10: 40,449,958 (GRCm39) |
Y131* |
probably null |
Het |
Slc28a2 |
T |
A |
2: 122,288,458 (GRCm39) |
M583K |
possibly damaging |
Het |
Slco1a6 |
G |
T |
6: 142,078,961 (GRCm39) |
|
probably null |
Het |
Slfn8 |
T |
A |
11: 82,894,078 (GRCm39) |
I854F |
probably damaging |
Het |
Strip1 |
T |
C |
3: 107,520,582 (GRCm39) |
R823G |
probably benign |
Het |
Stxbp2 |
A |
T |
8: 3,691,971 (GRCm39) |
I538F |
probably benign |
Het |
Tcl1b5 |
C |
T |
12: 105,145,273 (GRCm39) |
T79M |
probably benign |
Het |
Tmem104 |
G |
T |
11: 115,088,122 (GRCm39) |
A36S |
probably damaging |
Het |
Trim55 |
T |
A |
3: 19,725,116 (GRCm39) |
L211Q |
probably damaging |
Het |
Trim80 |
T |
C |
11: 115,332,419 (GRCm39) |
W204R |
possibly damaging |
Het |
Ttbk1 |
G |
A |
17: 46,757,256 (GRCm39) |
T1126I |
probably benign |
Het |
Ubqln2 |
C |
T |
X: 152,282,692 (GRCm39) |
Q415* |
probably null |
Het |
Unc13a |
C |
T |
8: 72,103,193 (GRCm39) |
R931H |
possibly damaging |
Het |
Utp4 |
T |
A |
8: 107,621,273 (GRCm39) |
S17T |
probably benign |
Het |
|
Other mutations in Emb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01406:Emb
|
APN |
13 |
117,405,466 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01613:Emb
|
APN |
13 |
117,408,614 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01780:Emb
|
APN |
13 |
117,386,007 (GRCm39) |
unclassified |
probably benign |
|
IGL02187:Emb
|
APN |
13 |
117,405,507 (GRCm39) |
splice site |
probably benign |
|
IGL02350:Emb
|
APN |
13 |
117,386,007 (GRCm39) |
unclassified |
probably benign |
|
IGL02357:Emb
|
APN |
13 |
117,386,007 (GRCm39) |
unclassified |
probably benign |
|
IGL02728:Emb
|
APN |
13 |
117,369,301 (GRCm39) |
missense |
probably benign |
0.39 |
R0098:Emb
|
UTSW |
13 |
117,404,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Emb
|
UTSW |
13 |
117,404,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R0540:Emb
|
UTSW |
13 |
117,369,286 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0607:Emb
|
UTSW |
13 |
117,369,286 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1421:Emb
|
UTSW |
13 |
117,408,624 (GRCm39) |
missense |
probably benign |
0.00 |
R1749:Emb
|
UTSW |
13 |
117,386,242 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2129:Emb
|
UTSW |
13 |
117,404,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R3896:Emb
|
UTSW |
13 |
117,409,598 (GRCm39) |
makesense |
probably null |
|
R4371:Emb
|
UTSW |
13 |
117,405,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R4990:Emb
|
UTSW |
13 |
117,401,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R5398:Emb
|
UTSW |
13 |
117,404,088 (GRCm39) |
missense |
probably damaging |
0.97 |
R5949:Emb
|
UTSW |
13 |
117,403,928 (GRCm39) |
missense |
probably benign |
0.13 |
R6330:Emb
|
UTSW |
13 |
117,385,666 (GRCm39) |
splice site |
probably null |
|
R7221:Emb
|
UTSW |
13 |
117,404,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R7479:Emb
|
UTSW |
13 |
117,385,962 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7548:Emb
|
UTSW |
13 |
117,408,590 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7557:Emb
|
UTSW |
13 |
117,386,252 (GRCm39) |
missense |
probably benign |
0.21 |
R7605:Emb
|
UTSW |
13 |
117,401,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R9314:Emb
|
UTSW |
13 |
117,408,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R9364:Emb
|
UTSW |
13 |
117,357,096 (GRCm39) |
intron |
probably benign |
|
R9366:Emb
|
UTSW |
13 |
117,357,096 (GRCm39) |
intron |
probably benign |
|
R9368:Emb
|
UTSW |
13 |
117,357,096 (GRCm39) |
intron |
probably benign |
|
R9369:Emb
|
UTSW |
13 |
117,357,096 (GRCm39) |
intron |
probably benign |
|
R9381:Emb
|
UTSW |
13 |
117,357,096 (GRCm39) |
intron |
probably benign |
|
|