Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
A |
G |
8: 120,884,227 (GRCm39) |
E330G |
possibly damaging |
Het |
Apob |
A |
C |
12: 8,057,752 (GRCm39) |
D2078A |
probably benign |
Het |
Arhgap21 |
T |
A |
2: 20,854,331 (GRCm39) |
Q1681L |
probably damaging |
Het |
Arsb |
A |
G |
13: 93,998,609 (GRCm39) |
T306A |
probably benign |
Het |
Brpf3 |
G |
A |
17: 29,047,394 (GRCm39) |
D1053N |
probably damaging |
Het |
Cenpf |
A |
T |
1: 189,384,795 (GRCm39) |
I2495N |
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,599,634 (GRCm39) |
K840E |
possibly damaging |
Het |
Cry1 |
A |
G |
10: 84,982,619 (GRCm39) |
L269P |
probably damaging |
Het |
Cyp21a1 |
C |
A |
17: 35,021,701 (GRCm39) |
E289* |
probably null |
Het |
Dcp2 |
A |
T |
18: 44,538,581 (GRCm39) |
K215* |
probably null |
Het |
Dnaaf11 |
A |
G |
15: 66,321,400 (GRCm39) |
I247T |
probably benign |
Het |
Ecm2 |
A |
G |
13: 49,683,632 (GRCm39) |
N537D |
probably damaging |
Het |
Emid1 |
G |
A |
11: 5,085,407 (GRCm39) |
T113M |
probably benign |
Het |
Exoc8 |
C |
T |
8: 125,622,918 (GRCm39) |
W483* |
probably null |
Het |
Fes |
A |
T |
7: 80,030,031 (GRCm39) |
N582K |
probably damaging |
Het |
Flnb |
G |
T |
14: 7,905,507 (GRCm38) |
E1086* |
probably null |
Het |
Flnc |
T |
A |
6: 29,455,844 (GRCm39) |
D2058E |
possibly damaging |
Het |
Gatb |
G |
A |
3: 85,561,112 (GRCm39) |
D543N |
probably benign |
Het |
Gm14412 |
A |
G |
2: 177,009,229 (GRCm39) |
V9A |
probably damaging |
Het |
Gm4884 |
T |
C |
7: 40,692,745 (GRCm39) |
V238A |
possibly damaging |
Het |
Igfbp5 |
A |
G |
1: 72,913,096 (GRCm39) |
V68A |
possibly damaging |
Het |
Igflr1 |
T |
A |
7: 30,267,222 (GRCm39) |
I330N |
probably damaging |
Het |
Il1r2 |
A |
G |
1: 40,154,298 (GRCm39) |
T222A |
probably benign |
Het |
Krt87 |
T |
C |
15: 101,330,989 (GRCm39) |
E419G |
probably benign |
Het |
Lman2 |
A |
G |
13: 55,499,315 (GRCm39) |
S187P |
probably damaging |
Het |
Mrpl38 |
T |
C |
11: 116,029,288 (GRCm39) |
E76G |
possibly damaging |
Het |
Mtx3 |
A |
G |
13: 92,984,112 (GRCm39) |
I130V |
probably benign |
Het |
Nkx2-1 |
T |
G |
12: 56,580,293 (GRCm39) |
M216L |
probably benign |
Het |
Notch1 |
C |
A |
2: 26,350,019 (GRCm39) |
V2374L |
probably benign |
Het |
Nrxn2 |
A |
G |
19: 6,543,037 (GRCm39) |
D1087G |
probably benign |
Het |
Nudt8 |
T |
C |
19: 4,051,902 (GRCm39) |
F171S |
probably damaging |
Het |
Or5an1 |
T |
G |
19: 12,261,224 (GRCm39) |
F271V |
probably benign |
Het |
Pds5a |
A |
T |
5: 65,785,357 (GRCm39) |
C916* |
probably null |
Het |
Phyhip |
A |
T |
14: 70,699,334 (GRCm39) |
N46Y |
probably damaging |
Het |
Pomt1 |
A |
G |
2: 32,140,874 (GRCm39) |
Y502C |
possibly damaging |
Het |
Prkcg |
A |
C |
7: 3,352,097 (GRCm39) |
|
probably benign |
Het |
Prl8a6 |
C |
T |
13: 27,619,369 (GRCm39) |
E118K |
probably benign |
Het |
Prpf39 |
T |
C |
12: 65,104,689 (GRCm39) |
|
probably null |
Het |
Ptprb |
A |
G |
10: 116,205,262 (GRCm39) |
H2159R |
probably damaging |
Het |
Ripor2 |
A |
T |
13: 24,885,595 (GRCm39) |
D571V |
probably damaging |
Het |
Rps19 |
C |
T |
7: 24,584,552 (GRCm39) |
L34F |
probably benign |
Het |
Rusc1 |
A |
G |
3: 88,996,128 (GRCm39) |
S145P |
probably damaging |
Het |
Scn4a |
T |
A |
11: 106,230,051 (GRCm39) |
T586S |
probably damaging |
Het |
Slc7a12 |
A |
G |
3: 14,546,124 (GRCm39) |
S90G |
possibly damaging |
Het |
Specc1l |
A |
G |
10: 75,082,410 (GRCm39) |
D619G |
probably damaging |
Het |
Src |
A |
G |
2: 157,304,710 (GRCm39) |
D143G |
probably benign |
Het |
Sst |
T |
C |
16: 23,708,558 (GRCm39) |
N91S |
probably benign |
Het |
Stxbp5l |
T |
A |
16: 37,036,398 (GRCm39) |
I406F |
probably damaging |
Het |
Thsd1 |
T |
A |
8: 22,748,887 (GRCm39) |
I525N |
probably damaging |
Het |
Ticam2 |
A |
T |
18: 46,693,467 (GRCm39) |
F207I |
probably damaging |
Het |
Tsc22d1 |
C |
A |
14: 76,656,180 (GRCm39) |
N31K |
probably damaging |
Het |
Tspan10 |
T |
C |
11: 120,336,989 (GRCm39) |
V253A |
probably benign |
Het |
Ttc33 |
A |
G |
15: 5,237,924 (GRCm39) |
K99R |
possibly damaging |
Het |
Vmn1r63 |
T |
A |
7: 5,806,212 (GRCm39) |
N140I |
probably damaging |
Het |
Yju2b |
C |
T |
8: 84,990,498 (GRCm39) |
V45I |
probably benign |
Het |
Zbtb25 |
A |
G |
12: 76,395,903 (GRCm39) |
*440Q |
probably null |
Het |
Zfhx4 |
T |
A |
3: 5,461,978 (GRCm39) |
C1218S |
probably damaging |
Het |
Zfp84 |
T |
A |
7: 29,476,607 (GRCm39) |
I433N |
probably damaging |
Het |
|
Other mutations in Naf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00806:Naf1
|
APN |
8 |
67,338,452 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01861:Naf1
|
APN |
8 |
67,317,185 (GRCm39) |
splice site |
probably benign |
|
IGL02817:Naf1
|
APN |
8 |
67,336,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Naf1
|
UTSW |
8 |
67,341,707 (GRCm39) |
splice site |
probably benign |
|
R0092:Naf1
|
UTSW |
8 |
67,341,760 (GRCm39) |
missense |
probably benign |
0.24 |
R2062:Naf1
|
UTSW |
8 |
67,340,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R2065:Naf1
|
UTSW |
8 |
67,340,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R2066:Naf1
|
UTSW |
8 |
67,340,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R2068:Naf1
|
UTSW |
8 |
67,340,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R4296:Naf1
|
UTSW |
8 |
67,342,114 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5186:Naf1
|
UTSW |
8 |
67,332,298 (GRCm39) |
missense |
probably benign |
0.10 |
R5560:Naf1
|
UTSW |
8 |
67,336,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R6122:Naf1
|
UTSW |
8 |
67,336,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R6143:Naf1
|
UTSW |
8 |
67,330,347 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6389:Naf1
|
UTSW |
8 |
67,313,680 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6827:Naf1
|
UTSW |
8 |
67,330,343 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7083:Naf1
|
UTSW |
8 |
67,313,138 (GRCm39) |
unclassified |
probably benign |
|
R7444:Naf1
|
UTSW |
8 |
67,313,200 (GRCm39) |
unclassified |
probably benign |
|
R7727:Naf1
|
UTSW |
8 |
67,313,200 (GRCm39) |
unclassified |
probably benign |
|
R7818:Naf1
|
UTSW |
8 |
67,342,028 (GRCm39) |
missense |
probably damaging |
0.97 |
R7860:Naf1
|
UTSW |
8 |
67,313,165 (GRCm39) |
missense |
unknown |
|
R7923:Naf1
|
UTSW |
8 |
67,313,200 (GRCm39) |
unclassified |
probably benign |
|
R7977:Naf1
|
UTSW |
8 |
67,313,146 (GRCm39) |
unclassified |
probably benign |
|
R8420:Naf1
|
UTSW |
8 |
67,313,200 (GRCm39) |
unclassified |
probably benign |
|
R8462:Naf1
|
UTSW |
8 |
67,313,200 (GRCm39) |
unclassified |
probably benign |
|
R8815:Naf1
|
UTSW |
8 |
67,317,333 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8989:Naf1
|
UTSW |
8 |
67,313,628 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9138:Naf1
|
UTSW |
8 |
67,317,198 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9231:Naf1
|
UTSW |
8 |
67,313,146 (GRCm39) |
unclassified |
probably benign |
|
R9283:Naf1
|
UTSW |
8 |
67,313,503 (GRCm39) |
missense |
unknown |
|
R9445:Naf1
|
UTSW |
8 |
67,336,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R9454:Naf1
|
UTSW |
8 |
67,313,200 (GRCm39) |
unclassified |
probably benign |
|
R9680:Naf1
|
UTSW |
8 |
67,313,200 (GRCm39) |
unclassified |
probably benign |
|
|