Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
C |
1: 71,333,959 (GRCm39) |
V1181G |
probably benign |
Het |
Adamts12 |
A |
T |
15: 11,217,915 (GRCm39) |
I291F |
probably damaging |
Het |
Aspm |
G |
C |
1: 139,407,282 (GRCm39) |
Q2056H |
probably benign |
Het |
C7 |
A |
T |
15: 5,076,406 (GRCm39) |
V122E |
probably benign |
Het |
Casp12 |
A |
T |
9: 5,352,844 (GRCm39) |
Q152L |
probably null |
Het |
Cdh16 |
T |
A |
8: 105,344,264 (GRCm39) |
T92S |
probably benign |
Het |
Chrd |
G |
C |
16: 20,553,058 (GRCm39) |
V162L |
possibly damaging |
Het |
Cpne8 |
A |
G |
15: 90,385,608 (GRCm39) |
|
probably benign |
Het |
Cspg4b |
T |
C |
13: 113,502,639 (GRCm39) |
Y115H |
probably damaging |
Het |
Cyp2j7 |
T |
A |
4: 96,090,384 (GRCm39) |
I347F |
probably damaging |
Het |
Cyp4a10 |
A |
T |
4: 115,378,304 (GRCm39) |
Q130L |
probably damaging |
Het |
Dach1 |
C |
T |
14: 98,406,184 (GRCm39) |
G188R |
probably damaging |
Het |
Dgkd |
T |
C |
1: 87,845,674 (GRCm39) |
S294P |
probably benign |
Het |
Dnah8 |
A |
G |
17: 30,882,290 (GRCm39) |
I621V |
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,144,346 (GRCm39) |
|
probably benign |
Het |
Echdc1 |
A |
T |
10: 29,198,417 (GRCm39) |
|
probably benign |
Het |
Elovl3 |
T |
A |
19: 46,120,597 (GRCm39) |
F30Y |
probably damaging |
Het |
Fa2h |
T |
C |
8: 112,120,146 (GRCm39) |
Y80C |
probably damaging |
Het |
Fgd3 |
C |
T |
13: 49,450,085 (GRCm39) |
D55N |
probably benign |
Het |
Fhod1 |
T |
C |
8: 106,058,287 (GRCm39) |
E823G |
possibly damaging |
Het |
Gapvd1 |
A |
G |
2: 34,589,925 (GRCm39) |
|
probably benign |
Het |
Gm17067 |
A |
T |
7: 42,358,046 (GRCm39) |
I152K |
probably benign |
Het |
Gvin3 |
G |
A |
7: 106,202,453 (GRCm39) |
L264F |
probably benign |
Het |
Kif27 |
A |
G |
13: 58,502,528 (GRCm39) |
V50A |
probably damaging |
Het |
Kpna2 |
T |
C |
11: 106,881,912 (GRCm39) |
T305A |
probably benign |
Het |
Krtap22-2 |
A |
G |
16: 88,807,407 (GRCm39) |
|
probably benign |
Het |
Lrp2bp |
T |
A |
8: 46,465,068 (GRCm39) |
F62L |
probably damaging |
Het |
Marf1 |
G |
A |
16: 13,970,129 (GRCm39) |
H197Y |
probably damaging |
Het |
Mob3b |
A |
G |
4: 35,083,947 (GRCm39) |
F81L |
probably benign |
Het |
Mon2 |
C |
T |
10: 122,871,451 (GRCm39) |
V389M |
probably damaging |
Het |
Myef2l |
A |
T |
3: 10,154,379 (GRCm39) |
M383L |
possibly damaging |
Het |
Myh8 |
A |
G |
11: 67,189,351 (GRCm39) |
K1176E |
probably damaging |
Het |
Nckap1l |
A |
G |
15: 103,384,063 (GRCm39) |
T554A |
probably benign |
Het |
Oog3 |
A |
G |
4: 143,884,641 (GRCm39) |
Y432H |
probably damaging |
Het |
Paxbp1 |
A |
T |
16: 90,832,924 (GRCm39) |
|
probably benign |
Het |
Phf20 |
A |
T |
2: 156,109,114 (GRCm39) |
K154* |
probably null |
Het |
Pip4p1 |
C |
T |
14: 51,166,351 (GRCm39) |
R213Q |
probably damaging |
Het |
Plekhj1 |
T |
C |
10: 80,632,250 (GRCm39) |
D74G |
possibly damaging |
Het |
Plpp4 |
T |
C |
7: 128,925,148 (GRCm39) |
C128R |
probably damaging |
Het |
Rcan3 |
A |
T |
4: 135,145,689 (GRCm39) |
|
probably null |
Het |
Sh3rf1 |
T |
A |
8: 61,827,172 (GRCm39) |
M642K |
probably benign |
Het |
Slc7a1 |
A |
G |
5: 148,271,393 (GRCm39) |
V522A |
probably benign |
Het |
Sorbs1 |
A |
G |
19: 40,303,182 (GRCm39) |
|
probably benign |
Het |
Spry2 |
C |
T |
14: 106,130,731 (GRCm39) |
V152M |
probably benign |
Het |
Srgap2 |
A |
G |
1: 131,277,200 (GRCm39) |
M349T |
possibly damaging |
Het |
Stag3 |
A |
G |
5: 138,289,643 (GRCm39) |
H271R |
possibly damaging |
Het |
Stat4 |
T |
C |
1: 52,107,939 (GRCm39) |
V136A |
probably benign |
Het |
Stc2 |
A |
T |
11: 31,310,177 (GRCm39) |
D286E |
probably benign |
Het |
Stk31 |
T |
C |
6: 49,414,311 (GRCm39) |
Y482H |
probably damaging |
Het |
Tasor2 |
A |
C |
13: 3,635,170 (GRCm39) |
|
probably null |
Het |
Ticrr |
C |
T |
7: 79,343,540 (GRCm39) |
P1135L |
probably benign |
Het |
Trim27 |
A |
T |
13: 21,375,399 (GRCm39) |
E310V |
probably benign |
Het |
Uvrag |
T |
C |
7: 98,641,188 (GRCm39) |
K284R |
probably benign |
Het |
Vmn1r78 |
A |
C |
7: 11,887,279 (GRCm39) |
S297R |
probably benign |
Het |
Xylt2 |
A |
G |
11: 94,560,466 (GRCm39) |
S270P |
probably damaging |
Het |
Zfhx3 |
T |
C |
8: 109,676,810 (GRCm39) |
M2620T |
probably benign |
Het |
Zkscan2 |
C |
A |
7: 123,099,219 (GRCm39) |
|
probably benign |
Het |
Zwint |
T |
C |
10: 72,493,030 (GRCm39) |
|
probably benign |
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 |
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 |
R2209:Naf1
|
UTSW |
8 |
67,313,188 (GRCm39) |
unclassified |
probably benign |
|
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 |
|
|