Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
A |
G |
5: 77,049,961 (GRCm39) |
S12P |
probably damaging |
Het |
Alx4 |
T |
A |
2: 93,498,953 (GRCm39) |
D228E |
probably damaging |
Het |
Antxr2 |
T |
C |
5: 98,177,455 (GRCm39) |
E71G |
probably benign |
Het |
Arhgap19 |
C |
A |
19: 41,790,417 (GRCm39) |
G17V |
probably benign |
Het |
C8a |
A |
C |
4: 104,719,791 (GRCm39) |
|
probably null |
Het |
Ccne2 |
T |
A |
4: 11,201,426 (GRCm39) |
|
probably benign |
Het |
Cdc42bpg |
G |
A |
19: 6,361,425 (GRCm39) |
C317Y |
probably damaging |
Het |
Cend1 |
C |
A |
7: 141,007,808 (GRCm39) |
R4L |
probably damaging |
Het |
Cfap44 |
T |
C |
16: 44,253,839 (GRCm39) |
|
probably null |
Het |
Cpt1c |
T |
C |
7: 44,608,999 (GRCm39) |
N774S |
probably benign |
Het |
Csmd1 |
C |
T |
8: 15,967,270 (GRCm39) |
D3198N |
probably damaging |
Het |
Dapk2 |
C |
T |
9: 66,176,168 (GRCm39) |
S323F |
probably damaging |
Het |
Ddx60 |
T |
G |
8: 62,470,783 (GRCm39) |
I1425R |
possibly damaging |
Het |
Edem1 |
T |
A |
6: 108,823,713 (GRCm39) |
Y370N |
probably damaging |
Het |
Elp5 |
A |
G |
11: 69,865,967 (GRCm39) |
V103A |
probably benign |
Het |
Fads1 |
C |
T |
19: 10,160,429 (GRCm39) |
P5L |
probably benign |
Het |
Fat1 |
A |
G |
8: 45,477,350 (GRCm39) |
D2132G |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,182,919 (GRCm39) |
|
probably benign |
Het |
G3bp1 |
T |
C |
11: 55,389,452 (GRCm39) |
F383L |
probably damaging |
Het |
Gp2 |
C |
T |
7: 119,053,791 (GRCm39) |
D57N |
probably damaging |
Het |
Gpr161 |
T |
C |
1: 165,144,805 (GRCm39) |
|
probably benign |
Het |
Gstcd |
G |
A |
3: 132,692,138 (GRCm39) |
|
probably benign |
Het |
Hipk3 |
A |
T |
2: 104,261,594 (GRCm39) |
C980* |
probably null |
Het |
Htr2a |
A |
T |
14: 74,879,649 (GRCm39) |
I93L |
probably damaging |
Het |
Itpr2 |
T |
G |
6: 146,135,506 (GRCm39) |
K1775N |
probably damaging |
Het |
Kcnt1 |
G |
A |
2: 25,797,640 (GRCm39) |
V864I |
probably damaging |
Het |
Kcnt2 |
A |
T |
1: 140,278,963 (GRCm39) |
Y38F |
probably damaging |
Het |
Limch1 |
G |
A |
5: 67,015,297 (GRCm39) |
|
probably null |
Het |
Lmtk2 |
C |
T |
5: 144,111,103 (GRCm39) |
R608C |
possibly damaging |
Het |
Loxhd1 |
C |
T |
18: 77,513,453 (GRCm39) |
|
probably benign |
Het |
Lpin2 |
A |
T |
17: 71,522,017 (GRCm39) |
E17V |
probably damaging |
Het |
Lrrc34 |
A |
T |
3: 30,684,142 (GRCm39) |
F342I |
probably benign |
Het |
Lyzl6 |
A |
G |
11: 103,527,578 (GRCm39) |
|
probably null |
Het |
Map3k4 |
A |
C |
17: 12,476,928 (GRCm39) |
|
probably benign |
Het |
Mocs3 |
C |
T |
2: 168,073,602 (GRCm39) |
P350S |
probably benign |
Het |
Myrf |
G |
C |
19: 10,195,526 (GRCm39) |
T428S |
probably benign |
Het |
Naip2 |
A |
C |
13: 100,298,290 (GRCm39) |
I582S |
probably benign |
Het |
Or1ad8 |
A |
G |
11: 50,897,904 (GRCm39) |
Y35C |
probably damaging |
Het |
Or4c52 |
A |
C |
2: 89,846,116 (GRCm39) |
I281L |
probably damaging |
Het |
Or7e168 |
G |
T |
9: 19,719,839 (GRCm39) |
S75I |
probably damaging |
Het |
Pcare |
G |
T |
17: 72,057,471 (GRCm39) |
F735L |
probably damaging |
Het |
Pdzrn4 |
A |
G |
15: 92,655,538 (GRCm39) |
E477G |
possibly damaging |
Het |
Rims2 |
G |
T |
15: 39,326,011 (GRCm39) |
|
probably null |
Het |
Samd4b |
C |
T |
7: 28,122,873 (GRCm39) |
A62T |
probably damaging |
Het |
Scamp1 |
T |
C |
13: 94,347,088 (GRCm39) |
N192S |
probably benign |
Het |
Scnn1g |
T |
C |
7: 121,345,802 (GRCm39) |
|
probably benign |
Het |
Setd1a |
T |
G |
7: 127,387,358 (GRCm39) |
|
probably benign |
Het |
Setdb1 |
A |
G |
3: 95,257,192 (GRCm39) |
|
probably benign |
Het |
Slc2a7 |
T |
C |
4: 150,250,823 (GRCm39) |
S415P |
probably benign |
Het |
Sp140l2 |
G |
T |
1: 85,247,824 (GRCm39) |
|
probably benign |
Het |
Strip2 |
A |
T |
6: 29,937,650 (GRCm39) |
Y526F |
possibly damaging |
Het |
Styxl2 |
T |
A |
1: 165,928,332 (GRCm39) |
T427S |
probably benign |
Het |
Syne2 |
A |
G |
12: 75,926,951 (GRCm39) |
D69G |
probably damaging |
Het |
Syt13 |
C |
A |
2: 92,745,596 (GRCm39) |
A22E |
probably benign |
Het |
Tm9sf2 |
T |
C |
14: 122,392,780 (GRCm39) |
F432S |
probably benign |
Het |
Vmn2r49 |
A |
T |
7: 9,710,357 (GRCm39) |
W792R |
probably damaging |
Het |
Zfp292 |
T |
C |
4: 34,808,227 (GRCm39) |
S1606G |
probably benign |
Het |
Zfp518a |
A |
T |
19: 40,900,665 (GRCm39) |
H198L |
probably damaging |
Het |
|
Other mutations in Rab5b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0038:Rab5b
|
UTSW |
10 |
128,518,772 (GRCm39) |
missense |
probably benign |
0.05 |
R0097:Rab5b
|
UTSW |
10 |
128,518,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R0097:Rab5b
|
UTSW |
10 |
128,518,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R0276:Rab5b
|
UTSW |
10 |
128,522,615 (GRCm39) |
critical splice donor site |
probably null |
|
R0366:Rab5b
|
UTSW |
10 |
128,518,772 (GRCm39) |
missense |
probably benign |
0.05 |
R0368:Rab5b
|
UTSW |
10 |
128,518,772 (GRCm39) |
missense |
probably benign |
0.05 |
R1120:Rab5b
|
UTSW |
10 |
128,515,483 (GRCm39) |
missense |
probably benign |
0.02 |
R1645:Rab5b
|
UTSW |
10 |
128,522,695 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4624:Rab5b
|
UTSW |
10 |
128,519,130 (GRCm39) |
missense |
probably benign |
0.27 |
R7107:Rab5b
|
UTSW |
10 |
128,519,062 (GRCm39) |
critical splice donor site |
probably null |
|
R7645:Rab5b
|
UTSW |
10 |
128,517,260 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8496:Rab5b
|
UTSW |
10 |
128,518,776 (GRCm39) |
nonsense |
probably null |
|
R8744:Rab5b
|
UTSW |
10 |
128,518,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R9211:Rab5b
|
UTSW |
10 |
128,519,063 (GRCm39) |
critical splice donor site |
probably null |
|
R9774:Rab5b
|
UTSW |
10 |
128,522,658 (GRCm39) |
missense |
probably benign |
0.18 |
|