Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam29 |
G |
A |
8: 56,324,754 (GRCm39) |
Q567* |
probably null |
Het |
Apol11a |
T |
C |
15: 77,395,219 (GRCm39) |
|
probably benign |
Het |
Arhgap29 |
A |
G |
3: 121,786,044 (GRCm39) |
H275R |
probably benign |
Het |
Arhgef17 |
C |
A |
7: 100,530,476 (GRCm39) |
E428* |
probably null |
Het |
Atm |
A |
T |
9: 53,367,830 (GRCm39) |
V2431E |
probably damaging |
Het |
Atn1 |
G |
T |
6: 124,724,750 (GRCm39) |
P161Q |
unknown |
Het |
Atp13a2 |
T |
C |
4: 140,721,113 (GRCm39) |
S99P |
probably damaging |
Het |
Atp8a1 |
A |
T |
5: 67,780,049 (GRCm39) |
|
probably benign |
Het |
Cdk18 |
T |
C |
1: 132,047,698 (GRCm39) |
|
probably benign |
Het |
Cep85 |
A |
G |
4: 133,894,711 (GRCm39) |
W32R |
probably damaging |
Het |
Cntn4 |
G |
T |
6: 106,486,363 (GRCm39) |
G264C |
probably damaging |
Het |
Col6a4 |
A |
G |
9: 105,940,052 (GRCm39) |
S1293P |
possibly damaging |
Het |
Col6a6 |
T |
C |
9: 105,658,290 (GRCm39) |
K641E |
probably damaging |
Het |
Dmd |
A |
T |
X: 82,922,126 (GRCm39) |
K1465N |
probably damaging |
Het |
Frs2 |
C |
T |
10: 116,916,979 (GRCm39) |
C5Y |
probably benign |
Het |
Gm5174 |
A |
G |
10: 86,492,866 (GRCm39) |
|
noncoding transcript |
Het |
Gpr61 |
A |
G |
3: 108,057,797 (GRCm39) |
V288A |
possibly damaging |
Het |
Grik3 |
G |
A |
4: 125,598,357 (GRCm39) |
|
probably benign |
Het |
Haao |
T |
A |
17: 84,146,267 (GRCm39) |
Q69L |
probably benign |
Het |
Ints6 |
T |
C |
14: 62,942,352 (GRCm39) |
|
probably benign |
Het |
Ints8 |
T |
C |
4: 11,221,204 (GRCm39) |
I724V |
possibly damaging |
Het |
Lrrk2 |
G |
A |
15: 91,613,123 (GRCm39) |
C749Y |
probably damaging |
Het |
Map4k1 |
A |
G |
7: 28,697,877 (GRCm39) |
D471G |
possibly damaging |
Het |
Mbtd1 |
A |
G |
11: 93,801,185 (GRCm39) |
Y122C |
probably damaging |
Het |
Mif-ps9 |
T |
A |
19: 56,743,766 (GRCm39) |
|
noncoding transcript |
Het |
Mrfap1 |
A |
G |
5: 36,953,817 (GRCm39) |
S41P |
possibly damaging |
Het |
Mrm2 |
T |
C |
5: 140,314,308 (GRCm39) |
T176A |
probably benign |
Het |
Mslnl |
T |
C |
17: 25,962,214 (GRCm39) |
L204P |
probably damaging |
Het |
Muc6 |
T |
C |
7: 141,238,144 (GRCm39) |
E112G |
probably benign |
Het |
Nfyb |
A |
G |
10: 82,586,665 (GRCm39) |
|
probably benign |
Het |
Nlgn3 |
T |
C |
X: 100,352,522 (GRCm39) |
|
probably benign |
Het |
Nr3c1 |
G |
A |
18: 39,620,051 (GRCm39) |
Q79* |
probably null |
Het |
Nxpe4 |
C |
G |
9: 48,307,793 (GRCm39) |
T299R |
probably benign |
Het |
Otud4 |
C |
A |
8: 80,400,603 (GRCm39) |
H1105N |
unknown |
Het |
Pcnx2 |
A |
G |
8: 126,500,572 (GRCm39) |
L1506P |
probably damaging |
Het |
Prl2c5 |
T |
A |
13: 13,364,009 (GRCm39) |
H88Q |
probably damaging |
Het |
Psmb2 |
A |
G |
4: 126,580,825 (GRCm39) |
Y73C |
probably damaging |
Het |
Rbl1 |
A |
T |
2: 157,011,891 (GRCm39) |
V688D |
probably benign |
Het |
Rhox2g |
C |
A |
X: 36,824,865 (GRCm39) |
|
probably benign |
Het |
Rmnd5a |
G |
A |
6: 71,375,439 (GRCm39) |
L80F |
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,702,765 (GRCm39) |
|
probably benign |
Het |
Sele |
T |
A |
1: 163,878,379 (GRCm39) |
S239R |
probably damaging |
Het |
Siglecf |
A |
T |
7: 43,005,344 (GRCm39) |
R435* |
probably null |
Het |
Slc23a1 |
C |
T |
18: 35,755,676 (GRCm39) |
V407M |
possibly damaging |
Het |
Slc6a14 |
G |
A |
X: 21,587,807 (GRCm39) |
V122I |
probably benign |
Het |
Spdl1 |
T |
A |
11: 34,704,434 (GRCm39) |
E466D |
unknown |
Het |
Stau2 |
A |
G |
1: 16,510,596 (GRCm39) |
F121L |
probably benign |
Het |
Stxbp1 |
A |
T |
2: 32,684,648 (GRCm39) |
S594T |
probably benign |
Het |
Sufu |
G |
A |
19: 46,443,159 (GRCm39) |
|
probably benign |
Het |
Tap2 |
G |
T |
17: 34,430,889 (GRCm39) |
V330L |
probably benign |
Het |
Tbc1d1 |
T |
C |
5: 64,421,775 (GRCm39) |
L389P |
probably damaging |
Het |
Tbx2 |
A |
G |
11: 85,725,592 (GRCm39) |
E181G |
probably damaging |
Het |
Tlcd4 |
A |
G |
3: 121,000,940 (GRCm39) |
V231A |
probably benign |
Het |
Tmprss9 |
G |
T |
10: 80,726,279 (GRCm39) |
A510S |
probably benign |
Het |
Tnxb |
G |
A |
17: 34,890,551 (GRCm39) |
C298Y |
probably damaging |
Het |
Tril |
G |
T |
6: 53,795,012 (GRCm39) |
R737S |
probably damaging |
Het |
Ugt2a3 |
A |
T |
5: 87,475,005 (GRCm39) |
L413Q |
probably damaging |
Het |
Vcan |
A |
G |
13: 89,805,675 (GRCm39) |
I2335T |
probably damaging |
Het |
Vmn2r28 |
T |
C |
7: 5,484,544 (GRCm39) |
N552S |
possibly damaging |
Het |
Zc3h7a |
C |
T |
16: 10,978,890 (GRCm39) |
R95H |
probably damaging |
Het |
Zfp598 |
A |
G |
17: 24,898,623 (GRCm39) |
N474S |
probably benign |
Het |
Zng1 |
A |
T |
19: 24,920,039 (GRCm39) |
|
probably benign |
Het |
Zpld1 |
T |
C |
16: 55,068,697 (GRCm39) |
D138G |
probably damaging |
Het |
|
Other mutations in Dus2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00966:Dus2
|
APN |
8 |
106,752,533 (GRCm39) |
splice site |
probably null |
|
IGL03000:Dus2
|
APN |
8 |
106,775,316 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03265:Dus2
|
APN |
8 |
106,760,423 (GRCm39) |
splice site |
probably benign |
|
R0400:Dus2
|
UTSW |
8 |
106,775,309 (GRCm39) |
missense |
probably benign |
0.08 |
R0733:Dus2
|
UTSW |
8 |
106,772,702 (GRCm39) |
critical splice donor site |
probably null |
|
R1109:Dus2
|
UTSW |
8 |
106,780,114 (GRCm39) |
missense |
probably benign |
0.16 |
R1190:Dus2
|
UTSW |
8 |
106,771,497 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1819:Dus2
|
UTSW |
8 |
106,778,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R2038:Dus2
|
UTSW |
8 |
106,775,294 (GRCm39) |
missense |
probably damaging |
0.99 |
R4282:Dus2
|
UTSW |
8 |
106,775,286 (GRCm39) |
missense |
probably benign |
0.17 |
R4621:Dus2
|
UTSW |
8 |
106,757,074 (GRCm39) |
missense |
probably damaging |
0.98 |
R4903:Dus2
|
UTSW |
8 |
106,771,437 (GRCm39) |
missense |
probably benign |
0.00 |
R5922:Dus2
|
UTSW |
8 |
106,780,037 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5997:Dus2
|
UTSW |
8 |
106,772,698 (GRCm39) |
missense |
probably benign |
0.14 |
R7235:Dus2
|
UTSW |
8 |
106,742,587 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7387:Dus2
|
UTSW |
8 |
106,772,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R7974:Dus2
|
UTSW |
8 |
106,762,652 (GRCm39) |
missense |
probably benign |
|
R8088:Dus2
|
UTSW |
8 |
106,757,073 (GRCm39) |
missense |
probably benign |
0.00 |
R8343:Dus2
|
UTSW |
8 |
106,722,645 (GRCm39) |
utr 3 prime |
probably benign |
|
R9086:Dus2
|
UTSW |
8 |
106,742,573 (GRCm39) |
nonsense |
probably null |
|
R9113:Dus2
|
UTSW |
8 |
106,775,333 (GRCm39) |
nonsense |
probably null |
|
R9383:Dus2
|
UTSW |
8 |
106,776,950 (GRCm39) |
missense |
probably benign |
0.02 |
R9480:Dus2
|
UTSW |
8 |
106,757,052 (GRCm39) |
nonsense |
probably null |
|
R9569:Dus2
|
UTSW |
8 |
106,771,507 (GRCm39) |
missense |
probably damaging |
0.99 |
R9766:Dus2
|
UTSW |
8 |
106,772,568 (GRCm39) |
missense |
probably damaging |
1.00 |
|