Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Accsl |
T |
C |
2: 93,686,086 (GRCm39) |
K577R |
probably benign |
Het |
Baiap3 |
A |
G |
17: 25,467,499 (GRCm39) |
S368P |
probably benign |
Het |
Brf2 |
T |
C |
8: 27,614,013 (GRCm39) |
E391G |
possibly damaging |
Het |
Casr |
T |
A |
16: 36,330,108 (GRCm39) |
M409L |
probably benign |
Het |
Ccdc83 |
G |
T |
7: 89,873,286 (GRCm39) |
Y356* |
probably null |
Het |
Clec10a |
A |
T |
11: 70,060,642 (GRCm39) |
N166Y |
probably damaging |
Het |
Copg1 |
T |
C |
6: 87,866,996 (GRCm39) |
F77S |
probably damaging |
Het |
Dnah7a |
T |
G |
1: 53,666,194 (GRCm39) |
K611T |
probably benign |
Het |
Dock10 |
G |
A |
1: 80,530,469 (GRCm39) |
H1025Y |
probably damaging |
Het |
Dock6 |
A |
T |
9: 21,741,596 (GRCm39) |
S876T |
possibly damaging |
Het |
Dop1b |
G |
T |
16: 93,573,881 (GRCm39) |
R1701L |
probably benign |
Het |
Fbxo43 |
C |
T |
15: 36,162,485 (GRCm39) |
V241I |
possibly damaging |
Het |
Gbx2 |
A |
T |
1: 89,856,550 (GRCm39) |
I280N |
probably damaging |
Het |
Gnai1 |
A |
G |
5: 18,496,504 (GRCm39) |
F140L |
|
Het |
Gne |
T |
C |
4: 44,084,061 (GRCm39) |
Y13C |
probably benign |
Het |
Heatr5b |
A |
T |
17: 79,121,662 (GRCm39) |
S688T |
probably benign |
Het |
Hectd2 |
T |
A |
19: 36,581,754 (GRCm39) |
D431E |
possibly damaging |
Het |
Hecw2 |
A |
G |
1: 54,079,546 (GRCm39) |
S36P |
probably benign |
Het |
Hpx |
A |
T |
7: 105,241,352 (GRCm39) |
I353N |
probably damaging |
Het |
Ints8 |
A |
T |
4: 11,204,534 (GRCm39) |
V974E |
probably damaging |
Het |
Jaml |
T |
A |
9: 45,000,110 (GRCm39) |
L136Q |
probably damaging |
Het |
Kazn |
A |
G |
4: 141,845,441 (GRCm39) |
V381A |
probably benign |
Het |
Krt79 |
T |
C |
15: 101,838,187 (GRCm39) |
T523A |
unknown |
Het |
Lrrc8e |
T |
G |
8: 4,285,140 (GRCm39) |
L455R |
probably damaging |
Het |
Mrps11 |
T |
C |
7: 78,433,125 (GRCm39) |
S7P |
possibly damaging |
Het |
Muc21 |
A |
G |
17: 35,933,722 (GRCm39) |
S155P |
unknown |
Het |
Neurl3 |
A |
G |
1: 36,308,662 (GRCm39) |
F50S |
probably damaging |
Het |
Nlgn1 |
T |
C |
3: 25,490,363 (GRCm39) |
T455A |
probably damaging |
Het |
Pbp2 |
T |
C |
6: 135,287,260 (GRCm39) |
Y29C |
probably damaging |
Het |
Pdcd11 |
T |
A |
19: 47,101,791 (GRCm39) |
L992* |
probably null |
Het |
Pla2g6 |
A |
G |
15: 79,171,322 (GRCm39) |
I756T |
probably benign |
Het |
Polm |
T |
A |
11: 5,781,707 (GRCm39) |
D263V |
possibly damaging |
Het |
Pspc1 |
T |
C |
14: 57,001,700 (GRCm39) |
T225A |
probably benign |
Het |
Rtca |
C |
A |
3: 116,301,473 (GRCm39) |
A25S |
probably benign |
Het |
Sirt2 |
G |
A |
7: 28,487,191 (GRCm39) |
V318M |
probably damaging |
Het |
Slc1a2 |
T |
A |
2: 102,568,197 (GRCm39) |
I78K |
probably damaging |
Het |
Slco3a1 |
A |
G |
7: 74,009,577 (GRCm39) |
I246T |
probably benign |
Het |
Smpd5 |
A |
G |
15: 76,179,926 (GRCm39) |
E325G |
probably benign |
Het |
Snw1 |
T |
C |
12: 87,500,673 (GRCm39) |
E362G |
probably benign |
Het |
Tmem63c |
A |
T |
12: 87,108,328 (GRCm39) |
M114L |
possibly damaging |
Het |
Trim24 |
T |
C |
6: 37,848,242 (GRCm39) |
L66P |
probably damaging |
Het |
Trpm3 |
T |
C |
19: 22,896,060 (GRCm39) |
F966L |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,609,643 (GRCm39) |
I17588V |
probably benign |
Het |
Vmn2r44 |
A |
T |
7: 8,371,227 (GRCm39) |
C606* |
probably null |
Het |
Vmn2r74 |
A |
T |
7: 85,601,454 (GRCm39) |
V728E |
probably benign |
Het |
Zfp503 |
T |
C |
14: 22,036,019 (GRCm39) |
D299G |
possibly damaging |
Het |
Zfp764l1 |
C |
T |
7: 126,992,496 (GRCm39) |
C38Y |
probably null |
Het |
|
Other mutations in Dus4l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:Dus4l
|
APN |
12 |
31,691,668 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01299:Dus4l
|
APN |
12 |
31,690,823 (GRCm39) |
missense |
probably benign |
|
IGL01443:Dus4l
|
APN |
12 |
31,702,409 (GRCm39) |
unclassified |
probably benign |
|
IGL01796:Dus4l
|
APN |
12 |
31,692,794 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02234:Dus4l
|
APN |
12 |
31,691,495 (GRCm39) |
splice site |
probably benign |
|
IGL02385:Dus4l
|
APN |
12 |
31,690,674 (GRCm39) |
utr 3 prime |
probably benign |
|
R0483:Dus4l
|
UTSW |
12 |
31,691,656 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1432:Dus4l
|
UTSW |
12 |
31,698,770 (GRCm39) |
missense |
probably benign |
0.03 |
R1514:Dus4l
|
UTSW |
12 |
31,690,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R1880:Dus4l
|
UTSW |
12 |
31,690,869 (GRCm39) |
missense |
probably benign |
0.00 |
R4362:Dus4l
|
UTSW |
12 |
31,698,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R5425:Dus4l
|
UTSW |
12 |
31,690,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R5568:Dus4l
|
UTSW |
12 |
31,696,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R7188:Dus4l
|
UTSW |
12 |
31,696,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R8900:Dus4l
|
UTSW |
12 |
31,690,692 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9696:Dus4l
|
UTSW |
12 |
31,696,647 (GRCm39) |
missense |
probably damaging |
0.97 |
R9801:Dus4l
|
UTSW |
12 |
31,698,827 (GRCm39) |
missense |
probably damaging |
0.99 |
|