Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad8 |
A |
G |
9: 26,901,890 (GRCm39) |
L158P |
probably damaging |
Het |
Aco1 |
A |
G |
4: 40,197,576 (GRCm39) |
Q860R |
probably benign |
Het |
Actl11 |
A |
T |
9: 107,806,181 (GRCm39) |
Q168L |
possibly damaging |
Het |
Adam26b |
T |
C |
8: 43,972,975 (GRCm39) |
I676V |
probably benign |
Het |
Aldoart2 |
A |
C |
12: 55,612,920 (GRCm39) |
I282L |
probably benign |
Het |
Capns1 |
G |
T |
7: 29,889,565 (GRCm39) |
S211R |
probably benign |
Het |
Cps1 |
T |
C |
1: 67,245,983 (GRCm39) |
V1158A |
probably damaging |
Het |
Cryl1 |
C |
T |
14: 57,523,821 (GRCm39) |
|
probably null |
Het |
Cxcr5 |
A |
G |
9: 44,425,607 (GRCm39) |
|
probably benign |
Het |
Dcaf13 |
A |
G |
15: 38,982,201 (GRCm39) |
K56E |
probably damaging |
Het |
Dlx6 |
T |
G |
6: 6,867,068 (GRCm39) |
S85A |
probably damaging |
Het |
Dsg2 |
C |
T |
18: 20,722,999 (GRCm39) |
|
probably benign |
Het |
Ebf3 |
C |
A |
7: 136,827,625 (GRCm39) |
|
probably benign |
Het |
Fads3 |
T |
C |
19: 10,030,366 (GRCm39) |
I168T |
probably benign |
Het |
Gm10295 |
G |
A |
7: 71,000,296 (GRCm39) |
P95S |
unknown |
Het |
Gm43638 |
T |
C |
5: 87,634,455 (GRCm39) |
T51A |
probably damaging |
Het |
Gm5114 |
G |
A |
7: 39,060,071 (GRCm39) |
|
probably benign |
Het |
Gucy2c |
G |
A |
6: 136,679,737 (GRCm39) |
T974M |
probably damaging |
Het |
Ighv1-19-1 |
T |
C |
12: 114,672,258 (GRCm39) |
|
probably benign |
Het |
Kri1 |
A |
T |
9: 21,191,723 (GRCm39) |
L173Q |
probably damaging |
Het |
Lztfl1 |
T |
C |
9: 123,531,338 (GRCm39) |
D210G |
probably benign |
Het |
Morc2a |
T |
A |
11: 3,638,149 (GRCm39) |
N958K |
probably damaging |
Het |
Msl3l2 |
G |
A |
10: 55,992,021 (GRCm39) |
A249T |
probably benign |
Het |
Nlrp4a |
A |
G |
7: 26,149,254 (GRCm39) |
E287G |
probably benign |
Het |
Nlrp9a |
A |
T |
7: 26,257,519 (GRCm39) |
N290I |
possibly damaging |
Het |
Or2b28 |
T |
G |
13: 21,531,185 (GRCm39) |
L29R |
probably damaging |
Het |
Or4e2 |
A |
G |
14: 52,688,484 (GRCm39) |
T205A |
probably benign |
Het |
Or5al6 |
C |
T |
2: 85,976,955 (GRCm39) |
G41D |
probably benign |
Het |
Pcsk7 |
A |
G |
9: 45,840,005 (GRCm39) |
D731G |
probably benign |
Het |
Plppr5 |
T |
A |
3: 117,480,298 (GRCm39) |
|
probably benign |
Het |
Podxl |
T |
C |
6: 31,505,639 (GRCm39) |
T135A |
possibly damaging |
Het |
Pole |
T |
G |
5: 110,485,106 (GRCm39) |
C407G |
possibly damaging |
Het |
Prl |
C |
A |
13: 27,249,024 (GRCm39) |
N224K |
possibly damaging |
Het |
Prnp |
A |
T |
2: 131,778,340 (GRCm39) |
|
probably benign |
Het |
Proser2 |
A |
G |
2: 6,105,149 (GRCm39) |
*472R |
probably null |
Het |
Rhag |
T |
C |
17: 41,122,178 (GRCm39) |
S38P |
possibly damaging |
Het |
Rnf146 |
T |
C |
10: 29,223,856 (GRCm39) |
D10G |
probably damaging |
Het |
Rps3a1 |
T |
C |
3: 86,049,085 (GRCm39) |
D29G |
probably benign |
Het |
Sv2a |
A |
T |
3: 96,097,012 (GRCm39) |
I446F |
probably benign |
Het |
Tbc1d30 |
C |
A |
10: 121,103,319 (GRCm39) |
R571L |
probably damaging |
Het |
Tfrc |
T |
A |
16: 32,443,646 (GRCm39) |
|
probably null |
Het |
Tnfaip1 |
G |
A |
11: 78,419,129 (GRCm39) |
P156S |
probably damaging |
Het |
Vmn1r226 |
T |
C |
17: 20,908,166 (GRCm39) |
S133P |
probably damaging |
Het |
Wnt9b |
C |
T |
11: 103,622,836 (GRCm39) |
R189K |
probably damaging |
Het |
Ythdc2 |
A |
G |
18: 44,983,726 (GRCm39) |
H564R |
probably benign |
Het |
Zfp442 |
C |
A |
2: 150,251,267 (GRCm39) |
E211* |
probably null |
Het |
|
Other mutations in Dync1li1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1510:Dync1li1
|
UTSW |
9 |
114,518,278 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1824:Dync1li1
|
UTSW |
9 |
114,538,252 (GRCm39) |
missense |
probably benign |
0.01 |
R1955:Dync1li1
|
UTSW |
9 |
114,550,814 (GRCm39) |
missense |
probably damaging |
0.99 |
R2000:Dync1li1
|
UTSW |
9 |
114,542,631 (GRCm39) |
missense |
probably benign |
0.05 |
R2520:Dync1li1
|
UTSW |
9 |
114,518,074 (GRCm39) |
missense |
probably null |
0.17 |
R2912:Dync1li1
|
UTSW |
9 |
114,544,743 (GRCm39) |
missense |
probably benign |
0.31 |
R4418:Dync1li1
|
UTSW |
9 |
114,535,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R4422:Dync1li1
|
UTSW |
9 |
114,538,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R4646:Dync1li1
|
UTSW |
9 |
114,538,237 (GRCm39) |
missense |
probably damaging |
0.96 |
R4693:Dync1li1
|
UTSW |
9 |
114,535,166 (GRCm39) |
missense |
probably damaging |
0.99 |
R4817:Dync1li1
|
UTSW |
9 |
114,534,162 (GRCm39) |
missense |
probably benign |
0.09 |
R5027:Dync1li1
|
UTSW |
9 |
114,542,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R5274:Dync1li1
|
UTSW |
9 |
114,544,273 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5363:Dync1li1
|
UTSW |
9 |
114,544,297 (GRCm39) |
missense |
probably damaging |
0.99 |
R5902:Dync1li1
|
UTSW |
9 |
114,546,929 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6359:Dync1li1
|
UTSW |
9 |
114,542,638 (GRCm39) |
missense |
probably benign |
0.29 |
R7235:Dync1li1
|
UTSW |
9 |
114,544,231 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7757:Dync1li1
|
UTSW |
9 |
114,538,345 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8161:Dync1li1
|
UTSW |
9 |
114,535,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R8191:Dync1li1
|
UTSW |
9 |
114,538,253 (GRCm39) |
missense |
probably benign |
0.02 |
R8703:Dync1li1
|
UTSW |
9 |
114,552,329 (GRCm39) |
missense |
probably damaging |
0.98 |
R8733:Dync1li1
|
UTSW |
9 |
114,534,178 (GRCm39) |
missense |
probably damaging |
0.97 |
R9211:Dync1li1
|
UTSW |
9 |
114,518,012 (GRCm39) |
nonsense |
probably null |
|
R9307:Dync1li1
|
UTSW |
9 |
114,535,076 (GRCm39) |
missense |
probably damaging |
0.98 |
|