Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agrp |
T |
C |
8: 106,294,000 (GRCm39) |
E41G |
probably benign |
Het |
Amph |
A |
T |
13: 19,230,186 (GRCm39) |
N45Y |
probably damaging |
Het |
Atp11a |
T |
A |
8: 12,882,522 (GRCm39) |
L470Q |
probably damaging |
Het |
Casp12 |
A |
T |
9: 5,354,548 (GRCm39) |
I306F |
probably benign |
Het |
Cobll1 |
A |
T |
2: 64,933,612 (GRCm39) |
M460K |
probably benign |
Het |
Col6a4 |
A |
T |
9: 105,890,895 (GRCm39) |
L1800I |
possibly damaging |
Het |
Ctdsp1 |
T |
C |
1: 74,433,227 (GRCm39) |
V131A |
probably damaging |
Het |
Ctnna3 |
A |
G |
10: 64,511,664 (GRCm39) |
H618R |
probably benign |
Het |
Dhx38 |
C |
A |
8: 110,283,534 (GRCm39) |
V538L |
possibly damaging |
Het |
Dtwd1 |
A |
G |
2: 126,001,733 (GRCm39) |
D151G |
probably damaging |
Het |
Fbxw28 |
A |
G |
9: 109,167,604 (GRCm39) |
L51P |
probably damaging |
Het |
Gm4781 |
C |
T |
10: 100,232,831 (GRCm39) |
|
noncoding transcript |
Het |
Gm5134 |
C |
A |
10: 75,840,594 (GRCm39) |
F479L |
probably benign |
Het |
H2bc27 |
A |
G |
11: 58,839,835 (GRCm39) |
K24E |
probably benign |
Het |
Hexa |
T |
G |
9: 59,468,243 (GRCm39) |
V290G |
probably damaging |
Het |
Ifi206 |
C |
T |
1: 173,308,928 (GRCm39) |
R356K |
possibly damaging |
Het |
Kcnj12 |
G |
A |
11: 60,961,277 (GRCm39) |
R525Q |
possibly damaging |
Het |
Lrp2 |
A |
T |
2: 69,285,869 (GRCm39) |
I3774N |
probably damaging |
Het |
Msh4 |
C |
A |
3: 153,569,076 (GRCm39) |
M832I |
probably benign |
Het |
Myh10 |
A |
G |
11: 68,676,685 (GRCm39) |
E852G |
probably damaging |
Het |
Ndufaf1 |
A |
T |
2: 119,490,963 (GRCm39) |
C32* |
probably null |
Het |
Nos2 |
A |
G |
11: 78,830,978 (GRCm39) |
E387G |
probably null |
Het |
Or4f58 |
C |
T |
2: 111,851,876 (GRCm39) |
G108R |
probably damaging |
Het |
Or55b10 |
A |
G |
7: 102,143,178 (GRCm39) |
V268A |
probably benign |
Het |
Or5h27 |
T |
A |
16: 59,006,266 (GRCm39) |
L193F |
unknown |
Het |
Or7a36 |
A |
C |
10: 78,820,512 (GRCm39) |
D296A |
possibly damaging |
Het |
Or7g29 |
A |
T |
9: 19,287,014 (GRCm39) |
H54Q |
probably benign |
Het |
Or8j3c |
A |
G |
2: 86,253,669 (GRCm39) |
V117A |
probably benign |
Het |
P3h3 |
T |
C |
6: 124,832,921 (GRCm39) |
T211A |
probably benign |
Het |
Pcdh7 |
A |
G |
5: 57,876,856 (GRCm39) |
N137S |
probably damaging |
Het |
Pgf |
T |
C |
12: 85,216,148 (GRCm39) |
T157A |
possibly damaging |
Het |
Prex1 |
T |
C |
2: 166,428,579 (GRCm39) |
D714G |
probably damaging |
Het |
Scn7a |
T |
C |
2: 66,522,913 (GRCm39) |
I930M |
probably damaging |
Het |
Siglecg |
T |
C |
7: 43,058,837 (GRCm39) |
S197P |
possibly damaging |
Het |
Skint7 |
T |
A |
4: 111,845,289 (GRCm39) |
I367N |
probably benign |
Het |
Slfn5 |
A |
T |
11: 82,851,830 (GRCm39) |
D652V |
probably damaging |
Het |
Stx1b |
G |
A |
7: 127,410,090 (GRCm39) |
Q3* |
probably null |
Het |
Tex35 |
T |
C |
1: 156,934,777 (GRCm39) |
M46V |
probably benign |
Het |
Tkt |
A |
C |
14: 30,280,733 (GRCm39) |
T55P |
possibly damaging |
Het |
Trim30c |
T |
C |
7: 104,032,538 (GRCm39) |
R263G |
probably benign |
Het |
U2af2 |
G |
A |
7: 5,069,450 (GRCm39) |
R33Q |
probably benign |
Het |
Washc4 |
T |
A |
10: 83,391,469 (GRCm39) |
V182D |
probably damaging |
Het |
Xirp2 |
T |
C |
2: 67,340,348 (GRCm39) |
V863A |
possibly damaging |
Het |
Zfp976 |
T |
G |
7: 42,263,504 (GRCm39) |
H111P |
probably benign |
Het |
Zfp982 |
A |
T |
4: 147,595,321 (GRCm39) |
N48Y |
probably damaging |
Het |
|
Other mutations in C130073F10Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02805:C130073F10Rik
|
APN |
4 |
101,748,171 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
IGL02869:C130073F10Rik
|
APN |
4 |
101,747,590 (GRCm39) |
nonsense |
probably null |
|
R0621:C130073F10Rik
|
UTSW |
4 |
101,747,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R1368:C130073F10Rik
|
UTSW |
4 |
101,747,953 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1471:C130073F10Rik
|
UTSW |
4 |
101,747,535 (GRCm39) |
missense |
probably benign |
0.01 |
R4732:C130073F10Rik
|
UTSW |
4 |
101,747,907 (GRCm39) |
missense |
probably benign |
0.03 |
R4733:C130073F10Rik
|
UTSW |
4 |
101,747,907 (GRCm39) |
missense |
probably benign |
0.03 |
R5372:C130073F10Rik
|
UTSW |
4 |
101,747,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R6510:C130073F10Rik
|
UTSW |
4 |
101,747,482 (GRCm39) |
missense |
probably benign |
0.01 |
R6888:C130073F10Rik
|
UTSW |
4 |
101,747,453 (GRCm39) |
missense |
probably benign |
0.12 |
R7229:C130073F10Rik
|
UTSW |
4 |
101,747,439 (GRCm39) |
missense |
probably benign |
0.00 |
R8186:C130073F10Rik
|
UTSW |
4 |
101,748,031 (GRCm39) |
nonsense |
probably null |
|
R8353:C130073F10Rik
|
UTSW |
4 |
101,747,881 (GRCm39) |
splice site |
probably null |
|
R8857:C130073F10Rik
|
UTSW |
4 |
101,747,555 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9559:C130073F10Rik
|
UTSW |
4 |
101,747,946 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9590:C130073F10Rik
|
UTSW |
4 |
101,747,618 (GRCm39) |
missense |
probably benign |
0.41 |
|