Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alpk2 |
G |
A |
18: 65,438,222 (GRCm39) |
T1524I |
probably damaging |
Het |
Ankrd29 |
G |
A |
18: 12,387,757 (GRCm39) |
A275V |
possibly damaging |
Het |
Arhgap26 |
T |
A |
18: 39,253,237 (GRCm39) |
F221L |
probably damaging |
Het |
Arhgap28 |
T |
C |
17: 68,208,361 (GRCm39) |
S36G |
probably damaging |
Het |
Bcl11a |
A |
G |
11: 24,113,890 (GRCm39) |
D411G |
probably damaging |
Het |
Cdh23 |
C |
A |
10: 60,163,149 (GRCm39) |
|
probably null |
Het |
Cnnm2 |
T |
A |
19: 46,750,990 (GRCm39) |
I260N |
probably damaging |
Het |
Coro6 |
T |
C |
11: 77,358,129 (GRCm39) |
F238S |
probably damaging |
Het |
Ddah1 |
G |
A |
3: 145,597,250 (GRCm39) |
M162I |
probably benign |
Het |
Dnah5 |
T |
C |
15: 28,387,937 (GRCm39) |
I3132T |
possibly damaging |
Het |
Drgx |
A |
T |
14: 32,350,818 (GRCm39) |
E218V |
probably damaging |
Het |
Dync2i1 |
C |
T |
12: 116,175,462 (GRCm39) |
W905* |
probably null |
Het |
Eif3f |
A |
T |
7: 108,539,482 (GRCm39) |
I251F |
probably benign |
Het |
Ephx4 |
T |
C |
5: 107,550,673 (GRCm39) |
F11L |
probably benign |
Het |
Esp1 |
T |
C |
17: 41,041,998 (GRCm39) |
S97P |
unknown |
Het |
Fbxw10 |
A |
T |
11: 62,759,983 (GRCm39) |
|
probably null |
Het |
Hsp90ab1 |
T |
C |
17: 45,882,440 (GRCm39) |
T85A |
possibly damaging |
Het |
Idh2 |
T |
C |
7: 79,748,895 (GRCm39) |
K129E |
probably damaging |
Het |
Kcnj6 |
A |
G |
16: 94,633,865 (GRCm39) |
I64T |
probably damaging |
Het |
Klk1b5 |
T |
A |
7: 43,500,251 (GRCm39) |
C280S |
probably damaging |
Het |
Lhx2 |
T |
A |
2: 38,250,111 (GRCm39) |
L269H |
probably damaging |
Het |
Lrrc71 |
T |
A |
3: 87,653,185 (GRCm39) |
|
probably null |
Het |
Lss |
T |
A |
10: 76,382,026 (GRCm39) |
L484Q |
probably damaging |
Het |
Mmp14 |
G |
A |
14: 54,669,389 (GRCm39) |
|
probably benign |
Het |
Muc5b |
A |
G |
7: 141,400,986 (GRCm39) |
T534A |
unknown |
Het |
Mysm1 |
T |
C |
4: 94,858,889 (GRCm39) |
K87E |
probably benign |
Het |
Or6f2 |
C |
G |
7: 139,756,127 (GRCm39) |
F37L |
possibly damaging |
Het |
Pcolce |
T |
C |
5: 137,607,309 (GRCm39) |
T61A |
probably damaging |
Het |
Phc3 |
C |
A |
3: 30,968,277 (GRCm39) |
D920Y |
probably damaging |
Het |
Pi4kb |
T |
C |
3: 94,901,599 (GRCm39) |
I422T |
probably benign |
Het |
Piezo1 |
C |
T |
8: 123,221,642 (GRCm39) |
R584H |
probably damaging |
Het |
Plce1 |
T |
A |
19: 38,693,781 (GRCm39) |
F768Y |
probably damaging |
Het |
Ppp1r21 |
T |
C |
17: 88,889,882 (GRCm39) |
S709P |
possibly damaging |
Het |
Prdx6 |
T |
C |
1: 161,074,858 (GRCm39) |
D74G |
probably damaging |
Het |
Rlf |
A |
G |
4: 121,008,060 (GRCm39) |
F307L |
possibly damaging |
Het |
Skic2 |
T |
C |
17: 35,068,879 (GRCm39) |
E40G |
probably benign |
Het |
Snapin |
G |
A |
3: 90,397,499 (GRCm39) |
R91* |
probably null |
Het |
Sort1 |
T |
A |
3: 108,263,955 (GRCm39) |
L838* |
probably null |
Het |
Sstr4 |
A |
G |
2: 148,238,273 (GRCm39) |
I295V |
possibly damaging |
Het |
Stk39 |
T |
A |
2: 68,222,462 (GRCm39) |
I201F |
probably damaging |
Het |
Tasp1 |
T |
C |
2: 139,752,474 (GRCm39) |
T322A |
probably benign |
Het |
Tepsin |
C |
T |
11: 119,982,579 (GRCm39) |
C491Y |
possibly damaging |
Het |
Tlr9 |
G |
A |
9: 106,101,278 (GRCm39) |
V190M |
probably damaging |
Het |
Ttf2 |
A |
G |
3: 100,858,324 (GRCm39) |
L755P |
probably damaging |
Het |
Txn2 |
G |
A |
15: 77,811,976 (GRCm39) |
T60M |
possibly damaging |
Het |
Vmn1r10 |
A |
G |
6: 57,091,287 (GRCm39) |
N293S |
probably benign |
Het |
Vmn1r232 |
A |
G |
17: 21,134,465 (GRCm39) |
L45P |
probably benign |
Het |
Vmn2r111 |
C |
T |
17: 22,790,142 (GRCm39) |
W288* |
probably null |
Het |
Vmn2r118 |
T |
C |
17: 55,915,421 (GRCm39) |
S510G |
possibly damaging |
Het |
Zgpat |
T |
A |
2: 181,007,439 (GRCm39) |
|
probably benign |
Het |
Zzef1 |
G |
T |
11: 72,777,598 (GRCm39) |
G1810C |
probably null |
Het |
|
Other mutations in Or6d13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01063:Or6d13
|
APN |
6 |
116,517,968 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02671:Or6d13
|
APN |
6 |
116,518,104 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL03107:Or6d13
|
APN |
6 |
116,517,900 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0041:Or6d13
|
UTSW |
6 |
116,518,295 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0426:Or6d13
|
UTSW |
6 |
116,517,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R0627:Or6d13
|
UTSW |
6 |
116,517,949 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0829:Or6d13
|
UTSW |
6 |
116,518,226 (GRCm39) |
missense |
probably benign |
0.01 |
R2111:Or6d13
|
UTSW |
6 |
116,517,611 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2112:Or6d13
|
UTSW |
6 |
116,517,611 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2120:Or6d13
|
UTSW |
6 |
116,517,416 (GRCm39) |
start codon destroyed |
probably null |
0.04 |
R3161:Or6d13
|
UTSW |
6 |
116,517,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R4710:Or6d13
|
UTSW |
6 |
116,517,611 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5244:Or6d13
|
UTSW |
6 |
116,518,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R5859:Or6d13
|
UTSW |
6 |
116,517,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R6273:Or6d13
|
UTSW |
6 |
116,518,277 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6505:Or6d13
|
UTSW |
6 |
116,517,561 (GRCm39) |
missense |
probably benign |
0.01 |
R7350:Or6d13
|
UTSW |
6 |
116,517,495 (GRCm39) |
missense |
probably benign |
0.28 |
R7380:Or6d13
|
UTSW |
6 |
116,517,894 (GRCm39) |
missense |
probably benign |
0.03 |
R7474:Or6d13
|
UTSW |
6 |
116,517,999 (GRCm39) |
missense |
probably damaging |
0.99 |
R8054:Or6d13
|
UTSW |
6 |
116,517,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R8476:Or6d13
|
UTSW |
6 |
116,517,507 (GRCm39) |
missense |
probably benign |
|
R8862:Or6d13
|
UTSW |
6 |
116,518,186 (GRCm39) |
missense |
probably benign |
0.03 |
R9082:Or6d13
|
UTSW |
6 |
116,517,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R9100:Or6d13
|
UTSW |
6 |
116,517,990 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9124:Or6d13
|
UTSW |
6 |
116,517,416 (GRCm39) |
start codon destroyed |
probably null |
0.04 |
R9151:Or6d13
|
UTSW |
6 |
116,517,990 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9321:Or6d13
|
UTSW |
6 |
116,518,370 (GRCm39) |
missense |
probably benign |
|
R9404:Or6d13
|
UTSW |
6 |
116,517,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|