Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts13 |
A |
G |
2: 26,873,986 (GRCm39) |
R412G |
probably damaging |
Het |
Adamts3 |
T |
A |
5: 89,832,326 (GRCm39) |
N927Y |
probably benign |
Het |
Adgra3 |
A |
G |
5: 50,117,901 (GRCm39) |
Y1216H |
probably benign |
Het |
Agpat3 |
C |
A |
10: 78,123,881 (GRCm39) |
|
probably benign |
Het |
AI182371 |
T |
A |
2: 34,975,733 (GRCm39) |
Q277L |
possibly damaging |
Het |
Arhgef15 |
A |
T |
11: 68,845,342 (GRCm39) |
L170Q |
possibly damaging |
Het |
Avpi1 |
C |
A |
19: 42,112,223 (GRCm39) |
E112* |
probably null |
Het |
Braf |
C |
T |
6: 39,617,413 (GRCm39) |
A534T |
probably damaging |
Het |
Bspry |
G |
C |
4: 62,404,791 (GRCm39) |
A196P |
probably damaging |
Het |
Cacna1c |
T |
A |
6: 118,570,988 (GRCm39) |
L2095F |
probably damaging |
Het |
Cdhr2 |
A |
T |
13: 54,874,651 (GRCm39) |
S908C |
probably damaging |
Het |
Cntnap5c |
C |
A |
17: 58,183,464 (GRCm39) |
Q57K |
probably benign |
Het |
Dtna |
C |
T |
18: 23,779,932 (GRCm39) |
|
probably benign |
Het |
Dynap |
A |
G |
18: 70,375,105 (GRCm39) |
S37P |
possibly damaging |
Het |
Efna5 |
A |
T |
17: 62,914,467 (GRCm39) |
|
probably benign |
Het |
Fancm |
T |
A |
12: 65,153,217 (GRCm39) |
C1224* |
probably null |
Het |
Fbxw16 |
T |
A |
9: 109,277,232 (GRCm39) |
S37C |
probably damaging |
Het |
Galnt4 |
A |
G |
10: 98,944,374 (GRCm39) |
Y33C |
probably benign |
Het |
Kcnk2 |
G |
T |
1: 189,027,888 (GRCm39) |
N122K |
probably benign |
Het |
Krt71 |
C |
A |
15: 101,647,753 (GRCm39) |
E222D |
probably damaging |
Het |
Ltf |
T |
A |
9: 110,858,636 (GRCm39) |
D461E |
possibly damaging |
Het |
Mapk4 |
A |
T |
18: 74,068,109 (GRCm39) |
L274Q |
probably damaging |
Het |
Mbd6 |
A |
G |
10: 127,122,741 (GRCm39) |
C103R |
probably damaging |
Het |
Nbeal1 |
A |
G |
1: 60,321,030 (GRCm39) |
N2047S |
probably benign |
Het |
Nefh |
C |
T |
11: 4,895,184 (GRCm39) |
S335N |
possibly damaging |
Het |
Obscn |
G |
T |
11: 58,934,803 (GRCm39) |
H4715N |
probably damaging |
Het |
Olfml1 |
A |
T |
7: 107,189,393 (GRCm39) |
I153L |
possibly damaging |
Het |
Or8g34 |
T |
A |
9: 39,372,772 (GRCm39) |
F12Y |
probably benign |
Het |
Pck1 |
A |
G |
2: 172,997,003 (GRCm39) |
E215G |
probably benign |
Het |
Peg12 |
T |
A |
7: 62,113,308 (GRCm39) |
E263V |
unknown |
Het |
Phkg1 |
T |
A |
5: 129,903,103 (GRCm39) |
T15S |
probably benign |
Het |
Plekhg1 |
T |
A |
10: 3,914,076 (GRCm39) |
L1120* |
probably null |
Het |
Prss59 |
A |
T |
6: 40,903,042 (GRCm39) |
L110* |
probably null |
Het |
Rlf |
T |
A |
4: 121,007,126 (GRCm39) |
H618L |
probably damaging |
Het |
Rnf112 |
T |
A |
11: 61,343,181 (GRCm39) |
R165W |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,293,401 (GRCm39) |
T51A |
probably benign |
Het |
Rnf220 |
A |
G |
4: 117,130,481 (GRCm39) |
L293P |
probably damaging |
Het |
Rock1 |
T |
C |
18: 10,140,240 (GRCm39) |
D117G |
probably damaging |
Het |
Rp1 |
A |
G |
1: 4,414,851 (GRCm39) |
V2087A |
probably benign |
Het |
Rpl7a |
A |
G |
2: 26,801,563 (GRCm39) |
|
probably null |
Het |
Serpinb6d |
A |
G |
13: 33,851,615 (GRCm39) |
D124G |
probably damaging |
Het |
Skor1 |
T |
G |
9: 63,053,133 (GRCm39) |
T279P |
probably damaging |
Het |
Son |
A |
T |
16: 91,456,221 (GRCm39) |
E1656V |
probably damaging |
Het |
Swap70 |
A |
G |
7: 109,878,562 (GRCm39) |
K511E |
probably benign |
Het |
Treh |
T |
C |
9: 44,594,910 (GRCm39) |
V262A |
probably benign |
Het |
Trpm4 |
A |
G |
7: 44,954,370 (GRCm39) |
|
probably null |
Het |
Ugt8a |
T |
C |
3: 125,708,739 (GRCm39) |
I124V |
probably benign |
Het |
Wdr53 |
T |
C |
16: 32,075,473 (GRCm39) |
V226A |
probably damaging |
Het |
Wdr64 |
G |
A |
1: 175,554,037 (GRCm39) |
W189* |
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 |
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 |
R3700:Or6d13
|
UTSW |
6 |
116,517,489 (GRCm39) |
missense |
probably benign |
0.10 |
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 |
|