Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A430005L14Rik |
G |
A |
4: 153,959,827 |
V32I |
probably benign |
Het |
Abcg4 |
A |
T |
9: 44,279,545 |
M19K |
probably benign |
Het |
Acsm1 |
A |
G |
7: 119,656,051 |
T392A |
probably benign |
Het |
Adam19 |
A |
T |
11: 46,125,026 |
I338F |
probably damaging |
Het |
Adamdec1 |
C |
T |
14: 68,570,163 |
M349I |
probably damaging |
Het |
Arhgef11 |
T |
A |
3: 87,679,752 |
|
probably benign |
Het |
Bptf |
T |
C |
11: 107,073,295 |
D1628G |
probably benign |
Het |
Camk2d |
C |
T |
3: 126,597,482 |
Q15* |
probably null |
Het |
Camk2g |
T |
G |
14: 20,793,931 |
D12A |
possibly damaging |
Het |
Cgn |
T |
C |
3: 94,779,990 |
M1V |
probably null |
Het |
Clec16a |
G |
A |
16: 10,731,679 |
C872Y |
probably damaging |
Het |
Dcbld1 |
C |
A |
10: 52,284,257 |
|
probably benign |
Het |
Ear-ps2 |
G |
A |
14: 44,047,060 |
|
noncoding transcript |
Het |
Espl1 |
T |
A |
15: 102,312,518 |
L903Q |
probably damaging |
Het |
Gm11639 |
T |
G |
11: 104,753,806 |
|
probably null |
Het |
Gm5150 |
T |
C |
3: 15,963,424 |
T228A |
probably benign |
Het |
Gm5435 |
A |
T |
12: 82,496,476 |
|
noncoding transcript |
Het |
Gpr156 |
T |
A |
16: 38,005,448 |
C676S |
probably benign |
Het |
Gstt3 |
C |
T |
10: 75,774,851 |
E230K |
possibly damaging |
Het |
Jarid2 |
A |
G |
13: 44,906,271 |
I660V |
possibly damaging |
Het |
Kif13a |
A |
G |
13: 46,775,401 |
|
probably null |
Het |
Kntc1 |
T |
A |
5: 123,764,191 |
V299D |
probably benign |
Het |
Lin9 |
T |
A |
1: 180,669,198 |
L351I |
probably benign |
Het |
Lipk |
T |
A |
19: 34,020,213 |
|
probably null |
Het |
Loxhd1 |
T |
C |
18: 77,332,682 |
L334P |
probably damaging |
Het |
Macc1 |
T |
A |
12: 119,446,477 |
Y327N |
probably damaging |
Het |
Man2a2 |
G |
A |
7: 80,361,128 |
S705L |
possibly damaging |
Het |
Mmp1b |
T |
C |
9: 7,384,897 |
I251V |
possibly damaging |
Het |
Ncam2 |
A |
T |
16: 81,434,819 |
Q57L |
probably damaging |
Het |
Nedd1 |
T |
C |
10: 92,686,240 |
E645G |
probably damaging |
Het |
Nfatc1 |
A |
T |
18: 80,708,117 |
M1K |
probably null |
Het |
Nlrp9b |
A |
T |
7: 20,023,991 |
R384S |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 89,813,584 |
H62R |
possibly damaging |
Het |
Olfr1097 |
A |
G |
2: 86,890,620 |
L185S |
probably damaging |
Het |
Olfr1233 |
T |
A |
2: 89,339,459 |
Y281F |
probably damaging |
Het |
Olfr640 |
T |
C |
7: 104,021,997 |
H107R |
probably damaging |
Het |
Olfr753-ps1 |
T |
A |
17: 37,170,000 |
Y216F |
probably damaging |
Het |
Olfr887 |
A |
T |
9: 38,085,126 |
M97L |
probably benign |
Het |
Pdzph1 |
T |
A |
17: 58,974,880 |
I136F |
probably damaging |
Het |
Pigg |
T |
C |
5: 108,314,160 |
I119T |
probably damaging |
Het |
R3hdm2 |
A |
G |
10: 127,458,893 |
H215R |
probably damaging |
Het |
Sept14 |
C |
T |
5: 129,685,914 |
|
probably null |
Het |
Slc9a3 |
T |
C |
13: 74,150,960 |
M166T |
possibly damaging |
Het |
Spock3 |
A |
G |
8: 63,345,782 |
D279G |
probably damaging |
Het |
Suco |
T |
C |
1: 161,833,430 |
I967V |
probably damaging |
Het |
Tgtp1 |
A |
G |
11: 48,987,176 |
L234P |
probably damaging |
Het |
Tmem176a |
A |
G |
6: 48,842,217 |
D4G |
probably benign |
Het |
Tmem2 |
T |
C |
19: 21,798,329 |
I312T |
probably benign |
Het |
Ugt1a10 |
G |
A |
1: 88,216,254 |
A199T |
probably damaging |
Het |
Uox |
A |
G |
3: 146,624,545 |
D152G |
probably damaging |
Het |
Vmn1r35 |
C |
T |
6: 66,679,506 |
W60* |
probably null |
Het |
Vmn2r103 |
T |
C |
17: 19,812,171 |
C736R |
probably damaging |
Het |
|