Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610010F05Rik |
A |
T |
11: 23,620,278 |
Y207* |
probably null |
Het |
Abca8b |
A |
C |
11: 109,941,607 |
H1231Q |
possibly damaging |
Het |
Acbd4 |
T |
A |
11: 103,103,851 |
|
probably null |
Het |
Atp13a4 |
T |
A |
16: 29,471,953 |
Y226F |
possibly damaging |
Het |
Brd3 |
A |
C |
2: 27,462,522 |
F132C |
probably damaging |
Het |
Btaf1 |
A |
T |
19: 36,956,524 |
N184I |
probably benign |
Het |
Ccdc180 |
A |
G |
4: 45,903,887 |
E351G |
possibly damaging |
Het |
Ccdc185 |
A |
T |
1: 182,747,353 |
Y590* |
probably null |
Het |
Chil1 |
G |
A |
1: 134,189,242 |
E315K |
probably benign |
Het |
Col6a6 |
T |
A |
9: 105,709,489 |
M1778L |
probably benign |
Het |
Cyp3a59 |
A |
C |
5: 146,104,711 |
Y355S |
probably damaging |
Het |
Cyp4a31 |
A |
G |
4: 115,574,711 |
T396A |
probably benign |
Het |
Dnah6 |
A |
T |
6: 73,144,965 |
I1373N |
probably damaging |
Het |
Dopey2 |
C |
A |
16: 93,777,386 |
H1598N |
probably benign |
Het |
Erich4 |
T |
A |
7: 25,615,134 |
K118M |
probably damaging |
Het |
Gkap1 |
A |
T |
13: 58,255,773 |
V179E |
probably benign |
Het |
Gpr107 |
T |
G |
2: 31,178,255 |
I243S |
possibly damaging |
Het |
Kcnq5 |
A |
T |
1: 21,479,378 |
I375N |
probably damaging |
Het |
Klhdc3 |
A |
T |
17: 46,676,966 |
H266Q |
probably benign |
Het |
Krt71 |
C |
T |
15: 101,735,466 |
G446R |
probably damaging |
Het |
L3mbtl2 |
A |
G |
15: 81,682,968 |
T423A |
probably benign |
Het |
Mical3 |
T |
C |
6: 120,952,469 |
E1812G |
probably damaging |
Het |
Nlrp1a |
A |
G |
11: 71,097,122 |
I1174T |
probably benign |
Het |
Npas2 |
C |
A |
1: 39,334,768 |
Q450K |
possibly damaging |
Het |
Nrp1 |
T |
A |
8: 128,468,389 |
I442N |
probably damaging |
Het |
Olfr1385 |
A |
T |
11: 49,495,021 |
M163L |
probably benign |
Het |
Olfr338 |
T |
A |
2: 36,376,994 |
S73T |
probably damaging |
Het |
Palld |
TGCGTAGCG |
TGCG |
8: 61,513,457 |
|
probably null |
Het |
Pih1d3 |
A |
T |
1: 31,223,215 |
I93F |
probably damaging |
Het |
Pold3 |
T |
A |
7: 100,119,683 |
Q36L |
possibly damaging |
Het |
Polg |
T |
C |
7: 79,459,786 |
T428A |
probably benign |
Het |
Rfx7 |
T |
A |
9: 72,577,047 |
V57E |
possibly damaging |
Het |
Rnf122 |
T |
G |
8: 31,112,149 |
M1R |
probably null |
Het |
Scn10a |
T |
A |
9: 119,617,733 |
T1410S |
probably damaging |
Het |
Serpinb13 |
T |
A |
1: 107,000,736 |
V362E |
probably damaging |
Het |
Setdb1 |
T |
C |
3: 95,327,611 |
N927S |
probably damaging |
Het |
Sft2d1 |
A |
G |
17: 8,320,638 |
K91R |
probably benign |
Het |
Shprh |
A |
G |
10: 11,159,530 |
H327R |
probably damaging |
Het |
Slc9b2 |
C |
A |
3: 135,336,395 |
H478Q |
probably benign |
Het |
Styxl1 |
G |
T |
5: 135,753,883 |
S117R |
probably damaging |
Het |
Synj2 |
T |
C |
17: 6,019,359 |
F150L |
probably damaging |
Het |
Tep1 |
C |
A |
14: 50,845,513 |
V1013L |
possibly damaging |
Het |
Tgfbi |
T |
A |
13: 56,630,655 |
L413Q |
probably damaging |
Het |
Tmc5 |
G |
A |
7: 118,666,870 |
R789Q |
probably damaging |
Het |
Tonsl |
T |
A |
15: 76,622,562 |
I115F |
possibly damaging |
Het |
Trim38 |
A |
G |
13: 23,791,134 |
Y352C |
probably damaging |
Het |
Txnl4a |
T |
A |
18: 80,207,321 |
V44D |
probably benign |
Het |
Vars2 |
A |
G |
17: 35,661,609 |
V39A |
probably damaging |
Het |
Vmn2r105 |
A |
G |
17: 20,208,322 |
C831R |
probably damaging |
Het |
Vmn2r26 |
T |
A |
6: 124,050,708 |
I469N |
probably benign |
Het |
Vmn2r53 |
T |
C |
7: 12,581,606 |
Y762C |
probably benign |
Het |
Vps13d |
T |
A |
4: 145,170,348 |
Q334L |
probably benign |
Het |
Zfp277 |
A |
T |
12: 40,364,165 |
I227N |
probably damaging |
Het |
|