Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
C |
3: 122,173,988 |
L2229P |
possibly damaging |
Het |
Acaca |
T |
A |
11: 84,260,634 |
M786K |
probably damaging |
Het |
Acta2 |
G |
A |
19: 34,252,531 |
T8I |
probably benign |
Het |
Adap1 |
T |
G |
5: 139,293,173 |
E117D |
possibly damaging |
Het |
Ap5z1 |
T |
C |
5: 142,477,298 |
S746P |
probably benign |
Het |
Appl2 |
A |
G |
10: 83,617,428 |
I208T |
possibly damaging |
Het |
Astn1 |
G |
A |
1: 158,667,638 |
|
probably null |
Het |
Astn1 |
A |
G |
1: 158,505,386 |
E346G |
possibly damaging |
Het |
Atp23 |
T |
A |
10: 126,868,725 |
I180L |
unknown |
Het |
Bean1 |
CT |
C |
8: 104,182,032 |
|
probably null |
Het |
Cdh23 |
A |
T |
10: 60,384,945 |
I1340N |
probably benign |
Het |
Cdh8 |
G |
A |
8: 99,098,885 |
Q493* |
probably null |
Het |
Ces1g |
T |
C |
8: 93,319,827 |
I357V |
probably benign |
Het |
Ddx46 |
A |
G |
13: 55,650,478 |
D226G |
probably damaging |
Het |
Eea1 |
C |
T |
10: 95,994,905 |
Q143* |
probably null |
Het |
Erlin2 |
G |
T |
8: 27,031,772 |
|
probably null |
Het |
Fat3 |
T |
A |
9: 15,938,319 |
D3929V |
probably damaging |
Het |
Flt3 |
T |
C |
5: 147,334,437 |
D898G |
probably damaging |
Het |
Gm16519 |
A |
G |
17: 70,929,356 |
N100S |
probably benign |
Het |
Gnl1 |
A |
G |
17: 35,988,536 |
H533R |
probably damaging |
Het |
Gphn |
A |
G |
12: 78,504,680 |
T301A |
possibly damaging |
Het |
Herc2 |
C |
T |
7: 56,219,779 |
R4295* |
probably null |
Het |
Insm2 |
T |
C |
12: 55,599,518 |
S16P |
possibly damaging |
Het |
Jak2 |
C |
T |
19: 29,298,637 |
T778I |
probably benign |
Het |
Lrriq3 |
A |
G |
3: 155,101,097 |
T128A |
probably damaging |
Het |
Lst1 |
A |
G |
17: 35,186,944 |
|
probably null |
Het |
Magi1 |
G |
T |
6: 93,708,110 |
Y762* |
probably null |
Het |
Man2b1 |
T |
A |
8: 85,090,965 |
C358* |
probably null |
Het |
Mga |
T |
C |
2: 119,935,551 |
V1432A |
probably damaging |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 |
|
probably null |
Het |
Morc2a |
C |
T |
11: 3,683,566 |
Q587* |
probably null |
Het |
Mrc2 |
T |
C |
11: 105,292,797 |
I4T |
probably benign |
Het |
Myl10 |
G |
C |
5: 136,697,971 |
V70L |
probably benign |
Het |
Myo3b |
A |
G |
2: 70,217,169 |
R340G |
probably benign |
Het |
Nipal3 |
T |
C |
4: 135,490,937 |
Y34C |
probably damaging |
Het |
Nktr |
T |
A |
9: 121,749,279 |
D804E |
unknown |
Het |
Nlrp4b |
A |
G |
7: 10,714,889 |
M340V |
probably benign |
Het |
Olfr1039 |
A |
G |
2: 86,131,264 |
V133A |
probably benign |
Het |
Olfr385 |
T |
A |
11: 73,589,268 |
T157S |
probably benign |
Het |
Olfr680-ps1 |
A |
T |
7: 105,092,771 |
M16K |
probably benign |
Het |
Olfr701 |
G |
A |
7: 106,818,374 |
C97Y |
probably damaging |
Het |
Pard3 |
T |
A |
8: 127,610,582 |
N1271K |
probably damaging |
Het |
Pcdhb11 |
A |
T |
18: 37,421,619 |
M1L |
possibly damaging |
Het |
Pclo |
T |
C |
5: 14,682,104 |
V3540A |
unknown |
Het |
Pemt |
A |
G |
11: 59,976,844 |
F154S |
probably damaging |
Het |
Ptpn18 |
G |
A |
1: 34,473,364 |
D417N |
possibly damaging |
Het |
Rnpc3 |
G |
T |
3: 113,613,832 |
T376K |
probably benign |
Het |
Rpe65 |
A |
G |
3: 159,604,609 |
Y143C |
probably damaging |
Het |
Sbk2 |
T |
C |
7: 4,963,149 |
E12G |
probably benign |
Het |
Slc2a5 |
T |
C |
4: 150,129,069 |
I106T |
possibly damaging |
Het |
Snx13 |
A |
G |
12: 35,085,982 |
D92G |
probably damaging |
Het |
Sorl1 |
C |
T |
9: 41,980,688 |
V1889I |
probably benign |
Het |
Spag17 |
A |
T |
3: 99,939,247 |
N29I |
possibly damaging |
Het |
Speg |
T |
C |
1: 75,401,464 |
V878A |
probably damaging |
Het |
Timp4 |
A |
G |
6: 115,250,460 |
S53P |
probably damaging |
Het |
Tssk1 |
G |
T |
16: 17,895,084 |
E244D |
probably benign |
Het |
Usp29 |
A |
C |
7: 6,961,220 |
T21P |
possibly damaging |
Het |
Vmn2r85 |
A |
T |
10: 130,422,866 |
V440E |
probably benign |
Het |
Wdr59 |
T |
C |
8: 111,490,369 |
D270G |
|
Het |
Zbbx |
G |
A |
3: 75,085,519 |
P223S |
probably damaging |
Het |
Zfp936 |
T |
A |
7: 43,189,815 |
C235* |
probably null |
Het |
Zranb3 |
A |
T |
1: 128,032,847 |
|
probably null |
Het |
|