Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700102P08Rik |
A |
G |
9: 108,393,275 |
T13A |
possibly damaging |
Het |
Abcg4 |
T |
C |
9: 44,275,348 |
T500A |
probably benign |
Het |
Adcy4 |
T |
A |
14: 55,769,224 |
I1051F |
probably damaging |
Het |
Adgrg6 |
A |
T |
10: 14,467,497 |
N235K |
probably benign |
Het |
Aldh3a2 |
A |
C |
11: 61,262,419 |
Y160* |
probably null |
Het |
Arhgef4 |
G |
A |
1: 34,723,477 |
A605T |
unknown |
Het |
Armt1 |
T |
C |
10: 4,450,859 |
M202T |
probably benign |
Het |
AU019823 |
T |
C |
9: 50,607,461 |
R284G |
probably benign |
Het |
Brd2 |
C |
A |
17: 34,112,898 |
V349F |
probably damaging |
Het |
Btnl10 |
A |
T |
11: 58,926,865 |
|
probably benign |
Het |
Ccdc178 |
A |
G |
18: 22,120,534 |
V216A |
possibly damaging |
Het |
Ccdc85c |
A |
T |
12: 108,274,709 |
L142Q |
unknown |
Het |
Cdc27 |
A |
T |
11: 104,528,694 |
S172T |
probably damaging |
Het |
Ceacam14 |
T |
C |
7: 17,814,312 |
I109T |
probably damaging |
Het |
Ces5a |
C |
T |
8: 93,534,583 |
G72E |
probably damaging |
Het |
Cfb |
A |
G |
17: 34,861,824 |
Y66H |
possibly damaging |
Het |
Clec14a |
G |
A |
12: 58,268,215 |
P207L |
probably damaging |
Het |
Clec16a |
G |
A |
16: 10,630,788 |
R599H |
probably damaging |
Het |
Csmd1 |
A |
T |
8: 15,903,212 |
I3423N |
probably damaging |
Het |
Cyp4a29 |
C |
A |
4: 115,250,199 |
N243K |
probably benign |
Het |
Ddx59 |
T |
C |
1: 136,416,872 |
F94L |
probably damaging |
Het |
Dusp3 |
A |
C |
11: 101,986,871 |
V19G |
probably benign |
Het |
Fgfr4 |
T |
A |
13: 55,166,108 |
V545E |
probably damaging |
Het |
Fxn |
G |
T |
19: 24,280,426 |
A47D |
probably damaging |
Het |
Gdpgp1 |
A |
T |
7: 80,239,150 |
I310F |
possibly damaging |
Het |
Gm7210 |
A |
T |
7: 11,594,113 |
|
noncoding transcript |
Het |
Grm7 |
G |
T |
6: 111,358,875 |
C749F |
probably damaging |
Het |
Hps4 |
T |
G |
5: 112,346,629 |
V26G |
probably damaging |
Het |
Igf1r |
A |
G |
7: 68,165,233 |
D294G |
probably benign |
Het |
Immp1l |
T |
C |
2: 105,930,827 |
F27S |
probably benign |
Het |
Kcnk3 |
T |
A |
5: 30,622,586 |
C327S |
probably damaging |
Het |
Kif13a |
T |
A |
13: 46,815,207 |
|
probably null |
Het |
Krtap5-4 |
T |
C |
7: 142,304,090 |
S166P |
unknown |
Het |
Lyst |
G |
A |
13: 13,743,311 |
D3319N |
possibly damaging |
Het |
Malrd1 |
T |
G |
2: 16,042,267 |
S1735A |
unknown |
Het |
Myh4 |
A |
G |
11: 67,243,442 |
T308A |
probably benign |
Het |
Myh8 |
A |
T |
11: 67,299,341 |
Q1269L |
probably benign |
Het |
Myo15b |
G |
A |
11: 115,890,831 |
V1367I |
probably damaging |
Het |
Nae1 |
T |
C |
8: 104,523,637 |
D208G |
probably benign |
Het |
Nelfe |
T |
A |
17: 34,854,456 |
V296D |
probably damaging |
Het |
Npepps |
A |
T |
11: 97,218,548 |
V734E |
probably damaging |
Het |
Ogdh |
A |
G |
11: 6,349,390 |
N752S |
probably damaging |
Het |
Olfr1094 |
A |
G |
2: 86,829,654 |
I301V |
possibly damaging |
Het |
Olfr266 |
T |
C |
3: 106,822,187 |
D124G |
probably damaging |
Het |
Olfr401 |
A |
T |
11: 74,121,721 |
Q144L |
possibly damaging |
Het |
Olfr906 |
T |
C |
9: 38,488,377 |
M116T |
probably benign |
Het |
Otof |
C |
A |
5: 30,414,544 |
G171V |
probably damaging |
Het |
Phtf2 |
A |
T |
5: 20,801,941 |
V208D |
probably damaging |
Het |
Pkn1 |
T |
A |
8: 83,683,591 |
T340S |
probably damaging |
Het |
Plcd4 |
C |
T |
1: 74,563,594 |
L668F |
possibly damaging |
Het |
Plch1 |
C |
T |
3: 63,781,390 |
W131* |
probably null |
Het |
Prss50 |
A |
T |
9: 110,861,299 |
D170V |
probably damaging |
Het |
Ptprg |
T |
C |
14: 12,237,118 |
V604A |
probably damaging |
Het |
Rab33b |
T |
C |
3: 51,493,405 |
V100A |
probably damaging |
Het |
Rbm26 |
T |
A |
14: 105,131,535 |
D736V |
probably damaging |
Het |
Rela |
C |
A |
19: 5,646,964 |
P400T |
probably benign |
Het |
Rpusd4 |
T |
C |
9: 35,268,038 |
L50P |
probably damaging |
Het |
Scn10a |
A |
C |
9: 119,627,115 |
Y1214D |
probably damaging |
Het |
Sema3c |
A |
G |
5: 17,672,432 |
E179G |
probably damaging |
Het |
Skint5 |
T |
A |
4: 113,517,133 |
D1253V |
unknown |
Het |
Sp4 |
G |
T |
12: 118,238,178 |
P771H |
probably damaging |
Het |
Sphkap |
T |
A |
1: 83,278,378 |
Y263F |
probably damaging |
Het |
Ssbp1 |
G |
A |
6: 40,476,753 |
V78I |
probably benign |
Het |
St3gal6 |
A |
G |
16: 58,486,406 |
I87T |
probably benign |
Het |
Tango6 |
T |
A |
8: 106,818,497 |
D997E |
probably benign |
Het |
Tpr |
C |
T |
1: 150,445,888 |
P2265S |
possibly damaging |
Het |
Ttc7b |
A |
T |
12: 100,325,677 |
F212Y |
probably damaging |
Het |
Ubc |
A |
G |
5: 125,388,260 |
M1T |
probably null |
Het |
Vill |
G |
C |
9: 119,063,648 |
Q376H |
probably benign |
Het |
Yes1 |
T |
C |
5: 32,651,686 |
I132T |
possibly damaging |
Het |
Ythdc2 |
A |
G |
18: 44,860,377 |
T830A |
probably benign |
Het |
Zbtb41 |
T |
A |
1: 139,430,306 |
F451I |
possibly damaging |
Het |
Zfp995 |
C |
T |
17: 21,880,512 |
C247Y |
probably benign |
Het |
|