Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9530077C05Rik |
G |
A |
9: 22,424,126 |
W13* |
probably null |
Het |
Abcc4 |
A |
G |
14: 118,490,566 |
L1268P |
possibly damaging |
Het |
Acot3 |
T |
A |
12: 84,057,086 |
V223E |
probably damaging |
Het |
Afap1 |
T |
G |
5: 35,997,551 |
S680A |
probably damaging |
Het |
Aox1 |
C |
T |
1: 58,077,513 |
A801V |
probably damaging |
Het |
Atp8b1 |
G |
T |
18: 64,577,616 |
T155K |
probably damaging |
Het |
B230118H07Rik |
A |
T |
2: 101,583,553 |
M133K |
possibly damaging |
Het |
Bard1 |
C |
A |
1: 71,030,750 |
V690F |
possibly damaging |
Het |
Btnl9 |
C |
A |
11: 49,182,965 |
|
probably null |
Het |
C1rl |
A |
G |
6: 124,493,188 |
N13S |
probably benign |
Het |
Cad |
C |
A |
5: 31,069,112 |
T1166K |
probably damaging |
Het |
Ckap5 |
T |
A |
2: 91,562,989 |
M405K |
probably damaging |
Het |
Csn1s1 |
T |
C |
5: 87,678,085 |
|
probably null |
Het |
Ctnna2 |
A |
G |
6: 76,915,828 |
L792P |
probably damaging |
Het |
Dennd3 |
T |
A |
15: 73,567,080 |
V1099D |
possibly damaging |
Het |
Dnaic2 |
A |
G |
11: 114,752,990 |
N482S |
probably benign |
Het |
Dock10 |
T |
C |
1: 80,606,173 |
T184A |
probably damaging |
Het |
Ear2 |
T |
A |
14: 44,103,089 |
L68H |
probably damaging |
Het |
Edn3 |
A |
G |
2: 174,779,732 |
T149A |
probably benign |
Het |
Erf |
C |
T |
7: 25,245,616 |
V131M |
probably benign |
Het |
Esp34 |
A |
G |
17: 38,554,227 |
|
probably benign |
Het |
Gm13128 |
C |
T |
4: 144,331,207 |
T128I |
probably benign |
Het |
Gm14548 |
G |
T |
7: 3,894,600 |
H499N |
probably damaging |
Het |
Gm7247 |
C |
T |
14: 51,364,348 |
S26F |
probably benign |
Het |
Golga1 |
A |
G |
2: 39,047,087 |
V161A |
probably benign |
Het |
Gpr17 |
T |
A |
18: 31,947,477 |
T178S |
probably benign |
Het |
Gsg1l2 |
T |
A |
11: 67,774,711 |
I35N |
possibly damaging |
Het |
Hmgn3 |
T |
A |
9: 83,112,231 |
T46S |
probably damaging |
Het |
Hydin |
A |
C |
8: 110,599,085 |
I4709L |
probably benign |
Het |
Ifna9 |
A |
T |
4: 88,592,363 |
L8Q |
probably null |
Het |
Kpna4 |
T |
C |
3: 69,126,733 |
E125G |
probably null |
Het |
Lrriq1 |
A |
G |
10: 103,170,464 |
S1267P |
probably damaging |
Het |
Mab21l1 |
G |
T |
3: 55,783,097 |
C35F |
possibly damaging |
Het |
Map3k2 |
A |
G |
18: 32,203,051 |
D97G |
probably damaging |
Het |
Mdn1 |
T |
A |
4: 32,741,073 |
I3799N |
probably damaging |
Het |
Mki67 |
G |
A |
7: 135,697,429 |
R1959C |
probably damaging |
Het |
Mroh1 |
A |
T |
15: 76,451,357 |
H1400L |
possibly damaging |
Het |
Mroh4 |
T |
A |
15: 74,625,472 |
K167* |
probably null |
Het |
Mroh8 |
A |
G |
2: 157,253,064 |
I334T |
probably benign |
Het |
Olfr559 |
T |
A |
7: 102,724,367 |
Y41F |
probably damaging |
Het |
Phf11d |
T |
A |
14: 59,365,449 |
|
probably benign |
Het |
Phf21a |
C |
T |
2: 92,351,752 |
T342I |
possibly damaging |
Het |
Plekhh3 |
T |
C |
11: 101,164,765 |
E483G |
possibly damaging |
Het |
Ppp1r3b |
G |
A |
8: 35,384,201 |
A65T |
probably damaging |
Het |
Prkcq |
A |
G |
2: 11,256,286 |
H383R |
probably damaging |
Het |
Pum1 |
T |
C |
4: 130,768,847 |
V961A |
probably damaging |
Het |
Scgb2b27 |
T |
C |
7: 34,012,136 |
E96G |
probably benign |
Het |
Sel1l2 |
T |
A |
2: 140,244,105 |
E522V |
probably damaging |
Het |
Socs4 |
T |
G |
14: 47,290,161 |
C184W |
probably damaging |
Het |
Spdye4c |
A |
T |
2: 128,596,633 |
I304F |
probably benign |
Het |
Sptbn2 |
A |
G |
19: 4,739,278 |
I1249V |
possibly damaging |
Het |
Sys1 |
T |
C |
2: 164,464,587 |
S154P |
probably benign |
Het |
Taf6l |
T |
C |
19: 8,778,166 |
Q275R |
possibly damaging |
Het |
Thada |
T |
A |
17: 84,436,634 |
I749F |
probably damaging |
Het |
Tubb1 |
T |
A |
2: 174,457,774 |
H416Q |
probably benign |
Het |
Vmn2r109 |
G |
A |
17: 20,540,719 |
T792I |
probably damaging |
Het |
Zfp988 |
A |
G |
4: 147,331,802 |
Q231R |
probably benign |
Het |
Zmynd8 |
T |
C |
2: 165,842,787 |
I182V |
possibly damaging |
Het |
Zzz3 |
T |
C |
3: 152,428,151 |
V282A |
probably benign |
Het |
|