Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
A |
G |
5: 8,896,587 |
E29G |
probably benign |
Het |
Abi3bp |
T |
C |
16: 56,671,265 |
S552P |
probably damaging |
Het |
Adgrg7 |
A |
G |
16: 56,773,466 |
I129T |
probably benign |
Het |
Adhfe1 |
A |
G |
1: 9,553,718 |
N148S |
probably damaging |
Het |
AI182371 |
A |
G |
2: 35,097,971 |
Y77H |
probably damaging |
Het |
Aldh5a1 |
C |
T |
13: 24,919,678 |
|
probably null |
Het |
Ankrd2 |
A |
G |
19: 42,040,105 |
T67A |
possibly damaging |
Het |
Anln |
A |
T |
9: 22,376,308 |
C232* |
probably null |
Het |
C330027C09Rik |
A |
T |
16: 48,994,329 |
K18* |
probably null |
Het |
Cchcr1 |
A |
G |
17: 35,528,578 |
D587G |
possibly damaging |
Het |
Cgn |
G |
T |
3: 94,767,125 |
Q901K |
possibly damaging |
Het |
Cluh |
G |
T |
11: 74,667,228 |
|
probably null |
Het |
Crebbp |
G |
A |
16: 4,084,623 |
Q2213* |
probably null |
Het |
Cyp2d22 |
T |
A |
15: 82,373,835 |
|
probably null |
Het |
Dcdc2a |
T |
C |
13: 25,205,457 |
V456A |
probably benign |
Het |
Depdc5 |
A |
G |
5: 32,968,731 |
E569G |
probably benign |
Het |
Dnah5 |
T |
C |
15: 28,459,185 |
F4517L |
probably benign |
Het |
Doc2b |
T |
C |
11: 75,773,595 |
K317E |
probably damaging |
Het |
Dysf |
T |
A |
6: 84,203,199 |
D1951E |
probably damaging |
Het |
Epha6 |
C |
A |
16: 60,424,835 |
A334S |
possibly damaging |
Het |
F2rl2 |
A |
C |
13: 95,700,641 |
I65L |
probably benign |
Het |
Fbxw17 |
A |
G |
13: 50,432,512 |
K417E |
probably benign |
Het |
Fkbpl |
G |
A |
17: 34,645,329 |
A24T |
probably benign |
Het |
Fxr2 |
A |
G |
11: 69,641,339 |
M96V |
possibly damaging |
Het |
Kcnj10 |
C |
A |
1: 172,369,325 |
Y135* |
probably null |
Het |
Kidins220 |
G |
A |
12: 25,052,813 |
R1238Q |
probably damaging |
Het |
Krt31 |
T |
C |
11: 100,048,230 |
N255S |
probably benign |
Het |
Lrp2 |
T |
C |
2: 69,511,001 |
D945G |
probably benign |
Het |
Lrrc66 |
T |
C |
5: 73,608,089 |
D537G |
probably benign |
Het |
Ltbp4 |
T |
A |
7: 27,319,724 |
I992F |
probably damaging |
Het |
Lzts1 |
A |
G |
8: 69,140,872 |
S28P |
probably benign |
Het |
Mrc2 |
C |
A |
11: 105,325,644 |
N86K |
probably damaging |
Het |
Mroh6 |
C |
A |
15: 75,886,637 |
A302S |
possibly damaging |
Het |
Muc16 |
T |
A |
9: 18,497,797 |
N198Y |
probably damaging |
Het |
Myo9a |
T |
C |
9: 59,871,229 |
S1423P |
probably benign |
Het |
Olfr1006 |
T |
A |
2: 85,674,594 |
K186* |
probably null |
Het |
Olfr1124 |
A |
T |
2: 87,435,318 |
D277V |
possibly damaging |
Het |
Olfr1141 |
A |
C |
2: 87,753,258 |
L245R |
probably damaging |
Het |
Olfr1367 |
A |
T |
13: 21,346,994 |
Y22F |
possibly damaging |
Het |
Olfr190 |
A |
G |
16: 59,074,714 |
V122A |
probably benign |
Het |
Olfr477 |
G |
T |
7: 107,990,413 |
G16V |
probably damaging |
Het |
Otogl |
G |
A |
10: 107,777,117 |
|
silent |
Het |
Polg |
T |
C |
7: 79,450,512 |
M1184V |
probably benign |
Het |
Prl8a8 |
T |
C |
13: 27,510,480 |
Y108C |
probably damaging |
Het |
Proser1 |
T |
A |
3: 53,478,119 |
I474N |
probably damaging |
Het |
Rbp1 |
C |
A |
9: 98,425,616 |
D79E |
possibly damaging |
Het |
Rnf213 |
T |
C |
11: 119,435,999 |
V1605A |
probably benign |
Het |
Rps24 |
A |
T |
14: 24,490,735 |
|
probably null |
Het |
Setd5 |
T |
C |
6: 113,121,812 |
|
probably null |
Het |
Slc38a3 |
T |
C |
9: 107,655,029 |
I435V |
probably benign |
Het |
Slco1a5 |
T |
A |
6: 142,234,808 |
M623L |
probably benign |
Het |
Spaca9 |
G |
A |
2: 28,693,781 |
R64W |
probably damaging |
Het |
Spn |
A |
G |
7: 127,136,307 |
S343P |
possibly damaging |
Het |
Sptan1 |
A |
G |
2: 30,004,523 |
T1168A |
probably benign |
Het |
Sptbn4 |
A |
T |
7: 27,364,587 |
L2138* |
probably null |
Het |
Tg |
T |
A |
15: 66,673,367 |
|
probably null |
Het |
Tigd5 |
T |
A |
15: 75,910,245 |
L152Q |
probably damaging |
Het |
Tmem163 |
C |
T |
1: 127,519,389 |
V170I |
probably benign |
Het |
Tpr |
T |
C |
1: 150,423,162 |
C1068R |
possibly damaging |
Het |
Ttc37 |
A |
G |
13: 76,185,240 |
E1536G |
probably damaging |
Het |
Ubr1 |
A |
T |
2: 120,893,209 |
Y1290N |
probably damaging |
Het |
Vmn1r184 |
T |
A |
7: 26,267,392 |
F188I |
probably benign |
Het |
Vmn2r100 |
G |
A |
17: 19,522,260 |
V299I |
probably benign |
Het |
Vmn2r91 |
T |
G |
17: 18,136,256 |
H728Q |
probably benign |
Het |
Vta1 |
T |
C |
10: 14,705,352 |
Y37C |
probably damaging |
Het |
Wbp2 |
C |
A |
11: 116,083,902 |
M35I |
probably benign |
Het |
Zcchc9 |
G |
A |
13: 91,805,867 |
Q90* |
probably null |
Het |
|