Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
A |
G |
9: 44,192,854 (GRCm39) |
|
probably null |
Het |
Akr1c14 |
T |
A |
13: 4,128,035 (GRCm39) |
C145* |
probably null |
Het |
Arhgef26 |
A |
G |
3: 62,367,145 (GRCm39) |
|
probably benign |
Het |
Asb9 |
A |
G |
X: 163,318,452 (GRCm39) |
M215V |
probably benign |
Het |
Atp6v1b1 |
T |
A |
6: 83,730,897 (GRCm39) |
|
probably benign |
Het |
Cep97 |
T |
C |
16: 55,735,868 (GRCm39) |
E310G |
probably damaging |
Het |
Ctrc |
C |
T |
4: 141,571,025 (GRCm39) |
D72N |
possibly damaging |
Het |
Dnah2 |
A |
G |
11: 69,349,011 (GRCm39) |
I2492T |
probably benign |
Het |
Emilin2 |
A |
G |
17: 71,582,144 (GRCm39) |
V194A |
probably damaging |
Het |
Epb41l5 |
T |
C |
1: 119,500,586 (GRCm39) |
T524A |
probably benign |
Het |
Fam91a1 |
A |
G |
15: 58,313,505 (GRCm39) |
N497S |
possibly damaging |
Het |
Gabpb1 |
A |
T |
2: 126,481,191 (GRCm39) |
C319* |
probably null |
Het |
Galnt10 |
A |
G |
11: 57,673,104 (GRCm39) |
T487A |
probably benign |
Het |
Hecw2 |
T |
A |
1: 53,981,961 (GRCm39) |
|
probably null |
Het |
Hmg20a |
C |
T |
9: 56,384,586 (GRCm39) |
Q119* |
probably null |
Het |
Ifi44l |
A |
G |
3: 151,468,477 (GRCm39) |
S18P |
unknown |
Het |
Immt |
T |
A |
6: 71,828,820 (GRCm39) |
V125E |
probably benign |
Het |
Ints13 |
T |
C |
6: 146,451,437 (GRCm39) |
|
probably benign |
Het |
Lrp1b |
C |
T |
2: 40,779,321 (GRCm39) |
G2574S |
probably benign |
Het |
Myoc |
T |
C |
1: 162,467,343 (GRCm39) |
C171R |
probably benign |
Het |
Ncbp1 |
C |
T |
4: 46,159,699 (GRCm39) |
T404M |
probably damaging |
Het |
Npy6r |
A |
G |
18: 44,408,998 (GRCm39) |
N140D |
probably damaging |
Het |
Nrxn2 |
A |
T |
19: 6,542,898 (GRCm39) |
M1041L |
possibly damaging |
Het |
Nsmaf |
G |
A |
4: 6,398,551 (GRCm39) |
P851L |
probably benign |
Het |
Nutm2 |
T |
A |
13: 50,627,829 (GRCm39) |
|
probably null |
Het |
Or10ak8 |
A |
G |
4: 118,773,947 (GRCm39) |
F239S |
probably damaging |
Het |
Or2g25 |
A |
G |
17: 37,970,579 (GRCm39) |
V215A |
probably benign |
Het |
Or4f61 |
A |
C |
2: 111,922,869 (GRCm39) |
M59R |
probably damaging |
Het |
Padi2 |
T |
G |
4: 140,654,468 (GRCm39) |
Y206* |
probably null |
Het |
Pcdh19 |
A |
T |
X: 132,582,007 (GRCm39) |
Y766* |
probably null |
Het |
Pde12 |
A |
G |
14: 26,387,619 (GRCm39) |
|
probably benign |
Het |
Ppl |
C |
T |
16: 4,907,680 (GRCm39) |
G872R |
probably benign |
Het |
Prkag3 |
C |
T |
1: 74,787,971 (GRCm39) |
|
probably benign |
Het |
Ptgfr |
T |
C |
3: 151,541,437 (GRCm39) |
T24A |
probably benign |
Het |
Rpe65 |
T |
C |
3: 159,321,283 (GRCm39) |
V365A |
probably benign |
Het |
Shank3 |
T |
C |
15: 89,388,118 (GRCm39) |
|
probably null |
Het |
Slco1a6 |
T |
C |
6: 142,032,200 (GRCm39) |
T642A |
probably benign |
Het |
Slco6d1 |
C |
A |
1: 98,371,468 (GRCm39) |
P275T |
probably damaging |
Het |
Smarca1 |
G |
T |
X: 46,964,109 (GRCm39) |
Q343K |
probably damaging |
Het |
Smoc2 |
A |
G |
17: 14,567,495 (GRCm39) |
T180A |
possibly damaging |
Het |
Tfrc |
G |
A |
16: 32,440,004 (GRCm39) |
V406I |
probably benign |
Het |
Tigit |
C |
T |
16: 43,469,473 (GRCm39) |
G206D |
probably benign |
Het |
Triobp |
G |
A |
15: 78,858,497 (GRCm39) |
|
probably benign |
Het |
Trmo |
T |
C |
4: 46,380,217 (GRCm39) |
Y384C |
probably damaging |
Het |
Vmn1r89 |
T |
A |
7: 12,953,465 (GRCm39) |
I67N |
probably damaging |
Het |
Wdr17 |
C |
A |
8: 55,140,771 (GRCm39) |
E194* |
probably null |
Het |
|
Other mutations in Atoh8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00925:Atoh8
|
APN |
6 |
72,211,553 (GRCm39) |
missense |
probably benign |
0.01 |
R2057:Atoh8
|
UTSW |
6 |
72,212,112 (GRCm39) |
missense |
probably damaging |
0.96 |
R2893:Atoh8
|
UTSW |
6 |
72,211,856 (GRCm39) |
missense |
probably benign |
|
R4787:Atoh8
|
UTSW |
6 |
72,200,761 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7529:Atoh8
|
UTSW |
6 |
72,200,825 (GRCm39) |
missense |
probably benign |
0.24 |
R9273:Atoh8
|
UTSW |
6 |
72,212,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R9782:Atoh8
|
UTSW |
6 |
72,200,848 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1177:Atoh8
|
UTSW |
6 |
72,212,110 (GRCm39) |
missense |
probably damaging |
1.00 |
|