Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J05Rik |
T |
C |
6: 146,853,841 (GRCm39) |
Q271R |
probably benign |
Het |
Abhd4 |
T |
A |
14: 54,500,164 (GRCm39) |
W63R |
probably damaging |
Het |
Adcy5 |
A |
G |
16: 35,120,018 (GRCm39) |
M1176V |
probably null |
Het |
Bach1 |
G |
A |
16: 87,516,179 (GRCm39) |
R240Q |
probably benign |
Het |
Brox |
G |
A |
1: 183,065,750 (GRCm39) |
P206L |
possibly damaging |
Het |
Ccn3 |
A |
G |
15: 54,611,171 (GRCm39) |
D102G |
possibly damaging |
Het |
Def6 |
A |
G |
17: 28,444,943 (GRCm39) |
K447R |
probably benign |
Het |
Dna2 |
T |
C |
10: 62,799,773 (GRCm39) |
S726P |
probably damaging |
Het |
Ell |
G |
A |
8: 71,031,879 (GRCm39) |
V15I |
probably damaging |
Het |
Entrep2 |
T |
A |
7: 64,409,075 (GRCm39) |
T440S |
probably benign |
Het |
Epha3 |
T |
A |
16: 63,593,698 (GRCm39) |
D130V |
probably benign |
Het |
Gys1 |
A |
G |
7: 45,089,008 (GRCm39) |
T200A |
possibly damaging |
Het |
Habp4 |
A |
T |
13: 64,309,939 (GRCm39) |
H47L |
probably benign |
Het |
Kcnj10 |
C |
A |
1: 172,196,563 (GRCm39) |
R26S |
probably benign |
Het |
Klhl1 |
T |
A |
14: 96,755,632 (GRCm39) |
D41V |
probably benign |
Het |
Lyn |
A |
G |
4: 3,782,996 (GRCm39) |
T410A |
probably damaging |
Het |
Mga |
A |
G |
2: 119,754,031 (GRCm39) |
T847A |
probably damaging |
Het |
Mrgpra3 |
G |
T |
7: 47,239,290 (GRCm39) |
T212N |
probably benign |
Het |
Myh4 |
T |
C |
11: 67,137,251 (GRCm39) |
F491L |
probably benign |
Het |
Neurl4 |
T |
A |
11: 69,801,562 (GRCm39) |
I1206N |
probably damaging |
Het |
Pcdhb15 |
T |
A |
18: 37,608,621 (GRCm39) |
W618R |
possibly damaging |
Het |
Pomc |
A |
G |
12: 4,010,146 (GRCm39) |
H129R |
probably damaging |
Het |
Ppm1l |
C |
A |
3: 69,460,399 (GRCm39) |
H325Q |
probably benign |
Het |
Psme4 |
A |
G |
11: 30,722,474 (GRCm39) |
|
probably benign |
Het |
Reep2 |
A |
G |
18: 34,978,342 (GRCm39) |
I74V |
probably null |
Het |
Robo2 |
T |
G |
16: 73,745,225 (GRCm39) |
E850A |
probably damaging |
Het |
Scrn2 |
T |
A |
11: 96,921,262 (GRCm39) |
|
probably benign |
Het |
Sfpq |
G |
A |
4: 126,923,675 (GRCm39) |
R673K |
probably benign |
Het |
Sh2d3c |
T |
C |
2: 32,644,581 (GRCm39) |
*703R |
probably null |
Het |
Spp1 |
A |
G |
5: 104,587,167 (GRCm39) |
M85V |
probably benign |
Het |
Srebf1 |
T |
C |
11: 60,097,810 (GRCm39) |
E98G |
probably damaging |
Het |
Srrm4 |
T |
A |
5: 116,582,851 (GRCm39) |
|
probably benign |
Het |
Ticam1 |
A |
T |
17: 56,578,154 (GRCm39) |
S314T |
possibly damaging |
Het |
Tie1 |
T |
C |
4: 118,341,823 (GRCm39) |
I209V |
possibly damaging |
Het |
Vapa |
G |
A |
17: 65,889,586 (GRCm39) |
R194* |
probably null |
Het |
Vcan |
C |
T |
13: 89,838,360 (GRCm39) |
D2395N |
probably damaging |
Het |
Whamm |
A |
G |
7: 81,241,574 (GRCm39) |
H295R |
probably benign |
Het |
Zdhhc14 |
A |
G |
17: 5,698,186 (GRCm39) |
Y85C |
probably damaging |
Het |
Zfp35 |
T |
A |
18: 24,136,583 (GRCm39) |
F309Y |
probably damaging |
Het |
Zfp423 |
C |
A |
8: 88,414,694 (GRCm39) |
C1187F |
probably damaging |
Het |
Zfp874b |
T |
C |
13: 67,622,392 (GRCm39) |
Y302C |
probably damaging |
Het |
|
Other mutations in Iqcn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R6811:Iqcn
|
UTSW |
8 |
71,169,422 (GRCm39) |
missense |
probably benign |
0.05 |
R6850:Iqcn
|
UTSW |
8 |
71,163,425 (GRCm39) |
missense |
probably damaging |
0.97 |
R7203:Iqcn
|
UTSW |
8 |
71,169,597 (GRCm39) |
missense |
probably benign |
0.26 |
R7260:Iqcn
|
UTSW |
8 |
71,161,397 (GRCm39) |
missense |
probably benign |
0.00 |
R7263:Iqcn
|
UTSW |
8 |
71,163,425 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7327:Iqcn
|
UTSW |
8 |
71,169,453 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7401:Iqcn
|
UTSW |
8 |
71,169,921 (GRCm39) |
missense |
probably benign |
0.03 |
R7542:Iqcn
|
UTSW |
8 |
71,161,415 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7572:Iqcn
|
UTSW |
8 |
71,162,075 (GRCm39) |
missense |
probably benign |
0.00 |
R7733:Iqcn
|
UTSW |
8 |
71,170,100 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7873:Iqcn
|
UTSW |
8 |
71,163,989 (GRCm39) |
missense |
probably benign |
0.29 |
R8015:Iqcn
|
UTSW |
8 |
71,169,441 (GRCm39) |
missense |
probably benign |
0.02 |
R8039:Iqcn
|
UTSW |
8 |
71,163,555 (GRCm39) |
missense |
probably benign |
0.09 |
R8061:Iqcn
|
UTSW |
8 |
71,161,224 (GRCm39) |
missense |
probably benign |
|
R8094:Iqcn
|
UTSW |
8 |
71,162,067 (GRCm39) |
missense |
probably benign |
|
R8498:Iqcn
|
UTSW |
8 |
71,162,625 (GRCm39) |
missense |
probably benign |
0.19 |
R8542:Iqcn
|
UTSW |
8 |
71,166,520 (GRCm39) |
splice site |
probably null |
|
R8709:Iqcn
|
UTSW |
8 |
71,162,372 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9141:Iqcn
|
UTSW |
8 |
71,162,421 (GRCm39) |
missense |
probably benign |
0.15 |
R9313:Iqcn
|
UTSW |
8 |
71,161,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R9324:Iqcn
|
UTSW |
8 |
71,161,794 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1177:Iqcn
|
UTSW |
8 |
71,169,752 (GRCm39) |
missense |
possibly damaging |
0.92 |
|