Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acap1 |
A |
T |
11: 69,773,202 (GRCm39) |
|
probably null |
Het |
Acat1 |
T |
C |
9: 53,496,183 (GRCm39) |
D318G |
probably benign |
Het |
Ahdc1 |
T |
C |
4: 132,791,002 (GRCm39) |
F748L |
probably benign |
Het |
Alkbh8 |
T |
A |
9: 3,347,916 (GRCm39) |
|
probably null |
Het |
Arhgef26 |
A |
G |
3: 62,247,449 (GRCm39) |
T178A |
probably benign |
Het |
Bid |
C |
T |
6: 120,874,216 (GRCm39) |
A110T |
possibly damaging |
Het |
Ccdc180 |
T |
C |
4: 45,909,359 (GRCm39) |
V509A |
possibly damaging |
Het |
Ccdc39 |
T |
C |
3: 33,869,634 (GRCm39) |
E731G |
probably benign |
Het |
Cenpf |
A |
G |
1: 189,374,998 (GRCm39) |
V2931A |
probably damaging |
Het |
Cobl |
A |
T |
11: 12,325,853 (GRCm39) |
N207K |
probably damaging |
Het |
Col14a1 |
T |
A |
15: 55,273,584 (GRCm39) |
W718R |
unknown |
Het |
Dnah7a |
A |
G |
1: 53,507,828 (GRCm39) |
I3081T |
probably damaging |
Het |
Dync1h1 |
T |
C |
12: 110,615,698 (GRCm39) |
V2977A |
probably damaging |
Het |
Ephb4 |
A |
G |
5: 137,364,796 (GRCm39) |
|
probably benign |
Het |
Fbxo24 |
A |
G |
5: 137,617,891 (GRCm39) |
V291A |
probably damaging |
Het |
Glra1 |
A |
C |
11: 55,405,896 (GRCm39) |
S282A |
probably benign |
Het |
Gm7589 |
C |
A |
9: 59,053,325 (GRCm39) |
|
noncoding transcript |
Het |
H6pd |
T |
C |
4: 150,066,872 (GRCm39) |
N505D |
probably benign |
Het |
Hdlbp |
T |
A |
1: 93,348,853 (GRCm39) |
N566Y |
probably damaging |
Het |
Hsp90aa1 |
C |
A |
12: 110,659,254 (GRCm39) |
K514N |
probably damaging |
Het |
Impdh1 |
A |
T |
6: 29,206,477 (GRCm39) |
V120D |
probably damaging |
Het |
Katnip |
A |
G |
7: 125,465,627 (GRCm39) |
T1360A |
probably benign |
Het |
Loxhd1 |
C |
T |
18: 77,490,632 (GRCm39) |
P1411S |
possibly damaging |
Het |
Lpl |
A |
G |
8: 69,349,281 (GRCm39) |
E269G |
probably damaging |
Het |
Map1a |
G |
T |
2: 121,136,701 (GRCm39) |
E2268* |
probably null |
Het |
Mark1 |
T |
C |
1: 184,660,245 (GRCm39) |
E137G |
probably damaging |
Het |
Mki67 |
A |
T |
7: 135,300,005 (GRCm39) |
S1676R |
possibly damaging |
Het |
Mogat2 |
T |
C |
7: 98,872,722 (GRCm39) |
Y154C |
possibly damaging |
Het |
Myo18a |
C |
G |
11: 77,732,405 (GRCm39) |
I859M |
probably benign |
Het |
Myo7a |
A |
G |
7: 97,756,215 (GRCm39) |
V39A |
probably benign |
Het |
Nedd4 |
T |
A |
9: 72,584,668 (GRCm39) |
I123N |
probably damaging |
Het |
Obscn |
A |
G |
11: 58,977,754 (GRCm39) |
V1966A |
probably benign |
Het |
Or7g33 |
T |
C |
9: 19,448,842 (GRCm39) |
N128S |
probably benign |
Het |
Orc3 |
T |
G |
4: 34,599,748 (GRCm39) |
N77T |
probably benign |
Het |
Penk |
A |
G |
4: 4,134,287 (GRCm39) |
M120T |
probably benign |
Het |
Phf7 |
G |
A |
14: 30,962,362 (GRCm39) |
Q148* |
probably null |
Het |
Pkhd1l1 |
G |
A |
15: 44,368,943 (GRCm39) |
V863I |
probably damaging |
Het |
Pkhd1l1 |
C |
T |
15: 44,452,993 (GRCm39) |
R3973C |
probably damaging |
Het |
Polq |
C |
T |
16: 36,862,109 (GRCm39) |
T264M |
probably damaging |
Het |
Ptprb |
A |
T |
10: 116,203,437 (GRCm39) |
T2070S |
probably damaging |
Het |
Ralgapb |
T |
C |
2: 158,272,453 (GRCm39) |
F169S |
probably damaging |
Het |
Rapgef5 |
G |
T |
12: 117,685,084 (GRCm39) |
A278S |
probably benign |
Het |
Ripor2 |
G |
T |
13: 24,861,824 (GRCm39) |
E203* |
probably null |
Het |
Setx |
T |
C |
2: 29,069,698 (GRCm39) |
L2501P |
probably benign |
Het |
Sh3bgrl2 |
C |
T |
9: 83,459,684 (GRCm39) |
|
probably benign |
Het |
Slc35b1 |
T |
A |
11: 95,276,689 (GRCm39) |
V56D |
probably damaging |
Het |
Slc45a4 |
C |
T |
15: 73,458,596 (GRCm39) |
D326N |
probably benign |
Het |
Stard9 |
C |
A |
2: 120,504,117 (GRCm39) |
S221R |
probably damaging |
Het |
Stat4 |
T |
A |
1: 52,053,086 (GRCm39) |
V89D |
probably benign |
Het |
Tek |
T |
A |
4: 94,627,943 (GRCm39) |
|
probably benign |
Het |
Tert |
T |
A |
13: 73,796,473 (GRCm39) |
F1068Y |
probably damaging |
Het |
Trim33 |
T |
A |
3: 103,217,670 (GRCm39) |
I205K |
probably damaging |
Het |
Vmn1r212 |
A |
T |
13: 23,067,562 (GRCm39) |
I257K |
probably benign |
Het |
|
Other mutations in Eri3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00678:Eri3
|
APN |
4 |
117,422,088 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01392:Eri3
|
APN |
4 |
117,446,356 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01781:Eri3
|
APN |
4 |
117,421,874 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02737:Eri3
|
APN |
4 |
117,422,057 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02969:Eri3
|
APN |
4 |
117,506,508 (GRCm39) |
missense |
probably damaging |
1.00 |
chewed_out
|
UTSW |
4 |
117,506,604 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4280001:Eri3
|
UTSW |
4 |
117,439,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0720:Eri3
|
UTSW |
4 |
117,410,242 (GRCm39) |
critical splice donor site |
probably null |
|
R0993:Eri3
|
UTSW |
4 |
117,421,860 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1538:Eri3
|
UTSW |
4 |
117,439,836 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1854:Eri3
|
UTSW |
4 |
117,506,562 (GRCm39) |
missense |
probably benign |
0.01 |
R1971:Eri3
|
UTSW |
4 |
117,421,964 (GRCm39) |
missense |
probably benign |
0.10 |
R5340:Eri3
|
UTSW |
4 |
117,530,991 (GRCm39) |
missense |
probably damaging |
0.99 |
R5511:Eri3
|
UTSW |
4 |
117,472,386 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5569:Eri3
|
UTSW |
4 |
117,506,553 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6052:Eri3
|
UTSW |
4 |
117,421,825 (GRCm39) |
missense |
probably damaging |
0.99 |
R7140:Eri3
|
UTSW |
4 |
117,506,604 (GRCm39) |
critical splice donor site |
probably null |
|
R7187:Eri3
|
UTSW |
4 |
117,446,343 (GRCm39) |
missense |
probably benign |
0.03 |
R7268:Eri3
|
UTSW |
4 |
117,506,580 (GRCm39) |
missense |
probably benign |
|
R8083:Eri3
|
UTSW |
4 |
117,450,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R8557:Eri3
|
UTSW |
4 |
117,472,520 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9430:Eri3
|
UTSW |
4 |
117,439,868 (GRCm39) |
nonsense |
probably null |
|
R9563:Eri3
|
UTSW |
4 |
117,422,013 (GRCm39) |
missense |
probably benign |
0.15 |
R9565:Eri3
|
UTSW |
4 |
117,422,013 (GRCm39) |
missense |
probably benign |
0.15 |
|