Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
G |
A |
8: 111,769,891 (GRCm39) |
R330Q |
possibly damaging |
Het |
Amph |
A |
T |
13: 19,284,823 (GRCm39) |
S250C |
possibly damaging |
Het |
Camsap2 |
C |
T |
1: 136,209,630 (GRCm39) |
E621K |
probably damaging |
Het |
Cpt2 |
A |
G |
4: 107,765,171 (GRCm39) |
S152P |
probably damaging |
Het |
Csmd1 |
T |
A |
8: 15,967,248 (GRCm39) |
Q3205L |
probably damaging |
Het |
Dag1 |
G |
T |
9: 108,084,552 (GRCm39) |
P863Q |
probably damaging |
Het |
Dclk1 |
A |
G |
3: 55,163,480 (GRCm39) |
I191V |
probably benign |
Het |
Ddhd1 |
A |
G |
14: 45,847,967 (GRCm39) |
L567P |
probably damaging |
Het |
Enox1 |
T |
C |
14: 77,936,750 (GRCm39) |
|
probably benign |
Het |
Exoc3 |
T |
C |
13: 74,347,658 (GRCm39) |
E104G |
probably damaging |
Het |
Foxp1 |
T |
A |
6: 99,139,930 (GRCm39) |
Q17L |
probably damaging |
Het |
Fscn1 |
A |
G |
5: 142,956,449 (GRCm39) |
|
probably benign |
Het |
Fut8 |
T |
C |
12: 77,411,811 (GRCm39) |
V91A |
probably benign |
Het |
Gm5475 |
T |
A |
15: 100,322,083 (GRCm39) |
Y77* |
probably null |
Het |
Gm5800 |
T |
C |
14: 51,953,605 (GRCm39) |
|
probably benign |
Het |
Hs2st1 |
T |
A |
3: 144,143,405 (GRCm39) |
K213* |
probably null |
Het |
Il5ra |
T |
A |
6: 106,719,647 (GRCm39) |
Y62F |
probably damaging |
Het |
Inpp5d |
A |
G |
1: 87,635,851 (GRCm39) |
E734G |
probably damaging |
Het |
Insig2 |
A |
T |
1: 121,234,649 (GRCm39) |
C194S |
probably damaging |
Het |
Lemd3 |
A |
C |
10: 120,761,361 (GRCm39) |
H898Q |
possibly damaging |
Het |
Lrp4 |
A |
G |
2: 91,301,548 (GRCm39) |
T43A |
probably benign |
Het |
Mast3 |
C |
T |
8: 71,236,343 (GRCm39) |
|
probably null |
Het |
Melk |
T |
C |
4: 44,360,864 (GRCm39) |
|
probably benign |
Het |
Myo10 |
C |
T |
15: 25,666,618 (GRCm39) |
|
probably benign |
Het |
Nlrc5 |
G |
A |
8: 95,216,163 (GRCm39) |
V967M |
probably benign |
Het |
Nlrp9b |
T |
A |
7: 19,757,647 (GRCm39) |
F295I |
probably damaging |
Het |
Phf3 |
A |
T |
1: 30,843,999 (GRCm39) |
D1653E |
probably benign |
Het |
Ppfia4 |
A |
T |
1: 134,251,827 (GRCm39) |
L449Q |
probably damaging |
Het |
Ppp1r16b |
T |
A |
2: 158,599,129 (GRCm39) |
I367N |
probably damaging |
Het |
Ralgapb |
T |
C |
2: 158,279,331 (GRCm39) |
L139S |
probably damaging |
Het |
Slc20a1 |
T |
C |
2: 129,052,692 (GRCm39) |
V658A |
probably damaging |
Het |
Son |
C |
A |
16: 91,461,616 (GRCm39) |
A347E |
probably damaging |
Het |
Tprg1l |
C |
A |
4: 154,244,594 (GRCm39) |
V134L |
possibly damaging |
Het |
Trim24 |
A |
T |
6: 37,934,484 (GRCm39) |
N733I |
probably damaging |
Het |
Uggt1 |
A |
T |
1: 36,225,013 (GRCm39) |
D540E |
probably benign |
Het |
Urb2 |
T |
A |
8: 124,773,934 (GRCm39) |
F1488L |
probably damaging |
Het |
Utp20 |
T |
C |
10: 88,634,266 (GRCm39) |
D810G |
probably benign |
Het |
Zfp473 |
T |
A |
7: 44,383,324 (GRCm39) |
K335N |
probably damaging |
Het |
|
Other mutations in Ankrd61 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01666:Ankrd61
|
APN |
5 |
143,827,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R0372:Ankrd61
|
UTSW |
5 |
143,827,993 (GRCm39) |
missense |
probably benign |
0.00 |
R0631:Ankrd61
|
UTSW |
5 |
143,831,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R2106:Ankrd61
|
UTSW |
5 |
143,828,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R2508:Ankrd61
|
UTSW |
5 |
143,833,894 (GRCm39) |
unclassified |
probably benign |
|
R3873:Ankrd61
|
UTSW |
5 |
143,828,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Ankrd61
|
UTSW |
5 |
143,831,613 (GRCm39) |
missense |
probably benign |
0.01 |
R5386:Ankrd61
|
UTSW |
5 |
143,828,482 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6651:Ankrd61
|
UTSW |
5 |
143,830,438 (GRCm39) |
missense |
probably damaging |
0.98 |
R8729:Ankrd61
|
UTSW |
5 |
143,827,803 (GRCm39) |
missense |
probably benign |
0.00 |
R8745:Ankrd61
|
UTSW |
5 |
143,828,237 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8815:Ankrd61
|
UTSW |
5 |
143,831,336 (GRCm39) |
missense |
probably benign |
|
R9005:Ankrd61
|
UTSW |
5 |
143,831,676 (GRCm39) |
missense |
probably benign |
0.01 |
R9110:Ankrd61
|
UTSW |
5 |
143,831,759 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9211:Ankrd61
|
UTSW |
5 |
143,828,358 (GRCm39) |
missense |
probably benign |
0.08 |
R9510:Ankrd61
|
UTSW |
5 |
143,828,322 (GRCm39) |
missense |
possibly damaging |
0.62 |
X0024:Ankrd61
|
UTSW |
5 |
143,828,619 (GRCm39) |
missense |
probably null |
1.00 |
X0024:Ankrd61
|
UTSW |
5 |
143,828,618 (GRCm39) |
missense |
probably damaging |
1.00 |
|