Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam34l |
T |
C |
8: 44,079,340 (GRCm39) |
I295V |
probably benign |
Het |
Adam5 |
T |
C |
8: 25,302,441 (GRCm39) |
Q101R |
probably benign |
Het |
C2cd4c |
T |
C |
10: 79,448,584 (GRCm39) |
N188D |
probably benign |
Het |
Cdc27 |
A |
G |
11: 104,416,875 (GRCm39) |
|
probably null |
Het |
Cdh11 |
T |
A |
8: 103,361,356 (GRCm39) |
I661L |
probably damaging |
Het |
Cimip1 |
T |
A |
2: 173,367,867 (GRCm39) |
S47T |
probably benign |
Het |
Csmd1 |
A |
G |
8: 16,760,634 (GRCm39) |
I167T |
probably benign |
Het |
Dennd3 |
T |
G |
15: 73,405,284 (GRCm39) |
F346V |
probably damaging |
Het |
Dis3l |
A |
T |
9: 64,248,412 (GRCm39) |
M1K |
probably null |
Het |
Dnajb6 |
A |
T |
5: 29,957,398 (GRCm39) |
K60I |
probably damaging |
Het |
Dock10 |
T |
A |
1: 80,514,657 (GRCm39) |
H1421L |
probably benign |
Het |
Elmod3 |
A |
T |
6: 72,545,921 (GRCm39) |
C274S |
probably damaging |
Het |
Eme1 |
T |
C |
11: 94,541,558 (GRCm39) |
E88G |
probably damaging |
Het |
Fam227a |
A |
T |
15: 79,505,006 (GRCm39) |
M475K |
probably benign |
Het |
Frem2 |
T |
C |
3: 53,561,394 (GRCm39) |
I1038V |
probably benign |
Het |
Gabpb1 |
T |
A |
2: 126,494,185 (GRCm39) |
N147Y |
probably damaging |
Het |
Gmnc |
A |
G |
16: 26,779,173 (GRCm39) |
L278P |
probably benign |
Het |
Gpr153 |
A |
G |
4: 152,366,331 (GRCm39) |
T299A |
probably benign |
Het |
H2-M11 |
T |
C |
17: 36,858,353 (GRCm39) |
V49A |
probably benign |
Het |
Hemgn |
T |
A |
4: 46,397,049 (GRCm39) |
K62N |
probably damaging |
Het |
Hormad2 |
G |
A |
11: 4,377,297 (GRCm39) |
T47M |
probably damaging |
Het |
Itgam |
T |
C |
7: 127,711,410 (GRCm39) |
F705L |
probably benign |
Het |
Klk1 |
T |
A |
7: 43,878,240 (GRCm39) |
|
probably null |
Het |
Myo1f |
A |
T |
17: 33,797,107 (GRCm39) |
I123F |
probably damaging |
Het |
Nup58 |
T |
C |
14: 60,457,590 (GRCm39) |
T538A |
probably damaging |
Het |
Or52j3 |
T |
A |
7: 102,836,030 (GRCm39) |
L74* |
probably null |
Het |
Or5p81 |
C |
T |
7: 108,267,400 (GRCm39) |
T259I |
probably benign |
Het |
Pdzd2 |
C |
T |
15: 12,399,356 (GRCm39) |
R790H |
probably damaging |
Het |
Pigv |
T |
C |
4: 133,389,960 (GRCm39) |
K74R |
probably benign |
Het |
Prmt8 |
T |
C |
6: 127,674,776 (GRCm39) |
K284R |
probably benign |
Het |
Rsl1d1 |
A |
T |
16: 11,017,553 (GRCm39) |
Y138N |
probably damaging |
Het |
Scara5 |
AC |
ACC |
14: 66,000,167 (GRCm39) |
|
probably benign |
Het |
Smc4 |
T |
A |
3: 68,913,548 (GRCm39) |
|
probably benign |
Het |
Spta1 |
G |
A |
1: 174,001,992 (GRCm39) |
V41I |
possibly damaging |
Het |
Tdrd7 |
C |
A |
4: 46,025,758 (GRCm39) |
N859K |
probably damaging |
Het |
Vps13d |
T |
G |
4: 144,883,121 (GRCm39) |
D824A |
probably damaging |
Het |
Wdfy2 |
A |
T |
14: 63,167,675 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Iqcf6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01598:Iqcf6
|
APN |
9 |
106,504,707 (GRCm39) |
missense |
probably benign |
|
IGL02006:Iqcf6
|
APN |
9 |
106,504,510 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02519:Iqcf6
|
APN |
9 |
106,504,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R1493:Iqcf6
|
UTSW |
9 |
106,504,641 (GRCm39) |
missense |
probably benign |
0.00 |
R4686:Iqcf6
|
UTSW |
9 |
106,504,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R6590:Iqcf6
|
UTSW |
9 |
106,504,501 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6690:Iqcf6
|
UTSW |
9 |
106,504,501 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7489:Iqcf6
|
UTSW |
9 |
106,504,656 (GRCm39) |
missense |
probably benign |
0.25 |
R8847:Iqcf6
|
UTSW |
9 |
106,504,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R8867:Iqcf6
|
UTSW |
9 |
106,504,698 (GRCm39) |
missense |
possibly damaging |
0.73 |
|