Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb3 |
A |
G |
10: 85,476,460 (GRCm39) |
T914A |
possibly damaging |
Het |
Acsl3 |
A |
C |
1: 78,665,999 (GRCm39) |
I142L |
probably benign |
Het |
Adgra2 |
C |
T |
8: 27,601,116 (GRCm39) |
P252L |
probably damaging |
Het |
Akap6 |
A |
G |
12: 53,186,303 (GRCm39) |
E1239G |
probably benign |
Het |
Arhgef17 |
TGGAGGAGGAGGAGGAGG |
TGGAGGAGGAGGAGG |
7: 100,580,244 (GRCm39) |
|
probably benign |
Het |
Calml4 |
A |
T |
9: 62,778,548 (GRCm39) |
D12V |
probably damaging |
Het |
Car9 |
G |
T |
4: 43,512,439 (GRCm39) |
|
probably null |
Het |
Ccar2 |
C |
A |
14: 70,377,558 (GRCm39) |
V699L |
possibly damaging |
Het |
Ccdc27 |
T |
C |
4: 154,126,226 (GRCm39) |
M88V |
unknown |
Het |
Ceacam15 |
T |
C |
7: 16,405,988 (GRCm39) |
R188G |
probably damaging |
Het |
Dcaf8 |
G |
A |
1: 172,001,619 (GRCm39) |
R272H |
probably benign |
Het |
Dchs1 |
A |
G |
7: 105,404,778 (GRCm39) |
V2588A |
probably benign |
Het |
Dst |
G |
A |
1: 34,250,313 (GRCm39) |
R1749H |
probably damaging |
Het |
Exog |
A |
G |
9: 119,291,572 (GRCm39) |
Q283R |
probably benign |
Het |
Fmnl1 |
A |
T |
11: 103,077,535 (GRCm39) |
|
probably null |
Het |
Gramd1c |
T |
C |
16: 43,811,085 (GRCm39) |
D213G |
probably damaging |
Het |
Iqgap1 |
A |
G |
7: 80,409,504 (GRCm39) |
|
probably null |
Het |
Itgae |
A |
G |
11: 73,016,188 (GRCm39) |
Y799C |
probably damaging |
Het |
Kalrn |
T |
C |
16: 33,809,173 (GRCm39) |
I903V |
probably benign |
Het |
Kcnh1 |
A |
G |
1: 192,188,071 (GRCm39) |
E844G |
probably benign |
Het |
Ly6g |
T |
C |
15: 75,028,615 (GRCm39) |
F25S |
probably benign |
Het |
Mapk1ip1 |
G |
A |
7: 138,438,456 (GRCm39) |
|
probably benign |
Het |
Mfsd3 |
A |
G |
15: 76,586,889 (GRCm39) |
H243R |
probably benign |
Het |
Mms22l |
T |
A |
4: 24,591,076 (GRCm39) |
Y1016N |
probably damaging |
Het |
Mrgprb5 |
A |
T |
7: 47,818,078 (GRCm39) |
V219E |
probably damaging |
Het |
Nars2 |
G |
A |
7: 96,652,036 (GRCm39) |
S209N |
probably benign |
Het |
Nckap5 |
T |
C |
1: 125,954,447 (GRCm39) |
T702A |
probably damaging |
Het |
Or1e26 |
T |
C |
11: 73,480,369 (GRCm39) |
N65S |
possibly damaging |
Het |
Paf1 |
A |
G |
7: 28,098,257 (GRCm39) |
|
probably benign |
Het |
Prl3d1 |
A |
T |
13: 27,282,693 (GRCm39) |
R145* |
probably null |
Het |
Rasl10b |
G |
A |
11: 83,308,665 (GRCm39) |
|
probably null |
Het |
Rnf13 |
T |
A |
3: 57,686,917 (GRCm39) |
N103K |
probably damaging |
Het |
Senp1 |
T |
C |
15: 97,973,734 (GRCm39) |
S170G |
probably benign |
Het |
Slc46a2 |
A |
G |
4: 59,914,620 (GRCm39) |
L101P |
probably damaging |
Het |
Tmem123 |
C |
T |
9: 7,791,107 (GRCm39) |
T136M |
probably damaging |
Het |
Tpo |
T |
A |
12: 30,153,109 (GRCm39) |
H415L |
probably damaging |
Het |
Vipr2 |
A |
G |
12: 116,100,950 (GRCm39) |
I255V |
probably benign |
Het |
Zc3h11a |
A |
T |
1: 133,561,541 (GRCm39) |
V310E |
probably damaging |
Het |
Zfp3 |
T |
A |
11: 70,663,462 (GRCm39) |
C474S |
probably damaging |
Het |
Zfp707 |
T |
A |
15: 75,846,465 (GRCm39) |
C99S |
probably damaging |
Het |
Zranb1 |
C |
T |
7: 132,573,062 (GRCm39) |
P410S |
probably damaging |
Het |
Zswim8 |
G |
T |
14: 20,760,816 (GRCm39) |
R30L |
probably damaging |
Het |
|
Other mutations in Khdc1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02090:Khdc1a
|
APN |
1 |
21,421,212 (GRCm39) |
missense |
probably benign |
0.00 |
R1169:Khdc1a
|
UTSW |
1 |
21,420,495 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1432:Khdc1a
|
UTSW |
1 |
21,420,542 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1629:Khdc1a
|
UTSW |
1 |
21,421,121 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1735:Khdc1a
|
UTSW |
1 |
21,421,189 (GRCm39) |
missense |
probably benign |
0.00 |
R2064:Khdc1a
|
UTSW |
1 |
21,421,196 (GRCm39) |
missense |
probably benign |
0.00 |
R2065:Khdc1a
|
UTSW |
1 |
21,421,196 (GRCm39) |
missense |
probably benign |
0.00 |
R4398:Khdc1a
|
UTSW |
1 |
21,420,617 (GRCm39) |
missense |
possibly damaging |
0.45 |
R4575:Khdc1a
|
UTSW |
1 |
21,420,653 (GRCm39) |
missense |
probably damaging |
0.97 |
R6030:Khdc1a
|
UTSW |
1 |
21,421,108 (GRCm39) |
missense |
probably benign |
0.01 |
R6030:Khdc1a
|
UTSW |
1 |
21,421,108 (GRCm39) |
missense |
probably benign |
0.01 |
R6183:Khdc1a
|
UTSW |
1 |
21,420,332 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7492:Khdc1a
|
UTSW |
1 |
21,420,542 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7861:Khdc1a
|
UTSW |
1 |
21,420,623 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7982:Khdc1a
|
UTSW |
1 |
21,421,130 (GRCm39) |
missense |
probably benign |
0.15 |
R9600:Khdc1a
|
UTSW |
1 |
21,421,204 (GRCm39) |
missense |
probably benign |
0.00 |
|