Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
A |
1: 71,325,648 (GRCm39) |
I1517L |
possibly damaging |
Het |
Akap12 |
A |
T |
10: 4,307,537 (GRCm39) |
D1449V |
probably benign |
Het |
Alg6 |
T |
A |
4: 99,630,643 (GRCm39) |
Y161N |
probably benign |
Het |
Arhgap45 |
A |
T |
10: 79,864,482 (GRCm39) |
|
probably benign |
Het |
Arhgap5 |
A |
T |
12: 52,565,023 (GRCm39) |
I665F |
probably damaging |
Het |
Bbs4 |
A |
G |
9: 59,247,131 (GRCm39) |
V123A |
possibly damaging |
Het |
Carm1 |
C |
T |
9: 21,498,598 (GRCm39) |
T480I |
probably benign |
Het |
Catsperb |
G |
A |
12: 101,591,513 (GRCm39) |
V1032M |
probably damaging |
Het |
Cdc42bpb |
A |
C |
12: 111,308,509 (GRCm39) |
I101S |
probably damaging |
Het |
Copa |
C |
A |
1: 171,915,155 (GRCm39) |
|
probably null |
Het |
Cramp1 |
T |
C |
17: 25,216,547 (GRCm39) |
I189V |
probably damaging |
Het |
Dhx33 |
G |
A |
11: 70,884,687 (GRCm39) |
Q40* |
probably null |
Het |
Egf |
A |
T |
3: 129,533,669 (GRCm39) |
F57Y |
probably damaging |
Het |
Flt4 |
T |
C |
11: 49,534,333 (GRCm39) |
I1168T |
probably benign |
Het |
Gm14178 |
A |
G |
11: 99,638,269 (GRCm39) |
S37P |
unknown |
Het |
Gpbp1 |
A |
T |
13: 111,563,075 (GRCm39) |
|
probably benign |
Het |
Herc1 |
T |
C |
9: 66,390,981 (GRCm39) |
S3980P |
probably benign |
Het |
Itga6 |
T |
C |
2: 71,617,670 (GRCm39) |
|
probably null |
Het |
Itgb4 |
T |
C |
11: 115,881,766 (GRCm39) |
S772P |
probably damaging |
Het |
Kcng4 |
C |
A |
8: 120,352,416 (GRCm39) |
G498V |
probably benign |
Het |
Lrp1 |
T |
G |
10: 127,381,689 (GRCm39) |
D3795A |
possibly damaging |
Het |
Lrrk2 |
T |
A |
15: 91,584,772 (GRCm39) |
|
probably null |
Het |
Mettl25 |
A |
T |
10: 105,659,058 (GRCm39) |
H408Q |
probably damaging |
Het |
Mki67 |
T |
C |
7: 135,307,505 (GRCm39) |
E457G |
probably damaging |
Het |
Mpl |
G |
A |
4: 118,312,858 (GRCm39) |
T158I |
possibly damaging |
Het |
Mtg2 |
C |
T |
2: 179,725,870 (GRCm39) |
T160I |
probably damaging |
Het |
Mtif2 |
A |
G |
11: 29,480,110 (GRCm39) |
I59V |
probably benign |
Het |
Ncapg |
C |
A |
5: 45,831,727 (GRCm39) |
S191* |
probably null |
Het |
Nup214 |
T |
C |
2: 31,928,190 (GRCm39) |
|
probably benign |
Het |
Or9m1 |
T |
C |
2: 87,733,871 (GRCm39) |
T50A |
probably benign |
Het |
Phf3 |
T |
A |
1: 30,847,809 (GRCm39) |
T1245S |
probably damaging |
Het |
Piezo2 |
T |
C |
18: 63,250,770 (GRCm39) |
D443G |
probably damaging |
Het |
Ptchd4 |
C |
A |
17: 42,627,936 (GRCm39) |
H132Q |
probably benign |
Het |
Pum1 |
T |
C |
4: 130,455,481 (GRCm39) |
|
probably benign |
Het |
Slc30a7 |
A |
T |
3: 115,783,765 (GRCm39) |
V136E |
probably damaging |
Het |
Slc5a10 |
A |
G |
11: 61,605,962 (GRCm39) |
V116A |
probably damaging |
Het |
Sos2 |
A |
T |
12: 69,637,574 (GRCm39) |
S1046T |
probably benign |
Het |
Svep1 |
A |
G |
4: 58,116,554 (GRCm39) |
S899P |
possibly damaging |
Het |
Tfr2 |
G |
A |
5: 137,569,953 (GRCm39) |
V120I |
probably benign |
Het |
Tnfrsf18 |
A |
T |
4: 156,112,493 (GRCm39) |
R117* |
probably null |
Het |
Trmt9b |
A |
G |
8: 36,979,713 (GRCm39) |
I439V |
probably benign |
Het |
Vmn1r77 |
T |
G |
7: 11,775,315 (GRCm39) |
F30L |
probably benign |
Het |
Vmn2r112 |
T |
C |
17: 22,837,603 (GRCm39) |
M688T |
probably benign |
Het |
Vmn2r93 |
T |
A |
17: 18,525,510 (GRCm39) |
D389E |
possibly damaging |
Het |
Zpld1 |
T |
G |
16: 55,046,748 (GRCm39) |
N407T |
probably benign |
Het |
Zranb3 |
C |
T |
1: 127,887,622 (GRCm39) |
W935* |
probably null |
Het |
Zyx |
G |
A |
6: 42,327,378 (GRCm39) |
R59Q |
probably damaging |
Het |
|
Other mutations in Pramel19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00484:Pramel19
|
APN |
4 |
101,798,898 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01837:Pramel19
|
APN |
4 |
101,798,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01870:Pramel19
|
APN |
4 |
101,797,887 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02040:Pramel19
|
APN |
4 |
101,798,331 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03264:Pramel19
|
APN |
4 |
101,798,329 (GRCm39) |
missense |
probably damaging |
0.99 |
R0033:Pramel19
|
UTSW |
4 |
101,798,881 (GRCm39) |
missense |
probably benign |
|
R0334:Pramel19
|
UTSW |
4 |
101,798,781 (GRCm39) |
missense |
probably benign |
0.01 |
R0846:Pramel19
|
UTSW |
4 |
101,798,447 (GRCm39) |
missense |
probably benign |
0.00 |
R1464:Pramel19
|
UTSW |
4 |
101,798,503 (GRCm39) |
missense |
probably damaging |
0.97 |
R1464:Pramel19
|
UTSW |
4 |
101,798,503 (GRCm39) |
missense |
probably damaging |
0.97 |
R1774:Pramel19
|
UTSW |
4 |
101,797,655 (GRCm39) |
missense |
probably benign |
0.27 |
R1888:Pramel19
|
UTSW |
4 |
101,798,335 (GRCm39) |
missense |
probably damaging |
0.99 |
R1888:Pramel19
|
UTSW |
4 |
101,798,335 (GRCm39) |
missense |
probably damaging |
0.99 |
R4510:Pramel19
|
UTSW |
4 |
101,798,757 (GRCm39) |
missense |
probably benign |
0.00 |
R4511:Pramel19
|
UTSW |
4 |
101,798,757 (GRCm39) |
missense |
probably benign |
0.00 |
R4890:Pramel19
|
UTSW |
4 |
101,798,788 (GRCm39) |
missense |
probably damaging |
0.99 |
R4960:Pramel19
|
UTSW |
4 |
101,798,661 (GRCm39) |
missense |
probably benign |
|
R5043:Pramel19
|
UTSW |
4 |
101,797,721 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5297:Pramel19
|
UTSW |
4 |
101,798,348 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5780:Pramel19
|
UTSW |
4 |
101,798,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R5957:Pramel19
|
UTSW |
4 |
101,798,898 (GRCm39) |
missense |
probably benign |
0.02 |
R6409:Pramel19
|
UTSW |
4 |
101,797,874 (GRCm39) |
nonsense |
probably null |
|
R6452:Pramel19
|
UTSW |
4 |
101,798,640 (GRCm39) |
missense |
probably benign |
0.02 |
R7619:Pramel19
|
UTSW |
4 |
101,798,497 (GRCm39) |
missense |
probably benign |
0.01 |
R8460:Pramel19
|
UTSW |
4 |
101,798,424 (GRCm39) |
missense |
probably benign |
0.00 |
R9202:Pramel19
|
UTSW |
4 |
101,797,860 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Pramel19
|
UTSW |
4 |
101,798,322 (GRCm39) |
nonsense |
probably null |
|
|