Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam22 |
T |
C |
5: 8,195,626 (GRCm39) |
I305V |
probably benign |
Het |
Aga |
T |
A |
8: 53,964,865 (GRCm39) |
L9Q |
possibly damaging |
Het |
Akna |
C |
T |
4: 63,313,409 (GRCm39) |
G238D |
probably benign |
Het |
Arhgap23 |
G |
A |
11: 97,354,525 (GRCm39) |
E813K |
probably damaging |
Het |
Atp13a2 |
T |
C |
4: 140,719,539 (GRCm39) |
|
probably null |
Het |
Atp8a1 |
C |
T |
5: 67,824,917 (GRCm39) |
G820S |
probably damaging |
Het |
Ccdc97 |
T |
G |
7: 25,415,459 (GRCm39) |
H68P |
possibly damaging |
Het |
Dclre1b |
A |
C |
3: 103,711,400 (GRCm39) |
|
probably null |
Het |
Erap1 |
T |
C |
13: 74,823,414 (GRCm39) |
I816T |
probably damaging |
Het |
Fubp1 |
G |
A |
3: 151,937,573 (GRCm39) |
A103T |
possibly damaging |
Het |
Gnal |
C |
G |
18: 67,221,654 (GRCm39) |
P19R |
unknown |
Het |
Gtf3c5 |
T |
C |
2: 28,461,196 (GRCm39) |
D306G |
probably damaging |
Het |
Hecw2 |
C |
T |
1: 53,871,804 (GRCm39) |
V1381M |
probably damaging |
Het |
Hsdl2 |
A |
T |
4: 59,594,417 (GRCm39) |
N16I |
probably damaging |
Het |
Kif14 |
G |
T |
1: 136,401,126 (GRCm39) |
M492I |
possibly damaging |
Het |
Kif27 |
A |
G |
13: 58,435,731 (GRCm39) |
V1354A |
probably damaging |
Het |
Kif9 |
G |
T |
9: 110,325,027 (GRCm39) |
|
probably null |
Het |
Lmtk3 |
G |
A |
7: 45,443,486 (GRCm39) |
C723Y |
possibly damaging |
Het |
Lrrc24 |
A |
G |
15: 76,602,176 (GRCm39) |
I193T |
possibly damaging |
Het |
Or2bd2 |
A |
G |
7: 6,441,901 (GRCm39) |
|
probably benign |
Het |
Or52b1 |
T |
C |
7: 104,979,355 (GRCm39) |
I15V |
probably benign |
Het |
Pkd1l1 |
C |
T |
11: 8,815,543 (GRCm39) |
R1456K |
possibly damaging |
Het |
Ranbp2 |
A |
G |
10: 58,314,686 (GRCm39) |
D1802G |
possibly damaging |
Het |
Resf1 |
T |
A |
6: 149,227,041 (GRCm39) |
M29K |
possibly damaging |
Het |
Satl1 |
A |
G |
X: 111,316,033 (GRCm39) |
S141P |
probably benign |
Het |
Scn11a |
C |
T |
9: 119,636,952 (GRCm39) |
V250M |
probably damaging |
Het |
Slitrk1 |
A |
G |
14: 109,149,994 (GRCm39) |
V239A |
possibly damaging |
Het |
Slitrk6 |
T |
A |
14: 110,988,171 (GRCm39) |
D512V |
probably damaging |
Het |
Snx8 |
A |
G |
5: 140,341,800 (GRCm39) |
L121P |
probably damaging |
Het |
Sumf1 |
A |
C |
6: 108,131,974 (GRCm39) |
V156G |
probably damaging |
Het |
Tamalin |
G |
T |
15: 101,122,418 (GRCm39) |
R79L |
possibly damaging |
Het |
Trp73 |
A |
G |
4: 154,149,089 (GRCm39) |
|
probably null |
Het |
Tsen2 |
A |
G |
6: 115,524,785 (GRCm39) |
|
probably benign |
Het |
Upp1 |
T |
C |
11: 9,084,815 (GRCm39) |
I178T |
probably benign |
Het |
Vmn2r73 |
A |
T |
7: 85,521,883 (GRCm39) |
L152Q |
probably damaging |
Het |
Vmn2r97 |
T |
C |
17: 19,167,542 (GRCm39) |
S599P |
possibly damaging |
Het |
Wrnip1 |
T |
C |
13: 32,990,866 (GRCm39) |
L375P |
probably damaging |
Het |
Zfp945 |
C |
T |
17: 23,069,583 (GRCm39) |
G793D |
probably damaging |
Het |
Zfyve9 |
C |
A |
4: 108,576,389 (GRCm39) |
A231S |
probably benign |
Het |
|
Other mutations in Pramel52-ps |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1985:Pramel52-ps
|
UTSW |
5 |
94,531,931 (GRCm39) |
missense |
probably benign |
0.13 |
R4607:Pramel52-ps
|
UTSW |
5 |
94,531,387 (GRCm39) |
missense |
probably benign |
0.35 |
R6186:Pramel52-ps
|
UTSW |
5 |
94,531,835 (GRCm39) |
missense |
probably benign |
0.28 |
R6585:Pramel52-ps
|
UTSW |
5 |
94,529,415 (GRCm39) |
missense |
probably benign |
|
R6755:Pramel52-ps
|
UTSW |
5 |
94,529,268 (GRCm39) |
missense |
probably benign |
0.03 |
R6945:Pramel52-ps
|
UTSW |
5 |
94,531,490 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7352:Pramel52-ps
|
UTSW |
5 |
94,531,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R7960:Pramel52-ps
|
UTSW |
5 |
94,531,739 (GRCm39) |
missense |
probably benign |
0.01 |
R8355:Pramel52-ps
|
UTSW |
5 |
94,531,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R8356:Pramel52-ps
|
UTSW |
5 |
94,531,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R8381:Pramel52-ps
|
UTSW |
5 |
94,531,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R8489:Pramel52-ps
|
UTSW |
5 |
94,531,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R8752:Pramel52-ps
|
UTSW |
5 |
94,529,354 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9101:Pramel52-ps
|
UTSW |
5 |
94,531,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R9577:Pramel52-ps
|
UTSW |
5 |
94,531,805 (GRCm39) |
nonsense |
probably null |
|
|