Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts16 |
G |
A |
13: 70,927,637 (GRCm39) |
|
probably benign |
Het |
Atad2b |
A |
C |
12: 5,068,053 (GRCm39) |
H1017P |
probably damaging |
Het |
Atp8a1 |
A |
T |
5: 67,813,317 (GRCm39) |
V943D |
probably benign |
Het |
Babam1 |
C |
T |
8: 71,856,951 (GRCm39) |
A304V |
probably damaging |
Het |
Cdk5rap2 |
G |
T |
4: 70,220,413 (GRCm39) |
A584D |
probably damaging |
Het |
Ddx21 |
A |
T |
10: 62,427,616 (GRCm39) |
L429* |
probably null |
Het |
Dsp |
T |
C |
13: 38,380,760 (GRCm39) |
Y2502H |
probably damaging |
Het |
Eaf1 |
G |
A |
14: 31,226,333 (GRCm39) |
D206N |
probably benign |
Het |
Fam43b |
T |
A |
4: 138,123,278 (GRCm39) |
D14V |
possibly damaging |
Het |
Fanca |
T |
A |
8: 124,044,889 (GRCm39) |
K34I |
probably damaging |
Het |
Fzd4 |
T |
C |
7: 89,056,525 (GRCm39) |
Y191H |
probably benign |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gm10479 |
A |
G |
12: 20,483,343 (GRCm39) |
T55A |
probably damaging |
Het |
Gsr |
T |
G |
8: 34,187,284 (GRCm39) |
I488M |
probably damaging |
Het |
Myh13 |
T |
C |
11: 67,232,377 (GRCm39) |
M517T |
possibly damaging |
Het |
Naip1 |
C |
G |
13: 100,580,791 (GRCm39) |
G152A |
probably benign |
Het |
Naip5 |
T |
A |
13: 100,356,338 (GRCm39) |
E1092D |
probably benign |
Het |
Nat10 |
G |
A |
2: 103,565,234 (GRCm39) |
T449I |
probably benign |
Het |
Nin |
A |
G |
12: 70,085,375 (GRCm39) |
S1619P |
probably damaging |
Het |
Or14c45 |
G |
A |
7: 86,175,969 (GRCm39) |
M1I |
probably null |
Het |
Or5m9b |
A |
G |
2: 85,905,923 (GRCm39) |
I280V |
probably benign |
Het |
Pcdh15 |
A |
G |
10: 74,479,439 (GRCm39) |
T448A |
probably benign |
Het |
Pcolce2 |
A |
G |
9: 95,519,930 (GRCm39) |
|
probably null |
Het |
Pnp |
C |
T |
14: 51,188,380 (GRCm39) |
R207* |
probably null |
Het |
Ppl |
A |
G |
16: 4,907,310 (GRCm39) |
V995A |
probably damaging |
Het |
Ppp2r2a |
G |
A |
14: 67,276,406 (GRCm39) |
T33I |
probably damaging |
Het |
Pramel20 |
C |
T |
4: 143,298,467 (GRCm39) |
R137C |
probably benign |
Het |
Pyroxd1 |
C |
G |
6: 142,300,467 (GRCm39) |
S199* |
probably null |
Het |
Rgs16 |
G |
T |
1: 153,617,781 (GRCm39) |
C97F |
probably damaging |
Het |
Sacs |
T |
A |
14: 61,444,717 (GRCm39) |
D2254E |
probably benign |
Het |
Slc6a17 |
T |
C |
3: 107,381,597 (GRCm39) |
M495V |
probably benign |
Het |
Svep1 |
T |
C |
4: 58,082,724 (GRCm39) |
I1967V |
probably benign |
Het |
Sympk |
G |
T |
7: 18,777,385 (GRCm39) |
R545L |
possibly damaging |
Het |
Tcp11l2 |
A |
G |
10: 84,420,800 (GRCm39) |
D13G |
probably damaging |
Het |
Vmn1r167 |
T |
C |
7: 23,205,011 (GRCm39) |
I2V |
probably benign |
Het |
Vwa5a |
T |
C |
9: 38,638,410 (GRCm39) |
|
probably null |
Het |
Wdr95 |
T |
C |
5: 149,505,279 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Mrs2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02323:Mrs2
|
APN |
13 |
25,188,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R0201:Mrs2
|
UTSW |
13 |
25,202,517 (GRCm39) |
missense |
probably benign |
0.02 |
R0371:Mrs2
|
UTSW |
13 |
25,177,078 (GRCm39) |
missense |
probably benign |
|
R0669:Mrs2
|
UTSW |
13 |
25,177,742 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1496:Mrs2
|
UTSW |
13 |
25,189,017 (GRCm39) |
missense |
probably benign |
0.01 |
R1600:Mrs2
|
UTSW |
13 |
25,179,393 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1796:Mrs2
|
UTSW |
13 |
25,181,111 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3964:Mrs2
|
UTSW |
13 |
25,185,746 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4837:Mrs2
|
UTSW |
13 |
25,183,040 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6953:Mrs2
|
UTSW |
13 |
25,185,771 (GRCm39) |
missense |
probably benign |
0.02 |
R7055:Mrs2
|
UTSW |
13 |
25,188,937 (GRCm39) |
missense |
probably benign |
|
R7752:Mrs2
|
UTSW |
13 |
25,202,549 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7877:Mrs2
|
UTSW |
13 |
25,181,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R7901:Mrs2
|
UTSW |
13 |
25,202,549 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7980:Mrs2
|
UTSW |
13 |
25,204,221 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8177:Mrs2
|
UTSW |
13 |
25,188,961 (GRCm39) |
missense |
probably benign |
0.00 |
R8879:Mrs2
|
UTSW |
13 |
25,185,767 (GRCm39) |
missense |
probably damaging |
0.96 |
|