Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts20 |
T |
A |
15: 94,226,726 (GRCm39) |
D1109V |
possibly damaging |
Het |
Apc2 |
G |
C |
10: 80,150,922 (GRCm39) |
R1992P |
possibly damaging |
Het |
Atmin |
A |
G |
8: 117,683,036 (GRCm39) |
N232S |
probably benign |
Het |
Brat1 |
A |
C |
5: 140,703,751 (GRCm39) |
D668A |
possibly damaging |
Het |
Casp16 |
A |
T |
17: 23,771,922 (GRCm39) |
V101E |
probably damaging |
Het |
Cass4 |
C |
T |
2: 172,274,478 (GRCm39) |
P753L |
probably damaging |
Het |
Clec7a |
A |
G |
6: 129,445,877 (GRCm39) |
S98P |
possibly damaging |
Het |
Cpne5 |
G |
A |
17: 29,378,082 (GRCm39) |
R566C |
unknown |
Het |
Csrnp1 |
C |
T |
9: 119,801,707 (GRCm39) |
E451K |
probably damaging |
Het |
Dlst |
A |
G |
12: 85,179,465 (GRCm39) |
T435A |
possibly damaging |
Het |
Dock8 |
A |
G |
19: 25,078,269 (GRCm39) |
T525A |
possibly damaging |
Het |
Dync2li1 |
A |
G |
17: 84,939,070 (GRCm39) |
T45A |
probably damaging |
Het |
Efcab3 |
A |
G |
11: 104,974,713 (GRCm39) |
N5307S |
possibly damaging |
Het |
Epha4 |
A |
G |
1: 77,357,539 (GRCm39) |
Y820H |
probably damaging |
Het |
F5 |
A |
G |
1: 164,003,798 (GRCm39) |
T198A |
probably benign |
Het |
Fbn2 |
T |
A |
18: 58,199,083 (GRCm39) |
N1395I |
probably damaging |
Het |
Fcnb |
T |
A |
2: 27,969,208 (GRCm39) |
Y163F |
probably damaging |
Het |
Gm5444 |
T |
C |
13: 4,884,278 (GRCm39) |
|
noncoding transcript |
Het |
Jph3 |
G |
T |
8: 122,480,158 (GRCm39) |
D279Y |
possibly damaging |
Het |
Kcnj3 |
A |
G |
2: 55,327,360 (GRCm39) |
N50D |
possibly damaging |
Het |
Kcnma1 |
A |
G |
14: 23,555,323 (GRCm39) |
I416T |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Kmt2e |
A |
G |
5: 23,706,640 (GRCm39) |
N1401S |
probably benign |
Het |
Lama5 |
C |
T |
2: 179,824,144 (GRCm39) |
|
probably benign |
Het |
Lrp1b |
A |
G |
2: 40,712,707 (GRCm39) |
V3095A |
probably damaging |
Het |
Mmp1a |
A |
G |
9: 7,475,346 (GRCm39) |
*372W |
probably null |
Het |
Or7d11 |
C |
T |
9: 19,966,169 (GRCm39) |
V197I |
probably benign |
Het |
Pdgfra |
T |
A |
5: 75,353,169 (GRCm39) |
N986K |
probably benign |
Het |
Pgap1 |
C |
T |
1: 54,532,507 (GRCm39) |
V671I |
probably benign |
Het |
Pla2g4e |
T |
C |
2: 119,999,085 (GRCm39) |
S760G |
probably benign |
Het |
Plk3 |
T |
C |
4: 116,990,633 (GRCm39) |
I94V |
probably benign |
Het |
Pogk |
C |
T |
1: 166,231,193 (GRCm39) |
V45I |
probably damaging |
Het |
Pou2f1 |
G |
C |
1: 165,722,538 (GRCm39) |
P349R |
probably damaging |
Het |
Rims1 |
T |
A |
1: 22,572,578 (GRCm39) |
Q541L |
probably benign |
Het |
Rptn |
A |
G |
3: 93,305,664 (GRCm39) |
Q999R |
probably benign |
Het |
Stxbp5 |
A |
G |
10: 9,645,163 (GRCm39) |
L911P |
probably damaging |
Het |
Tgfbr3 |
A |
G |
5: 107,362,753 (GRCm39) |
|
probably benign |
Het |
Trim7 |
A |
T |
11: 48,728,435 (GRCm39) |
T28S |
probably damaging |
Het |
Zfp595 |
T |
C |
13: 67,465,379 (GRCm39) |
I295V |
probably benign |
Het |
|
Other mutations in Cimip3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0675:Cimip3
|
UTSW |
17 |
47,724,701 (GRCm39) |
missense |
probably benign |
0.25 |
R1529:Cimip3
|
UTSW |
17 |
47,724,815 (GRCm39) |
missense |
probably benign |
0.11 |
R2256:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R2257:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R2512:Cimip3
|
UTSW |
17 |
47,724,651 (GRCm39) |
missense |
probably benign |
|
R2883:Cimip3
|
UTSW |
17 |
47,747,650 (GRCm39) |
missense |
probably damaging |
0.99 |
R3498:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R3499:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R3834:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R3835:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R3910:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R3911:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R3913:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R4191:Cimip3
|
UTSW |
17 |
47,747,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R4280:Cimip3
|
UTSW |
17 |
47,724,780 (GRCm39) |
missense |
probably benign |
0.02 |
R7054:Cimip3
|
UTSW |
17 |
47,748,114 (GRCm39) |
critical splice donor site |
probably null |
|
R8008:Cimip3
|
UTSW |
17 |
47,747,661 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Cimip3
|
UTSW |
17 |
47,724,659 (GRCm39) |
missense |
probably benign |
0.44 |
|