Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
T |
7: 119,917,985 (GRCm39) |
K1496* |
probably null |
Het |
Anapc1 |
C |
A |
2: 128,476,613 (GRCm39) |
R1335L |
probably damaging |
Het |
Arhgef10l |
A |
T |
4: 140,305,605 (GRCm39) |
S203T |
probably benign |
Het |
Astn1 |
C |
T |
1: 158,491,674 (GRCm39) |
T41I |
possibly damaging |
Het |
Avil |
A |
G |
10: 126,849,513 (GRCm39) |
N603S |
probably benign |
Het |
Brca1 |
T |
C |
11: 101,421,916 (GRCm39) |
D149G |
possibly damaging |
Het |
Col19a1 |
A |
C |
1: 24,598,849 (GRCm39) |
|
probably null |
Het |
Cps1 |
T |
C |
1: 67,268,577 (GRCm39) |
V1435A |
possibly damaging |
Het |
Cyp2j6 |
A |
T |
4: 96,406,394 (GRCm39) |
I459N |
probably damaging |
Het |
Cyth1 |
T |
C |
11: 118,073,132 (GRCm39) |
E242G |
probably damaging |
Het |
Dclk3 |
T |
G |
9: 111,296,738 (GRCm39) |
L94R |
possibly damaging |
Het |
Dsg3 |
T |
C |
18: 20,673,191 (GRCm39) |
V954A |
probably damaging |
Het |
Dync2h1 |
T |
A |
9: 7,111,487 (GRCm39) |
D309V |
probably damaging |
Het |
Efhd2 |
A |
G |
4: 141,601,878 (GRCm39) |
F101L |
probably benign |
Het |
Fgd5 |
T |
A |
6: 91,965,216 (GRCm39) |
M325K |
possibly damaging |
Het |
Fras1 |
T |
C |
5: 96,857,936 (GRCm39) |
S2077P |
probably benign |
Het |
Frmpd1 |
A |
T |
4: 45,279,340 (GRCm39) |
E688D |
probably benign |
Het |
Hspg2 |
T |
C |
4: 137,289,512 (GRCm39) |
V3824A |
probably benign |
Het |
Kctd16 |
A |
G |
18: 40,392,204 (GRCm39) |
E264G |
probably benign |
Het |
Miox |
G |
A |
15: 89,219,784 (GRCm39) |
V91I |
probably benign |
Het |
Nfyb |
G |
A |
10: 82,590,836 (GRCm39) |
A65V |
possibly damaging |
Het |
Or4a69 |
A |
G |
2: 89,313,147 (GRCm39) |
F111L |
probably benign |
Het |
Or52d1 |
T |
C |
7: 103,755,812 (GRCm39) |
S109P |
probably damaging |
Het |
Or5b94 |
C |
A |
19: 12,652,224 (GRCm39) |
F218L |
probably benign |
Het |
Parp9 |
T |
C |
16: 35,768,711 (GRCm39) |
I64T |
probably damaging |
Het |
Pfkfb4 |
T |
C |
9: 108,827,957 (GRCm39) |
V43A |
probably benign |
Het |
Pgap1 |
A |
T |
1: 54,533,984 (GRCm39) |
V643E |
probably damaging |
Het |
Pip5k1b |
T |
A |
19: 24,356,411 (GRCm39) |
M176L |
probably benign |
Het |
Ppfia4 |
A |
T |
1: 134,251,955 (GRCm39) |
|
probably null |
Het |
Prdx2 |
G |
A |
8: 85,696,880 (GRCm39) |
G4S |
probably benign |
Het |
Rin3 |
A |
G |
12: 102,279,340 (GRCm39) |
I50V |
possibly damaging |
Het |
Rtl1 |
G |
A |
12: 109,561,841 (GRCm39) |
|
probably benign |
Het |
Sgsm3 |
G |
C |
15: 80,893,667 (GRCm39) |
D434H |
probably damaging |
Het |
Shank2 |
T |
C |
7: 143,964,314 (GRCm39) |
S634P |
possibly damaging |
Het |
Sik2 |
A |
G |
9: 50,810,775 (GRCm39) |
M447T |
possibly damaging |
Het |
Sla2 |
A |
G |
2: 156,725,507 (GRCm39) |
|
probably null |
Het |
Spata16 |
T |
A |
3: 26,967,416 (GRCm39) |
F389I |
probably damaging |
Het |
Srebf1 |
G |
A |
11: 60,092,630 (GRCm39) |
A793V |
probably benign |
Het |
Tmed11 |
T |
A |
5: 108,925,278 (GRCm39) |
D178V |
probably damaging |
Het |
Traf7 |
A |
G |
17: 24,732,900 (GRCm39) |
F110L |
probably benign |
Het |
Ttn |
T |
A |
2: 76,555,908 (GRCm39) |
I30366F |
probably damaging |
Het |
Ubqlnl |
C |
T |
7: 103,799,399 (GRCm39) |
V33M |
probably damaging |
Het |
Vmn1r194 |
A |
G |
13: 22,429,217 (GRCm39) |
Y278C |
probably damaging |
Het |
Vmn2r100 |
C |
A |
17: 19,742,382 (GRCm39) |
P252Q |
possibly damaging |
Het |
Vmn2r114 |
A |
T |
17: 23,529,549 (GRCm39) |
Y184* |
probably null |
Het |
Vmn2r53 |
C |
T |
7: 12,315,993 (GRCm39) |
A609T |
probably damaging |
Het |
Vps13b |
A |
G |
15: 35,572,265 (GRCm39) |
T961A |
probably benign |
Het |
Xirp2 |
T |
A |
2: 67,349,622 (GRCm39) |
N3272K |
probably damaging |
Het |
Zfp217 |
C |
T |
2: 169,957,382 (GRCm39) |
A539T |
probably benign |
Het |
Zfp454 |
T |
A |
11: 50,774,602 (GRCm39) |
T24S |
possibly damaging |
Het |
|
Other mutations in Mapk15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01595:Mapk15
|
APN |
15 |
75,867,129 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02075:Mapk15
|
APN |
15 |
75,866,737 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02395:Mapk15
|
APN |
15 |
75,870,019 (GRCm39) |
missense |
probably benign |
|
IGL03052:Mapk15
|
UTSW |
15 |
75,865,731 (GRCm39) |
missense |
probably benign |
0.01 |
R0008:Mapk15
|
UTSW |
15 |
75,870,103 (GRCm39) |
missense |
probably benign |
0.08 |
R0109:Mapk15
|
UTSW |
15 |
75,867,926 (GRCm39) |
nonsense |
probably null |
|
R1148:Mapk15
|
UTSW |
15 |
75,870,004 (GRCm39) |
missense |
probably benign |
|
R1148:Mapk15
|
UTSW |
15 |
75,870,004 (GRCm39) |
missense |
probably benign |
|
R2406:Mapk15
|
UTSW |
15 |
75,870,697 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4526:Mapk15
|
UTSW |
15 |
75,867,104 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4572:Mapk15
|
UTSW |
15 |
75,870,599 (GRCm39) |
splice site |
probably benign |
|
R4613:Mapk15
|
UTSW |
15 |
75,867,759 (GRCm39) |
missense |
probably damaging |
0.98 |
R5861:Mapk15
|
UTSW |
15 |
75,868,208 (GRCm39) |
unclassified |
probably benign |
|
R6912:Mapk15
|
UTSW |
15 |
75,865,747 (GRCm39) |
missense |
probably damaging |
0.99 |
R7554:Mapk15
|
UTSW |
15 |
75,867,745 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7620:Mapk15
|
UTSW |
15 |
75,870,697 (GRCm39) |
missense |
probably benign |
0.00 |
R7923:Mapk15
|
UTSW |
15 |
75,868,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R9308:Mapk15
|
UTSW |
15 |
75,865,714 (GRCm39) |
nonsense |
probably null |
|
R9744:Mapk15
|
UTSW |
15 |
75,869,912 (GRCm39) |
missense |
possibly damaging |
0.78 |
Z1177:Mapk15
|
UTSW |
15 |
75,870,310 (GRCm39) |
nonsense |
probably null |
|
|