Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts2 |
T |
C |
11: 50,687,295 (GRCm39) |
Y1041H |
probably damaging |
Het |
Adck5 |
A |
C |
15: 76,479,816 (GRCm39) |
*568C |
probably null |
Het |
AK157302 |
T |
A |
13: 21,679,471 (GRCm39) |
|
probably benign |
Het |
Bmpr2 |
G |
T |
1: 59,852,836 (GRCm39) |
G56W |
probably damaging |
Het |
Capn11 |
A |
C |
17: 45,964,126 (GRCm39) |
I146S |
probably damaging |
Het |
Ccdc162 |
A |
T |
10: 41,456,302 (GRCm39) |
D1613E |
possibly damaging |
Het |
Ccdc167 |
T |
C |
17: 29,924,286 (GRCm39) |
E50G |
probably damaging |
Het |
Col5a2 |
G |
T |
1: 45,431,048 (GRCm39) |
P864Q |
possibly damaging |
Het |
Col7a1 |
C |
T |
9: 108,806,187 (GRCm39) |
|
probably benign |
Het |
Crebbp |
T |
A |
16: 3,944,370 (GRCm39) |
H556L |
probably damaging |
Het |
Dcpp1 |
T |
A |
17: 24,101,710 (GRCm39) |
I153N |
possibly damaging |
Het |
Dgke |
C |
T |
11: 88,946,212 (GRCm39) |
R196H |
probably benign |
Het |
Efr3a |
T |
A |
15: 65,722,999 (GRCm39) |
I459K |
probably benign |
Het |
Espl1 |
T |
A |
15: 102,228,271 (GRCm39) |
C1682S |
probably benign |
Het |
Exosc3 |
C |
T |
4: 45,317,747 (GRCm39) |
R185H |
probably damaging |
Het |
Fgd6 |
T |
C |
10: 93,879,338 (GRCm39) |
V64A |
possibly damaging |
Het |
Fhip2b |
G |
A |
14: 70,822,813 (GRCm39) |
R688C |
probably damaging |
Het |
Gata3 |
A |
G |
2: 9,882,276 (GRCm39) |
L42P |
probably damaging |
Het |
Ggta1 |
C |
A |
2: 35,292,462 (GRCm39) |
E282* |
probably null |
Het |
Ghr |
T |
C |
15: 3,349,669 (GRCm39) |
D503G |
probably damaging |
Het |
Gls |
C |
T |
1: 52,207,558 (GRCm39) |
G602D |
probably damaging |
Het |
Gm2058 |
A |
G |
7: 39,238,658 (GRCm39) |
|
noncoding transcript |
Het |
Grb7 |
T |
C |
11: 98,343,100 (GRCm39) |
|
probably benign |
Het |
Ifngr1 |
A |
T |
10: 19,485,348 (GRCm39) |
H449L |
probably damaging |
Het |
Ighg2b |
T |
G |
12: 113,270,656 (GRCm39) |
D158A |
possibly damaging |
Het |
Nphs2 |
T |
C |
1: 156,138,605 (GRCm39) |
V83A |
probably benign |
Het |
Parp6 |
T |
A |
9: 59,543,996 (GRCm39) |
M390K |
possibly damaging |
Het |
Pask |
T |
C |
1: 93,238,574 (GRCm39) |
K1304E |
probably benign |
Het |
Scai |
A |
G |
2: 38,996,973 (GRCm39) |
S274P |
probably benign |
Het |
Sik2 |
A |
G |
9: 50,818,763 (GRCm39) |
S404P |
probably damaging |
Het |
Slc7a8 |
A |
T |
14: 55,018,645 (GRCm39) |
I47N |
probably damaging |
Het |
Tas2r113 |
A |
T |
6: 132,870,760 (GRCm39) |
I263F |
probably benign |
Het |
Tdrd1 |
T |
A |
19: 56,843,734 (GRCm39) |
D737E |
probably benign |
Het |
Trio |
T |
C |
15: 27,732,954 (GRCm39) |
T2976A |
possibly damaging |
Het |
Ttc28 |
T |
C |
5: 111,233,037 (GRCm39) |
|
probably null |
Het |
Vmn1r21 |
A |
G |
6: 57,820,799 (GRCm39) |
I215T |
probably benign |
Het |
|
Other mutations in 2310002L09Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00561:2310002L09Rik
|
APN |
4 |
73,860,956 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02596:2310002L09Rik
|
APN |
4 |
73,868,904 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0841:2310002L09Rik
|
UTSW |
4 |
73,860,986 (GRCm39) |
missense |
probably benign |
|
R2919:2310002L09Rik
|
UTSW |
4 |
73,868,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R6056:2310002L09Rik
|
UTSW |
4 |
73,861,115 (GRCm39) |
missense |
probably benign |
0.00 |
R6795:2310002L09Rik
|
UTSW |
4 |
73,869,065 (GRCm39) |
start gained |
probably benign |
|
R6889:2310002L09Rik
|
UTSW |
4 |
73,861,290 (GRCm39) |
missense |
probably benign |
0.19 |
R7709:2310002L09Rik
|
UTSW |
4 |
73,861,091 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7793:2310002L09Rik
|
UTSW |
4 |
73,861,172 (GRCm39) |
missense |
probably benign |
0.05 |
R8517:2310002L09Rik
|
UTSW |
4 |
73,861,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R8671:2310002L09Rik
|
UTSW |
4 |
73,861,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R8867:2310002L09Rik
|
UTSW |
4 |
73,861,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R8938:2310002L09Rik
|
UTSW |
4 |
73,861,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R9618:2310002L09Rik
|
UTSW |
4 |
73,868,934 (GRCm39) |
start codon destroyed |
probably null |
0.46 |
|