Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Amy2a1 |
T |
C |
3: 113,325,363 (GRCm39) |
Y77C |
probably damaging |
Het |
Ankrd9 |
C |
A |
12: 110,944,202 (GRCm39) |
|
probably benign |
Het |
Arhgap28 |
C |
A |
17: 68,152,746 (GRCm39) |
W675L |
probably damaging |
Het |
Arhgap44 |
A |
G |
11: 64,900,834 (GRCm39) |
S595P |
probably damaging |
Het |
Brd10 |
A |
T |
19: 29,700,864 (GRCm39) |
H741Q |
possibly damaging |
Het |
Cacna1d |
C |
A |
14: 29,811,832 (GRCm39) |
D1273Y |
probably damaging |
Het |
Ccr4 |
T |
C |
9: 114,325,031 (GRCm39) |
|
probably benign |
Het |
Celsr1 |
A |
G |
15: 85,803,135 (GRCm39) |
V2468A |
probably damaging |
Het |
Chd2 |
T |
C |
7: 73,140,230 (GRCm39) |
E666G |
possibly damaging |
Het |
Ctnnd1 |
C |
A |
2: 84,439,986 (GRCm39) |
V775L |
probably damaging |
Het |
Cux2 |
C |
A |
5: 122,007,360 (GRCm39) |
R767L |
probably benign |
Het |
Dennd4c |
T |
A |
4: 86,717,626 (GRCm39) |
M541K |
possibly damaging |
Het |
Dnah7a |
T |
C |
1: 53,662,609 (GRCm39) |
R651G |
probably benign |
Het |
Fbrsl1 |
A |
T |
5: 110,525,963 (GRCm39) |
F80I |
probably damaging |
Het |
Fmnl2 |
C |
A |
2: 52,998,297 (GRCm39) |
P554Q |
probably damaging |
Het |
Gapvd1 |
C |
T |
2: 34,618,450 (GRCm39) |
D308N |
probably damaging |
Het |
Gatb |
A |
G |
3: 85,559,726 (GRCm39) |
|
probably null |
Het |
Jcad |
G |
A |
18: 4,675,256 (GRCm39) |
G1006D |
probably damaging |
Het |
Krt1c |
A |
G |
15: 101,724,398 (GRCm39) |
Y289H |
probably damaging |
Het |
Lrrc52 |
A |
G |
1: 167,293,922 (GRCm39) |
F121S |
probably damaging |
Het |
Lrrc63 |
G |
A |
14: 75,362,633 (GRCm39) |
T299I |
unknown |
Het |
Magi1 |
T |
C |
6: 93,920,289 (GRCm39) |
N109S |
probably benign |
Het |
Mbd4 |
C |
A |
6: 115,826,116 (GRCm39) |
E271* |
probably null |
Het |
Meis2 |
T |
A |
2: 115,694,751 (GRCm39) |
D457V |
probably damaging |
Het |
Mroh8 |
A |
G |
2: 157,067,547 (GRCm39) |
V604A |
probably benign |
Het |
Nedd4 |
T |
A |
9: 72,593,377 (GRCm39) |
V150E |
probably damaging |
Het |
Nes |
A |
G |
3: 87,884,243 (GRCm39) |
E790G |
probably damaging |
Het |
Or8h8 |
T |
C |
2: 86,753,492 (GRCm39) |
N128S |
probably benign |
Het |
Pik3c2a |
T |
C |
7: 115,967,993 (GRCm39) |
I834V |
possibly damaging |
Het |
Plxnb1 |
T |
C |
9: 108,933,367 (GRCm39) |
C666R |
possibly damaging |
Het |
Prg2 |
T |
C |
2: 84,813,620 (GRCm39) |
|
probably null |
Het |
Selenbp2 |
A |
G |
3: 94,609,821 (GRCm39) |
D257G |
probably damaging |
Het |
Slf1 |
T |
C |
13: 77,191,964 (GRCm39) |
R957G |
probably damaging |
Het |
Smim10l1 |
T |
A |
6: 133,082,513 (GRCm39) |
M46K |
possibly damaging |
Het |
Sptbn5 |
T |
C |
2: 119,902,856 (GRCm39) |
Y50C |
possibly damaging |
Het |
Tcea1 |
A |
G |
1: 4,928,652 (GRCm39) |
|
probably benign |
Het |
Tex14 |
A |
G |
11: 87,385,842 (GRCm39) |
E234G |
probably damaging |
Het |
Tmbim4 |
T |
C |
10: 120,060,556 (GRCm39) |
V181A |
probably benign |
Het |
Trappc9 |
A |
G |
15: 72,461,993 (GRCm39) |
S1091P |
possibly damaging |
Het |
Txnrd3 |
T |
A |
6: 89,631,134 (GRCm39) |
C143* |
probably null |
Het |
Ushbp1 |
C |
T |
8: 71,843,305 (GRCm39) |
C314Y |
unknown |
Het |
|
Other mutations in Decr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01657:Decr2
|
APN |
17 |
26,301,926 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02023:Decr2
|
APN |
17 |
26,306,354 (GRCm39) |
missense |
probably benign |
0.01 |
R0003:Decr2
|
UTSW |
17 |
26,302,027 (GRCm39) |
missense |
probably benign |
0.00 |
R0003:Decr2
|
UTSW |
17 |
26,302,027 (GRCm39) |
missense |
probably benign |
0.00 |
R1583:Decr2
|
UTSW |
17 |
26,301,998 (GRCm39) |
missense |
probably damaging |
0.99 |
R1588:Decr2
|
UTSW |
17 |
26,302,002 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1903:Decr2
|
UTSW |
17 |
26,306,387 (GRCm39) |
missense |
probably damaging |
0.99 |
R1968:Decr2
|
UTSW |
17 |
26,302,053 (GRCm39) |
missense |
probably benign |
0.00 |
R2269:Decr2
|
UTSW |
17 |
26,302,858 (GRCm39) |
missense |
probably benign |
0.03 |
R4758:Decr2
|
UTSW |
17 |
26,307,914 (GRCm39) |
missense |
probably damaging |
0.96 |
R5021:Decr2
|
UTSW |
17 |
26,301,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R5174:Decr2
|
UTSW |
17 |
26,306,443 (GRCm39) |
splice site |
probably null |
|
R6608:Decr2
|
UTSW |
17 |
26,302,858 (GRCm39) |
missense |
probably benign |
0.30 |
R8036:Decr2
|
UTSW |
17 |
26,301,962 (GRCm39) |
missense |
probably damaging |
0.97 |
R8799:Decr2
|
UTSW |
17 |
26,307,911 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8969:Decr2
|
UTSW |
17 |
26,306,355 (GRCm39) |
missense |
probably benign |
|
R9706:Decr2
|
UTSW |
17 |
26,302,869 (GRCm39) |
missense |
probably benign |
0.01 |
|