Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb3 |
A |
G |
1: 25,865,574 (GRCm39) |
F90L |
probably benign |
Het |
Anapc4 |
T |
A |
5: 53,021,968 (GRCm39) |
Y683* |
probably null |
Het |
Astn2 |
T |
G |
4: 65,570,186 (GRCm39) |
D773A |
probably damaging |
Het |
Atp2b3 |
T |
C |
X: 72,588,966 (GRCm39) |
|
probably benign |
Het |
Atp8b5 |
T |
C |
4: 43,291,693 (GRCm39) |
M22T |
probably benign |
Het |
Birc6 |
T |
A |
17: 74,967,606 (GRCm39) |
L4169H |
probably damaging |
Het |
Cdc42bpa |
T |
C |
1: 179,939,431 (GRCm39) |
V81A |
probably benign |
Het |
Clcn2 |
A |
T |
16: 20,532,369 (GRCm39) |
C80S |
probably damaging |
Het |
Clu |
C |
T |
14: 66,217,121 (GRCm39) |
A318V |
possibly damaging |
Het |
Csnk1g2 |
A |
G |
10: 80,475,463 (GRCm39) |
H378R |
probably benign |
Het |
Dpp3 |
T |
C |
19: 4,968,332 (GRCm39) |
T247A |
possibly damaging |
Het |
Eif4g1 |
A |
G |
16: 20,500,966 (GRCm39) |
N774D |
possibly damaging |
Het |
Epha4 |
A |
T |
1: 77,403,475 (GRCm39) |
V344E |
probably damaging |
Het |
Epha6 |
A |
C |
16: 59,659,666 (GRCm39) |
N817K |
probably benign |
Het |
Ggcx |
T |
A |
6: 72,406,941 (GRCm39) |
|
probably null |
Het |
Gm1965 |
C |
T |
6: 89,123,648 (GRCm39) |
|
noncoding transcript |
Het |
Gmnn |
T |
C |
13: 24,937,687 (GRCm39) |
E101G |
probably damaging |
Het |
Grik2 |
C |
T |
10: 49,404,082 (GRCm39) |
|
probably null |
Het |
H2-M11 |
T |
A |
17: 36,858,465 (GRCm39) |
D86E |
probably benign |
Het |
Il6st |
T |
A |
13: 112,618,077 (GRCm39) |
W164R |
probably damaging |
Het |
Ilvbl |
G |
T |
10: 78,412,602 (GRCm39) |
V108L |
possibly damaging |
Het |
Klk10 |
A |
G |
7: 43,431,013 (GRCm39) |
K19E |
possibly damaging |
Het |
Mbd4 |
G |
T |
6: 115,826,598 (GRCm39) |
T131N |
probably damaging |
Het |
Ncapd3 |
T |
C |
9: 26,983,120 (GRCm39) |
V956A |
possibly damaging |
Het |
Nif3l1 |
A |
C |
1: 58,494,771 (GRCm39) |
T247P |
probably damaging |
Het |
Nrcam |
T |
C |
12: 44,606,583 (GRCm39) |
V443A |
probably damaging |
Het |
Or4c35 |
A |
G |
2: 89,808,221 (GRCm39) |
Y33C |
probably damaging |
Het |
Pigk |
T |
A |
3: 152,428,157 (GRCm39) |
H61Q |
probably damaging |
Het |
Pla2g4d |
C |
A |
2: 120,105,768 (GRCm39) |
V431F |
possibly damaging |
Het |
Pxt1 |
A |
T |
17: 29,153,778 (GRCm39) |
H18Q |
possibly damaging |
Het |
Rpusd4 |
T |
C |
9: 35,184,757 (GRCm39) |
|
probably benign |
Het |
Slc22a18 |
T |
G |
7: 143,052,837 (GRCm39) |
L354R |
probably damaging |
Het |
Slc26a10 |
A |
G |
10: 127,010,903 (GRCm39) |
V443A |
probably damaging |
Het |
Smpx |
A |
G |
X: 156,497,676 (GRCm39) |
|
probably benign |
Het |
Sptan1 |
A |
G |
2: 29,908,491 (GRCm39) |
S1751G |
probably benign |
Het |
Ush2a |
C |
T |
1: 188,558,658 (GRCm39) |
T3629I |
probably benign |
Het |
Vcan |
C |
T |
13: 89,838,705 (GRCm39) |
V2280M |
probably damaging |
Het |
Vmn1r30 |
T |
C |
6: 58,412,619 (GRCm39) |
E71G |
probably benign |
Het |
Vmn2r100 |
A |
T |
17: 19,746,178 (GRCm39) |
I446F |
possibly damaging |
Het |
Vmn2r75 |
A |
T |
7: 85,813,455 (GRCm39) |
V449D |
probably damaging |
Het |
|
Other mutations in Decr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
R6661:Decr2
|
UTSW |
17 |
26,302,561 (GRCm39) |
missense |
possibly damaging |
0.53 |
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 |
|