Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,225,057 (GRCm39) |
L512* |
probably null |
Het |
Adam4 |
A |
T |
12: 81,467,485 (GRCm39) |
F379I |
probably benign |
Het |
Ano6 |
C |
G |
15: 95,863,906 (GRCm39) |
|
probably benign |
Het |
Apc2 |
A |
G |
10: 80,148,903 (GRCm39) |
E1319G |
possibly damaging |
Het |
Arfgef3 |
A |
G |
10: 18,473,535 (GRCm39) |
V1588A |
possibly damaging |
Het |
Arl8a |
T |
A |
1: 135,080,604 (GRCm39) |
V93E |
probably damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Cd200r2 |
T |
A |
16: 44,729,630 (GRCm39) |
I95N |
probably damaging |
Het |
Cep290 |
A |
G |
10: 100,397,100 (GRCm39) |
|
probably null |
Het |
Chd2 |
G |
T |
7: 73,157,631 (GRCm39) |
D171E |
possibly damaging |
Het |
Chrna7 |
G |
A |
7: 62,748,994 (GRCm39) |
A496V |
probably damaging |
Het |
Col9a2 |
C |
G |
4: 120,911,455 (GRCm39) |
R599G |
probably damaging |
Het |
Colgalt1 |
C |
G |
8: 72,076,385 (GRCm39) |
T612S |
probably benign |
Het |
Copg2 |
T |
C |
6: 30,787,893 (GRCm39) |
K602E |
probably benign |
Het |
Crtc1 |
T |
A |
8: 70,840,808 (GRCm39) |
T473S |
probably benign |
Het |
Ctbp2 |
A |
T |
7: 132,625,290 (GRCm39) |
|
probably null |
Het |
Edem1 |
T |
G |
6: 108,829,504 (GRCm39) |
M541R |
probably damaging |
Het |
Ehmt1 |
A |
C |
2: 24,696,229 (GRCm39) |
V953G |
probably damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fgfr2 |
T |
C |
7: 129,828,968 (GRCm39) |
|
probably null |
Het |
Focad |
A |
G |
4: 88,039,567 (GRCm39) |
D10G |
probably damaging |
Het |
Gfus |
G |
T |
15: 75,798,200 (GRCm39) |
L191I |
probably damaging |
Het |
Gm5901 |
G |
T |
7: 105,026,996 (GRCm39) |
V255F |
possibly damaging |
Het |
Hsp90aa1 |
T |
C |
12: 110,659,840 (GRCm39) |
N416S |
probably damaging |
Het |
Hspb1 |
T |
C |
5: 135,917,950 (GRCm39) |
F142L |
probably benign |
Het |
Il17re |
C |
T |
6: 113,439,314 (GRCm39) |
H75Y |
possibly damaging |
Het |
Kctd3 |
A |
G |
1: 188,713,568 (GRCm39) |
I389T |
probably damaging |
Het |
Lhx6 |
T |
C |
2: 35,981,402 (GRCm39) |
D63G |
probably benign |
Het |
Mepe |
A |
G |
5: 104,485,327 (GRCm39) |
T156A |
possibly damaging |
Het |
Met |
A |
G |
6: 17,534,197 (GRCm39) |
Y680C |
probably damaging |
Het |
Mrgpra3 |
T |
C |
7: 47,239,365 (GRCm39) |
Y187C |
possibly damaging |
Het |
Mst1 |
T |
G |
9: 107,960,151 (GRCm39) |
|
probably null |
Het |
Myh13 |
T |
A |
11: 67,231,184 (GRCm39) |
S394T |
possibly damaging |
Het |
Nbeal1 |
T |
A |
1: 60,290,529 (GRCm39) |
V1042E |
probably damaging |
Het |
Ndrg4 |
T |
A |
8: 96,432,839 (GRCm39) |
Y15* |
probably null |
Het |
Neurl4 |
G |
A |
11: 69,797,900 (GRCm39) |
R720H |
probably damaging |
Het |
Nfkbia |
A |
G |
12: 55,537,455 (GRCm39) |
|
probably benign |
Het |
Nwd1 |
T |
A |
8: 73,389,055 (GRCm39) |
M202K |
probably benign |
Het |
Or10d4 |
G |
T |
9: 39,580,569 (GRCm39) |
C72F |
possibly damaging |
Het |
Or2av9 |
T |
A |
11: 58,381,546 (GRCm39) |
I12F |
probably benign |
Het |
Pate2 |
T |
C |
9: 35,581,036 (GRCm39) |
|
probably benign |
Het |
Pibf1 |
A |
G |
14: 99,480,368 (GRCm39) |
T715A |
probably benign |
Het |
Pitpnm1 |
T |
C |
19: 4,160,935 (GRCm39) |
L858P |
probably benign |
Het |
Pla2g3 |
A |
C |
11: 3,443,115 (GRCm39) |
S483R |
probably benign |
Het |
Rad51ap2 |
T |
A |
12: 11,507,798 (GRCm39) |
D573E |
probably damaging |
Het |
Rho |
T |
C |
6: 115,912,352 (GRCm39) |
|
probably benign |
Het |
Rpl39l |
A |
T |
16: 9,992,328 (GRCm39) |
*52L |
probably null |
Het |
Slco1a5 |
T |
A |
6: 142,194,501 (GRCm39) |
R381W |
possibly damaging |
Het |
Spns3 |
T |
A |
11: 72,441,059 (GRCm39) |
|
probably benign |
Het |
Srgap2 |
A |
G |
1: 131,259,872 (GRCm39) |
S493P |
probably benign |
Het |
Tecpr2 |
T |
C |
12: 110,892,836 (GRCm39) |
S293P |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,583,211 (GRCm39) |
V20815M |
probably benign |
Het |
Ushbp1 |
T |
C |
8: 71,847,132 (GRCm39) |
I167V |
probably benign |
Het |
Wdr81 |
C |
T |
11: 75,340,231 (GRCm39) |
A1296T |
probably damaging |
Het |
Zmym2 |
A |
G |
14: 57,158,180 (GRCm39) |
Y573C |
probably benign |
Het |
|
Other mutations in Cd209d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01634:Cd209d
|
APN |
8 |
3,927,974 (GRCm39) |
splice site |
probably null |
|
IGL01707:Cd209d
|
APN |
8 |
3,928,296 (GRCm39) |
missense |
probably benign |
|
IGL02864:Cd209d
|
APN |
8 |
3,927,122 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03066:Cd209d
|
APN |
8 |
3,928,437 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03297:Cd209d
|
APN |
8 |
3,928,476 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0324:Cd209d
|
UTSW |
8 |
3,928,258 (GRCm39) |
missense |
probably benign |
0.31 |
R1335:Cd209d
|
UTSW |
8 |
3,922,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R1349:Cd209d
|
UTSW |
8 |
3,928,515 (GRCm39) |
unclassified |
probably benign |
|
R1372:Cd209d
|
UTSW |
8 |
3,928,515 (GRCm39) |
unclassified |
probably benign |
|
R1507:Cd209d
|
UTSW |
8 |
3,928,453 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1673:Cd209d
|
UTSW |
8 |
3,927,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R2567:Cd209d
|
UTSW |
8 |
3,926,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R4907:Cd209d
|
UTSW |
8 |
3,927,948 (GRCm39) |
missense |
probably benign |
0.01 |
R5349:Cd209d
|
UTSW |
8 |
3,928,320 (GRCm39) |
missense |
probably benign |
0.00 |
R5768:Cd209d
|
UTSW |
8 |
3,921,968 (GRCm39) |
missense |
probably benign |
0.05 |
R5949:Cd209d
|
UTSW |
8 |
3,927,949 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5953:Cd209d
|
UTSW |
8 |
3,927,979 (GRCm39) |
splice site |
probably null |
|
R6103:Cd209d
|
UTSW |
8 |
3,928,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R7382:Cd209d
|
UTSW |
8 |
3,927,965 (GRCm39) |
nonsense |
probably null |
|
R8714:Cd209d
|
UTSW |
8 |
3,923,772 (GRCm39) |
frame shift |
probably null |
|
R8715:Cd209d
|
UTSW |
8 |
3,923,772 (GRCm39) |
frame shift |
probably null |
|
R8716:Cd209d
|
UTSW |
8 |
3,923,772 (GRCm39) |
frame shift |
probably null |
|
R9672:Cd209d
|
UTSW |
8 |
3,922,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R9784:Cd209d
|
UTSW |
8 |
3,926,337 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Cd209d
|
UTSW |
8 |
3,927,961 (GRCm39) |
nonsense |
probably null |
|
|