Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ago2 |
T |
C |
15: 72,985,601 (GRCm39) |
I665V |
probably benign |
Het |
Aoc1l3 |
T |
G |
6: 48,964,508 (GRCm39) |
F172C |
probably damaging |
Het |
Arhgap32 |
A |
T |
9: 32,063,983 (GRCm39) |
M74L |
possibly damaging |
Het |
Asb4 |
T |
C |
6: 5,398,304 (GRCm39) |
C90R |
possibly damaging |
Het |
B3galt4 |
T |
A |
17: 34,169,821 (GRCm39) |
D139V |
probably damaging |
Het |
Camta2 |
A |
C |
11: 70,564,964 (GRCm39) |
I852S |
probably benign |
Het |
Cox4i2 |
G |
T |
2: 152,599,015 (GRCm39) |
E57D |
probably benign |
Het |
Dip2b |
T |
C |
15: 100,091,724 (GRCm39) |
I1055T |
probably benign |
Het |
Eif1ad18 |
T |
A |
12: 88,050,602 (GRCm39) |
W46R |
probably benign |
Het |
Eif4g3 |
C |
T |
4: 137,824,646 (GRCm39) |
P284S |
probably damaging |
Het |
Ephb1 |
C |
A |
9: 101,806,463 (GRCm39) |
|
probably null |
Het |
Fbxw7 |
A |
T |
3: 84,879,723 (GRCm39) |
|
probably null |
Het |
Frem1 |
C |
A |
4: 82,840,506 (GRCm39) |
D1789Y |
probably damaging |
Het |
Gm29106 |
A |
T |
1: 118,127,524 (GRCm39) |
R405S |
probably damaging |
Het |
Greb1l |
G |
A |
18: 10,547,482 (GRCm39) |
V1567M |
possibly damaging |
Het |
Hapstr1 |
A |
G |
16: 8,648,553 (GRCm39) |
|
probably null |
Het |
Heatr1 |
C |
A |
13: 12,449,956 (GRCm39) |
D1983E |
probably benign |
Het |
Lhfpl2 |
G |
T |
13: 94,311,029 (GRCm39) |
A100S |
probably damaging |
Het |
Lrp5 |
A |
T |
19: 3,655,301 (GRCm39) |
V1073D |
probably damaging |
Het |
Naip6 |
G |
A |
13: 100,438,706 (GRCm39) |
L364F |
possibly damaging |
Het |
Nek9 |
A |
G |
12: 85,350,311 (GRCm39) |
L921P |
probably damaging |
Het |
Nim1k |
C |
T |
13: 120,189,263 (GRCm39) |
E49K |
probably damaging |
Het |
Nsun5 |
A |
C |
5: 135,399,046 (GRCm39) |
N32T |
probably damaging |
Het |
Nuggc |
T |
C |
14: 65,855,092 (GRCm39) |
S325P |
probably damaging |
Het |
Or2d36 |
A |
G |
7: 106,747,290 (GRCm39) |
I256V |
probably damaging |
Het |
Or5w12 |
T |
A |
2: 87,501,797 (GRCm39) |
K305* |
probably null |
Het |
Pcdhga7 |
A |
G |
18: 37,848,710 (GRCm39) |
D239G |
probably damaging |
Het |
Pld2 |
A |
G |
11: 70,444,273 (GRCm39) |
D523G |
probably benign |
Het |
Prokr1 |
C |
A |
6: 87,565,455 (GRCm39) |
W130L |
probably damaging |
Het |
Prpf8 |
A |
G |
11: 75,381,562 (GRCm39) |
N266S |
probably damaging |
Het |
Rdh10 |
T |
C |
1: 16,176,255 (GRCm39) |
V5A |
probably benign |
Het |
Rp1l1 |
T |
C |
14: 64,267,834 (GRCm39) |
L1140P |
possibly damaging |
Het |
Sacs |
A |
G |
14: 61,448,874 (GRCm39) |
D3640G |
probably damaging |
Het |
Smarca2 |
A |
G |
19: 26,668,749 (GRCm39) |
E916G |
probably damaging |
Het |
Steap3 |
A |
T |
1: 120,171,624 (GRCm39) |
H160Q |
probably damaging |
Het |
Tlk2 |
T |
C |
11: 105,147,779 (GRCm39) |
|
probably null |
Het |
Tmprss4 |
A |
G |
9: 45,097,220 (GRCm39) |
V15A |
probably benign |
Het |
Togaram2 |
T |
C |
17: 72,014,129 (GRCm39) |
L559P |
probably damaging |
Het |
Topbp1 |
T |
A |
9: 103,213,045 (GRCm39) |
L990H |
probably damaging |
Het |
Ttll7 |
A |
G |
3: 146,615,369 (GRCm39) |
T278A |
possibly damaging |
Het |
Ttn |
G |
A |
2: 76,604,780 (GRCm39) |
L18385F |
probably damaging |
Het |
Upf3a |
G |
T |
8: 13,841,911 (GRCm39) |
A149S |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Zfp316 |
A |
T |
5: 143,239,280 (GRCm39) |
F913Y |
probably damaging |
Het |
|
Other mutations in Cd200l1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00435:Cd200l1
|
APN |
16 |
45,264,483 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02822:Cd200l1
|
APN |
16 |
45,262,968 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4618001:Cd200l1
|
UTSW |
16 |
45,264,297 (GRCm39) |
missense |
probably benign |
0.08 |
R0565:Cd200l1
|
UTSW |
16 |
45,264,536 (GRCm39) |
intron |
probably benign |
|
R1561:Cd200l1
|
UTSW |
16 |
45,262,875 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4632:Cd200l1
|
UTSW |
16 |
45,238,271 (GRCm39) |
missense |
probably benign |
0.34 |
R4667:Cd200l1
|
UTSW |
16 |
45,264,526 (GRCm39) |
missense |
probably benign |
0.01 |
R5887:Cd200l1
|
UTSW |
16 |
45,238,279 (GRCm39) |
missense |
probably damaging |
0.99 |
R6181:Cd200l1
|
UTSW |
16 |
45,238,260 (GRCm39) |
missense |
probably benign |
0.01 |
R6562:Cd200l1
|
UTSW |
16 |
45,264,442 (GRCm39) |
missense |
probably benign |
0.03 |
R6961:Cd200l1
|
UTSW |
16 |
45,264,366 (GRCm39) |
missense |
probably benign |
0.32 |
R7830:Cd200l1
|
UTSW |
16 |
45,262,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R8133:Cd200l1
|
UTSW |
16 |
45,264,304 (GRCm39) |
missense |
probably benign |
|
R8459:Cd200l1
|
UTSW |
16 |
45,238,271 (GRCm39) |
missense |
probably benign |
0.06 |
R8483:Cd200l1
|
UTSW |
16 |
45,240,235 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8810:Cd200l1
|
UTSW |
16 |
45,264,199 (GRCm39) |
missense |
probably benign |
0.04 |
R8950:Cd200l1
|
UTSW |
16 |
45,263,007 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8988:Cd200l1
|
UTSW |
16 |
45,238,271 (GRCm39) |
missense |
probably benign |
0.01 |
R9040:Cd200l1
|
UTSW |
16 |
45,264,509 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9729:Cd200l1
|
UTSW |
16 |
45,264,237 (GRCm39) |
missense |
possibly damaging |
0.63 |
X0011:Cd200l1
|
UTSW |
16 |
45,240,234 (GRCm39) |
missense |
possibly damaging |
0.92 |
X0019:Cd200l1
|
UTSW |
16 |
45,263,008 (GRCm39) |
missense |
probably benign |
|
|