Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl3 |
A |
C |
7: 82,189,525 (GRCm39) |
E583A |
probably damaging |
Het |
Aoah |
T |
A |
13: 21,099,108 (GRCm39) |
|
probably benign |
Het |
Atf7ip2 |
A |
G |
16: 10,058,476 (GRCm39) |
K305R |
possibly damaging |
Het |
Bltp1 |
T |
G |
3: 37,041,194 (GRCm39) |
V2524G |
probably damaging |
Het |
Cfap57 |
G |
A |
4: 118,463,873 (GRCm39) |
Q327* |
probably null |
Het |
Ckap2l |
A |
T |
2: 129,114,492 (GRCm39) |
|
probably benign |
Het |
Cul2 |
A |
G |
18: 3,419,335 (GRCm39) |
|
probably benign |
Het |
Ddx60 |
G |
A |
8: 62,395,578 (GRCm39) |
V172M |
probably damaging |
Het |
Drp2 |
T |
C |
X: 133,342,071 (GRCm39) |
L545P |
probably damaging |
Het |
Ezh1 |
A |
G |
11: 101,101,361 (GRCm39) |
|
probably benign |
Het |
Gipc2 |
A |
G |
3: 151,799,833 (GRCm39) |
F299S |
probably damaging |
Het |
Gsk3b |
T |
C |
16: 38,028,346 (GRCm39) |
|
probably benign |
Het |
Gtf3c3 |
C |
T |
1: 54,456,937 (GRCm39) |
A488T |
probably damaging |
Het |
Hikeshi |
A |
G |
7: 89,584,938 (GRCm39) |
S89P |
probably benign |
Het |
Hmcn1 |
C |
T |
1: 150,494,679 (GRCm39) |
A4137T |
possibly damaging |
Het |
Itprid1 |
T |
C |
6: 55,866,155 (GRCm39) |
F183L |
probably damaging |
Het |
Larp1b |
C |
A |
3: 40,987,963 (GRCm39) |
R62S |
possibly damaging |
Het |
Lgr5 |
A |
T |
10: 115,296,716 (GRCm39) |
|
probably null |
Het |
Lpin1 |
C |
A |
12: 16,613,722 (GRCm39) |
D449Y |
probably damaging |
Het |
Macrod2 |
A |
T |
2: 140,242,826 (GRCm39) |
I31L |
probably benign |
Het |
Meig1 |
T |
C |
2: 3,410,311 (GRCm39) |
D63G |
probably damaging |
Het |
Ndufa9 |
A |
T |
6: 126,799,031 (GRCm39) |
L362Q |
probably damaging |
Het |
Nlrp9c |
A |
T |
7: 26,083,862 (GRCm39) |
D572E |
probably benign |
Het |
Nxpe5 |
G |
A |
5: 138,237,658 (GRCm39) |
D61N |
probably benign |
Het |
Ogdh |
T |
A |
11: 6,290,544 (GRCm39) |
H376Q |
probably damaging |
Het |
P4ha3 |
T |
C |
7: 99,962,535 (GRCm39) |
I431T |
probably damaging |
Het |
Pcdhb14 |
G |
A |
18: 37,581,640 (GRCm39) |
V249M |
probably damaging |
Het |
Pcnp |
A |
G |
16: 55,844,754 (GRCm39) |
S49P |
probably damaging |
Het |
Pik3r6 |
C |
T |
11: 68,436,698 (GRCm39) |
T654I |
probably benign |
Het |
Rptn |
A |
G |
3: 93,303,552 (GRCm39) |
Y295C |
possibly damaging |
Het |
Sec16b |
A |
G |
1: 157,392,404 (GRCm39) |
D924G |
possibly damaging |
Het |
Setd1b |
C |
A |
5: 123,285,779 (GRCm39) |
T275K |
unknown |
Het |
Sgcb |
T |
A |
5: 73,801,757 (GRCm39) |
K36I |
probably damaging |
Het |
Smg7 |
A |
T |
1: 152,742,326 (GRCm39) |
|
probably benign |
Het |
Sned1 |
G |
A |
1: 93,209,376 (GRCm39) |
V830M |
possibly damaging |
Het |
Stab2 |
T |
C |
10: 86,695,619 (GRCm39) |
D599G |
possibly damaging |
Het |
Stk36 |
A |
G |
1: 74,671,925 (GRCm39) |
E875G |
probably benign |
Het |
Tagln3 |
C |
A |
16: 45,544,635 (GRCm39) |
R12L |
probably damaging |
Het |
Tax1bp1 |
C |
A |
6: 52,718,933 (GRCm39) |
|
probably benign |
Het |
Thnsl1 |
A |
G |
2: 21,217,857 (GRCm39) |
N16S |
probably damaging |
Het |
Ticrr |
C |
T |
7: 79,343,701 (GRCm39) |
P1189S |
probably benign |
Het |
Tnxb |
G |
A |
17: 34,904,017 (GRCm39) |
V1053M |
probably damaging |
Het |
Tpp2 |
T |
C |
1: 44,031,556 (GRCm39) |
|
probably null |
Het |
Trappc9 |
G |
A |
15: 72,897,816 (GRCm39) |
R377W |
probably damaging |
Het |
Vmn2r60 |
A |
T |
7: 41,844,365 (GRCm39) |
Q576L |
possibly damaging |
Het |
Zfp62 |
G |
T |
11: 49,107,517 (GRCm39) |
R536L |
probably damaging |
Het |
Zfp958 |
A |
T |
8: 4,676,169 (GRCm39) |
N46Y |
possibly damaging |
Het |
|
Other mutations in Cd200r2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00465:Cd200r2
|
APN |
16 |
44,729,651 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01019:Cd200r2
|
APN |
16 |
44,729,832 (GRCm39) |
splice site |
probably benign |
|
IGL01480:Cd200r2
|
APN |
16 |
44,729,629 (GRCm39) |
missense |
probably null |
1.00 |
IGL01510:Cd200r2
|
APN |
16 |
44,729,674 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02202:Cd200r2
|
APN |
16 |
44,729,723 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02492:Cd200r2
|
APN |
16 |
44,729,903 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02499:Cd200r2
|
APN |
16 |
44,734,948 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0066:Cd200r2
|
UTSW |
16 |
44,730,037 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0066:Cd200r2
|
UTSW |
16 |
44,730,037 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0503:Cd200r2
|
UTSW |
16 |
44,698,325 (GRCm39) |
start codon destroyed |
probably null |
0.93 |
R0526:Cd200r2
|
UTSW |
16 |
44,735,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R1118:Cd200r2
|
UTSW |
16 |
44,729,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R2393:Cd200r2
|
UTSW |
16 |
44,729,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R5450:Cd200r2
|
UTSW |
16 |
44,729,934 (GRCm39) |
missense |
probably benign |
0.04 |
R7466:Cd200r2
|
UTSW |
16 |
44,729,537 (GRCm39) |
missense |
probably damaging |
0.97 |
R9762:Cd200r2
|
UTSW |
16 |
44,729,420 (GRCm39) |
missense |
probably benign |
0.00 |
|