Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aida |
T |
C |
1: 183,095,012 (GRCm39) |
V151A |
possibly damaging |
Het |
Akap3 |
T |
C |
6: 126,842,377 (GRCm39) |
V332A |
probably damaging |
Het |
Apobec3 |
T |
A |
15: 79,790,653 (GRCm39) |
W332R |
|
Het |
Atf6 |
A |
G |
1: 170,668,402 (GRCm39) |
V166A |
probably benign |
Het |
Bcl6b |
A |
G |
11: 70,118,858 (GRCm39) |
|
probably null |
Het |
Brd3 |
G |
T |
2: 27,340,373 (GRCm39) |
P612Q |
probably damaging |
Het |
Btg1 |
T |
A |
10: 96,453,263 (GRCm39) |
L26H |
probably damaging |
Het |
Btg4 |
A |
G |
9: 51,030,560 (GRCm39) |
D220G |
probably damaging |
Het |
Cd209e |
T |
C |
8: 3,901,183 (GRCm39) |
D157G |
probably benign |
Het |
Cdhr18 |
A |
T |
14: 13,814,959 (GRCm38) |
L858Q |
unknown |
Het |
Cimip2b |
T |
G |
4: 43,427,329 (GRCm39) |
T332P |
unknown |
Het |
Dnah10 |
T |
C |
5: 124,907,107 (GRCm39) |
L4269P |
probably damaging |
Het |
Dync1li2 |
C |
A |
8: 105,154,752 (GRCm39) |
K285N |
possibly damaging |
Het |
Ehmt2 |
C |
A |
17: 35,118,740 (GRCm39) |
Q198K |
possibly damaging |
Het |
Foxn3 |
C |
A |
12: 99,359,294 (GRCm39) |
|
probably benign |
Het |
Fstl4 |
C |
T |
11: 52,664,694 (GRCm39) |
P8L |
probably benign |
Het |
G6pc1 |
T |
C |
11: 101,258,660 (GRCm39) |
I13T |
possibly damaging |
Het |
Ghrhr |
A |
G |
6: 55,362,470 (GRCm39) |
I356V |
probably benign |
Het |
Gm14410 |
A |
T |
2: 176,885,773 (GRCm39) |
C164S |
probably damaging |
Het |
Gpcpd1 |
A |
T |
2: 132,388,848 (GRCm39) |
M308K |
possibly damaging |
Het |
Gpr143 |
GTTTTTT |
GTTTTTTT |
X: 151,578,627 (GRCm39) |
|
probably null |
Het |
Gpr179 |
T |
C |
11: 97,225,727 (GRCm39) |
K2143E |
probably benign |
Het |
Grm2 |
G |
A |
9: 106,524,408 (GRCm39) |
T298I |
probably damaging |
Het |
H2-T24 |
A |
T |
17: 36,326,455 (GRCm39) |
L148Q |
probably damaging |
Het |
Hcn2 |
C |
T |
10: 79,560,559 (GRCm39) |
R297C |
probably damaging |
Het |
Hic1 |
T |
C |
11: 75,056,757 (GRCm39) |
T711A |
possibly damaging |
Het |
Ide |
T |
C |
19: 37,264,514 (GRCm39) |
D672G |
|
Het |
Impg1 |
A |
G |
9: 80,288,923 (GRCm39) |
F378S |
probably damaging |
Het |
Lipe |
T |
C |
7: 25,098,128 (GRCm39) |
|
probably benign |
Het |
Lmo7 |
A |
G |
14: 102,156,136 (GRCm39) |
D1270G |
probably null |
Het |
Mbnl1 |
A |
T |
3: 60,520,859 (GRCm39) |
H149L |
probably damaging |
Het |
Mmel1 |
T |
C |
4: 154,978,592 (GRCm39) |
Y675H |
probably benign |
Het |
Mrfap1 |
C |
A |
5: 36,953,807 (GRCm39) |
R44L |
probably damaging |
Het |
Nherf2 |
G |
T |
17: 24,868,922 (GRCm39) |
T68K |
probably damaging |
Het |
Notch2 |
A |
G |
3: 98,041,889 (GRCm39) |
T1303A |
possibly damaging |
Het |
Olfm3 |
A |
G |
3: 114,883,785 (GRCm39) |
D62G |
probably damaging |
Het |
Or10ak13 |
T |
C |
4: 118,638,952 (GRCm39) |
I277V |
probably benign |
Het |
Or2i1 |
C |
G |
17: 37,508,308 (GRCm39) |
A109P |
possibly damaging |
Het |
Or5g27 |
C |
T |
2: 85,409,882 (GRCm39) |
Q100* |
probably null |
Het |
Or5l13 |
T |
C |
2: 87,780,544 (GRCm39) |
E11G |
probably damaging |
Het |
Or5p59 |
T |
G |
7: 107,702,663 (GRCm39) |
I49S |
probably damaging |
Het |
Or6c8b |
T |
A |
10: 128,882,354 (GRCm39) |
I193F |
probably benign |
Het |
Pcbd2 |
A |
G |
13: 55,880,849 (GRCm39) |
Y68C |
probably benign |
Het |
Phf3 |
G |
C |
1: 30,869,003 (GRCm39) |
Q682E |
probably benign |
Het |
Ptpn6 |
C |
A |
6: 124,704,728 (GRCm39) |
R294L |
probably benign |
Het |
Ptprz1 |
T |
A |
6: 23,025,026 (GRCm39) |
V1754D |
probably damaging |
Het |
Rab36 |
T |
A |
10: 74,887,873 (GRCm39) |
I248K |
probably damaging |
Het |
Rabac1 |
A |
G |
7: 24,671,579 (GRCm39) |
Y114H |
probably benign |
Het |
Rag1 |
A |
G |
2: 101,474,701 (GRCm39) |
V147A |
probably benign |
Het |
Rnf150 |
T |
A |
8: 83,717,144 (GRCm39) |
V217D |
probably damaging |
Het |
Sh3glb2 |
C |
T |
2: 30,236,672 (GRCm39) |
R230Q |
probably damaging |
Het |
Slc13a1 |
A |
G |
6: 24,089,100 (GRCm39) |
V550A |
probably damaging |
Het |
Sp140 |
A |
G |
1: 85,560,235 (GRCm39) |
N289S |
possibly damaging |
Het |
Spmip6 |
T |
C |
4: 41,505,091 (GRCm39) |
E207G |
|
Het |
Stac3 |
T |
A |
10: 127,338,654 (GRCm39) |
M1K |
probably null |
Het |
Stk31 |
C |
T |
6: 49,424,221 (GRCm39) |
T845I |
possibly damaging |
Het |
Sufu |
T |
C |
19: 46,385,674 (GRCm39) |
Y45H |
probably damaging |
Het |
Tg |
T |
A |
15: 66,607,109 (GRCm39) |
C1834* |
probably null |
Het |
Tns3 |
G |
A |
11: 8,401,142 (GRCm39) |
T1052M |
possibly damaging |
Het |
Tpcn1 |
T |
C |
5: 120,686,021 (GRCm39) |
T427A |
possibly damaging |
Het |
Trim45 |
A |
G |
3: 100,830,265 (GRCm39) |
H13R |
probably benign |
Het |
Trpv5 |
A |
G |
6: 41,647,773 (GRCm39) |
F347L |
probably benign |
Het |
Vmn1r43 |
G |
A |
6: 89,846,877 (GRCm39) |
T203M |
probably damaging |
Het |
Zfp236 |
G |
T |
18: 82,664,238 (GRCm39) |
Q516K |
probably damaging |
Het |
|
Other mutations in Scarf2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01543:Scarf2
|
APN |
16 |
17,620,413 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02166:Scarf2
|
APN |
16 |
17,621,620 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02604:Scarf2
|
APN |
16 |
17,621,608 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03155:Scarf2
|
APN |
16 |
17,625,413 (GRCm39) |
missense |
probably benign |
0.00 |
R0639:Scarf2
|
UTSW |
16 |
17,624,369 (GRCm39) |
splice site |
probably null |
|
R1703:Scarf2
|
UTSW |
16 |
17,620,713 (GRCm39) |
missense |
probably damaging |
0.99 |
R2182:Scarf2
|
UTSW |
16 |
17,620,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R4730:Scarf2
|
UTSW |
16 |
17,620,877 (GRCm39) |
missense |
probably damaging |
0.99 |
R4744:Scarf2
|
UTSW |
16 |
17,621,380 (GRCm39) |
missense |
probably damaging |
0.99 |
R4798:Scarf2
|
UTSW |
16 |
17,621,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R5521:Scarf2
|
UTSW |
16 |
17,621,466 (GRCm39) |
critical splice donor site |
probably null |
|
R5994:Scarf2
|
UTSW |
16 |
17,624,243 (GRCm39) |
missense |
probably damaging |
0.99 |
R6742:Scarf2
|
UTSW |
16 |
17,624,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R7264:Scarf2
|
UTSW |
16 |
17,621,154 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7286:Scarf2
|
UTSW |
16 |
17,620,837 (GRCm39) |
nonsense |
probably null |
|
R7385:Scarf2
|
UTSW |
16 |
17,621,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R7409:Scarf2
|
UTSW |
16 |
17,624,918 (GRCm39) |
missense |
probably damaging |
0.99 |
R7812:Scarf2
|
UTSW |
16 |
17,621,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R8442:Scarf2
|
UTSW |
16 |
17,624,231 (GRCm39) |
missense |
probably benign |
0.43 |
R8803:Scarf2
|
UTSW |
16 |
17,620,695 (GRCm39) |
missense |
probably damaging |
0.98 |
R8865:Scarf2
|
UTSW |
16 |
17,620,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R8987:Scarf2
|
UTSW |
16 |
17,622,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R9047:Scarf2
|
UTSW |
16 |
17,624,270 (GRCm39) |
missense |
probably damaging |
0.96 |
|