Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
4930486L24Rik |
A |
G |
13: 60,992,132 (GRCm39) |
V298A |
probably damaging |
Het |
Abca12 |
A |
G |
1: 71,360,609 (GRCm39) |
V534A |
probably benign |
Het |
Abcb4 |
A |
G |
5: 8,980,906 (GRCm39) |
|
probably null |
Het |
Adam30 |
A |
T |
3: 98,070,170 (GRCm39) |
S668C |
probably damaging |
Het |
Ap1g1 |
T |
A |
8: 110,556,252 (GRCm39) |
V196D |
probably damaging |
Het |
Atp11b |
G |
A |
3: 35,888,543 (GRCm39) |
V738I |
probably benign |
Het |
Cast |
C |
T |
13: 74,946,834 (GRCm39) |
V27I |
probably damaging |
Het |
Cfap54 |
A |
G |
10: 92,651,780 (GRCm39) |
I3090T |
probably benign |
Het |
Cgn |
C |
A |
3: 94,686,748 (GRCm39) |
G185W |
probably damaging |
Het |
Cpm |
T |
C |
10: 117,511,890 (GRCm39) |
I278T |
probably damaging |
Het |
Dcaf15 |
T |
C |
8: 84,828,845 (GRCm39) |
T141A |
probably benign |
Het |
Dcun1d1 |
C |
T |
3: 35,949,819 (GRCm39) |
V244M |
probably damaging |
Het |
Defb8 |
A |
G |
8: 19,497,575 (GRCm39) |
L12P |
probably damaging |
Het |
Dlg1 |
A |
T |
16: 31,609,079 (GRCm39) |
I225F |
probably damaging |
Het |
Dync2h1 |
G |
T |
9: 7,118,932 (GRCm39) |
H2178N |
possibly damaging |
Het |
Enam |
A |
G |
5: 88,651,395 (GRCm39) |
E893G |
probably damaging |
Het |
Flt4 |
T |
A |
11: 49,518,034 (GRCm39) |
L358Q |
probably damaging |
Het |
Frmpd1 |
A |
G |
4: 45,284,785 (GRCm39) |
Q1202R |
probably benign |
Het |
Ghr |
T |
A |
15: 3,349,879 (GRCm39) |
D433V |
possibly damaging |
Het |
Grm7 |
G |
A |
6: 111,057,383 (GRCm39) |
D328N |
possibly damaging |
Het |
Haus4 |
T |
C |
14: 54,779,577 (GRCm39) |
D349G |
probably benign |
Het |
Helz |
T |
C |
11: 107,517,542 (GRCm39) |
|
probably null |
Het |
Hif3a |
A |
G |
7: 16,790,196 (GRCm39) |
L69P |
probably damaging |
Het |
Ifit1 |
A |
G |
19: 34,625,563 (GRCm39) |
E233G |
probably damaging |
Het |
Kcnc2 |
T |
C |
10: 112,291,733 (GRCm39) |
F307S |
possibly damaging |
Het |
Lrp1b |
A |
T |
2: 41,000,771 (GRCm39) |
V2151E |
possibly damaging |
Het |
Lrp5 |
T |
C |
19: 3,709,454 (GRCm39) |
N92S |
probably damaging |
Het |
Metrnl |
C |
T |
11: 121,606,839 (GRCm39) |
A216V |
probably damaging |
Het |
Msh2 |
A |
G |
17: 88,026,217 (GRCm39) |
T732A |
probably damaging |
Het |
Necab2 |
T |
C |
8: 120,194,334 (GRCm39) |
L270P |
probably damaging |
Het |
Noc3l |
T |
C |
19: 38,804,157 (GRCm39) |
K74E |
probably benign |
Het |
Oas2 |
A |
T |
5: 120,871,537 (GRCm39) |
L702Q |
probably damaging |
Het |
Or1j1 |
A |
T |
2: 36,703,047 (GRCm39) |
I19N |
probably benign |
Het |
Or2n1d |
A |
C |
17: 38,646,731 (GRCm39) |
I228L |
possibly damaging |
Het |
Or4k1 |
A |
G |
14: 50,377,436 (GRCm39) |
I220T |
possibly damaging |
Het |
Or4k6 |
C |
A |
14: 50,475,824 (GRCm39) |
V173L |
possibly damaging |
Het |
Or6c216 |
A |
T |
10: 129,678,814 (GRCm39) |
N32K |
probably damaging |
Het |
Pax6 |
A |
G |
2: 105,525,745 (GRCm39) |
H376R |
possibly damaging |
Het |
Pnkd |
C |
T |
1: 74,390,941 (GRCm39) |
R376C |
probably damaging |
Het |
Pnpla8 |
T |
C |
12: 44,342,696 (GRCm39) |
F484S |
probably damaging |
Het |
Psme4 |
T |
A |
11: 30,782,573 (GRCm39) |
H909Q |
probably benign |
Het |
Rasip1 |
CGG |
CGGG |
7: 45,281,820 (GRCm39) |
|
probably null |
Het |
Rbm47 |
A |
T |
5: 66,182,395 (GRCm39) |
Y413N |
probably damaging |
Het |
Rnf123 |
A |
G |
9: 107,929,638 (GRCm39) |
|
probably null |
Het |
Ruvbl1 |
T |
A |
6: 88,461,412 (GRCm39) |
M259K |
possibly damaging |
Het |
Sohlh2 |
A |
G |
3: 55,097,950 (GRCm39) |
H134R |
probably benign |
Het |
Sorbs2 |
A |
G |
8: 46,248,330 (GRCm39) |
D447G |
possibly damaging |
Het |
Tank |
C |
T |
2: 61,480,573 (GRCm39) |
P370S |
probably benign |
Het |
Tenm4 |
A |
G |
7: 96,544,131 (GRCm39) |
E2049G |
probably damaging |
Het |
Tnik |
A |
G |
3: 28,648,226 (GRCm39) |
H426R |
possibly damaging |
Het |
Trpm6 |
C |
A |
19: 18,831,564 (GRCm39) |
S1476R |
possibly damaging |
Het |
Trpm7 |
G |
A |
2: 126,682,703 (GRCm39) |
Q389* |
probably null |
Het |
Ttc28 |
G |
A |
5: 111,433,095 (GRCm39) |
R2043Q |
possibly damaging |
Het |
Tymp |
A |
G |
15: 89,260,510 (GRCm39) |
S103P |
probably damaging |
Het |
Usp40 |
C |
T |
1: 87,894,901 (GRCm39) |
|
probably null |
Het |
Vmn1r202 |
T |
A |
13: 22,685,977 (GRCm39) |
N147Y |
probably damaging |
Het |
Vmn2r89 |
T |
C |
14: 51,689,688 (GRCm39) |
S64P |
probably damaging |
Het |
Vps13a |
A |
T |
19: 16,727,220 (GRCm39) |
D229E |
probably benign |
Het |
Vps52 |
A |
G |
17: 34,180,153 (GRCm39) |
I354V |
probably benign |
Het |
Zbtb8os |
T |
C |
4: 129,235,557 (GRCm39) |
F90L |
probably damaging |
Het |
Zfp36l1 |
T |
C |
12: 80,157,270 (GRCm39) |
D37G |
possibly damaging |
Het |
Zfp467 |
A |
G |
6: 48,404,751 (GRCm39) |
S109P |
unknown |
Het |
Zzef1 |
T |
A |
11: 72,728,038 (GRCm39) |
C535S |
probably damaging |
Het |
|
Other mutations in Champ1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00530:Champ1
|
APN |
8 |
13,929,522 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL00775:Champ1
|
APN |
8 |
13,929,509 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02451:Champ1
|
APN |
8 |
13,928,739 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03283:Champ1
|
APN |
8 |
13,928,786 (GRCm39) |
missense |
probably benign |
0.04 |
PIT4810001:Champ1
|
UTSW |
8 |
13,929,234 (GRCm39) |
missense |
probably benign |
0.37 |
R0664:Champ1
|
UTSW |
8 |
13,929,485 (GRCm39) |
missense |
probably damaging |
0.96 |
R2219:Champ1
|
UTSW |
8 |
13,930,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R3077:Champ1
|
UTSW |
8 |
13,928,832 (GRCm39) |
missense |
probably benign |
|
R3735:Champ1
|
UTSW |
8 |
13,928,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R3838:Champ1
|
UTSW |
8 |
13,929,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R4933:Champ1
|
UTSW |
8 |
13,929,137 (GRCm39) |
missense |
probably benign |
0.14 |
R5294:Champ1
|
UTSW |
8 |
13,928,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R5893:Champ1
|
UTSW |
8 |
13,928,777 (GRCm39) |
missense |
probably benign |
0.08 |
R6548:Champ1
|
UTSW |
8 |
13,930,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R7261:Champ1
|
UTSW |
8 |
13,928,517 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7467:Champ1
|
UTSW |
8 |
13,928,579 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7747:Champ1
|
UTSW |
8 |
13,929,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R9328:Champ1
|
UTSW |
8 |
13,929,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R9464:Champ1
|
UTSW |
8 |
13,929,114 (GRCm39) |
missense |
probably damaging |
1.00 |
|