Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd29 |
A |
G |
18: 12,394,046 (GRCm39) |
V256A |
probably benign |
Het |
Arid4a |
A |
G |
12: 71,110,076 (GRCm39) |
D139G |
probably benign |
Het |
AU040320 |
T |
C |
4: 126,685,723 (GRCm39) |
W100R |
probably damaging |
Het |
C4bp |
T |
C |
1: 130,563,943 (GRCm39) |
*470W |
probably null |
Het |
Capn8 |
C |
A |
1: 182,456,234 (GRCm39) |
D661E |
possibly damaging |
Het |
Car14 |
T |
C |
3: 95,805,472 (GRCm39) |
T334A |
probably benign |
Het |
Cfhr4 |
G |
A |
1: 139,668,210 (GRCm39) |
P308S |
possibly damaging |
Het |
Chd6 |
T |
A |
2: 160,830,260 (GRCm39) |
T1012S |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 47,529,910 (GRCm39) |
|
probably null |
Het |
Dnaaf2 |
A |
G |
12: 69,244,437 (GRCm39) |
V208A |
probably benign |
Het |
Dnah11 |
A |
G |
12: 117,958,926 (GRCm39) |
W2986R |
probably damaging |
Het |
Epb42 |
G |
A |
2: 120,867,104 (GRCm39) |
|
probably benign |
Het |
Fam120a |
A |
G |
13: 49,045,497 (GRCm39) |
F780L |
probably benign |
Het |
Gpt2 |
G |
A |
8: 86,244,681 (GRCm39) |
E325K |
probably benign |
Het |
Grid2 |
T |
C |
6: 64,372,283 (GRCm39) |
F655S |
probably damaging |
Het |
Homer3 |
T |
C |
8: 70,737,955 (GRCm39) |
S2P |
probably damaging |
Het |
Hydin |
T |
C |
8: 111,038,883 (GRCm39) |
V207A |
probably benign |
Het |
Inpp5j |
T |
C |
11: 3,445,557 (GRCm39) |
|
probably null |
Het |
Jak1 |
C |
T |
4: 101,011,734 (GRCm39) |
|
probably null |
Het |
Jmjd1c |
A |
G |
10: 67,052,869 (GRCm39) |
I220V |
probably benign |
Het |
Kat6a |
T |
G |
8: 23,425,799 (GRCm39) |
S1115A |
possibly damaging |
Het |
Larp4 |
T |
G |
15: 99,905,611 (GRCm39) |
|
probably null |
Het |
Lrrc72 |
T |
G |
12: 36,259,717 (GRCm39) |
D43A |
probably damaging |
Het |
Nmbr |
A |
T |
10: 14,645,704 (GRCm39) |
*258Y |
probably null |
Het |
Nup210l |
C |
T |
3: 90,067,231 (GRCm39) |
A757V |
probably damaging |
Het |
Nup62 |
A |
G |
7: 44,479,157 (GRCm39) |
K391E |
possibly damaging |
Het |
Nup93 |
T |
A |
8: 94,970,314 (GRCm39) |
I71K |
probably damaging |
Het |
Or14a256 |
A |
T |
7: 86,265,323 (GRCm39) |
C177S |
probably damaging |
Het |
Or8b51 |
A |
C |
9: 38,569,385 (GRCm39) |
L101R |
probably damaging |
Het |
Pik3cg |
A |
G |
12: 32,254,346 (GRCm39) |
M547T |
possibly damaging |
Het |
Ropn1 |
A |
T |
16: 34,497,668 (GRCm39) |
I187F |
possibly damaging |
Het |
Rtp3 |
T |
C |
9: 110,816,264 (GRCm39) |
R96G |
possibly damaging |
Het |
Sfrp5 |
A |
T |
19: 42,188,227 (GRCm39) |
S197R |
probably damaging |
Het |
Slc12a6 |
A |
G |
2: 112,185,440 (GRCm39) |
H903R |
probably damaging |
Het |
Slc26a3 |
G |
T |
12: 31,513,523 (GRCm39) |
A482S |
probably damaging |
Het |
Slc2a12 |
G |
T |
10: 22,568,084 (GRCm39) |
A504S |
probably damaging |
Het |
Slitrk5 |
C |
A |
14: 111,919,085 (GRCm39) |
P903Q |
probably damaging |
Het |
Tas2r123 |
A |
T |
6: 132,824,133 (GRCm39) |
H10L |
probably benign |
Het |
Tex46 |
T |
C |
4: 136,340,212 (GRCm39) |
V99A |
probably benign |
Het |
Top2b |
T |
C |
14: 16,413,604 (GRCm38) |
V1024A |
probably benign |
Het |
Ugt2b36 |
G |
A |
5: 87,240,157 (GRCm39) |
T76I |
probably benign |
Het |
Usp31 |
G |
T |
7: 121,252,399 (GRCm39) |
T747K |
probably benign |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
|
Other mutations in Mptx2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Mptx2
|
APN |
1 |
173,102,455 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01737:Mptx2
|
APN |
1 |
173,102,408 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02212:Mptx2
|
APN |
1 |
173,102,248 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL03185:Mptx2
|
APN |
1 |
173,102,356 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1772:Mptx2
|
UTSW |
1 |
173,102,040 (GRCm39) |
missense |
probably damaging |
0.98 |
R2070:Mptx2
|
UTSW |
1 |
173,102,145 (GRCm39) |
nonsense |
probably null |
|
R3792:Mptx2
|
UTSW |
1 |
173,102,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R5673:Mptx2
|
UTSW |
1 |
173,102,414 (GRCm39) |
missense |
probably benign |
0.05 |
R5700:Mptx2
|
UTSW |
1 |
173,102,414 (GRCm39) |
missense |
probably benign |
0.05 |
R5701:Mptx2
|
UTSW |
1 |
173,102,414 (GRCm39) |
missense |
probably benign |
0.05 |
R6110:Mptx2
|
UTSW |
1 |
173,102,414 (GRCm39) |
missense |
probably benign |
0.05 |
R6118:Mptx2
|
UTSW |
1 |
173,102,414 (GRCm39) |
missense |
probably benign |
0.05 |
R6124:Mptx2
|
UTSW |
1 |
173,102,414 (GRCm39) |
missense |
probably benign |
0.05 |
R6738:Mptx2
|
UTSW |
1 |
173,102,422 (GRCm39) |
missense |
probably benign |
0.05 |
R8288:Mptx2
|
UTSW |
1 |
173,102,356 (GRCm39) |
missense |
probably benign |
0.00 |
R8737:Mptx2
|
UTSW |
1 |
173,105,256 (GRCm39) |
missense |
probably benign |
0.00 |
R8857:Mptx2
|
UTSW |
1 |
173,102,452 (GRCm39) |
missense |
probably benign |
0.32 |
R9070:Mptx2
|
UTSW |
1 |
173,102,119 (GRCm39) |
missense |
probably benign |
0.01 |
RF001:Mptx2
|
UTSW |
1 |
173,102,536 (GRCm39) |
missense |
probably benign |
0.01 |
|