Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam32 |
T |
A |
8: 25,368,770 (GRCm39) |
D538V |
probably damaging |
Het |
Akap9 |
T |
C |
5: 4,011,709 (GRCm39) |
I804T |
probably benign |
Het |
Amy1 |
T |
C |
3: 113,357,281 (GRCm39) |
E186G |
probably benign |
Het |
Best1 |
A |
G |
19: 9,974,446 (GRCm39) |
Y33H |
probably damaging |
Het |
Cacna1s |
C |
A |
1: 136,005,431 (GRCm39) |
N405K |
probably benign |
Het |
Casp7 |
T |
C |
19: 56,421,741 (GRCm39) |
Y60H |
probably damaging |
Het |
Ccdc61 |
T |
C |
7: 18,626,488 (GRCm39) |
N367S |
possibly damaging |
Het |
Cnksr3 |
A |
T |
10: 7,085,129 (GRCm39) |
|
probably null |
Het |
Col14a1 |
A |
C |
15: 55,308,044 (GRCm39) |
|
probably benign |
Het |
Cyp3a57 |
A |
T |
5: 145,323,784 (GRCm39) |
K424* |
probably null |
Het |
Dnai3 |
T |
C |
3: 145,786,184 (GRCm39) |
E366G |
probably damaging |
Het |
Ebf2 |
T |
A |
14: 67,475,008 (GRCm39) |
V81E |
probably benign |
Het |
Ehbp1 |
G |
T |
11: 21,964,945 (GRCm39) |
T1084K |
probably damaging |
Het |
Fastkd2 |
C |
T |
1: 63,770,953 (GRCm39) |
A103V |
possibly damaging |
Het |
Gtf3c2 |
T |
C |
5: 31,323,722 (GRCm39) |
K525E |
probably benign |
Het |
Hdac2 |
A |
G |
10: 36,873,003 (GRCm39) |
E287G |
probably damaging |
Het |
Ifi207 |
T |
A |
1: 173,555,208 (GRCm39) |
T832S |
possibly damaging |
Het |
Igf1 |
G |
C |
10: 87,700,722 (GRCm39) |
V49L |
probably damaging |
Het |
Lef1 |
A |
G |
3: 130,909,149 (GRCm39) |
D55G |
possibly damaging |
Het |
Lipo2 |
G |
T |
19: 33,698,407 (GRCm39) |
Y323* |
probably null |
Het |
Mettl24 |
C |
T |
10: 40,613,794 (GRCm39) |
R178C |
probably damaging |
Het |
Naa80 |
A |
G |
9: 107,460,225 (GRCm39) |
E40G |
probably damaging |
Het |
Ndrg4 |
C |
A |
8: 96,433,229 (GRCm39) |
C66* |
probably null |
Het |
Nemf |
A |
G |
12: 69,399,110 (GRCm39) |
V140A |
probably benign |
Het |
Nid2 |
T |
A |
14: 19,839,855 (GRCm39) |
F815I |
probably benign |
Het |
Or4c108 |
A |
G |
2: 88,804,143 (GRCm39) |
F31L |
probably benign |
Het |
Or5b106 |
A |
C |
19: 13,123,106 (GRCm39) |
S306A |
probably benign |
Het |
Or8b12c |
A |
C |
9: 37,716,141 (GRCm39) |
*311C |
probably null |
Het |
Or8b3b |
A |
T |
9: 38,584,355 (GRCm39) |
N141K |
possibly damaging |
Het |
Or8k30 |
A |
G |
2: 86,339,136 (GRCm39) |
E111G |
probably damaging |
Het |
Pcdhga3 |
T |
C |
18: 37,809,598 (GRCm39) |
S684P |
probably benign |
Het |
Plch1 |
A |
T |
3: 63,660,562 (GRCm39) |
C352* |
probably null |
Het |
Plscr2 |
G |
A |
9: 92,172,757 (GRCm39) |
V139I |
probably benign |
Het |
Ppa1 |
T |
A |
10: 61,508,182 (GRCm39) |
C270S |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,844,540 (GRCm39) |
M399L |
possibly damaging |
Het |
Scn3a |
A |
G |
2: 65,356,098 (GRCm39) |
V212A |
possibly damaging |
Het |
Serpina3b |
A |
G |
12: 104,099,285 (GRCm39) |
K267E |
probably benign |
Het |
Shroom3 |
A |
G |
5: 93,090,063 (GRCm39) |
T938A |
probably damaging |
Het |
Specc1 |
A |
C |
11: 62,023,279 (GRCm39) |
S115R |
probably benign |
Het |
Stim2 |
C |
T |
5: 54,210,787 (GRCm39) |
T74I |
probably benign |
Het |
Sult6b2 |
T |
A |
6: 142,750,025 (GRCm39) |
D31V |
possibly damaging |
Het |
Tbc1d24 |
A |
T |
17: 24,401,492 (GRCm39) |
W406R |
probably damaging |
Het |
Tmprss11b |
A |
G |
5: 86,811,245 (GRCm39) |
|
probably null |
Het |
Trappc9 |
A |
G |
15: 72,797,499 (GRCm39) |
Y575H |
possibly damaging |
Het |
Trim63 |
C |
T |
4: 134,050,412 (GRCm39) |
T232M |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,598,180 (GRCm39) |
S19578T |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Xpo4 |
T |
A |
14: 57,819,767 (GRCm39) |
E1139D |
probably benign |
Het |
|
Other mutations in Dpep3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Dpep3
|
APN |
8 |
106,705,779 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01078:Dpep3
|
APN |
8 |
106,704,860 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01543:Dpep3
|
APN |
8 |
106,702,814 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01996:Dpep3
|
APN |
8 |
106,701,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02036:Dpep3
|
APN |
8 |
106,700,417 (GRCm39) |
missense |
probably benign |
|
R0422:Dpep3
|
UTSW |
8 |
106,702,750 (GRCm39) |
critical splice donor site |
probably null |
|
R0627:Dpep3
|
UTSW |
8 |
106,705,363 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0747:Dpep3
|
UTSW |
8 |
106,704,018 (GRCm39) |
missense |
probably benign |
0.12 |
R1116:Dpep3
|
UTSW |
8 |
106,705,461 (GRCm39) |
missense |
probably damaging |
0.98 |
R1711:Dpep3
|
UTSW |
8 |
106,700,325 (GRCm39) |
missense |
probably benign |
0.01 |
R2085:Dpep3
|
UTSW |
8 |
106,701,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R4385:Dpep3
|
UTSW |
8 |
106,704,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R4860:Dpep3
|
UTSW |
8 |
106,702,821 (GRCm39) |
missense |
probably benign |
0.34 |
R4860:Dpep3
|
UTSW |
8 |
106,702,821 (GRCm39) |
missense |
probably benign |
0.34 |
R5784:Dpep3
|
UTSW |
8 |
106,705,375 (GRCm39) |
missense |
probably benign |
0.03 |
R6658:Dpep3
|
UTSW |
8 |
106,705,728 (GRCm39) |
missense |
probably benign |
|
R7536:Dpep3
|
UTSW |
8 |
106,704,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R9213:Dpep3
|
UTSW |
8 |
106,700,245 (GRCm39) |
missense |
probably benign |
0.15 |
R9528:Dpep3
|
UTSW |
8 |
106,704,251 (GRCm39) |
missense |
probably benign |
0.01 |
R9766:Dpep3
|
UTSW |
8 |
106,705,369 (GRCm39) |
missense |
probably damaging |
1.00 |
|