Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abat |
A |
T |
16: 8,618,531 |
K414* |
probably null |
Het |
Aco1 |
T |
A |
4: 40,186,376 |
I596N |
probably damaging |
Het |
Adgre1 |
A |
C |
17: 57,410,945 |
D319A |
probably damaging |
Het |
BC067074 |
C |
T |
13: 113,351,750 |
T102I |
probably benign |
Het |
Birc6 |
T |
C |
17: 74,609,345 |
V445A |
probably benign |
Het |
Btd |
A |
C |
14: 31,667,105 |
Q261P |
probably damaging |
Het |
Btd |
G |
T |
14: 31,667,106 |
Q261H |
possibly damaging |
Het |
C7 |
T |
A |
15: 5,045,682 |
Y176F |
probably benign |
Het |
Ccdc102a |
T |
C |
8: 94,909,803 |
S287G |
probably benign |
Het |
Ccdc178 |
T |
A |
18: 22,150,438 |
T12S |
probably benign |
Het |
Cnga4 |
G |
T |
7: 105,405,829 |
A104S |
probably benign |
Het |
Col10a1 |
G |
T |
10: 34,394,951 |
L306F |
probably damaging |
Het |
Cpne5 |
T |
C |
17: 29,226,222 |
D36G |
probably damaging |
Het |
Cstl1 |
A |
G |
2: 148,755,303 |
M75V |
probably benign |
Het |
Cyp26a1 |
T |
C |
19: 37,698,812 |
L149P |
probably damaging |
Het |
D630045J12Rik |
T |
G |
6: 38,194,635 |
E866A |
probably benign |
Het |
Dlec1 |
C |
T |
9: 119,112,422 |
P292L |
probably benign |
Het |
Dpp3 |
T |
G |
19: 4,916,789 |
E402A |
possibly damaging |
Het |
Egf |
T |
C |
3: 129,718,064 |
|
probably null |
Het |
Epha5 |
T |
C |
5: 84,416,462 |
Q15R |
possibly damaging |
Het |
Esyt3 |
A |
G |
9: 99,315,285 |
F831L |
probably benign |
Het |
Fam50b |
G |
A |
13: 34,747,101 |
E187K |
possibly damaging |
Het |
Fut7 |
A |
G |
2: 25,425,780 |
D350G |
probably benign |
Het |
Gab1 |
C |
A |
8: 80,784,817 |
E466D |
probably damaging |
Het |
Glrp1 |
A |
T |
1: 88,503,168 |
M160K |
unknown |
Het |
Gngt1 |
T |
C |
6: 3,994,088 |
|
probably null |
Het |
Gprc6a |
A |
T |
10: 51,631,412 |
V7E |
possibly damaging |
Het |
Idh3b |
A |
T |
2: 130,280,966 |
V301D |
probably damaging |
Het |
Ifi202b |
A |
C |
1: 173,963,958 |
C385G |
probably benign |
Het |
Ilvbl |
T |
A |
10: 78,579,086 |
L261Q |
probably damaging |
Het |
Irx6 |
T |
A |
8: 92,678,734 |
L410Q |
probably damaging |
Het |
Ism2 |
T |
C |
12: 87,299,663 |
M15V |
unknown |
Het |
Itih5 |
C |
A |
2: 10,190,327 |
R177S |
probably damaging |
Het |
Klra3 |
C |
T |
6: 130,327,124 |
G202R |
probably damaging |
Het |
Krt7 |
T |
C |
15: 101,413,970 |
V103A |
probably damaging |
Het |
Lama3 |
T |
C |
18: 12,528,418 |
S2145P |
probably damaging |
Het |
Mlph |
A |
G |
1: 90,941,706 |
R477G |
probably damaging |
Het |
Mybpc1 |
T |
A |
10: 88,543,719 |
L653F |
probably damaging |
Het |
Myrfl |
A |
G |
10: 116,781,947 |
|
probably null |
Het |
Myrip |
T |
G |
9: 120,422,507 |
L232R |
probably damaging |
Het |
Nrd1 |
A |
T |
4: 109,028,802 |
H126L |
probably benign |
Het |
Olfr251 |
T |
A |
9: 38,378,802 |
L307Q |
possibly damaging |
Het |
Olfr469 |
G |
T |
7: 107,823,158 |
L104I |
probably benign |
Het |
Olfr722 |
A |
T |
14: 49,895,667 |
I45N |
probably damaging |
Het |
Pcdhb10 |
T |
A |
18: 37,413,003 |
N377K |
probably damaging |
Het |
Pigt |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
2: 164,499,669 |
|
probably null |
Het |
Prkdc |
A |
C |
16: 15,769,966 |
I2572L |
probably benign |
Het |
Ptpro |
C |
A |
6: 137,380,478 |
D322E |
probably benign |
Het |
R3hcc1 |
A |
G |
14: 69,704,125 |
I332T |
probably damaging |
Het |
Rab8a |
T |
C |
8: 72,161,383 |
F9L |
probably damaging |
Het |
Ranbp3l |
A |
T |
15: 9,057,160 |
K165N |
probably damaging |
Het |
Rock2 |
T |
A |
12: 16,977,740 |
C1353S |
probably damaging |
Het |
Rsad2 |
T |
A |
12: 26,456,419 |
M1L |
possibly damaging |
Het |
Tymp |
A |
T |
15: 89,376,281 |
|
probably null |
Het |
Vmn1r104 |
A |
G |
7: 20,534,566 |
M244V |
probably benign |
Het |
Vmn1r232 |
G |
A |
17: 20,913,285 |
T351M |
possibly damaging |
Het |
Vmn2r50 |
A |
G |
7: 10,050,245 |
Y101H |
probably benign |
Het |
Vmn2r57 |
A |
G |
7: 41,428,665 |
L123P |
probably damaging |
Het |
Wdr17 |
T |
C |
8: 54,681,453 |
N331D |
probably damaging |
Het |
Wdr47 |
C |
T |
3: 108,614,355 |
Q89* |
probably null |
Het |
Zcchc4 |
A |
T |
5: 52,784,033 |
T57S |
probably benign |
Het |
|