Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
C |
A |
5: 63,898,469 |
P183T |
probably damaging |
Het |
6430573F11Rik |
G |
A |
8: 36,505,606 |
C70Y |
probably damaging |
Het |
Bcan |
G |
A |
3: 87,990,233 |
R682* |
probably null |
Het |
Bzw1 |
T |
A |
1: 58,404,259 |
L410Q |
probably damaging |
Het |
Cdh5 |
A |
T |
8: 104,113,040 |
I48F |
probably damaging |
Het |
Cdhr5 |
T |
C |
7: 141,274,057 |
N173D |
possibly damaging |
Het |
Cfap74 |
T |
C |
4: 155,429,171 |
M480T |
probably benign |
Het |
Col6a5 |
C |
T |
9: 105,940,012 |
A367T |
unknown |
Het |
Colca2 |
A |
G |
9: 51,270,655 |
F206L |
probably benign |
Het |
Cpsf1 |
A |
C |
15: 76,597,722 |
Y1064D |
possibly damaging |
Het |
Defb6 |
A |
T |
8: 19,228,074 |
H54L |
probably benign |
Het |
Dmtf1 |
A |
G |
5: 9,140,379 |
|
probably benign |
Het |
Dnah12 |
T |
C |
14: 26,734,603 |
L827S |
possibly damaging |
Het |
Dsc3 |
T |
C |
18: 20,001,865 |
T21A |
probably benign |
Het |
Epb41l1 |
G |
T |
2: 156,522,168 |
D866Y |
probably benign |
Het |
Epha1 |
T |
C |
6: 42,360,666 |
M860V |
probably damaging |
Het |
Far2 |
T |
C |
6: 148,173,409 |
L380P |
possibly damaging |
Het |
Fgd5 |
A |
G |
6: 91,989,299 |
I680V |
possibly damaging |
Het |
Fnbp4 |
T |
C |
2: 90,752,968 |
|
probably null |
Het |
Focad |
G |
A |
4: 88,359,905 |
|
probably null |
Het |
Gm14180 |
T |
A |
11: 99,730,313 |
|
probably benign |
Het |
Hbb-bh2 |
T |
C |
7: 103,840,415 |
T5A |
probably benign |
Het |
Ighv7-2 |
A |
G |
12: 113,912,480 |
F2L |
probably benign |
Het |
Igsf5 |
A |
G |
16: 96,364,081 |
T19A |
probably benign |
Het |
Kcnd3 |
C |
T |
3: 105,658,766 |
A421V |
probably damaging |
Het |
Klb |
A |
G |
5: 65,375,794 |
N482S |
probably benign |
Het |
Lipo2 |
A |
C |
19: 33,721,700 |
L310R |
probably damaging |
Het |
Mc3r |
A |
G |
2: 172,249,203 |
H115R |
possibly damaging |
Het |
Meioc |
A |
G |
11: 102,674,920 |
D398G |
possibly damaging |
Het |
Olfr1130 |
G |
A |
2: 87,607,392 |
M1I |
probably null |
Het |
Olfr1353 |
T |
C |
10: 78,970,317 |
S223P |
probably damaging |
Het |
Olfr683 |
A |
T |
7: 105,143,776 |
C172* |
probably null |
Het |
Pds5a |
T |
C |
5: 65,635,437 |
T718A |
probably benign |
Het |
Pdzd2 |
C |
T |
15: 12,385,637 |
D1016N |
possibly damaging |
Het |
Pla2g2c |
T |
C |
4: 138,734,408 |
|
probably null |
Het |
Plch1 |
T |
C |
3: 63,740,739 |
I404V |
probably damaging |
Het |
Ppp2r5c |
A |
T |
12: 110,580,522 |
D522V |
possibly damaging |
Het |
Prex2 |
T |
A |
1: 11,162,263 |
S851R |
probably benign |
Het |
Rapgef1 |
C |
T |
2: 29,719,656 |
P702S |
possibly damaging |
Het |
Rasal3 |
T |
A |
17: 32,391,385 |
D976V |
probably damaging |
Het |
Rasef |
A |
C |
4: 73,734,503 |
L587R |
probably damaging |
Het |
Rptn |
A |
T |
3: 93,396,511 |
R384* |
probably null |
Het |
Sema6a |
G |
A |
18: 47,306,457 |
|
probably benign |
Het |
Sycp2 |
G |
T |
2: 178,374,985 |
T608K |
probably damaging |
Het |
Syde1 |
C |
T |
10: 78,590,228 |
R35H |
probably benign |
Het |
Taf1 |
G |
T |
X: 101,543,059 |
M313I |
possibly damaging |
Het |
Taf15 |
A |
T |
11: 83,484,694 |
T31S |
probably benign |
Het |
Tktl2 |
T |
C |
8: 66,512,012 |
V74A |
probably damaging |
Het |
Tle4 |
A |
G |
19: 14,454,865 |
V489A |
probably damaging |
Het |
Tmem30a |
T |
C |
9: 79,777,285 |
H95R |
probably damaging |
Het |
Vmn1r75 |
C |
A |
7: 11,880,982 |
Q214K |
probably damaging |
Het |
Vps13c |
C |
T |
9: 67,910,193 |
T1049M |
probably benign |
Het |
Wdr78 |
T |
C |
4: 103,066,399 |
E411G |
probably benign |
Het |
Zfp37 |
T |
C |
4: 62,192,128 |
Q274R |
probably benign |
Het |
|