Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310061N02Rik |
T |
C |
16: 88,707,538 |
S124G |
possibly damaging |
Het |
4921539E11Rik |
T |
C |
4: 103,270,848 |
T27A |
probably benign |
Het |
Aspg |
T |
A |
12: 112,123,412 |
N461K |
probably benign |
Het |
B4galnt3 |
T |
A |
6: 120,218,967 |
T300S |
probably damaging |
Het |
BC035044 |
A |
G |
6: 128,885,007 |
|
probably benign |
Het |
Bmp5 |
C |
T |
9: 75,893,709 |
P374S |
probably damaging |
Het |
C330018D20Rik |
A |
T |
18: 56,957,856 |
F78L |
probably benign |
Het |
Cds2 |
T |
A |
2: 132,302,170 |
S289T |
probably benign |
Het |
Cerkl |
C |
T |
2: 79,341,335 |
C393Y |
probably damaging |
Het |
Ciita |
C |
T |
16: 10,523,792 |
R1020C |
probably damaging |
Het |
Dcaf13 |
C |
A |
15: 39,123,224 |
D130E |
probably benign |
Het |
Dnal4 |
C |
T |
15: 79,762,447 |
G50R |
probably damaging |
Het |
Elfn1 |
A |
G |
5: 139,971,568 |
N109S |
probably damaging |
Het |
Ep400 |
A |
G |
5: 110,676,554 |
V2435A |
unknown |
Het |
Fam178b |
T |
C |
1: 36,632,485 |
E185G |
probably damaging |
Het |
Fam227b |
C |
A |
2: 126,126,931 |
L74F |
probably benign |
Het |
Fam92b |
C |
A |
8: 120,167,303 |
|
probably null |
Het |
Fgfr4 |
G |
A |
13: 55,156,651 |
V138I |
probably benign |
Het |
Flnc |
A |
G |
6: 29,456,384 |
I2161V |
possibly damaging |
Het |
Frmd5 |
T |
C |
2: 121,562,909 |
N235S |
probably damaging |
Het |
Ggt6 |
A |
G |
11: 72,437,738 |
T355A |
possibly damaging |
Het |
Gm14393 |
G |
A |
2: 175,063,876 |
T41I |
probably damaging |
Het |
Gpr151 |
A |
C |
18: 42,578,867 |
S249A |
probably damaging |
Het |
Gpr152 |
T |
A |
19: 4,143,747 |
V429D |
probably benign |
Het |
Grm7 |
G |
A |
6: 111,358,426 |
M599I |
probably benign |
Het |
Hdac4 |
T |
A |
1: 91,972,790 |
R54* |
probably null |
Het |
Ice1 |
A |
G |
13: 70,592,650 |
L2146S |
probably damaging |
Het |
Igfbpl1 |
C |
T |
4: 45,815,588 |
V183I |
probably benign |
Het |
Kel |
G |
A |
6: 41,698,420 |
S299F |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,496,695 |
I1016T |
possibly damaging |
Het |
Lhx3 |
T |
C |
2: 26,201,118 |
D395G |
probably damaging |
Het |
Micu1 |
T |
C |
10: 59,750,521 |
Y140H |
possibly damaging |
Het |
Myt1l |
G |
A |
12: 29,832,332 |
G509R |
unknown |
Het |
Nbn |
C |
T |
4: 15,986,593 |
H665Y |
probably benign |
Het |
Pkhd1 |
G |
T |
1: 20,117,836 |
T3416K |
probably benign |
Het |
Plxnb1 |
T |
C |
9: 109,100,772 |
F232S |
probably damaging |
Het |
Pus7l |
T |
C |
15: 94,529,486 |
N472D |
probably damaging |
Het |
Rfx1 |
C |
T |
8: 84,082,720 |
Q225* |
probably null |
Het |
Rnase2a |
T |
C |
14: 51,255,563 |
Y115C |
possibly damaging |
Het |
Ryr1 |
T |
A |
7: 29,109,812 |
D386V |
probably benign |
Het |
Sfi1 |
A |
ATCTTCCCAAAGCCAGTGC |
11: 3,153,384 |
|
probably benign |
Homo |
Sgcz |
T |
A |
8: 37,639,984 |
T125S |
probably damaging |
Het |
Sntb1 |
C |
G |
15: 55,642,795 |
G461R |
probably damaging |
Het |
Syt2 |
A |
G |
1: 134,740,957 |
S36G |
probably benign |
Het |
Tcaf3 |
A |
G |
6: 42,597,185 |
L31P |
probably damaging |
Het |
Tenm3 |
C |
A |
8: 48,367,377 |
E142* |
probably null |
Het |
Tgfbr2 |
G |
T |
9: 116,131,601 |
S94R |
probably damaging |
Het |
Vmn2r12 |
A |
G |
5: 109,091,818 |
I293T |
probably damaging |
Het |
Wrap73 |
G |
A |
4: 154,145,274 |
R34Q |
probably damaging |
Het |
Zc3h14 |
A |
G |
12: 98,780,065 |
D511G |
possibly damaging |
Het |
Zcchc11 |
T |
A |
4: 108,491,412 |
I297N |
probably damaging |
Het |
|