Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932431P20Rik |
C |
A |
7: 29,537,463 |
|
noncoding transcript |
Het |
5430419D17Rik |
T |
A |
7: 131,243,107 |
Y692* |
probably null |
Het |
Acad11 |
A |
G |
9: 104,126,656 |
E649G |
probably damaging |
Het |
Adgre1 |
C |
A |
17: 57,419,335 |
T402K |
probably benign |
Het |
Agap3 |
A |
G |
5: 24,501,002 |
|
probably benign |
Het |
Amy1 |
T |
C |
3: 113,556,040 |
I494V |
probably benign |
Het |
Arhgef40 |
G |
A |
14: 51,991,698 |
|
probably null |
Het |
Atp2c2 |
T |
C |
8: 119,745,590 |
V461A |
probably benign |
Het |
Bub1 |
A |
G |
2: 127,810,663 |
S595P |
probably damaging |
Het |
Cnbd1 |
T |
C |
4: 18,906,988 |
|
probably benign |
Het |
Cux1 |
A |
T |
5: 136,311,491 |
|
probably benign |
Het |
Dsg3 |
T |
A |
18: 20,523,607 |
I178N |
probably benign |
Het |
Dus2 |
T |
A |
8: 106,025,901 |
|
probably null |
Het |
Enpp1 |
G |
A |
10: 24,654,031 |
H570Y |
probably damaging |
Het |
Ephb3 |
A |
C |
16: 21,217,294 |
T57P |
probably benign |
Het |
Fat3 |
C |
A |
9: 15,999,094 |
V1871F |
possibly damaging |
Het |
Fbll1 |
T |
C |
11: 35,798,047 |
T130A |
probably benign |
Het |
Fbxl20 |
C |
T |
11: 98,110,974 |
S99N |
probably damaging |
Het |
Folr2 |
T |
C |
7: 101,840,386 |
E182G |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,555,221 |
D281G |
probably benign |
Het |
Gm17175 |
G |
T |
14: 51,573,069 |
Q34K |
possibly damaging |
Het |
Gm5592 |
T |
A |
7: 41,289,095 |
D600E |
probably damaging |
Het |
Gtf2e1 |
T |
C |
16: 37,515,730 |
E294G |
probably benign |
Het |
Gtf3c2 |
A |
G |
5: 31,170,173 |
|
probably benign |
Het |
Heg1 |
T |
C |
16: 33,710,607 |
L151P |
probably damaging |
Het |
Hmcn2 |
T |
G |
2: 31,428,994 |
V3902G |
probably damaging |
Het |
Ift140 |
A |
G |
17: 25,018,802 |
Y4C |
probably damaging |
Het |
Ighv1-19 |
A |
C |
12: 114,708,949 |
V17G |
possibly damaging |
Het |
Iqca |
T |
A |
1: 90,045,657 |
I770F |
probably benign |
Het |
Jak3 |
T |
A |
8: 71,679,012 |
C115S |
probably benign |
Het |
Kif18b |
A |
T |
11: 102,914,675 |
M252K |
probably damaging |
Het |
Klhdc7a |
A |
T |
4: 139,966,925 |
V237D |
probably benign |
Het |
Klhl11 |
C |
T |
11: 100,463,205 |
V597I |
possibly damaging |
Het |
Krt72 |
T |
A |
15: 101,780,961 |
Y312F |
probably damaging |
Het |
Lonp2 |
T |
A |
8: 86,633,972 |
I191N |
probably damaging |
Het |
Npc2 |
A |
T |
12: 84,772,845 |
I8N |
possibly damaging |
Het |
Nr4a1 |
T |
C |
15: 101,272,788 |
L413P |
probably damaging |
Het |
Nup133 |
T |
C |
8: 123,911,906 |
N895S |
probably damaging |
Het |
Olfr869 |
T |
C |
9: 20,137,235 |
F40L |
probably benign |
Het |
Ppef1 |
A |
G |
X: 160,685,294 |
I94T |
probably benign |
Het |
Prrt4 |
G |
A |
6: 29,176,456 |
T290I |
probably benign |
Het |
Ptpru |
A |
T |
4: 131,772,616 |
V1239E |
probably damaging |
Het |
Rab8b |
T |
G |
9: 66,852,992 |
M117L |
probably benign |
Het |
S1pr5 |
T |
A |
9: 21,244,216 |
I305F |
possibly damaging |
Het |
Sdr39u1 |
A |
G |
14: 55,898,006 |
V160A |
probably damaging |
Het |
Slc6a21 |
C |
T |
7: 45,288,244 |
T653M |
probably benign |
Het |
Stk39 |
T |
A |
2: 68,211,958 |
E544D |
probably benign |
Het |
Tgfbr3 |
T |
C |
5: 107,142,501 |
T313A |
probably benign |
Het |
Tle6 |
A |
T |
10: 81,594,458 |
L287M |
probably damaging |
Het |
Tmc2 |
A |
G |
2: 130,264,012 |
H821R |
probably benign |
Het |
Tmem230 |
G |
T |
2: 132,245,977 |
D26E |
probably benign |
Het |
Tnfaip3 |
A |
G |
10: 19,005,137 |
F394S |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,811,377 |
L13458F |
probably damaging |
Het |
Vwa5a |
A |
T |
9: 38,723,379 |
N161I |
probably benign |
Het |
|