Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930438A08Rik |
T |
G |
11: 58,180,594 (GRCm39) |
|
probably null |
Het |
Adra2c |
G |
A |
5: 35,438,143 (GRCm39) |
R305Q |
probably benign |
Het |
Ahnak |
A |
G |
19: 9,014,617 (GRCm39) |
D147G |
|
Het |
Arhgap30 |
T |
A |
1: 171,225,114 (GRCm39) |
S57T |
probably damaging |
Het |
Aspm |
T |
C |
1: 139,408,607 (GRCm39) |
I2498T |
probably damaging |
Het |
Atr |
C |
T |
9: 95,792,610 (GRCm39) |
A1644V |
possibly damaging |
Het |
Cc2d1a |
G |
T |
8: 84,870,744 (GRCm39) |
D101E |
probably benign |
Het |
Cntfr |
A |
G |
4: 41,661,995 (GRCm39) |
L249P |
probably damaging |
Het |
D130043K22Rik |
T |
C |
13: 25,071,876 (GRCm39) |
I940T |
possibly damaging |
Het |
Dnah12 |
T |
G |
14: 26,572,494 (GRCm39) |
C2862G |
probably null |
Het |
Dnah8 |
CGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTT |
CGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTT |
17: 30,979,841 (GRCm39) |
|
probably null |
Het |
Dnah9 |
A |
G |
11: 65,976,309 (GRCm39) |
F1247L |
possibly damaging |
Het |
Dpp10 |
T |
C |
1: 123,264,611 (GRCm39) |
Q737R |
probably damaging |
Het |
Dpp3 |
A |
G |
19: 4,959,897 (GRCm39) |
V673A |
possibly damaging |
Het |
Eif2a |
A |
T |
3: 58,448,467 (GRCm39) |
K100I |
possibly damaging |
Het |
Flnc |
C |
A |
6: 29,461,109 (GRCm39) |
N2694K |
probably damaging |
Het |
Fv1 |
T |
A |
4: 147,953,768 (GRCm39) |
D111E |
possibly damaging |
Het |
Gcnt3 |
G |
A |
9: 69,941,569 (GRCm39) |
A333V |
probably damaging |
Het |
Gpr151 |
T |
C |
18: 42,712,710 (GRCm39) |
|
probably benign |
Het |
Gxylt2 |
A |
G |
6: 100,727,416 (GRCm39) |
T177A |
probably benign |
Het |
Hnmt |
G |
A |
2: 23,893,880 (GRCm39) |
L205F |
possibly damaging |
Het |
Ikbkb |
A |
T |
8: 23,172,740 (GRCm39) |
|
probably null |
Het |
Ikzf2 |
T |
C |
1: 69,578,337 (GRCm39) |
S391G |
probably benign |
Het |
Kif26a |
C |
T |
12: 112,140,286 (GRCm39) |
T505M |
probably damaging |
Het |
Kif3b |
A |
T |
2: 153,159,460 (GRCm39) |
K420N |
probably benign |
Het |
Kmt2a |
A |
G |
9: 44,730,294 (GRCm39) |
V3341A |
unknown |
Het |
Lce1i |
T |
C |
3: 92,685,081 (GRCm39) |
K32E |
unknown |
Het |
Lmf1 |
A |
G |
17: 25,881,514 (GRCm39) |
Y521C |
probably damaging |
Het |
Mki67 |
C |
T |
7: 135,305,913 (GRCm39) |
C655Y |
probably damaging |
Het |
Morc3 |
T |
A |
16: 93,667,401 (GRCm39) |
V593E |
probably benign |
Het |
Muc16 |
A |
G |
9: 18,497,314 (GRCm39) |
F6613L |
probably benign |
Het |
Naip1 |
G |
A |
13: 100,563,101 (GRCm39) |
T688I |
probably benign |
Het |
Or2n1d |
T |
A |
17: 38,646,540 (GRCm39) |
L164* |
probably null |
Het |
Otop2 |
T |
A |
11: 115,214,503 (GRCm39) |
C87S |
probably benign |
Het |
Picalm |
T |
A |
7: 89,810,484 (GRCm39) |
L97* |
probably null |
Het |
Pik3c2g |
T |
A |
6: 139,606,768 (GRCm39) |
W272R |
probably damaging |
Het |
Plekhg4 |
G |
A |
8: 106,101,398 (GRCm39) |
G20R |
unknown |
Het |
Ppp1r35 |
G |
A |
5: 137,777,304 (GRCm39) |
A17T |
unknown |
Het |
Ppp2r5e |
A |
T |
12: 75,509,167 (GRCm39) |
Y371N |
possibly damaging |
Het |
Rtl1 |
T |
C |
12: 109,556,973 (GRCm39) |
E1622G |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 28,723,600 (GRCm39) |
E4181G |
probably damaging |
Het |
Saxo1 |
C |
A |
4: 86,397,132 (GRCm39) |
M135I |
probably benign |
Het |
Shank2 |
C |
A |
7: 143,964,183 (GRCm39) |
P597Q |
possibly damaging |
Het |
Shld2 |
G |
A |
14: 33,971,245 (GRCm39) |
Q547* |
probably null |
Het |
Slc44a1 |
G |
A |
4: 53,542,389 (GRCm39) |
V308I |
probably benign |
Het |
Slc6a21 |
A |
G |
7: 44,937,785 (GRCm39) |
H367R |
probably benign |
Het |
Snx11 |
G |
T |
11: 96,660,023 (GRCm39) |
T222K |
probably benign |
Het |
Snx4 |
C |
T |
16: 33,112,228 (GRCm39) |
Q388* |
probably null |
Het |
Sulf1 |
T |
C |
1: 12,918,622 (GRCm39) |
L831P |
probably damaging |
Het |
Ugt2a3 |
A |
T |
5: 87,485,018 (GRCm39) |
V2D |
|
Het |
Unc5c |
T |
C |
3: 141,494,683 (GRCm39) |
V406A |
possibly damaging |
Het |
Unc5d |
A |
C |
8: 29,365,639 (GRCm39) |
N115K |
probably damaging |
Het |
Usp28 |
C |
A |
9: 48,947,026 (GRCm39) |
T819N |
probably damaging |
Het |
Usp42 |
T |
C |
5: 143,702,704 (GRCm39) |
D639G |
possibly damaging |
Het |
Vmn2r102 |
T |
A |
17: 19,897,564 (GRCm39) |
M193K |
possibly damaging |
Het |
Vmn2r12 |
A |
G |
5: 109,239,823 (GRCm39) |
Y247H |
probably damaging |
Het |
Vps13d |
T |
C |
4: 144,822,814 (GRCm39) |
D2989G |
|
Het |
Vsig2 |
A |
G |
9: 37,455,335 (GRCm39) |
E295G |
probably benign |
Het |
Wdfy3 |
T |
A |
5: 102,055,333 (GRCm39) |
N1579I |
probably benign |
Het |
Zfp521 |
T |
C |
18: 13,980,173 (GRCm39) |
D80G |
possibly damaging |
Het |
Zfp663 |
A |
C |
2: 165,195,607 (GRCm39) |
L204R |
probably damaging |
Het |
|
Other mutations in Rexo1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00970:Rexo1
|
APN |
10 |
80,386,798 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01128:Rexo1
|
APN |
10 |
80,385,573 (GRCm39) |
missense |
probably benign |
|
IGL01890:Rexo1
|
APN |
10 |
80,378,845 (GRCm39) |
missense |
possibly damaging |
0.85 |
PIT4453001:Rexo1
|
UTSW |
10 |
80,386,231 (GRCm39) |
missense |
probably damaging |
0.97 |
R0044:Rexo1
|
UTSW |
10 |
80,380,212 (GRCm39) |
missense |
probably benign |
0.16 |
R0365:Rexo1
|
UTSW |
10 |
80,378,410 (GRCm39) |
missense |
probably damaging |
0.99 |
R0573:Rexo1
|
UTSW |
10 |
80,380,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R1146:Rexo1
|
UTSW |
10 |
80,380,239 (GRCm39) |
missense |
probably benign |
0.04 |
R1146:Rexo1
|
UTSW |
10 |
80,380,239 (GRCm39) |
missense |
probably benign |
0.04 |
R1511:Rexo1
|
UTSW |
10 |
80,385,884 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1523:Rexo1
|
UTSW |
10 |
80,378,585 (GRCm39) |
missense |
probably benign |
0.41 |
R1807:Rexo1
|
UTSW |
10 |
80,378,413 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1868:Rexo1
|
UTSW |
10 |
80,378,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:Rexo1
|
UTSW |
10 |
80,386,303 (GRCm39) |
missense |
probably benign |
0.00 |
R1936:Rexo1
|
UTSW |
10 |
80,386,303 (GRCm39) |
missense |
probably benign |
0.00 |
R1957:Rexo1
|
UTSW |
10 |
80,379,200 (GRCm39) |
missense |
probably damaging |
0.96 |
R2084:Rexo1
|
UTSW |
10 |
80,397,100 (GRCm39) |
missense |
probably benign |
0.01 |
R2153:Rexo1
|
UTSW |
10 |
80,379,943 (GRCm39) |
nonsense |
probably null |
|
R2262:Rexo1
|
UTSW |
10 |
80,385,403 (GRCm39) |
missense |
probably benign |
0.02 |
R4471:Rexo1
|
UTSW |
10 |
80,378,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R4472:Rexo1
|
UTSW |
10 |
80,378,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R4690:Rexo1
|
UTSW |
10 |
80,382,255 (GRCm39) |
missense |
probably benign |
0.01 |
R4972:Rexo1
|
UTSW |
10 |
80,385,527 (GRCm39) |
missense |
probably damaging |
0.96 |
R6335:Rexo1
|
UTSW |
10 |
80,379,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R6505:Rexo1
|
UTSW |
10 |
80,378,845 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6615:Rexo1
|
UTSW |
10 |
80,379,848 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6949:Rexo1
|
UTSW |
10 |
80,386,470 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7612:Rexo1
|
UTSW |
10 |
80,385,497 (GRCm39) |
missense |
probably benign |
0.40 |
R7807:Rexo1
|
UTSW |
10 |
80,385,970 (GRCm39) |
missense |
probably benign |
0.09 |
R7840:Rexo1
|
UTSW |
10 |
80,386,572 (GRCm39) |
missense |
probably benign |
|
R8779:Rexo1
|
UTSW |
10 |
80,384,292 (GRCm39) |
missense |
probably benign |
0.26 |
R8897:Rexo1
|
UTSW |
10 |
80,378,437 (GRCm39) |
missense |
probably damaging |
0.98 |
R8995:Rexo1
|
UTSW |
10 |
80,386,095 (GRCm39) |
missense |
probably damaging |
0.96 |
R9094:Rexo1
|
UTSW |
10 |
80,378,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R9411:Rexo1
|
UTSW |
10 |
80,397,248 (GRCm39) |
missense |
|
|
R9438:Rexo1
|
UTSW |
10 |
80,378,848 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9648:Rexo1
|
UTSW |
10 |
80,385,540 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Rexo1
|
UTSW |
10 |
80,385,609 (GRCm39) |
missense |
probably damaging |
1.00 |
|