Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
C |
T |
6: 142,591,604 (GRCm39) |
|
probably benign |
Het |
Ankrd10 |
G |
T |
8: 11,685,482 (GRCm39) |
R46S |
possibly damaging |
Het |
Atp13a5 |
A |
G |
16: 29,085,681 (GRCm39) |
|
probably benign |
Het |
Baz1a |
A |
G |
12: 54,965,221 (GRCm39) |
|
probably null |
Het |
Bicd2 |
C |
T |
13: 49,533,346 (GRCm39) |
T644M |
probably damaging |
Het |
Ccr9 |
A |
T |
9: 123,609,035 (GRCm39) |
H239L |
probably benign |
Het |
Cd180 |
A |
T |
13: 102,842,408 (GRCm39) |
N485Y |
probably damaging |
Het |
Ces1d |
T |
A |
8: 93,919,400 (GRCm39) |
S131C |
probably damaging |
Het |
Cnpy2 |
T |
A |
10: 128,162,076 (GRCm39) |
S116R |
probably benign |
Het |
Crym |
T |
C |
7: 119,788,972 (GRCm39) |
K285R |
probably benign |
Het |
Cyp2a4 |
A |
T |
7: 26,012,293 (GRCm39) |
I359F |
possibly damaging |
Het |
Cyp2b10 |
T |
A |
7: 25,614,359 (GRCm39) |
|
probably benign |
Het |
Dcpp3 |
A |
T |
17: 24,136,925 (GRCm39) |
|
probably benign |
Het |
Dnah8 |
T |
A |
17: 30,927,364 (GRCm39) |
I1340K |
probably benign |
Het |
Fbln1 |
T |
C |
15: 85,111,277 (GRCm39) |
C144R |
probably damaging |
Het |
Gm1553 |
T |
C |
10: 82,328,010 (GRCm39) |
R66G |
unknown |
Het |
Il10rb |
G |
A |
16: 91,208,898 (GRCm39) |
V103I |
probably benign |
Het |
Irak1bp1 |
T |
A |
9: 82,728,614 (GRCm39) |
W182R |
probably benign |
Het |
Kcna3 |
T |
C |
3: 106,944,315 (GRCm39) |
S193P |
probably damaging |
Het |
Kif14 |
C |
T |
1: 136,410,156 (GRCm39) |
H628Y |
probably damaging |
Het |
Krt31 |
A |
G |
11: 99,941,079 (GRCm39) |
L77P |
probably damaging |
Het |
Krt36 |
C |
T |
11: 99,994,940 (GRCm39) |
A211T |
possibly damaging |
Het |
L3mbtl2 |
C |
T |
15: 81,552,942 (GRCm39) |
A125V |
probably damaging |
Het |
Lmo7 |
A |
G |
14: 102,137,892 (GRCm39) |
T743A |
probably benign |
Het |
Lyst |
C |
T |
13: 13,821,664 (GRCm39) |
T1346M |
probably benign |
Het |
Mapkbp1 |
T |
A |
2: 119,843,384 (GRCm39) |
|
probably null |
Het |
Mif |
T |
C |
10: 75,695,638 (GRCm39) |
D55G |
probably benign |
Het |
Mlh3 |
G |
T |
12: 85,314,361 (GRCm39) |
C608* |
probably null |
Het |
Mlip |
A |
T |
9: 77,146,859 (GRCm39) |
C85S |
probably benign |
Het |
Mug1 |
T |
C |
6: 121,826,809 (GRCm39) |
S211P |
possibly damaging |
Het |
Mybl2 |
T |
A |
2: 162,903,528 (GRCm39) |
|
probably benign |
Het |
Myh8 |
C |
T |
11: 67,196,843 (GRCm39) |
|
probably benign |
Het |
Nanos1 |
A |
G |
19: 60,745,368 (GRCm39) |
Y222C |
probably damaging |
Het |
Or10ag52 |
A |
T |
2: 87,044,037 (GRCm39) |
Y267F |
probably benign |
Het |
Or2n1e |
G |
T |
17: 38,585,774 (GRCm39) |
M37I |
probably benign |
Het |
Or5d16 |
T |
C |
2: 87,773,909 (GRCm39) |
D21G |
possibly damaging |
Het |
Papolb |
A |
G |
5: 142,515,211 (GRCm39) |
V144A |
probably damaging |
Het |
Pctp |
A |
G |
11: 89,876,945 (GRCm39) |
S185P |
probably benign |
Het |
Plod1 |
A |
T |
4: 148,003,298 (GRCm39) |
L509Q |
probably null |
Het |
Ppp1r13b |
C |
A |
12: 111,802,122 (GRCm39) |
M290I |
probably benign |
Het |
Ralb |
G |
C |
1: 119,405,856 (GRCm39) |
|
probably null |
Het |
Rxylt1 |
T |
C |
10: 121,931,841 (GRCm39) |
|
probably benign |
Het |
Slc4a8 |
T |
A |
15: 100,672,519 (GRCm39) |
D18E |
probably damaging |
Het |
Speg |
A |
C |
1: 75,400,568 (GRCm39) |
H2576P |
possibly damaging |
Het |
Spock1 |
T |
C |
13: 57,588,349 (GRCm39) |
D241G |
probably damaging |
Het |
Tcam1 |
T |
A |
11: 106,175,040 (GRCm39) |
V165E |
probably benign |
Het |
Thbs1 |
T |
A |
2: 117,943,472 (GRCm39) |
V30E |
possibly damaging |
Het |
Tll2 |
A |
G |
19: 41,077,265 (GRCm39) |
Y834H |
possibly damaging |
Het |
Trpm6 |
G |
A |
19: 18,756,008 (GRCm39) |
D84N |
probably damaging |
Het |
Ubr1 |
T |
A |
2: 120,737,427 (GRCm39) |
Q1039L |
probably damaging |
Het |
Ubr4 |
A |
G |
4: 139,138,171 (GRCm39) |
|
probably benign |
Het |
Vmn1r74 |
T |
C |
7: 11,581,242 (GRCm39) |
Y181H |
possibly damaging |
Het |
Vmn2r13 |
T |
C |
5: 109,304,395 (GRCm39) |
T679A |
probably benign |
Het |
Vmn2r91 |
A |
T |
17: 18,325,712 (GRCm39) |
Y110F |
probably damaging |
Het |
Zbtb40 |
A |
C |
4: 136,745,842 (GRCm39) |
S64A |
probably benign |
Het |
Zfp184 |
T |
A |
13: 22,131,252 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Akr1b7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01402:Akr1b7
|
APN |
6 |
34,398,052 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02006:Akr1b7
|
APN |
6 |
34,392,385 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02238:Akr1b7
|
APN |
6 |
34,392,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R1809:Akr1b7
|
UTSW |
6 |
34,396,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R2114:Akr1b7
|
UTSW |
6 |
34,395,929 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2115:Akr1b7
|
UTSW |
6 |
34,395,929 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2117:Akr1b7
|
UTSW |
6 |
34,395,929 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4277:Akr1b7
|
UTSW |
6 |
34,397,955 (GRCm39) |
intron |
probably benign |
|
R5396:Akr1b7
|
UTSW |
6 |
34,389,411 (GRCm39) |
critical splice donor site |
probably null |
|
R5504:Akr1b7
|
UTSW |
6 |
34,396,453 (GRCm39) |
splice site |
probably null |
|
R6181:Akr1b7
|
UTSW |
6 |
34,392,313 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6657:Akr1b7
|
UTSW |
6 |
34,393,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R6815:Akr1b7
|
UTSW |
6 |
34,389,269 (GRCm39) |
splice site |
probably null |
|
R7211:Akr1b7
|
UTSW |
6 |
34,398,049 (GRCm39) |
missense |
probably benign |
0.39 |
R7246:Akr1b7
|
UTSW |
6 |
34,392,404 (GRCm39) |
missense |
probably benign |
0.04 |
R7417:Akr1b7
|
UTSW |
6 |
34,394,300 (GRCm39) |
splice site |
probably null |
|
R7572:Akr1b7
|
UTSW |
6 |
34,396,343 (GRCm39) |
missense |
probably damaging |
0.99 |
R7608:Akr1b7
|
UTSW |
6 |
34,397,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R9068:Akr1b7
|
UTSW |
6 |
34,395,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R9468:Akr1b7
|
UTSW |
6 |
34,392,316 (GRCm39) |
missense |
probably benign |
0.02 |
|