Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
T |
7: 119,807,106 (GRCm39) |
T51S |
probably benign |
Het |
Abcc1 |
A |
G |
16: 14,214,336 (GRCm39) |
D204G |
possibly damaging |
Het |
Acaa1b |
C |
T |
9: 118,980,915 (GRCm39) |
E172K |
probably benign |
Het |
Adamts5 |
G |
A |
16: 85,696,806 (GRCm39) |
T117I |
probably benign |
Het |
Alg9 |
C |
T |
9: 50,690,361 (GRCm39) |
A121V |
probably damaging |
Het |
Atf7ip2 |
T |
C |
16: 10,027,032 (GRCm39) |
I100T |
possibly damaging |
Het |
Calm2 |
T |
C |
17: 87,750,165 (GRCm39) |
|
probably null |
Het |
Cfap44 |
A |
T |
16: 44,301,775 (GRCm39) |
M1838L |
probably benign |
Het |
Cym |
A |
G |
3: 107,127,009 (GRCm39) |
Y49H |
probably benign |
Het |
Dchs1 |
G |
A |
7: 105,404,338 (GRCm39) |
R2735* |
probably null |
Het |
Dnajc6 |
T |
C |
4: 101,463,808 (GRCm39) |
I187T |
probably benign |
Het |
Fam151a |
G |
T |
4: 106,592,725 (GRCm39) |
R69L |
possibly damaging |
Het |
Gm4779 |
TCGGGGCCGGGGCCGGGGCCG |
TCGGGGCCGGGGCCGGGGCCGGGGCCG |
X: 100,837,777 (GRCm39) |
|
probably benign |
Het |
Gm9922 |
C |
A |
14: 101,966,961 (GRCm39) |
G97V |
unknown |
Het |
Hacl1 |
A |
T |
14: 31,338,443 (GRCm39) |
M378K |
probably damaging |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Ighv1-82 |
A |
T |
12: 115,916,574 (GRCm39) |
I6N |
possibly damaging |
Het |
Kctd19 |
A |
C |
8: 106,109,616 (GRCm39) |
V942G |
probably benign |
Het |
Lce1l |
C |
T |
3: 92,757,483 (GRCm39) |
C125Y |
unknown |
Het |
Mmp8 |
T |
C |
9: 7,560,449 (GRCm39) |
F42S |
probably damaging |
Het |
Myom2 |
T |
C |
8: 15,148,411 (GRCm39) |
L529P |
probably damaging |
Het |
Nectin3 |
A |
T |
16: 46,268,759 (GRCm39) |
Y548N |
probably damaging |
Het |
Olfml3 |
T |
C |
3: 103,643,176 (GRCm39) |
K402E |
probably damaging |
Het |
Or4c12b |
T |
C |
2: 89,646,865 (GRCm39) |
F59S |
probably damaging |
Het |
Or6aa1 |
T |
A |
7: 86,044,131 (GRCm39) |
T192S |
probably damaging |
Het |
Otof |
T |
A |
5: 30,545,614 (GRCm39) |
I514F |
probably damaging |
Het |
Pira12 |
T |
A |
7: 3,898,264 (GRCm39) |
I353F |
possibly damaging |
Het |
Plch1 |
G |
T |
3: 63,623,458 (GRCm39) |
S603* |
probably null |
Het |
Ppa1 |
T |
A |
10: 61,502,691 (GRCm39) |
D171E |
probably benign |
Het |
Pramel23 |
C |
A |
4: 143,425,075 (GRCm39) |
D123Y |
probably benign |
Het |
Prss34 |
T |
C |
17: 25,518,737 (GRCm39) |
C240R |
probably damaging |
Het |
Ptpre |
A |
G |
7: 135,285,016 (GRCm39) |
D714G |
probably damaging |
Het |
Ranbp9 |
A |
G |
13: 43,633,936 (GRCm39) |
F157L |
probably benign |
Het |
Rbbp6 |
A |
G |
7: 122,600,417 (GRCm39) |
K1475E |
unknown |
Het |
Retnlg |
A |
G |
16: 48,693,237 (GRCm39) |
N5D |
probably benign |
Het |
Rev1 |
T |
C |
1: 38,092,185 (GRCm39) |
T1245A |
probably damaging |
Het |
Rngtt |
G |
T |
4: 33,362,927 (GRCm39) |
L360F |
probably damaging |
Het |
Scrib |
A |
C |
15: 75,936,610 (GRCm39) |
V447G |
probably damaging |
Het |
Slc22a6 |
C |
A |
19: 8,598,684 (GRCm39) |
A247E |
possibly damaging |
Het |
Slc25a20 |
G |
A |
9: 108,539,343 (GRCm39) |
|
probably benign |
Het |
Spag16 |
T |
A |
1: 69,958,585 (GRCm39) |
|
probably null |
Het |
Stx3 |
C |
T |
19: 11,767,412 (GRCm39) |
W87* |
probably null |
Het |
Syngap1 |
T |
A |
17: 27,181,961 (GRCm39) |
M1158K |
possibly damaging |
Het |
Tmed9 |
C |
A |
13: 55,741,107 (GRCm39) |
H41N |
possibly damaging |
Het |
Trav15-2-dv6-2 |
G |
A |
14: 53,887,242 (GRCm39) |
S54N |
probably benign |
Het |
Tyk2 |
C |
T |
9: 21,020,156 (GRCm39) |
V1001I |
probably benign |
Het |
Ugt8a |
A |
G |
3: 125,709,065 (GRCm39) |
V15A |
probably benign |
Het |
Uhrf2 |
A |
G |
19: 30,065,949 (GRCm39) |
E661G |
probably benign |
Het |
Vmn2r77 |
T |
A |
7: 86,449,979 (GRCm39) |
I75N |
probably benign |
Het |
Zfp346 |
T |
G |
13: 55,278,416 (GRCm39) |
V258G |
probably damaging |
Het |
Zfp87 |
T |
A |
13: 74,520,513 (GRCm39) |
K188N |
possibly damaging |
Het |
Zgrf1 |
C |
A |
3: 127,377,299 (GRCm39) |
S848* |
probably null |
Het |
|
Other mutations in Agmat |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02870:Agmat
|
APN |
4 |
141,474,253 (GRCm39) |
missense |
probably benign |
0.02 |
3-1:Agmat
|
UTSW |
4 |
141,476,921 (GRCm39) |
missense |
possibly damaging |
0.49 |
3-1:Agmat
|
UTSW |
4 |
141,476,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R1635:Agmat
|
UTSW |
4 |
141,474,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R2103:Agmat
|
UTSW |
4 |
141,483,214 (GRCm39) |
missense |
probably damaging |
0.97 |
R2215:Agmat
|
UTSW |
4 |
141,476,899 (GRCm39) |
missense |
probably benign |
0.01 |
R3767:Agmat
|
UTSW |
4 |
141,483,273 (GRCm39) |
missense |
probably benign |
0.00 |
R4379:Agmat
|
UTSW |
4 |
141,484,802 (GRCm39) |
missense |
probably benign |
0.10 |
R5422:Agmat
|
UTSW |
4 |
141,483,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R5640:Agmat
|
UTSW |
4 |
141,483,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R5750:Agmat
|
UTSW |
4 |
141,476,998 (GRCm39) |
missense |
probably benign |
0.03 |
R6728:Agmat
|
UTSW |
4 |
141,476,897 (GRCm39) |
missense |
probably benign |
0.00 |
R6891:Agmat
|
UTSW |
4 |
141,483,192 (GRCm39) |
missense |
probably benign |
0.01 |
R7293:Agmat
|
UTSW |
4 |
141,483,246 (GRCm39) |
nonsense |
probably null |
|
R7361:Agmat
|
UTSW |
4 |
141,474,163 (GRCm39) |
missense |
probably benign |
0.23 |
R7585:Agmat
|
UTSW |
4 |
141,477,056 (GRCm39) |
missense |
probably benign |
0.09 |
R8832:Agmat
|
UTSW |
4 |
141,474,320 (GRCm39) |
missense |
probably benign |
0.08 |
R9288:Agmat
|
UTSW |
4 |
141,474,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R9400:Agmat
|
UTSW |
4 |
141,476,981 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Agmat
|
UTSW |
4 |
141,474,290 (GRCm39) |
missense |
possibly damaging |
0.72 |
|