Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057N15Rik |
A |
T |
16: 88,570,496 (GRCm39) |
Y181* |
probably null |
Het |
Adgrf2 |
T |
G |
17: 43,025,271 (GRCm39) |
K71T |
possibly damaging |
Het |
Brca2 |
T |
A |
5: 150,464,076 (GRCm39) |
M1280K |
probably benign |
Het |
Card14 |
T |
C |
11: 119,224,405 (GRCm39) |
S541P |
possibly damaging |
Het |
Cd19 |
G |
T |
7: 126,013,496 (GRCm39) |
Q98K |
possibly damaging |
Het |
Ceacam5 |
T |
A |
7: 17,493,341 (GRCm39) |
I788N |
possibly damaging |
Het |
Cpne2 |
A |
T |
8: 95,284,048 (GRCm39) |
I290L |
probably benign |
Het |
Cpsf1 |
C |
T |
15: 76,481,209 (GRCm39) |
V1216I |
probably benign |
Het |
Csad |
G |
A |
15: 102,097,357 (GRCm39) |
|
probably benign |
Het |
Depdc7 |
T |
A |
2: 104,560,853 (GRCm39) |
Q47L |
probably benign |
Het |
Dnajc6 |
T |
A |
4: 101,455,123 (GRCm39) |
S105T |
probably benign |
Het |
Dsg4 |
C |
A |
18: 20,604,047 (GRCm39) |
P838Q |
probably damaging |
Het |
Efcab3 |
T |
A |
11: 104,999,647 (GRCm39) |
Y179N |
possibly damaging |
Het |
Egfr |
A |
T |
11: 16,809,025 (GRCm39) |
N73I |
possibly damaging |
Het |
Eya2 |
T |
C |
2: 165,529,657 (GRCm39) |
|
probably null |
Het |
Fubp1 |
A |
G |
3: 151,923,652 (GRCm39) |
Q123R |
possibly damaging |
Het |
Galns |
A |
G |
8: 123,311,693 (GRCm39) |
I439T |
possibly damaging |
Het |
Gm57858 |
A |
T |
3: 36,079,506 (GRCm39) |
S261R |
possibly damaging |
Het |
Gsdmd |
T |
G |
15: 75,736,803 (GRCm39) |
L140R |
probably damaging |
Het |
Hcrtr1 |
A |
G |
4: 130,029,478 (GRCm39) |
V201A |
possibly damaging |
Het |
Ildr2 |
T |
A |
1: 166,135,361 (GRCm39) |
M371K |
probably benign |
Het |
Kalrn |
G |
A |
16: 34,134,582 (GRCm39) |
T412I |
possibly damaging |
Het |
Kdm5b |
C |
T |
1: 134,552,656 (GRCm39) |
Q1211* |
probably null |
Het |
Loxhd1 |
T |
C |
18: 77,517,671 (GRCm39) |
S1840P |
possibly damaging |
Het |
Maml2 |
A |
G |
9: 13,617,781 (GRCm39) |
M376V |
probably benign |
Het |
Mgat4e |
T |
C |
1: 134,469,745 (GRCm39) |
T100A |
probably damaging |
Het |
Myo18b |
T |
A |
5: 113,013,168 (GRCm39) |
T812S |
possibly damaging |
Het |
Nanp |
T |
A |
2: 150,881,158 (GRCm39) |
E30V |
probably null |
Het |
Or2w1b |
G |
T |
13: 21,300,217 (GRCm39) |
M118I |
probably damaging |
Het |
Or4c107 |
T |
G |
2: 88,788,849 (GRCm39) |
L13R |
probably damaging |
Het |
Or5ac21 |
A |
T |
16: 59,123,990 (GRCm39) |
H158L |
probably damaging |
Het |
Parp3 |
T |
A |
9: 106,351,393 (GRCm39) |
N241I |
probably benign |
Het |
Piezo2 |
T |
C |
18: 63,175,610 (GRCm39) |
N1924D |
probably benign |
Het |
Pou1f1 |
A |
G |
16: 65,326,811 (GRCm39) |
N137S |
probably damaging |
Het |
Ptgdr |
A |
G |
14: 45,096,094 (GRCm39) |
M206T |
probably damaging |
Het |
Ptprd |
T |
C |
4: 76,004,696 (GRCm39) |
T20A |
probably benign |
Het |
Rexo1 |
G |
C |
10: 80,385,497 (GRCm39) |
S520R |
probably benign |
Het |
Sgip1 |
T |
A |
4: 102,727,005 (GRCm39) |
S94T |
probably benign |
Het |
Slc35e3 |
A |
G |
10: 117,576,785 (GRCm39) |
V182A |
probably benign |
Het |
Slfn2 |
A |
G |
11: 82,961,089 (GRCm39) |
E356G |
probably damaging |
Het |
Spry4 |
C |
A |
18: 38,722,982 (GRCm39) |
K260N |
probably damaging |
Het |
Sync |
A |
T |
4: 129,187,375 (GRCm39) |
M136L |
probably benign |
Het |
Tm7sf2 |
A |
G |
19: 6,120,638 (GRCm39) |
V425A |
probably benign |
Het |
Trim21 |
T |
A |
7: 102,208,742 (GRCm39) |
M326L |
probably benign |
Het |
Tubgcp2 |
T |
A |
7: 139,580,964 (GRCm39) |
K663M |
probably damaging |
Het |
Uggt1 |
T |
C |
1: 36,202,316 (GRCm39) |
I1094V |
probably damaging |
Het |
Urb1 |
A |
G |
16: 90,594,798 (GRCm39) |
S245P |
probably damaging |
Het |
Vwa3a |
A |
T |
7: 120,351,838 (GRCm39) |
D34V |
probably null |
Het |
Zbtb45 |
C |
T |
7: 12,741,326 (GRCm39) |
A311T |
possibly damaging |
Het |
Zfp655 |
T |
C |
5: 145,173,999 (GRCm39) |
S135P |
unknown |
Het |
|
Other mutations in Trim62 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01530:Trim62
|
APN |
4 |
128,778,252 (GRCm39) |
missense |
probably benign |
0.05 |
R0201:Trim62
|
UTSW |
4 |
128,796,343 (GRCm39) |
missense |
probably benign |
|
R0744:Trim62
|
UTSW |
4 |
128,778,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R1619:Trim62
|
UTSW |
4 |
128,803,281 (GRCm39) |
missense |
probably damaging |
0.98 |
R1834:Trim62
|
UTSW |
4 |
128,803,018 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5223:Trim62
|
UTSW |
4 |
128,803,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R5494:Trim62
|
UTSW |
4 |
128,778,999 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6909:Trim62
|
UTSW |
4 |
128,778,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R6959:Trim62
|
UTSW |
4 |
128,802,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R7507:Trim62
|
UTSW |
4 |
128,790,664 (GRCm39) |
missense |
probably benign |
0.01 |
R7544:Trim62
|
UTSW |
4 |
128,796,346 (GRCm39) |
missense |
probably benign |
0.04 |
R7624:Trim62
|
UTSW |
4 |
128,777,471 (GRCm39) |
start gained |
probably benign |
|
R7817:Trim62
|
UTSW |
4 |
128,794,478 (GRCm39) |
missense |
probably benign |
|
R8404:Trim62
|
UTSW |
4 |
128,803,233 (GRCm39) |
missense |
probably benign |
0.01 |
R8502:Trim62
|
UTSW |
4 |
128,803,233 (GRCm39) |
missense |
probably benign |
0.01 |
R8692:Trim62
|
UTSW |
4 |
128,794,465 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9061:Trim62
|
UTSW |
4 |
128,802,963 (GRCm39) |
missense |
probably damaging |
1.00 |
|