Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alms1 |
T |
C |
6: 85,604,986 (GRCm39) |
F2212S |
possibly damaging |
Het |
Anpep |
T |
C |
7: 79,475,098 (GRCm39) |
I155V |
possibly damaging |
Het |
Aoc1 |
G |
A |
6: 48,885,223 (GRCm39) |
V653M |
probably damaging |
Het |
Arl8b |
T |
C |
6: 108,798,518 (GRCm39) |
|
probably benign |
Het |
Bax |
A |
C |
7: 45,115,552 (GRCm39) |
|
probably null |
Het |
Cpne7 |
G |
A |
8: 123,852,382 (GRCm39) |
E195K |
probably damaging |
Het |
Csmd3 |
A |
G |
15: 47,539,168 (GRCm39) |
I2330T |
possibly damaging |
Het |
Dnajc16 |
A |
G |
4: 141,501,940 (GRCm39) |
S297P |
probably benign |
Het |
Farp2 |
A |
G |
1: 93,504,155 (GRCm39) |
K311E |
probably damaging |
Het |
Fhad1 |
A |
G |
4: 141,691,906 (GRCm39) |
L410P |
probably damaging |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gm12185 |
T |
C |
11: 48,798,886 (GRCm39) |
T536A |
possibly damaging |
Het |
Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
Hydin |
C |
T |
8: 111,245,806 (GRCm39) |
T2173I |
possibly damaging |
Het |
Kpnb1 |
A |
G |
11: 97,055,556 (GRCm39) |
V783A |
probably benign |
Het |
Krt1 |
A |
G |
15: 101,754,811 (GRCm39) |
V509A |
unknown |
Het |
Lrwd1 |
A |
T |
5: 136,164,729 (GRCm39) |
L26* |
probably null |
Het |
Mal2 |
T |
A |
15: 54,451,728 (GRCm39) |
W50R |
probably damaging |
Het |
Map3k21 |
A |
T |
8: 126,668,871 (GRCm39) |
E819V |
probably damaging |
Het |
Mrgprx3-ps |
T |
C |
7: 46,959,959 (GRCm39) |
T11A |
probably benign |
Het |
Mroh2b |
T |
C |
15: 4,953,170 (GRCm39) |
F635L |
probably benign |
Het |
Mylip |
G |
A |
13: 45,562,178 (GRCm39) |
E327K |
probably damaging |
Het |
Nfix |
T |
C |
8: 85,453,103 (GRCm39) |
D308G |
probably damaging |
Het |
Or1l8 |
G |
A |
2: 36,817,824 (GRCm39) |
Q101* |
probably null |
Het |
Or7e166 |
G |
A |
9: 19,624,638 (GRCm39) |
V172I |
probably benign |
Het |
Psma6 |
A |
G |
12: 55,454,254 (GRCm39) |
E26G |
probably damaging |
Het |
Rgs16 |
T |
A |
1: 153,617,804 (GRCm39) |
S105T |
probably damaging |
Het |
Slc25a23 |
T |
A |
17: 57,354,291 (GRCm39) |
N372Y |
possibly damaging |
Het |
Slc35e2 |
A |
G |
4: 155,697,187 (GRCm39) |
M234V |
probably benign |
Het |
Tbc1d8 |
A |
G |
1: 39,431,334 (GRCm39) |
V346A |
probably damaging |
Het |
Tgfb1i1 |
C |
T |
7: 127,847,654 (GRCm39) |
|
probably benign |
Het |
Triml2 |
A |
C |
8: 43,643,349 (GRCm39) |
T177P |
probably damaging |
Het |
Uba6 |
T |
C |
5: 86,267,245 (GRCm39) |
T959A |
probably benign |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in 2700062C07Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02217:2700062C07Rik
|
APN |
18 |
24,603,955 (GRCm39) |
utr 5 prime |
probably benign |
|
R1108:2700062C07Rik
|
UTSW |
18 |
24,610,333 (GRCm39) |
missense |
probably benign |
0.09 |
R1422:2700062C07Rik
|
UTSW |
18 |
24,610,333 (GRCm39) |
missense |
probably benign |
0.09 |
R2212:2700062C07Rik
|
UTSW |
18 |
24,603,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R4030:2700062C07Rik
|
UTSW |
18 |
24,608,715 (GRCm39) |
missense |
probably benign |
0.00 |
R4246:2700062C07Rik
|
UTSW |
18 |
24,606,013 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4248:2700062C07Rik
|
UTSW |
18 |
24,606,013 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4249:2700062C07Rik
|
UTSW |
18 |
24,606,013 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4734:2700062C07Rik
|
UTSW |
18 |
24,603,961 (GRCm39) |
start codon destroyed |
probably null |
0.86 |
R7269:2700062C07Rik
|
UTSW |
18 |
24,606,013 (GRCm39) |
missense |
probably damaging |
0.98 |
R7903:2700062C07Rik
|
UTSW |
18 |
24,608,783 (GRCm39) |
critical splice donor site |
probably null |
|
R8125:2700062C07Rik
|
UTSW |
18 |
24,608,709 (GRCm39) |
missense |
probably benign |
|
R9577:2700062C07Rik
|
UTSW |
18 |
24,608,663 (GRCm39) |
missense |
probably benign |
0.01 |
|