Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
A |
G |
5: 114,326,503 (GRCm39) |
T290A |
possibly damaging |
Het |
Apip |
G |
A |
2: 102,917,486 (GRCm39) |
V62M |
probably damaging |
Het |
Appbp2 |
T |
C |
11: 85,105,143 (GRCm39) |
K141R |
possibly damaging |
Het |
Arhgef18 |
T |
A |
8: 3,501,624 (GRCm39) |
|
probably benign |
Het |
B3galt2 |
A |
G |
1: 143,522,583 (GRCm39) |
T240A |
probably benign |
Het |
Bivm |
A |
T |
1: 44,180,973 (GRCm39) |
N385I |
probably damaging |
Het |
Brd4 |
A |
T |
17: 32,417,649 (GRCm39) |
|
probably benign |
Het |
Cage1 |
T |
C |
13: 38,206,789 (GRCm39) |
D352G |
possibly damaging |
Het |
Ceacam10 |
A |
G |
7: 24,480,535 (GRCm39) |
Y102C |
probably damaging |
Het |
Diaph3 |
T |
C |
14: 87,156,282 (GRCm39) |
D677G |
probably benign |
Het |
Dis3l |
T |
C |
9: 64,226,536 (GRCm39) |
|
probably null |
Het |
Dnah6 |
C |
T |
6: 73,165,360 (GRCm39) |
V582M |
probably benign |
Het |
Fndc3b |
A |
G |
3: 27,521,552 (GRCm39) |
L541P |
probably damaging |
Het |
Folh1 |
T |
C |
7: 86,391,444 (GRCm39) |
T384A |
possibly damaging |
Het |
Gdpd3 |
T |
C |
7: 126,365,695 (GRCm39) |
L18P |
probably damaging |
Het |
Grxcr2 |
T |
A |
18: 42,132,047 (GRCm39) |
K7N |
probably damaging |
Het |
Inpp4b |
A |
T |
8: 82,723,968 (GRCm39) |
D500V |
probably benign |
Het |
Ints4 |
C |
T |
7: 97,175,849 (GRCm39) |
L647F |
probably benign |
Het |
Kif17 |
T |
A |
4: 138,013,876 (GRCm39) |
L264Q |
possibly damaging |
Het |
Kif21a |
T |
C |
15: 90,843,948 (GRCm39) |
N1104S |
possibly damaging |
Het |
Ly6e |
T |
G |
15: 74,830,546 (GRCm39) |
L132R |
probably benign |
Het |
Mis18bp1 |
T |
A |
12: 65,185,452 (GRCm39) |
H905L |
probably damaging |
Het |
Nr2f2 |
A |
G |
7: 70,004,446 (GRCm39) |
S269P |
probably damaging |
Het |
Or2b2b |
C |
A |
13: 21,858,787 (GRCm39) |
C109F |
probably benign |
Het |
Or2o1 |
G |
A |
11: 49,051,354 (GRCm39) |
C171Y |
probably damaging |
Het |
Or5d46 |
T |
A |
2: 88,170,771 (GRCm39) |
N287K |
probably damaging |
Het |
Pde8b |
T |
C |
13: 95,166,910 (GRCm39) |
I757V |
probably damaging |
Het |
Psg23 |
A |
T |
7: 18,346,122 (GRCm39) |
I191N |
possibly damaging |
Het |
Slc12a4 |
A |
T |
8: 106,672,475 (GRCm39) |
|
probably null |
Het |
Snph |
A |
T |
2: 151,436,093 (GRCm39) |
Y209* |
probably null |
Het |
Tnfaip3 |
T |
C |
10: 18,882,649 (GRCm39) |
H256R |
probably damaging |
Het |
Tnip3 |
T |
A |
6: 65,573,107 (GRCm39) |
|
probably benign |
Het |
Ttc3 |
T |
A |
16: 94,243,386 (GRCm39) |
F1130Y |
probably damaging |
Het |
Twnk |
T |
G |
19: 44,998,627 (GRCm39) |
V515G |
probably damaging |
Het |
Usp24 |
T |
A |
4: 106,280,658 (GRCm39) |
I2324K |
probably benign |
Het |
Vwa7 |
T |
C |
17: 35,238,827 (GRCm39) |
F305S |
probably damaging |
Het |
Ythdc2 |
A |
T |
18: 44,983,735 (GRCm39) |
Q567L |
probably damaging |
Het |
Zbtb11 |
T |
A |
16: 55,818,523 (GRCm39) |
I649K |
probably damaging |
Het |
Zbtb49 |
T |
C |
5: 38,358,204 (GRCm39) |
Y683C |
probably damaging |
Het |
Zfhx4 |
A |
T |
3: 5,309,152 (GRCm39) |
M793L |
possibly damaging |
Het |
Zmym6 |
T |
G |
4: 127,002,437 (GRCm39) |
I556R |
probably damaging |
Het |
Zswim8 |
C |
T |
14: 20,764,780 (GRCm39) |
P717S |
probably benign |
Het |
|
Other mutations in Gulo |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00325:Gulo
|
APN |
14 |
66,243,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R0599:Gulo
|
UTSW |
14 |
66,227,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Gulo
|
UTSW |
14 |
66,246,496 (GRCm39) |
start codon destroyed |
probably benign |
|
R2058:Gulo
|
UTSW |
14 |
66,228,608 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2079:Gulo
|
UTSW |
14 |
66,227,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R2405:Gulo
|
UTSW |
14 |
66,228,477 (GRCm39) |
critical splice donor site |
probably null |
|
R4196:Gulo
|
UTSW |
14 |
66,225,702 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4807:Gulo
|
UTSW |
14 |
66,227,833 (GRCm39) |
missense |
probably benign |
0.00 |
R5341:Gulo
|
UTSW |
14 |
66,225,707 (GRCm39) |
missense |
probably benign |
0.12 |
R5913:Gulo
|
UTSW |
14 |
66,237,470 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5915:Gulo
|
UTSW |
14 |
66,245,570 (GRCm39) |
missense |
probably benign |
0.29 |
R6328:Gulo
|
UTSW |
14 |
66,240,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R6628:Gulo
|
UTSW |
14 |
66,241,619 (GRCm39) |
missense |
probably benign |
0.00 |
R7725:Gulo
|
UTSW |
14 |
66,245,522 (GRCm39) |
missense |
probably damaging |
0.99 |
R7935:Gulo
|
UTSW |
14 |
66,237,288 (GRCm39) |
missense |
probably benign |
|
R8720:Gulo
|
UTSW |
14 |
66,225,074 (GRCm39) |
missense |
probably benign |
0.01 |
R8940:Gulo
|
UTSW |
14 |
66,235,040 (GRCm39) |
missense |
probably benign |
0.04 |
R9458:Gulo
|
UTSW |
14 |
66,235,043 (GRCm39) |
missense |
probably benign |
0.01 |
R9716:Gulo
|
UTSW |
14 |
66,234,348 (GRCm39) |
missense |
probably benign |
0.00 |
R9746:Gulo
|
UTSW |
14 |
66,225,630 (GRCm39) |
critical splice donor site |
probably null |
|
|