Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam9 |
A |
T |
8: 25,453,026 (GRCm39) |
N760K |
probably benign |
Het |
Ahcyl |
T |
A |
16: 45,974,955 (GRCm39) |
T141S |
probably benign |
Het |
Akr1b10 |
A |
G |
6: 34,369,920 (GRCm39) |
T216A |
possibly damaging |
Het |
Arsj |
A |
G |
3: 126,232,993 (GRCm39) |
R580G |
probably benign |
Het |
C9 |
A |
T |
15: 6,474,918 (GRCm39) |
I26F |
probably damaging |
Het |
Cacna2d1 |
A |
G |
5: 16,533,041 (GRCm39) |
E578G |
probably damaging |
Het |
Clca4b |
C |
T |
3: 144,622,536 (GRCm39) |
V510I |
probably benign |
Het |
Dab2 |
C |
T |
15: 6,464,895 (GRCm39) |
T561I |
possibly damaging |
Het |
Golga5 |
A |
T |
12: 102,450,752 (GRCm39) |
E12D |
possibly damaging |
Het |
Hsd17b12 |
A |
T |
2: 93,874,280 (GRCm39) |
F208I |
probably damaging |
Het |
Inf2 |
A |
G |
12: 112,579,008 (GRCm39) |
|
probably benign |
Het |
Kcnh3 |
T |
A |
15: 99,127,337 (GRCm39) |
W378R |
probably damaging |
Het |
Klhdc8b |
G |
C |
9: 108,326,422 (GRCm39) |
R158G |
possibly damaging |
Het |
Klhl41 |
G |
A |
2: 69,500,554 (GRCm39) |
R5Q |
probably benign |
Het |
Mppe1 |
A |
G |
18: 67,370,419 (GRCm39) |
|
probably null |
Het |
Muc20 |
G |
A |
16: 32,614,300 (GRCm39) |
A359V |
probably damaging |
Het |
Myh14 |
T |
C |
7: 44,263,105 (GRCm39) |
D1765G |
probably damaging |
Het |
Or10j2 |
T |
C |
1: 173,098,372 (GRCm39) |
M210T |
probably benign |
Het |
Or4c10b |
C |
T |
2: 89,711,235 (GRCm39) |
Q22* |
probably null |
Het |
Or5p58 |
A |
G |
7: 107,693,985 (GRCm39) |
M264T |
probably benign |
Het |
Pbrm1 |
T |
A |
14: 30,757,916 (GRCm39) |
L182Q |
probably damaging |
Het |
Pde8a |
A |
G |
7: 80,967,095 (GRCm39) |
N412S |
probably benign |
Het |
Phyh |
A |
G |
2: 4,940,912 (GRCm39) |
T271A |
probably damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,352,942 (GRCm39) |
S258P |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Pyroxd1 |
A |
G |
6: 142,291,463 (GRCm39) |
E2G |
probably benign |
Het |
Ralgapa1 |
G |
T |
12: 55,723,550 (GRCm39) |
Q2115K |
probably benign |
Het |
Rufy3 |
A |
G |
5: 88,732,129 (GRCm39) |
E44G |
possibly damaging |
Het |
Slit2 |
A |
T |
5: 48,395,721 (GRCm39) |
N712I |
probably damaging |
Het |
Sptbn1 |
A |
G |
11: 30,095,985 (GRCm39) |
M303T |
possibly damaging |
Het |
Ssbp4 |
A |
G |
8: 71,052,509 (GRCm39) |
I154T |
probably benign |
Het |
Syne2 |
A |
G |
12: 75,977,778 (GRCm39) |
K1409E |
probably benign |
Het |
Tfap2b |
T |
C |
1: 19,304,449 (GRCm39) |
Y420H |
probably damaging |
Het |
Tlr5 |
A |
G |
1: 182,803,261 (GRCm39) |
|
probably null |
Het |
Tmprss15 |
C |
T |
16: 78,821,637 (GRCm39) |
|
probably null |
Het |
Tns1 |
A |
T |
1: 73,959,722 (GRCm39) |
I418N |
probably damaging |
Het |
Txlna |
A |
T |
4: 129,522,984 (GRCm39) |
V452D |
probably benign |
Het |
Wdr17 |
C |
T |
8: 55,146,131 (GRCm39) |
A90T |
possibly damaging |
Het |
Zfp563 |
A |
T |
17: 33,323,659 (GRCm39) |
S85C |
possibly damaging |
Het |
Zfp764l1 |
A |
T |
7: 126,991,504 (GRCm39) |
I161N |
possibly damaging |
Het |
|
Other mutations in Lcn3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02041:Lcn3
|
APN |
2 |
25,655,636 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02139:Lcn3
|
APN |
2 |
25,656,646 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02221:Lcn3
|
APN |
2 |
25,656,172 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02665:Lcn3
|
APN |
2 |
25,656,416 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03049:Lcn3
|
APN |
2 |
25,655,586 (GRCm39) |
start codon destroyed |
probably null |
0.02 |
R3522:Lcn3
|
UTSW |
2 |
25,656,133 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4227:Lcn3
|
UTSW |
2 |
25,656,123 (GRCm39) |
missense |
probably benign |
0.00 |
R6684:Lcn3
|
UTSW |
2 |
25,656,170 (GRCm39) |
missense |
probably benign |
0.00 |
R6937:Lcn3
|
UTSW |
2 |
25,657,823 (GRCm39) |
nonsense |
probably null |
|
R7010:Lcn3
|
UTSW |
2 |
25,656,068 (GRCm39) |
missense |
probably damaging |
0.99 |
R7487:Lcn3
|
UTSW |
2 |
25,656,174 (GRCm39) |
critical splice donor site |
probably null |
|
R7966:Lcn3
|
UTSW |
2 |
25,656,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R8553:Lcn3
|
UTSW |
2 |
25,656,347 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9544:Lcn3
|
UTSW |
2 |
25,656,151 (GRCm39) |
missense |
probably benign |
|
R9609:Lcn3
|
UTSW |
2 |
25,657,596 (GRCm39) |
missense |
possibly damaging |
0.88 |
|