Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap5 |
T |
A |
12: 52,565,136 (GRCm39) |
N702K |
probably damaging |
Het |
Atm |
T |
C |
9: 53,390,995 (GRCm39) |
T1860A |
probably benign |
Het |
Bicdl1 |
A |
T |
5: 115,811,217 (GRCm39) |
H231Q |
probably damaging |
Het |
C2cd5 |
A |
C |
6: 142,987,218 (GRCm39) |
D470E |
probably damaging |
Het |
Chd5 |
T |
C |
4: 152,451,751 (GRCm39) |
F688L |
probably damaging |
Het |
Cul3 |
T |
C |
1: 80,300,619 (GRCm39) |
Y74C |
probably damaging |
Het |
Dhx16 |
A |
G |
17: 36,203,429 (GRCm39) |
E1042G |
probably damaging |
Het |
Dnah11 |
A |
G |
12: 118,020,915 (GRCm39) |
L1966P |
probably damaging |
Het |
Dpy19l1 |
A |
T |
9: 24,386,682 (GRCm39) |
I204N |
possibly damaging |
Het |
Drd2 |
T |
C |
9: 49,313,559 (GRCm39) |
|
probably benign |
Het |
Fasn |
A |
G |
11: 120,711,166 (GRCm39) |
V228A |
probably damaging |
Het |
Fggy |
T |
C |
4: 95,737,846 (GRCm39) |
W148R |
probably benign |
Het |
Gm9631 |
G |
A |
11: 121,834,478 (GRCm39) |
|
|
Het |
Gpr89 |
A |
T |
3: 96,804,741 (GRCm39) |
Y38* |
probably null |
Het |
H2-M1 |
G |
A |
17: 36,983,026 (GRCm39) |
H22Y |
possibly damaging |
Het |
Kdm3b |
T |
A |
18: 34,941,630 (GRCm39) |
S574T |
probably benign |
Het |
Kmt2c |
C |
T |
5: 25,578,018 (GRCm39) |
V753I |
probably benign |
Het |
Lnpep |
T |
C |
17: 17,765,165 (GRCm39) |
T762A |
possibly damaging |
Het |
Lrp2 |
C |
T |
2: 69,291,649 (GRCm39) |
C3510Y |
probably damaging |
Het |
Nlrp3 |
T |
A |
11: 59,456,849 (GRCm39) |
|
probably benign |
Het |
Or14c39 |
A |
G |
7: 86,344,027 (GRCm39) |
Y121C |
probably damaging |
Het |
Or1j18 |
A |
T |
2: 36,624,356 (GRCm39) |
I8F |
probably benign |
Het |
Or5b3 |
A |
G |
19: 13,388,259 (GRCm39) |
T109A |
possibly damaging |
Het |
Pcnx3 |
A |
T |
19: 5,736,509 (GRCm39) |
V176E |
possibly damaging |
Het |
Phlpp1 |
T |
C |
1: 106,320,444 (GRCm39) |
S1480P |
probably benign |
Het |
Ppfia3 |
T |
C |
7: 44,991,141 (GRCm39) |
R1027G |
probably damaging |
Het |
Rnf216 |
A |
G |
5: 143,054,665 (GRCm39) |
Y628H |
possibly damaging |
Het |
Sh3bp1 |
G |
A |
15: 78,785,699 (GRCm39) |
R4Q |
probably damaging |
Het |
Skint9 |
A |
G |
4: 112,271,335 (GRCm39) |
|
probably benign |
Het |
Slc25a51 |
A |
G |
4: 45,400,074 (GRCm39) |
S39P |
probably benign |
Het |
Smarca4 |
C |
T |
9: 21,612,386 (GRCm39) |
R1558C |
probably damaging |
Het |
Spag9 |
A |
G |
11: 94,007,567 (GRCm39) |
S1224G |
probably benign |
Het |
Spdl1 |
G |
T |
11: 34,704,181 (GRCm39) |
Q551K |
probably benign |
Het |
Sugt1 |
A |
G |
14: 79,847,698 (GRCm39) |
I183V |
probably benign |
Het |
Th |
G |
A |
7: 142,453,643 (GRCm39) |
S19L |
probably damaging |
Het |
Tmprss11g |
A |
G |
5: 86,638,750 (GRCm39) |
V246A |
probably benign |
Het |
Tnfaip8l2 |
T |
C |
3: 95,047,714 (GRCm39) |
T50A |
probably benign |
Het |
Tox3 |
G |
T |
8: 90,984,759 (GRCm39) |
T140K |
possibly damaging |
Het |
Unc50 |
T |
A |
1: 37,476,531 (GRCm39) |
Y205* |
probably null |
Het |
Vmn2r83 |
A |
T |
10: 79,314,881 (GRCm39) |
K376N |
probably benign |
Het |
|
Other mutations in Lcn9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01952:Lcn9
|
APN |
2 |
25,714,550 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4418001:Lcn9
|
UTSW |
2 |
25,714,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R1479:Lcn9
|
UTSW |
2 |
25,713,715 (GRCm39) |
splice site |
probably benign |
|
R1657:Lcn9
|
UTSW |
2 |
25,714,722 (GRCm39) |
missense |
probably benign |
0.17 |
R4199:Lcn9
|
UTSW |
2 |
25,714,773 (GRCm39) |
missense |
probably benign |
0.15 |
R4526:Lcn9
|
UTSW |
2 |
25,714,520 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4570:Lcn9
|
UTSW |
2 |
25,713,591 (GRCm39) |
missense |
probably benign |
0.04 |
R5232:Lcn9
|
UTSW |
2 |
25,714,067 (GRCm39) |
critical splice donor site |
probably null |
|
R5577:Lcn9
|
UTSW |
2 |
25,713,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R5849:Lcn9
|
UTSW |
2 |
25,713,268 (GRCm39) |
critical splice donor site |
probably null |
|
R6059:Lcn9
|
UTSW |
2 |
25,714,737 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7748:Lcn9
|
UTSW |
2 |
25,714,926 (GRCm39) |
makesense |
probably null |
|
R9257:Lcn9
|
UTSW |
2 |
25,714,784 (GRCm39) |
critical splice donor site |
probably null |
|
|