Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930438A08Rik |
A |
G |
11: 58,179,176 (GRCm39) |
Y170C |
probably damaging |
Het |
Adcy2 |
C |
T |
13: 69,036,161 (GRCm39) |
V167I |
probably benign |
Het |
Agl |
A |
G |
3: 116,545,825 (GRCm39) |
Y1324H |
probably damaging |
Het |
Arhgef37 |
G |
T |
18: 61,641,860 (GRCm39) |
Q170K |
probably damaging |
Het |
Asah2 |
A |
G |
19: 31,994,176 (GRCm39) |
S390P |
probably damaging |
Het |
Atp8a1 |
A |
T |
5: 67,932,068 (GRCm39) |
H240Q |
probably benign |
Het |
Btbd16 |
T |
A |
7: 130,390,557 (GRCm39) |
N151K |
probably damaging |
Het |
Ccdc73 |
T |
A |
2: 104,803,499 (GRCm39) |
|
probably benign |
Het |
Cecr2 |
G |
T |
6: 120,735,159 (GRCm39) |
M21I |
probably benign |
Het |
Ckap2l |
T |
C |
2: 129,127,636 (GRCm39) |
T181A |
probably benign |
Het |
Col4a3 |
T |
C |
1: 82,629,879 (GRCm39) |
|
probably benign |
Het |
Cplane1 |
T |
A |
15: 8,252,576 (GRCm39) |
C1933S |
probably benign |
Het |
Dnah9 |
A |
G |
11: 65,972,074 (GRCm39) |
|
probably benign |
Het |
Efcab3 |
T |
C |
11: 104,611,706 (GRCm39) |
L516P |
possibly damaging |
Het |
Fat3 |
T |
C |
9: 16,286,419 (GRCm39) |
T1035A |
probably benign |
Het |
Fzd8 |
A |
G |
18: 9,212,947 (GRCm39) |
T10A |
unknown |
Het |
Gm9631 |
C |
A |
11: 121,833,328 (GRCm39) |
C636F |
probably damaging |
Het |
Gp1ba |
A |
G |
11: 70,531,614 (GRCm39) |
|
probably benign |
Het |
Gsk3a |
A |
G |
7: 24,931,134 (GRCm39) |
V277A |
probably damaging |
Het |
H2-M1 |
T |
A |
17: 36,981,120 (GRCm39) |
|
probably benign |
Het |
Hesx1 |
T |
A |
14: 26,722,809 (GRCm39) |
W45R |
probably damaging |
Het |
Il23r |
T |
A |
6: 67,463,317 (GRCm39) |
M59L |
possibly damaging |
Het |
Insc |
T |
A |
7: 114,444,312 (GRCm39) |
V433E |
probably benign |
Het |
Itga8 |
T |
C |
2: 12,196,053 (GRCm39) |
|
probably benign |
Het |
Kif13a |
T |
A |
13: 46,966,299 (GRCm39) |
E436V |
probably damaging |
Het |
Liph |
A |
G |
16: 21,814,100 (GRCm39) |
F7S |
probably benign |
Het |
Lpar2 |
T |
C |
8: 70,276,823 (GRCm39) |
V204A |
probably damaging |
Het |
Man2b2 |
A |
T |
5: 36,983,402 (GRCm39) |
D182E |
probably benign |
Het |
Mmp27 |
T |
C |
9: 7,581,156 (GRCm39) |
|
probably benign |
Het |
Mrm1 |
A |
G |
11: 84,705,639 (GRCm39) |
|
probably benign |
Het |
Mtx3 |
T |
C |
13: 92,986,869 (GRCm39) |
S271P |
probably damaging |
Het |
Myh11 |
A |
T |
16: 14,044,480 (GRCm39) |
M641K |
possibly damaging |
Het |
Necab2 |
A |
G |
8: 120,197,670 (GRCm39) |
D332G |
probably damaging |
Het |
Ngfr |
A |
G |
11: 95,465,065 (GRCm39) |
I261T |
possibly damaging |
Het |
Nrap |
T |
C |
19: 56,345,757 (GRCm39) |
E617G |
probably damaging |
Het |
Obscn |
G |
T |
11: 58,941,306 (GRCm39) |
T4505K |
probably benign |
Het |
Or8b37 |
G |
T |
9: 37,959,123 (GRCm39) |
V202L |
probably benign |
Het |
Or8b57 |
A |
G |
9: 40,003,807 (GRCm39) |
Y148H |
probably damaging |
Het |
Osbpl11 |
T |
A |
16: 33,062,100 (GRCm39) |
|
probably benign |
Het |
Otof |
A |
G |
5: 30,552,041 (GRCm39) |
V301A |
probably damaging |
Het |
Phf3 |
A |
T |
1: 30,850,919 (GRCm39) |
L1145Q |
probably damaging |
Het |
Phospho2 |
T |
A |
2: 69,626,540 (GRCm39) |
I232N |
possibly damaging |
Het |
Pomgnt2 |
T |
A |
9: 121,811,127 (GRCm39) |
K551N |
probably damaging |
Het |
Ptchd3 |
A |
G |
11: 121,721,984 (GRCm39) |
T286A |
possibly damaging |
Het |
Rnf213 |
A |
G |
11: 119,331,976 (GRCm39) |
D2396G |
probably damaging |
Het |
Sh3pxd2b |
A |
G |
11: 32,373,341 (GRCm39) |
E836G |
possibly damaging |
Het |
Simc1 |
G |
T |
13: 54,673,468 (GRCm39) |
M605I |
possibly damaging |
Het |
Slc12a3 |
G |
A |
8: 95,056,061 (GRCm39) |
E66K |
possibly damaging |
Het |
Spg11 |
T |
C |
2: 121,915,464 (GRCm39) |
N1060S |
probably benign |
Het |
Supt5 |
A |
T |
7: 28,028,462 (GRCm39) |
W178R |
probably damaging |
Het |
Tmem41a |
G |
T |
16: 21,756,740 (GRCm39) |
F126L |
probably benign |
Het |
Ube2m |
T |
A |
7: 12,771,553 (GRCm39) |
Q35L |
probably benign |
Het |
Usp33 |
A |
G |
3: 152,086,211 (GRCm39) |
D658G |
probably damaging |
Het |
Vmn2r12 |
A |
T |
5: 109,238,373 (GRCm39) |
C456S |
probably benign |
Het |
Vmn2r81 |
T |
A |
10: 79,104,434 (GRCm39) |
D352E |
probably damaging |
Het |
Zfp516 |
A |
G |
18: 83,005,388 (GRCm39) |
Y764C |
probably damaging |
Het |
Zswim7 |
A |
G |
11: 62,167,473 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Lrfn4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1103:Lrfn4
|
UTSW |
19 |
4,663,299 (GRCm39) |
missense |
probably benign |
0.00 |
R1629:Lrfn4
|
UTSW |
19 |
4,663,523 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4406:Lrfn4
|
UTSW |
19 |
4,663,299 (GRCm39) |
missense |
probably benign |
0.00 |
R4459:Lrfn4
|
UTSW |
19 |
4,662,662 (GRCm39) |
missense |
probably benign |
|
R5543:Lrfn4
|
UTSW |
19 |
4,662,191 (GRCm39) |
missense |
probably benign |
0.41 |
R6115:Lrfn4
|
UTSW |
19 |
4,663,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R6554:Lrfn4
|
UTSW |
19 |
4,663,914 (GRCm39) |
missense |
probably damaging |
0.98 |
R7626:Lrfn4
|
UTSW |
19 |
4,663,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R7779:Lrfn4
|
UTSW |
19 |
4,663,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R7968:Lrfn4
|
UTSW |
19 |
4,663,343 (GRCm39) |
missense |
probably benign |
0.06 |
R8008:Lrfn4
|
UTSW |
19 |
4,663,565 (GRCm39) |
missense |
probably benign |
0.21 |
R8356:Lrfn4
|
UTSW |
19 |
4,662,256 (GRCm39) |
missense |
probably benign |
0.44 |
R8482:Lrfn4
|
UTSW |
19 |
4,664,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R9180:Lrfn4
|
UTSW |
19 |
4,663,353 (GRCm39) |
missense |
probably benign |
0.01 |
R9507:Lrfn4
|
UTSW |
19 |
4,664,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R9520:Lrfn4
|
UTSW |
19 |
4,664,237 (GRCm39) |
missense |
probably damaging |
0.99 |
|