Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apof |
T |
C |
10: 128,104,891 (GRCm39) |
L15P |
probably damaging |
Het |
BC048671 |
T |
C |
6: 90,282,095 (GRCm39) |
F84S |
probably benign |
Het |
Bsn |
G |
A |
9: 107,988,651 (GRCm39) |
A2367V |
probably benign |
Het |
C2cd4a |
C |
T |
9: 67,739,039 (GRCm39) |
M1I |
probably null |
Het |
Cd72 |
T |
A |
4: 43,450,109 (GRCm39) |
K266N |
possibly damaging |
Het |
Col12a1 |
A |
G |
9: 79,542,781 (GRCm39) |
F2328S |
probably damaging |
Het |
Cubn |
T |
C |
2: 13,318,855 (GRCm39) |
Y2948C |
probably damaging |
Het |
Dagla |
A |
G |
19: 10,240,456 (GRCm39) |
|
probably null |
Het |
Dagla |
A |
G |
19: 10,248,883 (GRCm39) |
F24L |
probably damaging |
Het |
Dnah14 |
A |
G |
1: 181,568,849 (GRCm39) |
T2860A |
probably damaging |
Het |
Efcab2 |
A |
T |
1: 178,265,001 (GRCm39) |
K22N |
probably benign |
Het |
Flt1 |
C |
T |
5: 147,512,983 (GRCm39) |
R1118Q |
probably damaging |
Het |
Foxl1 |
T |
A |
8: 121,855,224 (GRCm39) |
L175Q |
possibly damaging |
Het |
Gm572 |
G |
T |
4: 148,743,450 (GRCm39) |
R140L |
possibly damaging |
Het |
Gucy2g |
T |
C |
19: 55,205,833 (GRCm39) |
R676G |
probably benign |
Het |
Hmcn2 |
C |
A |
2: 31,281,088 (GRCm39) |
L1867I |
probably benign |
Het |
Hspb8 |
T |
C |
5: 116,560,504 (GRCm39) |
Y12C |
probably damaging |
Het |
Igf2bp2 |
A |
C |
16: 21,883,841 (GRCm39) |
|
probably null |
Het |
Igkv9-129 |
T |
A |
6: 67,816,784 (GRCm39) |
M3K |
probably damaging |
Het |
Il5 |
C |
T |
11: 53,612,651 (GRCm39) |
P54S |
probably damaging |
Het |
Kif18a |
T |
C |
2: 109,125,318 (GRCm39) |
I245T |
possibly damaging |
Het |
Kif2b |
T |
A |
11: 91,467,140 (GRCm39) |
N381I |
possibly damaging |
Het |
Lrrc49 |
A |
G |
9: 60,500,908 (GRCm39) |
F679S |
probably benign |
Het |
Med24 |
A |
G |
11: 98,598,383 (GRCm39) |
F742L |
probably benign |
Het |
Msh3 |
T |
C |
13: 92,349,020 (GRCm39) |
T1071A |
probably benign |
Het |
Neb |
T |
C |
2: 52,177,220 (GRCm39) |
T1374A |
probably damaging |
Het |
Or4d6 |
A |
T |
19: 12,086,091 (GRCm39) |
I47N |
probably damaging |
Het |
Or5p75-ps1 |
A |
C |
7: 108,107,851 (GRCm39) |
Q196P |
unknown |
Het |
P3h2 |
A |
G |
16: 25,805,955 (GRCm39) |
I296T |
probably benign |
Het |
Pcdhb21 |
A |
T |
18: 37,646,841 (GRCm39) |
|
probably benign |
Het |
Prkab2 |
G |
T |
3: 97,566,002 (GRCm39) |
G25C |
probably damaging |
Het |
Ptprm |
C |
A |
17: 67,251,312 (GRCm39) |
A522S |
possibly damaging |
Het |
Scarf2 |
A |
G |
16: 17,624,231 (GRCm39) |
D512G |
probably benign |
Het |
Sema3d |
A |
G |
5: 12,592,608 (GRCm39) |
T346A |
probably damaging |
Het |
Septin7 |
T |
C |
9: 25,163,938 (GRCm39) |
S2P |
unknown |
Het |
Sfrp5 |
A |
G |
19: 42,187,236 (GRCm39) |
V278A |
probably benign |
Het |
Taar1 |
T |
A |
10: 23,796,522 (GRCm39) |
C73* |
probably null |
Het |
Tek |
T |
A |
4: 94,715,922 (GRCm39) |
L448Q |
probably benign |
Het |
Tmem132a |
A |
C |
19: 10,835,833 (GRCm39) |
L899R |
probably damaging |
Het |
Txndc5 |
T |
C |
13: 38,711,845 (GRCm39) |
|
probably benign |
Het |
Uck1 |
C |
A |
2: 32,150,153 (GRCm39) |
|
probably benign |
Het |
Uggt1 |
A |
G |
1: 36,212,568 (GRCm39) |
S925P |
probably damaging |
Het |
Unc13d |
A |
T |
11: 115,958,657 (GRCm39) |
D786E |
probably damaging |
Het |
|
Other mutations in Vmn1r26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02517:Vmn1r26
|
APN |
6 |
57,986,127 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02609:Vmn1r26
|
APN |
6 |
57,985,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R1121:Vmn1r26
|
UTSW |
6 |
57,985,647 (GRCm39) |
missense |
probably benign |
0.43 |
R1881:Vmn1r26
|
UTSW |
6 |
57,985,650 (GRCm39) |
missense |
probably benign |
0.20 |
R1958:Vmn1r26
|
UTSW |
6 |
57,985,286 (GRCm39) |
missense |
probably benign |
0.01 |
R1978:Vmn1r26
|
UTSW |
6 |
57,986,111 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2106:Vmn1r26
|
UTSW |
6 |
57,985,710 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2117:Vmn1r26
|
UTSW |
6 |
57,985,335 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2323:Vmn1r26
|
UTSW |
6 |
57,985,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R4917:Vmn1r26
|
UTSW |
6 |
57,985,808 (GRCm39) |
missense |
probably damaging |
0.99 |
R5695:Vmn1r26
|
UTSW |
6 |
57,985,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R6355:Vmn1r26
|
UTSW |
6 |
57,985,536 (GRCm39) |
missense |
probably benign |
0.02 |
R6948:Vmn1r26
|
UTSW |
6 |
57,985,718 (GRCm39) |
missense |
probably damaging |
0.98 |
R7114:Vmn1r26
|
UTSW |
6 |
57,985,755 (GRCm39) |
missense |
probably benign |
0.02 |
R7977:Vmn1r26
|
UTSW |
6 |
57,985,264 (GRCm39) |
nonsense |
probably null |
|
R7987:Vmn1r26
|
UTSW |
6 |
57,985,264 (GRCm39) |
nonsense |
probably null |
|
R8311:Vmn1r26
|
UTSW |
6 |
57,985,518 (GRCm39) |
missense |
probably benign |
0.39 |
R8784:Vmn1r26
|
UTSW |
6 |
57,985,440 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9129:Vmn1r26
|
UTSW |
6 |
57,985,373 (GRCm39) |
missense |
|
|
RF020:Vmn1r26
|
UTSW |
6 |
57,985,705 (GRCm39) |
missense |
probably benign |
0.35 |
Z1176:Vmn1r26
|
UTSW |
6 |
57,985,582 (GRCm39) |
missense |
probably damaging |
1.00 |
|