Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg8 |
T |
C |
17: 84,999,249 (GRCm39) |
L115P |
probably damaging |
Het |
Adgrb3 |
A |
C |
1: 25,133,033 (GRCm39) |
M481R |
possibly damaging |
Het |
Adgrd1 |
C |
A |
5: 129,199,647 (GRCm39) |
N161K |
probably benign |
Het |
Alx4 |
T |
A |
2: 93,507,725 (GRCm39) |
V340D |
probably damaging |
Het |
Arid1a |
A |
G |
4: 133,407,716 (GRCm39) |
S2264P |
unknown |
Het |
Azi2 |
A |
T |
9: 117,876,526 (GRCm39) |
H14L |
probably damaging |
Het |
Camsap2 |
A |
G |
1: 136,202,629 (GRCm39) |
|
probably benign |
Het |
Ccpg1 |
T |
A |
9: 72,919,354 (GRCm39) |
L323* |
probably null |
Het |
Cpsf1 |
A |
T |
15: 76,483,148 (GRCm39) |
I943N |
probably damaging |
Het |
Crebrf |
T |
A |
17: 26,978,739 (GRCm39) |
Y476N |
probably damaging |
Het |
Defb10 |
T |
A |
8: 22,351,894 (GRCm39) |
Y46* |
probably null |
Het |
Dock3 |
A |
G |
9: 106,863,269 (GRCm39) |
L703P |
probably damaging |
Het |
Ebf2 |
A |
T |
14: 67,484,518 (GRCm39) |
I181F |
probably damaging |
Het |
Eif3e |
T |
A |
15: 43,114,917 (GRCm39) |
M420L |
probably benign |
Het |
Emilin3 |
T |
A |
2: 160,751,185 (GRCm39) |
Q188L |
probably damaging |
Het |
Fbxl4 |
C |
T |
4: 22,376,840 (GRCm39) |
T92M |
probably damaging |
Het |
Fer1l6 |
C |
T |
15: 58,453,752 (GRCm39) |
Q687* |
probably null |
Het |
Fkrp |
T |
C |
7: 16,544,635 (GRCm39) |
E409G |
possibly damaging |
Het |
Fzd9 |
T |
C |
5: 135,278,460 (GRCm39) |
D475G |
probably benign |
Het |
Gabbr1 |
C |
T |
17: 37,380,958 (GRCm39) |
T767I |
possibly damaging |
Het |
Gdf2 |
G |
A |
14: 33,663,451 (GRCm39) |
|
probably null |
Het |
Gpatch1 |
T |
C |
7: 35,008,776 (GRCm39) |
N82D |
probably benign |
Het |
Heg1 |
T |
A |
16: 33,583,961 (GRCm39) |
L1256Q |
probably damaging |
Het |
Ireb2 |
T |
A |
9: 54,803,885 (GRCm39) |
|
probably null |
Het |
Kansl1 |
T |
G |
11: 104,247,640 (GRCm39) |
H570P |
probably benign |
Het |
Kcna10 |
T |
G |
3: 107,101,744 (GRCm39) |
M125R |
probably damaging |
Het |
Lrp1b |
T |
G |
2: 40,741,805 (GRCm39) |
I3041L |
possibly damaging |
Het |
Mbtd1 |
T |
C |
11: 93,815,474 (GRCm39) |
F354S |
possibly damaging |
Het |
Mideas |
A |
T |
12: 84,199,661 (GRCm39) |
F1020I |
probably benign |
Het |
Mov10 |
T |
C |
3: 104,709,894 (GRCm39) |
T331A |
probably benign |
Het |
Ms4a8a |
A |
T |
19: 11,045,780 (GRCm39) |
S243T |
probably damaging |
Het |
Ndufa11 |
T |
C |
17: 57,024,867 (GRCm39) |
S10P |
probably benign |
Het |
Olfml3 |
A |
G |
3: 103,643,737 (GRCm39) |
Y215H |
possibly damaging |
Het |
Or2t45 |
T |
A |
11: 58,669,705 (GRCm39) |
F251I |
possibly damaging |
Het |
Or56b2j |
A |
G |
7: 104,353,529 (GRCm39) |
I252V |
possibly damaging |
Het |
Pclo |
T |
C |
5: 14,763,574 (GRCm39) |
S4016P |
probably benign |
Het |
Pcyox1 |
G |
C |
6: 86,368,726 (GRCm39) |
A264G |
probably damaging |
Het |
Pdzrn3 |
C |
T |
6: 101,130,272 (GRCm39) |
D515N |
probably damaging |
Het |
Pnisr |
A |
G |
4: 21,874,587 (GRCm39) |
|
probably benign |
Het |
Prc1 |
T |
C |
7: 79,962,927 (GRCm39) |
S574P |
probably damaging |
Het |
Ranbp3l |
T |
A |
15: 9,037,186 (GRCm39) |
V16D |
probably damaging |
Het |
Rfx1 |
T |
C |
8: 84,800,687 (GRCm39) |
V96A |
probably damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Sfmbt1 |
T |
C |
14: 30,537,211 (GRCm39) |
|
probably null |
Het |
Siglecf |
T |
C |
7: 43,001,364 (GRCm39) |
Y111H |
probably damaging |
Het |
Snx14 |
G |
A |
9: 88,280,347 (GRCm39) |
T536I |
possibly damaging |
Het |
Spindoc |
A |
G |
19: 7,351,512 (GRCm39) |
V204A |
probably benign |
Het |
Sptbn5 |
A |
G |
2: 119,915,812 (GRCm39) |
|
probably benign |
Het |
Swt1 |
G |
A |
1: 151,278,727 (GRCm39) |
Q227* |
probably null |
Het |
Tg |
A |
G |
15: 66,631,416 (GRCm39) |
I562V |
possibly damaging |
Het |
Trip11 |
T |
A |
12: 101,851,179 (GRCm39) |
I677F |
probably damaging |
Het |
Vmn1r90 |
T |
C |
7: 14,295,601 (GRCm39) |
K166E |
possibly damaging |
Het |
Vmn2r124 |
T |
C |
17: 18,269,819 (GRCm39) |
I25T |
possibly damaging |
Het |
Vps13d |
A |
T |
4: 144,907,777 (GRCm39) |
|
probably null |
Het |
Zfp106 |
T |
C |
2: 120,354,449 (GRCm39) |
I170V |
probably benign |
Het |
|
Other mutations in Vmn1r49 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01293:Vmn1r49
|
APN |
6 |
90,049,394 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03230:Vmn1r49
|
APN |
6 |
90,049,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03308:Vmn1r49
|
APN |
6 |
90,049,341 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0517:Vmn1r49
|
UTSW |
6 |
90,049,720 (GRCm39) |
missense |
probably damaging |
0.98 |
R0638:Vmn1r49
|
UTSW |
6 |
90,049,648 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1498:Vmn1r49
|
UTSW |
6 |
90,049,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R1649:Vmn1r49
|
UTSW |
6 |
90,049,623 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1668:Vmn1r49
|
UTSW |
6 |
90,049,764 (GRCm39) |
missense |
probably benign |
0.07 |
R1816:Vmn1r49
|
UTSW |
6 |
90,049,785 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2071:Vmn1r49
|
UTSW |
6 |
90,049,184 (GRCm39) |
missense |
probably benign |
0.00 |
R2155:Vmn1r49
|
UTSW |
6 |
90,049,441 (GRCm39) |
missense |
probably damaging |
0.99 |
R2274:Vmn1r49
|
UTSW |
6 |
90,049,126 (GRCm39) |
missense |
probably benign |
0.23 |
R4222:Vmn1r49
|
UTSW |
6 |
90,049,228 (GRCm39) |
missense |
probably benign |
0.06 |
R4614:Vmn1r49
|
UTSW |
6 |
90,049,534 (GRCm39) |
missense |
probably benign |
0.00 |
R4797:Vmn1r49
|
UTSW |
6 |
90,049,612 (GRCm39) |
missense |
probably benign |
0.13 |
R4978:Vmn1r49
|
UTSW |
6 |
90,049,872 (GRCm39) |
missense |
probably benign |
0.30 |
R5959:Vmn1r49
|
UTSW |
6 |
90,049,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R6741:Vmn1r49
|
UTSW |
6 |
90,049,195 (GRCm39) |
missense |
probably benign |
0.19 |
R6744:Vmn1r49
|
UTSW |
6 |
90,049,184 (GRCm39) |
missense |
probably benign |
0.00 |
R7173:Vmn1r49
|
UTSW |
6 |
90,049,250 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7457:Vmn1r49
|
UTSW |
6 |
90,049,534 (GRCm39) |
missense |
probably benign |
0.00 |
R7573:Vmn1r49
|
UTSW |
6 |
90,049,843 (GRCm39) |
missense |
probably benign |
0.06 |
R8360:Vmn1r49
|
UTSW |
6 |
90,049,991 (GRCm39) |
missense |
probably benign |
0.06 |
R8399:Vmn1r49
|
UTSW |
6 |
90,049,689 (GRCm39) |
nonsense |
probably null |
|
R9560:Vmn1r49
|
UTSW |
6 |
90,049,382 (GRCm39) |
missense |
probably benign |
0.03 |
|