Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9630041A04Rik |
T |
C |
9: 101,815,968 (GRCm39) |
L51P |
probably damaging |
Het |
Adgrb3 |
A |
T |
1: 25,133,003 (GRCm39) |
M1121K |
probably benign |
Het |
Ank2 |
T |
C |
3: 126,825,778 (GRCm39) |
N371S |
|
Het |
Arhgef5 |
T |
A |
6: 43,260,885 (GRCm39) |
C1437S |
probably damaging |
Het |
Atp8b1 |
A |
T |
18: 64,690,058 (GRCm39) |
L558Q |
probably damaging |
Het |
Bsn |
T |
C |
9: 108,016,729 (GRCm39) |
K94R |
probably benign |
Het |
Cacna2d1 |
T |
A |
5: 16,519,935 (GRCm39) |
V435D |
probably damaging |
Het |
Chd3 |
T |
C |
11: 69,241,711 (GRCm39) |
N1474S |
probably damaging |
Het |
Chd7 |
A |
G |
4: 8,855,038 (GRCm39) |
D2089G |
probably damaging |
Het |
Col11a2 |
T |
A |
17: 34,270,264 (GRCm39) |
M492K |
unknown |
Het |
Col16a1 |
A |
T |
4: 129,954,262 (GRCm39) |
T502S |
unknown |
Het |
Csl |
A |
T |
10: 99,594,182 (GRCm39) |
N294K |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,350,850 (GRCm39) |
M2624K |
possibly damaging |
Het |
Dync1li1 |
C |
A |
9: 114,535,251 (GRCm39) |
H172N |
probably damaging |
Het |
Eef1a1 |
C |
T |
9: 78,387,672 (GRCm39) |
V59I |
probably benign |
Het |
Ephb1 |
T |
C |
9: 102,072,012 (GRCm39) |
K256E |
probably damaging |
Het |
Erlin2 |
C |
A |
8: 27,518,970 (GRCm39) |
T78N |
probably damaging |
Het |
Fbxo10 |
A |
G |
4: 45,044,793 (GRCm39) |
L614P |
probably damaging |
Het |
Fer1l4 |
A |
T |
2: 155,866,555 (GRCm39) |
D1555E |
probably benign |
Het |
Gabrr2 |
A |
G |
4: 33,082,566 (GRCm39) |
D230G |
probably damaging |
Het |
Gen1 |
A |
T |
12: 11,291,465 (GRCm39) |
S840T |
probably benign |
Het |
Glyctk |
G |
A |
9: 106,034,892 (GRCm39) |
T58I |
probably benign |
Het |
Gm12258 |
G |
A |
11: 58,750,138 (GRCm39) |
A438T |
unknown |
Het |
Gm14305 |
A |
G |
2: 176,413,298 (GRCm39) |
T397A |
probably benign |
Het |
Hnrnpu |
G |
T |
1: 178,165,067 (GRCm39) |
R24S |
possibly damaging |
Het |
Iffo2 |
A |
G |
4: 139,302,265 (GRCm39) |
N3D |
possibly damaging |
Het |
Insr |
C |
T |
8: 3,308,660 (GRCm39) |
M125I |
probably damaging |
Het |
Itsn1 |
G |
A |
16: 91,615,446 (GRCm39) |
R397H |
unknown |
Het |
Kcnj16 |
T |
A |
11: 110,915,341 (GRCm39) |
M1K |
probably null |
Het |
Kcns3 |
G |
A |
12: 11,169,764 (GRCm39) |
|
probably benign |
Het |
Kmt2c |
A |
G |
5: 25,579,562 (GRCm39) |
V578A |
probably benign |
Het |
Krt79 |
T |
C |
15: 101,839,137 (GRCm39) |
K444R |
probably damaging |
Het |
Mtg2 |
T |
C |
2: 179,727,368 (GRCm39) |
V340A |
probably benign |
Het |
Mtr |
A |
C |
13: 12,236,372 (GRCm39) |
L618R |
probably damaging |
Het |
Myo6 |
T |
A |
9: 80,124,991 (GRCm39) |
D23E |
unknown |
Het |
Nos1ap |
A |
G |
1: 170,218,328 (GRCm39) |
V27A |
probably damaging |
Het |
Npc1 |
A |
T |
18: 12,328,129 (GRCm39) |
I1060K |
possibly damaging |
Het |
Nrbp1 |
T |
A |
5: 31,401,193 (GRCm39) |
L23* |
probably null |
Het |
Or10ag52 |
T |
C |
2: 87,044,148 (GRCm39) |
I304T |
probably damaging |
Het |
Or1p1c |
A |
T |
11: 74,160,544 (GRCm39) |
M110L |
probably benign |
Het |
Or6c6c |
A |
T |
10: 129,540,753 (GRCm39) |
K2I |
possibly damaging |
Het |
Or8b3 |
C |
A |
9: 38,314,803 (GRCm39) |
T211K |
probably damaging |
Het |
Or9s13 |
G |
A |
1: 92,548,078 (GRCm39) |
R150H |
probably benign |
Het |
Pcdhgc5 |
A |
T |
18: 37,954,615 (GRCm39) |
T630S |
probably damaging |
Het |
Pgm2 |
C |
A |
5: 64,269,503 (GRCm39) |
T530K |
probably damaging |
Het |
Phf20l1 |
A |
T |
15: 66,475,922 (GRCm39) |
N185I |
probably damaging |
Het |
Pkp2 |
A |
G |
16: 16,031,313 (GRCm39) |
D26G |
probably damaging |
Het |
Rangap1 |
C |
T |
15: 81,594,696 (GRCm39) |
E378K |
probably benign |
Het |
Rapgef1 |
A |
C |
2: 29,569,210 (GRCm39) |
I43L |
probably benign |
Het |
Rbfox1 |
A |
G |
16: 7,094,892 (GRCm39) |
T111A |
|
Het |
Rptn |
GCAAGACCAGAGTTCTCACCAGGGTCAGAAAGGCAGACAAGACCAGAGTTCTCACCAGGGTCAGAAAGGCAGACAAGACCAGAGTTCTCACCAGGGTCA |
GCAAGACCAGAGTTCTCACCAGGGTCAGAAAGGCAGACAAGACCAGAGTTCTCACCAGGGTCA |
3: 93,304,000 (GRCm39) |
|
probably benign |
Het |
Spata16 |
A |
T |
3: 26,894,811 (GRCm39) |
M287L |
probably benign |
Het |
Speer4a2 |
T |
C |
5: 26,289,690 (GRCm39) |
S246G |
possibly damaging |
Het |
Stau2 |
A |
G |
1: 16,416,049 (GRCm39) |
M470T |
probably benign |
Het |
Tcf12 |
T |
C |
9: 71,922,933 (GRCm39) |
Y70C |
probably damaging |
Het |
Tsc22d1 |
C |
T |
14: 76,654,460 (GRCm39) |
T313M |
probably benign |
Het |
Zbtb48 |
A |
T |
4: 152,106,567 (GRCm39) |
C345S |
probably damaging |
Het |
Zfp628 |
G |
A |
7: 4,921,958 (GRCm39) |
R60Q |
probably damaging |
Het |
Zfp638 |
T |
C |
6: 83,906,713 (GRCm39) |
S293P |
possibly damaging |
Het |
Zkscan17 |
G |
A |
11: 59,393,770 (GRCm39) |
P183S |
probably benign |
Het |
Zscan12 |
G |
T |
13: 21,547,897 (GRCm39) |
K26N |
probably benign |
Het |
|
Other mutations in Vmn1r52 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01721:Vmn1r52
|
APN |
6 |
90,155,905 (GRCm39) |
missense |
probably benign |
|
IGL02102:Vmn1r52
|
APN |
6 |
90,156,189 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02583:Vmn1r52
|
APN |
6 |
90,156,126 (GRCm39) |
nonsense |
probably null |
|
IGL02938:Vmn1r52
|
APN |
6 |
90,156,295 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0233:Vmn1r52
|
UTSW |
6 |
90,156,593 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0233:Vmn1r52
|
UTSW |
6 |
90,156,593 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0904:Vmn1r52
|
UTSW |
6 |
90,156,446 (GRCm39) |
missense |
probably damaging |
0.98 |
R2190:Vmn1r52
|
UTSW |
6 |
90,156,151 (GRCm39) |
missense |
probably benign |
0.12 |
R4184:Vmn1r52
|
UTSW |
6 |
90,156,219 (GRCm39) |
missense |
probably benign |
0.00 |
R4906:Vmn1r52
|
UTSW |
6 |
90,155,930 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5475:Vmn1r52
|
UTSW |
6 |
90,155,894 (GRCm39) |
missense |
probably benign |
0.04 |
R5689:Vmn1r52
|
UTSW |
6 |
90,156,232 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5740:Vmn1r52
|
UTSW |
6 |
90,156,176 (GRCm39) |
missense |
probably benign |
0.02 |
R7263:Vmn1r52
|
UTSW |
6 |
90,156,535 (GRCm39) |
missense |
probably benign |
0.00 |
R7337:Vmn1r52
|
UTSW |
6 |
90,156,605 (GRCm39) |
missense |
probably benign |
0.31 |
R7374:Vmn1r52
|
UTSW |
6 |
90,156,118 (GRCm39) |
missense |
probably benign |
0.08 |
R8699:Vmn1r52
|
UTSW |
6 |
90,155,742 (GRCm39) |
missense |
probably benign |
0.02 |
R8747:Vmn1r52
|
UTSW |
6 |
90,156,451 (GRCm39) |
missense |
probably benign |
0.36 |
R9721:Vmn1r52
|
UTSW |
6 |
90,156,008 (GRCm39) |
missense |
probably damaging |
1.00 |
|