Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb8 |
T |
C |
5: 24,611,723 (GRCm39) |
V513A |
probably damaging |
Het |
Acsf2 |
C |
T |
11: 94,453,714 (GRCm39) |
V416M |
probably damaging |
Het |
Adrm1 |
G |
A |
2: 179,817,002 (GRCm39) |
A225T |
unknown |
Het |
Aldh9a1 |
T |
C |
1: 167,180,236 (GRCm39) |
|
probably null |
Het |
Apbb2 |
T |
C |
5: 66,608,987 (GRCm39) |
D220G |
probably benign |
Het |
Bace2 |
T |
C |
16: 97,238,052 (GRCm39) |
V501A |
probably benign |
Het |
Camsap1 |
T |
C |
2: 25,828,214 (GRCm39) |
N1170S |
probably benign |
Het |
Casr |
A |
G |
16: 36,315,979 (GRCm39) |
V697A |
probably damaging |
Het |
Clcn1 |
T |
C |
6: 42,284,595 (GRCm39) |
|
probably null |
Het |
Cobl |
T |
C |
11: 12,203,459 (GRCm39) |
K1081R |
probably benign |
Het |
Ctr9 |
T |
A |
7: 110,633,099 (GRCm39) |
L116I |
probably damaging |
Het |
Dennd4a |
T |
C |
9: 64,780,312 (GRCm39) |
F616S |
probably damaging |
Het |
Dynlt1a |
C |
T |
17: 6,362,089 (GRCm39) |
G30S |
possibly damaging |
Het |
Eif1 |
T |
C |
11: 100,211,274 (GRCm39) |
S23P |
possibly damaging |
Het |
Eml6 |
A |
C |
11: 29,699,973 (GRCm39) |
L1721R |
possibly damaging |
Het |
Fscb |
A |
G |
12: 64,521,049 (GRCm39) |
I139T |
probably benign |
Het |
Fstl4 |
A |
G |
11: 52,959,496 (GRCm39) |
E179G |
probably damaging |
Het |
Fuom |
T |
C |
7: 139,680,067 (GRCm39) |
T95A |
|
Het |
Gigyf1 |
C |
T |
5: 137,523,740 (GRCm39) |
H1001Y |
probably damaging |
Het |
Helz2 |
G |
A |
2: 180,881,998 (GRCm39) |
T265I |
probably benign |
Het |
Hs6st3 |
G |
T |
14: 120,106,968 (GRCm39) |
V459F |
probably damaging |
Het |
Ido2 |
A |
G |
8: 25,025,156 (GRCm39) |
|
probably null |
Het |
Idua |
A |
G |
5: 108,818,115 (GRCm39) |
I96V |
probably benign |
Het |
Iftap |
A |
T |
2: 101,400,989 (GRCm39) |
|
probably benign |
Het |
Inpp5j |
A |
G |
11: 3,445,171 (GRCm39) |
S494P |
|
Het |
Krt19 |
A |
G |
11: 100,032,209 (GRCm39) |
V285A |
probably damaging |
Het |
Krt71 |
T |
G |
15: 101,646,817 (GRCm39) |
D297A |
possibly damaging |
Het |
L3hypdh |
G |
A |
12: 72,131,723 (GRCm39) |
R70C |
probably damaging |
Het |
Masp1 |
T |
C |
16: 23,303,156 (GRCm39) |
Y324C |
probably damaging |
Het |
Mfap2 |
A |
G |
4: 140,741,114 (GRCm39) |
D25G |
possibly damaging |
Het |
Mmp17 |
G |
A |
5: 129,672,148 (GRCm39) |
|
probably null |
Het |
Mroh7 |
G |
A |
4: 106,578,634 (GRCm39) |
P15S |
probably benign |
Het |
Muc5b |
T |
A |
7: 141,417,373 (GRCm39) |
C3440S |
probably benign |
Het |
Naip5 |
C |
A |
13: 100,382,406 (GRCm39) |
S101I |
probably damaging |
Het |
Neb |
A |
T |
2: 52,113,060 (GRCm39) |
Y1066N |
|
Het |
Nop56 |
T |
A |
2: 130,119,188 (GRCm39) |
C38S |
probably benign |
Het |
Nup214 |
T |
A |
2: 31,923,362 (GRCm39) |
L1297Q |
possibly damaging |
Het |
Oasl2 |
C |
A |
5: 115,040,329 (GRCm39) |
|
probably benign |
Het |
Or4a70 |
A |
G |
2: 89,324,132 (GRCm39) |
F175L |
probably damaging |
Het |
Or4c58 |
T |
C |
2: 89,675,273 (GRCm39) |
N15D |
probably benign |
Het |
Or51b4 |
A |
G |
7: 103,530,904 (GRCm39) |
V182A |
possibly damaging |
Het |
Or52a5 |
T |
A |
7: 103,427,547 (GRCm39) |
I2F |
probably benign |
Het |
Or5h24 |
T |
C |
16: 58,918,731 (GRCm39) |
H208R |
unknown |
Het |
Or8g4 |
T |
C |
9: 39,662,092 (GRCm39) |
S137P |
possibly damaging |
Het |
Pacrg |
C |
T |
17: 10,795,496 (GRCm39) |
V155I |
probably benign |
Het |
Patz1 |
A |
T |
11: 3,257,658 (GRCm39) |
M96L |
probably benign |
Het |
Pcca |
A |
G |
14: 122,875,794 (GRCm39) |
D141G |
probably benign |
Het |
Ptprr |
A |
G |
10: 115,884,075 (GRCm39) |
Y44C |
probably damaging |
Het |
Rad51ap1 |
A |
G |
6: 126,911,675 (GRCm39) |
|
probably null |
Het |
Raet1e |
A |
C |
10: 22,057,198 (GRCm39) |
D174A |
probably damaging |
Het |
Rhobtb2 |
T |
G |
14: 70,034,214 (GRCm39) |
D337A |
probably benign |
Het |
Sbf2 |
T |
C |
7: 109,934,594 (GRCm39) |
K1377E |
probably damaging |
Het |
Sh3pxd2b |
A |
G |
11: 32,361,567 (GRCm39) |
K260E |
probably damaging |
Het |
Slc4a8 |
A |
T |
15: 100,685,170 (GRCm39) |
I234F |
possibly damaging |
Het |
Srgap3 |
C |
T |
6: 112,716,325 (GRCm39) |
R625H |
probably benign |
Het |
Tbxas1 |
C |
T |
6: 39,004,830 (GRCm39) |
T359I |
probably benign |
Het |
Trim9 |
T |
A |
12: 70,337,161 (GRCm39) |
S309C |
probably benign |
Het |
Ttn |
G |
A |
2: 76,659,483 (GRCm39) |
P12191S |
unknown |
Het |
Unc80 |
A |
G |
1: 66,522,463 (GRCm39) |
R222G |
possibly damaging |
Het |
Vmn1r202 |
A |
T |
13: 22,686,314 (GRCm39) |
H34Q |
possibly damaging |
Het |
Vmn2r61 |
T |
A |
7: 41,916,141 (GRCm39) |
N251K |
probably benign |
Het |
Vmn2r67 |
A |
T |
7: 84,785,924 (GRCm39) |
Y694N |
probably damaging |
Het |
Vwde |
A |
G |
6: 13,205,782 (GRCm39) |
F255S |
probably benign |
Het |
Zfp532 |
T |
G |
18: 65,758,227 (GRCm39) |
I720R |
possibly damaging |
Het |
Zfp819 |
A |
G |
7: 43,267,319 (GRCm39) |
T601A |
probably benign |
Het |
Zfp853 |
G |
T |
5: 143,274,280 (GRCm39) |
Q462K |
unknown |
Het |
|
Other mutations in Gm21886 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1679:Gm21886
|
UTSW |
18 |
80,132,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R1902:Gm21886
|
UTSW |
18 |
80,132,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R3779:Gm21886
|
UTSW |
18 |
80,132,649 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7146:Gm21886
|
UTSW |
18 |
80,132,697 (GRCm39) |
small deletion |
probably benign |
|
R7254:Gm21886
|
UTSW |
18 |
80,132,950 (GRCm39) |
nonsense |
probably null |
|
R7405:Gm21886
|
UTSW |
18 |
80,133,040 (GRCm39) |
small deletion |
probably benign |
|
R7412:Gm21886
|
UTSW |
18 |
80,132,967 (GRCm39) |
small deletion |
probably benign |
|
R7427:Gm21886
|
UTSW |
18 |
80,132,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R7428:Gm21886
|
UTSW |
18 |
80,132,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R7526:Gm21886
|
UTSW |
18 |
80,133,040 (GRCm39) |
small deletion |
probably benign |
|
R7756:Gm21886
|
UTSW |
18 |
80,133,040 (GRCm39) |
small deletion |
probably benign |
|
R7880:Gm21886
|
UTSW |
18 |
80,133,040 (GRCm39) |
small deletion |
probably benign |
|
R7891:Gm21886
|
UTSW |
18 |
80,132,972 (GRCm39) |
missense |
probably null |
0.17 |
R8295:Gm21886
|
UTSW |
18 |
80,133,040 (GRCm39) |
small deletion |
probably benign |
|
R8950:Gm21886
|
UTSW |
18 |
80,133,040 (GRCm39) |
small deletion |
probably benign |
|
R9659:Gm21886
|
UTSW |
18 |
80,132,776 (GRCm39) |
small deletion |
probably benign |
|
R9731:Gm21886
|
UTSW |
18 |
80,133,040 (GRCm39) |
small deletion |
probably benign |
|
Z1176:Gm21886
|
UTSW |
18 |
80,133,138 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Gm21886
|
UTSW |
18 |
80,132,602 (GRCm39) |
nonsense |
probably null |
|
Z1191:Gm21886
|
UTSW |
18 |
80,133,040 (GRCm39) |
small deletion |
probably benign |
|
|