Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730596B20Rik |
C |
T |
6: 52,156,014 (GRCm39) |
P27S |
unknown |
Het |
Abi3bp |
A |
T |
16: 56,435,109 (GRCm39) |
K602* |
probably null |
Het |
Adam29 |
G |
T |
8: 56,326,230 (GRCm39) |
H75N |
probably damaging |
Het |
Ajap1 |
C |
T |
4: 153,469,312 (GRCm39) |
E373K |
probably damaging |
Het |
Alg6 |
C |
A |
4: 99,632,113 (GRCm39) |
H206N |
probably damaging |
Het |
Alox5 |
A |
T |
6: 116,392,394 (GRCm39) |
S376T |
probably benign |
Het |
Arhgap19 |
A |
T |
19: 41,770,802 (GRCm39) |
Y321N |
probably benign |
Het |
Brip1 |
A |
G |
11: 86,048,634 (GRCm39) |
V236A |
probably benign |
Het |
C1ra |
C |
T |
6: 124,499,658 (GRCm39) |
P615S |
probably damaging |
Het |
Ccdc69 |
C |
T |
11: 54,942,024 (GRCm39) |
V161I |
possibly damaging |
Het |
Chil5 |
G |
A |
3: 105,927,323 (GRCm39) |
R163C |
possibly damaging |
Het |
Cldnd1 |
A |
G |
16: 58,549,907 (GRCm39) |
D30G |
probably damaging |
Het |
Csmd1 |
A |
G |
8: 15,945,731 (GRCm39) |
C3561R |
probably damaging |
Het |
Daxx |
T |
G |
17: 34,130,255 (GRCm39) |
V90G |
probably damaging |
Het |
Dgkg |
T |
A |
16: 22,441,054 (GRCm39) |
|
probably benign |
Het |
Dmrta2 |
A |
G |
4: 109,839,222 (GRCm39) |
H323R |
probably damaging |
Het |
Dysf |
A |
T |
6: 84,041,878 (GRCm39) |
T161S |
probably benign |
Het |
Fat1 |
G |
T |
8: 45,484,311 (GRCm39) |
R3183L |
probably benign |
Het |
Fcho1 |
C |
A |
8: 72,166,190 (GRCm39) |
D347Y |
probably damaging |
Het |
Gm21798 |
T |
C |
15: 64,689,555 (GRCm39) |
C5R |
unknown |
Het |
Hmcn1 |
T |
C |
1: 150,456,018 (GRCm39) |
R5301G |
probably damaging |
Het |
Hoxd11 |
T |
C |
2: 74,514,459 (GRCm39) |
F330L |
probably damaging |
Het |
Lactbl1 |
A |
G |
4: 136,364,950 (GRCm39) |
D434G |
probably benign |
Het |
Lgals8 |
A |
T |
13: 12,463,362 (GRCm39) |
N191K |
probably damaging |
Het |
Malrd1 |
T |
C |
2: 16,147,115 (GRCm39) |
S1986P |
unknown |
Het |
Map3k9 |
C |
T |
12: 81,790,582 (GRCm39) |
D324N |
probably damaging |
Het |
Mcmbp |
C |
A |
7: 128,305,306 (GRCm39) |
K487N |
probably damaging |
Het |
Mrpl4 |
G |
T |
9: 20,914,067 (GRCm39) |
|
probably benign |
Het |
Nectin2 |
T |
C |
7: 19,451,546 (GRCm39) |
D496G |
possibly damaging |
Het |
Nom1 |
T |
C |
5: 29,647,534 (GRCm39) |
S590P |
probably benign |
Het |
Noto |
T |
C |
6: 85,402,481 (GRCm39) |
F156L |
probably damaging |
Het |
Nrf1 |
T |
A |
6: 30,116,271 (GRCm39) |
D314E |
probably damaging |
Het |
Nup93 |
T |
C |
8: 95,030,260 (GRCm39) |
L373P |
probably damaging |
Het |
Or2w1b |
A |
C |
13: 21,300,191 (GRCm39) |
I110L |
probably benign |
Het |
Or4a2 |
T |
C |
2: 89,247,843 (GRCm39) |
K305E |
possibly damaging |
Het |
Or4c11c |
A |
G |
2: 88,661,932 (GRCm39) |
Q157R |
probably benign |
Het |
Or5d40 |
A |
T |
2: 88,015,310 (GRCm39) |
M30L |
probably benign |
Het |
Or5g25 |
T |
A |
2: 85,478,512 (GRCm39) |
Q51L |
not run |
Het |
Or9s27 |
A |
C |
1: 92,516,986 (GRCm39) |
R311S |
probably benign |
Het |
Pclo |
A |
T |
5: 14,571,345 (GRCm39) |
K243N |
probably damaging |
Het |
Pdgfra |
T |
A |
5: 75,331,264 (GRCm39) |
C290S |
probably damaging |
Het |
Pnlip |
G |
A |
19: 58,668,066 (GRCm39) |
|
probably null |
Het |
Pou2af3 |
G |
A |
9: 51,188,900 (GRCm39) |
A19V |
possibly damaging |
Het |
Ptprm |
A |
T |
17: 67,032,786 (GRCm39) |
H1022Q |
probably benign |
Het |
Rfx2 |
T |
C |
17: 57,110,527 (GRCm39) |
D153G |
probably benign |
Het |
Rps6ka2 |
T |
C |
17: 7,539,032 (GRCm39) |
F317L |
probably damaging |
Het |
Rtl1 |
T |
A |
12: 109,557,539 (GRCm39) |
E1433D |
unknown |
Het |
Sarnp |
A |
G |
10: 128,669,223 (GRCm39) |
T27A |
probably benign |
Het |
Shc3 |
A |
T |
13: 51,602,042 (GRCm39) |
M295K |
probably benign |
Het |
Slc1a3 |
T |
A |
15: 8,672,568 (GRCm39) |
M304L |
probably damaging |
Het |
Slco1a6 |
G |
T |
6: 142,048,727 (GRCm39) |
T351K |
possibly damaging |
Het |
Snrk |
A |
G |
9: 121,986,288 (GRCm39) |
N219S |
probably damaging |
Het |
Spats2 |
T |
A |
15: 99,110,022 (GRCm39) |
V473E |
probably benign |
Het |
Stk35 |
T |
C |
2: 129,652,645 (GRCm39) |
L382P |
probably damaging |
Het |
Tbx10 |
T |
C |
19: 4,049,034 (GRCm39) |
V315A |
probably benign |
Het |
Tdpoz1 |
A |
G |
3: 93,578,082 (GRCm39) |
L234P |
probably damaging |
Het |
Ttn |
T |
G |
2: 76,544,489 (GRCm39) |
E32832D |
probably benign |
Het |
Ttn |
T |
C |
2: 76,601,530 (GRCm39) |
Y18678C |
probably damaging |
Het |
Ugt2a2 |
A |
T |
5: 87,622,353 (GRCm39) |
M205K |
probably damaging |
Het |
Utrn |
C |
A |
10: 12,516,695 (GRCm39) |
V2300L |
probably benign |
Het |
Vmn1r175 |
T |
C |
7: 23,507,847 (GRCm39) |
N260S |
probably benign |
Het |
Vmn1r63 |
T |
A |
7: 5,806,000 (GRCm39) |
I211L |
probably benign |
Het |
Vmn1r83 |
A |
G |
7: 12,055,542 (GRCm39) |
W172R |
possibly damaging |
Het |
Xirp2 |
T |
C |
2: 67,340,978 (GRCm39) |
L1073P |
probably benign |
Het |
Zfp82 |
A |
G |
7: 29,755,597 (GRCm39) |
V495A |
possibly damaging |
Het |
|
Other mutations in Lmod2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00340:Lmod2
|
APN |
6 |
24,598,051 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01013:Lmod2
|
APN |
6 |
24,604,134 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02164:Lmod2
|
APN |
6 |
24,603,909 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02328:Lmod2
|
APN |
6 |
24,603,832 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02956:Lmod2
|
APN |
6 |
24,603,631 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03213:Lmod2
|
APN |
6 |
24,603,615 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03351:Lmod2
|
APN |
6 |
24,598,015 (GRCm39) |
missense |
probably benign |
0.00 |
P0035:Lmod2
|
UTSW |
6 |
24,597,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R1764:Lmod2
|
UTSW |
6 |
24,603,376 (GRCm39) |
missense |
probably damaging |
0.99 |
R3104:Lmod2
|
UTSW |
6 |
24,604,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R3955:Lmod2
|
UTSW |
6 |
24,603,870 (GRCm39) |
missense |
probably benign |
0.02 |
R4410:Lmod2
|
UTSW |
6 |
24,604,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R4876:Lmod2
|
UTSW |
6 |
24,604,278 (GRCm39) |
missense |
probably benign |
0.06 |
R4957:Lmod2
|
UTSW |
6 |
24,603,871 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5509:Lmod2
|
UTSW |
6 |
24,603,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Lmod2
|
UTSW |
6 |
24,603,853 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6114:Lmod2
|
UTSW |
6 |
24,603,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R6462:Lmod2
|
UTSW |
6 |
24,604,300 (GRCm39) |
missense |
probably benign |
0.06 |
R6834:Lmod2
|
UTSW |
6 |
24,597,782 (GRCm39) |
start gained |
probably benign |
|
R6869:Lmod2
|
UTSW |
6 |
24,604,126 (GRCm39) |
missense |
probably benign |
0.06 |
R6909:Lmod2
|
UTSW |
6 |
24,604,157 (GRCm39) |
missense |
probably benign |
0.00 |
R6918:Lmod2
|
UTSW |
6 |
24,603,594 (GRCm39) |
missense |
probably benign |
0.23 |
R7352:Lmod2
|
UTSW |
6 |
24,598,110 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7425:Lmod2
|
UTSW |
6 |
24,603,475 (GRCm39) |
missense |
probably benign |
|
R7986:Lmod2
|
UTSW |
6 |
24,603,448 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8417:Lmod2
|
UTSW |
6 |
24,603,384 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9063:Lmod2
|
UTSW |
6 |
24,603,364 (GRCm39) |
missense |
probably benign |
0.01 |
R9286:Lmod2
|
UTSW |
6 |
24,603,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R9326:Lmod2
|
UTSW |
6 |
24,597,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R9461:Lmod2
|
UTSW |
6 |
24,603,568 (GRCm39) |
missense |
probably benign |
0.01 |
R9716:Lmod2
|
UTSW |
6 |
24,604,182 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9780:Lmod2
|
UTSW |
6 |
24,604,233 (GRCm39) |
missense |
probably damaging |
1.00 |
|