Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy7 |
T |
C |
8: 89,048,431 (GRCm39) |
S625P |
probably damaging |
Het |
Agpat1 |
T |
C |
17: 34,830,586 (GRCm39) |
V170A |
probably damaging |
Het |
Alg9 |
C |
T |
9: 50,720,080 (GRCm39) |
Q519* |
probably null |
Het |
Apol8 |
C |
T |
15: 77,634,336 (GRCm39) |
R80H |
probably benign |
Het |
Arhgap25 |
G |
T |
6: 87,465,287 (GRCm39) |
S118* |
probably null |
Het |
Arhgap30 |
T |
A |
1: 171,225,086 (GRCm39) |
Y47* |
probably null |
Het |
Arhgap42 |
C |
T |
9: 9,011,434 (GRCm39) |
D451N |
probably damaging |
Het |
Cabp2 |
T |
A |
19: 4,135,582 (GRCm39) |
F91I |
probably damaging |
Het |
Ccdc30 |
T |
C |
4: 119,230,943 (GRCm39) |
E108G |
probably benign |
Het |
Cfap99 |
T |
C |
5: 34,458,763 (GRCm39) |
S53P |
probably damaging |
Het |
Clec5a |
C |
T |
6: 40,556,361 (GRCm39) |
R135H |
possibly damaging |
Het |
Cops8 |
T |
G |
1: 90,531,325 (GRCm39) |
D18E |
probably benign |
Het |
Cped1 |
A |
T |
6: 22,233,480 (GRCm39) |
M779L |
possibly damaging |
Het |
Cyp4x1 |
G |
A |
4: 114,967,263 (GRCm39) |
H438Y |
probably damaging |
Het |
Disc1 |
A |
T |
8: 125,815,014 (GRCm39) |
T293S |
probably benign |
Het |
Ercc1 |
T |
C |
7: 19,084,102 (GRCm39) |
L113S |
probably damaging |
Het |
Ermp1 |
G |
T |
19: 29,593,196 (GRCm39) |
N765K |
probably benign |
Het |
Fam83c |
A |
G |
2: 155,676,740 (GRCm39) |
I10T |
probably benign |
Het |
Farp1 |
T |
C |
14: 121,513,008 (GRCm39) |
V788A |
probably benign |
Het |
Fbn1 |
C |
G |
2: 125,319,489 (GRCm39) |
G92R |
probably damaging |
Het |
Fsd1 |
T |
A |
17: 56,302,881 (GRCm39) |
M328K |
probably benign |
Het |
Fzd3 |
C |
A |
14: 65,440,262 (GRCm39) |
S636I |
probably benign |
Het |
Gapvd1 |
A |
G |
2: 34,594,330 (GRCm39) |
S886P |
probably damaging |
Het |
Gatad2b |
T |
A |
3: 90,249,029 (GRCm39) |
D22E |
probably benign |
Het |
Gm7168 |
A |
T |
17: 14,169,238 (GRCm39) |
K202* |
probably null |
Het |
Gmps |
T |
C |
3: 63,887,690 (GRCm39) |
I54T |
probably damaging |
Het |
Gp6 |
A |
G |
7: 4,397,114 (GRCm39) |
I107T |
probably benign |
Het |
Gpat2 |
T |
C |
2: 127,273,267 (GRCm39) |
V217A |
possibly damaging |
Het |
Hdlbp |
T |
A |
1: 93,344,917 (GRCm39) |
I863F |
probably damaging |
Het |
Hmcn1 |
A |
C |
1: 150,624,841 (GRCm39) |
I1021M |
possibly damaging |
Het |
Igkv6-14 |
C |
T |
6: 70,412,087 (GRCm39) |
A66T |
probably benign |
Het |
Ippk |
C |
T |
13: 49,599,818 (GRCm39) |
P226S |
|
Het |
Iqch |
A |
G |
9: 63,361,855 (GRCm39) |
I925T |
probably benign |
Het |
Kcnt1 |
A |
G |
2: 25,791,223 (GRCm39) |
E522G |
possibly damaging |
Het |
Kremen2 |
C |
G |
17: 23,962,776 (GRCm39) |
E103D |
probably damaging |
Het |
Lig4 |
G |
T |
8: 10,023,485 (GRCm39) |
N98K |
probably benign |
Het |
Lrrc3b |
T |
G |
14: 15,358,232 (GRCm38) |
I125L |
probably benign |
Het |
Lrrc4 |
T |
C |
6: 28,829,902 (GRCm39) |
D148G |
probably damaging |
Het |
Mmrn2 |
G |
A |
14: 34,119,593 (GRCm39) |
V191I |
probably benign |
Het |
Nadk |
T |
A |
4: 155,655,127 (GRCm39) |
|
probably null |
Het |
Napb |
C |
A |
2: 148,551,351 (GRCm39) |
A61S |
possibly damaging |
Het |
Ncan |
T |
A |
8: 70,561,221 (GRCm39) |
D582V |
possibly damaging |
Het |
Ncl |
T |
C |
1: 86,284,364 (GRCm39) |
D244G |
possibly damaging |
Het |
Nlrp14 |
A |
G |
7: 106,791,715 (GRCm39) |
N800S |
possibly damaging |
Het |
Nlrp9b |
C |
T |
7: 19,753,260 (GRCm39) |
T55M |
probably benign |
Het |
Nobox |
G |
A |
6: 43,282,951 (GRCm39) |
T228I |
probably benign |
Het |
Npffr1 |
C |
A |
10: 61,449,750 (GRCm39) |
P8H |
possibly damaging |
Het |
Nrg2 |
T |
C |
18: 36,154,156 (GRCm39) |
Y587C |
probably damaging |
Het |
Nsd1 |
T |
G |
13: 55,393,434 (GRCm39) |
V448G |
probably benign |
Het |
Or2w1 |
T |
A |
13: 21,317,371 (GRCm39) |
V142D |
probably benign |
Het |
Or5e1 |
G |
T |
7: 108,354,438 (GRCm39) |
C125F |
probably damaging |
Het |
Or8k41 |
T |
G |
2: 86,313,412 (GRCm39) |
I225L |
probably damaging |
Het |
Or9g20 |
A |
G |
2: 85,630,011 (GRCm39) |
L201P |
probably damaging |
Het |
Peg10 |
T |
TCCC |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Ppp5c |
T |
C |
7: 16,742,932 (GRCm39) |
T229A |
probably benign |
Het |
Pramel51 |
T |
C |
12: 88,143,850 (GRCm39) |
Y329C |
probably benign |
Het |
Prr5 |
C |
T |
15: 84,577,993 (GRCm39) |
R101C |
probably damaging |
Het |
Psg22 |
T |
C |
7: 18,456,987 (GRCm39) |
M290T |
probably benign |
Het |
Pzp |
C |
T |
6: 128,490,694 (GRCm39) |
|
probably null |
Het |
Rapgef6 |
T |
C |
11: 54,516,784 (GRCm39) |
V347A |
probably benign |
Het |
Rttn |
A |
T |
18: 89,029,040 (GRCm39) |
H586L |
probably damaging |
Het |
Sema3f |
A |
T |
9: 107,565,275 (GRCm39) |
I259K |
possibly damaging |
Het |
Sgpp1 |
A |
T |
12: 75,763,374 (GRCm39) |
L269Q |
probably damaging |
Het |
Slc22a8 |
A |
C |
19: 8,582,903 (GRCm39) |
I195L |
probably benign |
Het |
Slc35a5 |
T |
C |
16: 44,962,551 (GRCm39) |
T425A |
unknown |
Het |
Spata31e1 |
G |
A |
13: 49,939,548 (GRCm39) |
R721C |
probably benign |
Het |
Stard13 |
G |
A |
5: 150,986,970 (GRCm39) |
T180I |
probably damaging |
Het |
Stard9 |
G |
A |
2: 120,534,911 (GRCm39) |
G3723S |
probably benign |
Het |
Svil |
A |
T |
18: 5,062,385 (GRCm39) |
T902S |
probably damaging |
Het |
Tnfaip8l3 |
T |
A |
9: 53,934,421 (GRCm39) |
R185W |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,590,393 (GRCm39) |
D21105E |
probably benign |
Het |
Vmn2r109 |
T |
A |
17: 20,774,729 (GRCm39) |
M209L |
probably benign |
Het |
Vmn2r125 |
A |
G |
4: 156,703,642 (GRCm39) |
H340R |
probably damaging |
Het |
Zfp946 |
T |
C |
17: 22,674,481 (GRCm39) |
C412R |
probably damaging |
Het |
|
Other mutations in Lrsam1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01393:Lrsam1
|
APN |
2 |
32,845,185 (GRCm39) |
splice site |
probably benign |
|
IGL01407:Lrsam1
|
APN |
2 |
32,837,915 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01565:Lrsam1
|
APN |
2 |
32,826,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01985:Lrsam1
|
APN |
2 |
32,818,103 (GRCm39) |
missense |
probably benign |
|
IGL02743:Lrsam1
|
APN |
2 |
32,818,661 (GRCm39) |
splice site |
probably null |
|
R0240:Lrsam1
|
UTSW |
2 |
32,845,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R0591:Lrsam1
|
UTSW |
2 |
32,823,935 (GRCm39) |
splice site |
probably benign |
|
R0845:Lrsam1
|
UTSW |
2 |
32,843,455 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0945:Lrsam1
|
UTSW |
2 |
32,837,921 (GRCm39) |
missense |
probably benign |
0.04 |
R1475:Lrsam1
|
UTSW |
2 |
32,844,277 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2147:Lrsam1
|
UTSW |
2 |
32,835,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R3790:Lrsam1
|
UTSW |
2 |
32,848,171 (GRCm39) |
missense |
probably null |
1.00 |
R4374:Lrsam1
|
UTSW |
2 |
32,845,203 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4822:Lrsam1
|
UTSW |
2 |
32,816,804 (GRCm39) |
missense |
probably damaging |
0.99 |
R5014:Lrsam1
|
UTSW |
2 |
32,826,407 (GRCm39) |
intron |
probably benign |
|
R5472:Lrsam1
|
UTSW |
2 |
32,835,870 (GRCm39) |
frame shift |
probably null |
|
R5566:Lrsam1
|
UTSW |
2 |
32,831,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R5640:Lrsam1
|
UTSW |
2 |
32,835,864 (GRCm39) |
missense |
probably benign |
0.13 |
R5992:Lrsam1
|
UTSW |
2 |
32,845,234 (GRCm39) |
missense |
probably benign |
0.00 |
R7513:Lrsam1
|
UTSW |
2 |
32,843,497 (GRCm39) |
missense |
probably benign |
0.02 |
R7515:Lrsam1
|
UTSW |
2 |
32,830,251 (GRCm39) |
critical splice donor site |
probably null |
|
R9731:Lrsam1
|
UTSW |
2 |
32,835,452 (GRCm39) |
critical splice donor site |
probably null |
|
R9766:Lrsam1
|
UTSW |
2 |
32,818,077 (GRCm39) |
missense |
probably benign |
|
Z1176:Lrsam1
|
UTSW |
2 |
32,831,826 (GRCm39) |
missense |
probably damaging |
1.00 |
|