Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A430005L14Rik |
G |
A |
4: 154,044,284 (GRCm39) |
V32I |
probably benign |
Het |
Abcg4 |
A |
T |
9: 44,190,842 (GRCm39) |
M19K |
probably benign |
Het |
Acsm1 |
A |
G |
7: 119,255,274 (GRCm39) |
T392A |
probably benign |
Het |
Adam19 |
A |
T |
11: 46,015,853 (GRCm39) |
I338F |
probably damaging |
Het |
Adamdec1 |
C |
T |
14: 68,807,612 (GRCm39) |
M349I |
probably damaging |
Het |
Arhgef11 |
T |
A |
3: 87,587,059 (GRCm39) |
|
probably benign |
Het |
Bptf |
T |
C |
11: 106,964,121 (GRCm39) |
D1628G |
probably benign |
Het |
Camk2d |
C |
T |
3: 126,391,131 (GRCm39) |
Q15* |
probably null |
Het |
Camk2g |
T |
G |
14: 20,843,999 (GRCm39) |
D12A |
possibly damaging |
Het |
Cemip2 |
T |
C |
19: 21,775,693 (GRCm39) |
I312T |
probably benign |
Het |
Cgn |
T |
C |
3: 94,687,300 (GRCm39) |
M1V |
probably null |
Het |
Clec16a |
G |
A |
16: 10,549,543 (GRCm39) |
C872Y |
probably damaging |
Het |
Dcbld1 |
C |
A |
10: 52,160,353 (GRCm39) |
|
probably benign |
Het |
Ear-ps2 |
G |
A |
14: 44,284,517 (GRCm39) |
|
noncoding transcript |
Het |
Efcab3 |
T |
G |
11: 104,644,632 (GRCm39) |
|
probably null |
Het |
Espl1 |
T |
A |
15: 102,220,953 (GRCm39) |
L903Q |
probably damaging |
Het |
Gm5150 |
T |
C |
3: 16,017,588 (GRCm39) |
T228A |
probably benign |
Het |
Gm5435 |
A |
T |
12: 82,543,250 (GRCm39) |
|
noncoding transcript |
Het |
Gpr156 |
T |
A |
16: 37,825,810 (GRCm39) |
C676S |
probably benign |
Het |
Gstt3 |
C |
T |
10: 75,610,685 (GRCm39) |
E230K |
possibly damaging |
Het |
Jarid2 |
A |
G |
13: 45,059,747 (GRCm39) |
I660V |
possibly damaging |
Het |
Kif13a |
A |
G |
13: 46,928,877 (GRCm39) |
|
probably null |
Het |
Kntc1 |
T |
A |
5: 123,902,254 (GRCm39) |
V299D |
probably benign |
Het |
Lin9 |
T |
A |
1: 180,496,763 (GRCm39) |
L351I |
probably benign |
Het |
Lipk |
T |
A |
19: 33,997,613 (GRCm39) |
|
probably null |
Het |
Loxhd1 |
T |
C |
18: 77,420,378 (GRCm39) |
L334P |
probably damaging |
Het |
Macc1 |
T |
A |
12: 119,410,212 (GRCm39) |
Y327N |
probably damaging |
Het |
Man2a2 |
G |
A |
7: 80,010,876 (GRCm39) |
S705L |
possibly damaging |
Het |
Mmp1b |
T |
C |
9: 7,384,897 (GRCm39) |
I251V |
possibly damaging |
Het |
Ncam2 |
A |
T |
16: 81,231,707 (GRCm39) |
Q57L |
probably damaging |
Het |
Nedd1 |
T |
C |
10: 92,522,102 (GRCm39) |
E645G |
probably damaging |
Het |
Nfatc1 |
A |
T |
18: 80,751,332 (GRCm39) |
M1K |
probably null |
Het |
Nlrp9b |
A |
T |
7: 19,757,916 (GRCm39) |
R384S |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 89,780,354 (GRCm39) |
H62R |
possibly damaging |
Het |
Or2h2b-ps1 |
T |
A |
17: 37,480,891 (GRCm39) |
Y216F |
probably damaging |
Het |
Or4c125 |
T |
A |
2: 89,169,803 (GRCm39) |
Y281F |
probably damaging |
Het |
Or51i1 |
T |
C |
7: 103,671,204 (GRCm39) |
H107R |
probably damaging |
Het |
Or8b39 |
A |
T |
9: 37,996,422 (GRCm39) |
M97L |
probably benign |
Het |
Or8h7 |
A |
G |
2: 86,720,964 (GRCm39) |
L185S |
probably damaging |
Het |
Pdzph1 |
T |
A |
17: 59,281,875 (GRCm39) |
I136F |
probably damaging |
Het |
Pigg |
T |
C |
5: 108,462,026 (GRCm39) |
I119T |
probably damaging |
Het |
R3hdm2 |
A |
G |
10: 127,294,762 (GRCm39) |
H215R |
probably damaging |
Het |
Septin14 |
C |
T |
5: 129,762,978 (GRCm39) |
|
probably null |
Het |
Slc9a3 |
T |
C |
13: 74,299,079 (GRCm39) |
M166T |
possibly damaging |
Het |
Spock3 |
A |
G |
8: 63,798,816 (GRCm39) |
D279G |
probably damaging |
Het |
Suco |
T |
C |
1: 161,660,999 (GRCm39) |
I967V |
probably damaging |
Het |
Tgtp1 |
A |
G |
11: 48,878,003 (GRCm39) |
L234P |
probably damaging |
Het |
Tmem176a |
A |
G |
6: 48,819,151 (GRCm39) |
D4G |
probably benign |
Het |
Ugt1a10 |
G |
A |
1: 88,143,976 (GRCm39) |
A199T |
probably damaging |
Het |
Uox |
A |
G |
3: 146,330,300 (GRCm39) |
D152G |
probably damaging |
Het |
Vmn1r35 |
C |
T |
6: 66,656,490 (GRCm39) |
W60* |
probably null |
Het |
Vmn2r103 |
T |
C |
17: 20,032,433 (GRCm39) |
C736R |
probably damaging |
Het |
|
Other mutations in Gm5117 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01022:Gm5117
|
APN |
8 |
32,228,515 (GRCm39) |
exon |
noncoding transcript |
|
IGL01362:Gm5117
|
APN |
8 |
32,227,947 (GRCm39) |
exon |
noncoding transcript |
|
IGL01972:Gm5117
|
APN |
8 |
32,227,787 (GRCm39) |
exon |
noncoding transcript |
|
IGL02100:Gm5117
|
APN |
8 |
32,227,412 (GRCm39) |
exon |
noncoding transcript |
|
IGL02339:Gm5117
|
APN |
8 |
32,228,254 (GRCm39) |
exon |
noncoding transcript |
|
IGL02366:Gm5117
|
APN |
8 |
32,227,887 (GRCm39) |
exon |
noncoding transcript |
|
IGL02505:Gm5117
|
APN |
8 |
32,228,344 (GRCm39) |
exon |
noncoding transcript |
|
IGL02698:Gm5117
|
APN |
8 |
32,229,767 (GRCm39) |
exon |
noncoding transcript |
|
IGL03310:Gm5117
|
APN |
8 |
32,228,836 (GRCm39) |
exon |
noncoding transcript |
|
IGL02835:Gm5117
|
UTSW |
8 |
32,227,198 (GRCm39) |
unclassified |
noncoding transcript |
|
R1816:Gm5117
|
UTSW |
8 |
32,228,986 (GRCm39) |
exon |
noncoding transcript |
|
R2157:Gm5117
|
UTSW |
8 |
32,228,222 (GRCm39) |
exon |
noncoding transcript |
|
R2353:Gm5117
|
UTSW |
8 |
32,229,223 (GRCm39) |
exon |
noncoding transcript |
|
R2404:Gm5117
|
UTSW |
8 |
32,227,306 (GRCm39) |
exon |
noncoding transcript |
|
R2408:Gm5117
|
UTSW |
8 |
32,227,306 (GRCm39) |
exon |
noncoding transcript |
|
R2409:Gm5117
|
UTSW |
8 |
32,227,306 (GRCm39) |
exon |
noncoding transcript |
|
R2510:Gm5117
|
UTSW |
8 |
32,228,383 (GRCm39) |
exon |
noncoding transcript |
|
R4686:Gm5117
|
UTSW |
8 |
32,229,284 (GRCm39) |
exon |
noncoding transcript |
|
R4953:Gm5117
|
UTSW |
8 |
32,228,608 (GRCm39) |
exon |
noncoding transcript |
|
R5244:Gm5117
|
UTSW |
8 |
32,228,305 (GRCm39) |
exon |
noncoding transcript |
|
R5275:Gm5117
|
UTSW |
8 |
32,229,595 (GRCm39) |
exon |
noncoding transcript |
|
|