Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acnat1 |
A |
G |
4: 49,450,785 (GRCm39) |
Y109H |
possibly damaging |
Het |
Adgrf3 |
T |
A |
5: 30,401,522 (GRCm39) |
K835N |
possibly damaging |
Het |
Afg1l |
T |
C |
10: 42,194,712 (GRCm39) |
D360G |
probably damaging |
Het |
Ap3s1 |
C |
T |
18: 46,887,448 (GRCm39) |
T27M |
probably benign |
Het |
Atp8b4 |
A |
G |
2: 126,256,284 (GRCm39) |
L225P |
probably damaging |
Het |
Bicra |
G |
A |
7: 15,713,056 (GRCm39) |
T997I |
probably benign |
Het |
Bod1l |
T |
C |
5: 41,995,411 (GRCm39) |
R112G |
probably damaging |
Het |
Cabin1 |
T |
C |
10: 75,561,535 (GRCm39) |
T989A |
possibly damaging |
Het |
Cog1 |
C |
A |
11: 113,546,887 (GRCm39) |
Q494K |
probably benign |
Het |
Cyb5rl |
T |
C |
4: 106,942,550 (GRCm39) |
Y160H |
probably benign |
Het |
Dnajb8 |
A |
G |
6: 88,200,057 (GRCm39) |
N198D |
probably damaging |
Het |
Eif1ad11 |
T |
C |
12: 87,994,117 (GRCm39) |
I115T |
probably damaging |
Het |
Eif3l |
C |
A |
15: 78,970,778 (GRCm39) |
Q351K |
possibly damaging |
Het |
Esr1 |
T |
C |
10: 4,916,301 (GRCm39) |
|
probably benign |
Het |
Fam3c |
G |
T |
6: 22,329,607 (GRCm39) |
A40D |
probably damaging |
Het |
Fcrla |
A |
G |
1: 170,749,797 (GRCm39) |
S87P |
probably damaging |
Het |
Glra1 |
A |
G |
11: 55,411,822 (GRCm39) |
Y246H |
probably damaging |
Het |
Gm45871 |
T |
A |
18: 90,609,844 (GRCm39) |
C361S |
probably damaging |
Het |
Greb1l |
A |
G |
18: 10,547,347 (GRCm39) |
N1522D |
possibly damaging |
Het |
Hcn4 |
T |
C |
9: 58,731,435 (GRCm39) |
M214T |
unknown |
Het |
Heatr5b |
A |
T |
17: 79,070,418 (GRCm39) |
V1665E |
probably damaging |
Het |
Hemgn |
C |
A |
4: 46,395,990 (GRCm39) |
M415I |
possibly damaging |
Het |
Hibadh |
G |
A |
6: 52,524,013 (GRCm39) |
T295I |
probably damaging |
Het |
Iars1 |
T |
C |
13: 49,878,745 (GRCm39) |
L947P |
probably damaging |
Het |
Icam2 |
G |
A |
11: 106,269,585 (GRCm39) |
T178I |
probably damaging |
Het |
Lbr |
A |
G |
1: 181,663,763 (GRCm39) |
S86P |
probably damaging |
Het |
Lipe |
G |
A |
7: 25,082,749 (GRCm39) |
T801I |
probably benign |
Het |
Lrp6 |
T |
C |
6: 134,518,934 (GRCm39) |
T44A |
possibly damaging |
Het |
Malrd1 |
A |
G |
2: 15,847,439 (GRCm39) |
H1193R |
probably benign |
Het |
Mroh2a |
GCCC |
GC |
1: 88,159,979 (GRCm39) |
|
probably null |
Het |
Myh10 |
A |
G |
11: 68,699,676 (GRCm39) |
I1671V |
probably benign |
Het |
Or2c1 |
A |
G |
16: 3,656,894 (GRCm39) |
D19G |
probably benign |
Het |
Osbpl9 |
T |
C |
4: 108,930,129 (GRCm39) |
D334G |
possibly damaging |
Het |
Pdcd11 |
A |
G |
19: 47,098,117 (GRCm39) |
D801G |
probably damaging |
Het |
Pfdn4 |
C |
A |
2: 170,358,556 (GRCm39) |
D16E |
probably benign |
Het |
Pmp22 |
C |
T |
11: 63,049,099 (GRCm39) |
A114V |
probably damaging |
Het |
Rrp9 |
C |
T |
9: 106,360,778 (GRCm39) |
T253I |
probably damaging |
Het |
Speer1m |
A |
T |
5: 11,970,612 (GRCm39) |
K62* |
probably null |
Het |
Tnrc6a |
A |
G |
7: 122,769,133 (GRCm39) |
T308A |
probably damaging |
Het |
Trgv4 |
T |
A |
13: 19,369,250 (GRCm39) |
C34S |
probably benign |
Het |
Trhr |
A |
G |
15: 44,092,602 (GRCm39) |
M280V |
possibly damaging |
Het |
Trp53bp1 |
G |
A |
2: 121,059,084 (GRCm39) |
H926Y |
probably damaging |
Het |
Trpv5 |
A |
T |
6: 41,652,903 (GRCm39) |
I90K |
probably benign |
Het |
Ttn |
T |
C |
2: 76,719,259 (GRCm39) |
|
probably benign |
Het |
Vav1 |
A |
C |
17: 57,612,280 (GRCm39) |
R513S |
probably damaging |
Het |
Vmn2r100 |
A |
T |
17: 19,741,671 (GRCm39) |
T128S |
probably benign |
Het |
Zfp687 |
T |
C |
3: 94,915,700 (GRCm39) |
Y1024C |
probably damaging |
Het |
Zfp938 |
C |
A |
10: 82,061,160 (GRCm39) |
G487* |
probably null |
Het |
Znrf2 |
A |
G |
6: 54,855,430 (GRCm39) |
Y73C |
probably damaging |
Het |
|
Other mutations in 2900026A02Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02810:2900026A02Rik
|
APN |
5 |
113,249,401 (GRCm39) |
missense |
probably damaging |
1.00 |
oyster
|
UTSW |
5 |
113,330,833 (GRCm39) |
missense |
probably benign |
0.14 |
pimento
|
UTSW |
5 |
113,243,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R1394:2900026A02Rik
|
UTSW |
5 |
113,249,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R1395:2900026A02Rik
|
UTSW |
5 |
113,249,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R4329:2900026A02Rik
|
UTSW |
5 |
113,243,455 (GRCm39) |
critical splice donor site |
probably null |
|
R4766:2900026A02Rik
|
UTSW |
5 |
113,245,502 (GRCm39) |
missense |
probably benign |
0.01 |
R6124:2900026A02Rik
|
UTSW |
5 |
113,331,622 (GRCm39) |
missense |
probably benign |
|
R6336:2900026A02Rik
|
UTSW |
5 |
113,331,349 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6365:2900026A02Rik
|
UTSW |
5 |
113,330,510 (GRCm39) |
missense |
probably benign |
0.00 |
R6759:2900026A02Rik
|
UTSW |
5 |
113,331,692 (GRCm39) |
missense |
probably benign |
0.00 |
R7117:2900026A02Rik
|
UTSW |
5 |
113,339,250 (GRCm39) |
missense |
probably benign |
0.00 |
R7168:2900026A02Rik
|
UTSW |
5 |
113,285,659 (GRCm39) |
missense |
probably damaging |
0.96 |
R7339:2900026A02Rik
|
UTSW |
5 |
113,330,938 (GRCm39) |
missense |
probably benign |
0.09 |
R7450:2900026A02Rik
|
UTSW |
5 |
113,331,977 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7458:2900026A02Rik
|
UTSW |
5 |
113,338,510 (GRCm39) |
missense |
probably benign |
0.05 |
R7525:2900026A02Rik
|
UTSW |
5 |
113,331,221 (GRCm39) |
missense |
probably damaging |
0.99 |
R7707:2900026A02Rik
|
UTSW |
5 |
113,285,852 (GRCm39) |
start codon destroyed |
probably benign |
0.14 |
R7848:2900026A02Rik
|
UTSW |
5 |
113,340,007 (GRCm39) |
missense |
probably damaging |
0.96 |
R7869:2900026A02Rik
|
UTSW |
5 |
113,332,001 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7871:2900026A02Rik
|
UTSW |
5 |
113,331,092 (GRCm39) |
missense |
probably benign |
0.02 |
R8327:2900026A02Rik
|
UTSW |
5 |
113,331,685 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8411:2900026A02Rik
|
UTSW |
5 |
113,285,588 (GRCm39) |
missense |
probably benign |
|
R8429:2900026A02Rik
|
UTSW |
5 |
113,331,302 (GRCm39) |
missense |
probably benign |
0.29 |
R8940:2900026A02Rik
|
UTSW |
5 |
113,241,068 (GRCm39) |
missense |
probably benign |
0.07 |
R9065:2900026A02Rik
|
UTSW |
5 |
113,323,084 (GRCm39) |
missense |
probably benign |
0.00 |
R9096:2900026A02Rik
|
UTSW |
5 |
113,339,793 (GRCm39) |
missense |
|
|
R9182:2900026A02Rik
|
UTSW |
5 |
113,243,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R9191:2900026A02Rik
|
UTSW |
5 |
113,330,564 (GRCm39) |
missense |
probably benign |
0.34 |
R9330:2900026A02Rik
|
UTSW |
5 |
113,330,833 (GRCm39) |
missense |
probably benign |
0.14 |
R9336:2900026A02Rik
|
UTSW |
5 |
113,240,966 (GRCm39) |
critical splice donor site |
probably null |
|
R9375:2900026A02Rik
|
UTSW |
5 |
113,332,567 (GRCm39) |
missense |
probably benign |
|
R9388:2900026A02Rik
|
UTSW |
5 |
113,338,714 (GRCm39) |
missense |
probably benign |
0.00 |
R9483:2900026A02Rik
|
UTSW |
5 |
113,339,010 (GRCm39) |
missense |
probably benign |
0.01 |
R9529:2900026A02Rik
|
UTSW |
5 |
113,331,682 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9675:2900026A02Rik
|
UTSW |
5 |
113,339,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R9784:2900026A02Rik
|
UTSW |
5 |
113,338,527 (GRCm39) |
missense |
possibly damaging |
0.93 |
|