Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
A |
3: 137,771,611 (GRCm39) |
S267T |
possibly damaging |
Het |
Abca9 |
T |
C |
11: 109,998,052 (GRCm39) |
D1514G |
probably benign |
Het |
Adamtsl4 |
T |
A |
3: 95,584,980 (GRCm39) |
D896V |
probably damaging |
Het |
Arglu1 |
T |
A |
8: 8,733,843 (GRCm39) |
R158W |
probably damaging |
Het |
Arhgef7 |
A |
G |
8: 11,778,388 (GRCm39) |
E46G |
probably benign |
Het |
Atg2b |
A |
G |
12: 105,613,055 (GRCm39) |
V1172A |
probably benign |
Het |
Bhlhe23 |
T |
A |
2: 180,417,886 (GRCm39) |
K217N |
probably damaging |
Het |
Birc6 |
A |
C |
17: 74,977,369 (GRCm39) |
N4388T |
probably damaging |
Het |
Ccp110 |
C |
T |
7: 118,328,919 (GRCm39) |
A845V |
probably damaging |
Het |
Cd63 |
A |
G |
10: 128,747,722 (GRCm39) |
Y105C |
probably damaging |
Het |
Cdk11b |
T |
C |
4: 155,723,072 (GRCm39) |
|
probably null |
Het |
Clip1 |
T |
A |
5: 123,768,744 (GRCm39) |
R618S |
probably benign |
Het |
Crybg1 |
A |
T |
10: 43,843,739 (GRCm39) |
F1731L |
possibly damaging |
Het |
Dock1 |
A |
C |
7: 134,390,923 (GRCm39) |
K728Q |
possibly damaging |
Het |
Emc2 |
A |
G |
15: 43,374,240 (GRCm39) |
E180G |
probably damaging |
Het |
F13b |
A |
T |
1: 139,440,725 (GRCm39) |
I394F |
probably benign |
Het |
Fnta |
A |
G |
8: 26,499,735 (GRCm39) |
I155T |
probably benign |
Het |
Fshr |
T |
A |
17: 89,293,685 (GRCm39) |
E331V |
probably benign |
Het |
Fshr |
T |
A |
17: 89,293,684 (GRCm39) |
E331D |
probably benign |
Het |
Gas2l1 |
A |
T |
11: 5,011,108 (GRCm39) |
C574S |
probably benign |
Het |
Ggnbp2 |
T |
A |
11: 84,744,847 (GRCm39) |
|
probably benign |
Het |
Gm3371 |
A |
C |
14: 44,641,111 (GRCm39) |
|
probably benign |
Het |
Gm7489 |
T |
A |
15: 53,749,016 (GRCm39) |
|
probably benign |
Het |
Hand1 |
A |
C |
11: 57,722,273 (GRCm39) |
F114V |
probably damaging |
Het |
Itga4 |
A |
C |
2: 79,110,939 (GRCm39) |
H259P |
probably damaging |
Het |
Jakmip1 |
A |
T |
5: 37,262,245 (GRCm39) |
H183L |
probably benign |
Het |
Kifbp |
A |
T |
10: 62,398,908 (GRCm39) |
|
probably benign |
Het |
Krt8 |
G |
T |
15: 101,906,402 (GRCm39) |
A369D |
possibly damaging |
Het |
Krt82 |
T |
C |
15: 101,453,484 (GRCm39) |
S301G |
probably damaging |
Het |
Lig3 |
A |
G |
11: 82,678,504 (GRCm39) |
T248A |
probably benign |
Het |
Madcam1 |
C |
G |
10: 79,504,179 (GRCm39) |
T255S |
probably benign |
Het |
Med20 |
T |
C |
17: 47,929,775 (GRCm39) |
Y71H |
probably benign |
Het |
Mtss2 |
A |
G |
8: 111,455,850 (GRCm39) |
I107V |
probably damaging |
Het |
Nans |
T |
C |
4: 46,502,547 (GRCm39) |
F328S |
possibly damaging |
Het |
Ncbp3 |
A |
G |
11: 72,944,373 (GRCm39) |
|
probably benign |
Het |
Nek8 |
T |
C |
11: 78,063,342 (GRCm39) |
M1V |
probably null |
Het |
Nufip1 |
A |
T |
14: 76,370,538 (GRCm39) |
N413I |
possibly damaging |
Het |
Pbx3 |
T |
C |
2: 34,178,793 (GRCm39) |
|
probably benign |
Het |
Plppr3 |
C |
T |
10: 79,698,279 (GRCm39) |
G419R |
probably benign |
Het |
Rfx1 |
G |
T |
8: 84,793,221 (GRCm39) |
|
probably benign |
Het |
Rnpepl1 |
C |
T |
1: 92,839,045 (GRCm39) |
A68V |
probably benign |
Het |
Rsbn1l |
A |
T |
5: 21,101,212 (GRCm39) |
M776K |
probably benign |
Het |
Setd7 |
A |
T |
3: 51,450,238 (GRCm39) |
Y63N |
probably damaging |
Het |
Slc45a2 |
C |
T |
15: 11,027,871 (GRCm39) |
T480I |
probably damaging |
Het |
Snap47 |
T |
C |
11: 59,319,178 (GRCm39) |
E320G |
probably damaging |
Het |
Spaca6 |
C |
A |
17: 18,058,656 (GRCm39) |
P68Q |
probably benign |
Het |
Tdrd3 |
G |
C |
14: 87,743,651 (GRCm39) |
R527P |
probably damaging |
Het |
Tmprss2 |
G |
T |
16: 97,377,492 (GRCm39) |
Q202K |
probably benign |
Het |
Tmprss6 |
A |
G |
15: 78,330,460 (GRCm39) |
V69A |
probably damaging |
Het |
Trav6-1 |
A |
T |
14: 52,876,161 (GRCm39) |
Q27L |
probably benign |
Het |
Ttn |
C |
T |
2: 76,731,957 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
C |
2: 76,619,945 (GRCm39) |
I15908V |
probably benign |
Het |
Ttn |
T |
A |
2: 76,628,019 (GRCm39) |
D12931V |
probably damaging |
Het |
Ush2a |
T |
A |
1: 188,176,902 (GRCm39) |
|
probably null |
Het |
Wls |
A |
G |
3: 159,578,645 (GRCm39) |
N69S |
probably benign |
Het |
|
Other mutations in Amer2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01844:Amer2
|
APN |
14 |
60,617,356 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03306:Amer2
|
APN |
14 |
60,616,001 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03382:Amer2
|
APN |
14 |
60,617,331 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0365:Amer2
|
UTSW |
14 |
60,616,984 (GRCm39) |
missense |
probably damaging |
0.99 |
R0433:Amer2
|
UTSW |
14 |
60,616,032 (GRCm39) |
missense |
probably damaging |
0.99 |
R1696:Amer2
|
UTSW |
14 |
60,617,123 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1754:Amer2
|
UTSW |
14 |
60,617,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R1991:Amer2
|
UTSW |
14 |
60,617,269 (GRCm39) |
missense |
probably damaging |
0.96 |
R2018:Amer2
|
UTSW |
14 |
60,615,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R2423:Amer2
|
UTSW |
14 |
60,616,656 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3160:Amer2
|
UTSW |
14 |
60,616,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R3161:Amer2
|
UTSW |
14 |
60,616,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Amer2
|
UTSW |
14 |
60,616,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R4928:Amer2
|
UTSW |
14 |
60,616,894 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4981:Amer2
|
UTSW |
14 |
60,617,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R5535:Amer2
|
UTSW |
14 |
60,616,302 (GRCm39) |
small deletion |
probably benign |
|
R5685:Amer2
|
UTSW |
14 |
60,617,026 (GRCm39) |
nonsense |
probably null |
|
R6002:Amer2
|
UTSW |
14 |
60,616,231 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6247:Amer2
|
UTSW |
14 |
60,616,321 (GRCm39) |
missense |
probably damaging |
0.96 |
R6408:Amer2
|
UTSW |
14 |
60,617,674 (GRCm39) |
missense |
probably damaging |
0.96 |
R7271:Amer2
|
UTSW |
14 |
60,617,123 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7407:Amer2
|
UTSW |
14 |
60,616,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R8116:Amer2
|
UTSW |
14 |
60,616,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R8122:Amer2
|
UTSW |
14 |
60,616,791 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8758:Amer2
|
UTSW |
14 |
60,616,326 (GRCm39) |
missense |
probably damaging |
0.99 |
R9005:Amer2
|
UTSW |
14 |
60,617,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R9006:Amer2
|
UTSW |
14 |
60,617,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R9007:Amer2
|
UTSW |
14 |
60,617,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R9016:Amer2
|
UTSW |
14 |
60,617,376 (GRCm39) |
missense |
probably damaging |
1.00 |
|