Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
A |
G |
11: 119,912,277 (GRCm39) |
I56T |
probably benign |
Het |
Adissp |
T |
C |
2: 130,993,682 (GRCm39) |
|
probably null |
Het |
Akr1c12 |
A |
G |
13: 4,325,796 (GRCm39) |
L99S |
probably damaging |
Het |
Azin1 |
C |
A |
15: 38,493,871 (GRCm39) |
V251F |
possibly damaging |
Het |
Btbd16 |
C |
T |
7: 130,417,516 (GRCm39) |
R344C |
probably damaging |
Het |
C2cd3 |
A |
T |
7: 100,065,262 (GRCm39) |
M305L |
|
Het |
Casz1 |
A |
G |
4: 149,023,320 (GRCm39) |
T742A |
probably damaging |
Het |
Cbfa2t2 |
A |
G |
2: 154,352,426 (GRCm39) |
|
probably null |
Het |
Clec2e |
T |
A |
6: 129,071,420 (GRCm39) |
Y139F |
possibly damaging |
Het |
Crisp2 |
T |
A |
17: 41,094,724 (GRCm39) |
N117I |
possibly damaging |
Het |
Ddx52 |
A |
T |
11: 83,833,008 (GRCm39) |
D2V |
probably damaging |
Het |
Dmpk |
T |
A |
7: 18,824,946 (GRCm39) |
V442E |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,368,942 (GRCm39) |
M1654K |
probably benign |
Het |
Eln |
AGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCAGGGACACCAGC |
AGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCAGGGACACCAGC |
5: 134,739,935 (GRCm39) |
|
probably benign |
Het |
Fktn |
G |
A |
4: 53,734,854 (GRCm39) |
G125D |
probably benign |
Het |
Fry |
A |
G |
5: 150,356,994 (GRCm39) |
E1847G |
possibly damaging |
Het |
Gck |
A |
G |
11: 5,899,553 (GRCm39) |
|
probably null |
Het |
Gga2 |
T |
C |
7: 121,603,195 (GRCm39) |
D167G |
probably damaging |
Het |
Gprc6a |
A |
G |
10: 51,491,506 (GRCm39) |
S748P |
probably damaging |
Het |
H2-M10.2 |
T |
C |
17: 36,595,643 (GRCm39) |
R216G |
probably benign |
Het |
H2-M2 |
T |
A |
17: 37,792,215 (GRCm39) |
I312F |
probably benign |
Het |
Havcr2 |
A |
T |
11: 46,347,350 (GRCm39) |
Y109F |
probably damaging |
Het |
Hoga1 |
T |
C |
19: 42,048,333 (GRCm39) |
V67A |
|
Het |
Ift70b |
T |
A |
2: 75,768,391 (GRCm39) |
I121F |
possibly damaging |
Het |
Kcnk12 |
C |
A |
17: 88,104,507 (GRCm39) |
V126L |
possibly damaging |
Het |
Klc1 |
A |
G |
12: 111,738,950 (GRCm39) |
E66G |
probably damaging |
Het |
Klhl2 |
A |
T |
8: 65,205,870 (GRCm39) |
Y350* |
probably null |
Het |
Letm1 |
T |
C |
5: 33,926,802 (GRCm39) |
H165R |
probably damaging |
Het |
Luc7l2 |
T |
C |
6: 38,547,489 (GRCm39) |
C36R |
probably damaging |
Het |
Mab21l1 |
A |
G |
3: 55,690,674 (GRCm39) |
N87S |
probably damaging |
Het |
Mdn1 |
A |
G |
4: 32,678,414 (GRCm39) |
T681A |
probably damaging |
Het |
Mrc1 |
C |
T |
2: 14,312,790 (GRCm39) |
T904I |
possibly damaging |
Het |
Mrpl38 |
A |
G |
11: 116,023,276 (GRCm39) |
S326P |
probably damaging |
Het |
Mtr |
T |
G |
13: 12,268,764 (GRCm39) |
K32N |
probably benign |
Het |
Mybpc3 |
T |
A |
2: 90,965,478 (GRCm39) |
C1128* |
probably null |
Het |
Ncdn |
T |
C |
4: 126,645,762 (GRCm39) |
D49G |
probably damaging |
Het |
Nfkbiz |
G |
A |
16: 55,642,337 (GRCm39) |
T27I |
probably damaging |
Het |
Npnt |
A |
T |
3: 132,653,866 (GRCm39) |
Y38* |
probably null |
Het |
Nrxn2 |
A |
G |
19: 6,581,931 (GRCm39) |
E1622G |
probably benign |
Het |
Nutm2 |
T |
C |
13: 50,626,964 (GRCm39) |
I373T |
probably damaging |
Het |
Or4c58 |
T |
C |
2: 89,674,715 (GRCm39) |
I201V |
probably benign |
Het |
Or51m1 |
T |
C |
7: 103,578,980 (GRCm39) |
S317P |
possibly damaging |
Het |
Osbp2 |
A |
G |
11: 3,662,170 (GRCm39) |
S228P |
probably damaging |
Het |
Pbx3 |
C |
T |
2: 34,103,348 (GRCm39) |
R208Q |
probably damaging |
Het |
Pcdhgb5 |
T |
C |
18: 37,864,838 (GRCm39) |
V211A |
probably benign |
Het |
Pi16 |
C |
T |
17: 29,544,899 (GRCm39) |
T151M |
probably damaging |
Het |
Pramel39-ps |
G |
T |
5: 94,451,001 (GRCm39) |
P375H |
probably damaging |
Het |
Ptpro |
T |
C |
6: 137,420,933 (GRCm39) |
I1068T |
probably benign |
Het |
Rbl1 |
A |
T |
2: 157,035,154 (GRCm39) |
Y309N |
probably damaging |
Het |
Rsf1 |
GGCGGCGGC |
GGCGGCGGCCGCGGCGGC |
7: 97,229,134 (GRCm39) |
|
probably benign |
Het |
Serpina3g |
G |
C |
12: 104,206,518 (GRCm39) |
E106D |
probably benign |
Het |
Slc4a11 |
C |
T |
2: 130,533,664 (GRCm39) |
A100T |
probably damaging |
Het |
Son |
G |
C |
16: 91,454,508 (GRCm39) |
R1085P |
probably damaging |
Het |
Tasor |
A |
T |
14: 27,163,927 (GRCm39) |
I238F |
probably damaging |
Het |
Tbx18 |
C |
A |
9: 87,612,675 (GRCm39) |
A75S |
probably benign |
Het |
Tmem232 |
C |
A |
17: 65,792,881 (GRCm39) |
Q105H |
probably damaging |
Het |
Ttc29 |
A |
G |
8: 79,060,390 (GRCm39) |
I437V |
probably benign |
Het |
Ttn |
T |
A |
2: 76,621,887 (GRCm39) |
I15552L |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,750,313 (GRCm39) |
T3579S |
probably benign |
Het |
Vps11 |
A |
G |
9: 44,267,719 (GRCm39) |
F298L |
probably benign |
Het |
Wbp11 |
T |
C |
6: 136,791,259 (GRCm39) |
T625A |
unknown |
Het |
Xylb |
T |
A |
9: 119,215,428 (GRCm39) |
N460K |
probably damaging |
Het |
Znrf4 |
C |
A |
17: 56,819,218 (GRCm39) |
V30F |
probably damaging |
Het |
|
Other mutations in Erlec1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00326:Erlec1
|
APN |
11 |
30,898,510 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL00537:Erlec1
|
APN |
11 |
30,889,591 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00766:Erlec1
|
APN |
11 |
30,900,623 (GRCm39) |
nonsense |
probably null |
|
IGL01760:Erlec1
|
APN |
11 |
30,884,731 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02505:Erlec1
|
APN |
11 |
30,900,767 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02633:Erlec1
|
APN |
11 |
30,898,430 (GRCm39) |
nonsense |
probably null |
|
R0674:Erlec1
|
UTSW |
11 |
30,885,073 (GRCm39) |
intron |
probably benign |
|
R1211:Erlec1
|
UTSW |
11 |
30,898,298 (GRCm39) |
critical splice donor site |
probably null |
|
R1974:Erlec1
|
UTSW |
11 |
30,889,604 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4326:Erlec1
|
UTSW |
11 |
30,899,972 (GRCm39) |
missense |
probably benign |
|
R4328:Erlec1
|
UTSW |
11 |
30,899,972 (GRCm39) |
missense |
probably benign |
|
R4392:Erlec1
|
UTSW |
11 |
30,893,697 (GRCm39) |
critical splice donor site |
probably null |
|
R4641:Erlec1
|
UTSW |
11 |
30,898,442 (GRCm39) |
nonsense |
probably null |
|
R4697:Erlec1
|
UTSW |
11 |
30,902,640 (GRCm39) |
missense |
probably benign |
0.27 |
R4917:Erlec1
|
UTSW |
11 |
30,884,710 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5486:Erlec1
|
UTSW |
11 |
30,885,047 (GRCm39) |
missense |
probably damaging |
0.98 |
R5735:Erlec1
|
UTSW |
11 |
30,900,591 (GRCm39) |
missense |
probably benign |
0.00 |
R5775:Erlec1
|
UTSW |
11 |
30,893,848 (GRCm39) |
missense |
probably benign |
0.11 |
R6475:Erlec1
|
UTSW |
11 |
30,898,442 (GRCm39) |
nonsense |
probably null |
|
R7027:Erlec1
|
UTSW |
11 |
30,900,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R7235:Erlec1
|
UTSW |
11 |
30,900,751 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7440:Erlec1
|
UTSW |
11 |
30,900,818 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8551:Erlec1
|
UTSW |
11 |
30,881,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R8848:Erlec1
|
UTSW |
11 |
30,898,411 (GRCm39) |
missense |
probably damaging |
1.00 |
|