Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110009E18Rik |
A |
C |
1: 120,078,472 (GRCm39) |
K43T |
probably damaging |
Het |
Abca12 |
A |
G |
1: 71,297,380 (GRCm39) |
V2370A |
possibly damaging |
Het |
Abca13 |
T |
A |
11: 9,243,667 (GRCm39) |
C1843* |
probably null |
Het |
Abr |
C |
T |
11: 76,399,751 (GRCm39) |
S82N |
probably benign |
Het |
Acot2 |
T |
C |
12: 84,039,384 (GRCm39) |
S298P |
probably benign |
Het |
Acrbp |
A |
G |
6: 125,038,062 (GRCm39) |
D421G |
probably benign |
Het |
Adam25 |
A |
T |
8: 41,206,736 (GRCm39) |
M1L |
probably benign |
Het |
Ano8 |
A |
G |
8: 71,934,784 (GRCm39) |
V441A |
possibly damaging |
Het |
Aoc1l1 |
T |
C |
6: 48,955,540 (GRCm39) |
S717P |
probably benign |
Het |
Atg2b |
T |
C |
12: 105,624,549 (GRCm39) |
H650R |
probably benign |
Het |
Atp11a |
C |
T |
8: 12,894,490 (GRCm39) |
T695I |
probably damaging |
Het |
AU018091 |
A |
G |
7: 3,214,023 (GRCm39) |
S74P |
probably benign |
Het |
Cadps2 |
A |
G |
6: 23,427,238 (GRCm39) |
Y597H |
probably benign |
Het |
Ccdc15 |
C |
T |
9: 37,215,665 (GRCm39) |
E619K |
probably damaging |
Het |
Ceacam11 |
G |
T |
7: 17,709,468 (GRCm39) |
C222F |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,177,822 (GRCm39) |
*3677W |
probably null |
Het |
Col11a1 |
G |
C |
3: 114,005,752 (GRCm39) |
C1628S |
probably benign |
Het |
Dhx8 |
T |
C |
11: 101,654,808 (GRCm39) |
I1032T |
possibly damaging |
Het |
Dpp10 |
T |
C |
1: 123,281,159 (GRCm39) |
D630G |
probably damaging |
Het |
Eif2a |
A |
G |
3: 58,448,475 (GRCm39) |
T103A |
probably benign |
Het |
Frem1 |
T |
C |
4: 82,920,057 (GRCm39) |
E432G |
probably damaging |
Het |
Gdnf |
C |
T |
15: 7,840,423 (GRCm39) |
|
probably benign |
Het |
Hace1 |
T |
A |
10: 45,547,230 (GRCm39) |
M471K |
probably benign |
Het |
Hydin |
A |
G |
8: 111,326,877 (GRCm39) |
T4739A |
possibly damaging |
Het |
Ilf2 |
A |
G |
3: 90,394,570 (GRCm39) |
I320V |
probably benign |
Het |
Iqgap3 |
C |
A |
3: 88,016,176 (GRCm39) |
F986L |
probably damaging |
Het |
Klhl21 |
T |
C |
4: 152,093,419 (GRCm39) |
L7S |
probably benign |
Het |
Lrrc61 |
G |
T |
6: 48,545,761 (GRCm39) |
E195* |
probably null |
Het |
Maz |
G |
T |
7: 126,622,292 (GRCm39) |
A443E |
possibly damaging |
Het |
Mcm5 |
C |
T |
8: 75,844,168 (GRCm39) |
S313F |
probably benign |
Het |
Mtor |
T |
A |
4: 148,568,801 (GRCm39) |
L1107Q |
probably damaging |
Het |
Nectin3 |
T |
C |
16: 46,215,511 (GRCm39) |
H494R |
probably benign |
Het |
Nlgn1 |
G |
T |
3: 25,488,480 (GRCm39) |
Y618* |
probably null |
Het |
Nup98 |
C |
T |
7: 101,778,252 (GRCm39) |
E1372K |
probably benign |
Het |
Or12e9 |
A |
G |
2: 87,201,960 (GRCm39) |
N28S |
probably benign |
Het |
Or5af1 |
T |
C |
11: 58,722,610 (GRCm39) |
V210A |
probably benign |
Het |
Otud6b |
A |
G |
4: 14,818,349 (GRCm39) |
I184T |
probably damaging |
Het |
Pcsk6 |
A |
G |
7: 65,697,346 (GRCm39) |
N891S |
probably benign |
Het |
Pde4a |
T |
A |
9: 21,106,096 (GRCm39) |
L237Q |
probably damaging |
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Perm1 |
TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT |
TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT |
4: 156,302,525 (GRCm39) |
|
probably benign |
Het |
Pou3f1 |
A |
G |
4: 124,552,179 (GRCm39) |
H227R |
possibly damaging |
Het |
Prss53 |
G |
A |
7: 127,488,802 (GRCm39) |
R31C |
probably damaging |
Het |
Psmb8 |
T |
A |
17: 34,417,435 (GRCm39) |
D21E |
probably benign |
Het |
Ptprq |
A |
G |
10: 107,478,813 (GRCm39) |
Y1277H |
probably damaging |
Het |
Rexo2 |
T |
C |
9: 48,380,176 (GRCm39) |
T219A |
probably benign |
Het |
Rfc3 |
A |
G |
5: 151,566,411 (GRCm39) |
F346S |
probably damaging |
Het |
Rhoq |
A |
T |
17: 87,304,373 (GRCm39) |
Q168L |
|
Het |
Sgk1 |
A |
G |
10: 21,874,096 (GRCm39) |
N452S |
probably damaging |
Het |
Slc35f3 |
A |
G |
8: 127,048,026 (GRCm39) |
K122R |
probably damaging |
Het |
Slc4a2 |
T |
A |
5: 24,644,761 (GRCm39) |
M1021K |
probably benign |
Het |
Sorcs2 |
A |
G |
5: 36,186,484 (GRCm39) |
V886A |
probably benign |
Het |
Spata20 |
T |
A |
11: 94,374,444 (GRCm39) |
M308L |
probably damaging |
Het |
Spen |
A |
T |
4: 141,199,098 (GRCm39) |
H3176Q |
probably benign |
Het |
Stat5b |
T |
A |
11: 100,692,361 (GRCm39) |
H141L |
probably benign |
Het |
Syne2 |
T |
A |
12: 75,995,839 (GRCm39) |
H2126Q |
possibly damaging |
Het |
Traj46 |
A |
G |
14: 54,409,851 (GRCm39) |
T20A |
|
Het |
Trim30a |
G |
T |
7: 104,078,330 (GRCm39) |
Q249K |
probably damaging |
Het |
Trmt13 |
A |
G |
3: 116,388,281 (GRCm39) |
Y52H |
probably benign |
Het |
Trpv3 |
A |
G |
11: 73,187,267 (GRCm39) |
I700V |
probably damaging |
Het |
Tyr |
G |
A |
7: 87,121,704 (GRCm39) |
H363Y |
probably damaging |
Het |
Tyr |
C |
G |
7: 87,121,705 (GRCm39) |
M362I |
possibly damaging |
Het |
Ubb |
G |
A |
11: 62,442,984 (GRCm39) |
V5M |
probably damaging |
Het |
Unc5a |
T |
C |
13: 55,150,288 (GRCm39) |
L519P |
probably damaging |
Het |
Uso1 |
A |
G |
5: 92,315,191 (GRCm39) |
D185G |
possibly damaging |
Het |
Vmn1r228 |
C |
T |
17: 20,996,862 (GRCm39) |
E219K |
probably damaging |
Het |
Wdr49 |
A |
G |
3: 75,240,669 (GRCm39) |
V400A |
probably damaging |
Het |
Zfp292 |
A |
G |
4: 34,810,794 (GRCm39) |
M755T |
probably benign |
Het |
|
Other mutations in Eci3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01933:Eci3
|
APN |
13 |
35,132,772 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02636:Eci3
|
APN |
13 |
35,130,963 (GRCm39) |
splice site |
probably null |
|
R0217:Eci3
|
UTSW |
13 |
35,132,072 (GRCm39) |
missense |
probably benign |
0.01 |
R0627:Eci3
|
UTSW |
13 |
35,132,126 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1529:Eci3
|
UTSW |
13 |
35,140,903 (GRCm39) |
missense |
probably benign |
0.00 |
R1840:Eci3
|
UTSW |
13 |
35,144,024 (GRCm39) |
missense |
probably benign |
0.38 |
R1856:Eci3
|
UTSW |
13 |
35,137,011 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4620:Eci3
|
UTSW |
13 |
35,132,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R5186:Eci3
|
UTSW |
13 |
35,130,961 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5427:Eci3
|
UTSW |
13 |
35,143,931 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7400:Eci3
|
UTSW |
13 |
35,143,960 (GRCm39) |
missense |
probably benign |
|
R8083:Eci3
|
UTSW |
13 |
35,140,873 (GRCm39) |
missense |
probably benign |
0.00 |
R8345:Eci3
|
UTSW |
13 |
35,132,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R8684:Eci3
|
UTSW |
13 |
35,143,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R8730:Eci3
|
UTSW |
13 |
35,144,405 (GRCm39) |
missense |
probably benign |
0.43 |
R9104:Eci3
|
UTSW |
13 |
35,144,382 (GRCm39) |
critical splice donor site |
probably null |
|
|