Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
A |
G |
2: 68,539,281 (GRCm39) |
M1V |
probably null |
Het |
Abca13 |
T |
A |
11: 9,247,177 (GRCm39) |
L2308H |
probably damaging |
Het |
Abcc8 |
T |
C |
7: 45,764,463 (GRCm39) |
T1161A |
probably benign |
Het |
Acin1 |
T |
A |
14: 54,901,130 (GRCm39) |
T659S |
probably benign |
Het |
Actl7a |
G |
T |
4: 56,743,827 (GRCm39) |
R118L |
probably damaging |
Het |
Acyp2 |
C |
T |
11: 30,456,354 (GRCm39) |
E98K |
possibly damaging |
Het |
Alkbh8 |
A |
G |
9: 3,385,414 (GRCm39) |
K569E |
probably benign |
Het |
Anxa3 |
A |
T |
5: 96,960,712 (GRCm39) |
K39* |
probably null |
Het |
Aoc2 |
A |
G |
11: 101,220,072 (GRCm39) |
E659G |
probably damaging |
Het |
Atg7 |
C |
T |
6: 114,650,639 (GRCm39) |
T83M |
possibly damaging |
Het |
AU022252 |
T |
C |
4: 119,084,101 (GRCm39) |
D104G |
probably benign |
Het |
Car6 |
T |
C |
4: 150,271,956 (GRCm39) |
Y231C |
possibly damaging |
Het |
Cdh10 |
T |
G |
15: 18,985,341 (GRCm39) |
|
probably null |
Het |
Cebpz |
A |
C |
17: 79,233,366 (GRCm39) |
M787R |
probably benign |
Het |
Chst2 |
A |
G |
9: 95,287,662 (GRCm39) |
L228P |
probably damaging |
Het |
Clic4 |
T |
C |
4: 134,999,869 (GRCm39) |
K11R |
probably benign |
Het |
Col6a3 |
C |
T |
1: 90,729,921 (GRCm39) |
|
probably null |
Het |
Commd7 |
T |
A |
2: 153,463,737 (GRCm39) |
T144S |
probably damaging |
Het |
Ctla2a |
T |
A |
13: 61,082,834 (GRCm39) |
*138Y |
probably null |
Het |
Dhx33 |
A |
T |
11: 70,879,957 (GRCm39) |
V351D |
probably damaging |
Het |
Dnah9 |
G |
A |
11: 65,916,013 (GRCm39) |
T2313I |
probably benign |
Het |
Dspp |
A |
T |
5: 104,325,977 (GRCm39) |
D780V |
unknown |
Het |
Dync1li1 |
A |
G |
9: 114,546,929 (GRCm39) |
|
probably null |
Het |
Fan1 |
T |
C |
7: 64,023,070 (GRCm39) |
|
probably null |
Het |
Gart |
A |
G |
16: 91,425,415 (GRCm39) |
S617P |
probably damaging |
Het |
Ggcx |
A |
G |
6: 72,406,979 (GRCm39) |
N705S |
possibly damaging |
Het |
Gm4841 |
A |
T |
18: 60,403,868 (GRCm39) |
V75E |
probably damaging |
Het |
Greb1l |
A |
G |
18: 10,538,302 (GRCm39) |
E1105G |
probably benign |
Het |
Hr |
C |
A |
14: 70,795,231 (GRCm39) |
Q288K |
probably benign |
Het |
Hus1 |
T |
C |
11: 8,960,669 (GRCm39) |
|
probably benign |
Het |
Ifi47 |
C |
A |
11: 48,986,213 (GRCm39) |
|
probably null |
Het |
Irf2bp1 |
T |
C |
7: 18,738,372 (GRCm39) |
V4A |
probably benign |
Het |
Kprp |
C |
T |
3: 92,731,835 (GRCm39) |
C405Y |
unknown |
Het |
Lacc1 |
T |
C |
14: 77,272,239 (GRCm39) |
I186V |
possibly damaging |
Het |
Lifr |
A |
G |
15: 7,220,231 (GRCm39) |
T954A |
probably benign |
Het |
Lonrf2 |
T |
C |
1: 38,846,174 (GRCm39) |
M333V |
probably benign |
Het |
Mthfd1 |
A |
T |
12: 76,337,826 (GRCm39) |
H400L |
probably benign |
Het |
Myh4 |
A |
G |
11: 67,141,733 (GRCm39) |
K864R |
possibly damaging |
Het |
Nup50 |
C |
T |
15: 84,819,641 (GRCm39) |
A305V |
probably benign |
Het |
Or4a74 |
T |
A |
2: 89,439,595 (GRCm39) |
I284L |
probably damaging |
Het |
Or4k44 |
C |
T |
2: 111,367,739 (GRCm39) |
M298I |
probably benign |
Het |
Pax4 |
G |
T |
6: 28,447,126 (GRCm39) |
Q3K |
probably benign |
Het |
Pced1b |
T |
G |
15: 97,282,970 (GRCm39) |
Y336* |
probably null |
Het |
Postn |
C |
A |
3: 54,279,510 (GRCm39) |
N329K |
probably benign |
Het |
Prickle1 |
T |
C |
15: 93,408,553 (GRCm39) |
E82G |
probably null |
Het |
Prtn3 |
T |
C |
10: 79,718,766 (GRCm39) |
Y241H |
probably damaging |
Het |
Rasgrf2 |
A |
T |
13: 92,068,011 (GRCm39) |
I260K |
probably damaging |
Het |
Sh3glb1 |
T |
C |
3: 144,418,431 (GRCm39) |
N44S |
possibly damaging |
Het |
Sis |
A |
T |
3: 72,867,589 (GRCm39) |
|
probably null |
Het |
Slc4a9 |
A |
G |
18: 36,662,386 (GRCm39) |
|
probably null |
Het |
Slc4a9 |
A |
T |
18: 36,664,560 (GRCm39) |
D406V |
probably damaging |
Het |
Slc8a1 |
C |
T |
17: 81,715,511 (GRCm39) |
G841R |
probably damaging |
Het |
Smn1 |
C |
T |
13: 100,263,412 (GRCm39) |
P60L |
probably benign |
Het |
Snai1 |
G |
A |
2: 167,383,930 (GRCm39) |
C241Y |
probably damaging |
Het |
Spock3 |
A |
G |
8: 63,808,336 (GRCm39) |
D411G |
unknown |
Het |
Szt2 |
T |
A |
4: 118,248,700 (GRCm39) |
T607S |
probably benign |
Het |
Tcap |
A |
T |
11: 98,274,673 (GRCm39) |
M1L |
probably benign |
Het |
Tex29 |
A |
T |
8: 11,905,723 (GRCm39) |
|
probably benign |
Het |
Tex29 |
C |
A |
8: 11,904,276 (GRCm39) |
|
probably benign |
Het |
Tex29 |
C |
T |
8: 11,904,277 (GRCm39) |
|
probably benign |
Het |
Tln2 |
T |
C |
9: 67,269,999 (GRCm39) |
T467A |
probably benign |
Het |
Trim34a |
C |
T |
7: 103,910,328 (GRCm39) |
Q377* |
probably null |
Het |
Ube2q1 |
T |
A |
3: 89,683,487 (GRCm39) |
L144* |
probably null |
Het |
Vps13c |
A |
G |
9: 67,841,729 (GRCm39) |
E1917G |
probably benign |
Het |
Wdr19 |
T |
A |
5: 65,384,482 (GRCm39) |
N525K |
probably benign |
Het |
Wdr3 |
A |
T |
3: 100,051,807 (GRCm39) |
|
probably benign |
Het |
Wnt5b |
T |
A |
6: 119,425,199 (GRCm39) |
H6L |
probably benign |
Het |
Yju2 |
A |
G |
17: 56,269,077 (GRCm39) |
T62A |
probably damaging |
Het |
Zdbf2 |
T |
C |
1: 63,345,685 (GRCm39) |
S1355P |
possibly damaging |
Het |
Zfp11 |
T |
A |
5: 129,734,976 (GRCm39) |
I162F |
probably damaging |
Het |
Zpbp |
T |
C |
11: 11,365,332 (GRCm39) |
T172A |
probably benign |
Het |
|
Other mutations in E2f3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00770:E2f3
|
APN |
13 |
30,102,687 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00774:E2f3
|
APN |
13 |
30,102,687 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02541:E2f3
|
APN |
13 |
30,100,827 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02669:E2f3
|
APN |
13 |
30,100,974 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03119:E2f3
|
APN |
13 |
30,169,348 (GRCm39) |
missense |
probably benign |
0.21 |
Crumble
|
UTSW |
13 |
30,095,301 (GRCm39) |
missense |
probably damaging |
1.00 |
Hillside
|
UTSW |
13 |
30,102,652 (GRCm39) |
missense |
probably damaging |
1.00 |
Slippery
|
UTSW |
13 |
30,102,568 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0830:E2f3
|
UTSW |
13 |
30,169,543 (GRCm39) |
missense |
probably benign |
0.02 |
R0948:E2f3
|
UTSW |
13 |
30,169,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R1442:E2f3
|
UTSW |
13 |
30,102,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:E2f3
|
UTSW |
13 |
30,104,159 (GRCm39) |
missense |
probably damaging |
0.97 |
R2496:E2f3
|
UTSW |
13 |
30,095,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R4715:E2f3
|
UTSW |
13 |
30,095,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R5202:E2f3
|
UTSW |
13 |
30,102,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R6796:E2f3
|
UTSW |
13 |
30,102,568 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7546:E2f3
|
UTSW |
13 |
30,094,112 (GRCm39) |
missense |
probably damaging |
0.98 |
R7705:E2f3
|
UTSW |
13 |
30,169,306 (GRCm39) |
missense |
probably benign |
0.39 |
R7779:E2f3
|
UTSW |
13 |
30,102,598 (GRCm39) |
missense |
probably damaging |
0.99 |
R8354:E2f3
|
UTSW |
13 |
30,169,787 (GRCm39) |
unclassified |
probably benign |
|
R8518:E2f3
|
UTSW |
13 |
30,097,453 (GRCm39) |
missense |
probably damaging |
0.98 |
R8868:E2f3
|
UTSW |
13 |
30,095,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R9017:E2f3
|
UTSW |
13 |
30,097,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R9041:E2f3
|
UTSW |
13 |
30,093,939 (GRCm39) |
missense |
probably damaging |
0.97 |
R9272:E2f3
|
UTSW |
13 |
30,102,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R9336:E2f3
|
UTSW |
13 |
30,095,239 (GRCm39) |
missense |
possibly damaging |
0.87 |
|