Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
G |
A |
11: 84,154,138 (GRCm39) |
R953Q |
possibly damaging |
Het |
Aldh1a1 |
A |
T |
19: 20,579,434 (GRCm39) |
H20L |
probably benign |
Het |
Ankrd52 |
T |
A |
10: 128,219,526 (GRCm39) |
C487S |
probably benign |
Het |
Ap1s3 |
T |
C |
1: 79,602,845 (GRCm39) |
E54G |
probably benign |
Het |
Arglu1 |
A |
C |
8: 8,717,361 (GRCm39) |
M236R |
probably benign |
Het |
Baz1b |
T |
A |
5: 135,246,293 (GRCm39) |
F581I |
probably benign |
Het |
Bbox1 |
T |
G |
2: 110,122,884 (GRCm39) |
D135A |
probably benign |
Het |
Bcl2l14 |
T |
A |
6: 134,400,786 (GRCm39) |
V69E |
probably damaging |
Het |
Brinp3 |
C |
T |
1: 146,390,627 (GRCm39) |
Q58* |
probably null |
Het |
Ccnb1ip1 |
T |
A |
14: 51,029,724 (GRCm39) |
K113* |
probably null |
Het |
Cep128 |
T |
C |
12: 91,200,878 (GRCm39) |
I830M |
probably damaging |
Het |
Ces2f |
C |
T |
8: 105,681,284 (GRCm39) |
T541I |
probably damaging |
Het |
Chsy3 |
C |
A |
18: 59,309,149 (GRCm39) |
P134Q |
possibly damaging |
Het |
Cobl |
T |
G |
11: 12,328,271 (GRCm39) |
T112P |
probably damaging |
Het |
Cplane2 |
A |
T |
4: 140,947,159 (GRCm39) |
Y180F |
probably benign |
Het |
Dcc |
T |
A |
18: 71,680,469 (GRCm39) |
K589I |
probably benign |
Het |
Depdc1b |
T |
A |
13: 108,523,505 (GRCm39) |
I460K |
possibly damaging |
Het |
Dlst |
T |
C |
12: 85,157,705 (GRCm39) |
F12S |
probably benign |
Het |
Dnah1 |
G |
C |
14: 31,019,067 (GRCm39) |
F1342L |
probably damaging |
Het |
Dtnb |
A |
G |
12: 3,798,480 (GRCm39) |
Q438R |
possibly damaging |
Het |
Dusp4 |
C |
A |
8: 35,275,065 (GRCm39) |
S61R |
probably damaging |
Het |
E130308A19Rik |
A |
G |
4: 59,737,688 (GRCm39) |
Y433C |
probably damaging |
Het |
Elapor2 |
A |
G |
5: 9,460,709 (GRCm39) |
N210S |
probably benign |
Het |
Eya1 |
C |
T |
1: 14,301,636 (GRCm39) |
|
probably null |
Het |
Fsd1 |
G |
A |
17: 56,300,876 (GRCm39) |
R245H |
probably damaging |
Het |
Fzr1 |
T |
A |
10: 81,204,463 (GRCm39) |
D379V |
probably damaging |
Het |
Gk2 |
T |
A |
5: 97,604,195 (GRCm39) |
E214D |
probably benign |
Het |
Gm10837 |
C |
G |
14: 122,728,142 (GRCm39) |
A6G |
unknown |
Het |
Gmnc |
A |
T |
16: 26,779,272 (GRCm39) |
V251E |
probably benign |
Het |
Golga3 |
A |
G |
5: 110,340,953 (GRCm39) |
Q549R |
probably damaging |
Het |
Gsdmd |
T |
G |
15: 75,736,204 (GRCm39) |
V111G |
probably damaging |
Het |
Gtf3c1 |
T |
C |
7: 125,244,914 (GRCm39) |
T1707A |
possibly damaging |
Het |
Gucy2c |
C |
T |
6: 136,674,937 (GRCm39) |
V1049M |
probably benign |
Het |
Gucy2g |
A |
G |
19: 55,229,583 (GRCm39) |
V29A |
probably damaging |
Het |
Hecw1 |
A |
T |
13: 14,609,044 (GRCm39) |
M1K |
probably null |
Het |
Hmcn1 |
T |
C |
1: 150,736,118 (GRCm39) |
D117G |
probably damaging |
Het |
Ifnab |
T |
A |
4: 88,609,350 (GRCm39) |
T39S |
possibly damaging |
Het |
Lcorl |
A |
G |
5: 45,904,566 (GRCm39) |
Y171H |
probably damaging |
Het |
Ly6g6c |
C |
T |
17: 35,288,437 (GRCm39) |
P103L |
probably damaging |
Het |
Macf1 |
T |
G |
4: 123,325,936 (GRCm39) |
E5189A |
probably damaging |
Het |
Mapkap1 |
A |
G |
2: 34,453,151 (GRCm39) |
E348G |
probably damaging |
Het |
Med25 |
G |
T |
7: 44,534,325 (GRCm39) |
A280D |
probably damaging |
Het |
Mep1b |
C |
A |
18: 21,233,108 (GRCm39) |
A703E |
probably benign |
Het |
Morn5 |
T |
A |
2: 35,944,990 (GRCm39) |
N71K |
probably benign |
Het |
Mtmr10 |
T |
A |
7: 63,970,375 (GRCm39) |
Y373N |
possibly damaging |
Het |
Myo1d |
C |
T |
11: 80,565,460 (GRCm39) |
E426K |
probably damaging |
Het |
Ncbp1 |
G |
C |
4: 46,155,756 (GRCm39) |
V302L |
probably benign |
Het |
Notch4 |
A |
G |
17: 34,801,520 (GRCm39) |
T1123A |
possibly damaging |
Het |
Nudt18 |
T |
A |
14: 70,816,452 (GRCm39) |
M88K |
possibly damaging |
Het |
Or12k8 |
A |
G |
2: 36,975,608 (GRCm39) |
S51P |
possibly damaging |
Het |
Or5b100-ps1 |
A |
T |
19: 12,994,097 (GRCm39) |
D170V |
possibly damaging |
Het |
Or6d12 |
T |
A |
6: 116,493,632 (GRCm39) |
L298Q |
probably damaging |
Het |
Or8g4 |
A |
T |
9: 39,661,787 (GRCm39) |
Y35F |
possibly damaging |
Het |
Pdcd6ip |
T |
C |
9: 113,488,953 (GRCm39) |
N694S |
probably benign |
Het |
Pecam1 |
T |
A |
11: 106,579,773 (GRCm39) |
T430S |
probably benign |
Het |
Plaa |
T |
G |
4: 94,462,288 (GRCm39) |
T530P |
probably benign |
Het |
Ppfia3 |
G |
T |
7: 45,010,019 (GRCm39) |
Q95K |
probably damaging |
Het |
Ppp4r2 |
T |
C |
6: 100,843,274 (GRCm39) |
S331P |
probably benign |
Het |
Prg4 |
T |
C |
1: 150,334,014 (GRCm39) |
T117A |
possibly damaging |
Het |
Prrc2b |
A |
T |
2: 32,103,531 (GRCm39) |
D1003V |
probably benign |
Het |
Ptk2 |
G |
A |
15: 73,093,658 (GRCm39) |
P854S |
possibly damaging |
Het |
Rasef |
T |
C |
4: 73,698,626 (GRCm39) |
I12V |
probably benign |
Het |
Robo2 |
T |
G |
16: 74,149,504 (GRCm39) |
Y108S |
probably damaging |
Het |
Rp1 |
T |
A |
1: 4,277,014 (GRCm39) |
E762V |
unknown |
Het |
Rsrc1 |
T |
C |
3: 66,901,987 (GRCm39) |
S46P |
unknown |
Het |
Rttn |
A |
T |
18: 89,027,546 (GRCm39) |
T554S |
probably benign |
Het |
Sall3 |
C |
T |
18: 81,017,314 (GRCm39) |
V205M |
probably damaging |
Het |
Scn3a |
C |
A |
2: 65,327,944 (GRCm39) |
V849L |
probably damaging |
Het |
Sec23a |
A |
G |
12: 59,039,069 (GRCm39) |
C277R |
probably benign |
Het |
Sf3b3 |
C |
T |
8: 111,539,639 (GRCm39) |
A1075T |
possibly damaging |
Het |
Sfxn5 |
T |
C |
6: 85,309,366 (GRCm39) |
D113G |
unknown |
Het |
Slc22a22 |
C |
T |
15: 57,126,876 (GRCm39) |
M64I |
probably benign |
Het |
Slc5a11 |
C |
T |
7: 122,857,669 (GRCm39) |
P253S |
probably damaging |
Het |
Smarcd3 |
A |
G |
5: 24,798,067 (GRCm39) |
F449S |
probably damaging |
Het |
Sspo |
C |
T |
6: 48,437,313 (GRCm39) |
T1357M |
probably damaging |
Het |
Styx |
C |
T |
14: 45,609,873 (GRCm39) |
T179I |
probably benign |
Het |
Syt7 |
A |
T |
19: 10,412,963 (GRCm39) |
T297S |
probably benign |
Het |
Tbx19 |
T |
A |
1: 164,988,135 (GRCm39) |
|
probably benign |
Het |
Tg |
T |
A |
15: 66,545,392 (GRCm39) |
V149E |
probably damaging |
Het |
Tgfbr3l |
T |
A |
8: 4,299,238 (GRCm39) |
L35Q |
probably damaging |
Het |
Tmem161b |
C |
A |
13: 84,370,537 (GRCm39) |
|
probably benign |
Het |
Tmem219 |
T |
A |
7: 126,490,975 (GRCm39) |
T161S |
probably damaging |
Het |
Tox2 |
T |
A |
2: 163,162,501 (GRCm39) |
L68H |
|
Het |
Trim5 |
T |
A |
7: 103,927,681 (GRCm39) |
D153V |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,580,651 (GRCm39) |
Y23414C |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,582,153 (GRCm39) |
N22913K |
probably damaging |
Het |
Ubr2 |
A |
C |
17: 47,266,779 (GRCm39) |
M1124R |
possibly damaging |
Het |
Vmn2r75 |
A |
G |
7: 85,815,568 (GRCm39) |
S99P |
probably damaging |
Het |
Wdr83 |
T |
C |
8: 85,802,680 (GRCm39) |
D219G |
probably damaging |
Het |
Wdr90 |
C |
T |
17: 26,068,623 (GRCm39) |
V1285M |
probably damaging |
Het |
Zmynd15 |
A |
T |
11: 70,351,581 (GRCm39) |
L62F |
probably damaging |
Het |
|
Other mutations in Ebf2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01636:Ebf2
|
APN |
14 |
67,476,927 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01808:Ebf2
|
APN |
14 |
67,651,932 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02087:Ebf2
|
APN |
14 |
67,665,545 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02094:Ebf2
|
APN |
14 |
67,472,689 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02270:Ebf2
|
APN |
14 |
67,476,402 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03222:Ebf2
|
APN |
14 |
67,649,441 (GRCm39) |
splice site |
probably null |
|
IGL03390:Ebf2
|
APN |
14 |
67,661,558 (GRCm39) |
missense |
probably benign |
0.19 |
G1Funyon:Ebf2
|
UTSW |
14 |
67,476,431 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0044:Ebf2
|
UTSW |
14 |
67,548,417 (GRCm39) |
intron |
probably benign |
|
R0062:Ebf2
|
UTSW |
14 |
67,475,989 (GRCm39) |
splice site |
probably benign |
|
R0062:Ebf2
|
UTSW |
14 |
67,475,989 (GRCm39) |
splice site |
probably benign |
|
R0069:Ebf2
|
UTSW |
14 |
67,647,499 (GRCm39) |
missense |
probably damaging |
0.99 |
R0069:Ebf2
|
UTSW |
14 |
67,647,499 (GRCm39) |
missense |
probably damaging |
0.99 |
R0505:Ebf2
|
UTSW |
14 |
67,609,185 (GRCm39) |
nonsense |
probably null |
|
R2103:Ebf2
|
UTSW |
14 |
67,625,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R2438:Ebf2
|
UTSW |
14 |
67,625,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R3789:Ebf2
|
UTSW |
14 |
67,476,942 (GRCm39) |
critical splice donor site |
probably null |
|
R4153:Ebf2
|
UTSW |
14 |
67,472,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R4348:Ebf2
|
UTSW |
14 |
67,476,871 (GRCm39) |
missense |
probably damaging |
0.99 |
R4793:Ebf2
|
UTSW |
14 |
67,647,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R4991:Ebf2
|
UTSW |
14 |
67,627,106 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5164:Ebf2
|
UTSW |
14 |
67,627,970 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5222:Ebf2
|
UTSW |
14 |
67,551,043 (GRCm39) |
intron |
probably benign |
|
R5227:Ebf2
|
UTSW |
14 |
67,484,518 (GRCm39) |
missense |
probably damaging |
0.99 |
R5459:Ebf2
|
UTSW |
14 |
67,472,650 (GRCm39) |
missense |
probably benign |
0.34 |
R5622:Ebf2
|
UTSW |
14 |
67,628,007 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6035:Ebf2
|
UTSW |
14 |
67,476,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R6035:Ebf2
|
UTSW |
14 |
67,476,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R6265:Ebf2
|
UTSW |
14 |
67,661,509 (GRCm39) |
missense |
probably benign |
0.00 |
R6893:Ebf2
|
UTSW |
14 |
67,475,008 (GRCm39) |
missense |
probably benign |
0.22 |
R7394:Ebf2
|
UTSW |
14 |
67,474,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R7449:Ebf2
|
UTSW |
14 |
67,647,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R7652:Ebf2
|
UTSW |
14 |
67,628,016 (GRCm39) |
critical splice donor site |
probably null |
|
R7724:Ebf2
|
UTSW |
14 |
67,661,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R8143:Ebf2
|
UTSW |
14 |
67,649,386 (GRCm39) |
nonsense |
probably null |
|
R8153:Ebf2
|
UTSW |
14 |
67,627,914 (GRCm39) |
missense |
probably damaging |
0.97 |
R8301:Ebf2
|
UTSW |
14 |
67,476,431 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8963:Ebf2
|
UTSW |
14 |
67,665,554 (GRCm39) |
missense |
probably benign |
0.34 |
R8978:Ebf2
|
UTSW |
14 |
67,661,548 (GRCm39) |
missense |
probably benign |
|
R9031:Ebf2
|
UTSW |
14 |
67,472,594 (GRCm39) |
missense |
probably benign |
0.01 |
R9409:Ebf2
|
UTSW |
14 |
67,472,665 (GRCm39) |
missense |
probably damaging |
0.99 |
|