Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd5 |
T |
C |
9: 122,194,278 (GRCm39) |
M1T |
probably null |
Het |
Ager |
G |
A |
17: 34,818,092 (GRCm39) |
G183E |
probably damaging |
Het |
Alcam |
C |
A |
16: 52,125,982 (GRCm39) |
V112L |
probably damaging |
Het |
Amot |
T |
A |
X: 144,270,024 (GRCm39) |
Q204H |
probably damaging |
Het |
Ankar |
C |
T |
1: 72,697,808 (GRCm39) |
|
probably null |
Het |
Armc9 |
A |
G |
1: 86,104,587 (GRCm39) |
M279V |
possibly damaging |
Het |
Bpifb1 |
C |
T |
2: 154,051,849 (GRCm39) |
T218I |
probably benign |
Het |
Cacna1f |
A |
C |
X: 7,480,234 (GRCm39) |
|
probably benign |
Het |
Cacna2d2 |
T |
C |
9: 107,395,474 (GRCm39) |
|
probably null |
Het |
Ccdc57 |
A |
T |
11: 120,752,069 (GRCm39) |
C837* |
probably null |
Het |
Ctbp2 |
G |
A |
7: 132,592,885 (GRCm39) |
A808V |
probably damaging |
Het |
Dcbld2 |
T |
C |
16: 58,268,889 (GRCm39) |
|
probably null |
Het |
Dis3 |
T |
C |
14: 99,328,754 (GRCm39) |
|
probably benign |
Het |
Disp2 |
T |
C |
2: 118,620,450 (GRCm39) |
F394S |
probably damaging |
Het |
Dnah1 |
T |
C |
14: 31,005,246 (GRCm39) |
N2336S |
probably damaging |
Het |
Drap1 |
C |
A |
19: 5,473,871 (GRCm39) |
L66F |
probably damaging |
Het |
Eif5a2 |
C |
T |
3: 28,847,888 (GRCm39) |
R109C |
probably benign |
Het |
Enpp1 |
A |
T |
10: 24,553,872 (GRCm39) |
D105E |
probably damaging |
Het |
Evi5l |
G |
A |
8: 4,241,293 (GRCm39) |
M275I |
probably damaging |
Het |
Fndc3c1 |
T |
C |
X: 105,516,340 (GRCm39) |
|
probably benign |
Het |
Git1 |
T |
C |
11: 77,396,813 (GRCm39) |
V645A |
possibly damaging |
Het |
Gm7735 |
T |
A |
16: 88,966,437 (GRCm39) |
C20* |
probably null |
Het |
Ighv1-42 |
G |
T |
12: 114,900,906 (GRCm39) |
P60T |
probably benign |
Het |
Jakmip2 |
A |
T |
18: 43,696,350 (GRCm39) |
L533Q |
probably damaging |
Het |
Kdm2b |
C |
T |
5: 123,085,898 (GRCm39) |
E238K |
probably damaging |
Het |
Lpin2 |
T |
C |
17: 71,550,921 (GRCm39) |
S694P |
probably damaging |
Het |
Mab21l2 |
C |
T |
3: 86,454,562 (GRCm39) |
R146Q |
possibly damaging |
Het |
Mmp1b |
A |
T |
9: 7,386,400 (GRCm39) |
S174T |
probably benign |
Het |
Neb |
T |
C |
2: 52,181,211 (GRCm39) |
Y1132C |
probably damaging |
Het |
Nhsl1 |
A |
T |
10: 18,387,383 (GRCm39) |
H219L |
possibly damaging |
Het |
Nwd2 |
T |
A |
5: 63,948,996 (GRCm39) |
|
probably null |
Het |
Obp1a |
A |
C |
X: 77,134,449 (GRCm39) |
M18R |
possibly damaging |
Het |
Or13a19 |
A |
T |
7: 139,903,505 (GRCm39) |
K298* |
probably null |
Het |
Or2ag13 |
T |
C |
7: 106,473,180 (GRCm39) |
T91A |
probably benign |
Het |
Pabpc5 |
T |
A |
X: 118,837,688 (GRCm39) |
M1K |
probably null |
Het |
Paxip1 |
A |
G |
5: 27,980,596 (GRCm39) |
|
probably benign |
Het |
Perm1 |
A |
G |
4: 156,302,500 (GRCm39) |
E348G |
probably benign |
Het |
Pfkfb1 |
T |
C |
X: 149,405,138 (GRCm39) |
F170L |
probably damaging |
Het |
Pou3f3 |
A |
G |
1: 42,737,686 (GRCm39) |
M461V |
probably benign |
Het |
Ppfia2 |
G |
A |
10: 106,693,360 (GRCm39) |
D622N |
probably damaging |
Het |
Prtg |
T |
G |
9: 72,799,606 (GRCm39) |
S801R |
probably damaging |
Het |
Rars2 |
T |
A |
4: 34,623,404 (GRCm39) |
|
probably benign |
Het |
Rasal1 |
A |
G |
5: 120,790,917 (GRCm39) |
D35G |
probably damaging |
Het |
Repin1 |
T |
A |
6: 48,574,055 (GRCm39) |
L272Q |
probably damaging |
Het |
Spmip5 |
C |
A |
19: 58,777,684 (GRCm39) |
R34L |
possibly damaging |
Het |
Stk36 |
T |
C |
1: 74,655,728 (GRCm39) |
|
probably benign |
Het |
Tbxa2r |
A |
G |
10: 81,170,320 (GRCm39) |
T269A |
probably benign |
Het |
Tmem132c |
G |
A |
5: 127,640,466 (GRCm39) |
R879Q |
probably benign |
Het |
Vmn1r78 |
C |
A |
7: 11,886,407 (GRCm39) |
A6E |
probably benign |
Het |
Vps45 |
A |
T |
3: 95,941,133 (GRCm39) |
N369K |
probably benign |
Het |
Vps45 |
T |
C |
3: 95,926,958 (GRCm39) |
I530V |
probably benign |
Het |
Zkscan16 |
G |
A |
4: 58,956,911 (GRCm39) |
G398R |
probably damaging |
Het |
|
Other mutations in Flt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Flt1
|
APN |
5 |
147,517,110 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00469:Flt1
|
APN |
5 |
147,540,415 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00897:Flt1
|
APN |
5 |
147,526,664 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01111:Flt1
|
APN |
5 |
147,515,146 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01154:Flt1
|
APN |
5 |
147,512,966 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01744:Flt1
|
APN |
5 |
147,508,271 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01973:Flt1
|
APN |
5 |
147,620,699 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02079:Flt1
|
APN |
5 |
147,505,641 (GRCm39) |
splice site |
probably benign |
|
IGL02156:Flt1
|
APN |
5 |
147,618,551 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02345:Flt1
|
APN |
5 |
147,519,436 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02548:Flt1
|
APN |
5 |
147,576,058 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02631:Flt1
|
APN |
5 |
147,610,384 (GRCm39) |
nonsense |
probably null |
|
IGL02686:Flt1
|
APN |
5 |
147,525,412 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02938:Flt1
|
APN |
5 |
147,615,109 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03057:Flt1
|
APN |
5 |
147,618,734 (GRCm39) |
nonsense |
probably null |
|
IGL03196:Flt1
|
APN |
5 |
147,551,937 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03205:Flt1
|
APN |
5 |
147,636,631 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03255:Flt1
|
APN |
5 |
147,525,331 (GRCm39) |
splice site |
probably benign |
|
flywheels
|
UTSW |
5 |
147,536,456 (GRCm39) |
missense |
probably damaging |
1.00 |
BB008:Flt1
|
UTSW |
5 |
147,525,382 (GRCm39) |
missense |
probably damaging |
1.00 |
BB018:Flt1
|
UTSW |
5 |
147,525,382 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02837:Flt1
|
UTSW |
5 |
147,591,980 (GRCm39) |
missense |
probably benign |
0.32 |
PIT4402001:Flt1
|
UTSW |
5 |
147,615,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Flt1
|
UTSW |
5 |
147,507,824 (GRCm39) |
splice site |
probably benign |
|
R0380:Flt1
|
UTSW |
5 |
147,525,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R0448:Flt1
|
UTSW |
5 |
147,503,204 (GRCm39) |
splice site |
probably benign |
|
R0789:Flt1
|
UTSW |
5 |
147,576,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R1005:Flt1
|
UTSW |
5 |
147,618,695 (GRCm39) |
missense |
probably damaging |
0.99 |
R1241:Flt1
|
UTSW |
5 |
147,536,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R1302:Flt1
|
UTSW |
5 |
147,501,050 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1411:Flt1
|
UTSW |
5 |
147,517,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R1615:Flt1
|
UTSW |
5 |
147,576,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1634:Flt1
|
UTSW |
5 |
147,613,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R1749:Flt1
|
UTSW |
5 |
147,591,929 (GRCm39) |
missense |
probably benign |
0.00 |
R1768:Flt1
|
UTSW |
5 |
147,609,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R1972:Flt1
|
UTSW |
5 |
147,591,903 (GRCm39) |
splice site |
probably benign |
|
R2074:Flt1
|
UTSW |
5 |
147,536,416 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2081:Flt1
|
UTSW |
5 |
147,576,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R2864:Flt1
|
UTSW |
5 |
147,531,431 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2865:Flt1
|
UTSW |
5 |
147,531,431 (GRCm39) |
missense |
possibly damaging |
0.68 |
R3740:Flt1
|
UTSW |
5 |
147,536,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R3820:Flt1
|
UTSW |
5 |
147,636,827 (GRCm39) |
splice site |
probably benign |
|
R4089:Flt1
|
UTSW |
5 |
147,501,051 (GRCm39) |
missense |
probably benign |
0.03 |
R4299:Flt1
|
UTSW |
5 |
147,620,717 (GRCm39) |
missense |
probably benign |
0.00 |
R4570:Flt1
|
UTSW |
5 |
147,531,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R4812:Flt1
|
UTSW |
5 |
147,620,749 (GRCm39) |
missense |
probably benign |
0.30 |
R4853:Flt1
|
UTSW |
5 |
147,620,749 (GRCm39) |
missense |
probably benign |
0.30 |
R4865:Flt1
|
UTSW |
5 |
147,620,749 (GRCm39) |
missense |
probably benign |
0.30 |
R4900:Flt1
|
UTSW |
5 |
147,620,749 (GRCm39) |
missense |
probably benign |
0.30 |
R4906:Flt1
|
UTSW |
5 |
147,620,749 (GRCm39) |
missense |
probably benign |
0.30 |
R4907:Flt1
|
UTSW |
5 |
147,620,749 (GRCm39) |
missense |
probably benign |
0.30 |
R4909:Flt1
|
UTSW |
5 |
147,620,749 (GRCm39) |
missense |
probably benign |
0.30 |
R5072:Flt1
|
UTSW |
5 |
147,620,749 (GRCm39) |
missense |
probably benign |
0.30 |
R5073:Flt1
|
UTSW |
5 |
147,620,749 (GRCm39) |
missense |
probably benign |
0.30 |
R5074:Flt1
|
UTSW |
5 |
147,620,749 (GRCm39) |
missense |
probably benign |
0.30 |
R5218:Flt1
|
UTSW |
5 |
147,618,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R5547:Flt1
|
UTSW |
5 |
147,591,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R5731:Flt1
|
UTSW |
5 |
147,614,962 (GRCm39) |
missense |
probably benign |
0.16 |
R5732:Flt1
|
UTSW |
5 |
147,571,293 (GRCm39) |
nonsense |
probably null |
|
R5804:Flt1
|
UTSW |
5 |
147,517,247 (GRCm39) |
splice site |
probably null |
|
R6107:Flt1
|
UTSW |
5 |
147,540,403 (GRCm39) |
missense |
probably benign |
0.15 |
R6440:Flt1
|
UTSW |
5 |
147,501,115 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6453:Flt1
|
UTSW |
5 |
147,620,751 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6539:Flt1
|
UTSW |
5 |
147,515,186 (GRCm39) |
missense |
probably benign |
0.27 |
R7068:Flt1
|
UTSW |
5 |
147,610,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R7112:Flt1
|
UTSW |
5 |
147,540,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R7195:Flt1
|
UTSW |
5 |
147,540,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R7255:Flt1
|
UTSW |
5 |
147,517,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R7347:Flt1
|
UTSW |
5 |
147,517,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R7469:Flt1
|
UTSW |
5 |
147,540,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R7473:Flt1
|
UTSW |
5 |
147,531,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R7663:Flt1
|
UTSW |
5 |
147,591,930 (GRCm39) |
missense |
probably benign |
|
R7688:Flt1
|
UTSW |
5 |
147,613,135 (GRCm39) |
missense |
probably benign |
|
R7729:Flt1
|
UTSW |
5 |
147,637,177 (GRCm39) |
missense |
probably benign |
0.00 |
R7931:Flt1
|
UTSW |
5 |
147,525,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R8051:Flt1
|
UTSW |
5 |
147,519,501 (GRCm39) |
missense |
probably benign |
0.02 |
R8275:Flt1
|
UTSW |
5 |
147,614,957 (GRCm39) |
missense |
probably damaging |
0.99 |
R8434:Flt1
|
UTSW |
5 |
147,576,253 (GRCm39) |
missense |
probably damaging |
0.97 |
R8442:Flt1
|
UTSW |
5 |
147,512,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R8756:Flt1
|
UTSW |
5 |
147,576,224 (GRCm39) |
missense |
probably benign |
0.07 |
R8855:Flt1
|
UTSW |
5 |
147,618,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R8855:Flt1
|
UTSW |
5 |
147,507,682 (GRCm39) |
missense |
probably benign |
0.00 |
R9165:Flt1
|
UTSW |
5 |
147,552,047 (GRCm39) |
missense |
probably damaging |
0.99 |
R9240:Flt1
|
UTSW |
5 |
147,618,676 (GRCm39) |
missense |
probably benign |
|
R9439:Flt1
|
UTSW |
5 |
147,515,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R9658:Flt1
|
UTSW |
5 |
147,525,377 (GRCm39) |
missense |
probably damaging |
0.97 |
X0064:Flt1
|
UTSW |
5 |
147,610,423 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Flt1
|
UTSW |
5 |
147,618,459 (GRCm39) |
missense |
possibly damaging |
0.79 |
|