Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5930422O12Rik |
A |
G |
8: 33,919,353 (GRCm39) |
I58V |
unknown |
Het |
Abca4 |
G |
T |
3: 121,926,242 (GRCm39) |
G18V |
probably damaging |
Het |
Arl9 |
T |
C |
5: 77,154,374 (GRCm39) |
V34A |
possibly damaging |
Het |
Bpifb9a |
A |
T |
2: 154,104,163 (GRCm39) |
N202I |
possibly damaging |
Het |
C1qtnf6 |
A |
T |
15: 78,411,514 (GRCm39) |
M54K |
probably benign |
Het |
Ccdc62 |
T |
C |
5: 124,089,352 (GRCm39) |
|
probably null |
Het |
Cd177 |
A |
G |
7: 24,443,846 (GRCm39) |
C751R |
probably damaging |
Het |
Clcn3 |
T |
C |
8: 61,375,923 (GRCm39) |
I657V |
possibly damaging |
Het |
Cmtm1 |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
8: 105,036,102 (GRCm39) |
|
probably benign |
Het |
Dag1 |
T |
C |
9: 108,095,310 (GRCm39) |
T61A |
probably benign |
Het |
Fam184b |
C |
T |
5: 45,710,471 (GRCm39) |
G553E |
probably benign |
Het |
Fkbp15 |
G |
C |
4: 62,225,166 (GRCm39) |
A831G |
probably benign |
Het |
Fmnl2 |
T |
A |
2: 53,008,149 (GRCm39) |
|
probably null |
Het |
Gm5431 |
A |
G |
11: 48,785,275 (GRCm39) |
Y89H |
probably damaging |
Het |
Gprin2 |
C |
A |
14: 33,917,397 (GRCm39) |
L124F |
probably damaging |
Het |
Hacd2 |
T |
A |
16: 34,922,374 (GRCm39) |
Y188N |
probably damaging |
Het |
Itgad |
A |
G |
7: 127,797,726 (GRCm39) |
T950A |
probably benign |
Het |
Kit |
T |
A |
5: 75,815,075 (GRCm39) |
I933N |
possibly damaging |
Het |
Klhl11 |
A |
T |
11: 100,354,589 (GRCm39) |
Y411N |
probably damaging |
Het |
N4bp2 |
T |
C |
5: 65,966,500 (GRCm39) |
S1313P |
probably damaging |
Het |
Neurog1 |
T |
C |
13: 56,399,354 (GRCm39) |
K131R |
probably damaging |
Het |
Or11h6 |
T |
C |
14: 50,880,248 (GRCm39) |
L170P |
probably damaging |
Het |
Or5d16 |
T |
A |
2: 87,773,771 (GRCm39) |
H67L |
possibly damaging |
Het |
Otogl |
T |
C |
10: 107,717,325 (GRCm39) |
D382G |
probably damaging |
Het |
Pcdh1 |
A |
C |
18: 38,331,651 (GRCm39) |
F590V |
probably damaging |
Het |
Pcdha5 |
G |
A |
18: 37,093,820 (GRCm39) |
V110M |
probably damaging |
Het |
Pdlim3 |
A |
G |
8: 46,368,284 (GRCm39) |
N261D |
probably benign |
Het |
Pou4f1 |
T |
C |
14: 104,703,347 (GRCm39) |
T362A |
unknown |
Het |
Prlr |
A |
G |
15: 10,314,221 (GRCm39) |
T9A |
probably benign |
Het |
Psmb7 |
T |
C |
2: 38,478,289 (GRCm39) |
Y245C |
probably damaging |
Het |
Ryr3 |
T |
A |
2: 112,471,917 (GRCm39) |
D4515V |
probably damaging |
Het |
Svop |
T |
C |
5: 114,198,124 (GRCm39) |
K149E |
probably damaging |
Het |
Tlr3 |
A |
G |
8: 45,851,157 (GRCm39) |
V56A |
probably benign |
Het |
Tm4sf20 |
T |
G |
1: 82,738,013 (GRCm39) |
I93L |
probably benign |
Het |
Ugt2b5 |
T |
A |
5: 87,288,111 (GRCm39) |
R19* |
probably null |
Het |
Vmn2r28 |
G |
T |
7: 5,491,668 (GRCm39) |
T193K |
probably benign |
Het |
Vps13c |
A |
G |
9: 67,802,661 (GRCm39) |
D654G |
probably damaging |
Het |
Zfyve16 |
T |
A |
13: 92,644,701 (GRCm39) |
Q1167L |
probably benign |
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 |
|
IGL02143:Flt1
|
APN |
5 |
147,515,246 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
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 |
|