Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn1 |
T |
C |
12: 80,240,446 (GRCm39) |
R214G |
probably benign |
Het |
Cacna1e |
T |
A |
1: 154,348,123 (GRCm39) |
K817N |
probably benign |
Het |
Cyp3a16 |
A |
G |
5: 145,377,244 (GRCm39) |
F448L |
probably damaging |
Het |
Dpp6 |
T |
A |
5: 27,869,760 (GRCm39) |
|
probably null |
Het |
Eif2ak3 |
C |
T |
6: 70,869,710 (GRCm39) |
T799M |
probably damaging |
Het |
Erbb4 |
A |
T |
1: 68,383,090 (GRCm39) |
S302R |
probably damaging |
Het |
Fam217a |
T |
A |
13: 35,099,632 (GRCm39) |
|
probably benign |
Het |
Fpr-rs7 |
G |
A |
17: 20,334,454 (GRCm39) |
S12L |
probably damaging |
Het |
Fsd1 |
C |
T |
17: 56,303,733 (GRCm39) |
S491F |
probably damaging |
Het |
Hpcal4 |
T |
C |
4: 123,083,035 (GRCm39) |
|
probably null |
Het |
Intu |
A |
T |
3: 40,647,017 (GRCm39) |
D630V |
probably damaging |
Het |
Jak3 |
A |
G |
8: 72,136,933 (GRCm39) |
D703G |
probably damaging |
Het |
Lama4 |
A |
G |
10: 38,887,060 (GRCm39) |
I122V |
probably benign |
Het |
Mrpl11 |
A |
C |
19: 5,013,409 (GRCm39) |
K92T |
probably null |
Het |
Mtarc2 |
A |
G |
1: 184,551,413 (GRCm39) |
|
probably benign |
Het |
Mylk |
A |
G |
16: 34,791,610 (GRCm39) |
|
probably null |
Het |
Or52ab4 |
A |
T |
7: 102,987,974 (GRCm39) |
K238* |
probably null |
Het |
Parpbp |
A |
C |
10: 87,975,848 (GRCm39) |
Y88* |
probably null |
Het |
Plod2 |
G |
A |
9: 92,488,655 (GRCm39) |
R627Q |
probably damaging |
Het |
Rapsn |
G |
T |
2: 90,867,144 (GRCm39) |
A149S |
probably damaging |
Het |
Ripk3 |
T |
G |
14: 56,023,484 (GRCm39) |
Q109P |
probably damaging |
Het |
Scaf11 |
T |
C |
15: 96,318,361 (GRCm39) |
D401G |
probably damaging |
Het |
Serpine2 |
G |
A |
1: 79,779,268 (GRCm39) |
T150I |
probably damaging |
Het |
Sh2d6 |
T |
A |
6: 72,495,945 (GRCm39) |
T98S |
probably benign |
Het |
Slc28a1 |
G |
T |
7: 80,814,427 (GRCm39) |
A513S |
probably benign |
Het |
Tanc2 |
T |
C |
11: 105,777,207 (GRCm39) |
F795S |
probably damaging |
Het |
Tcim |
T |
A |
8: 24,928,705 (GRCm39) |
I70F |
probably benign |
Het |
Thbd |
G |
A |
2: 148,249,602 (GRCm39) |
Q89* |
probably null |
Het |
Tmem115 |
C |
T |
9: 107,411,859 (GRCm39) |
T61I |
probably damaging |
Het |
Tsc2 |
A |
T |
17: 24,832,259 (GRCm39) |
V650E |
probably damaging |
Het |
Tubgcp6 |
A |
T |
15: 88,992,199 (GRCm39) |
Y595* |
probably null |
Het |
Uroc1 |
C |
T |
6: 90,323,747 (GRCm39) |
A398V |
probably damaging |
Het |
Vmn1r31 |
T |
C |
6: 58,449,587 (GRCm39) |
T93A |
probably benign |
Het |
Vmn2r113 |
A |
G |
17: 23,175,024 (GRCm39) |
E545G |
possibly damaging |
Het |
Vps13a |
A |
G |
19: 16,678,516 (GRCm39) |
V1155A |
possibly damaging |
Het |
Zfp667 |
A |
G |
7: 6,307,869 (GRCm39) |
H179R |
probably benign |
Het |
|
Other mutations in Flt4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00499:Flt4
|
APN |
11 |
49,526,088 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01140:Flt4
|
APN |
11 |
49,525,770 (GRCm39) |
nonsense |
probably null |
|
IGL01360:Flt4
|
APN |
11 |
49,534,333 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01769:Flt4
|
APN |
11 |
49,525,998 (GRCm39) |
splice site |
probably benign |
|
IGL02189:Flt4
|
APN |
11 |
49,516,830 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02206:Flt4
|
APN |
11 |
49,521,217 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02324:Flt4
|
APN |
11 |
49,536,822 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02433:Flt4
|
APN |
11 |
49,521,400 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03009:Flt4
|
APN |
11 |
49,517,951 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03035:Flt4
|
APN |
11 |
49,536,724 (GRCm39) |
nonsense |
probably null |
|
IGL03059:Flt4
|
APN |
11 |
49,533,134 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03350:Flt4
|
APN |
11 |
49,525,620 (GRCm39) |
nonsense |
probably null |
|
PIT4802001:Flt4
|
UTSW |
11 |
49,523,996 (GRCm39) |
missense |
probably benign |
|
R0360:Flt4
|
UTSW |
11 |
49,527,818 (GRCm39) |
missense |
probably benign |
0.02 |
R0364:Flt4
|
UTSW |
11 |
49,527,818 (GRCm39) |
missense |
probably benign |
0.02 |
R0386:Flt4
|
UTSW |
11 |
49,535,213 (GRCm39) |
missense |
probably benign |
0.00 |
R0395:Flt4
|
UTSW |
11 |
49,521,170 (GRCm39) |
missense |
probably benign |
0.00 |
R0600:Flt4
|
UTSW |
11 |
49,527,166 (GRCm39) |
splice site |
probably benign |
|
R0666:Flt4
|
UTSW |
11 |
49,516,274 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0720:Flt4
|
UTSW |
11 |
49,527,166 (GRCm39) |
splice site |
probably benign |
|
R0734:Flt4
|
UTSW |
11 |
49,517,544 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0973:Flt4
|
UTSW |
11 |
49,527,166 (GRCm39) |
splice site |
probably benign |
|
R1013:Flt4
|
UTSW |
11 |
49,527,166 (GRCm39) |
splice site |
probably benign |
|
R1103:Flt4
|
UTSW |
11 |
49,527,166 (GRCm39) |
splice site |
probably benign |
|
R1104:Flt4
|
UTSW |
11 |
49,527,166 (GRCm39) |
splice site |
probably benign |
|
R1162:Flt4
|
UTSW |
11 |
49,527,166 (GRCm39) |
splice site |
probably benign |
|
R1241:Flt4
|
UTSW |
11 |
49,527,166 (GRCm39) |
splice site |
probably benign |
|
R1401:Flt4
|
UTSW |
11 |
49,527,166 (GRCm39) |
splice site |
probably benign |
|
R1487:Flt4
|
UTSW |
11 |
49,523,971 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1546:Flt4
|
UTSW |
11 |
49,522,808 (GRCm39) |
missense |
probably benign |
0.03 |
R1999:Flt4
|
UTSW |
11 |
49,536,824 (GRCm39) |
missense |
probably benign |
0.00 |
R2110:Flt4
|
UTSW |
11 |
49,516,131 (GRCm39) |
missense |
probably benign |
0.03 |
R2150:Flt4
|
UTSW |
11 |
49,536,824 (GRCm39) |
missense |
probably benign |
0.00 |
R2189:Flt4
|
UTSW |
11 |
49,526,525 (GRCm39) |
missense |
probably benign |
0.24 |
R2217:Flt4
|
UTSW |
11 |
49,515,555 (GRCm39) |
missense |
probably benign |
0.00 |
R2218:Flt4
|
UTSW |
11 |
49,515,555 (GRCm39) |
missense |
probably benign |
0.00 |
R2249:Flt4
|
UTSW |
11 |
49,536,786 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2402:Flt4
|
UTSW |
11 |
49,528,646 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3508:Flt4
|
UTSW |
11 |
49,524,941 (GRCm39) |
missense |
probably damaging |
0.99 |
R3974:Flt4
|
UTSW |
11 |
49,527,567 (GRCm39) |
missense |
probably damaging |
0.99 |
R4168:Flt4
|
UTSW |
11 |
49,521,400 (GRCm39) |
missense |
probably benign |
0.01 |
R4700:Flt4
|
UTSW |
11 |
49,517,271 (GRCm39) |
intron |
probably benign |
|
R4701:Flt4
|
UTSW |
11 |
49,517,635 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4714:Flt4
|
UTSW |
11 |
49,518,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R4817:Flt4
|
UTSW |
11 |
49,516,242 (GRCm39) |
missense |
probably damaging |
0.98 |
R4921:Flt4
|
UTSW |
11 |
49,517,970 (GRCm39) |
missense |
probably damaging |
0.98 |
R5066:Flt4
|
UTSW |
11 |
49,524,990 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5095:Flt4
|
UTSW |
11 |
49,517,986 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5166:Flt4
|
UTSW |
11 |
49,524,084 (GRCm39) |
splice site |
probably null |
|
R5245:Flt4
|
UTSW |
11 |
49,541,861 (GRCm39) |
frame shift |
probably null |
|
R5250:Flt4
|
UTSW |
11 |
49,521,227 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5400:Flt4
|
UTSW |
11 |
49,541,861 (GRCm39) |
frame shift |
probably null |
|
R5401:Flt4
|
UTSW |
11 |
49,541,861 (GRCm39) |
frame shift |
probably null |
|
R5402:Flt4
|
UTSW |
11 |
49,541,861 (GRCm39) |
frame shift |
probably null |
|
R5527:Flt4
|
UTSW |
11 |
49,525,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R5686:Flt4
|
UTSW |
11 |
49,521,430 (GRCm39) |
missense |
probably benign |
0.00 |
R5766:Flt4
|
UTSW |
11 |
49,517,513 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5996:Flt4
|
UTSW |
11 |
49,541,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R6037:Flt4
|
UTSW |
11 |
49,527,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R6037:Flt4
|
UTSW |
11 |
49,527,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R6352:Flt4
|
UTSW |
11 |
49,534,333 (GRCm39) |
missense |
probably benign |
0.04 |
R6361:Flt4
|
UTSW |
11 |
49,521,405 (GRCm39) |
missense |
probably benign |
0.00 |
R6574:Flt4
|
UTSW |
11 |
49,516,199 (GRCm39) |
missense |
probably benign |
|
R7205:Flt4
|
UTSW |
11 |
49,525,125 (GRCm39) |
missense |
probably null |
0.78 |
R7216:Flt4
|
UTSW |
11 |
49,525,508 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7257:Flt4
|
UTSW |
11 |
49,516,836 (GRCm39) |
missense |
probably benign |
0.22 |
R7457:Flt4
|
UTSW |
11 |
49,521,155 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7559:Flt4
|
UTSW |
11 |
49,535,198 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8181:Flt4
|
UTSW |
11 |
49,525,723 (GRCm39) |
missense |
probably damaging |
0.99 |
R8286:Flt4
|
UTSW |
11 |
49,528,089 (GRCm39) |
missense |
probably benign |
0.00 |
R8885:Flt4
|
UTSW |
11 |
49,527,160 (GRCm39) |
splice site |
probably benign |
|
R9051:Flt4
|
UTSW |
11 |
49,527,598 (GRCm39) |
missense |
probably benign |
0.02 |
R9104:Flt4
|
UTSW |
11 |
49,525,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R9112:Flt4
|
UTSW |
11 |
49,524,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R9301:Flt4
|
UTSW |
11 |
49,516,241 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9721:Flt4
|
UTSW |
11 |
49,535,260 (GRCm39) |
critical splice donor site |
probably null |
|
X0017:Flt4
|
UTSW |
11 |
49,517,560 (GRCm39) |
missense |
possibly damaging |
0.89 |
|