Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
A |
T |
5: 109,885,662 (GRCm39) |
N65K |
probably benign |
Het |
Abcc9 |
T |
C |
6: 142,536,162 (GRCm39) |
Y1524C |
probably benign |
Het |
Acap1 |
A |
G |
11: 69,778,019 (GRCm39) |
I102T |
probably damaging |
Het |
Acvr2a |
T |
C |
2: 48,783,553 (GRCm39) |
V284A |
possibly damaging |
Het |
Adam3 |
T |
C |
8: 25,174,630 (GRCm39) |
M712V |
probably benign |
Het |
Adck1 |
T |
C |
12: 88,407,908 (GRCm39) |
V213A |
probably benign |
Het |
Adgrl3 |
G |
T |
5: 81,659,957 (GRCm39) |
W242L |
probably damaging |
Het |
Alk |
T |
C |
17: 72,211,310 (GRCm39) |
T857A |
probably benign |
Het |
Alms1 |
A |
G |
6: 85,605,528 (GRCm39) |
T2393A |
probably benign |
Het |
Ank3 |
C |
T |
10: 69,837,939 (GRCm39) |
P240L |
probably damaging |
Het |
Ankrd35 |
C |
A |
3: 96,592,140 (GRCm39) |
L809M |
possibly damaging |
Het |
Birc6 |
T |
A |
17: 74,957,094 (GRCm39) |
L3690Q |
probably damaging |
Het |
Bmp3 |
C |
A |
5: 99,019,920 (GRCm39) |
F114L |
probably damaging |
Het |
Cage1 |
G |
A |
13: 38,203,184 (GRCm39) |
H627Y |
probably benign |
Het |
Cars1 |
T |
C |
7: 143,123,212 (GRCm39) |
D468G |
probably damaging |
Het |
Ccdc148 |
T |
C |
2: 58,719,814 (GRCm39) |
E487G |
probably damaging |
Het |
Ccdc80 |
A |
T |
16: 44,938,530 (GRCm39) |
I746F |
probably damaging |
Het |
Ccl25 |
A |
G |
8: 4,403,913 (GRCm39) |
Q119R |
possibly damaging |
Het |
Cdh24 |
C |
T |
14: 54,870,672 (GRCm39) |
D178N |
probably damaging |
Het |
Cdk12 |
A |
T |
11: 98,113,513 (GRCm39) |
T766S |
unknown |
Het |
Chst15 |
T |
A |
7: 131,849,613 (GRCm39) |
T443S |
probably benign |
Het |
Cnbp |
T |
C |
6: 87,822,128 (GRCm39) |
D125G |
possibly damaging |
Het |
Cntn2 |
A |
T |
1: 132,443,770 (GRCm39) |
V1003E |
possibly damaging |
Het |
Crct1 |
A |
G |
3: 92,922,132 (GRCm39) |
|
probably benign |
Het |
Dand5 |
C |
T |
8: 85,543,113 (GRCm39) |
C121Y |
probably damaging |
Het |
Dmkn |
A |
T |
7: 30,470,658 (GRCm39) |
D382V |
probably damaging |
Het |
Dnase2b |
T |
A |
3: 146,299,196 (GRCm39) |
T86S |
probably damaging |
Het |
Dusp8 |
GCCACCACCACCACCACCACCACC |
GCCACCACCACCACCACCACC |
7: 141,635,891 (GRCm39) |
|
probably benign |
Het |
Eef1akmt1 |
C |
T |
14: 57,788,089 (GRCm39) |
V90M |
probably damaging |
Het |
Egfl7 |
G |
T |
2: 26,480,992 (GRCm39) |
W168L |
probably benign |
Het |
Ep400 |
A |
G |
5: 110,813,676 (GRCm39) |
C2908R |
probably damaging |
Het |
Espl1 |
A |
G |
15: 102,223,676 (GRCm39) |
K1076E |
probably damaging |
Het |
Exoc4 |
A |
G |
6: 33,887,452 (GRCm39) |
N747D |
probably benign |
Het |
Fancm |
T |
C |
12: 65,123,915 (GRCm39) |
V191A |
probably benign |
Het |
Fbxo17 |
A |
G |
7: 28,432,214 (GRCm39) |
D97G |
probably benign |
Het |
Fer1l6 |
G |
T |
15: 58,472,160 (GRCm39) |
|
probably null |
Het |
Fpr-rs7 |
T |
C |
17: 20,334,082 (GRCm39) |
H136R |
possibly damaging |
Het |
Frem3 |
T |
A |
8: 81,339,765 (GRCm39) |
I686N |
possibly damaging |
Het |
Galnt9 |
A |
G |
5: 110,725,315 (GRCm39) |
K84R |
probably damaging |
Het |
Gfm2 |
T |
A |
13: 97,312,184 (GRCm39) |
M760K |
probably damaging |
Het |
Glis3 |
T |
C |
19: 28,643,504 (GRCm39) |
T13A |
probably damaging |
Het |
H2-K2 |
A |
G |
17: 34,216,050 (GRCm39) |
V323A |
possibly damaging |
Het |
Hbb-bs |
G |
A |
7: 103,475,927 (GRCm39) |
A130V |
probably damaging |
Het |
Herc2 |
T |
A |
7: 55,879,438 (GRCm39) |
H4685Q |
probably benign |
Het |
Ighv5-9-1 |
C |
T |
12: 113,699,914 (GRCm39) |
R56H |
possibly damaging |
Het |
Itgb4 |
A |
G |
11: 115,897,431 (GRCm39) |
N1548S |
probably benign |
Het |
Itpr3 |
T |
C |
17: 27,316,979 (GRCm39) |
Y745H |
probably damaging |
Het |
Kank3 |
G |
T |
17: 34,036,174 (GRCm39) |
G14V |
probably damaging |
Het |
Kif24 |
G |
T |
4: 41,394,329 (GRCm39) |
S982Y |
probably damaging |
Het |
Kifc5b |
C |
T |
17: 27,139,997 (GRCm39) |
R53W |
probably damaging |
Het |
Krt39 |
A |
G |
11: 99,405,575 (GRCm39) |
S442P |
possibly damaging |
Het |
Lcat |
G |
A |
8: 106,669,074 (GRCm39) |
P67L |
possibly damaging |
Het |
Maml2 |
T |
C |
9: 13,532,471 (GRCm39) |
S562P |
probably damaging |
Het |
Map3k8 |
G |
A |
18: 4,349,124 (GRCm39) |
R65W |
possibly damaging |
Het |
Mbd3 |
G |
T |
10: 80,231,410 (GRCm39) |
R12S |
probably damaging |
Het |
Msr1 |
T |
C |
8: 40,077,292 (GRCm39) |
E106G |
possibly damaging |
Het |
Myh4 |
T |
A |
11: 67,144,854 (GRCm39) |
L1256Q |
probably damaging |
Het |
Mypn |
G |
A |
10: 62,983,715 (GRCm39) |
T511M |
possibly damaging |
Het |
Nub1 |
A |
T |
5: 24,906,467 (GRCm39) |
N331I |
probably benign |
Het |
Nup107 |
A |
G |
10: 117,606,416 (GRCm39) |
V440A |
possibly damaging |
Het |
Ofcc1 |
A |
G |
13: 40,367,993 (GRCm39) |
F174L |
probably benign |
Het |
Or10d5 |
A |
C |
9: 39,861,521 (GRCm39) |
V182G |
probably damaging |
Het |
Or52ab2 |
A |
T |
7: 102,969,750 (GRCm39) |
N44I |
probably damaging |
Het |
Or9q2 |
T |
C |
19: 13,772,829 (GRCm39) |
I49V |
probably benign |
Het |
Parp2 |
C |
A |
14: 51,056,725 (GRCm39) |
L310I |
probably damaging |
Het |
Pcdh20 |
A |
G |
14: 88,707,162 (GRCm39) |
V46A |
probably benign |
Het |
Pcdhgb6 |
A |
G |
18: 37,876,525 (GRCm39) |
D411G |
probably damaging |
Het |
Pkd1l2 |
T |
C |
8: 117,781,624 (GRCm39) |
E807G |
probably benign |
Het |
Pkd1l2 |
A |
T |
8: 117,799,288 (GRCm39) |
N267K |
probably damaging |
Het |
Pramel24 |
A |
T |
4: 143,454,896 (GRCm39) |
K398M |
possibly damaging |
Het |
Rell1 |
C |
A |
5: 64,093,376 (GRCm39) |
M126I |
probably damaging |
Het |
Robo4 |
G |
A |
9: 37,313,856 (GRCm39) |
E36K |
probably benign |
Het |
Rpgrip1l |
T |
C |
8: 91,987,637 (GRCm39) |
S807G |
probably benign |
Het |
Rpl10a |
T |
C |
17: 28,549,826 (GRCm39) |
V169A |
probably benign |
Het |
Rubcn |
C |
T |
16: 32,667,664 (GRCm39) |
V166I |
probably damaging |
Het |
Sall2 |
T |
C |
14: 52,552,850 (GRCm39) |
E113G |
possibly damaging |
Het |
Sars2 |
T |
C |
7: 28,451,863 (GRCm39) |
S423P |
possibly damaging |
Het |
Scaper |
A |
G |
9: 55,799,519 (GRCm39) |
I182T |
probably benign |
Het |
Selp |
A |
G |
1: 163,968,966 (GRCm39) |
D522G |
possibly damaging |
Het |
Sema4b |
T |
A |
7: 79,848,504 (GRCm39) |
I35N |
possibly damaging |
Het |
Sgce |
A |
T |
6: 4,694,153 (GRCm39) |
F268I |
probably damaging |
Het |
Slc14a2 |
G |
T |
18: 78,235,403 (GRCm39) |
A258E |
probably damaging |
Het |
Slc17a9 |
T |
C |
2: 180,377,742 (GRCm39) |
Y213H |
probably benign |
Het |
Slc22a7 |
T |
G |
17: 46,747,859 (GRCm39) |
I233L |
probably benign |
Het |
Slc35f1 |
A |
G |
10: 52,938,698 (GRCm39) |
Q210R |
probably damaging |
Het |
Slc6a21 |
A |
G |
7: 44,937,734 (GRCm39) |
E350G |
possibly damaging |
Het |
Spata21 |
A |
T |
4: 140,839,402 (GRCm39) |
D639V |
probably damaging |
Het |
Svil |
A |
G |
18: 5,108,631 (GRCm39) |
D1519G |
probably damaging |
Het |
Tbccd1 |
T |
C |
16: 22,660,649 (GRCm39) |
T56A |
probably benign |
Het |
Tigit |
A |
T |
16: 43,482,380 (GRCm39) |
I118N |
probably damaging |
Het |
Tlr11 |
A |
T |
14: 50,600,342 (GRCm39) |
Q776L |
possibly damaging |
Het |
Tspan12 |
A |
C |
6: 21,835,448 (GRCm39) |
I9S |
possibly damaging |
Het |
Unc5c |
T |
A |
3: 141,494,727 (GRCm39) |
Y347N |
probably damaging |
Het |
Unk |
A |
G |
11: 115,945,771 (GRCm39) |
T481A |
probably benign |
Het |
Vmn1r192 |
A |
C |
13: 22,371,650 (GRCm39) |
V190G |
probably damaging |
Het |
Vnn3 |
A |
T |
10: 23,740,473 (GRCm39) |
M259L |
probably benign |
Het |
Zan |
T |
C |
5: 137,406,632 (GRCm39) |
|
probably benign |
Het |
Zdhhc6 |
T |
C |
19: 55,301,642 (GRCm39) |
H113R |
probably damaging |
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 |
IGL01386:Flt4
|
APN |
11 |
49,528,162 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
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 |
|