Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
Abi2 |
C |
A |
1: 60,503,738 (GRCm39) |
P212T |
probably damaging |
Het |
Ano4 |
A |
G |
10: 89,153,108 (GRCm39) |
F68S |
possibly damaging |
Het |
Art5 |
C |
A |
7: 101,747,591 (GRCm39) |
A63S |
probably benign |
Het |
Asgr1 |
T |
A |
11: 69,947,247 (GRCm39) |
S96R |
probably benign |
Het |
Bdp1 |
A |
T |
13: 100,163,957 (GRCm39) |
V2248D |
possibly damaging |
Het |
Cacna1s |
C |
T |
1: 135,998,705 (GRCm39) |
A200V |
possibly damaging |
Het |
Cacna2d2 |
A |
G |
9: 107,390,738 (GRCm39) |
K357E |
probably damaging |
Het |
Cdhr18 |
T |
C |
14: 13,864,282 (GRCm38) |
N348S |
probably damaging |
Het |
Cfap52 |
C |
T |
11: 67,837,126 (GRCm39) |
G212R |
probably benign |
Het |
Dcun1d3 |
A |
G |
7: 119,456,965 (GRCm39) |
F249S |
probably damaging |
Het |
Ece2 |
A |
G |
16: 20,449,112 (GRCm39) |
Y17C |
probably damaging |
Het |
Efemp1 |
C |
T |
11: 28,871,760 (GRCm39) |
T425I |
probably damaging |
Het |
Eprs1 |
A |
G |
1: 185,128,306 (GRCm39) |
E562G |
probably damaging |
Het |
Fbn2 |
T |
C |
18: 58,177,295 (GRCm39) |
T2001A |
probably benign |
Het |
Fry |
T |
A |
5: 150,351,644 (GRCm39) |
M1716K |
probably benign |
Het |
Gm10684 |
T |
A |
9: 45,019,039 (GRCm39) |
|
probably benign |
Het |
Hivep1 |
G |
A |
13: 42,311,416 (GRCm39) |
V1219I |
probably damaging |
Het |
Hyls1 |
G |
A |
9: 35,472,480 (GRCm39) |
S312F |
probably benign |
Het |
Il23r |
C |
T |
6: 67,455,938 (GRCm39) |
V177M |
probably damaging |
Het |
Klf12 |
T |
C |
14: 100,137,650 (GRCm39) |
S299G |
probably benign |
Het |
Lama5 |
G |
A |
2: 179,848,806 (GRCm39) |
R265C |
probably damaging |
Het |
Lifr |
A |
G |
15: 7,216,424 (GRCm39) |
T800A |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,063,831 (GRCm39) |
L2729P |
probably damaging |
Het |
Mki67 |
A |
C |
7: 135,298,532 (GRCm39) |
S2167R |
possibly damaging |
Het |
Mus81 |
T |
C |
19: 5,534,032 (GRCm39) |
K400E |
probably damaging |
Het |
Nomo1 |
T |
A |
7: 45,712,423 (GRCm39) |
I656N |
possibly damaging |
Het |
Oas3 |
T |
C |
5: 120,907,384 (GRCm39) |
T418A |
probably benign |
Het |
Olr1 |
A |
G |
6: 129,470,504 (GRCm39) |
L221P |
probably damaging |
Het |
Or14c44 |
C |
T |
7: 86,062,478 (GRCm39) |
L303F |
probably benign |
Het |
Or5m9 |
T |
C |
2: 85,876,928 (GRCm39) |
M34T |
probably benign |
Het |
Or8b3 |
T |
A |
9: 38,314,601 (GRCm39) |
C144S |
probably benign |
Het |
Or8g22 |
A |
G |
9: 38,958,403 (GRCm39) |
V104A |
probably damaging |
Het |
Or8k28 |
T |
A |
2: 86,286,133 (GRCm39) |
I161L |
probably benign |
Het |
Pih1d1 |
C |
T |
7: 44,805,738 (GRCm39) |
A69V |
probably damaging |
Het |
Pkdrej |
A |
C |
15: 85,703,967 (GRCm39) |
S656R |
probably damaging |
Het |
Polr3f |
A |
G |
2: 144,377,943 (GRCm39) |
D171G |
probably damaging |
Het |
Rasal1 |
T |
C |
5: 120,787,566 (GRCm39) |
V11A |
possibly damaging |
Het |
Rsf1 |
G |
GACGGCGGCT |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Sptbn4 |
T |
A |
7: 27,063,595 (GRCm39) |
Y2277F |
probably damaging |
Het |
St6galnac6 |
A |
G |
2: 32,502,240 (GRCm39) |
Q7R |
probably damaging |
Het |
Thrsp |
T |
G |
7: 97,066,499 (GRCm39) |
D71A |
possibly damaging |
Het |
Vmn2r1 |
C |
A |
3: 63,989,150 (GRCm39) |
Q30K |
probably benign |
Het |
Vmn2r125 |
C |
A |
4: 156,703,396 (GRCm39) |
A258D |
probably benign |
Het |
Wipf2 |
C |
T |
11: 98,787,005 (GRCm39) |
P345S |
probably benign |
Het |
Zeb2 |
G |
T |
2: 44,878,652 (GRCm39) |
S1170* |
probably null |
Het |
Zfp947 |
A |
G |
17: 22,366,415 (GRCm39) |
Y38H |
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 |
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 |
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 |
|