Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acta2 |
G |
A |
19: 34,229,931 (GRCm39) |
T8I |
probably benign |
Het |
Alox5 |
T |
C |
6: 116,390,756 (GRCm39) |
D465G |
possibly damaging |
Het |
Arhgef16 |
T |
A |
4: 154,367,339 (GRCm39) |
K355N |
possibly damaging |
Het |
Camkk2 |
T |
A |
5: 122,902,363 (GRCm39) |
|
probably benign |
Het |
Ccdc171 |
C |
T |
4: 83,499,012 (GRCm39) |
Q237* |
probably null |
Het |
Ces2b |
T |
C |
8: 105,564,017 (GRCm39) |
Y464H |
possibly damaging |
Het |
Cntfr |
A |
G |
4: 41,662,013 (GRCm39) |
F243S |
possibly damaging |
Het |
Crip3 |
A |
T |
17: 46,740,791 (GRCm39) |
R65S |
probably benign |
Het |
Dcn |
A |
G |
10: 97,319,340 (GRCm39) |
Y39C |
possibly damaging |
Het |
Degs2 |
T |
C |
12: 108,658,332 (GRCm39) |
S216G |
possibly damaging |
Het |
Dmxl1 |
A |
G |
18: 50,035,861 (GRCm39) |
I2295V |
probably benign |
Het |
Dnah2 |
A |
G |
11: 69,389,511 (GRCm39) |
S794P |
probably damaging |
Het |
Eri1 |
A |
C |
8: 35,941,554 (GRCm39) |
Y264* |
probably null |
Het |
Etl4 |
T |
C |
2: 20,718,189 (GRCm39) |
L179P |
probably damaging |
Het |
F5 |
T |
G |
1: 164,014,481 (GRCm39) |
M584R |
possibly damaging |
Het |
Fam98c |
G |
T |
7: 28,852,248 (GRCm39) |
R104S |
probably damaging |
Het |
Hbp1 |
T |
C |
12: 31,993,899 (GRCm39) |
E43G |
probably benign |
Het |
Hivep3 |
CGG |
CG |
4: 119,955,108 (GRCm39) |
1141 |
probably null |
Het |
Kcnj3 |
T |
A |
2: 55,484,833 (GRCm39) |
C310* |
probably null |
Het |
Lct |
T |
C |
1: 128,212,932 (GRCm39) |
Y1907C |
probably damaging |
Het |
Loxhd1 |
T |
C |
18: 77,518,882 (GRCm39) |
V1896A |
possibly damaging |
Het |
Lrfn4 |
C |
A |
19: 4,663,679 (GRCm39) |
R285L |
probably damaging |
Het |
Ltb4r2 |
T |
A |
14: 56,000,338 (GRCm39) |
S320T |
probably damaging |
Het |
Mmd |
G |
T |
11: 90,148,378 (GRCm39) |
R20L |
probably damaging |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Nbas |
T |
C |
12: 13,608,661 (GRCm39) |
S2146P |
probably benign |
Het |
Nop14 |
A |
G |
5: 34,809,135 (GRCm39) |
F319L |
probably damaging |
Het |
Numa1 |
C |
A |
7: 101,648,630 (GRCm39) |
T787K |
probably benign |
Het |
Or10q12 |
T |
G |
19: 13,745,709 (GRCm39) |
M1R |
probably null |
Het |
Or2t46 |
A |
C |
11: 58,471,999 (GRCm39) |
T110P |
probably damaging |
Het |
Or6c208 |
T |
G |
10: 129,223,726 (GRCm39) |
C75G |
possibly damaging |
Het |
Patj |
T |
C |
4: 98,435,224 (GRCm39) |
V2A |
probably benign |
Het |
Pisd |
T |
C |
5: 32,898,032 (GRCm39) |
H52R |
probably benign |
Het |
Plekhg6 |
A |
T |
6: 125,340,631 (GRCm39) |
D576E |
probably benign |
Het |
Plekhn1 |
T |
A |
4: 156,310,110 (GRCm39) |
H68L |
probably benign |
Het |
Ppp1r37 |
T |
A |
7: 19,295,778 (GRCm39) |
I60F |
probably damaging |
Het |
Ppp2r1b |
C |
T |
9: 50,789,476 (GRCm39) |
T513M |
possibly damaging |
Het |
Pramel32 |
A |
T |
4: 88,548,279 (GRCm39) |
I42N |
probably damaging |
Het |
Rhobtb2 |
C |
A |
14: 70,034,386 (GRCm39) |
A280S |
probably damaging |
Het |
Rnf40 |
A |
G |
7: 127,189,047 (GRCm39) |
D140G |
probably benign |
Het |
Rxfp1 |
A |
G |
3: 79,555,397 (GRCm39) |
L653P |
probably damaging |
Het |
Satb1 |
A |
T |
17: 52,074,995 (GRCm39) |
D500E |
probably benign |
Het |
Slc15a1 |
A |
T |
14: 121,713,377 (GRCm39) |
D383E |
probably benign |
Het |
Smarcad1 |
C |
A |
6: 65,073,033 (GRCm39) |
S604R |
possibly damaging |
Het |
St7 |
A |
G |
6: 17,934,216 (GRCm39) |
T533A |
probably damaging |
Het |
Sv2c |
T |
A |
13: 96,122,451 (GRCm39) |
T442S |
probably benign |
Het |
Tbx2 |
A |
G |
11: 85,731,622 (GRCm39) |
T640A |
probably benign |
Het |
Tenm4 |
T |
A |
7: 96,542,221 (GRCm39) |
N1948K |
probably damaging |
Het |
Tll1 |
T |
C |
8: 64,551,268 (GRCm39) |
|
probably null |
Het |
Tmem135 |
A |
T |
7: 88,805,718 (GRCm39) |
|
probably null |
Het |
Tonsl |
A |
T |
15: 76,518,136 (GRCm39) |
L582Q |
probably null |
Het |
Unc13c |
T |
A |
9: 73,641,799 (GRCm39) |
K1231N |
probably damaging |
Het |
Vmn2r101 |
T |
A |
17: 19,832,192 (GRCm39) |
Y729* |
probably null |
Het |
Zcchc2 |
A |
G |
1: 105,928,742 (GRCm39) |
T334A |
possibly damaging |
Het |
Zfp655 |
T |
C |
5: 145,173,917 (GRCm39) |
L136P |
probably damaging |
Het |
Zfp729a |
A |
T |
13: 67,768,437 (GRCm39) |
C597* |
probably null |
Het |
|
Other mutations in Flad1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00422:Flad1
|
APN |
3 |
89,313,160 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02065:Flad1
|
APN |
3 |
89,316,294 (GRCm39) |
missense |
probably damaging |
1.00 |
brick
|
UTSW |
3 |
89,318,494 (GRCm39) |
missense |
probably damaging |
1.00 |
Impaler
|
UTSW |
3 |
89,310,758 (GRCm39) |
missense |
probably damaging |
0.99 |
stone
|
UTSW |
3 |
89,316,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Flad1
|
UTSW |
3 |
89,309,552 (GRCm39) |
nonsense |
probably null |
|
R3821:Flad1
|
UTSW |
3 |
89,318,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R3822:Flad1
|
UTSW |
3 |
89,318,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R4458:Flad1
|
UTSW |
3 |
89,316,241 (GRCm39) |
missense |
probably benign |
0.14 |
R4838:Flad1
|
UTSW |
3 |
89,313,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R5296:Flad1
|
UTSW |
3 |
89,318,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R6522:Flad1
|
UTSW |
3 |
89,310,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R6703:Flad1
|
UTSW |
3 |
89,315,897 (GRCm39) |
missense |
probably benign |
|
R7000:Flad1
|
UTSW |
3 |
89,309,549 (GRCm39) |
utr 3 prime |
probably benign |
|
R7114:Flad1
|
UTSW |
3 |
89,314,837 (GRCm39) |
missense |
probably benign |
0.00 |
R7127:Flad1
|
UTSW |
3 |
89,310,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R7365:Flad1
|
UTSW |
3 |
89,315,972 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7662:Flad1
|
UTSW |
3 |
89,310,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R8097:Flad1
|
UTSW |
3 |
89,316,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R8296:Flad1
|
UTSW |
3 |
89,316,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R8332:Flad1
|
UTSW |
3 |
89,314,828 (GRCm39) |
missense |
probably benign |
|
R8531:Flad1
|
UTSW |
3 |
89,310,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R8711:Flad1
|
UTSW |
3 |
89,316,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R9090:Flad1
|
UTSW |
3 |
89,315,858 (GRCm39) |
nonsense |
probably null |
|
R9271:Flad1
|
UTSW |
3 |
89,315,858 (GRCm39) |
nonsense |
probably null |
|
R9767:Flad1
|
UTSW |
3 |
89,310,718 (GRCm39) |
missense |
probably benign |
0.01 |
|