Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
G |
A |
6: 121,618,349 (GRCm39) |
R214H |
probably benign |
Het |
Abca4 |
A |
G |
3: 121,906,096 (GRCm39) |
S822G |
probably benign |
Het |
Adgrv1 |
T |
A |
13: 81,707,621 (GRCm39) |
I1262F |
probably benign |
Het |
Agbl2 |
A |
G |
2: 90,632,088 (GRCm39) |
D482G |
probably damaging |
Het |
Asph |
T |
A |
4: 9,630,947 (GRCm39) |
T134S |
possibly damaging |
Het |
Cacna1a |
C |
T |
8: 85,286,070 (GRCm39) |
A905V |
probably benign |
Het |
Cacna1b |
C |
T |
2: 24,569,530 (GRCm39) |
R798H |
probably benign |
Het |
Cpne8 |
G |
T |
15: 90,486,044 (GRCm39) |
Q140K |
probably benign |
Het |
Crocc2 |
A |
T |
1: 93,120,847 (GRCm39) |
N538I |
probably benign |
Het |
Cyp2j9 |
T |
A |
4: 96,462,184 (GRCm39) |
I366F |
probably damaging |
Het |
Dchs1 |
A |
T |
7: 105,410,064 (GRCm39) |
D1769E |
probably damaging |
Het |
Def6 |
A |
T |
17: 28,435,972 (GRCm39) |
I44F |
probably damaging |
Het |
Dnah7a |
G |
A |
1: 53,462,422 (GRCm39) |
T3723M |
probably damaging |
Het |
Ecd |
T |
A |
14: 20,387,140 (GRCm39) |
Y198F |
probably damaging |
Het |
Ecel1 |
A |
C |
1: 87,079,760 (GRCm39) |
M451R |
probably damaging |
Het |
Eea1 |
A |
G |
10: 95,831,506 (GRCm39) |
D199G |
probably benign |
Het |
Efna5 |
A |
T |
17: 62,914,374 (GRCm39) |
I217N |
unknown |
Het |
F13a1 |
A |
T |
13: 37,100,859 (GRCm39) |
D428E |
probably damaging |
Het |
Fads1 |
T |
G |
19: 10,170,276 (GRCm39) |
I272S |
probably benign |
Het |
Fam149a |
C |
T |
8: 45,834,611 (GRCm39) |
A63T |
|
Het |
Fam83a |
A |
T |
15: 57,872,977 (GRCm39) |
N269Y |
probably damaging |
Het |
Fasn |
G |
A |
11: 120,708,979 (GRCm39) |
T568I |
possibly damaging |
Het |
Fbn1 |
A |
G |
2: 125,156,637 (GRCm39) |
S2363P |
probably damaging |
Het |
Fbxl4 |
T |
A |
4: 22,390,803 (GRCm39) |
W329R |
probably damaging |
Het |
Fgf12 |
A |
T |
16: 28,008,233 (GRCm39) |
V189E |
probably damaging |
Het |
Galm |
A |
G |
17: 80,490,661 (GRCm39) |
T273A |
possibly damaging |
Het |
Gm43302 |
A |
G |
5: 105,438,739 (GRCm39) |
S50P |
probably damaging |
Het |
Gm45861 |
C |
T |
8: 28,010,788 (GRCm39) |
S561L |
unknown |
Het |
Gnao1 |
A |
G |
8: 94,538,045 (GRCm39) |
I28V |
probably benign |
Het |
Golga4 |
A |
G |
9: 118,385,779 (GRCm39) |
N967S |
probably damaging |
Het |
Gpr155 |
A |
T |
2: 73,203,993 (GRCm39) |
F274I |
probably benign |
Het |
Grm1 |
A |
C |
10: 10,595,092 (GRCm39) |
N845K |
probably damaging |
Het |
Hnrnpa2b1 |
A |
T |
6: 51,443,120 (GRCm39) |
|
probably null |
Het |
Hsf4 |
G |
T |
8: 105,996,628 (GRCm39) |
D18Y |
probably null |
Het |
Htt |
T |
A |
5: 35,060,675 (GRCm39) |
D2774E |
probably benign |
Het |
Iars2 |
A |
G |
1: 185,028,621 (GRCm39) |
I679T |
probably benign |
Het |
Irf4 |
T |
C |
13: 30,945,414 (GRCm39) |
F387L |
probably damaging |
Het |
Itgb5 |
A |
G |
16: 33,720,962 (GRCm39) |
Y342C |
probably damaging |
Het |
Kcnmb4 |
A |
G |
10: 116,282,299 (GRCm39) |
W133R |
possibly damaging |
Het |
Ldhc |
A |
T |
7: 46,525,999 (GRCm39) |
H271L |
probably benign |
Het |
Lmtk2 |
C |
A |
5: 144,113,079 (GRCm39) |
D1266E |
probably damaging |
Het |
Lrrtm1 |
C |
A |
6: 77,221,807 (GRCm39) |
N421K |
possibly damaging |
Het |
Ly9 |
G |
A |
1: 171,432,587 (GRCm39) |
T142I |
probably benign |
Het |
Manba |
A |
G |
3: 135,223,764 (GRCm39) |
Y217C |
probably damaging |
Het |
Mapkbp1 |
T |
C |
2: 119,845,109 (GRCm39) |
L330P |
probably damaging |
Het |
Marchf2 |
A |
T |
17: 33,915,165 (GRCm39) |
V143E |
probably benign |
Het |
Mmel1 |
A |
T |
4: 154,969,478 (GRCm39) |
D191V |
possibly damaging |
Het |
Mrgpra1 |
A |
T |
7: 46,985,583 (GRCm39) |
I32N |
probably benign |
Het |
Mroh2b |
C |
T |
15: 4,960,510 (GRCm39) |
Q748* |
probably null |
Het |
Mrpl34 |
T |
G |
8: 71,918,024 (GRCm39) |
W66G |
probably damaging |
Het |
Muc21 |
T |
C |
17: 35,931,865 (GRCm39) |
T774A |
unknown |
Het |
Nde1 |
T |
A |
16: 14,001,446 (GRCm39) |
S165T |
|
Het |
Nek10 |
T |
G |
14: 14,937,610 (GRCm38) |
I776M |
probably damaging |
Het |
Nell2 |
A |
G |
15: 95,281,552 (GRCm39) |
S385P |
probably damaging |
Het |
Nsf |
A |
T |
11: 103,821,568 (GRCm39) |
F29Y |
possibly damaging |
Het |
Nsmaf |
A |
T |
4: 6,433,320 (GRCm39) |
Y133* |
probably null |
Het |
Ogfr |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
2: 180,237,059 (GRCm39) |
|
probably benign |
Het |
Or14j8 |
A |
T |
17: 38,263,091 (GRCm39) |
S275T |
possibly damaging |
Het |
Pcdhb8 |
A |
G |
18: 37,489,776 (GRCm39) |
I485V |
probably benign |
Het |
Poteg |
T |
A |
8: 27,938,033 (GRCm39) |
M1K |
probably null |
Het |
Pramel24 |
A |
T |
4: 143,453,303 (GRCm39) |
N137I |
probably benign |
Het |
Prdm5 |
G |
A |
6: 65,860,569 (GRCm39) |
V418I |
possibly damaging |
Het |
Psmc6 |
T |
A |
14: 45,578,320 (GRCm39) |
C228S |
probably damaging |
Het |
Ptgfrn |
C |
T |
3: 100,963,927 (GRCm39) |
A562T |
possibly damaging |
Het |
Ralgapa2 |
G |
T |
2: 146,184,139 (GRCm39) |
Q1576K |
probably benign |
Het |
Ranbp9 |
C |
T |
13: 43,567,506 (GRCm39) |
G400D |
probably damaging |
Het |
Rgs11 |
A |
T |
17: 26,423,484 (GRCm39) |
I134F |
probably damaging |
Het |
Rnf150 |
T |
A |
8: 83,762,715 (GRCm39) |
C317S |
probably damaging |
Het |
Rrm2b |
G |
A |
15: 37,960,858 (GRCm39) |
|
probably benign |
Het |
Scai |
T |
C |
2: 38,996,978 (GRCm39) |
Q272R |
probably benign |
Het |
Sec62 |
C |
T |
3: 30,847,506 (GRCm39) |
R4C |
possibly damaging |
Het |
Sgo2b |
C |
A |
8: 64,393,091 (GRCm39) |
L115F |
probably null |
Het |
Slc44a3 |
G |
A |
3: 121,307,456 (GRCm39) |
P177S |
probably damaging |
Het |
Slc45a4 |
G |
A |
15: 73,457,966 (GRCm39) |
L528F |
probably damaging |
Het |
Slco1a1 |
G |
T |
6: 141,857,624 (GRCm39) |
A569D |
probably damaging |
Het |
Stam2 |
G |
T |
2: 52,604,984 (GRCm39) |
Q184K |
probably damaging |
Het |
Tada2b |
A |
T |
5: 36,641,166 (GRCm39) |
L79Q |
probably damaging |
Het |
Tecpr1 |
T |
C |
5: 144,153,117 (GRCm39) |
E204G |
possibly damaging |
Het |
Tecta |
A |
T |
9: 42,284,597 (GRCm39) |
D829E |
probably benign |
Het |
Tepsin |
A |
G |
11: 119,982,654 (GRCm39) |
V472A |
probably benign |
Het |
Tnfrsf1a |
G |
A |
6: 125,334,688 (GRCm39) |
M109I |
possibly damaging |
Het |
Trim42 |
A |
T |
9: 97,245,275 (GRCm39) |
Y508* |
probably null |
Het |
Trmo |
T |
G |
4: 46,387,625 (GRCm39) |
N65T |
probably benign |
Het |
Tspear |
G |
T |
10: 77,665,471 (GRCm39) |
E86* |
probably null |
Het |
Ubr1 |
A |
T |
2: 120,734,523 (GRCm39) |
S1126T |
probably damaging |
Het |
Usp50 |
C |
A |
2: 126,622,477 (GRCm39) |
D28Y |
probably damaging |
Het |
Utp6 |
T |
A |
11: 79,842,455 (GRCm39) |
I225F |
probably benign |
Het |
Utrn |
T |
C |
10: 12,543,351 (GRCm39) |
T1766A |
probably benign |
Het |
Vcl |
T |
A |
14: 21,045,160 (GRCm39) |
N288K |
probably benign |
Het |
Vmn2r69 |
T |
C |
7: 85,061,663 (GRCm39) |
N104D |
probably benign |
Het |
Zc3h7b |
G |
A |
15: 81,656,681 (GRCm39) |
R166Q |
probably benign |
Het |
Zfhx4 |
T |
A |
3: 5,455,484 (GRCm39) |
S1159R |
probably benign |
Het |
|
Other mutations in Frmd4b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00849:Frmd4b
|
APN |
6 |
97,285,021 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01478:Frmd4b
|
APN |
6 |
97,305,254 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01760:Frmd4b
|
APN |
6 |
97,285,663 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01777:Frmd4b
|
APN |
6 |
97,272,905 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01960:Frmd4b
|
APN |
6 |
97,272,741 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02408:Frmd4b
|
APN |
6 |
97,272,770 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02429:Frmd4b
|
APN |
6 |
97,302,390 (GRCm39) |
splice site |
probably benign |
|
IGL02525:Frmd4b
|
APN |
6 |
97,389,494 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02618:Frmd4b
|
APN |
6 |
97,285,066 (GRCm39) |
nonsense |
probably null |
|
IGL03051:Frmd4b
|
APN |
6 |
97,272,943 (GRCm39) |
nonsense |
probably null |
|
IGL03120:Frmd4b
|
APN |
6 |
97,373,206 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03218:Frmd4b
|
APN |
6 |
97,285,075 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03260:Frmd4b
|
APN |
6 |
97,373,185 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02984:Frmd4b
|
UTSW |
6 |
97,273,221 (GRCm39) |
missense |
probably damaging |
0.96 |
P0031:Frmd4b
|
UTSW |
6 |
97,330,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Frmd4b
|
UTSW |
6 |
97,300,610 (GRCm39) |
splice site |
probably benign |
|
R0055:Frmd4b
|
UTSW |
6 |
97,300,610 (GRCm39) |
splice site |
probably benign |
|
R0058:Frmd4b
|
UTSW |
6 |
97,400,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R0255:Frmd4b
|
UTSW |
6 |
97,285,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R0437:Frmd4b
|
UTSW |
6 |
97,400,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R0594:Frmd4b
|
UTSW |
6 |
97,302,387 (GRCm39) |
splice site |
probably benign |
|
R1525:Frmd4b
|
UTSW |
6 |
97,273,347 (GRCm39) |
missense |
probably damaging |
0.97 |
R1640:Frmd4b
|
UTSW |
6 |
97,285,634 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1768:Frmd4b
|
UTSW |
6 |
97,283,725 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1923:Frmd4b
|
UTSW |
6 |
97,265,415 (GRCm39) |
missense |
probably benign |
0.33 |
R2056:Frmd4b
|
UTSW |
6 |
97,389,448 (GRCm39) |
critical splice donor site |
probably null |
|
R2192:Frmd4b
|
UTSW |
6 |
97,464,577 (GRCm39) |
missense |
probably damaging |
0.98 |
R3809:Frmd4b
|
UTSW |
6 |
97,300,690 (GRCm39) |
missense |
possibly damaging |
0.49 |
R3831:Frmd4b
|
UTSW |
6 |
97,389,486 (GRCm39) |
nonsense |
probably null |
|
R4466:Frmd4b
|
UTSW |
6 |
97,300,614 (GRCm39) |
critical splice donor site |
probably null |
|
R4536:Frmd4b
|
UTSW |
6 |
97,287,693 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4652:Frmd4b
|
UTSW |
6 |
97,272,716 (GRCm39) |
missense |
probably benign |
0.38 |
R4679:Frmd4b
|
UTSW |
6 |
97,272,627 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4735:Frmd4b
|
UTSW |
6 |
97,436,220 (GRCm39) |
start gained |
probably benign |
|
R4793:Frmd4b
|
UTSW |
6 |
97,272,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4940:Frmd4b
|
UTSW |
6 |
97,275,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R4948:Frmd4b
|
UTSW |
6 |
97,283,691 (GRCm39) |
missense |
probably benign |
0.06 |
R5092:Frmd4b
|
UTSW |
6 |
97,272,941 (GRCm39) |
missense |
probably damaging |
0.98 |
R5119:Frmd4b
|
UTSW |
6 |
97,277,275 (GRCm39) |
missense |
probably benign |
0.03 |
R5289:Frmd4b
|
UTSW |
6 |
97,279,309 (GRCm39) |
splice site |
probably null |
|
R5610:Frmd4b
|
UTSW |
6 |
97,283,752 (GRCm39) |
missense |
probably benign |
|
R5690:Frmd4b
|
UTSW |
6 |
97,330,164 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6248:Frmd4b
|
UTSW |
6 |
97,436,173 (GRCm39) |
missense |
probably benign |
0.10 |
R6437:Frmd4b
|
UTSW |
6 |
97,273,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R6459:Frmd4b
|
UTSW |
6 |
97,464,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R6825:Frmd4b
|
UTSW |
6 |
97,302,437 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6964:Frmd4b
|
UTSW |
6 |
97,282,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R7110:Frmd4b
|
UTSW |
6 |
97,273,192 (GRCm39) |
nonsense |
probably null |
|
R7154:Frmd4b
|
UTSW |
6 |
97,283,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R7764:Frmd4b
|
UTSW |
6 |
97,272,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R8073:Frmd4b
|
UTSW |
6 |
97,283,674 (GRCm39) |
missense |
probably benign |
0.03 |
R8382:Frmd4b
|
UTSW |
6 |
97,282,209 (GRCm39) |
missense |
probably benign |
|
R8746:Frmd4b
|
UTSW |
6 |
97,269,370 (GRCm39) |
missense |
probably benign |
|
R8881:Frmd4b
|
UTSW |
6 |
97,272,735 (GRCm39) |
missense |
probably benign |
0.00 |
R8885:Frmd4b
|
UTSW |
6 |
97,389,480 (GRCm39) |
missense |
probably benign |
0.01 |
R8907:Frmd4b
|
UTSW |
6 |
97,273,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R8975:Frmd4b
|
UTSW |
6 |
97,283,477 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9032:Frmd4b
|
UTSW |
6 |
97,269,334 (GRCm39) |
missense |
probably benign |
0.00 |
R9085:Frmd4b
|
UTSW |
6 |
97,269,334 (GRCm39) |
missense |
probably benign |
0.00 |
R9094:Frmd4b
|
UTSW |
6 |
97,398,559 (GRCm39) |
missense |
|
|
R9429:Frmd4b
|
UTSW |
6 |
97,279,252 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Frmd4b
|
UTSW |
6 |
97,282,326 (GRCm39) |
nonsense |
probably null |
|
|