Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
T |
C |
11: 109,982,425 (GRCm39) |
I6V |
probably null |
Het |
Aox1 |
A |
G |
1: 58,107,529 (GRCm39) |
D601G |
probably damaging |
Het |
Asic1 |
GCACC |
GCACCACC |
15: 99,596,684 (GRCm39) |
|
probably benign |
Het |
Cacna1g |
T |
G |
11: 94,333,674 (GRCm39) |
N931T |
probably damaging |
Het |
Ccdc14 |
T |
C |
16: 34,541,955 (GRCm39) |
F511L |
probably damaging |
Het |
Cd177 |
T |
A |
7: 24,444,348 (GRCm39) |
E710V |
probably benign |
Het |
Cep112 |
T |
C |
11: 108,643,386 (GRCm39) |
C49R |
probably benign |
Het |
Clip2 |
G |
A |
5: 134,551,645 (GRCm39) |
T159M |
possibly damaging |
Het |
Dnah2 |
T |
C |
11: 69,326,710 (GRCm39) |
N3575S |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,044,410 (GRCm39) |
I3234F |
probably damaging |
Het |
Eci3 |
G |
T |
13: 35,130,961 (GRCm39) |
A302E |
possibly damaging |
Het |
Fam204a |
T |
C |
19: 60,188,421 (GRCm39) |
K214E |
probably damaging |
Het |
Fam78a |
T |
C |
2: 31,972,666 (GRCm39) |
T85A |
possibly damaging |
Het |
Flnb |
T |
C |
14: 7,909,748 (GRCm38) |
Y1401H |
probably damaging |
Het |
Foxl2 |
A |
T |
9: 98,838,108 (GRCm39) |
D132V |
probably damaging |
Het |
Gm26558 |
G |
T |
2: 70,491,761 (GRCm39) |
|
probably benign |
Het |
Gpr139 |
A |
G |
7: 118,744,063 (GRCm39) |
V174A |
probably benign |
Het |
Grik5 |
T |
C |
7: 24,715,244 (GRCm39) |
T676A |
probably damaging |
Het |
H60c |
T |
C |
10: 3,209,273 (GRCm39) |
|
probably null |
Het |
Hspa1l |
A |
G |
17: 35,197,445 (GRCm39) |
K495E |
probably damaging |
Het |
Irgm1 |
C |
T |
11: 48,757,044 (GRCm39) |
V256I |
probably benign |
Het |
Kat7 |
T |
A |
11: 95,177,242 (GRCm39) |
T293S |
probably benign |
Het |
Lipg |
C |
T |
18: 75,094,009 (GRCm39) |
V13I |
probably benign |
Het |
Lrrn1 |
A |
T |
6: 107,546,185 (GRCm39) |
Y661F |
probably damaging |
Het |
Mllt3 |
A |
G |
4: 87,759,232 (GRCm39) |
V272A |
probably benign |
Het |
Mx1 |
G |
A |
16: 97,256,694 (GRCm39) |
R162C |
probably benign |
Het |
Myo18b |
T |
A |
5: 113,019,336 (GRCm39) |
D647V |
probably damaging |
Het |
Naf1 |
G |
A |
8: 67,332,298 (GRCm39) |
V329I |
probably benign |
Het |
Or4k40 |
A |
T |
2: 111,251,119 (GRCm39) |
M59K |
probably damaging |
Het |
Or52u1 |
A |
T |
7: 104,237,418 (GRCm39) |
I153F |
probably damaging |
Het |
Or8g22 |
A |
T |
9: 38,958,265 (GRCm39) |
C194* |
probably null |
Het |
P2rx5 |
G |
A |
11: 73,062,616 (GRCm39) |
V442M |
possibly damaging |
Het |
Pcdhb9 |
A |
G |
18: 37,534,285 (GRCm39) |
E93G |
probably damaging |
Het |
Pcdhga4 |
A |
T |
18: 37,820,479 (GRCm39) |
N676I |
probably benign |
Het |
Pgm5 |
A |
G |
19: 24,797,492 (GRCm39) |
M230T |
probably damaging |
Het |
Pik3c2g |
T |
C |
6: 139,599,016 (GRCm39) |
V44A |
probably damaging |
Het |
Pp2d1 |
T |
C |
17: 53,815,168 (GRCm39) |
M519V |
probably benign |
Het |
Ppp1r10 |
A |
G |
17: 36,239,403 (GRCm39) |
E404G |
probably damaging |
Het |
Prpf8 |
A |
T |
11: 75,380,609 (GRCm39) |
E104V |
possibly damaging |
Het |
Ptpra |
T |
C |
2: 30,328,367 (GRCm39) |
|
probably null |
Het |
Pygl |
A |
C |
12: 70,248,118 (GRCm39) |
N248K |
probably damaging |
Het |
Rbm8a |
A |
G |
3: 96,538,248 (GRCm39) |
D102G |
probably damaging |
Het |
Sema3d |
A |
G |
5: 12,634,875 (GRCm39) |
D647G |
probably benign |
Het |
Serpinb11 |
A |
T |
1: 107,307,484 (GRCm39) |
D305V |
probably damaging |
Het |
Slc12a8 |
T |
C |
16: 33,437,578 (GRCm39) |
I337T |
probably damaging |
Het |
Slc29a2 |
G |
A |
19: 5,078,995 (GRCm39) |
R286Q |
probably benign |
Het |
Slc2a3 |
T |
A |
6: 122,712,542 (GRCm39) |
D234V |
probably damaging |
Het |
Slco4a1 |
T |
C |
2: 180,114,901 (GRCm39) |
V608A |
probably damaging |
Het |
Spata31d1e |
A |
T |
13: 59,891,553 (GRCm39) |
L89H |
probably damaging |
Het |
Srrm2 |
C |
T |
17: 24,035,561 (GRCm39) |
T831I |
probably benign |
Het |
St18 |
T |
A |
1: 6,872,541 (GRCm39) |
|
probably null |
Het |
Tesk2 |
G |
C |
4: 116,599,093 (GRCm39) |
G67A |
probably damaging |
Het |
Tlr1 |
A |
T |
5: 65,082,564 (GRCm39) |
L671H |
probably damaging |
Het |
Tmem63b |
A |
T |
17: 45,972,403 (GRCm39) |
Y735N |
possibly damaging |
Het |
Tmprss11a |
C |
T |
5: 86,567,938 (GRCm39) |
C263Y |
probably damaging |
Het |
Trio |
A |
T |
15: 27,898,077 (GRCm39) |
V345E |
probably damaging |
Het |
Tut7 |
A |
G |
13: 59,964,470 (GRCm39) |
|
probably null |
Het |
Ubr5 |
A |
G |
15: 37,998,160 (GRCm39) |
S1674P |
probably damaging |
Het |
Uchl3 |
T |
A |
14: 101,933,353 (GRCm39) |
C209S |
probably damaging |
Het |
Uhmk1 |
T |
C |
1: 170,038,736 (GRCm39) |
N206S |
probably damaging |
Het |
Uhrf1 |
C |
T |
17: 56,625,340 (GRCm39) |
R588W |
probably damaging |
Het |
Usp28 |
T |
C |
9: 48,921,550 (GRCm39) |
V256A |
probably damaging |
Het |
Utrn |
C |
A |
10: 12,604,521 (GRCm39) |
L552F |
probably damaging |
Het |
Vmn1r55 |
A |
T |
7: 5,149,985 (GRCm39) |
M146K |
probably damaging |
Het |
Vmn1r57 |
A |
C |
7: 5,224,107 (GRCm39) |
I211L |
probably benign |
Het |
Zar1 |
C |
T |
5: 72,734,742 (GRCm39) |
C316Y |
probably damaging |
Het |
Zc3h11a |
A |
T |
1: 133,549,412 (GRCm39) |
S750T |
probably damaging |
Het |
Zfp366 |
G |
A |
13: 99,382,676 (GRCm39) |
C613Y |
probably benign |
Het |
Zfp37 |
A |
T |
4: 62,109,493 (GRCm39) |
C524S |
probably damaging |
Het |
Zfp516 |
T |
C |
18: 82,975,218 (GRCm39) |
V472A |
probably benign |
Het |
Zhx1 |
A |
T |
15: 57,915,819 (GRCm39) |
M809K |
probably damaging |
Het |
Zic1 |
T |
C |
9: 91,246,424 (GRCm39) |
Y216C |
probably damaging |
Het |
|
Other mutations in Frs2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00807:Frs2
|
APN |
10 |
116,910,791 (GRCm39) |
splice site |
probably benign |
|
IGL02300:Frs2
|
APN |
10 |
116,913,496 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL03028:Frs2
|
APN |
10 |
116,909,838 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0001:Frs2
|
UTSW |
10 |
116,910,781 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0513:Frs2
|
UTSW |
10 |
116,910,570 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0708:Frs2
|
UTSW |
10 |
116,909,997 (GRCm39) |
missense |
probably damaging |
0.99 |
R0735:Frs2
|
UTSW |
10 |
116,910,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R1296:Frs2
|
UTSW |
10 |
116,916,979 (GRCm39) |
missense |
probably benign |
0.30 |
R1934:Frs2
|
UTSW |
10 |
116,914,806 (GRCm39) |
missense |
probably damaging |
0.99 |
R1938:Frs2
|
UTSW |
10 |
116,917,011 (GRCm39) |
start gained |
probably benign |
|
R1992:Frs2
|
UTSW |
10 |
116,910,459 (GRCm39) |
missense |
probably benign |
|
R2095:Frs2
|
UTSW |
10 |
116,910,507 (GRCm39) |
missense |
probably benign |
0.00 |
R3878:Frs2
|
UTSW |
10 |
116,914,815 (GRCm39) |
missense |
probably benign |
0.01 |
R4732:Frs2
|
UTSW |
10 |
116,909,998 (GRCm39) |
missense |
probably benign |
0.31 |
R4733:Frs2
|
UTSW |
10 |
116,909,998 (GRCm39) |
missense |
probably benign |
0.31 |
R5326:Frs2
|
UTSW |
10 |
116,913,468 (GRCm39) |
missense |
probably benign |
0.00 |
R5894:Frs2
|
UTSW |
10 |
116,917,011 (GRCm39) |
start gained |
probably benign |
|
R6084:Frs2
|
UTSW |
10 |
116,912,714 (GRCm39) |
critical splice donor site |
probably null |
|
R7468:Frs2
|
UTSW |
10 |
116,910,007 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7603:Frs2
|
UTSW |
10 |
116,909,968 (GRCm39) |
missense |
probably benign |
0.03 |
R8179:Frs2
|
UTSW |
10 |
116,912,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R8190:Frs2
|
UTSW |
10 |
116,910,784 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8721:Frs2
|
UTSW |
10 |
116,909,935 (GRCm39) |
missense |
probably benign |
0.00 |
R9104:Frs2
|
UTSW |
10 |
116,910,070 (GRCm39) |
missense |
probably benign |
0.19 |
Z1177:Frs2
|
UTSW |
10 |
116,910,284 (GRCm39) |
missense |
probably damaging |
1.00 |
|