Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A1cf |
A |
T |
19: 31,904,526 (GRCm39) |
K263M |
probably damaging |
Het |
Adam26a |
G |
A |
8: 44,023,073 (GRCm39) |
T139M |
possibly damaging |
Het |
Agrp |
G |
T |
8: 106,293,467 (GRCm39) |
T106K |
probably damaging |
Het |
Akap9 |
C |
T |
5: 4,007,645 (GRCm39) |
Q238* |
probably null |
Het |
Ankrd6 |
A |
T |
4: 32,828,774 (GRCm39) |
V85E |
probably damaging |
Het |
Ap2b1 |
C |
A |
11: 83,215,430 (GRCm39) |
P125T |
probably damaging |
Het |
Arhgef7 |
C |
A |
8: 11,858,713 (GRCm39) |
|
probably null |
Het |
Cblc |
A |
T |
7: 19,524,399 (GRCm39) |
D280E |
probably benign |
Het |
Cdk11b |
T |
C |
4: 155,732,854 (GRCm39) |
|
probably benign |
Het |
Cela2a |
G |
T |
4: 141,545,257 (GRCm39) |
F239L |
probably damaging |
Het |
Cfap57 |
A |
T |
4: 118,463,828 (GRCm39) |
C342S |
probably benign |
Het |
Clca4a |
C |
A |
3: 144,669,516 (GRCm39) |
W345L |
probably damaging |
Het |
Col6a5 |
T |
C |
9: 105,808,492 (GRCm39) |
D852G |
unknown |
Het |
Cyp4a32 |
T |
C |
4: 115,468,505 (GRCm39) |
V329A |
possibly damaging |
Het |
Dcaf8 |
C |
T |
1: 172,003,062 (GRCm39) |
P287S |
probably damaging |
Het |
Dmxl1 |
T |
A |
18: 50,067,704 (GRCm39) |
D2654E |
probably damaging |
Het |
Dpep1 |
A |
T |
8: 123,927,486 (GRCm39) |
I347F |
possibly damaging |
Het |
Dtnb |
T |
A |
12: 3,693,936 (GRCm39) |
Y56* |
probably null |
Het |
Duox1 |
T |
C |
2: 122,169,125 (GRCm39) |
Y1182H |
possibly damaging |
Het |
Dusp10 |
T |
A |
1: 183,769,422 (GRCm39) |
S129R |
probably benign |
Het |
Dync2i1 |
T |
C |
12: 116,219,532 (GRCm39) |
I137V |
probably benign |
Het |
Epcam |
G |
A |
17: 87,949,556 (GRCm39) |
R173Q |
probably damaging |
Het |
Ephb3 |
A |
G |
16: 21,039,400 (GRCm39) |
E384G |
probably damaging |
Het |
Exosc10 |
A |
T |
4: 148,652,960 (GRCm39) |
D525V |
probably damaging |
Het |
Fam186a |
T |
A |
15: 99,840,227 (GRCm39) |
T2006S |
possibly damaging |
Het |
Fbxw21 |
T |
A |
9: 108,977,242 (GRCm39) |
T156S |
possibly damaging |
Het |
Fcrl5 |
A |
G |
3: 87,364,704 (GRCm39) |
E568G |
probably damaging |
Het |
Fmn2 |
C |
T |
1: 174,436,024 (GRCm39) |
|
probably benign |
Het |
Garre1 |
A |
T |
7: 33,947,631 (GRCm39) |
M459K |
probably damaging |
Het |
Gas2l1 |
G |
A |
11: 5,014,266 (GRCm39) |
H65Y |
probably damaging |
Het |
Gjd2 |
A |
T |
2: 113,843,614 (GRCm39) |
M1K |
probably null |
Het |
Hdgfl3 |
T |
C |
7: 81,549,432 (GRCm39) |
Y149C |
probably damaging |
Het |
Hmcn2 |
T |
C |
2: 31,244,733 (GRCm39) |
V730A |
probably damaging |
Het |
Inpp4a |
A |
T |
1: 37,437,880 (GRCm39) |
S223C |
probably damaging |
Het |
Ip6k1 |
G |
A |
9: 107,918,195 (GRCm39) |
E77K |
possibly damaging |
Het |
Knl1 |
T |
A |
2: 118,902,219 (GRCm39) |
W1307R |
probably benign |
Het |
Kpna3 |
A |
G |
14: 61,624,926 (GRCm39) |
L139P |
probably damaging |
Het |
Lama3 |
T |
C |
18: 12,612,929 (GRCm39) |
|
probably null |
Het |
Lin54 |
G |
A |
5: 100,633,108 (GRCm39) |
P192L |
possibly damaging |
Het |
Lpo |
T |
A |
11: 87,700,018 (GRCm39) |
|
probably null |
Het |
Lrrc37 |
T |
A |
11: 103,507,897 (GRCm39) |
|
probably benign |
Het |
Lrrd1 |
T |
G |
5: 3,900,483 (GRCm39) |
|
probably null |
Het |
Nbas |
T |
A |
12: 13,610,978 (GRCm39) |
|
probably null |
Het |
Nemp1 |
G |
A |
10: 127,532,117 (GRCm39) |
G341D |
probably damaging |
Het |
Nrp1 |
T |
C |
8: 129,152,366 (GRCm39) |
F192L |
probably damaging |
Het |
Nufip2 |
T |
A |
11: 77,583,916 (GRCm39) |
V610E |
probably damaging |
Het |
Nup160 |
T |
G |
2: 90,530,780 (GRCm39) |
Y479* |
probably null |
Het |
Oas1d |
A |
T |
5: 121,058,025 (GRCm39) |
D323V |
possibly damaging |
Het |
Or10ak14 |
A |
G |
4: 118,610,797 (GRCm39) |
W315R |
possibly damaging |
Het |
Or14j1 |
A |
G |
17: 38,146,244 (GRCm39) |
D118G |
possibly damaging |
Het |
Or4c3d |
T |
C |
2: 89,882,128 (GRCm39) |
Y180C |
probably damaging |
Het |
Or52e4 |
C |
A |
7: 104,706,001 (GRCm39) |
H183N |
probably damaging |
Het |
Or5ac22 |
T |
A |
16: 59,135,069 (GRCm39) |
R234* |
probably null |
Het |
Or8b3 |
G |
A |
9: 38,314,550 (GRCm39) |
V127M |
possibly damaging |
Het |
Or8c9 |
A |
T |
9: 38,241,803 (GRCm39) |
T307S |
probably benign |
Het |
Pcm1 |
T |
A |
8: 41,766,396 (GRCm39) |
M1567K |
possibly damaging |
Het |
Pdxk |
A |
G |
10: 78,279,730 (GRCm39) |
V215A |
probably benign |
Het |
Phf12 |
T |
A |
11: 77,914,427 (GRCm39) |
L74Q |
probably damaging |
Het |
Plcg1 |
A |
G |
2: 160,595,663 (GRCm39) |
E537G |
probably null |
Het |
Plxna2 |
C |
T |
1: 194,326,678 (GRCm39) |
P204L |
possibly damaging |
Het |
Ppp3cb |
T |
G |
14: 20,574,131 (GRCm39) |
M236L |
probably benign |
Het |
Qrsl1 |
A |
T |
10: 43,772,026 (GRCm39) |
S55T |
probably damaging |
Het |
Rbm5 |
T |
C |
9: 107,621,112 (GRCm39) |
|
probably null |
Het |
Sipa1l2 |
A |
G |
8: 126,171,274 (GRCm39) |
S1403P |
probably damaging |
Het |
Sis |
C |
T |
3: 72,872,937 (GRCm39) |
C67Y |
probably damaging |
Het |
Specc1 |
A |
G |
11: 62,019,218 (GRCm39) |
I686V |
possibly damaging |
Het |
Speg |
G |
A |
1: 75,394,507 (GRCm39) |
E1739K |
probably benign |
Het |
Sprtn |
C |
A |
8: 125,628,372 (GRCm39) |
H154Q |
probably damaging |
Het |
St7l |
A |
G |
3: 104,778,303 (GRCm39) |
T147A |
probably benign |
Het |
Stab1 |
G |
A |
14: 30,867,985 (GRCm39) |
Q1630* |
probably null |
Het |
Stpg2 |
A |
G |
3: 138,937,960 (GRCm39) |
D173G |
probably benign |
Het |
Tcf20 |
G |
A |
15: 82,736,978 (GRCm39) |
T1491I |
probably benign |
Het |
Themis2 |
A |
T |
4: 132,516,960 (GRCm39) |
I180N |
possibly damaging |
Het |
Timd5 |
T |
C |
11: 46,417,121 (GRCm39) |
L13P |
probably damaging |
Het |
Tktl2 |
G |
A |
8: 66,964,999 (GRCm39) |
V186M |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,638,340 (GRCm39) |
V13980A |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,575,978 (GRCm39) |
V24972M |
probably damaging |
Het |
Usp5 |
A |
T |
6: 124,800,423 (GRCm39) |
M286K |
possibly damaging |
Het |
Vmn2r22 |
G |
A |
6: 123,614,802 (GRCm39) |
R263C |
possibly damaging |
Het |
Vmn2r71 |
T |
G |
7: 85,270,435 (GRCm39) |
C534G |
probably damaging |
Het |
Wnk2 |
C |
T |
13: 49,214,202 (GRCm39) |
S1460N |
possibly damaging |
Het |
Zfp445 |
G |
A |
9: 122,681,707 (GRCm39) |
P745S |
probably damaging |
Het |
Zfp957 |
C |
T |
14: 79,451,436 (GRCm39) |
G121D |
probably damaging |
Het |
Zscan4f |
A |
G |
7: 11,135,254 (GRCm39) |
E220G |
possibly damaging |
Het |
|
Other mutations in Fut9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00919:Fut9
|
APN |
4 |
25,620,316 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01134:Fut9
|
APN |
4 |
25,620,446 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01330:Fut9
|
APN |
4 |
25,619,791 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01732:Fut9
|
APN |
4 |
25,619,867 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02824:Fut9
|
APN |
4 |
25,620,037 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU74:Fut9
|
UTSW |
4 |
25,620,802 (GRCm39) |
missense |
probably benign |
0.25 |
R0280:Fut9
|
UTSW |
4 |
25,619,852 (GRCm39) |
missense |
probably benign |
0.00 |
R0408:Fut9
|
UTSW |
4 |
25,620,319 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0594:Fut9
|
UTSW |
4 |
25,620,526 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0609:Fut9
|
UTSW |
4 |
25,620,811 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
R0709:Fut9
|
UTSW |
4 |
25,620,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R1567:Fut9
|
UTSW |
4 |
25,620,344 (GRCm39) |
missense |
probably damaging |
0.99 |
R1856:Fut9
|
UTSW |
4 |
25,620,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R2036:Fut9
|
UTSW |
4 |
25,620,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R2165:Fut9
|
UTSW |
4 |
25,619,734 (GRCm39) |
makesense |
probably null |
|
R2165:Fut9
|
UTSW |
4 |
25,619,733 (GRCm39) |
makesense |
probably null |
|
R2332:Fut9
|
UTSW |
4 |
25,619,823 (GRCm39) |
nonsense |
probably null |
|
R4539:Fut9
|
UTSW |
4 |
25,619,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R4722:Fut9
|
UTSW |
4 |
25,799,734 (GRCm39) |
utr 5 prime |
probably benign |
|
R4766:Fut9
|
UTSW |
4 |
25,799,191 (GRCm39) |
intron |
probably benign |
|
R4937:Fut9
|
UTSW |
4 |
25,799,591 (GRCm39) |
splice site |
probably benign |
|
R5025:Fut9
|
UTSW |
4 |
25,620,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Fut9
|
UTSW |
4 |
25,799,245 (GRCm39) |
intron |
probably benign |
|
R5158:Fut9
|
UTSW |
4 |
25,620,731 (GRCm39) |
missense |
probably benign |
0.01 |
R5601:Fut9
|
UTSW |
4 |
25,620,299 (GRCm39) |
missense |
probably benign |
0.00 |
R5974:Fut9
|
UTSW |
4 |
25,620,090 (GRCm39) |
nonsense |
probably null |
|
R6315:Fut9
|
UTSW |
4 |
25,619,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R6385:Fut9
|
UTSW |
4 |
25,620,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R6652:Fut9
|
UTSW |
4 |
25,620,619 (GRCm39) |
missense |
probably benign |
0.44 |
R6809:Fut9
|
UTSW |
4 |
25,620,647 (GRCm39) |
missense |
probably benign |
|
R6825:Fut9
|
UTSW |
4 |
25,619,925 (GRCm39) |
missense |
probably benign |
|
R7145:Fut9
|
UTSW |
4 |
25,620,507 (GRCm39) |
missense |
probably damaging |
0.96 |
R7573:Fut9
|
UTSW |
4 |
25,620,691 (GRCm39) |
missense |
probably benign |
0.04 |
R8933:Fut9
|
UTSW |
4 |
25,619,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R9715:Fut9
|
UTSW |
4 |
25,620,679 (GRCm39) |
missense |
probably benign |
0.00 |
X0057:Fut9
|
UTSW |
4 |
25,799,686 (GRCm39) |
start gained |
probably benign |
|
|