Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
C |
T |
5: 113,097,636 (GRCm38) |
V1584I |
probably benign |
Het |
Adamts12 |
A |
G |
15: 11,285,901 (GRCm38) |
D732G |
probably benign |
Het |
Agpat4 |
A |
G |
17: 12,151,750 (GRCm38) |
|
probably benign |
Het |
AI182371 |
T |
C |
2: 35,095,817 (GRCm38) |
D140G |
possibly damaging |
Het |
Apol11b |
T |
A |
15: 77,634,933 (GRCm38) |
T316S |
probably benign |
Het |
Arsi |
G |
A |
18: 60,916,651 (GRCm38) |
G202E |
probably benign |
Het |
Bard1 |
T |
C |
1: 71,075,174 (GRCm38) |
E216G |
probably benign |
Het |
Bdp1 |
C |
A |
13: 100,049,868 (GRCm38) |
R1692L |
probably damaging |
Het |
Capn10 |
T |
C |
1: 92,943,419 (GRCm38) |
I101T |
probably damaging |
Het |
Ccdc175 |
C |
T |
12: 72,112,205 (GRCm38) |
M653I |
probably benign |
Het |
Ccdc9b |
C |
A |
2: 118,759,577 (GRCm38) |
R262L |
probably damaging |
Het |
Ccr8 |
G |
A |
9: 120,094,464 (GRCm38) |
C215Y |
probably damaging |
Het |
Cct3 |
T |
A |
3: 88,311,785 (GRCm38) |
L241* |
probably null |
Het |
Cd2ap |
A |
T |
17: 42,852,459 (GRCm38) |
I25N |
probably damaging |
Het |
Cdh19 |
T |
C |
1: 110,893,260 (GRCm38) |
K583E |
probably benign |
Het |
Cela3a |
A |
G |
4: 137,402,675 (GRCm38) |
S212P |
unknown |
Het |
Cfap44 |
T |
A |
16: 44,415,883 (GRCm38) |
|
probably null |
Het |
Clca3a1 |
A |
T |
3: 144,749,712 (GRCm38) |
L440Q |
probably damaging |
Het |
Crybg2 |
A |
G |
4: 134,089,352 (GRCm38) |
Y1676C |
probably damaging |
Het |
Dscam |
T |
C |
16: 96,643,988 (GRCm38) |
D1501G |
probably benign |
Het |
Eml6 |
C |
A |
11: 29,805,757 (GRCm38) |
L832F |
probably benign |
Het |
Enpp3 |
A |
G |
10: 24,773,927 (GRCm38) |
L867P |
probably damaging |
Het |
Erbb3 |
A |
G |
10: 128,586,238 (GRCm38) |
Y46H |
possibly damaging |
Het |
Fads3 |
T |
C |
19: 10,056,020 (GRCm38) |
I342T |
possibly damaging |
Het |
Flvcr1 |
A |
T |
1: 191,021,106 (GRCm38) |
S290T |
probably benign |
Het |
Gad2 |
C |
T |
2: 22,622,667 (GRCm38) |
A2V |
probably damaging |
Het |
Gkn3 |
C |
T |
6: 87,383,525 (GRCm38) |
A163T |
probably damaging |
Het |
Gm10715 |
T |
G |
9: 3,038,073 (GRCm38) |
|
probably benign |
Het |
Herc1 |
T |
G |
9: 66,441,929 (GRCm38) |
D2023E |
probably benign |
Het |
Hsd3b3 |
A |
G |
3: 98,742,485 (GRCm38) |
L174P |
probably damaging |
Het |
Impg2 |
TACCACCACCACCACCACCACCACCA |
TACCACCACCACCACCACCACCA |
16: 56,257,939 (GRCm38) |
|
probably benign |
Het |
Iqcf3 |
A |
G |
9: 106,560,949 (GRCm38) |
|
probably null |
Het |
Kcna4 |
G |
A |
2: 107,296,543 (GRCm38) |
V541M |
probably damaging |
Het |
Kcnj11 |
T |
C |
7: 46,099,816 (GRCm38) |
T28A |
probably benign |
Het |
Kcnmb2 |
T |
A |
3: 32,181,867 (GRCm38) |
N88K |
probably damaging |
Het |
Kdm2a |
TTCCTCCTCCTCCTCCTCTTCCTCCTCCTC |
TTCCTCCTCCTCCTCTTCCTCCTCCTC |
19: 4,324,507 (GRCm38) |
|
probably benign |
Het |
Krt2 |
T |
C |
15: 101,813,960 (GRCm38) |
E430G |
probably damaging |
Het |
Lins1 |
C |
T |
7: 66,710,641 (GRCm38) |
L384F |
possibly damaging |
Het |
Man1c1 |
G |
C |
4: 134,703,438 (GRCm38) |
P11R |
probably damaging |
Het |
Mfge8 |
T |
C |
7: 79,134,525 (GRCm38) |
N389D |
probably damaging |
Het |
Mug1 |
C |
T |
6: 121,884,254 (GRCm38) |
T1278I |
probably benign |
Het |
Myh9 |
T |
C |
15: 77,807,877 (GRCm38) |
M161V |
probably damaging |
Het |
Myl7 |
T |
A |
11: 5,898,171 (GRCm38) |
Y61F |
probably benign |
Het |
Nlrp4d |
A |
T |
7: 10,362,779 (GRCm38) |
|
unknown |
Het |
Nol3 |
A |
G |
8: 105,281,933 (GRCm38) |
|
probably null |
Het |
Nup85 |
T |
A |
11: 115,577,925 (GRCm38) |
|
probably null |
Het |
Obscn |
T |
A |
11: 59,012,742 (GRCm38) |
T7619S |
probably damaging |
Het |
Or2t49 |
T |
A |
11: 58,501,668 (GRCm38) |
N296I |
probably damaging |
Het |
Or4k48 |
T |
C |
2: 111,645,881 (GRCm38) |
M39V |
probably benign |
Het |
Or52a24 |
C |
T |
7: 103,732,250 (GRCm38) |
T108I |
possibly damaging |
Het |
Or7g26 |
G |
A |
9: 19,318,845 (GRCm38) |
V104I |
probably benign |
Het |
Pax5 |
T |
A |
4: 44,679,494 (GRCm38) |
I184F |
probably damaging |
Het |
Pcdha7 |
T |
A |
18: 36,974,507 (GRCm38) |
V195D |
probably damaging |
Het |
Phf3 |
A |
T |
1: 30,813,939 (GRCm38) |
|
probably benign |
Het |
Pla2g15 |
G |
T |
8: 106,163,071 (GRCm38) |
G325V |
probably damaging |
Het |
Ppp1r21 |
T |
C |
17: 88,572,615 (GRCm38) |
F487L |
probably benign |
Het |
Ppp1r9a |
A |
G |
6: 5,157,016 (GRCm38) |
I965V |
probably benign |
Het |
Ptpru |
A |
G |
4: 131,820,964 (GRCm38) |
V74A |
probably damaging |
Het |
Rif1 |
T |
A |
2: 52,098,934 (GRCm38) |
Y780N |
probably damaging |
Het |
Rps25 |
T |
A |
9: 44,408,749 (GRCm38) |
Y23N |
possibly damaging |
Het |
Ryr1 |
T |
C |
7: 29,085,833 (GRCm38) |
D1811G |
probably damaging |
Het |
Scamp5 |
T |
G |
9: 57,452,036 (GRCm38) |
|
probably null |
Het |
Senp1 |
T |
C |
15: 98,045,896 (GRCm38) |
D602G |
probably damaging |
Het |
Sh2b2 |
T |
G |
5: 136,231,957 (GRCm38) |
D135A |
probably damaging |
Het |
Slc26a8 |
G |
A |
17: 28,638,661 (GRCm38) |
T836M |
probably benign |
Het |
Slfn4 |
T |
G |
11: 83,186,821 (GRCm38) |
I145S |
possibly damaging |
Het |
Spag6l |
G |
A |
16: 16,777,390 (GRCm38) |
T377I |
probably benign |
Het |
Spdye4b |
T |
C |
5: 143,196,334 (GRCm38) |
F129S |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,470,580 (GRCm38) |
G2360E |
probably benign |
Het |
Taar2 |
A |
T |
10: 23,940,771 (GRCm38) |
I70F |
probably damaging |
Het |
Taar7e |
A |
G |
10: 24,038,566 (GRCm38) |
N318S |
probably damaging |
Het |
Tor1a |
C |
A |
2: 30,967,730 (GRCm38) |
R42L |
probably benign |
Het |
Trdn |
A |
T |
10: 33,474,506 (GRCm38) |
Q690H |
probably benign |
Het |
Trim56 |
C |
A |
5: 137,112,725 (GRCm38) |
V646L |
probably benign |
Het |
Tspan15 |
T |
A |
10: 62,191,544 (GRCm38) |
K165I |
probably benign |
Het |
Usp24 |
A |
G |
4: 106,416,048 (GRCm38) |
Y2210C |
probably damaging |
Het |
Usp45 |
A |
G |
4: 21,797,307 (GRCm38) |
T76A |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,878,224 (GRCm38) |
|
probably null |
Het |
Zfp512b |
T |
C |
2: 181,585,095 (GRCm38) |
|
probably benign |
Het |
Zyx |
C |
A |
6: 42,356,159 (GRCm38) |
|
probably null |
Het |
|
Other mutations in Fut9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00919:Fut9
|
APN |
4 |
25,620,316 (GRCm38) |
missense |
possibly damaging |
0.71 |
IGL01134:Fut9
|
APN |
4 |
25,620,446 (GRCm38) |
missense |
probably benign |
0.13 |
IGL01330:Fut9
|
APN |
4 |
25,619,791 (GRCm38) |
missense |
possibly damaging |
0.95 |
IGL01732:Fut9
|
APN |
4 |
25,619,867 (GRCm38) |
missense |
possibly damaging |
0.58 |
IGL02824:Fut9
|
APN |
4 |
25,620,037 (GRCm38) |
missense |
probably damaging |
1.00 |
ANU74:Fut9
|
UTSW |
4 |
25,620,802 (GRCm38) |
missense |
probably benign |
0.25 |
R0280:Fut9
|
UTSW |
4 |
25,619,852 (GRCm38) |
missense |
probably benign |
0.00 |
R0408:Fut9
|
UTSW |
4 |
25,620,319 (GRCm38) |
missense |
possibly damaging |
0.69 |
R0594:Fut9
|
UTSW |
4 |
25,620,526 (GRCm38) |
missense |
possibly damaging |
0.94 |
R0609:Fut9
|
UTSW |
4 |
25,620,811 (GRCm38) |
start codon destroyed |
probably null |
0.98 |
R0709:Fut9
|
UTSW |
4 |
25,620,359 (GRCm38) |
missense |
probably damaging |
1.00 |
R1567:Fut9
|
UTSW |
4 |
25,620,344 (GRCm38) |
missense |
probably damaging |
0.99 |
R1719:Fut9
|
UTSW |
4 |
25,619,744 (GRCm38) |
missense |
possibly damaging |
0.62 |
R1856:Fut9
|
UTSW |
4 |
25,620,352 (GRCm38) |
missense |
probably damaging |
1.00 |
R2036:Fut9
|
UTSW |
4 |
25,620,322 (GRCm38) |
missense |
probably damaging |
1.00 |
R2165:Fut9
|
UTSW |
4 |
25,619,734 (GRCm38) |
makesense |
probably null |
|
R2165:Fut9
|
UTSW |
4 |
25,619,733 (GRCm38) |
makesense |
probably null |
|
R2332:Fut9
|
UTSW |
4 |
25,619,823 (GRCm38) |
nonsense |
probably null |
|
R4539:Fut9
|
UTSW |
4 |
25,619,793 (GRCm38) |
missense |
probably damaging |
1.00 |
R4722:Fut9
|
UTSW |
4 |
25,799,734 (GRCm38) |
utr 5 prime |
probably benign |
|
R4937:Fut9
|
UTSW |
4 |
25,799,591 (GRCm38) |
splice site |
probably benign |
|
R5025:Fut9
|
UTSW |
4 |
25,620,502 (GRCm38) |
missense |
probably damaging |
1.00 |
R5032:Fut9
|
UTSW |
4 |
25,799,245 (GRCm38) |
intron |
probably benign |
|
R5158:Fut9
|
UTSW |
4 |
25,620,731 (GRCm38) |
missense |
probably benign |
0.01 |
R5601:Fut9
|
UTSW |
4 |
25,620,299 (GRCm38) |
missense |
probably benign |
0.00 |
R5974:Fut9
|
UTSW |
4 |
25,620,090 (GRCm38) |
nonsense |
probably null |
|
R6315:Fut9
|
UTSW |
4 |
25,619,774 (GRCm38) |
missense |
probably damaging |
1.00 |
R6385:Fut9
|
UTSW |
4 |
25,620,328 (GRCm38) |
missense |
probably damaging |
1.00 |
R6652:Fut9
|
UTSW |
4 |
25,620,619 (GRCm38) |
missense |
probably benign |
0.44 |
R6809:Fut9
|
UTSW |
4 |
25,620,647 (GRCm38) |
missense |
probably benign |
|
R6825:Fut9
|
UTSW |
4 |
25,619,925 (GRCm38) |
missense |
probably benign |
|
R7145:Fut9
|
UTSW |
4 |
25,620,507 (GRCm38) |
missense |
probably damaging |
0.96 |
R7573:Fut9
|
UTSW |
4 |
25,620,691 (GRCm38) |
missense |
probably benign |
0.04 |
R8933:Fut9
|
UTSW |
4 |
25,619,861 (GRCm38) |
missense |
probably damaging |
1.00 |
R9715:Fut9
|
UTSW |
4 |
25,620,679 (GRCm38) |
missense |
probably benign |
0.00 |
X0057:Fut9
|
UTSW |
4 |
25,799,686 (GRCm38) |
start gained |
probably benign |
|
|