Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
A |
T |
10: 100,445,115 (GRCm39) |
K165N |
probably damaging |
Het |
Adam6b |
T |
A |
12: 113,453,615 (GRCm39) |
M144K |
probably damaging |
Het |
Arhgap44 |
T |
C |
11: 64,922,903 (GRCm39) |
|
probably benign |
Het |
Arl5c |
T |
A |
11: 97,885,939 (GRCm39) |
I21F |
probably damaging |
Het |
Bglap2 |
C |
T |
3: 88,285,552 (GRCm39) |
G40D |
probably damaging |
Het |
Bptf |
T |
C |
11: 106,964,940 (GRCm39) |
E1303G |
probably damaging |
Het |
Calhm1 |
T |
C |
19: 47,129,896 (GRCm39) |
T209A |
probably damaging |
Het |
Ccr8 |
A |
G |
9: 119,923,976 (GRCm39) |
|
probably null |
Het |
Chkb |
C |
T |
15: 89,313,610 (GRCm39) |
R65Q |
probably benign |
Het |
Col4a1 |
T |
C |
8: 11,249,838 (GRCm39) |
|
probably benign |
Het |
Cryzl2 |
A |
G |
1: 157,292,014 (GRCm39) |
T98A |
probably benign |
Het |
D430041D05Rik |
T |
C |
2: 103,998,509 (GRCm39) |
T1080A |
probably damaging |
Het |
Dhx8 |
C |
A |
11: 101,643,223 (GRCm39) |
T765N |
probably damaging |
Het |
Dicer1 |
T |
C |
12: 104,697,323 (GRCm39) |
D78G |
probably benign |
Het |
Drd2 |
A |
G |
9: 49,316,271 (GRCm39) |
I344V |
probably benign |
Het |
Edil3 |
A |
T |
13: 89,347,570 (GRCm39) |
|
probably benign |
Het |
Fbxw19 |
C |
T |
9: 109,313,493 (GRCm39) |
G235D |
probably benign |
Het |
Fzd1 |
T |
C |
5: 4,805,702 (GRCm39) |
K627E |
possibly damaging |
Het |
Garin4 |
T |
C |
1: 190,896,637 (GRCm39) |
D2G |
probably benign |
Het |
Gm10638 |
A |
G |
8: 87,472,828 (GRCm39) |
|
probably benign |
Het |
H6pd |
G |
T |
4: 150,080,773 (GRCm39) |
A24E |
probably damaging |
Het |
Hectd2 |
G |
T |
19: 36,578,929 (GRCm39) |
|
probably null |
Het |
Hps5 |
A |
G |
7: 46,440,333 (GRCm39) |
|
probably benign |
Het |
Irx3 |
T |
C |
8: 92,527,296 (GRCm39) |
N136S |
possibly damaging |
Het |
Kcmf1 |
T |
C |
6: 72,826,568 (GRCm39) |
M1V |
probably null |
Het |
Klrb1 |
A |
T |
6: 128,687,583 (GRCm39) |
F104I |
probably benign |
Het |
Lrfn5 |
T |
C |
12: 61,886,803 (GRCm39) |
M197T |
probably benign |
Het |
Mpdz |
A |
C |
4: 81,279,677 (GRCm39) |
M51R |
possibly damaging |
Het |
Mtbp |
G |
T |
15: 55,432,466 (GRCm39) |
E258* |
probably null |
Het |
Mylk3 |
T |
A |
8: 86,079,539 (GRCm39) |
H373L |
probably damaging |
Het |
Myrfl |
A |
G |
10: 116,664,882 (GRCm39) |
S383P |
probably damaging |
Het |
Nt5c |
T |
C |
11: 115,381,468 (GRCm39) |
*195W |
probably null |
Het |
Ocstamp |
A |
G |
2: 165,238,184 (GRCm39) |
V360A |
possibly damaging |
Het |
Or10ak16 |
A |
T |
4: 118,750,426 (GRCm39) |
I49F |
possibly damaging |
Het |
Or10al6 |
T |
A |
17: 38,083,284 (GRCm39) |
C247S |
probably damaging |
Het |
Or4k35 |
A |
G |
2: 111,100,208 (GRCm39) |
F168S |
probably damaging |
Het |
Or4p19 |
A |
T |
2: 88,242,378 (GRCm39) |
V208D |
probably damaging |
Het |
Or5an9 |
A |
G |
19: 12,186,953 (GRCm39) |
T8A |
probably damaging |
Het |
Otop2 |
T |
C |
11: 115,217,234 (GRCm39) |
|
probably benign |
Het |
Pom121l2 |
A |
T |
13: 22,172,649 (GRCm39) |
|
probably benign |
Het |
Pon2 |
T |
A |
6: 5,272,410 (GRCm39) |
K137* |
probably null |
Het |
Ppip5k2 |
T |
A |
1: 97,647,579 (GRCm39) |
Q1049L |
probably benign |
Het |
Ralgapa2 |
C |
T |
2: 146,276,729 (GRCm39) |
V504M |
probably damaging |
Het |
Rph3a |
G |
A |
5: 121,080,317 (GRCm39) |
H654Y |
probably damaging |
Het |
Sh2d1b1 |
T |
C |
1: 170,107,342 (GRCm39) |
|
probably benign |
Het |
Slc15a2 |
G |
A |
16: 36,595,960 (GRCm39) |
T154I |
probably benign |
Het |
Slc45a3 |
T |
C |
1: 131,905,265 (GRCm39) |
V96A |
possibly damaging |
Het |
Slc7a4 |
A |
G |
16: 17,393,497 (GRCm39) |
S101P |
probably damaging |
Het |
Smco2 |
T |
C |
6: 146,772,633 (GRCm39) |
|
probably benign |
Het |
Spata2 |
A |
T |
2: 167,325,580 (GRCm39) |
V413E |
probably benign |
Het |
Specc1l |
A |
G |
10: 75,082,260 (GRCm39) |
E552G |
probably damaging |
Het |
Sstr5 |
C |
T |
17: 25,711,008 (GRCm39) |
V74M |
probably benign |
Het |
Timm50 |
G |
A |
7: 28,006,280 (GRCm39) |
R274W |
probably damaging |
Het |
Tll2 |
A |
G |
19: 41,087,132 (GRCm39) |
V573A |
possibly damaging |
Het |
Tm7sf3 |
C |
A |
6: 146,507,685 (GRCm39) |
R459M |
possibly damaging |
Het |
Txk |
A |
G |
5: 72,889,105 (GRCm39) |
|
probably null |
Het |
Uroc1 |
A |
G |
6: 90,324,284 (GRCm39) |
D436G |
probably damaging |
Het |
Vmn1r13 |
T |
A |
6: 57,187,083 (GRCm39) |
Y81N |
possibly damaging |
Het |
Vmn2r19 |
A |
G |
6: 123,313,141 (GRCm39) |
E737G |
probably damaging |
Het |
Wfs1 |
A |
G |
5: 37,134,324 (GRCm39) |
|
probably benign |
Het |
Zfp1 |
G |
A |
8: 112,396,875 (GRCm39) |
E285K |
probably damaging |
Het |
Zfp1005 |
T |
A |
2: 150,111,136 (GRCm39) |
C609S |
possibly damaging |
Het |
Zfp661 |
G |
A |
2: 127,419,640 (GRCm39) |
Q167* |
probably null |
Het |
Zswim8 |
T |
C |
14: 20,760,834 (GRCm39) |
F36S |
probably damaging |
Het |
Zw10 |
A |
G |
9: 48,980,023 (GRCm39) |
T385A |
probably benign |
Het |
|
Other mutations in Garin1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01434:Garin1b
|
APN |
6 |
29,320,700 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02342:Garin1b
|
APN |
6 |
29,323,829 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0467:Garin1b
|
UTSW |
6 |
29,326,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R0610:Garin1b
|
UTSW |
6 |
29,326,576 (GRCm39) |
missense |
probably benign |
0.01 |
R1773:Garin1b
|
UTSW |
6 |
29,334,152 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1950:Garin1b
|
UTSW |
6 |
29,335,815 (GRCm39) |
splice site |
probably null |
|
R4259:Garin1b
|
UTSW |
6 |
29,320,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R4305:Garin1b
|
UTSW |
6 |
29,326,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R4351:Garin1b
|
UTSW |
6 |
29,320,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R4508:Garin1b
|
UTSW |
6 |
29,323,764 (GRCm39) |
missense |
probably benign |
0.04 |
R5014:Garin1b
|
UTSW |
6 |
29,326,723 (GRCm39) |
intron |
probably benign |
|
R5249:Garin1b
|
UTSW |
6 |
29,323,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R5506:Garin1b
|
UTSW |
6 |
29,319,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R6212:Garin1b
|
UTSW |
6 |
29,319,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R6456:Garin1b
|
UTSW |
6 |
29,334,045 (GRCm39) |
missense |
probably benign |
|
R6949:Garin1b
|
UTSW |
6 |
29,323,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R7047:Garin1b
|
UTSW |
6 |
29,323,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R7562:Garin1b
|
UTSW |
6 |
29,323,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R8346:Garin1b
|
UTSW |
6 |
29,334,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R9061:Garin1b
|
UTSW |
6 |
29,323,902 (GRCm39) |
missense |
probably benign |
0.27 |
X0065:Garin1b
|
UTSW |
6 |
29,326,660 (GRCm39) |
missense |
probably damaging |
1.00 |
|