Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr1a1 |
T |
A |
4: 116,495,217 (GRCm39) |
I261F |
probably damaging |
Het |
Aldh1l1 |
T |
C |
6: 90,541,371 (GRCm39) |
V255A |
probably benign |
Het |
Ambn |
T |
A |
5: 88,612,340 (GRCm39) |
M172K |
probably benign |
Het |
Arhgef18 |
A |
G |
8: 3,439,094 (GRCm39) |
|
probably benign |
Het |
BC034090 |
T |
C |
1: 155,101,319 (GRCm39) |
H315R |
possibly damaging |
Het |
Btaf1 |
T |
A |
19: 36,959,122 (GRCm39) |
D707E |
probably benign |
Het |
C6 |
T |
C |
15: 4,764,739 (GRCm39) |
L145P |
possibly damaging |
Het |
Cav3 |
T |
A |
6: 112,449,207 (GRCm39) |
L75Q |
probably damaging |
Het |
Cavin2 |
T |
A |
1: 51,339,939 (GRCm39) |
D205E |
probably benign |
Het |
Cdadc1 |
T |
C |
14: 59,811,242 (GRCm39) |
T423A |
probably damaging |
Het |
Cep120 |
A |
T |
18: 53,857,648 (GRCm39) |
H272Q |
probably damaging |
Het |
Chd9 |
A |
T |
8: 91,659,229 (GRCm39) |
Q63L |
possibly damaging |
Het |
Clspn |
T |
C |
4: 126,460,228 (GRCm39) |
|
probably benign |
Het |
Cramp1 |
G |
T |
17: 25,202,217 (GRCm39) |
H422N |
probably damaging |
Het |
Csn1s2b |
A |
T |
5: 87,966,943 (GRCm39) |
M71L |
probably benign |
Het |
D630045J12Rik |
C |
A |
6: 38,158,366 (GRCm39) |
A1104S |
probably damaging |
Het |
D930048N14Rik |
A |
G |
11: 51,545,663 (GRCm39) |
|
probably benign |
Het |
Ern2 |
G |
A |
7: 121,776,623 (GRCm39) |
P366S |
probably damaging |
Het |
Gm1527 |
T |
C |
3: 28,952,880 (GRCm39) |
I60T |
probably damaging |
Het |
Gse1 |
T |
C |
8: 121,305,254 (GRCm39) |
|
probably benign |
Het |
Ildr1 |
T |
C |
16: 36,528,681 (GRCm39) |
L42P |
probably damaging |
Het |
Itih2 |
G |
A |
2: 10,110,546 (GRCm39) |
T515I |
probably benign |
Het |
Jcad |
C |
A |
18: 4,673,309 (GRCm39) |
P357Q |
probably damaging |
Het |
Kitl |
A |
G |
10: 99,899,976 (GRCm39) |
T94A |
probably benign |
Het |
Klri1 |
C |
T |
6: 129,675,204 (GRCm39) |
M185I |
probably benign |
Het |
Lsamp |
A |
T |
16: 41,775,661 (GRCm39) |
M171L |
probably benign |
Het |
Macf1 |
T |
G |
4: 123,377,846 (GRCm39) |
I1460L |
probably damaging |
Het |
Map1b |
C |
G |
13: 99,652,986 (GRCm39) |
V4L |
probably benign |
Het |
Mboat7 |
A |
T |
7: 3,688,817 (GRCm39) |
V237D |
probably benign |
Het |
Mctp2 |
A |
T |
7: 71,811,006 (GRCm39) |
I656K |
probably damaging |
Het |
Ms4a6b |
A |
G |
19: 11,497,806 (GRCm39) |
D35G |
possibly damaging |
Het |
Nipsnap2 |
T |
A |
5: 129,830,301 (GRCm39) |
I205N |
probably damaging |
Het |
Nsd2 |
T |
C |
5: 34,011,984 (GRCm39) |
V264A |
probably damaging |
Het |
Oacyl |
C |
T |
18: 65,883,167 (GRCm39) |
T582I |
probably damaging |
Het |
Olfm1 |
A |
T |
2: 28,119,279 (GRCm39) |
T333S |
possibly damaging |
Het |
Olfm4 |
G |
A |
14: 80,249,422 (GRCm39) |
E180K |
probably damaging |
Het |
Or14j6 |
T |
C |
17: 38,215,060 (GRCm39) |
F208L |
probably benign |
Het |
Or2ad1 |
A |
T |
13: 21,326,912 (GRCm39) |
L105Q |
probably damaging |
Het |
Or8g17 |
T |
G |
9: 38,930,776 (GRCm39) |
Q20H |
probably benign |
Het |
Parp4 |
T |
A |
14: 56,827,885 (GRCm39) |
V212E |
possibly damaging |
Het |
Pcdhb21 |
T |
A |
18: 37,648,666 (GRCm39) |
N598K |
probably damaging |
Het |
Piezo2 |
C |
A |
18: 63,250,743 (GRCm39) |
W452L |
probably benign |
Het |
Plec |
C |
A |
15: 76,090,011 (GRCm39) |
A110S |
possibly damaging |
Het |
Popdc3 |
T |
C |
10: 45,191,320 (GRCm39) |
Y144H |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,421,015 (GRCm39) |
Y246* |
probably null |
Het |
Pyroxd2 |
T |
C |
19: 42,726,573 (GRCm39) |
D247G |
probably damaging |
Het |
Robo2 |
T |
C |
16: 73,695,889 (GRCm39) |
E1418G |
probably benign |
Het |
Rtp3 |
T |
C |
9: 110,815,772 (GRCm39) |
T198A |
probably benign |
Het |
Sec16a |
A |
T |
2: 26,315,536 (GRCm39) |
V1767D |
probably damaging |
Het |
Septin14 |
T |
C |
5: 129,774,819 (GRCm39) |
N119D |
probably benign |
Het |
Serpina5 |
A |
T |
12: 104,071,484 (GRCm39) |
T364S |
possibly damaging |
Het |
Setd2 |
A |
G |
9: 110,378,932 (GRCm39) |
S632G |
probably benign |
Het |
Sh3bp2 |
C |
T |
5: 34,716,348 (GRCm39) |
A253V |
possibly damaging |
Het |
Slc6a5 |
G |
T |
7: 49,586,010 (GRCm39) |
G443C |
probably damaging |
Het |
Spag9 |
T |
A |
11: 93,999,278 (GRCm39) |
|
probably null |
Het |
Sptbn1 |
T |
C |
11: 30,087,301 (GRCm39) |
E1033G |
probably damaging |
Het |
Timm17a |
T |
G |
1: 135,237,540 (GRCm39) |
Q39P |
probably damaging |
Het |
Tmem26 |
A |
T |
10: 68,587,103 (GRCm39) |
T184S |
probably damaging |
Het |
Tpi1 |
A |
T |
6: 124,789,891 (GRCm39) |
|
probably null |
Het |
Tssk5 |
T |
C |
15: 76,258,003 (GRCm39) |
Y118C |
possibly damaging |
Het |
Ttll4 |
T |
A |
1: 74,736,629 (GRCm39) |
L1118Q |
possibly damaging |
Het |
Ttll5 |
T |
A |
12: 85,969,788 (GRCm39) |
L691Q |
probably damaging |
Het |
Vmn1r49 |
A |
T |
6: 90,049,623 (GRCm39) |
H126Q |
possibly damaging |
Het |
Zfp518b |
A |
T |
5: 38,829,224 (GRCm39) |
V927E |
probably damaging |
Het |
Zfp618 |
T |
C |
4: 63,013,774 (GRCm39) |
F213S |
probably damaging |
Het |
Zfp759 |
T |
A |
13: 67,287,668 (GRCm39) |
N406K |
probably benign |
Het |
|
Other mutations in Ptgdr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02548:Ptgdr
|
APN |
14 |
45,096,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R1036:Ptgdr
|
UTSW |
14 |
45,096,572 (GRCm39) |
missense |
probably damaging |
0.98 |
R1368:Ptgdr
|
UTSW |
14 |
45,090,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Ptgdr
|
UTSW |
14 |
45,096,036 (GRCm39) |
nonsense |
probably null |
|
R1786:Ptgdr
|
UTSW |
14 |
45,096,036 (GRCm39) |
nonsense |
probably null |
|
R1921:Ptgdr
|
UTSW |
14 |
45,090,738 (GRCm39) |
missense |
probably benign |
0.00 |
R2312:Ptgdr
|
UTSW |
14 |
45,096,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R4867:Ptgdr
|
UTSW |
14 |
45,096,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R5198:Ptgdr
|
UTSW |
14 |
45,096,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R6917:Ptgdr
|
UTSW |
14 |
45,096,067 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7186:Ptgdr
|
UTSW |
14 |
45,096,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R7291:Ptgdr
|
UTSW |
14 |
45,096,649 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7399:Ptgdr
|
UTSW |
14 |
45,095,689 (GRCm39) |
splice site |
probably null |
|
R7612:Ptgdr
|
UTSW |
14 |
45,096,094 (GRCm39) |
missense |
probably damaging |
0.98 |
R7763:Ptgdr
|
UTSW |
14 |
45,096,535 (GRCm39) |
missense |
probably damaging |
0.99 |
R7850:Ptgdr
|
UTSW |
14 |
45,090,828 (GRCm39) |
missense |
probably benign |
0.05 |
R8139:Ptgdr
|
UTSW |
14 |
45,096,142 (GRCm39) |
missense |
probably benign |
0.13 |
R8262:Ptgdr
|
UTSW |
14 |
45,090,858 (GRCm39) |
missense |
probably benign |
0.01 |
R8392:Ptgdr
|
UTSW |
14 |
45,096,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R8992:Ptgdr
|
UTSW |
14 |
45,096,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R9359:Ptgdr
|
UTSW |
14 |
45,090,715 (GRCm39) |
missense |
|
|
R9403:Ptgdr
|
UTSW |
14 |
45,090,715 (GRCm39) |
missense |
|
|
|