Other mutations in this stock |
Total: 114 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aaas |
C |
T |
15: 102,247,068 (GRCm39) |
|
probably benign |
Het |
Aadacl4fm5 |
G |
A |
4: 144,504,389 (GRCm39) |
T254I |
possibly damaging |
Het |
Abce1 |
A |
G |
8: 80,412,578 (GRCm39) |
I583T |
probably benign |
Het |
Abtb3 |
T |
C |
10: 85,469,563 (GRCm39) |
L828P |
probably damaging |
Het |
Adcy1 |
A |
T |
11: 7,111,945 (GRCm39) |
T937S |
probably benign |
Het |
Adgra2 |
A |
G |
8: 27,601,196 (GRCm39) |
I279V |
possibly damaging |
Het |
Adgrl4 |
A |
T |
3: 151,216,416 (GRCm39) |
N533I |
possibly damaging |
Het |
Adipor1 |
T |
C |
1: 134,350,771 (GRCm39) |
S7P |
probably benign |
Het |
Amelx |
A |
T |
X: 167,965,153 (GRCm39) |
|
probably null |
Het |
Anks1b |
A |
T |
10: 89,885,792 (GRCm39) |
T163S |
probably damaging |
Het |
Apc |
A |
G |
18: 34,450,388 (GRCm39) |
E2394G |
probably damaging |
Het |
Arhgef39 |
C |
T |
4: 43,499,309 (GRCm39) |
G56E |
probably damaging |
Het |
Arnt |
C |
T |
3: 95,355,704 (GRCm39) |
S16L |
possibly damaging |
Het |
Arsj |
A |
G |
3: 126,232,670 (GRCm39) |
N472S |
probably benign |
Het |
Atg2b |
T |
C |
12: 105,635,677 (GRCm39) |
Y197C |
probably damaging |
Het |
B3gat1 |
A |
T |
9: 26,667,248 (GRCm39) |
D160V |
possibly damaging |
Het |
Bmp7 |
T |
C |
2: 172,781,714 (GRCm39) |
E50G |
probably damaging |
Het |
Bms1 |
T |
C |
6: 118,369,939 (GRCm39) |
E869G |
probably damaging |
Het |
Brd4 |
G |
A |
17: 32,440,340 (GRCm39) |
P332L |
possibly damaging |
Het |
C130074G19Rik |
T |
C |
1: 184,615,095 (GRCm39) |
T32A |
probably benign |
Het |
C1rl |
A |
T |
6: 124,486,021 (GRCm39) |
Y464F |
probably damaging |
Het |
Ccdc150 |
T |
A |
1: 54,303,068 (GRCm39) |
M193K |
probably benign |
Het |
Ccdc7a |
A |
G |
8: 129,706,616 (GRCm39) |
S338P |
probably damaging |
Het |
Cenpu |
T |
C |
8: 47,025,872 (GRCm39) |
|
probably benign |
Het |
Cep170 |
A |
C |
1: 176,597,013 (GRCm39) |
V448G |
probably benign |
Het |
Col27a1 |
G |
T |
4: 63,196,031 (GRCm39) |
A879S |
probably benign |
Het |
Crtac1 |
C |
T |
19: 42,276,383 (GRCm39) |
S515N |
possibly damaging |
Het |
Cstad |
G |
A |
2: 30,498,293 (GRCm39) |
V43M |
unknown |
Het |
Daam1 |
T |
C |
12: 72,029,529 (GRCm39) |
|
probably null |
Het |
Dnmt1 |
C |
T |
9: 20,838,442 (GRCm39) |
R207H |
probably benign |
Het |
Dsg3 |
A |
G |
18: 20,655,162 (GRCm39) |
N153S |
probably damaging |
Het |
Dzip3 |
C |
A |
16: 48,747,956 (GRCm39) |
L1151F |
probably damaging |
Het |
Eml5 |
A |
T |
12: 98,826,220 (GRCm39) |
H644Q |
probably damaging |
Het |
Emsy |
A |
G |
7: 98,297,027 (GRCm39) |
L52P |
probably damaging |
Het |
Eno1 |
T |
A |
4: 150,331,232 (GRCm39) |
|
probably null |
Het |
Epha3 |
T |
A |
16: 63,593,315 (GRCm39) |
T258S |
probably benign |
Het |
Ern1 |
T |
C |
11: 106,317,723 (GRCm39) |
T134A |
probably damaging |
Het |
Fam151b |
G |
T |
13: 92,614,410 (GRCm39) |
T26K |
probably damaging |
Het |
Fam151b |
T |
A |
13: 92,614,411 (GRCm39) |
T26S |
probably damaging |
Het |
Fat1 |
T |
C |
8: 45,493,719 (GRCm39) |
V3955A |
probably damaging |
Het |
Fbn1 |
T |
C |
2: 125,209,574 (GRCm39) |
N930S |
possibly damaging |
Het |
Fgr |
A |
G |
4: 132,725,673 (GRCm39) |
M361V |
probably benign |
Het |
Fmo4 |
G |
A |
1: 162,631,259 (GRCm39) |
T236I |
probably benign |
Het |
Fndc7 |
G |
A |
3: 108,790,825 (GRCm39) |
T67I |
probably damaging |
Het |
Fxr2 |
A |
G |
11: 69,534,766 (GRCm39) |
T216A |
probably benign |
Het |
Gdf10 |
G |
A |
14: 33,654,710 (GRCm39) |
A406T |
probably benign |
Het |
Gm42669 |
A |
T |
5: 107,656,738 (GRCm39) |
E355D |
possibly damaging |
Het |
Gm5174 |
A |
T |
10: 86,492,617 (GRCm39) |
|
noncoding transcript |
Het |
Gm5431 |
A |
T |
11: 48,779,224 (GRCm39) |
L844* |
probably null |
Het |
Gm6489 |
T |
C |
1: 31,326,452 (GRCm39) |
|
noncoding transcript |
Het |
Gna11 |
A |
G |
10: 81,366,678 (GRCm39) |
V344A |
probably damaging |
Het |
Gtpbp3 |
A |
G |
8: 71,943,099 (GRCm39) |
E170G |
probably damaging |
Het |
H2az1 |
A |
C |
3: 137,571,275 (GRCm39) |
|
probably benign |
Het |
Heatr1 |
A |
G |
13: 12,411,419 (GRCm39) |
N87D |
probably damaging |
Het |
Iars2 |
T |
C |
1: 185,027,868 (GRCm39) |
K687E |
possibly damaging |
Het |
Ica1 |
T |
C |
6: 8,749,736 (GRCm39) |
D71G |
possibly damaging |
Het |
Ifnlr1 |
T |
C |
4: 135,413,881 (GRCm39) |
L10P |
probably damaging |
Het |
Il1r1 |
T |
A |
1: 40,352,300 (GRCm39) |
L490* |
probably null |
Het |
Ip6k3 |
A |
T |
17: 27,370,142 (GRCm39) |
L92Q |
probably benign |
Het |
Itgbl1 |
T |
A |
14: 124,204,090 (GRCm39) |
F394I |
probably damaging |
Het |
Kat6b |
T |
C |
14: 21,678,947 (GRCm39) |
Y437H |
probably damaging |
Het |
Kcnh5 |
G |
C |
12: 74,944,358 (GRCm39) |
Q964E |
probably benign |
Het |
Krt27 |
A |
T |
11: 99,237,309 (GRCm39) |
|
probably null |
Het |
Mki67 |
A |
T |
7: 135,300,128 (GRCm39) |
D1635E |
probably benign |
Het |
Mmp23 |
G |
T |
4: 155,736,509 (GRCm39) |
H177Q |
possibly damaging |
Het |
Myef2l |
G |
T |
3: 10,154,346 (GRCm39) |
V372F |
probably benign |
Het |
Mylk2 |
C |
A |
2: 152,759,527 (GRCm39) |
Q406K |
possibly damaging |
Het |
Myo1g |
A |
G |
11: 6,462,159 (GRCm39) |
|
probably null |
Het |
Myrf |
T |
C |
19: 10,197,160 (GRCm39) |
T261A |
probably benign |
Het |
Nmt2 |
C |
T |
2: 3,326,419 (GRCm39) |
P486L |
possibly damaging |
Het |
Oard1 |
T |
A |
17: 48,722,304 (GRCm39) |
L100* |
probably null |
Het |
Oca2 |
T |
C |
7: 55,971,246 (GRCm39) |
I391T |
possibly damaging |
Het |
Or51v14 |
T |
A |
7: 103,260,618 (GRCm39) |
*314L |
probably null |
Het |
Or5k17 |
T |
A |
16: 58,746,530 (GRCm39) |
M135L |
probably benign |
Het |
Or5p64 |
A |
C |
7: 107,854,403 (GRCm39) |
L314* |
probably null |
Het |
Or6c68 |
A |
T |
10: 129,157,740 (GRCm39) |
I83F |
possibly damaging |
Het |
Or8b39 |
T |
A |
9: 37,996,419 (GRCm39) |
C96S |
probably damaging |
Het |
Or9k2b |
C |
A |
10: 130,015,847 (GRCm39) |
A301S |
possibly damaging |
Het |
Pabpc4 |
T |
A |
4: 123,180,658 (GRCm39) |
S127T |
probably damaging |
Het |
Pcdhb1 |
A |
G |
18: 37,398,760 (GRCm39) |
D237G |
probably damaging |
Het |
Pdcd6ip |
T |
C |
9: 113,537,090 (GRCm39) |
Y29C |
probably damaging |
Het |
Phf3 |
C |
A |
1: 30,870,601 (GRCm39) |
R95L |
probably damaging |
Het |
Pkd1l2 |
A |
T |
8: 117,757,421 (GRCm39) |
V1539D |
probably damaging |
Het |
Plxna1 |
A |
T |
6: 89,308,273 (GRCm39) |
D1271E |
probably damaging |
Het |
Ppp3r2 |
A |
G |
4: 49,681,726 (GRCm39) |
F75L |
probably damaging |
Het |
Rabgap1 |
T |
C |
2: 37,373,774 (GRCm39) |
F262S |
possibly damaging |
Het |
Rbbp6 |
T |
C |
7: 122,589,511 (GRCm39) |
S438P |
probably benign |
Het |
Rexo1 |
G |
A |
10: 80,379,200 (GRCm39) |
R1038C |
probably damaging |
Het |
Rnf10 |
A |
G |
5: 115,398,381 (GRCm39) |
|
probably benign |
Het |
Scyl1 |
C |
A |
19: 5,810,132 (GRCm39) |
A565S |
probably benign |
Het |
Septin4 |
A |
G |
11: 87,481,193 (GRCm39) |
T378A |
probably benign |
Het |
Sh3yl1 |
A |
G |
12: 30,992,787 (GRCm39) |
|
probably null |
Het |
Slc1a7 |
G |
T |
4: 107,825,782 (GRCm39) |
D14Y |
probably benign |
Het |
Slc32a1 |
T |
C |
2: 158,455,963 (GRCm39) |
V206A |
probably damaging |
Het |
Smyd5 |
G |
A |
6: 85,415,121 (GRCm39) |
R43Q |
probably benign |
Het |
Snrnp200 |
G |
A |
2: 127,058,095 (GRCm39) |
A286T |
possibly damaging |
Het |
Sp110 |
A |
C |
1: 85,505,050 (GRCm39) |
F434C |
probably benign |
Het |
Srebf2 |
T |
A |
15: 82,079,155 (GRCm39) |
H794Q |
probably benign |
Het |
Ssbp2 |
T |
C |
13: 91,812,303 (GRCm39) |
|
probably benign |
Het |
Sspo |
G |
A |
6: 48,455,207 (GRCm39) |
G3023D |
probably damaging |
Het |
St6galnac5 |
T |
A |
3: 152,552,120 (GRCm39) |
Q149L |
probably benign |
Het |
Stab2 |
A |
G |
10: 86,697,334 (GRCm39) |
Y1985H |
probably benign |
Het |
Suz12 |
A |
G |
11: 79,889,926 (GRCm39) |
M146V |
probably benign |
Het |
Tac2 |
A |
G |
10: 127,564,349 (GRCm39) |
|
probably null |
Het |
Thbd |
T |
C |
2: 148,248,899 (GRCm39) |
E323G |
probably damaging |
Het |
Tnfrsf26 |
T |
A |
7: 143,171,660 (GRCm39) |
T98S |
probably damaging |
Het |
Trim15 |
T |
C |
17: 37,173,215 (GRCm39) |
|
probably benign |
Het |
Trpt1 |
T |
C |
19: 6,975,561 (GRCm39) |
V105A |
possibly damaging |
Het |
Vcam1 |
T |
C |
3: 115,919,606 (GRCm39) |
Y226C |
probably damaging |
Het |
Vmn1r175 |
A |
G |
7: 23,507,808 (GRCm39) |
V273A |
probably benign |
Het |
Vmn2r109 |
A |
G |
17: 20,784,969 (GRCm39) |
V17A |
probably benign |
Het |
Vmn2r84 |
G |
A |
10: 130,226,677 (GRCm39) |
A387V |
probably benign |
Het |
Wdfy4 |
A |
T |
14: 32,693,641 (GRCm39) |
L2728Q |
probably damaging |
Het |
Zfp934 |
T |
A |
13: 62,666,108 (GRCm39) |
T178S |
possibly damaging |
Het |
|
Other mutations in Pth2r |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01333:Pth2r
|
APN |
1 |
65,427,884 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02054:Pth2r
|
APN |
1 |
65,375,940 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02429:Pth2r
|
APN |
1 |
65,385,998 (GRCm39) |
missense |
probably benign |
0.05 |
R0277:Pth2r
|
UTSW |
1 |
65,427,775 (GRCm39) |
missense |
probably benign |
|
R0323:Pth2r
|
UTSW |
1 |
65,427,775 (GRCm39) |
missense |
probably benign |
|
R0415:Pth2r
|
UTSW |
1 |
65,427,598 (GRCm39) |
missense |
probably benign |
|
R1067:Pth2r
|
UTSW |
1 |
65,411,507 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1463:Pth2r
|
UTSW |
1 |
65,402,436 (GRCm39) |
missense |
probably damaging |
0.96 |
R1566:Pth2r
|
UTSW |
1 |
65,427,697 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1690:Pth2r
|
UTSW |
1 |
65,411,462 (GRCm39) |
missense |
probably benign |
0.02 |
R1710:Pth2r
|
UTSW |
1 |
65,375,997 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2062:Pth2r
|
UTSW |
1 |
65,382,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R2232:Pth2r
|
UTSW |
1 |
65,375,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R2942:Pth2r
|
UTSW |
1 |
65,427,635 (GRCm39) |
missense |
probably benign |
0.00 |
R3011:Pth2r
|
UTSW |
1 |
65,376,147 (GRCm39) |
missense |
probably benign |
0.05 |
R3857:Pth2r
|
UTSW |
1 |
65,361,206 (GRCm39) |
missense |
probably damaging |
0.98 |
R3858:Pth2r
|
UTSW |
1 |
65,361,206 (GRCm39) |
missense |
probably damaging |
0.98 |
R3859:Pth2r
|
UTSW |
1 |
65,361,206 (GRCm39) |
missense |
probably damaging |
0.98 |
R4540:Pth2r
|
UTSW |
1 |
65,321,360 (GRCm39) |
missense |
probably benign |
|
R4694:Pth2r
|
UTSW |
1 |
65,375,920 (GRCm39) |
missense |
probably benign |
|
R4777:Pth2r
|
UTSW |
1 |
65,427,676 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4926:Pth2r
|
UTSW |
1 |
65,361,143 (GRCm39) |
missense |
probably benign |
0.27 |
R5209:Pth2r
|
UTSW |
1 |
65,427,856 (GRCm39) |
missense |
probably benign |
0.04 |
R5871:Pth2r
|
UTSW |
1 |
65,427,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R6868:Pth2r
|
UTSW |
1 |
65,427,638 (GRCm39) |
missense |
probably benign |
0.02 |
R7132:Pth2r
|
UTSW |
1 |
65,361,225 (GRCm39) |
missense |
probably benign |
0.00 |
R7242:Pth2r
|
UTSW |
1 |
65,427,779 (GRCm39) |
missense |
probably benign |
0.42 |
R7677:Pth2r
|
UTSW |
1 |
65,427,605 (GRCm39) |
missense |
probably benign |
0.00 |
R7836:Pth2r
|
UTSW |
1 |
65,390,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R8061:Pth2r
|
UTSW |
1 |
65,382,660 (GRCm39) |
missense |
possibly damaging |
0.64 |
Z1176:Pth2r
|
UTSW |
1 |
65,402,467 (GRCm39) |
missense |
probably benign |
0.20 |
|