Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ambp |
C |
T |
4: 63,066,977 (GRCm39) |
V188I |
probably benign |
Het |
Bbs9 |
G |
T |
9: 22,582,221 (GRCm39) |
E638* |
probably null |
Het |
Bmp6 |
A |
G |
13: 38,682,904 (GRCm39) |
M465V |
probably damaging |
Het |
Ccdc192 |
T |
A |
18: 57,800,417 (GRCm39) |
C171* |
probably null |
Het |
Cemip |
T |
C |
7: 83,632,440 (GRCm39) |
E374G |
possibly damaging |
Het |
Cnbd1 |
A |
T |
4: 18,895,141 (GRCm39) |
Y200* |
probably null |
Het |
Cox6b1 |
G |
T |
7: 30,323,929 (GRCm39) |
Y34* |
probably null |
Het |
Cyp2d26 |
A |
C |
15: 82,675,619 (GRCm39) |
I303M |
probably benign |
Het |
Diaph1 |
T |
A |
18: 38,026,469 (GRCm39) |
|
probably null |
Het |
Dmp1 |
T |
C |
5: 104,359,731 (GRCm39) |
S136P |
probably damaging |
Het |
Dpy19l1 |
C |
T |
9: 24,396,365 (GRCm39) |
R117Q |
probably damaging |
Het |
Eea1 |
A |
G |
10: 95,832,877 (GRCm39) |
T241A |
probably damaging |
Het |
Erap1 |
C |
A |
13: 74,814,291 (GRCm39) |
T25K |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,906,007 (GRCm39) |
E3137G |
probably benign |
Het |
Fryl |
C |
T |
5: 73,179,844 (GRCm39) |
|
probably null |
Het |
Gldc |
T |
G |
19: 30,078,165 (GRCm39) |
D944A |
possibly damaging |
Het |
Igkv1-122 |
G |
A |
6: 67,993,728 (GRCm39) |
M1I |
probably null |
Het |
Jag2 |
G |
A |
12: 112,879,969 (GRCm39) |
P380S |
possibly damaging |
Het |
Kcnc2 |
T |
C |
10: 112,108,311 (GRCm39) |
|
probably null |
Het |
Kmt2a |
T |
C |
9: 44,736,781 (GRCm39) |
|
probably benign |
Het |
Lrrc55 |
A |
G |
2: 85,022,333 (GRCm39) |
V286A |
probably damaging |
Het |
Mllt10 |
C |
A |
2: 18,127,128 (GRCm39) |
H82N |
probably damaging |
Het |
Myh11 |
C |
A |
16: 14,039,639 (GRCm39) |
R837L |
probably damaging |
Het |
Nsg1 |
C |
A |
5: 38,313,035 (GRCm39) |
D55Y |
probably damaging |
Het |
Nup107 |
C |
A |
10: 117,617,247 (GRCm39) |
R221M |
probably damaging |
Het |
Nup153 |
G |
T |
13: 46,837,583 (GRCm39) |
A1213D |
possibly damaging |
Het |
Ovgp1 |
G |
A |
3: 105,885,665 (GRCm39) |
G174S |
probably damaging |
Het |
Papss2 |
C |
T |
19: 32,629,482 (GRCm39) |
A357V |
probably benign |
Het |
Pclo |
A |
G |
5: 14,763,881 (GRCm39) |
K4118R |
unknown |
Het |
Pde2a |
T |
C |
7: 101,156,918 (GRCm39) |
I628T |
possibly damaging |
Het |
Pla2r1 |
A |
G |
2: 60,325,708 (GRCm39) |
W521R |
probably damaging |
Het |
Pld1 |
A |
T |
3: 28,153,813 (GRCm39) |
Q744L |
probably damaging |
Het |
Pnpo |
T |
A |
11: 96,829,775 (GRCm39) |
E251V |
possibly damaging |
Het |
Rdh10 |
C |
T |
1: 16,178,246 (GRCm39) |
H173Y |
possibly damaging |
Het |
Sgpp2 |
A |
T |
1: 78,393,533 (GRCm39) |
I179F |
probably damaging |
Het |
Slc11a1 |
C |
T |
1: 74,423,899 (GRCm39) |
P409L |
probably damaging |
Het |
Slc35b4 |
T |
A |
6: 34,135,364 (GRCm39) |
N316I |
probably benign |
Het |
Snrnp200 |
A |
G |
2: 127,064,148 (GRCm39) |
I712V |
probably benign |
Het |
Spr |
T |
C |
6: 85,111,222 (GRCm39) |
D216G |
possibly damaging |
Het |
Sri |
G |
A |
5: 8,113,755 (GRCm39) |
|
probably null |
Het |
Tas2r124 |
T |
C |
6: 132,732,332 (GRCm39) |
S214P |
probably damaging |
Het |
Tg |
T |
A |
15: 66,549,936 (GRCm39) |
S233T |
probably damaging |
Het |
Tgfbr3 |
A |
T |
5: 107,269,279 (GRCm39) |
|
probably benign |
Het |
Vmn2r45 |
A |
G |
7: 8,486,337 (GRCm39) |
F317S |
probably benign |
Het |
Vmn2r99 |
C |
A |
17: 19,613,920 (GRCm39) |
|
probably benign |
Het |
Zfp957 |
T |
C |
14: 79,451,331 (GRCm39) |
E156G |
probably benign |
Het |
|
Other mutations in Grm5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Grm5
|
APN |
7 |
87,779,989 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00970:Grm5
|
APN |
7 |
87,453,104 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01286:Grm5
|
APN |
7 |
87,251,773 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01307:Grm5
|
APN |
7 |
87,724,220 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01603:Grm5
|
APN |
7 |
87,252,386 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01705:Grm5
|
APN |
7 |
87,779,254 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02184:Grm5
|
APN |
7 |
87,675,650 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02504:Grm5
|
APN |
7 |
87,779,980 (GRCm39) |
missense |
probably benign |
|
IGL02689:Grm5
|
APN |
7 |
87,251,918 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02725:Grm5
|
APN |
7 |
87,723,873 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02851:Grm5
|
APN |
7 |
87,723,918 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03106:Grm5
|
APN |
7 |
87,685,278 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03257:Grm5
|
APN |
7 |
87,252,106 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL03291:Grm5
|
APN |
7 |
87,780,004 (GRCm39) |
missense |
probably damaging |
1.00 |
BB004:Grm5
|
UTSW |
7 |
87,685,382 (GRCm39) |
missense |
probably benign |
0.16 |
BB014:Grm5
|
UTSW |
7 |
87,685,382 (GRCm39) |
missense |
probably benign |
0.16 |
R0078:Grm5
|
UTSW |
7 |
87,724,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R0314:Grm5
|
UTSW |
7 |
87,252,163 (GRCm39) |
missense |
probably damaging |
0.97 |
R0318:Grm5
|
UTSW |
7 |
87,252,175 (GRCm39) |
missense |
probably damaging |
0.99 |
R0364:Grm5
|
UTSW |
7 |
87,723,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R0380:Grm5
|
UTSW |
7 |
87,723,584 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0454:Grm5
|
UTSW |
7 |
87,779,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Grm5
|
UTSW |
7 |
87,779,989 (GRCm39) |
missense |
probably benign |
0.00 |
R0562:Grm5
|
UTSW |
7 |
87,252,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R1695:Grm5
|
UTSW |
7 |
87,685,311 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2012:Grm5
|
UTSW |
7 |
87,724,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R2384:Grm5
|
UTSW |
7 |
87,251,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R2510:Grm5
|
UTSW |
7 |
87,685,299 (GRCm39) |
missense |
probably benign |
0.21 |
R2870:Grm5
|
UTSW |
7 |
87,251,930 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2870:Grm5
|
UTSW |
7 |
87,251,930 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3861:Grm5
|
UTSW |
7 |
87,779,202 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4451:Grm5
|
UTSW |
7 |
87,724,340 (GRCm39) |
critical splice donor site |
probably null |
|
R4626:Grm5
|
UTSW |
7 |
87,779,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R4728:Grm5
|
UTSW |
7 |
87,624,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R4914:Grm5
|
UTSW |
7 |
87,779,337 (GRCm39) |
missense |
probably benign |
0.00 |
R5122:Grm5
|
UTSW |
7 |
87,724,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R5352:Grm5
|
UTSW |
7 |
87,724,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R5361:Grm5
|
UTSW |
7 |
87,723,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R5684:Grm5
|
UTSW |
7 |
87,779,853 (GRCm39) |
missense |
probably benign |
|
R5715:Grm5
|
UTSW |
7 |
87,779,464 (GRCm39) |
missense |
probably benign |
0.05 |
R5759:Grm5
|
UTSW |
7 |
87,675,808 (GRCm39) |
missense |
probably damaging |
0.96 |
R5844:Grm5
|
UTSW |
7 |
87,453,232 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5889:Grm5
|
UTSW |
7 |
87,252,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R6048:Grm5
|
UTSW |
7 |
87,675,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R6145:Grm5
|
UTSW |
7 |
87,675,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R6232:Grm5
|
UTSW |
7 |
87,251,638 (GRCm39) |
unclassified |
probably benign |
|
R6972:Grm5
|
UTSW |
7 |
87,252,131 (GRCm39) |
missense |
probably benign |
0.02 |
R7072:Grm5
|
UTSW |
7 |
87,723,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R7258:Grm5
|
UTSW |
7 |
87,723,914 (GRCm39) |
missense |
probably damaging |
0.96 |
R7316:Grm5
|
UTSW |
7 |
87,624,473 (GRCm39) |
missense |
probably benign |
|
R7434:Grm5
|
UTSW |
7 |
87,779,682 (GRCm39) |
missense |
probably benign |
0.10 |
R7521:Grm5
|
UTSW |
7 |
87,723,480 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7616:Grm5
|
UTSW |
7 |
87,765,409 (GRCm39) |
missense |
probably benign |
|
R7631:Grm5
|
UTSW |
7 |
87,624,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R7655:Grm5
|
UTSW |
7 |
87,779,459 (GRCm39) |
missense |
probably benign |
0.00 |
R7656:Grm5
|
UTSW |
7 |
87,779,459 (GRCm39) |
missense |
probably benign |
0.00 |
R7739:Grm5
|
UTSW |
7 |
87,779,266 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7897:Grm5
|
UTSW |
7 |
87,780,069 (GRCm39) |
missense |
probably benign |
0.14 |
R7927:Grm5
|
UTSW |
7 |
87,685,382 (GRCm39) |
missense |
probably benign |
0.16 |
R7967:Grm5
|
UTSW |
7 |
87,624,569 (GRCm39) |
missense |
probably damaging |
0.99 |
R8260:Grm5
|
UTSW |
7 |
87,724,340 (GRCm39) |
critical splice donor site |
probably null |
|
R8345:Grm5
|
UTSW |
7 |
87,723,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R8460:Grm5
|
UTSW |
7 |
87,252,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R8473:Grm5
|
UTSW |
7 |
87,252,278 (GRCm39) |
missense |
probably damaging |
0.97 |
R8531:Grm5
|
UTSW |
7 |
87,779,724 (GRCm39) |
missense |
probably benign |
0.05 |
R8671:Grm5
|
UTSW |
7 |
87,765,498 (GRCm39) |
critical splice donor site |
probably null |
|
R8805:Grm5
|
UTSW |
7 |
87,453,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R9036:Grm5
|
UTSW |
7 |
87,685,397 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9106:Grm5
|
UTSW |
7 |
87,723,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R9136:Grm5
|
UTSW |
7 |
87,689,254 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9189:Grm5
|
UTSW |
7 |
87,724,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R9196:Grm5
|
UTSW |
7 |
87,723,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Grm5
|
UTSW |
7 |
87,723,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R9234:Grm5
|
UTSW |
7 |
87,723,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R9384:Grm5
|
UTSW |
7 |
87,723,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R9424:Grm5
|
UTSW |
7 |
87,765,484 (GRCm39) |
missense |
probably benign |
0.00 |
R9531:Grm5
|
UTSW |
7 |
87,780,075 (GRCm39) |
makesense |
probably null |
|
R9631:Grm5
|
UTSW |
7 |
87,624,560 (GRCm39) |
missense |
probably damaging |
0.98 |
R9691:Grm5
|
UTSW |
7 |
87,723,903 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Grm5
|
UTSW |
7 |
87,251,923 (GRCm39) |
missense |
probably damaging |
1.00 |
|