Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057N15Rik |
A |
G |
16: 88,570,498 (GRCm39) |
Y181H |
probably benign |
Het |
A530084C06Rik |
A |
G |
13: 31,742,813 (GRCm39) |
|
probably benign |
Het |
Adamtsl1 |
A |
G |
4: 86,274,592 (GRCm39) |
D1208G |
probably benign |
Het |
Ankrd55 |
T |
C |
13: 112,504,757 (GRCm39) |
F501S |
probably benign |
Het |
Aox1 |
G |
A |
1: 58,349,201 (GRCm39) |
D656N |
probably damaging |
Het |
Atr |
A |
T |
9: 95,781,218 (GRCm39) |
|
probably benign |
Het |
Bicra |
G |
A |
7: 15,706,173 (GRCm39) |
R1423W |
probably damaging |
Het |
Cabyr |
T |
A |
18: 12,884,073 (GRCm39) |
S187T |
probably benign |
Het |
Car5b |
G |
A |
X: 162,762,297 (GRCm39) |
R282C |
probably damaging |
Het |
Cdon |
A |
T |
9: 35,368,794 (GRCm39) |
T343S |
possibly damaging |
Het |
Cep350 |
C |
T |
1: 155,777,181 (GRCm39) |
|
probably null |
Het |
Cimap1a |
A |
G |
7: 140,428,728 (GRCm39) |
|
probably null |
Het |
Copa |
T |
C |
1: 171,949,254 (GRCm39) |
|
probably benign |
Het |
Cyp4f18 |
T |
C |
8: 72,749,854 (GRCm39) |
D265G |
probably benign |
Het |
Dgkb |
T |
A |
12: 38,654,157 (GRCm39) |
C759S |
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,021,757 (GRCm39) |
M3470V |
probably benign |
Het |
Eif4g2 |
T |
C |
7: 110,677,500 (GRCm39) |
N177S |
probably damaging |
Het |
Etfb |
C |
T |
7: 43,104,002 (GRCm39) |
Q145* |
probably null |
Het |
Flnb |
T |
A |
14: 7,912,943 (GRCm38) |
|
probably null |
Het |
G430095P16Rik |
G |
A |
8: 85,453,271 (GRCm39) |
|
probably benign |
Het |
Gfral |
A |
T |
9: 76,115,924 (GRCm39) |
S17T |
probably benign |
Het |
Greb1 |
T |
A |
12: 16,773,412 (GRCm39) |
T221S |
probably benign |
Het |
Haus5 |
A |
T |
7: 30,358,508 (GRCm39) |
S289T |
probably damaging |
Het |
Ighv6-4 |
T |
C |
12: 114,370,221 (GRCm39) |
Y77C |
probably damaging |
Het |
Il23r |
A |
T |
6: 67,400,685 (GRCm39) |
D548E |
probably benign |
Het |
Il23r |
A |
T |
6: 67,463,235 (GRCm39) |
F86Y |
possibly damaging |
Het |
Inppl1 |
A |
T |
7: 101,480,210 (GRCm39) |
M424K |
probably benign |
Het |
Jam3 |
A |
G |
9: 27,010,184 (GRCm39) |
Y267H |
probably damaging |
Het |
Lrrc37 |
T |
C |
11: 103,510,990 (GRCm39) |
N326S |
unknown |
Het |
Mms19 |
A |
T |
19: 41,951,857 (GRCm39) |
M160K |
probably damaging |
Het |
Muc2 |
CGTG |
CGTGTG |
7: 141,699,185 (GRCm38) |
|
probably null |
Het |
Mup5 |
A |
G |
4: 61,751,237 (GRCm39) |
L137P |
probably damaging |
Het |
Mylk |
G |
C |
16: 34,699,845 (GRCm39) |
E403Q |
possibly damaging |
Het |
Ntrk2 |
G |
A |
13: 59,022,184 (GRCm39) |
S413N |
probably damaging |
Het |
Nuak2 |
C |
A |
1: 132,259,941 (GRCm39) |
T573N |
probably benign |
Het |
Or4m1 |
A |
T |
14: 50,557,575 (GRCm39) |
I239K |
probably benign |
Het |
Or52h9 |
G |
A |
7: 104,202,563 (GRCm39) |
V146M |
probably benign |
Het |
Padi4 |
GCTGCGTACCTCCAC |
GC |
4: 140,475,760 (GRCm39) |
|
probably benign |
Het |
Pclo |
T |
A |
5: 14,842,086 (GRCm39) |
I4787N |
unknown |
Het |
Pde8a |
G |
T |
7: 80,973,878 (GRCm39) |
V612L |
probably benign |
Het |
Pear1 |
A |
T |
3: 87,696,107 (GRCm39) |
|
probably null |
Het |
Pgbd1 |
A |
G |
13: 21,607,688 (GRCm39) |
Y169H |
probably damaging |
Het |
Pkd1l1 |
A |
G |
11: 8,786,448 (GRCm39) |
|
probably benign |
Het |
Prkag3 |
C |
T |
1: 74,783,879 (GRCm39) |
|
probably null |
Het |
Rsph9 |
A |
T |
17: 46,455,050 (GRCm39) |
S9T |
possibly damaging |
Het |
Rxfp1 |
A |
T |
3: 79,612,876 (GRCm39) |
|
probably null |
Het |
Senp7 |
A |
G |
16: 55,996,189 (GRCm39) |
E756G |
probably damaging |
Het |
Serpina1e |
G |
T |
12: 103,915,450 (GRCm39) |
T252K |
probably benign |
Het |
Sipa1l1 |
T |
A |
12: 82,484,510 (GRCm39) |
S1555T |
probably benign |
Het |
Slain1 |
T |
C |
14: 103,932,711 (GRCm39) |
S432P |
probably damaging |
Het |
Slc37a2 |
A |
T |
9: 37,144,418 (GRCm39) |
|
probably null |
Het |
Thg1l |
C |
T |
11: 45,845,018 (GRCm39) |
R18Q |
probably damaging |
Het |
Tnn |
A |
G |
1: 159,943,907 (GRCm39) |
|
probably benign |
Het |
Trim32 |
G |
A |
4: 65,531,491 (GRCm39) |
R16Q |
probably damaging |
Het |
Tshz3 |
A |
G |
7: 36,470,842 (GRCm39) |
T944A |
probably damaging |
Het |
Ttn |
C |
G |
2: 76,684,774 (GRCm39) |
|
probably benign |
Het |
Ythdc2 |
T |
C |
18: 44,973,331 (GRCm39) |
S323P |
possibly damaging |
Het |
Zfp827 |
A |
G |
8: 79,786,939 (GRCm39) |
N35S |
probably damaging |
Het |
|
Other mutations in Gpr26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01065:Gpr26
|
APN |
7 |
131,569,230 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01345:Gpr26
|
APN |
7 |
131,569,161 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01658:Gpr26
|
APN |
7 |
131,585,834 (GRCm39) |
missense |
probably benign |
|
IGL02724:Gpr26
|
APN |
7 |
131,576,121 (GRCm39) |
critical splice donor site |
probably null |
|
R0408:Gpr26
|
UTSW |
7 |
131,576,001 (GRCm39) |
splice site |
probably null |
|
R0408:Gpr26
|
UTSW |
7 |
131,569,249 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2508:Gpr26
|
UTSW |
7 |
131,568,823 (GRCm39) |
missense |
probably damaging |
0.98 |
R4088:Gpr26
|
UTSW |
7 |
131,568,805 (GRCm39) |
missense |
probably benign |
0.00 |
R4630:Gpr26
|
UTSW |
7 |
131,568,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R4680:Gpr26
|
UTSW |
7 |
131,576,082 (GRCm39) |
missense |
probably benign |
0.34 |
R4756:Gpr26
|
UTSW |
7 |
131,569,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R5229:Gpr26
|
UTSW |
7 |
131,585,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R5610:Gpr26
|
UTSW |
7 |
131,568,694 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6605:Gpr26
|
UTSW |
7 |
131,585,893 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6653:Gpr26
|
UTSW |
7 |
131,585,830 (GRCm39) |
missense |
probably benign |
0.00 |
R7213:Gpr26
|
UTSW |
7 |
131,569,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R7351:Gpr26
|
UTSW |
7 |
131,576,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R7768:Gpr26
|
UTSW |
7 |
131,576,077 (GRCm39) |
missense |
probably damaging |
0.99 |
R7887:Gpr26
|
UTSW |
7 |
131,568,702 (GRCm39) |
missense |
probably benign |
|
R8822:Gpr26
|
UTSW |
7 |
131,568,997 (GRCm39) |
missense |
probably damaging |
0.98 |
R9382:Gpr26
|
UTSW |
7 |
131,568,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R9508:Gpr26
|
UTSW |
7 |
131,585,830 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Gpr26
|
UTSW |
7 |
131,585,823 (GRCm39) |
frame shift |
probably null |
|
Z1176:Gpr26
|
UTSW |
7 |
131,568,954 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Gpr26
|
UTSW |
7 |
131,568,777 (GRCm39) |
missense |
probably damaging |
1.00 |
|