Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abitram |
A |
G |
4: 56,804,218 (GRCm39) |
I78V |
probably benign |
Het |
Acot2 |
A |
G |
12: 84,039,691 (GRCm39) |
Y400C |
probably benign |
Het |
Agbl1 |
A |
G |
7: 76,059,080 (GRCm39) |
M237V |
|
Het |
Atrnl1 |
C |
A |
19: 57,599,811 (GRCm39) |
S9* |
probably null |
Het |
BC031181 |
A |
T |
18: 75,142,406 (GRCm39) |
K71* |
probably null |
Het |
Bmal2 |
A |
G |
6: 146,707,940 (GRCm39) |
T21A |
probably benign |
Het |
Brpf1 |
A |
T |
6: 113,291,835 (GRCm39) |
M294L |
probably benign |
Het |
Camk2g |
T |
G |
14: 20,789,410 (GRCm39) |
D382A |
possibly damaging |
Het |
Ccdc33 |
T |
A |
9: 58,025,748 (GRCm39) |
R94W |
probably damaging |
Het |
Cd244a |
T |
A |
1: 171,404,823 (GRCm39) |
L225Q |
probably damaging |
Het |
Chsy1 |
G |
T |
7: 65,820,778 (GRCm39) |
V338F |
probably damaging |
Het |
Col14a1 |
A |
G |
15: 55,225,846 (GRCm39) |
I170V |
unknown |
Het |
Col6a2 |
G |
T |
10: 76,443,590 (GRCm39) |
Q492K |
probably benign |
Het |
Dnah12 |
G |
T |
14: 26,581,273 (GRCm39) |
V3168L |
probably benign |
Het |
Dnah7a |
T |
C |
1: 53,535,164 (GRCm39) |
S2699G |
possibly damaging |
Het |
Efhc1 |
A |
G |
1: 21,031,281 (GRCm39) |
|
probably null |
Het |
Fsip2 |
A |
G |
2: 82,807,886 (GRCm39) |
K1402E |
possibly damaging |
Het |
Ghdc |
C |
T |
11: 100,660,493 (GRCm39) |
A127T |
probably benign |
Het |
Gm19410 |
A |
T |
8: 36,276,253 (GRCm39) |
M1637L |
probably benign |
Het |
Grm5 |
T |
G |
7: 87,779,459 (GRCm39) |
D998E |
probably benign |
Het |
Krtcap3 |
A |
G |
5: 31,409,904 (GRCm39) |
T157A |
probably damaging |
Het |
Ltf |
A |
T |
9: 110,853,462 (GRCm39) |
K18* |
probably null |
Het |
Luc7l2 |
A |
G |
6: 38,580,399 (GRCm39) |
R333G |
unknown |
Het |
Mdc1 |
T |
G |
17: 36,161,773 (GRCm39) |
S895R |
probably benign |
Het |
Mef2a |
G |
A |
7: 66,945,142 (GRCm39) |
T80M |
probably damaging |
Het |
Mitd1 |
T |
A |
1: 37,924,356 (GRCm39) |
I65F |
probably benign |
Het |
Mms19 |
A |
G |
19: 41,933,011 (GRCm39) |
L1026P |
probably damaging |
Het |
Mtbp |
G |
T |
15: 55,472,922 (GRCm39) |
V629L |
unknown |
Het |
Ncapd3 |
T |
A |
9: 26,966,801 (GRCm39) |
I545N |
possibly damaging |
Het |
Nin |
G |
A |
12: 70,089,542 (GRCm39) |
T1291M |
|
Het |
Or10z1 |
T |
A |
1: 174,077,784 (GRCm39) |
K236N |
probably damaging |
Het |
Or5b123 |
A |
T |
19: 13,597,197 (GRCm39) |
I181F |
probably damaging |
Het |
Orc3 |
G |
T |
4: 34,587,032 (GRCm39) |
C352* |
probably null |
Het |
Oxct2b |
G |
A |
4: 123,011,550 (GRCm39) |
G490D |
probably benign |
Het |
Pcdhb16 |
A |
T |
18: 37,612,458 (GRCm39) |
T473S |
probably benign |
Het |
Phkg2 |
G |
A |
7: 127,182,074 (GRCm39) |
G365D |
probably damaging |
Het |
Pira1 |
T |
C |
7: 3,742,281 (GRCm39) |
E82G |
probably damaging |
Het |
Plekhd1 |
A |
G |
12: 80,768,934 (GRCm39) |
|
probably null |
Het |
Ppp2r3d |
A |
T |
9: 101,088,911 (GRCm39) |
F471I |
probably benign |
Het |
Prl3d1 |
T |
C |
13: 27,284,018 (GRCm39) |
C196R |
possibly damaging |
Het |
Prmt1 |
A |
T |
7: 44,633,552 (GRCm39) |
F14L |
probably benign |
Het |
Prox1 |
A |
G |
1: 189,894,418 (GRCm39) |
L9P |
probably damaging |
Het |
Ptpn13 |
T |
A |
5: 103,688,849 (GRCm39) |
F881I |
probably benign |
Het |
Rab3ip |
A |
G |
10: 116,750,044 (GRCm39) |
I363T |
probably benign |
Het |
Rapgef3 |
T |
C |
15: 97,659,090 (GRCm39) |
E134G |
probably damaging |
Het |
Rapgef6 |
C |
T |
11: 54,585,279 (GRCm39) |
P1559L |
probably benign |
Het |
Rnf180 |
T |
C |
13: 105,304,096 (GRCm39) |
K507E |
probably damaging |
Het |
Rpl3l |
T |
C |
17: 24,949,960 (GRCm39) |
I53T |
probably benign |
Het |
Rtl1 |
T |
C |
12: 109,557,442 (GRCm39) |
I1466V |
unknown |
Het |
Saxo2 |
A |
G |
7: 82,284,559 (GRCm39) |
Y100H |
probably damaging |
Het |
Selenoh |
G |
T |
2: 84,500,724 (GRCm39) |
R39S |
probably damaging |
Het |
Sgsm2 |
A |
G |
11: 74,756,323 (GRCm39) |
V342A |
probably damaging |
Het |
Slc26a9 |
T |
A |
1: 131,690,982 (GRCm39) |
F587I |
possibly damaging |
Het |
Smoc1 |
A |
T |
12: 81,152,682 (GRCm39) |
Q91L |
possibly damaging |
Het |
Spag9 |
A |
C |
11: 93,887,389 (GRCm39) |
H98P |
possibly damaging |
Het |
Spata31e3 |
T |
G |
13: 50,401,122 (GRCm39) |
K401N |
probably benign |
Het |
T2 |
T |
A |
17: 8,637,047 (GRCm39) |
C337* |
probably null |
Het |
Tbc1d19 |
A |
G |
5: 54,054,377 (GRCm39) |
Y455C |
probably damaging |
Het |
Thbd |
A |
G |
2: 148,249,340 (GRCm39) |
L176P |
probably damaging |
Het |
Tmem116 |
A |
G |
5: 121,590,252 (GRCm39) |
|
probably null |
Het |
Tmem25 |
C |
T |
9: 44,709,640 (GRCm39) |
V54I |
possibly damaging |
Het |
Trpm4 |
C |
T |
7: 44,971,233 (GRCm39) |
V378I |
probably benign |
Het |
Trrap |
G |
T |
5: 144,779,422 (GRCm39) |
W3129C |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,558,660 (GRCm39) |
D29740E |
probably damaging |
Het |
Vcan |
C |
T |
13: 89,833,233 (GRCm39) |
C3073Y |
probably damaging |
Het |
Xrra1 |
T |
A |
7: 99,560,189 (GRCm39) |
D388E |
probably benign |
Het |
|
Other mutations in Glp1r |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Glp1r
|
APN |
17 |
31,120,891 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL00516:Glp1r
|
APN |
17 |
31,144,532 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00653:Glp1r
|
APN |
17 |
31,149,734 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00917:Glp1r
|
APN |
17 |
31,138,443 (GRCm39) |
splice site |
probably benign |
|
IGL02005:Glp1r
|
APN |
17 |
31,143,585 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02411:Glp1r
|
APN |
17 |
31,143,485 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02889:Glp1r
|
APN |
17 |
31,150,118 (GRCm39) |
splice site |
probably benign |
|
IGL02928:Glp1r
|
APN |
17 |
31,137,911 (GRCm39) |
missense |
probably benign |
0.00 |
N/A:Glp1r
|
UTSW |
17 |
31,150,257 (GRCm39) |
missense |
probably damaging |
0.98 |
R0135:Glp1r
|
UTSW |
17 |
31,143,551 (GRCm39) |
missense |
probably benign |
0.00 |
R0395:Glp1r
|
UTSW |
17 |
31,155,312 (GRCm39) |
missense |
probably benign |
0.34 |
R0481:Glp1r
|
UTSW |
17 |
31,150,191 (GRCm39) |
missense |
probably benign |
0.03 |
R0602:Glp1r
|
UTSW |
17 |
31,128,201 (GRCm39) |
missense |
probably benign |
0.12 |
R0841:Glp1r
|
UTSW |
17 |
31,138,406 (GRCm39) |
missense |
probably benign |
0.01 |
R1145:Glp1r
|
UTSW |
17 |
31,138,406 (GRCm39) |
missense |
probably benign |
0.01 |
R1145:Glp1r
|
UTSW |
17 |
31,138,406 (GRCm39) |
missense |
probably benign |
0.01 |
R1232:Glp1r
|
UTSW |
17 |
31,137,905 (GRCm39) |
missense |
probably benign |
|
R1804:Glp1r
|
UTSW |
17 |
31,149,687 (GRCm39) |
splice site |
probably null |
|
R1846:Glp1r
|
UTSW |
17 |
31,148,909 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1982:Glp1r
|
UTSW |
17 |
31,144,601 (GRCm39) |
nonsense |
probably null |
|
R1990:Glp1r
|
UTSW |
17 |
31,149,722 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2091:Glp1r
|
UTSW |
17 |
31,144,523 (GRCm39) |
missense |
probably damaging |
0.97 |
R3432:Glp1r
|
UTSW |
17 |
31,143,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R4456:Glp1r
|
UTSW |
17 |
31,137,949 (GRCm39) |
nonsense |
probably null |
|
R4488:Glp1r
|
UTSW |
17 |
31,137,905 (GRCm39) |
missense |
probably benign |
|
R4610:Glp1r
|
UTSW |
17 |
31,150,221 (GRCm39) |
missense |
probably benign |
0.03 |
R4884:Glp1r
|
UTSW |
17 |
31,155,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Glp1r
|
UTSW |
17 |
31,137,861 (GRCm39) |
missense |
probably benign |
|
R6358:Glp1r
|
UTSW |
17 |
31,151,618 (GRCm39) |
missense |
probably benign |
0.07 |
R6359:Glp1r
|
UTSW |
17 |
31,148,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R6490:Glp1r
|
UTSW |
17 |
31,143,546 (GRCm39) |
missense |
probably damaging |
0.98 |
R6698:Glp1r
|
UTSW |
17 |
31,155,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R7063:Glp1r
|
UTSW |
17 |
31,144,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R7165:Glp1r
|
UTSW |
17 |
31,128,297 (GRCm39) |
missense |
probably benign |
0.23 |
R7293:Glp1r
|
UTSW |
17 |
31,143,599 (GRCm39) |
missense |
probably benign |
0.00 |
R7646:Glp1r
|
UTSW |
17 |
31,155,257 (GRCm39) |
missense |
probably benign |
0.38 |
R7655:Glp1r
|
UTSW |
17 |
31,149,572 (GRCm39) |
critical splice donor site |
probably null |
|
R7686:Glp1r
|
UTSW |
17 |
31,144,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R8531:Glp1r
|
UTSW |
17 |
31,143,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R9050:Glp1r
|
UTSW |
17 |
31,137,892 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Glp1r
|
UTSW |
17 |
31,138,437 (GRCm39) |
critical splice donor site |
probably null |
|
|