Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
C |
T |
3: 137,771,419 (GRCm39) |
R203* |
probably null |
Het |
Acp6 |
T |
C |
3: 97,083,054 (GRCm39) |
L355P |
probably damaging |
Het |
Aebp2 |
T |
C |
6: 140,579,464 (GRCm39) |
S234P |
probably damaging |
Het |
Anapc7 |
A |
G |
5: 122,577,567 (GRCm39) |
D374G |
probably benign |
Het |
Apob |
A |
T |
12: 8,051,039 (GRCm39) |
I1088F |
probably damaging |
Het |
Arid4b |
T |
C |
13: 14,307,021 (GRCm39) |
V92A |
probably damaging |
Het |
Armc3 |
T |
C |
2: 19,297,953 (GRCm39) |
Y575H |
probably damaging |
Het |
Asxl2 |
G |
T |
12: 3,534,558 (GRCm39) |
G252* |
probably null |
Het |
Atl1 |
A |
T |
12: 70,010,102 (GRCm39) |
K556M |
probably damaging |
Het |
AU018091 |
A |
G |
7: 3,212,104 (GRCm39) |
V206A |
probably benign |
Het |
Bcas1 |
A |
T |
2: 170,212,397 (GRCm39) |
D383E |
possibly damaging |
Het |
Bmx |
A |
G |
X: 163,015,192 (GRCm39) |
W257R |
probably benign |
Het |
Bpifb6 |
T |
C |
2: 153,747,270 (GRCm39) |
|
probably null |
Het |
Cacna1b |
G |
A |
2: 24,622,318 (GRCm39) |
P222L |
probably damaging |
Het |
Cand1 |
A |
G |
10: 119,045,972 (GRCm39) |
S978P |
probably damaging |
Het |
Cap2 |
T |
A |
13: 46,791,357 (GRCm39) |
Y175N |
possibly damaging |
Het |
Caps2 |
G |
A |
10: 112,036,591 (GRCm39) |
A384T |
probably benign |
Het |
Catsperg2 |
A |
T |
7: 29,420,470 (GRCm39) |
Y223* |
probably null |
Het |
Cd81 |
G |
T |
7: 142,620,938 (GRCm39) |
G206* |
probably null |
Het |
Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
Cdkn2aip |
G |
T |
8: 48,165,211 (GRCm39) |
N167K |
probably benign |
Het |
Ceacam14 |
T |
A |
7: 17,549,290 (GRCm39) |
L227* |
probably null |
Het |
Ceacam5 |
A |
T |
7: 17,491,805 (GRCm39) |
D725V |
probably damaging |
Het |
Cldn34a |
A |
T |
X: 151,346,841 (GRCm39) |
H171L |
probably benign |
Het |
Col18a1 |
T |
C |
10: 76,916,988 (GRCm39) |
I114V |
unknown |
Het |
Cp |
A |
G |
3: 20,033,177 (GRCm39) |
D667G |
probably damaging |
Het |
Cr2 |
G |
A |
1: 194,836,458 (GRCm39) |
P1278S |
possibly damaging |
Het |
Crat |
A |
G |
2: 30,295,060 (GRCm39) |
Y452H |
possibly damaging |
Het |
Cyp4f13 |
T |
A |
17: 33,144,542 (GRCm39) |
H318L |
probably damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dmbt1 |
A |
G |
7: 130,660,018 (GRCm39) |
N527S |
probably damaging |
Het |
Fcgbpl1 |
A |
T |
7: 27,853,785 (GRCm39) |
D1583V |
probably damaging |
Het |
Fgb |
G |
T |
3: 82,951,560 (GRCm39) |
Y256* |
probably null |
Het |
Frmd3 |
T |
A |
4: 74,105,676 (GRCm39) |
S441T |
probably damaging |
Het |
Gm14190 |
G |
T |
11: 99,581,431 (GRCm39) |
Q46K |
unknown |
Het |
Golt1b |
T |
A |
6: 142,338,080 (GRCm39) |
F17Y |
probably damaging |
Het |
Gsdmc |
A |
G |
15: 63,673,748 (GRCm39) |
I179T |
probably benign |
Het |
Gsdmc2 |
T |
A |
15: 63,700,086 (GRCm39) |
M229L |
probably benign |
Het |
Gulp1 |
A |
C |
1: 44,805,274 (GRCm39) |
N121T |
possibly damaging |
Het |
Ift122 |
T |
A |
6: 115,901,328 (GRCm39) |
F1037I |
probably damaging |
Het |
Ildr1 |
A |
T |
16: 36,536,568 (GRCm39) |
Y199F |
probably damaging |
Het |
Ints2 |
T |
A |
11: 86,139,760 (GRCm39) |
H278L |
possibly damaging |
Het |
Invs |
T |
C |
4: 48,392,599 (GRCm39) |
V271A |
possibly damaging |
Het |
Kcnj2 |
T |
C |
11: 110,963,709 (GRCm39) |
I367T |
probably benign |
Het |
Kif21b |
T |
C |
1: 136,089,508 (GRCm39) |
S1115P |
probably damaging |
Het |
Lce1k |
A |
T |
3: 92,714,125 (GRCm39) |
C20S |
unknown |
Het |
Lcmt2 |
C |
A |
2: 120,970,762 (GRCm39) |
R107L |
probably benign |
Het |
Letm1 |
A |
AG |
5: 33,926,859 (GRCm39) |
|
probably null |
Het |
Lrrc9 |
A |
C |
12: 72,544,635 (GRCm39) |
R71S |
probably damaging |
Het |
Mcc |
C |
A |
18: 44,624,382 (GRCm39) |
E213* |
probably null |
Het |
Mis18bp1 |
T |
C |
12: 65,205,468 (GRCm39) |
T235A |
probably benign |
Het |
Mta2 |
C |
T |
19: 8,919,696 (GRCm39) |
|
probably benign |
Het |
Nebl |
T |
A |
2: 17,457,321 (GRCm39) |
I80F |
probably damaging |
Het |
Nek10 |
A |
G |
14: 14,860,764 (GRCm38) |
T467A |
probably benign |
Het |
Nexn |
A |
T |
3: 151,958,576 (GRCm39) |
F106I |
probably damaging |
Het |
Nrdc |
T |
A |
4: 108,896,972 (GRCm39) |
Y282* |
probably null |
Het |
Nxf3 |
G |
A |
X: 134,976,583 (GRCm39) |
P380S |
possibly damaging |
Het |
Oma1 |
C |
T |
4: 103,178,971 (GRCm39) |
T208I |
probably damaging |
Het |
Or1a1 |
T |
C |
11: 74,086,989 (GRCm39) |
V220A |
probably damaging |
Het |
Or4c31 |
A |
G |
2: 88,291,686 (GRCm39) |
M1V |
probably null |
Het |
Or4d10c |
C |
A |
19: 12,065,620 (GRCm39) |
V179F |
probably damaging |
Het |
Or4p21 |
A |
G |
2: 88,277,033 (GRCm39) |
L83P |
probably damaging |
Het |
Or51a42 |
A |
T |
7: 103,708,335 (GRCm39) |
I158N |
possibly damaging |
Het |
Or52l1 |
A |
T |
7: 104,830,221 (GRCm39) |
C115S |
probably damaging |
Het |
Or5p66 |
C |
A |
7: 107,885,566 (GRCm39) |
G256* |
probably null |
Het |
Or5p70 |
A |
G |
7: 107,995,041 (GRCm39) |
Y238C |
probably benign |
Het |
Panx2 |
A |
T |
15: 88,953,941 (GRCm39) |
Y632F |
possibly damaging |
Het |
Pdia4 |
T |
C |
6: 47,773,589 (GRCm39) |
T587A |
probably benign |
Het |
Piezo2 |
A |
T |
18: 63,207,733 (GRCm39) |
L1426Q |
probably null |
Het |
Pigk |
T |
A |
3: 152,450,131 (GRCm39) |
Y212N |
probably damaging |
Het |
Pramel22 |
T |
A |
4: 143,380,838 (GRCm39) |
Y395F |
probably damaging |
Het |
Prl3b1 |
C |
T |
13: 27,429,775 (GRCm39) |
T71I |
possibly damaging |
Het |
Rab3gap1 |
A |
G |
1: 127,870,166 (GRCm39) |
E929G |
possibly damaging |
Het |
Rabl3 |
T |
C |
16: 37,384,079 (GRCm39) |
I162T |
probably benign |
Het |
Rasgrf2 |
T |
A |
13: 92,172,473 (GRCm39) |
T188S |
probably damaging |
Het |
Slc12a2 |
A |
G |
18: 58,043,358 (GRCm39) |
I601V |
possibly damaging |
Het |
Slc25a42 |
A |
T |
8: 70,644,519 (GRCm39) |
I60N |
probably benign |
Het |
Slc2a3 |
C |
T |
6: 122,713,694 (GRCm39) |
G173S |
probably damaging |
Het |
Slc46a3 |
G |
A |
5: 147,823,404 (GRCm39) |
T146M |
probably damaging |
Het |
Specc1 |
C |
A |
11: 61,920,120 (GRCm39) |
P7T |
possibly damaging |
Het |
Sptbn4 |
T |
C |
7: 27,123,235 (GRCm39) |
D229G |
probably benign |
Het |
Sspo |
T |
C |
6: 48,427,984 (GRCm39) |
I154T |
probably benign |
Het |
Stx5a |
T |
C |
19: 8,726,254 (GRCm39) |
|
probably null |
Het |
Stxbp6 |
A |
T |
12: 44,902,640 (GRCm39) |
C210* |
probably null |
Het |
Tagap1 |
C |
T |
17: 7,224,285 (GRCm39) |
R137Q |
probably benign |
Het |
Tbc1d9 |
A |
G |
8: 83,997,932 (GRCm39) |
Y1163C |
probably damaging |
Het |
Tex14 |
T |
G |
11: 87,440,296 (GRCm39) |
L1367R |
probably damaging |
Het |
Tnnt3 |
C |
T |
7: 142,065,262 (GRCm39) |
R131C |
possibly damaging |
Het |
Tpx2 |
T |
A |
2: 152,732,544 (GRCm39) |
M606K |
probably benign |
Het |
Trim46 |
A |
T |
3: 89,145,008 (GRCm39) |
Y489N |
probably damaging |
Het |
Ttc28 |
C |
T |
5: 111,424,188 (GRCm39) |
S1485L |
probably benign |
Het |
Txnl1 |
T |
C |
18: 63,812,585 (GRCm39) |
T70A |
probably benign |
Het |
Unc80 |
T |
C |
1: 66,731,708 (GRCm39) |
L3053P |
probably damaging |
Het |
Wars1 |
G |
T |
12: 108,854,359 (GRCm39) |
N18K |
possibly damaging |
Het |
Wnt8a |
A |
G |
18: 34,677,937 (GRCm39) |
D115G |
probably damaging |
Het |
Xndc1 |
T |
A |
7: 101,722,398 (GRCm39) |
V21E |
probably damaging |
Het |
Zfp493 |
T |
A |
13: 67,934,388 (GRCm39) |
C114S |
probably damaging |
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 |
|
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 |
|
R7656: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 |
|
|