Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438H23Rik |
A |
G |
16: 90,852,515 (GRCm39) |
F207S |
probably damaging |
Het |
Abhd8 |
T |
A |
8: 71,910,718 (GRCm39) |
K363N |
probably benign |
Het |
Adam11 |
T |
A |
11: 102,667,399 (GRCm39) |
V653E |
probably damaging |
Het |
Adam18 |
T |
C |
8: 25,155,558 (GRCm39) |
S154G |
possibly damaging |
Het |
Adamts1 |
T |
C |
16: 85,595,591 (GRCm39) |
|
probably benign |
Het |
Afm |
G |
T |
5: 90,698,181 (GRCm39) |
V528L |
probably benign |
Het |
Alox12b |
C |
T |
11: 69,053,574 (GRCm39) |
H145Y |
probably benign |
Het |
Ankmy2 |
C |
A |
12: 36,220,434 (GRCm39) |
|
probably benign |
Het |
Aox3 |
G |
A |
1: 58,164,247 (GRCm39) |
|
probably benign |
Het |
Arhgap28 |
T |
C |
17: 68,171,583 (GRCm39) |
D396G |
probably damaging |
Het |
B430203G13Rik |
T |
C |
12: 17,974,489 (GRCm39) |
|
noncoding transcript |
Het |
Bean1 |
C |
T |
8: 104,943,807 (GRCm39) |
P121S |
probably damaging |
Het |
Bok |
T |
C |
1: 93,614,229 (GRCm39) |
S21P |
probably damaging |
Het |
Brwd1 |
A |
C |
16: 95,848,304 (GRCm39) |
N572K |
probably damaging |
Het |
C5ar1 |
A |
T |
7: 15,982,864 (GRCm39) |
V52E |
probably damaging |
Het |
Cblif |
G |
T |
19: 11,735,118 (GRCm39) |
C246F |
probably damaging |
Het |
Cdr2l |
C |
A |
11: 115,284,497 (GRCm39) |
P278T |
probably damaging |
Het |
Cnga4 |
T |
A |
7: 105,056,055 (GRCm39) |
I219N |
probably damaging |
Het |
Cpne2 |
C |
T |
8: 95,281,553 (GRCm39) |
|
probably benign |
Het |
D430041D05Rik |
A |
G |
2: 104,085,379 (GRCm39) |
S1057P |
possibly damaging |
Het |
Def8 |
G |
A |
8: 124,183,234 (GRCm39) |
A278T |
probably damaging |
Het |
Dgcr2 |
A |
G |
16: 17,676,306 (GRCm39) |
S152P |
probably damaging |
Het |
Dstyk |
A |
T |
1: 132,390,672 (GRCm39) |
D828V |
probably damaging |
Het |
Eml2 |
T |
C |
7: 18,937,877 (GRCm39) |
S582P |
probably damaging |
Het |
Engase |
T |
C |
11: 118,375,304 (GRCm39) |
Y359H |
possibly damaging |
Het |
Fat3 |
T |
C |
9: 15,918,073 (GRCm39) |
D1450G |
probably damaging |
Het |
Fbxw8 |
A |
T |
5: 118,208,552 (GRCm39) |
I467N |
probably damaging |
Het |
Fhdc1 |
A |
T |
3: 84,352,925 (GRCm39) |
Y767N |
probably damaging |
Het |
Flii |
T |
C |
11: 60,614,204 (GRCm39) |
D105G |
probably damaging |
Het |
Gaa |
C |
T |
11: 119,169,716 (GRCm39) |
T590I |
probably benign |
Het |
Gabrr1 |
T |
A |
4: 33,160,224 (GRCm39) |
S303T |
probably damaging |
Het |
Garre1 |
T |
C |
7: 33,945,382 (GRCm39) |
I499M |
probably damaging |
Het |
Glp1r |
A |
G |
17: 31,143,551 (GRCm39) |
I196V |
probably benign |
Het |
Helz2 |
A |
C |
2: 180,874,062 (GRCm39) |
L2144R |
probably damaging |
Het |
Itpr1 |
A |
T |
6: 108,465,443 (GRCm39) |
|
probably benign |
Het |
Kcns1 |
A |
T |
2: 164,006,875 (GRCm39) |
S363T |
possibly damaging |
Het |
Kif13a |
A |
T |
13: 46,947,419 (GRCm39) |
V855E |
probably damaging |
Het |
Krt42 |
T |
C |
11: 100,153,985 (GRCm39) |
T424A |
possibly damaging |
Het |
Lct |
A |
T |
1: 128,212,860 (GRCm39) |
F1931Y |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 41,159,251 (GRCm39) |
V1563E |
probably damaging |
Het |
Lrrc37 |
C |
A |
11: 103,508,873 (GRCm39) |
|
probably benign |
Het |
Lzts2 |
T |
C |
19: 45,014,626 (GRCm39) |
|
probably benign |
Het |
Mamdc4 |
C |
T |
2: 25,456,932 (GRCm39) |
R615Q |
possibly damaging |
Het |
Mei1 |
C |
T |
15: 81,956,170 (GRCm39) |
Q133* |
probably null |
Het |
Mif4gd |
T |
C |
11: 115,499,291 (GRCm39) |
E197G |
probably damaging |
Het |
Ncdn |
A |
T |
4: 126,640,462 (GRCm39) |
S544T |
probably benign |
Het |
Nfat5 |
C |
T |
8: 108,065,707 (GRCm39) |
R156W |
probably damaging |
Het |
Or52a5 |
T |
A |
7: 103,426,970 (GRCm39) |
D194V |
probably damaging |
Het |
Padi6 |
T |
C |
4: 140,464,663 (GRCm39) |
T114A |
probably benign |
Het |
Pigk |
G |
T |
3: 152,450,343 (GRCm39) |
|
probably benign |
Het |
Pkd1 |
T |
A |
17: 24,784,045 (GRCm39) |
F197Y |
possibly damaging |
Het |
Pld5 |
A |
T |
1: 175,798,155 (GRCm39) |
F415I |
probably damaging |
Het |
Pnpla5 |
A |
G |
15: 83,998,150 (GRCm39) |
L364P |
probably damaging |
Het |
Prrc2c |
G |
A |
1: 162,543,052 (GRCm39) |
|
probably benign |
Het |
Rab32 |
C |
T |
10: 10,426,584 (GRCm39) |
D121N |
probably damaging |
Het |
Rab44 |
A |
T |
17: 29,357,106 (GRCm39) |
T79S |
probably benign |
Het |
Reln |
G |
T |
5: 22,333,647 (GRCm39) |
N258K |
probably damaging |
Het |
Retsat |
A |
G |
6: 72,579,755 (GRCm39) |
T177A |
probably damaging |
Het |
Serpinf2 |
T |
A |
11: 75,327,219 (GRCm39) |
H236L |
probably damaging |
Het |
Slc26a6 |
A |
T |
9: 108,737,794 (GRCm39) |
|
probably benign |
Het |
Slitrk1 |
T |
A |
14: 109,149,061 (GRCm39) |
E550V |
probably benign |
Het |
Smarcd3 |
A |
T |
5: 24,800,497 (GRCm39) |
|
probably benign |
Het |
Spdye4a |
A |
C |
5: 143,210,857 (GRCm39) |
|
probably null |
Het |
Susd2 |
C |
T |
10: 75,474,348 (GRCm39) |
G572D |
probably damaging |
Het |
Tcaf3 |
C |
T |
6: 42,566,692 (GRCm39) |
R799K |
probably benign |
Het |
Tg |
A |
G |
15: 66,566,719 (GRCm39) |
S1256G |
probably benign |
Het |
Them4 |
A |
T |
3: 94,230,877 (GRCm39) |
|
probably benign |
Het |
Tmem210 |
C |
T |
2: 25,178,480 (GRCm39) |
A47V |
probably damaging |
Het |
Tnfrsf1b |
A |
G |
4: 144,955,616 (GRCm39) |
Y47H |
probably benign |
Het |
Tnik |
T |
G |
3: 28,661,394 (GRCm39) |
N598K |
possibly damaging |
Het |
Ttc3 |
A |
G |
16: 94,263,127 (GRCm39) |
N1498D |
possibly damaging |
Het |
Ttll4 |
C |
A |
1: 74,719,087 (GRCm39) |
H313N |
possibly damaging |
Het |
Vipr2 |
A |
G |
12: 116,106,447 (GRCm39) |
I348V |
probably benign |
Het |
Vps13a |
A |
G |
19: 16,758,129 (GRCm39) |
V2A |
probably damaging |
Het |
Vps72 |
G |
A |
3: 95,026,508 (GRCm39) |
R151K |
probably damaging |
Het |
Zfp106 |
A |
G |
2: 120,350,968 (GRCm39) |
V1561A |
probably damaging |
Het |
Zfp658 |
C |
A |
7: 43,223,019 (GRCm39) |
Y431* |
probably null |
Het |
Zkscan2 |
T |
C |
7: 123,079,864 (GRCm39) |
K698E |
possibly damaging |
Het |
|
Other mutations in Grm6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00432:Grm6
|
APN |
11 |
50,754,124 (GRCm39) |
splice site |
probably benign |
|
IGL01305:Grm6
|
APN |
11 |
50,750,346 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02121:Grm6
|
APN |
11 |
50,750,483 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02413:Grm6
|
APN |
11 |
50,750,766 (GRCm39) |
missense |
probably damaging |
0.99 |
ANU22:Grm6
|
UTSW |
11 |
50,750,346 (GRCm39) |
missense |
probably benign |
0.27 |
R0089:Grm6
|
UTSW |
11 |
50,750,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R0147:Grm6
|
UTSW |
11 |
50,750,144 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1498:Grm6
|
UTSW |
11 |
50,748,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R1577:Grm6
|
UTSW |
11 |
50,753,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R1666:Grm6
|
UTSW |
11 |
50,750,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R2923:Grm6
|
UTSW |
11 |
50,755,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R4060:Grm6
|
UTSW |
11 |
50,744,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R4486:Grm6
|
UTSW |
11 |
50,750,816 (GRCm39) |
missense |
probably damaging |
0.99 |
R4488:Grm6
|
UTSW |
11 |
50,750,816 (GRCm39) |
missense |
probably damaging |
0.99 |
R4489:Grm6
|
UTSW |
11 |
50,750,816 (GRCm39) |
missense |
probably damaging |
0.99 |
R4646:Grm6
|
UTSW |
11 |
50,748,033 (GRCm39) |
missense |
probably benign |
0.03 |
R4701:Grm6
|
UTSW |
11 |
50,753,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Grm6
|
UTSW |
11 |
50,748,104 (GRCm39) |
missense |
probably benign |
0.00 |
R4860:Grm6
|
UTSW |
11 |
50,755,439 (GRCm39) |
missense |
probably benign |
0.31 |
R5603:Grm6
|
UTSW |
11 |
50,747,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R6104:Grm6
|
UTSW |
11 |
50,750,144 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6746:Grm6
|
UTSW |
11 |
50,747,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R6791:Grm6
|
UTSW |
11 |
50,750,601 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6802:Grm6
|
UTSW |
11 |
50,744,216 (GRCm39) |
missense |
probably benign |
0.24 |
R6856:Grm6
|
UTSW |
11 |
50,750,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R7102:Grm6
|
UTSW |
11 |
50,753,804 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7221:Grm6
|
UTSW |
11 |
50,753,870 (GRCm39) |
missense |
probably damaging |
0.97 |
R7727:Grm6
|
UTSW |
11 |
50,742,369 (GRCm39) |
missense |
probably benign |
0.02 |
R7783:Grm6
|
UTSW |
11 |
50,753,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R7876:Grm6
|
UTSW |
11 |
50,750,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R8006:Grm6
|
UTSW |
11 |
50,755,484 (GRCm39) |
makesense |
probably null |
|
R8985:Grm6
|
UTSW |
11 |
50,746,537 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9666:Grm6
|
UTSW |
11 |
50,750,877 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Grm6
|
UTSW |
11 |
50,753,922 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Grm6
|
UTSW |
11 |
50,750,364 (GRCm39) |
missense |
probably benign |
0.43 |
Z1177:Grm6
|
UTSW |
11 |
50,750,694 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Grm6
|
UTSW |
11 |
50,742,327 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Grm6
|
UTSW |
11 |
50,742,089 (GRCm39) |
missense |
probably benign |
0.40 |
|