Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930568D16Rik |
T |
A |
2: 35,244,811 (GRCm39) |
E180D |
probably damaging |
Het |
Add3 |
A |
G |
19: 53,232,720 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
A |
T |
13: 81,590,620 (GRCm39) |
I4396N |
probably damaging |
Het |
Apc |
C |
T |
18: 34,450,199 (GRCm39) |
S2331L |
possibly damaging |
Het |
Apoh |
G |
T |
11: 108,286,729 (GRCm39) |
C51F |
probably damaging |
Het |
Arid4b |
T |
C |
13: 14,317,648 (GRCm39) |
V177A |
possibly damaging |
Het |
Atp13a1 |
T |
A |
8: 70,249,935 (GRCm39) |
I343N |
probably damaging |
Het |
Bcar1 |
T |
C |
8: 112,440,032 (GRCm39) |
D654G |
probably benign |
Het |
Brox |
T |
C |
1: 183,064,072 (GRCm39) |
K245R |
probably damaging |
Het |
Ccdc146 |
A |
T |
5: 21,524,577 (GRCm39) |
S258R |
possibly damaging |
Het |
Ccdc169 |
A |
C |
3: 55,047,562 (GRCm39) |
K18Q |
probably damaging |
Het |
Cenps |
C |
A |
4: 149,214,658 (GRCm39) |
|
probably benign |
Het |
Crot |
C |
A |
5: 9,019,120 (GRCm39) |
E478* |
probably null |
Het |
Dgkq |
A |
T |
5: 108,802,236 (GRCm39) |
M443K |
probably damaging |
Het |
Dhx32 |
A |
T |
7: 133,339,057 (GRCm39) |
L326Q |
probably damaging |
Het |
Dtwd1 |
A |
G |
2: 126,000,342 (GRCm39) |
I93V |
probably benign |
Het |
Ehmt2 |
C |
T |
17: 35,118,357 (GRCm39) |
T44I |
probably benign |
Het |
Enc1 |
T |
C |
13: 97,381,765 (GRCm39) |
S92P |
probably benign |
Het |
Epha5 |
T |
C |
5: 84,479,051 (GRCm39) |
|
probably benign |
Het |
Eya4 |
T |
A |
10: 23,031,892 (GRCm39) |
S244C |
probably damaging |
Het |
Fmnl3 |
G |
A |
15: 99,223,791 (GRCm39) |
R302W |
probably damaging |
Het |
Fscn3 |
A |
T |
6: 28,436,173 (GRCm39) |
I490F |
possibly damaging |
Het |
Galntl6 |
A |
G |
8: 58,415,436 (GRCm39) |
V239A |
probably benign |
Het |
Glg1 |
T |
C |
8: 111,892,323 (GRCm39) |
I841V |
possibly damaging |
Het |
Gm15455 |
T |
C |
1: 33,876,893 (GRCm39) |
|
noncoding transcript |
Het |
Gpd1l |
C |
T |
9: 114,743,473 (GRCm39) |
M142I |
probably benign |
Het |
Helb |
A |
G |
10: 119,927,653 (GRCm39) |
V819A |
possibly damaging |
Het |
Hnrnpul2 |
T |
G |
19: 8,802,255 (GRCm39) |
F374C |
probably damaging |
Het |
Hoxc10 |
G |
A |
15: 102,875,753 (GRCm39) |
S154N |
possibly damaging |
Het |
Ice2 |
A |
T |
9: 69,319,651 (GRCm39) |
T367S |
possibly damaging |
Het |
Iqca1 |
A |
T |
1: 90,067,819 (GRCm39) |
|
probably null |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Klhl14 |
T |
A |
18: 21,784,677 (GRCm39) |
H250L |
probably damaging |
Het |
Kmt2c |
A |
T |
5: 25,535,801 (GRCm39) |
D1447E |
probably benign |
Het |
Larp1 |
G |
T |
11: 57,940,765 (GRCm39) |
M630I |
probably benign |
Het |
Lrp2 |
A |
G |
2: 69,326,667 (GRCm39) |
|
probably null |
Het |
Map4k3 |
G |
T |
17: 80,911,427 (GRCm39) |
Q673K |
probably benign |
Het |
Mettl16 |
A |
G |
11: 74,686,823 (GRCm39) |
N201D |
possibly damaging |
Het |
Mrpl15 |
C |
A |
1: 4,855,956 (GRCm39) |
|
probably benign |
Het |
Mthfd1l |
T |
A |
10: 3,998,222 (GRCm39) |
V655D |
probably damaging |
Het |
Odf1 |
T |
C |
15: 38,226,531 (GRCm39) |
Y144H |
probably damaging |
Het |
Or2f1b |
G |
T |
6: 42,739,493 (GRCm39) |
C169F |
probably damaging |
Het |
Or5t5 |
G |
T |
2: 86,616,571 (GRCm39) |
V166L |
probably benign |
Het |
Padi1 |
T |
C |
4: 140,542,140 (GRCm39) |
Y594C |
probably damaging |
Het |
Palm3 |
T |
A |
8: 84,756,049 (GRCm39) |
D520E |
probably benign |
Het |
Paox |
G |
A |
7: 139,707,567 (GRCm39) |
C130Y |
probably damaging |
Het |
Parpbp |
T |
A |
10: 87,975,769 (GRCm39) |
S115C |
probably damaging |
Het |
Pcnx3 |
A |
G |
19: 5,721,708 (GRCm39) |
V1438A |
possibly damaging |
Het |
Pdlim2 |
T |
A |
14: 70,405,229 (GRCm39) |
D212V |
probably benign |
Het |
Pi4ka |
A |
G |
16: 17,121,006 (GRCm39) |
F53L |
probably damaging |
Het |
Pik3c2a |
A |
T |
7: 115,967,419 (GRCm39) |
D839E |
probably damaging |
Het |
Pou2f1 |
T |
C |
1: 165,710,625 (GRCm39) |
|
probably benign |
Het |
Ppl |
A |
T |
16: 4,906,492 (GRCm39) |
Y1268N |
probably benign |
Het |
Prelid3a |
C |
T |
18: 67,598,011 (GRCm39) |
S6L |
probably benign |
Het |
Ptk2 |
T |
G |
15: 73,175,682 (GRCm39) |
D285A |
possibly damaging |
Het |
Rasd2 |
T |
G |
8: 75,948,811 (GRCm39) |
Y246D |
probably damaging |
Het |
Rhobtb1 |
T |
A |
10: 69,106,085 (GRCm39) |
F217I |
probably damaging |
Het |
Serhl |
T |
C |
15: 82,987,237 (GRCm39) |
|
probably benign |
Het |
Sh3tc2 |
A |
G |
18: 62,123,078 (GRCm39) |
E613G |
probably damaging |
Het |
Slc26a3 |
A |
G |
12: 31,502,714 (GRCm39) |
|
probably benign |
Het |
Steap4 |
T |
C |
5: 8,025,769 (GRCm39) |
I110T |
probably benign |
Het |
Syde1 |
C |
A |
10: 78,425,150 (GRCm39) |
R287L |
possibly damaging |
Het |
Tmem184c |
C |
T |
8: 78,325,291 (GRCm39) |
|
probably null |
Het |
Trmt44 |
C |
A |
5: 35,730,032 (GRCm39) |
|
probably benign |
Het |
Ttbk2 |
G |
T |
2: 120,603,764 (GRCm39) |
S256R |
probably benign |
Het |
Ttll6 |
A |
T |
11: 96,036,336 (GRCm39) |
I322F |
probably damaging |
Het |
Ubap2 |
A |
T |
4: 41,205,753 (GRCm39) |
|
probably null |
Het |
Wsb2 |
A |
T |
5: 117,515,600 (GRCm39) |
T402S |
probably damaging |
Het |
|
Other mutations in Rhbdl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01389:Rhbdl2
|
APN |
4 |
123,723,450 (GRCm39) |
missense |
probably benign |
|
IGL02111:Rhbdl2
|
APN |
4 |
123,716,630 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03381:Rhbdl2
|
APN |
4 |
123,716,610 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03410:Rhbdl2
|
APN |
4 |
123,723,463 (GRCm39) |
nonsense |
probably null |
|
R0039:Rhbdl2
|
UTSW |
4 |
123,703,822 (GRCm39) |
missense |
probably benign |
0.02 |
R1292:Rhbdl2
|
UTSW |
4 |
123,723,435 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2024:Rhbdl2
|
UTSW |
4 |
123,720,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R2120:Rhbdl2
|
UTSW |
4 |
123,718,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R4364:Rhbdl2
|
UTSW |
4 |
123,703,728 (GRCm39) |
start codon destroyed |
probably null |
0.87 |
R4366:Rhbdl2
|
UTSW |
4 |
123,703,728 (GRCm39) |
start codon destroyed |
probably null |
0.87 |
R4413:Rhbdl2
|
UTSW |
4 |
123,703,880 (GRCm39) |
missense |
probably benign |
0.04 |
R4749:Rhbdl2
|
UTSW |
4 |
123,720,694 (GRCm39) |
critical splice donor site |
probably null |
|
R5069:Rhbdl2
|
UTSW |
4 |
123,711,710 (GRCm39) |
nonsense |
probably null |
|
R5303:Rhbdl2
|
UTSW |
4 |
123,704,014 (GRCm39) |
intron |
probably benign |
|
R7147:Rhbdl2
|
UTSW |
4 |
123,703,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R7171:Rhbdl2
|
UTSW |
4 |
123,708,049 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7337:Rhbdl2
|
UTSW |
4 |
123,711,659 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7374:Rhbdl2
|
UTSW |
4 |
123,711,658 (GRCm39) |
missense |
probably benign |
0.01 |
R7411:Rhbdl2
|
UTSW |
4 |
123,723,435 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7718:Rhbdl2
|
UTSW |
4 |
123,718,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R8152:Rhbdl2
|
UTSW |
4 |
123,718,711 (GRCm39) |
missense |
probably benign |
0.13 |
|