Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
A |
G |
6: 121,623,788 (GRCm39) |
I385V |
probably benign |
Het |
Ablim2 |
A |
G |
5: 36,032,241 (GRCm39) |
D622G |
probably damaging |
Het |
Acsbg1 |
A |
T |
9: 54,549,946 (GRCm39) |
S86T |
probably damaging |
Het |
Adam34l |
T |
A |
8: 44,079,133 (GRCm39) |
I364L |
probably benign |
Het |
Ank2 |
A |
C |
3: 126,846,397 (GRCm39) |
D199E |
probably damaging |
Het |
Art2a |
T |
A |
7: 101,204,452 (GRCm39) |
M29L |
probably benign |
Het |
Bbs2 |
C |
A |
8: 94,824,863 (GRCm39) |
|
probably null |
Het |
Brwd1 |
A |
T |
16: 95,815,074 (GRCm39) |
I1402N |
probably damaging |
Het |
C1qtnf9 |
C |
A |
14: 61,017,069 (GRCm39) |
P200T |
possibly damaging |
Het |
Ciita |
T |
C |
16: 10,329,767 (GRCm39) |
Y684H |
probably damaging |
Het |
Dennd1c |
T |
C |
17: 57,373,272 (GRCm39) |
N734D |
probably benign |
Het |
Depdc1b |
A |
T |
13: 108,460,653 (GRCm39) |
I88F |
possibly damaging |
Het |
Dsg2 |
A |
G |
18: 20,723,274 (GRCm39) |
|
probably null |
Het |
Foxp2 |
A |
G |
6: 15,394,761 (GRCm39) |
T154A |
probably damaging |
Het |
Gmeb1 |
A |
T |
4: 131,969,688 (GRCm39) |
V95D |
possibly damaging |
Het |
Gmeb1 |
A |
G |
4: 131,973,324 (GRCm39) |
S62P |
probably benign |
Het |
Golga5 |
T |
A |
12: 102,438,732 (GRCm39) |
V149D |
probably damaging |
Het |
H1f7 |
A |
C |
15: 98,154,652 (GRCm39) |
S166A |
unknown |
Het |
Hivep1 |
T |
C |
13: 42,311,846 (GRCm39) |
L1362P |
probably benign |
Het |
Ift81 |
T |
C |
5: 122,740,414 (GRCm39) |
M205V |
probably benign |
Het |
Iglv3 |
T |
A |
16: 19,059,968 (GRCm39) |
Q120L |
possibly damaging |
Het |
Ints9 |
C |
T |
14: 65,217,659 (GRCm39) |
T62I |
possibly damaging |
Het |
Itga1 |
G |
T |
13: 115,096,673 (GRCm39) |
|
probably null |
Het |
Katnip |
C |
T |
7: 125,472,006 (GRCm39) |
H1532Y |
probably benign |
Het |
Krt77 |
A |
C |
15: 101,773,988 (GRCm39) |
I222S |
probably damaging |
Het |
Mrps25 |
A |
G |
6: 92,160,819 (GRCm39) |
|
probably null |
Het |
Mrps27 |
A |
G |
13: 99,548,754 (GRCm39) |
T297A |
probably benign |
Het |
Mup15 |
A |
T |
4: 61,357,850 (GRCm39) |
L7Q |
unknown |
Het |
Naip1 |
T |
A |
13: 100,562,169 (GRCm39) |
I999F |
probably damaging |
Het |
Ndst1 |
A |
G |
18: 60,836,901 (GRCm39) |
F387L |
probably damaging |
Het |
Nudt9 |
T |
C |
5: 104,202,151 (GRCm39) |
S71P |
probably damaging |
Het |
Or14c41 |
C |
A |
7: 86,235,245 (GRCm39) |
A254D |
probably benign |
Het |
Or2b4 |
A |
G |
17: 38,116,432 (GRCm39) |
Y132C |
probably damaging |
Het |
Or5al1 |
T |
G |
2: 85,990,380 (GRCm39) |
E111D |
probably damaging |
Het |
Pak4 |
C |
T |
7: 28,264,690 (GRCm39) |
V71I |
possibly damaging |
Het |
Pcolce |
A |
C |
5: 137,603,496 (GRCm39) |
S446A |
probably benign |
Het |
Per2 |
T |
A |
1: 91,349,251 (GRCm39) |
N1040I |
probably damaging |
Het |
Pla2g6 |
A |
T |
15: 79,188,592 (GRCm39) |
S422T |
probably benign |
Het |
Pla2r1 |
G |
T |
2: 60,332,543 (GRCm39) |
|
probably null |
Het |
Plcb4 |
T |
C |
2: 135,752,094 (GRCm39) |
V100A |
possibly damaging |
Het |
Polr1d |
C |
T |
5: 147,015,533 (GRCm39) |
T72M |
probably benign |
Het |
Psd3 |
A |
C |
8: 68,270,791 (GRCm39) |
|
probably benign |
Het |
Radil |
T |
C |
5: 142,480,697 (GRCm39) |
E586G |
probably damaging |
Het |
Serpina1b |
T |
A |
12: 103,695,515 (GRCm39) |
|
probably null |
Het |
Setd3 |
C |
T |
12: 108,124,114 (GRCm39) |
E192K |
probably benign |
Het |
Ssu2 |
G |
A |
6: 112,351,781 (GRCm39) |
H315Y |
probably damaging |
Het |
Taok3 |
T |
A |
5: 117,410,262 (GRCm39) |
M818K |
probably benign |
Het |
Tmem131l |
T |
C |
3: 83,829,471 (GRCm39) |
N1062S |
probably benign |
Het |
Tmx4 |
C |
T |
2: 134,481,425 (GRCm39) |
|
probably benign |
Het |
Traip |
G |
A |
9: 107,845,933 (GRCm39) |
C342Y |
probably benign |
Het |
Traj9 |
G |
T |
14: 54,446,890 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Vegfc |
T |
C |
8: 54,634,289 (GRCm39) |
S323P |
probably benign |
Het |
Vinac1 |
T |
C |
2: 128,879,301 (GRCm39) |
D875G |
possibly damaging |
Het |
|
Other mutations in Rnf150 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02183:Rnf150
|
APN |
8 |
83,730,234 (GRCm39) |
missense |
probably damaging |
0.96 |
R0512:Rnf150
|
UTSW |
8 |
83,590,807 (GRCm39) |
missense |
probably benign |
0.01 |
R1848:Rnf150
|
UTSW |
8 |
83,590,639 (GRCm39) |
start codon destroyed |
possibly damaging |
0.67 |
R2078:Rnf150
|
UTSW |
8 |
83,730,234 (GRCm39) |
missense |
probably damaging |
0.96 |
R2192:Rnf150
|
UTSW |
8 |
83,591,020 (GRCm39) |
missense |
probably damaging |
0.98 |
R3918:Rnf150
|
UTSW |
8 |
83,591,090 (GRCm39) |
missense |
probably benign |
0.25 |
R4365:Rnf150
|
UTSW |
8 |
83,590,744 (GRCm39) |
missense |
probably benign |
0.05 |
R4781:Rnf150
|
UTSW |
8 |
83,590,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R4810:Rnf150
|
UTSW |
8 |
83,716,991 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4859:Rnf150
|
UTSW |
8 |
83,590,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R5677:Rnf150
|
UTSW |
8 |
83,730,228 (GRCm39) |
nonsense |
probably null |
|
R6022:Rnf150
|
UTSW |
8 |
83,769,358 (GRCm39) |
missense |
probably benign |
0.00 |
R6283:Rnf150
|
UTSW |
8 |
83,717,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R6306:Rnf150
|
UTSW |
8 |
83,810,131 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7014:Rnf150
|
UTSW |
8 |
83,769,292 (GRCm39) |
missense |
probably benign |
|
R7023:Rnf150
|
UTSW |
8 |
83,590,706 (GRCm39) |
missense |
probably damaging |
0.97 |
R7394:Rnf150
|
UTSW |
8 |
83,717,100 (GRCm39) |
nonsense |
probably null |
|
R7710:Rnf150
|
UTSW |
8 |
83,590,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R7771:Rnf150
|
UTSW |
8 |
83,590,832 (GRCm39) |
missense |
probably benign |
0.00 |
R8073:Rnf150
|
UTSW |
8 |
83,590,546 (GRCm39) |
start gained |
probably benign |
|
R8856:Rnf150
|
UTSW |
8 |
83,762,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R8980:Rnf150
|
UTSW |
8 |
83,717,087 (GRCm39) |
missense |
probably benign |
0.19 |
R9139:Rnf150
|
UTSW |
8 |
83,590,588 (GRCm39) |
start gained |
probably benign |
|
R9289:Rnf150
|
UTSW |
8 |
83,716,982 (GRCm39) |
missense |
probably benign |
|
R9410:Rnf150
|
UTSW |
8 |
83,762,722 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9594:Rnf150
|
UTSW |
8 |
83,717,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R9603:Rnf150
|
UTSW |
8 |
83,717,208 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9763:Rnf150
|
UTSW |
8 |
83,732,968 (GRCm39) |
missense |
probably benign |
|
|