Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc3 |
A |
G |
11: 94,249,627 (GRCm39) |
L1106P |
probably damaging |
Het |
Alx3 |
C |
G |
3: 107,512,135 (GRCm39) |
P258A |
probably damaging |
Het |
Bbs9 |
A |
G |
9: 22,582,128 (GRCm39) |
T607A |
probably benign |
Het |
Catsperg1 |
A |
T |
7: 28,891,111 (GRCm39) |
V644E |
possibly damaging |
Het |
Cep85 |
T |
C |
4: 133,875,472 (GRCm39) |
K499E |
possibly damaging |
Het |
Chd5 |
A |
T |
4: 152,463,923 (GRCm39) |
H1464L |
probably damaging |
Het |
Chrne |
A |
G |
11: 70,507,856 (GRCm39) |
L281P |
probably damaging |
Het |
Col3a1 |
A |
G |
1: 45,379,472 (GRCm39) |
|
probably benign |
Het |
Cpsf4l |
A |
G |
11: 113,600,279 (GRCm39) |
F13L |
possibly damaging |
Het |
Dgcr8 |
T |
C |
16: 18,077,825 (GRCm39) |
I603V |
probably benign |
Het |
Dhx16 |
A |
G |
17: 36,192,267 (GRCm39) |
D102G |
probably benign |
Het |
Dnm1 |
G |
T |
2: 32,206,987 (GRCm39) |
D564E |
probably benign |
Het |
Dync1li1 |
T |
A |
9: 114,534,178 (GRCm39) |
Y93N |
probably damaging |
Het |
Esp31 |
A |
G |
17: 38,955,509 (GRCm39) |
I51V |
probably benign |
Het |
Grap |
G |
T |
11: 61,562,517 (GRCm39) |
A163S |
possibly damaging |
Het |
Hgs |
G |
A |
11: 120,360,954 (GRCm39) |
|
probably null |
Het |
Icosl |
A |
T |
10: 77,909,697 (GRCm39) |
N214I |
probably damaging |
Het |
Ints6 |
G |
A |
14: 62,934,297 (GRCm39) |
P737S |
probably benign |
Het |
Irag1 |
C |
T |
7: 110,477,425 (GRCm39) |
V564M |
probably benign |
Het |
Lima1 |
A |
G |
15: 99,678,699 (GRCm39) |
S581P |
probably damaging |
Het |
Lrfn2 |
G |
A |
17: 49,403,824 (GRCm39) |
R649H |
probably damaging |
Het |
Muc5b |
A |
G |
7: 141,417,532 (GRCm39) |
T3493A |
possibly damaging |
Het |
Mup4 |
A |
T |
4: 59,958,587 (GRCm39) |
N104K |
probably damaging |
Het |
Nedd4 |
T |
C |
9: 72,633,766 (GRCm39) |
V424A |
possibly damaging |
Het |
Or6c88 |
T |
A |
10: 129,406,579 (GRCm39) |
D18E |
possibly damaging |
Het |
Or8d23 |
A |
G |
9: 38,841,985 (GRCm39) |
I173V |
probably benign |
Het |
Otop1 |
G |
A |
5: 38,457,117 (GRCm39) |
R292H |
probably damaging |
Het |
Otop1 |
T |
A |
5: 38,457,796 (GRCm39) |
C518* |
probably null |
Het |
Parp3 |
C |
T |
9: 106,353,150 (GRCm39) |
V9M |
probably benign |
Het |
Pcdhb20 |
C |
T |
18: 37,638,437 (GRCm39) |
A321V |
probably damaging |
Het |
Pik3c2g |
C |
T |
6: 139,714,426 (GRCm39) |
Q311* |
probably null |
Het |
Pkd1l1 |
A |
T |
11: 8,883,657 (GRCm39) |
V855D |
|
Het |
Polr2k |
T |
A |
15: 36,176,913 (GRCm39) |
D97E |
probably benign |
Het |
Psmd11 |
A |
G |
11: 80,325,342 (GRCm39) |
|
probably benign |
Het |
Ralgapa2 |
G |
A |
2: 146,266,683 (GRCm39) |
T631M |
probably damaging |
Het |
Ralgps1 |
C |
A |
2: 33,174,836 (GRCm39) |
|
probably null |
Het |
Rbm18 |
A |
G |
2: 36,024,211 (GRCm39) |
S17P |
probably damaging |
Het |
Rcc1 |
C |
A |
4: 132,065,515 (GRCm39) |
L49F |
probably benign |
Het |
Rgma |
T |
C |
7: 73,059,036 (GRCm39) |
S63P |
possibly damaging |
Het |
Scn1a |
T |
A |
2: 66,154,944 (GRCm39) |
I672L |
probably benign |
Het |
Sema4c |
T |
C |
1: 36,591,954 (GRCm39) |
T270A |
probably damaging |
Het |
Serac1 |
A |
G |
17: 6,100,303 (GRCm39) |
L479P |
probably damaging |
Het |
Slc22a16 |
A |
G |
10: 40,450,061 (GRCm39) |
M187V |
probably benign |
Het |
Slc41a3 |
A |
T |
6: 90,610,710 (GRCm39) |
T191S |
possibly damaging |
Het |
Slu7 |
G |
A |
11: 43,334,167 (GRCm39) |
V398M |
probably damaging |
Het |
Sphk1 |
A |
G |
11: 116,426,451 (GRCm39) |
T136A |
probably benign |
Het |
Sqstm1 |
G |
T |
11: 50,101,493 (GRCm39) |
P31Q |
possibly damaging |
Het |
Trappc11 |
A |
T |
8: 47,954,883 (GRCm39) |
V885D |
probably damaging |
Het |
Trav6-1 |
T |
A |
14: 52,876,213 (GRCm39) |
Y44* |
probably null |
Het |
Trav9-2 |
T |
A |
14: 53,828,755 (GRCm39) |
C42S |
probably damaging |
Het |
Zc2hc1a |
A |
G |
3: 7,593,168 (GRCm39) |
T194A |
probably benign |
Het |
Zfp729a |
A |
G |
13: 67,769,104 (GRCm39) |
V375A |
probably damaging |
Het |
|
Other mutations in Or10ag55-ps1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R6154:Or10ag55-ps1
|
UTSW |
2 |
87,139,902 (GRCm39) |
missense |
probably benign |
0.01 |
R6464:Or10ag55-ps1
|
UTSW |
2 |
87,139,951 (GRCm39) |
missense |
probably damaging |
0.97 |
R6494:Or10ag55-ps1
|
UTSW |
2 |
87,139,520 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6692:Or10ag55-ps1
|
UTSW |
2 |
87,139,336 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6826:Or10ag55-ps1
|
UTSW |
2 |
87,114,672 (GRCm39) |
missense |
probably benign |
0.02 |
R7054:Or10ag55-ps1
|
UTSW |
2 |
87,114,775 (GRCm39) |
missense |
probably benign |
0.42 |
R7176:Or10ag55-ps1
|
UTSW |
2 |
87,115,378 (GRCm39) |
missense |
probably damaging |
0.99 |
R7271:Or10ag55-ps1
|
UTSW |
2 |
87,114,725 (GRCm39) |
missense |
probably benign |
0.23 |
R7616:Or10ag55-ps1
|
UTSW |
2 |
87,115,617 (GRCm39) |
makesense |
probably null |
|
R8434:Or10ag55-ps1
|
UTSW |
2 |
87,114,978 (GRCm39) |
missense |
probably benign |
0.01 |
R8673:Or10ag55-ps1
|
UTSW |
2 |
87,114,658 (GRCm39) |
missense |
probably benign |
0.05 |
R8981:Or10ag55-ps1
|
UTSW |
2 |
87,115,561 (GRCm39) |
missense |
probably benign |
0.01 |
R9567:Or10ag55-ps1
|
UTSW |
2 |
87,115,037 (GRCm39) |
nonsense |
probably null |
|
R9654:Or10ag55-ps1
|
UTSW |
2 |
87,115,071 (GRCm39) |
missense |
probably benign |
0.12 |
R9716:Or10ag55-ps1
|
UTSW |
2 |
87,115,491 (GRCm39) |
missense |
probably damaging |
1.00 |
|