Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy10 |
T |
A |
1: 165,337,906 (GRCm39) |
D173E |
probably benign |
Het |
Ahctf1 |
T |
C |
1: 179,605,371 (GRCm39) |
D721G |
possibly damaging |
Het |
Allc |
T |
C |
12: 28,607,356 (GRCm39) |
T299A |
probably damaging |
Het |
Ankrd55 |
T |
A |
13: 112,459,575 (GRCm39) |
|
probably benign |
Het |
Axl |
C |
T |
7: 25,463,379 (GRCm39) |
D633N |
probably benign |
Het |
Brf2 |
G |
T |
8: 27,614,621 (GRCm39) |
R30S |
|
Het |
Bsn |
A |
G |
9: 107,984,890 (GRCm39) |
S283P |
possibly damaging |
Het |
Ccng2 |
C |
G |
5: 93,421,202 (GRCm39) |
S237R |
probably benign |
Het |
Ces1d |
A |
T |
8: 93,912,740 (GRCm39) |
S233T |
possibly damaging |
Het |
Chst15 |
T |
A |
7: 131,871,879 (GRCm39) |
H134L |
probably benign |
Het |
Col14a1 |
A |
G |
15: 55,284,276 (GRCm39) |
T846A |
unknown |
Het |
Cwh43 |
A |
T |
5: 73,591,572 (GRCm39) |
D555V |
probably damaging |
Het |
Cyld |
C |
A |
8: 89,432,043 (GRCm39) |
P14T |
probably benign |
Het |
Dctn1 |
G |
A |
6: 83,176,738 (GRCm39) |
R1264H |
possibly damaging |
Het |
Dkk3 |
T |
A |
7: 111,717,489 (GRCm39) |
S327C |
probably damaging |
Het |
Dnmbp |
T |
G |
19: 43,879,005 (GRCm39) |
H22P |
unknown |
Het |
Duxf4 |
T |
G |
10: 58,072,148 (GRCm39) |
Q22P |
possibly damaging |
Het |
Fabp4 |
T |
A |
3: 10,270,342 (GRCm39) |
T103S |
probably benign |
Het |
Fam43a |
T |
C |
16: 30,420,106 (GRCm39) |
L230P |
probably damaging |
Het |
Fam83h |
ACTCCCCTTGCGCTCAGGGTAAGCTGGGGTAGGGCTCCCCTTGCGCTCAGGGTAAGCTGGGGTAGGGCTCCCCTTGCGCTCAGGGTAAGCTGGGGTAGGGCTCCCCTTGCGCTCAGGGTAAGCTGGGGT |
ACTCCCCTTGCGCTCAGGGTAAGCTGGGGTAGGGCTCCCCTTGCGCTCAGGGTAAGCTGGGGTAGGGCTCCCCTTGCGCTCAGGGTAAGCTGGGGT |
15: 75,874,624 (GRCm39) |
|
probably benign |
Het |
Fank1 |
T |
A |
7: 133,478,493 (GRCm39) |
Y186N |
probably damaging |
Het |
Fbxo8 |
G |
A |
8: 57,044,555 (GRCm39) |
R286K |
possibly damaging |
Het |
Fmnl2 |
G |
A |
2: 52,997,678 (GRCm39) |
|
probably null |
Het |
Gli2 |
T |
A |
1: 118,765,701 (GRCm39) |
S817C |
probably damaging |
Het |
Gm10110 |
C |
T |
14: 90,135,677 (GRCm39) |
V76M |
noncoding transcript |
Het |
Gstt2 |
C |
G |
10: 75,668,291 (GRCm39) |
A155P |
probably benign |
Het |
Ints9 |
T |
A |
14: 65,244,757 (GRCm39) |
M213K |
probably benign |
Het |
Jak1 |
G |
A |
4: 101,036,738 (GRCm39) |
R301* |
probably null |
Het |
Kdsr |
T |
C |
1: 106,652,727 (GRCm39) |
T302A |
probably benign |
Het |
Khsrp |
T |
C |
17: 57,331,123 (GRCm39) |
E460G |
probably damaging |
Het |
Larp1b |
G |
A |
3: 40,991,245 (GRCm39) |
R193H |
probably damaging |
Het |
Nedd4l |
A |
G |
18: 65,324,560 (GRCm39) |
K487R |
probably damaging |
Het |
Niban2 |
A |
G |
2: 32,809,029 (GRCm39) |
E205G |
probably benign |
Het |
Nwd1 |
T |
A |
8: 73,431,580 (GRCm39) |
S1193T |
probably damaging |
Het |
Or10ag57 |
A |
T |
2: 87,218,852 (GRCm39) |
T268S |
probably benign |
Het |
Or5k3 |
T |
A |
16: 58,969,529 (GRCm39) |
C105* |
probably null |
Het |
Padi1 |
T |
C |
4: 140,542,014 (GRCm39) |
H636R |
probably damaging |
Het |
Pdilt |
A |
G |
7: 119,097,293 (GRCm39) |
I266T |
probably damaging |
Het |
Rell2 |
A |
T |
18: 38,090,665 (GRCm39) |
Q114L |
probably benign |
Het |
Rfc1 |
A |
G |
5: 65,426,289 (GRCm39) |
|
probably null |
Het |
Rpia |
T |
C |
6: 70,748,002 (GRCm39) |
N265D |
possibly damaging |
Het |
Rsf1 |
CGGCGGCGG |
CGGCGGCGGGGCGGCGG |
7: 97,229,127 (GRCm39) |
|
probably null |
Het |
Samd12 |
T |
C |
15: 53,723,645 (GRCm39) |
D16G |
probably damaging |
Het |
Slc25a54 |
T |
C |
3: 109,006,005 (GRCm39) |
|
probably null |
Het |
Slc6a3 |
T |
A |
13: 73,705,200 (GRCm39) |
D230E |
probably benign |
Het |
Sorbs1 |
G |
C |
19: 40,365,244 (GRCm39) |
R180G |
probably benign |
Het |
Synpo2l |
A |
G |
14: 20,711,204 (GRCm39) |
V472A |
probably benign |
Het |
Taf6l |
A |
G |
19: 8,750,714 (GRCm39) |
I120T |
possibly damaging |
Het |
Tent5c |
A |
G |
3: 100,380,327 (GRCm39) |
V143A |
probably damaging |
Het |
Trappc11 |
T |
C |
8: 47,969,624 (GRCm39) |
D328G |
probably damaging |
Het |
Trp53bp1 |
A |
G |
2: 121,029,523 (GRCm39) |
S1836P |
probably damaging |
Het |
Ugt2b37 |
G |
A |
5: 87,402,440 (GRCm39) |
L64F |
probably benign |
Het |
Vmn2r56 |
A |
T |
7: 12,449,601 (GRCm39) |
Y212* |
probably null |
Het |
Vps54 |
T |
A |
11: 21,250,464 (GRCm39) |
|
probably benign |
Het |
Zfp268 |
A |
T |
4: 145,349,547 (GRCm39) |
D328V |
possibly damaging |
Het |
Zfp648 |
T |
A |
1: 154,080,535 (GRCm39) |
H231Q |
probably benign |
Het |
Zscan4d |
T |
A |
7: 10,896,369 (GRCm39) |
T334S |
possibly damaging |
Het |
Zswim9 |
T |
C |
7: 12,995,536 (GRCm39) |
M207V |
probably benign |
Het |
|
Other mutations in Or8b54 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00948:Or8b54
|
APN |
9 |
38,687,108 (GRCm39) |
nonsense |
probably null |
|
IGL01016:Or8b54
|
APN |
9 |
38,686,737 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01391:Or8b54
|
APN |
9 |
38,686,826 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01451:Or8b54
|
APN |
9 |
38,687,225 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02250:Or8b54
|
APN |
9 |
38,686,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R0026:Or8b54
|
UTSW |
9 |
38,686,892 (GRCm39) |
missense |
probably benign |
0.01 |
R0334:Or8b54
|
UTSW |
9 |
38,686,535 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0655:Or8b54
|
UTSW |
9 |
38,686,850 (GRCm39) |
nonsense |
probably null |
|
R1024:Or8b54
|
UTSW |
9 |
38,686,631 (GRCm39) |
missense |
probably damaging |
0.97 |
R3522:Or8b54
|
UTSW |
9 |
38,687,016 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3967:Or8b54
|
UTSW |
9 |
38,686,664 (GRCm39) |
missense |
probably benign |
0.09 |
R3968:Or8b54
|
UTSW |
9 |
38,686,664 (GRCm39) |
missense |
probably benign |
0.09 |
R3969:Or8b54
|
UTSW |
9 |
38,686,664 (GRCm39) |
missense |
probably benign |
0.09 |
R4761:Or8b54
|
UTSW |
9 |
38,687,133 (GRCm39) |
missense |
probably benign |
0.05 |
R4796:Or8b54
|
UTSW |
9 |
38,686,670 (GRCm39) |
missense |
probably benign |
0.15 |
R4880:Or8b54
|
UTSW |
9 |
38,686,843 (GRCm39) |
nonsense |
probably null |
|
R5237:Or8b54
|
UTSW |
9 |
38,687,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R5756:Or8b54
|
UTSW |
9 |
38,686,554 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R6230:Or8b54
|
UTSW |
9 |
38,687,073 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6487:Or8b54
|
UTSW |
9 |
38,686,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R7514:Or8b54
|
UTSW |
9 |
38,686,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R7573:Or8b54
|
UTSW |
9 |
38,686,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R7755:Or8b54
|
UTSW |
9 |
38,687,073 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8195:Or8b54
|
UTSW |
9 |
38,686,577 (GRCm39) |
missense |
noncoding transcript |
|
R8196:Or8b54
|
UTSW |
9 |
38,686,577 (GRCm39) |
missense |
noncoding transcript |
|
R8197:Or8b54
|
UTSW |
9 |
38,686,577 (GRCm39) |
missense |
noncoding transcript |
|
R8199:Or8b54
|
UTSW |
9 |
38,686,577 (GRCm39) |
missense |
noncoding transcript |
|
R8211:Or8b54
|
UTSW |
9 |
38,686,577 (GRCm39) |
missense |
noncoding transcript |
|
R8212:Or8b54
|
UTSW |
9 |
38,686,577 (GRCm39) |
missense |
noncoding transcript |
|
R8236:Or8b54
|
UTSW |
9 |
38,686,577 (GRCm39) |
missense |
noncoding transcript |
|
R8239:Or8b54
|
UTSW |
9 |
38,686,577 (GRCm39) |
missense |
noncoding transcript |
|
R8279:Or8b54
|
UTSW |
9 |
38,686,577 (GRCm39) |
missense |
noncoding transcript |
|
R8283:Or8b54
|
UTSW |
9 |
38,686,577 (GRCm39) |
missense |
noncoding transcript |
|
R9207:Or8b54
|
UTSW |
9 |
38,686,960 (GRCm39) |
missense |
possibly damaging |
0.48 |
|