Incidental Mutation 'R4008:Or5h24'
ID |
475055 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Or5h24
|
Ensembl Gene |
ENSMUSG00000059041 |
Gene Name |
olfactory receptor family 5 subfamily H member 24, pseudogene 1 |
Synonyms |
Olfr192, MOR183-11_p, GA_x54KRFPKG5P-55327126-55326203 |
MMRRC Submission |
040946-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.185)
|
Stock # |
R4008 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
16 |
Chromosomal Location |
58918429-58922216 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 58919124 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Isoleucine
at position 77
(T77I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000145941
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000080251]
[ENSMUST00000205727]
[ENSMUST00000206214]
|
AlphaFold |
no structure available at present |
Predicted Effect |
unknown
Transcript: ENSMUST00000080251
AA Change: T77I
|
Predicted Effect |
unknown
Transcript: ENSMUST00000205727
AA Change: T77I
|
Predicted Effect |
unknown
Transcript: ENSMUST00000206214
AA Change: T77I
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 93.8%
|
Validation Efficiency |
97% (32/33) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acss2 |
T |
A |
2: 155,399,548 (GRCm39) |
L529Q |
probably damaging |
Het |
Adsl |
T |
C |
15: 80,850,357 (GRCm39) |
S359P |
probably benign |
Het |
Batf2 |
G |
A |
19: 6,221,378 (GRCm39) |
E63K |
probably damaging |
Het |
Chd1l |
A |
T |
3: 97,477,718 (GRCm39) |
M679K |
probably benign |
Het |
Clvs2 |
G |
A |
10: 33,419,458 (GRCm39) |
H199Y |
probably damaging |
Het |
F830045P16Rik |
A |
T |
2: 129,305,467 (GRCm39) |
N302K |
probably damaging |
Het |
H2-K2 |
G |
A |
17: 34,218,525 (GRCm39) |
|
probably benign |
Het |
Ifit2 |
G |
T |
19: 34,551,445 (GRCm39) |
M328I |
probably benign |
Het |
Larp7 |
T |
C |
3: 127,334,519 (GRCm39) |
D490G |
probably benign |
Het |
Map9 |
T |
C |
3: 82,266,390 (GRCm39) |
Y12H |
probably damaging |
Het |
Mn1 |
G |
T |
5: 111,568,035 (GRCm39) |
E668D |
probably benign |
Het |
Mrps18c |
T |
C |
5: 100,950,982 (GRCm39) |
|
probably benign |
Het |
Npdc1 |
T |
A |
2: 25,298,992 (GRCm39) |
Y237* |
probably null |
Het |
Oprm1 |
A |
G |
10: 6,782,520 (GRCm39) |
M388V |
probably benign |
Het |
Or10ag57 |
A |
T |
2: 87,218,924 (GRCm39) |
I292F |
possibly damaging |
Het |
Or4n5 |
A |
G |
14: 50,132,464 (GRCm39) |
L265P |
probably benign |
Het |
Pkn2 |
T |
C |
3: 142,516,219 (GRCm39) |
D568G |
possibly damaging |
Het |
Pwp1 |
A |
G |
10: 85,717,898 (GRCm39) |
T279A |
possibly damaging |
Het |
Rabep2 |
C |
A |
7: 126,044,546 (GRCm39) |
D547E |
probably damaging |
Het |
Rbm34 |
T |
C |
8: 127,676,037 (GRCm39) |
K426R |
probably benign |
Het |
Rgs14 |
T |
G |
13: 55,517,726 (GRCm39) |
L8V |
probably damaging |
Het |
Ripor2 |
A |
G |
13: 24,880,521 (GRCm39) |
H407R |
probably benign |
Het |
Serpina3a |
A |
T |
12: 104,084,902 (GRCm39) |
D99V |
probably benign |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Slc39a12 |
T |
C |
2: 14,456,928 (GRCm39) |
F603L |
probably damaging |
Het |
Smg5 |
T |
C |
3: 88,256,465 (GRCm39) |
S244P |
probably benign |
Het |
St3gal3 |
T |
C |
4: 117,797,637 (GRCm39) |
I252V |
probably benign |
Het |
Tars3 |
T |
A |
7: 65,327,876 (GRCm39) |
D528E |
probably damaging |
Het |
Try10 |
A |
G |
6: 41,333,608 (GRCm39) |
T118A |
probably benign |
Het |
Tshr |
C |
T |
12: 91,504,268 (GRCm39) |
S402L |
probably benign |
Het |
|
Other mutations in Or5h24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R3807:Or5h24
|
UTSW |
16 |
58,919,206 (GRCm39) |
makesense |
probably null |
|
R3872:Or5h24
|
UTSW |
16 |
58,919,124 (GRCm39) |
missense |
unknown |
|
R4009:Or5h24
|
UTSW |
16 |
58,919,124 (GRCm39) |
missense |
unknown |
|
R4011:Or5h24
|
UTSW |
16 |
58,919,124 (GRCm39) |
missense |
unknown |
|
R4043:Or5h24
|
UTSW |
16 |
58,919,124 (GRCm39) |
missense |
unknown |
|
R4044:Or5h24
|
UTSW |
16 |
58,919,124 (GRCm39) |
missense |
unknown |
|
R4296:Or5h24
|
UTSW |
16 |
58,919,124 (GRCm39) |
missense |
unknown |
|
R4300:Or5h24
|
UTSW |
16 |
58,918,641 (GRCm39) |
missense |
unknown |
|
R4948:Or5h24
|
UTSW |
16 |
58,919,340 (GRCm39) |
missense |
probably damaging |
0.99 |
R5411:Or5h24
|
UTSW |
16 |
58,919,067 (GRCm39) |
missense |
unknown |
|
R5426:Or5h24
|
UTSW |
16 |
58,918,665 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5436:Or5h24
|
UTSW |
16 |
58,919,182 (GRCm39) |
missense |
unknown |
|
R5597:Or5h24
|
UTSW |
16 |
58,918,710 (GRCm39) |
missense |
unknown |
|
R6758:Or5h24
|
UTSW |
16 |
58,919,328 (GRCm39) |
missense |
probably damaging |
0.96 |
R6882:Or5h24
|
UTSW |
16 |
58,918,990 (GRCm39) |
missense |
unknown |
|
R8026:Or5h24
|
UTSW |
16 |
58,918,731 (GRCm39) |
missense |
unknown |
|
R8224:Or5h24
|
UTSW |
16 |
58,919,117 (GRCm39) |
missense |
unknown |
|
R8313:Or5h24
|
UTSW |
16 |
58,919,004 (GRCm39) |
missense |
unknown |
|
R8827:Or5h24
|
UTSW |
16 |
58,919,061 (GRCm39) |
missense |
unknown |
|
|
Predicted Primers |
|
Posted On |
2017-04-14 |