Incidental Mutation 'R4009:Or5h24'
ID |
475060 |
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 |
040846-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.185)
|
Stock # |
R4009 (G1)
|
Quality Score |
214 |
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: 99.2%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 93.5%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
A |
T |
11: 109,980,933 (GRCm39) |
L35Q |
probably damaging |
Het |
Acss2 |
T |
A |
2: 155,399,548 (GRCm39) |
L529Q |
probably damaging |
Het |
Apc2 |
T |
A |
10: 80,149,426 (GRCm39) |
D1464E |
probably benign |
Het |
Atp8a2 |
A |
G |
14: 60,265,434 (GRCm39) |
S301P |
possibly damaging |
Het |
Cntln |
A |
G |
4: 84,981,452 (GRCm39) |
T877A |
probably benign |
Het |
Cntn6 |
T |
C |
6: 104,810,783 (GRCm39) |
I537T |
probably damaging |
Het |
Cyp2d12 |
T |
G |
15: 82,440,493 (GRCm39) |
L94R |
probably damaging |
Het |
Dnah7a |
A |
G |
1: 53,564,164 (GRCm39) |
L1965P |
probably damaging |
Het |
Dock10 |
T |
C |
1: 80,510,148 (GRCm39) |
N1560S |
probably damaging |
Het |
F830045P16Rik |
A |
T |
2: 129,305,467 (GRCm39) |
N302K |
probably damaging |
Het |
Fxr1 |
G |
T |
3: 34,119,171 (GRCm39) |
R580L |
probably benign |
Het |
Gm5592 |
G |
T |
7: 40,938,934 (GRCm39) |
V739L |
probably benign |
Het |
Gna13 |
A |
G |
11: 109,286,843 (GRCm39) |
D222G |
probably damaging |
Het |
Grm7 |
T |
A |
6: 111,472,683 (GRCm39) |
Y841N |
probably damaging |
Het |
Kat2b |
G |
A |
17: 53,951,769 (GRCm39) |
|
probably null |
Het |
Kcng4 |
A |
G |
8: 120,352,824 (GRCm39) |
V362A |
probably damaging |
Het |
Kcnh1 |
T |
A |
1: 191,959,448 (GRCm39) |
I334N |
probably benign |
Het |
Mapkbp1 |
T |
C |
2: 119,854,086 (GRCm39) |
S1222P |
probably benign |
Het |
Or10a3m |
A |
T |
7: 108,313,366 (GRCm39) |
I269L |
probably benign |
Het |
Or10ag57 |
A |
T |
2: 87,218,924 (GRCm39) |
I292F |
possibly damaging |
Het |
Or11g26 |
T |
C |
14: 50,753,419 (GRCm39) |
S253P |
possibly damaging |
Het |
Pik3cb |
A |
G |
9: 98,922,982 (GRCm39) |
Y1017H |
probably damaging |
Het |
Plpp5 |
A |
G |
8: 26,210,338 (GRCm39) |
E36G |
probably damaging |
Het |
Pnma8a |
A |
T |
7: 16,695,301 (GRCm39) |
K385N |
probably damaging |
Het |
Ptprd |
T |
G |
4: 75,874,634 (GRCm39) |
M1272L |
possibly damaging |
Het |
Rad51ap2 |
A |
G |
12: 11,507,052 (GRCm39) |
I325V |
probably benign |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Skint4 |
T |
C |
4: 111,977,306 (GRCm39) |
V232A |
possibly damaging |
Het |
Slc30a5 |
G |
A |
13: 100,945,741 (GRCm39) |
A537V |
probably damaging |
Het |
Tcerg1 |
CAATTGAAAA |
CAA |
18: 42,697,201 (GRCm39) |
|
probably null |
Het |
Tenm3 |
C |
A |
8: 48,802,258 (GRCm39) |
K162N |
probably damaging |
Het |
Vmn2r44 |
T |
A |
7: 8,380,987 (GRCm39) |
Q302L |
possibly damaging |
Het |
Zfp618 |
G |
A |
4: 63,051,801 (GRCm39) |
A861T |
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 |
|
R4008: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 |