Incidental Mutation 'R4008:Or4n5'
| ID |
311578 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or4n5
|
| Ensembl Gene |
ENSMUSG00000048933 |
| Gene Name |
olfactory receptor family 4 subfamily N member 5 |
| Synonyms |
GA_x6K02T2PMLR-5566715-5565789, MOR241-3, Olfr722 |
| MMRRC Submission |
040946-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.087)
|
| Stock # |
R4008 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
14 |
| Chromosomal Location |
50131715-50139398 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 50132464 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Proline
at position 265
(L265P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000059721
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053290]
|
| AlphaFold |
Q8VFC8 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000053290
AA Change: L265P
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000059721
Gene: ENSMUSG00000048933
AA Change: L265P
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
305 |
4.3e-44 |
PFAM |
|
Pfam:7tm_1
|
41 |
288 |
2.5e-19 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000213271
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 93.8%
|
| Validation Efficiency |
97% (32/33) |
| MGI Phenotype |
FUNCTION: Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]
|
| 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 |
| Or5h24 |
G |
A |
16: 58,919,124 (GRCm39) |
T77I |
unknown |
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 Or4n5 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
R1229:Or4n5
|
UTSW |
14 |
50,132,711 (GRCm39) |
nonsense |
probably null |
|
|
R1400:Or4n5
|
UTSW |
14 |
50,133,148 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R1417:Or4n5
|
UTSW |
14 |
50,133,020 (GRCm39) |
nonsense |
probably null |
|
|
R2126:Or4n5
|
UTSW |
14 |
50,132,524 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3968:Or4n5
|
UTSW |
14 |
50,132,983 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4032:Or4n5
|
UTSW |
14 |
50,132,433 (GRCm39) |
missense |
probably benign |
0.22 |
|
R4409:Or4n5
|
UTSW |
14 |
50,133,230 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4934:Or4n5
|
UTSW |
14 |
50,133,206 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5110:Or4n5
|
UTSW |
14 |
50,133,032 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R5232:Or4n5
|
UTSW |
14 |
50,133,155 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7019:Or4n5
|
UTSW |
14 |
50,133,124 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8963:Or4n5
|
UTSW |
14 |
50,132,509 (GRCm39) |
missense |
probably benign |
0.27 |
|
R9188:Or4n5
|
UTSW |
14 |
50,132,366 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GAAGTACCTAACACAGCATTTGC -3'
(R):5'- TACCTTTGCTGTGGAGCTCC -3'
Sequencing Primer
(F):5'- GCTAAAGAACTGATTCAATGCATG -3'
(R):5'- AGCTCCTGATGGTTTCTAACAG -3'
|
| Posted On |
2015-04-29 |
Incidental Mutation