Incidental Mutation 'R1166:Or4a81'
| ID |
100994 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or4a81
|
| Ensembl Gene |
ENSMUSG00000075074 |
| Gene Name |
olfactory receptor family 4 subfamily A member 81 |
| Synonyms |
Olfr1254, GA_x6K02T2Q125-51230155-51229211, MOR231-13 |
| MMRRC Submission |
039239-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.078)
|
| Stock # |
R1166 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
89618750-89619694 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 89619675 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 7
(V7A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149507
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099764]
[ENSMUST00000111523]
[ENSMUST00000216587]
|
| AlphaFold |
Q8VFB1 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000099764
AA Change: V7A
PolyPhen 2
Score 0.744 (Sensitivity: 0.85; Specificity: 0.92)
|
| SMART Domains |
Protein: ENSMUSP00000097352
Gene: ENSMUSG00000075074
AA Change: V7A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_1
|
39 |
285 |
9.7e-30 |
PFAM |
|
Pfam:7tm_4
|
137 |
278 |
1.3e-39 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000111523
AA Change: V7A
PolyPhen 2
Score 0.744 (Sensitivity: 0.85; Specificity: 0.92)
|
| SMART Domains |
Protein: ENSMUSP00000107148
Gene: ENSMUSG00000075074
AA Change: V7A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
303 |
2.4e-46 |
PFAM |
|
Pfam:7tm_1
|
39 |
285 |
5.6e-18 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000216587
AA Change: V7A
PolyPhen 2
Score 0.744 (Sensitivity: 0.85; Specificity: 0.92)
|
| Meta Mutation Damage Score |
0.1795 |
| Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.3%
- 10x: 95.0%
- 20x: 86.3%
|
| Validation Efficiency |
96% (43/45) |
| 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: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A2ml1 |
T |
C |
6: 128,547,880 (GRCm39) |
K286R |
probably benign |
Het |
| Arhgef10l |
T |
C |
4: 140,302,581 (GRCm39) |
|
probably benign |
Het |
| Ccdc175 |
T |
G |
12: 72,152,706 (GRCm39) |
K733T |
probably damaging |
Het |
| Cenpn |
T |
G |
8: 117,652,946 (GRCm39) |
I39R |
probably damaging |
Het |
| Cfap53 |
A |
T |
18: 74,433,251 (GRCm39) |
Y112F |
possibly damaging |
Het |
| Cngb1 |
C |
A |
8: 95,986,809 (GRCm39) |
C361F |
probably damaging |
Het |
| Ctf2 |
T |
C |
7: 127,318,685 (GRCm39) |
T105A |
probably benign |
Het |
| Dnah7b |
A |
T |
1: 46,364,970 (GRCm39) |
T3584S |
probably damaging |
Het |
| Ebf3 |
C |
T |
7: 136,914,896 (GRCm39) |
|
probably benign |
Het |
| Ep300 |
A |
G |
15: 81,514,265 (GRCm39) |
|
probably benign |
Het |
| Fbxo17 |
T |
A |
7: 28,432,953 (GRCm39) |
V158E |
probably damaging |
Het |
| Fbxw24 |
T |
C |
9: 109,436,066 (GRCm39) |
E322G |
probably benign |
Het |
| Gm5698 |
G |
T |
1: 31,016,366 (GRCm39) |
D228E |
probably damaging |
Het |
| Hfm1 |
A |
T |
5: 107,059,277 (GRCm39) |
D248E |
probably benign |
Het |
| Insm2 |
T |
C |
12: 55,647,281 (GRCm39) |
S342P |
probably benign |
Het |
| Krt36 |
G |
A |
11: 99,993,654 (GRCm39) |
R395C |
probably benign |
Het |
| Lrrc37 |
A |
G |
11: 103,506,209 (GRCm39) |
S1920P |
probably benign |
Het |
| Lsm14b |
T |
A |
2: 179,673,334 (GRCm39) |
|
probably benign |
Het |
| Map1a |
A |
G |
2: 121,130,741 (GRCm39) |
E519G |
probably damaging |
Het |
| Mfsd14a |
T |
C |
3: 116,427,543 (GRCm39) |
|
probably benign |
Het |
| Mfsd4b5 |
T |
C |
10: 39,846,419 (GRCm39) |
Y387C |
probably damaging |
Het |
| Mybpc2 |
T |
C |
7: 44,154,449 (GRCm39) |
N1063D |
possibly damaging |
Het |
| Nlrp10 |
T |
A |
7: 108,524,217 (GRCm39) |
H421L |
probably damaging |
Het |
| Nup155 |
A |
T |
15: 8,187,244 (GRCm39) |
H1391L |
probably damaging |
Het |
| Pacrg |
A |
T |
17: 10,622,268 (GRCm39) |
Y235* |
probably null |
Het |
| Pde4dip |
T |
A |
3: 97,620,512 (GRCm39) |
D1629V |
possibly damaging |
Het |
| Prl8a2 |
G |
T |
13: 27,537,935 (GRCm39) |
S204I |
possibly damaging |
Het |
| Sec24a |
A |
T |
11: 51,624,294 (GRCm39) |
M356K |
possibly damaging |
Het |
| Sh3tc2 |
A |
C |
18: 62,124,247 (GRCm39) |
S972R |
probably damaging |
Het |
| Shc2 |
C |
T |
10: 79,456,946 (GRCm39) |
V557M |
probably damaging |
Het |
| Slc2a9 |
A |
G |
5: 38,539,384 (GRCm39) |
|
probably null |
Het |
| Tcaf1 |
T |
C |
6: 42,655,612 (GRCm39) |
I455V |
probably benign |
Het |
| Umodl1 |
T |
G |
17: 31,221,772 (GRCm39) |
|
probably benign |
Het |
| Wdr27 |
T |
C |
17: 15,112,733 (GRCm39) |
T658A |
probably damaging |
Het |
| Zfp318 |
T |
C |
17: 46,720,618 (GRCm39) |
Y1119H |
possibly damaging |
Het |
| Zfp939 |
C |
A |
7: 39,122,763 (GRCm39) |
|
noncoding transcript |
Het |
|
| Other mutations in Or4a81 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01631:Or4a81
|
APN |
2 |
89,619,129 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02822:Or4a81
|
APN |
2 |
89,619,444 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R1639:Or4a81
|
UTSW |
2 |
89,619,589 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2248:Or4a81
|
UTSW |
2 |
89,619,524 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R2256:Or4a81
|
UTSW |
2 |
89,618,814 (GRCm39) |
missense |
probably benign |
|
|
R2351:Or4a81
|
UTSW |
2 |
89,619,522 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4432:Or4a81
|
UTSW |
2 |
89,619,078 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R4649:Or4a81
|
UTSW |
2 |
89,619,637 (GRCm39) |
missense |
probably benign |
0.19 |
|
R4788:Or4a81
|
UTSW |
2 |
89,619,480 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6454:Or4a81
|
UTSW |
2 |
89,619,522 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6591:Or4a81
|
UTSW |
2 |
89,619,332 (GRCm39) |
nonsense |
probably null |
|
|
R6691:Or4a81
|
UTSW |
2 |
89,619,332 (GRCm39) |
nonsense |
probably null |
|
|
R7418:Or4a81
|
UTSW |
2 |
89,619,320 (GRCm39) |
nonsense |
probably null |
|
|
R7451:Or4a81
|
UTSW |
2 |
89,619,453 (GRCm39) |
missense |
probably benign |
|
|
R8024:Or4a81
|
UTSW |
2 |
89,619,390 (GRCm39) |
missense |
probably benign |
0.07 |
|
R8080:Or4a81
|
UTSW |
2 |
89,618,971 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R8251:Or4a81
|
UTSW |
2 |
89,619,567 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8318:Or4a81
|
UTSW |
2 |
89,619,321 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R8475:Or4a81
|
UTSW |
2 |
89,619,586 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9166:Or4a81
|
UTSW |
2 |
89,619,291 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9460:Or4a81
|
UTSW |
2 |
89,618,778 (GRCm39) |
missense |
probably benign |
|
|
R9474:Or4a81
|
UTSW |
2 |
89,619,506 (GRCm39) |
nonsense |
probably null |
|
|
R9677:Or4a81
|
UTSW |
2 |
89,619,161 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
X0022:Or4a81
|
UTSW |
2 |
89,619,075 (GRCm39) |
missense |
probably benign |
0.02 |
|
| Predicted Primers |
|
| Posted On |
2014-01-15 |
Incidental Mutation