Incidental Mutation 'R0152:Or10ak9'
| ID |
22773 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or10ak9
|
| Ensembl Gene |
ENSMUSG00000073769 |
| Gene Name |
olfactory receptor family 10 subfamily AK member 9 |
| Synonyms |
MOR259-3P, GA_x6K02T2QD9B-18670866-18669913, Olfr1331 |
| MMRRC Submission |
038435-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.054)
|
| Stock # |
R0152 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
(trace)
|
| Chromosome |
4 |
| Chromosomal Location |
118725980-118726933 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 118726083 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Asparagine
at position 34
(I34N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000154685
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000094831]
[ENSMUST00000106360]
[ENSMUST00000216589]
|
| AlphaFold |
K7N684 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000094831
AA Change: I35N
PolyPhen 2
Score 0.794 (Sensitivity: 0.85; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000092426
Gene: ENSMUSG00000073769
AA Change: I35N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
32 |
308 |
2.1e-53 |
PFAM |
|
Pfam:7tm_1
|
42 |
291 |
3.9e-22 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000106360
AA Change: I35N
PolyPhen 2
Score 0.794 (Sensitivity: 0.85; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000101967
Gene: ENSMUSG00000073769
AA Change: I35N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_1
|
41 |
290 |
1.2e-28 |
PFAM |
|
Pfam:7tm_4
|
139 |
283 |
2.8e-45 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000216589
AA Change: I34N
PolyPhen 2
Score 0.887 (Sensitivity: 0.82; Specificity: 0.94)
|
| Meta Mutation Damage Score |
0.1795 |
| Coding Region Coverage |
- 1x: 98.9%
- 3x: 97.9%
- 10x: 95.3%
- 20x: 89.5%
|
| Validation Efficiency |
87% (40/46) |
| 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: 45 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aass |
T |
C |
6: 23,074,688 (GRCm39) |
D834G |
probably damaging |
Het |
| Abca13 |
T |
A |
11: 9,531,724 (GRCm39) |
H4650Q |
probably damaging |
Het |
| Aqr |
T |
A |
2: 113,989,491 (GRCm39) |
T111S |
probably benign |
Het |
| Arfip2 |
G |
A |
7: 105,286,430 (GRCm39) |
T124M |
probably damaging |
Het |
| Arhgap44 |
G |
T |
11: 64,902,745 (GRCm39) |
A574E |
probably benign |
Het |
| Arhgef26 |
T |
C |
3: 62,330,965 (GRCm39) |
S560P |
probably damaging |
Het |
| Car5a |
T |
A |
8: 122,643,185 (GRCm39) |
N273I |
probably damaging |
Het |
| Cd4 |
G |
A |
6: 124,844,709 (GRCm39) |
Q359* |
probably null |
Het |
| Cgrrf1 |
G |
A |
14: 47,091,370 (GRCm39) |
C298Y |
probably damaging |
Het |
| Clip3 |
G |
A |
7: 30,002,857 (GRCm39) |
A416T |
probably benign |
Het |
| Dst |
C |
T |
1: 34,228,200 (GRCm39) |
P1606L |
probably damaging |
Het |
| Eif3e |
G |
A |
15: 43,115,632 (GRCm39) |
A378V |
possibly damaging |
Het |
| Ercc6 |
C |
G |
14: 32,268,862 (GRCm39) |
|
probably benign |
Het |
| Eri2 |
A |
G |
7: 119,389,606 (GRCm39) |
V104A |
probably damaging |
Het |
| Exph5 |
T |
A |
9: 53,264,504 (GRCm39) |
|
probably null |
Het |
| Hmcn1 |
A |
T |
1: 150,539,630 (GRCm39) |
Y2954N |
probably benign |
Het |
| Itga2 |
C |
T |
13: 115,002,850 (GRCm39) |
G547R |
probably benign |
Het |
| Kbtbd11 |
T |
C |
8: 15,077,428 (GRCm39) |
V9A |
probably damaging |
Het |
| Ldb2 |
T |
C |
5: 44,699,141 (GRCm39) |
D99G |
possibly damaging |
Het |
| Mfsd12 |
G |
T |
10: 81,193,633 (GRCm39) |
D68Y |
probably damaging |
Het |
| Mgarp |
T |
C |
3: 51,296,384 (GRCm39) |
D228G |
probably benign |
Het |
| Myh14 |
A |
T |
7: 44,272,605 (GRCm39) |
L1441Q |
probably damaging |
Het |
| Obscn |
T |
C |
11: 58,943,402 (GRCm39) |
D4810G |
probably benign |
Het |
| Or14c40 |
A |
T |
7: 86,313,719 (GRCm39) |
Y283F |
probably damaging |
Het |
| Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
| Or5b12 |
A |
G |
19: 12,897,472 (GRCm39) |
V67A |
possibly damaging |
Het |
| Or8g30 |
A |
G |
9: 39,230,757 (GRCm39) |
I51T |
probably benign |
Het |
| Pdhx |
A |
G |
2: 102,858,625 (GRCm39) |
V393A |
probably benign |
Het |
| Pdpk1 |
C |
T |
17: 24,325,920 (GRCm39) |
R92H |
possibly damaging |
Het |
| Pgr |
A |
T |
9: 8,965,023 (GRCm39) |
I889F |
probably benign |
Het |
| Pum2 |
T |
A |
12: 8,778,754 (GRCm39) |
I468K |
possibly damaging |
Het |
| Recql5 |
A |
G |
11: 115,785,499 (GRCm39) |
S666P |
probably benign |
Het |
| Rims4 |
C |
T |
2: 163,705,849 (GRCm39) |
V262M |
possibly damaging |
Het |
| Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
| Slc26a4 |
T |
C |
12: 31,579,497 (GRCm39) |
I588M |
probably damaging |
Het |
| Slc9a2 |
A |
G |
1: 40,781,964 (GRCm39) |
T398A |
probably damaging |
Het |
| Snapc1 |
C |
T |
12: 74,021,806 (GRCm39) |
R81C |
probably damaging |
Het |
| Tub |
A |
T |
7: 108,620,134 (GRCm39) |
N93Y |
probably damaging |
Het |
| Usp3 |
T |
C |
9: 66,447,432 (GRCm39) |
T181A |
probably damaging |
Het |
| Vars2 |
A |
G |
17: 35,970,919 (GRCm39) |
L637P |
probably damaging |
Het |
| Vmn2r1 |
T |
C |
3: 63,989,240 (GRCm39) |
S60P |
possibly damaging |
Het |
| Wdcp |
A |
G |
12: 4,901,583 (GRCm39) |
S480G |
probably benign |
Het |
| Zbtb38 |
T |
C |
9: 96,568,333 (GRCm39) |
Y917C |
probably damaging |
Het |
| Zfp68 |
T |
C |
5: 138,604,875 (GRCm39) |
K445E |
probably damaging |
Het |
| Zmynd10 |
A |
G |
9: 107,428,144 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Or10ak9 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00090:Or10ak9
|
APN |
4 |
118,726,484 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01314:Or10ak9
|
APN |
4 |
118,726,328 (GRCm39) |
missense |
probably benign |
0.26 |
|
IGL02025:Or10ak9
|
APN |
4 |
118,726,362 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02458:Or10ak9
|
APN |
4 |
118,726,497 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
IGL02793:Or10ak9
|
APN |
4 |
118,726,794 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02827:Or10ak9
|
APN |
4 |
118,726,157 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02863:Or10ak9
|
APN |
4 |
118,726,083 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
IGL03125:Or10ak9
|
APN |
4 |
118,726,118 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0078:Or10ak9
|
UTSW |
4 |
118,726,424 (GRCm39) |
missense |
probably benign |
|
|
R0299:Or10ak9
|
UTSW |
4 |
118,726,613 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3881:Or10ak9
|
UTSW |
4 |
118,726,550 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3928:Or10ak9
|
UTSW |
4 |
118,726,179 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3929:Or10ak9
|
UTSW |
4 |
118,726,179 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5288:Or10ak9
|
UTSW |
4 |
118,726,772 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5552:Or10ak9
|
UTSW |
4 |
118,726,665 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5672:Or10ak9
|
UTSW |
4 |
118,726,379 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R5773:Or10ak9
|
UTSW |
4 |
118,726,718 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6117:Or10ak9
|
UTSW |
4 |
118,726,341 (GRCm39) |
missense |
probably benign |
0.39 |
|
R6910:Or10ak9
|
UTSW |
4 |
118,726,335 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6911:Or10ak9
|
UTSW |
4 |
118,726,335 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6912:Or10ak9
|
UTSW |
4 |
118,726,335 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7164:Or10ak9
|
UTSW |
4 |
118,726,922 (GRCm39) |
missense |
probably benign |
0.30 |
|
R7446:Or10ak9
|
UTSW |
4 |
118,726,019 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R9747:Or10ak9
|
UTSW |
4 |
118,726,217 (GRCm39) |
missense |
probably damaging |
1.00 |
|
T0975:Or10ak9
|
UTSW |
4 |
118,726,500 (GRCm39) |
missense |
probably benign |
0.02 |
|
| Predicted Primers |
PCR Primer
(F):5'- ACCAATCTTCTGGGCTGCACTG -3'
(R):5'- ATGCAAGCCAAGCTACGCACTG -3'
Sequencing Primer
(F):5'- CTGCACTGTTTCAGGTGTTAC -3'
(R):5'- GACCTTCACACAAGTAGTGGTTG -3'
|
| Posted On |
2013-04-16 |
Incidental Mutation