Incidental Mutation 'IGL02228:Or6aa1'
| ID |
285395 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or6aa1
|
| Ensembl Gene |
ENSMUSG00000039608 |
| Gene Name |
olfactory receptor family 6 subfamily AA member 1 |
| Synonyms |
MOR104-2, Olfr303, GA_x6K02T2NHDJ-9712819-9713778 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.082)
|
| Stock # |
IGL02228
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
86043704-86044743 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to C
at 86044286 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Serine
at position 140
(I140S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149419
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053958]
[ENSMUST00000215234]
[ENSMUST00000215532]
[ENSMUST00000215733]
[ENSMUST00000216409]
|
| AlphaFold |
Q8VFP0 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000053958
AA Change: I140S
PolyPhen 2
Score 0.500 (Sensitivity: 0.88; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000062459
Gene: ENSMUSG00000039608
AA Change: I140S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
1.2e-52 |
PFAM |
|
Pfam:7tm_1
|
41 |
307 |
4.9e-20 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000215234
AA Change: I140S
PolyPhen 2
Score 0.500 (Sensitivity: 0.88; Specificity: 0.90)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000215532
AA Change: I140S
PolyPhen 2
Score 0.500 (Sensitivity: 0.88; Specificity: 0.90)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000215733
AA Change: I140S
PolyPhen 2
Score 0.500 (Sensitivity: 0.88; Specificity: 0.90)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000216409
AA Change: I140S
PolyPhen 2
Score 0.500 (Sensitivity: 0.88; Specificity: 0.90)
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| 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: 34 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acot1 |
T |
C |
12: 84,063,738 (GRCm39) |
V282A |
probably benign |
Het |
| Acsm5 |
A |
G |
7: 119,131,089 (GRCm39) |
D169G |
probably damaging |
Het |
| Adam8 |
C |
T |
7: 139,568,719 (GRCm39) |
|
probably null |
Het |
| Agpat1 |
T |
C |
17: 34,829,536 (GRCm39) |
F37L |
possibly damaging |
Het |
| Asah2 |
A |
T |
19: 31,994,114 (GRCm39) |
D410E |
probably benign |
Het |
| Atg2a |
T |
A |
19: 6,296,830 (GRCm39) |
V378D |
probably benign |
Het |
| Atp1a4 |
T |
C |
1: 172,082,452 (GRCm39) |
Y130C |
possibly damaging |
Het |
| Bnc2 |
T |
C |
4: 84,211,313 (GRCm39) |
H419R |
possibly damaging |
Het |
| Capza3 |
A |
G |
6: 139,987,641 (GRCm39) |
D80G |
probably benign |
Het |
| Col6a4 |
C |
T |
9: 105,945,277 (GRCm39) |
D946N |
probably benign |
Het |
| Crat |
T |
C |
2: 30,303,194 (GRCm39) |
H31R |
probably damaging |
Het |
| Dsc2 |
A |
G |
18: 20,176,790 (GRCm39) |
V419A |
probably damaging |
Het |
| Ebf1 |
T |
C |
11: 44,863,739 (GRCm39) |
V363A |
probably damaging |
Het |
| Lcp2 |
T |
C |
11: 33,997,424 (GRCm39) |
F24S |
probably damaging |
Het |
| Lgmn |
G |
A |
12: 102,361,973 (GRCm39) |
T376I |
probably benign |
Het |
| Lrrc8d |
C |
T |
5: 105,959,730 (GRCm39) |
L47F |
probably benign |
Het |
| Mier1 |
T |
A |
4: 102,988,259 (GRCm39) |
M44K |
possibly damaging |
Het |
| Ogfod1 |
C |
A |
8: 94,789,615 (GRCm39) |
Q439K |
probably benign |
Het |
| Pcgf6 |
A |
C |
19: 47,036,421 (GRCm39) |
F216C |
probably damaging |
Het |
| Pcnt |
C |
T |
10: 76,225,308 (GRCm39) |
R1732K |
probably benign |
Het |
| Pramel17 |
T |
C |
4: 101,694,055 (GRCm39) |
Y276C |
probably benign |
Het |
| Pramel31 |
A |
G |
4: 144,089,231 (GRCm39) |
K183R |
probably damaging |
Het |
| Rbbp4 |
A |
T |
4: 129,211,543 (GRCm39) |
H370Q |
probably damaging |
Het |
| Reln |
A |
G |
5: 22,109,729 (GRCm39) |
V3127A |
probably damaging |
Het |
| Rttn |
T |
A |
18: 89,060,355 (GRCm39) |
V1019E |
probably damaging |
Het |
| Serpina9 |
C |
T |
12: 103,974,859 (GRCm39) |
R98Q |
probably benign |
Het |
| Slc16a7 |
C |
A |
10: 125,066,667 (GRCm39) |
G324V |
probably damaging |
Het |
| Slc22a3 |
A |
G |
17: 12,678,697 (GRCm39) |
L209P |
probably damaging |
Het |
| Tet1 |
T |
A |
10: 62,649,513 (GRCm39) |
T1695S |
probably damaging |
Het |
| Tulp3 |
G |
A |
6: 128,311,448 (GRCm39) |
T74M |
probably damaging |
Het |
| Ube3a |
A |
G |
7: 58,938,144 (GRCm39) |
|
probably benign |
Het |
| Ufl1 |
A |
T |
4: 25,281,686 (GRCm39) |
S23T |
probably benign |
Het |
| Unc80 |
A |
G |
1: 66,647,587 (GRCm39) |
E1509G |
possibly damaging |
Het |
| Wnk2 |
A |
T |
13: 49,210,416 (GRCm39) |
I1801N |
probably damaging |
Het |
|
| Other mutations in Or6aa1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02902:Or6aa1
|
APN |
7 |
86,043,743 (GRCm39) |
utr 3 prime |
probably benign |
|
|
IGL02937:Or6aa1
|
APN |
7 |
86,043,798 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
BB001:Or6aa1
|
UTSW |
7 |
86,043,938 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB011:Or6aa1
|
UTSW |
7 |
86,043,938 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1455:Or6aa1
|
UTSW |
7 |
86,043,803 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1524:Or6aa1
|
UTSW |
7 |
86,044,020 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1762:Or6aa1
|
UTSW |
7 |
86,044,353 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R3014:Or6aa1
|
UTSW |
7 |
86,043,884 (GRCm39) |
missense |
probably benign |
0.19 |
|
R3027:Or6aa1
|
UTSW |
7 |
86,043,761 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4073:Or6aa1
|
UTSW |
7 |
86,044,155 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4502:Or6aa1
|
UTSW |
7 |
86,044,485 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R4503:Or6aa1
|
UTSW |
7 |
86,044,485 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R4607:Or6aa1
|
UTSW |
7 |
86,043,718 (GRCm39) |
splice site |
probably null |
|
|
R4608:Or6aa1
|
UTSW |
7 |
86,043,718 (GRCm39) |
splice site |
probably null |
|
|
R7134:Or6aa1
|
UTSW |
7 |
86,044,752 (GRCm39) |
start gained |
probably benign |
|
|
R7298:Or6aa1
|
UTSW |
7 |
86,044,131 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7827:Or6aa1
|
UTSW |
7 |
86,043,765 (GRCm39) |
nonsense |
probably null |
|
|
R7924:Or6aa1
|
UTSW |
7 |
86,043,938 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8160:Or6aa1
|
UTSW |
7 |
86,044,473 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R8294:Or6aa1
|
UTSW |
7 |
86,044,487 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9465:Or6aa1
|
UTSW |
7 |
86,043,864 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9725:Or6aa1
|
UTSW |
7 |
86,043,973 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Posted On |
2015-04-16 |
Incidental Mutation