Incidental Mutation 'IGL02554:Or10a3m'
| ID |
298410 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or10a3m
|
| Ensembl Gene |
ENSMUSG00000056946 |
| Gene Name |
olfactory receptor family 10 subfamily A member 3M |
| Synonyms |
Olfr512, MOR268-3, GA_x6K02T2PBJ9-11043421-11044365 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.115)
|
| Stock # |
IGL02554
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
108312562-108313542 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 108312949 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Valine
at position 118
(M118V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000147972
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000074730]
[ENSMUST00000209620]
|
| AlphaFold |
Q8VFZ4 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000074730
AA Change: M130V
PolyPhen 2
Score 0.942 (Sensitivity: 0.80; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000074291
Gene: ENSMUSG00000056946
AA Change: M130V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
43 |
320 |
7.8e-62 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
47 |
317 |
2.5e-6 |
PFAM |
|
Pfam:7tm_1
|
53 |
302 |
2.3e-25 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000209620
AA Change: M118V
PolyPhen 2
Score 0.942 (Sensitivity: 0.80; Specificity: 0.94)
|
| 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: 46 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 9930111J21Rik1 |
T |
A |
11: 48,838,830 (GRCm39) |
M586L |
probably damaging |
Het |
| Abcg3 |
T |
C |
5: 105,117,318 (GRCm39) |
D204G |
possibly damaging |
Het |
| Acox3 |
C |
A |
5: 35,765,710 (GRCm39) |
L588I |
probably damaging |
Het |
| Adamts9 |
G |
T |
6: 92,857,828 (GRCm39) |
L849I |
probably benign |
Het |
| Alkbh3 |
T |
G |
2: 93,826,692 (GRCm39) |
T170P |
probably damaging |
Het |
| Anks1b |
A |
T |
10: 90,757,240 (GRCm39) |
H300L |
probably damaging |
Het |
| Arhgap29 |
T |
C |
3: 121,786,173 (GRCm39) |
|
probably benign |
Het |
| Brd8dc |
A |
G |
18: 34,726,068 (GRCm39) |
S112P |
probably benign |
Het |
| Cd86 |
C |
T |
16: 36,438,847 (GRCm39) |
G181D |
probably benign |
Het |
| Cep68 |
A |
T |
11: 20,190,096 (GRCm39) |
H305Q |
possibly damaging |
Het |
| Cimip4 |
A |
G |
15: 78,262,736 (GRCm39) |
M245T |
possibly damaging |
Het |
| Clptm1l |
A |
T |
13: 73,755,879 (GRCm39) |
D165V |
probably benign |
Het |
| Dctn1 |
T |
C |
6: 83,159,704 (GRCm39) |
Y61H |
probably damaging |
Het |
| Dnah7a |
A |
T |
1: 53,657,205 (GRCm39) |
M857K |
possibly damaging |
Het |
| Gpr158 |
A |
G |
2: 21,831,407 (GRCm39) |
M836V |
probably benign |
Het |
| Gria1 |
G |
T |
11: 57,180,314 (GRCm39) |
A755S |
possibly damaging |
Het |
| Helb |
G |
A |
10: 119,925,617 (GRCm39) |
T920M |
probably damaging |
Het |
| Hr |
T |
C |
14: 70,797,306 (GRCm39) |
|
probably benign |
Het |
| Igf2bp1 |
A |
G |
11: 95,864,994 (GRCm39) |
S152P |
probably damaging |
Het |
| Iqsec1 |
T |
C |
6: 90,646,327 (GRCm39) |
Y784C |
probably damaging |
Het |
| Ldah |
T |
A |
12: 8,333,935 (GRCm39) |
C275* |
probably null |
Het |
| Lpin3 |
T |
C |
2: 160,738,707 (GRCm39) |
S220P |
probably damaging |
Het |
| Med23 |
T |
C |
10: 24,774,473 (GRCm39) |
|
probably null |
Het |
| Mllt1 |
T |
C |
17: 57,206,806 (GRCm39) |
D346G |
probably benign |
Het |
| Myef2 |
A |
C |
2: 124,942,345 (GRCm39) |
|
probably null |
Het |
| Myh2 |
A |
G |
11: 67,079,991 (GRCm39) |
S1095G |
probably benign |
Het |
| Nav1 |
A |
G |
1: 135,512,651 (GRCm39) |
|
silent |
Het |
| Piwil2 |
G |
A |
14: 70,628,935 (GRCm39) |
|
probably benign |
Het |
| Pkhd1l1 |
T |
A |
15: 44,441,896 (GRCm39) |
F3612I |
probably damaging |
Het |
| Ror2 |
C |
T |
13: 53,264,764 (GRCm39) |
S764N |
probably damaging |
Het |
| S100pbp |
A |
T |
4: 129,075,644 (GRCm39) |
|
probably null |
Het |
| Scnn1b |
T |
C |
7: 121,516,746 (GRCm39) |
I495T |
probably damaging |
Het |
| Sgo2b |
A |
C |
8: 64,379,571 (GRCm39) |
V1087G |
probably damaging |
Het |
| Sil1 |
A |
T |
18: 35,481,786 (GRCm39) |
V91E |
probably damaging |
Het |
| Slc5a4b |
A |
G |
10: 75,946,685 (GRCm39) |
I29T |
possibly damaging |
Het |
| Spink5 |
A |
T |
18: 44,148,661 (GRCm39) |
N908I |
probably benign |
Het |
| Svopl |
A |
C |
6: 37,993,978 (GRCm39) |
I351S |
probably damaging |
Het |
| Syngr3 |
A |
G |
17: 24,905,302 (GRCm39) |
V198A |
probably benign |
Het |
| Tbck |
C |
A |
3: 132,456,953 (GRCm39) |
Y622* |
probably null |
Het |
| Tkt |
T |
A |
14: 30,280,737 (GRCm39) |
M56K |
probably damaging |
Het |
| Trip10 |
T |
C |
17: 57,570,135 (GRCm39) |
V544A |
probably damaging |
Het |
| Txndc16 |
T |
C |
14: 45,409,995 (GRCm39) |
E195G |
probably damaging |
Het |
| Vmn2r69 |
G |
A |
7: 85,059,014 (GRCm39) |
P516S |
probably damaging |
Het |
| Vmn2r74 |
T |
C |
7: 85,606,581 (GRCm39) |
N255S |
probably benign |
Het |
| Xpo4 |
T |
C |
14: 57,827,545 (GRCm39) |
T884A |
probably benign |
Het |
| Zdhhc2 |
A |
G |
8: 40,915,155 (GRCm39) |
N167S |
probably damaging |
Het |
|
| Other mutations in Or10a3m |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01889:Or10a3m
|
APN |
7 |
108,313,089 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01912:Or10a3m
|
APN |
7 |
108,313,465 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
IGL02182:Or10a3m
|
APN |
7 |
108,313,075 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02409:Or10a3m
|
APN |
7 |
108,313,366 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03210:Or10a3m
|
APN |
7 |
108,312,775 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03373:Or10a3m
|
APN |
7 |
108,313,339 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03400:Or10a3m
|
APN |
7 |
108,312,733 (GRCm39) |
missense |
probably benign |
0.28 |
|
R0092:Or10a3m
|
UTSW |
7 |
108,313,031 (GRCm39) |
missense |
probably benign |
|
|
R0741:Or10a3m
|
UTSW |
7 |
108,312,811 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1515:Or10a3m
|
UTSW |
7 |
108,313,148 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R1982:Or10a3m
|
UTSW |
7 |
108,312,902 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2176:Or10a3m
|
UTSW |
7 |
108,313,339 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3967:Or10a3m
|
UTSW |
7 |
108,313,060 (GRCm39) |
missense |
probably benign |
|
|
R4009:Or10a3m
|
UTSW |
7 |
108,313,366 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4010:Or10a3m
|
UTSW |
7 |
108,313,366 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4011:Or10a3m
|
UTSW |
7 |
108,313,366 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5095:Or10a3m
|
UTSW |
7 |
108,313,019 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5271:Or10a3m
|
UTSW |
7 |
108,313,424 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5864:Or10a3m
|
UTSW |
7 |
108,312,671 (GRCm39) |
missense |
probably benign |
|
|
R5926:Or10a3m
|
UTSW |
7 |
108,312,794 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6295:Or10a3m
|
UTSW |
7 |
108,312,845 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6528:Or10a3m
|
UTSW |
7 |
108,312,638 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6624:Or10a3m
|
UTSW |
7 |
108,312,743 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R8029:Or10a3m
|
UTSW |
7 |
108,313,037 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R8443:Or10a3m
|
UTSW |
7 |
108,313,418 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R8737:Or10a3m
|
UTSW |
7 |
108,312,964 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9415:Or10a3m
|
UTSW |
7 |
108,313,042 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9622:Or10a3m
|
UTSW |
7 |
108,312,677 (GRCm39) |
missense |
probably benign |
0.30 |
|
X0023:Or10a3m
|
UTSW |
7 |
108,313,217 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
Z1088:Or10a3m
|
UTSW |
7 |
108,312,745 (GRCm39) |
missense |
probably benign |
0.06 |
|
| Posted On |
2015-04-16 |
Incidental Mutation