Incidental Mutation 'IGL01142:Or7g17'
| ID |
52006 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or7g17
|
| Ensembl Gene |
ENSMUSG00000051414 |
| Gene Name |
olfactory receptor family 7 subfamily G member 17 |
| Synonyms |
Olfr829, GA_x6K02T2PVTD-12599710-12600648, MOR147-1 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.198)
|
| Stock # |
IGL01142
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
18767923-18768888 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 18768830 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Serine
at position 303
(N303S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000058101
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000058411]
[ENSMUST00000212229]
|
| AlphaFold |
Q8VGX1 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000058411
AA Change: N303S
PolyPhen 2
Score 0.969 (Sensitivity: 0.77; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000058101
Gene: ENSMUSG00000051414
AA Change: N303S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
40 |
317 |
2e-52 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
44 |
174 |
1e-10 |
PFAM |
|
Pfam:7tm_1
|
50 |
299 |
1.6e-21 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000212229
AA Change: N294S
PolyPhen 2
Score 0.962 (Sensitivity: 0.78; Specificity: 0.95)
|
| 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: 22 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Armc3 |
C |
T |
2: 19,302,709 (GRCm39) |
|
probably benign |
Het |
| Cacnb3 |
T |
A |
15: 98,539,883 (GRCm39) |
L269* |
probably null |
Het |
| Calu |
T |
C |
6: 29,366,207 (GRCm39) |
|
probably null |
Het |
| Cep97 |
A |
G |
16: 55,742,561 (GRCm39) |
S129P |
probably damaging |
Het |
| Cpt1b |
T |
C |
15: 89,303,196 (GRCm39) |
M620V |
probably benign |
Het |
| Dnah7b |
T |
C |
1: 46,234,538 (GRCm39) |
|
probably null |
Het |
| Evi5 |
T |
C |
5: 107,963,477 (GRCm39) |
K410R |
probably benign |
Het |
| Gad2 |
T |
C |
2: 22,571,297 (GRCm39) |
|
probably benign |
Het |
| Helb |
A |
T |
10: 119,947,049 (GRCm39) |
V88D |
probably damaging |
Het |
| Hexim2 |
A |
G |
11: 103,024,960 (GRCm39) |
E19G |
probably benign |
Het |
| Klhl25 |
T |
C |
7: 75,516,344 (GRCm39) |
Y112H |
probably damaging |
Het |
| Lin52 |
T |
C |
12: 84,503,009 (GRCm39) |
|
probably benign |
Het |
| Ms4a4c |
A |
G |
19: 11,403,614 (GRCm39) |
T157A |
probably benign |
Het |
| Or12e8 |
T |
C |
2: 87,187,889 (GRCm39) |
F34L |
possibly damaging |
Het |
| Plxnb1 |
A |
G |
9: 108,931,765 (GRCm39) |
T472A |
probably benign |
Het |
| Sez6 |
T |
G |
11: 77,864,642 (GRCm39) |
V534G |
probably damaging |
Het |
| Sim1 |
C |
A |
10: 50,786,767 (GRCm39) |
T333K |
probably damaging |
Het |
| Tedc1 |
C |
T |
12: 113,126,808 (GRCm39) |
R357* |
probably null |
Het |
| Tmem115 |
A |
G |
9: 107,411,844 (GRCm39) |
N56S |
possibly damaging |
Het |
| Ubac1 |
T |
C |
2: 25,896,580 (GRCm39) |
I150V |
probably damaging |
Het |
| Vps13a |
T |
C |
19: 16,664,479 (GRCm39) |
K1455E |
possibly damaging |
Het |
| Yrdc |
T |
C |
4: 124,747,787 (GRCm39) |
F97L |
probably damaging |
Het |
|
| Other mutations in Or7g17 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01696:Or7g17
|
APN |
9 |
18,768,352 (GRCm39) |
missense |
probably benign |
0.19 |
|
IGL02285:Or7g17
|
APN |
9 |
18,768,286 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R0133:Or7g17
|
UTSW |
9 |
18,767,925 (GRCm39) |
start codon destroyed |
probably null |
|
|
R0173:Or7g17
|
UTSW |
9 |
18,768,325 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0270:Or7g17
|
UTSW |
9 |
18,768,127 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0449:Or7g17
|
UTSW |
9 |
18,767,945 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1111:Or7g17
|
UTSW |
9 |
18,768,888 (GRCm39) |
makesense |
probably null |
|
|
R1462:Or7g17
|
UTSW |
9 |
18,768,407 (GRCm39) |
missense |
probably benign |
0.30 |
|
R1462:Or7g17
|
UTSW |
9 |
18,768,407 (GRCm39) |
missense |
probably benign |
0.30 |
|
R1845:Or7g17
|
UTSW |
9 |
18,768,782 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4090:Or7g17
|
UTSW |
9 |
18,768,398 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4096:Or7g17
|
UTSW |
9 |
18,767,933 (GRCm39) |
missense |
probably benign |
|
|
R4097:Or7g17
|
UTSW |
9 |
18,767,933 (GRCm39) |
missense |
probably benign |
|
|
R4755:Or7g17
|
UTSW |
9 |
18,768,476 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4867:Or7g17
|
UTSW |
9 |
18,768,862 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5084:Or7g17
|
UTSW |
9 |
18,768,632 (GRCm39) |
missense |
probably benign |
0.43 |
|
R7216:Or7g17
|
UTSW |
9 |
18,768,632 (GRCm39) |
missense |
probably benign |
0.43 |
|
R7252:Or7g17
|
UTSW |
9 |
18,768,548 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7300:Or7g17
|
UTSW |
9 |
18,768,530 (GRCm39) |
missense |
not run |
|
|
R7412:Or7g17
|
UTSW |
9 |
18,768,085 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R8079:Or7g17
|
UTSW |
9 |
18,768,725 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R9083:Or7g17
|
UTSW |
9 |
18,768,550 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9648:Or7g17
|
UTSW |
9 |
18,768,748 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
X0024:Or7g17
|
UTSW |
9 |
18,768,320 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0057:Or7g17
|
UTSW |
9 |
18,767,933 (GRCm39) |
missense |
probably benign |
|
|
| Posted On |
2013-06-21 |
Incidental Mutation