Incidental Mutation 'IGL00309:Or5g26'
| ID |
12846 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or5g26
|
| Ensembl Gene |
ENSMUSG00000075212 |
| Gene Name |
olfactory receptor family 5 subfamily G member 26 |
| Synonyms |
MOR175-1, Olfr154, 912-93, Olfr4-3, OR93, GA_x6K02T2Q125-47143827-47142871 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.084)
|
| Stock # |
IGL00309
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
85493721-85494799 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 85494700 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Aspartic acid
at position 26
(V26D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000097502
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099918]
|
| AlphaFold |
Q9QY00 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099918
AA Change: V26D
PolyPhen 2
Score 0.230 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000097502
Gene: ENSMUSG00000075212
AA Change: V26D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
3.2e-49 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
1.7e-17 |
PFAM |
|
| 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: 25 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4933430I17Rik |
T |
C |
4: 62,450,903 (GRCm39) |
|
probably benign |
Het |
| Abca9 |
T |
A |
11: 110,051,342 (GRCm39) |
D118V |
probably benign |
Het |
| Adgrb2 |
T |
A |
4: 129,912,598 (GRCm39) |
I1241N |
probably damaging |
Het |
| Arsb |
A |
G |
13: 93,926,608 (GRCm39) |
D126G |
probably benign |
Het |
| BB014433 |
G |
T |
8: 15,092,510 (GRCm39) |
N114K |
probably benign |
Het |
| Ccne2 |
T |
A |
4: 11,199,322 (GRCm39) |
V241E |
probably benign |
Het |
| Ccnjl |
A |
T |
11: 43,474,023 (GRCm39) |
K199N |
probably benign |
Het |
| Cyp2c55 |
A |
G |
19: 39,000,190 (GRCm39) |
T130A |
probably benign |
Het |
| Cyp2c70 |
A |
T |
19: 40,145,270 (GRCm39) |
N395K |
probably benign |
Het |
| Dst |
T |
C |
1: 34,199,733 (GRCm39) |
V67A |
probably damaging |
Het |
| Dysf |
G |
A |
6: 84,085,081 (GRCm39) |
R806H |
probably damaging |
Het |
| Extl3 |
G |
A |
14: 65,314,438 (GRCm39) |
P248L |
probably benign |
Het |
| Fcgbp |
A |
G |
7: 27,784,555 (GRCm39) |
D205G |
probably damaging |
Het |
| Gga1 |
G |
T |
15: 78,767,555 (GRCm39) |
V98L |
possibly damaging |
Het |
| Gpr6 |
C |
T |
10: 40,946,812 (GRCm39) |
A257T |
probably damaging |
Het |
| Mex3c |
C |
T |
18: 73,722,960 (GRCm39) |
T351M |
probably damaging |
Het |
| Or10d4c |
T |
A |
9: 39,558,636 (GRCm39) |
S205T |
probably benign |
Het |
| Or10g3b |
A |
G |
14: 52,587,167 (GRCm39) |
V112A |
probably benign |
Het |
| Or5ar1 |
A |
T |
2: 85,671,706 (GRCm39) |
V143D |
probably benign |
Het |
| Prex1 |
A |
G |
2: 166,451,743 (GRCm39) |
Y412H |
probably damaging |
Het |
| Slc25a25 |
A |
T |
2: 32,309,172 (GRCm39) |
V75E |
probably benign |
Het |
| Sv2c |
A |
G |
13: 96,184,937 (GRCm39) |
C247R |
probably damaging |
Het |
| Trpm5 |
A |
T |
7: 142,636,728 (GRCm39) |
V403E |
probably benign |
Het |
| Wdr17 |
A |
G |
8: 55,140,746 (GRCm39) |
V202A |
probably damaging |
Het |
| Zscan25 |
A |
G |
5: 145,220,559 (GRCm39) |
E118G |
probably damaging |
Het |
|
| Other mutations in Or5g26 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01745:Or5g26
|
APN |
2 |
85,493,921 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R1937:Or5g26
|
UTSW |
2 |
85,494,341 (GRCm39) |
missense |
probably benign |
|
|
R2086:Or5g26
|
UTSW |
2 |
85,494,090 (GRCm39) |
missense |
probably benign |
|
|
R2876:Or5g26
|
UTSW |
2 |
85,494,034 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3881:Or5g26
|
UTSW |
2 |
85,494,769 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4801:Or5g26
|
UTSW |
2 |
85,494,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4802:Or5g26
|
UTSW |
2 |
85,494,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6010:Or5g26
|
UTSW |
2 |
85,494,374 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6944:Or5g26
|
UTSW |
2 |
85,494,195 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7089:Or5g26
|
UTSW |
2 |
85,494,518 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R7443:Or5g26
|
UTSW |
2 |
85,493,912 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7453:Or5g26
|
UTSW |
2 |
85,494,524 (GRCm39) |
missense |
probably benign |
|
|
R7736:Or5g26
|
UTSW |
2 |
85,494,758 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7853:Or5g26
|
UTSW |
2 |
85,494,689 (GRCm39) |
missense |
probably benign |
|
|
R9719:Or5g26
|
UTSW |
2 |
85,494,608 (GRCm39) |
missense |
probably benign |
0.30 |
|
Z1088:Or5g26
|
UTSW |
2 |
85,493,960 (GRCm39) |
missense |
probably benign |
0.02 |
|
| Posted On |
2012-12-06 |
Incidental Mutation