Incidental Mutation 'IGL02087:Or5p68'
| ID |
279275 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or5p68
|
| Ensembl Gene |
ENSMUSG00000093980 |
| Gene Name |
olfactory receptor family 5 subfamily P member 68 |
| Synonyms |
MOR204-35, GA_x6K02T2PBJ9-10676998-10676054, Olfr493 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.083)
|
| Stock # |
IGL02087
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
107945242-107946186 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 107946173 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Histidine to Leucine
at position 5
(H5L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000079005
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000080106]
|
| AlphaFold |
Q8VEW5 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000080106
AA Change: H5L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000079005
Gene: ENSMUSG00000093980
AA Change: H5L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
34 |
311 |
7.1e-55 |
PFAM |
|
Pfam:7tm_1
|
44 |
293 |
1.1e-22 |
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 |
|---|
| Asl |
C |
T |
5: 130,040,442 (GRCm39) |
W450* |
probably null |
Het |
| Copg1 |
T |
C |
6: 87,879,192 (GRCm39) |
Y413H |
possibly damaging |
Het |
| Ctsll3 |
G |
T |
13: 60,947,423 (GRCm39) |
H254Q |
possibly damaging |
Het |
| Ebf2 |
A |
G |
14: 67,665,545 (GRCm39) |
T568A |
probably benign |
Het |
| Etnppl |
C |
A |
3: 130,420,194 (GRCm39) |
S8R |
probably benign |
Het |
| Fry |
C |
A |
5: 150,327,059 (GRCm39) |
N1248K |
probably benign |
Het |
| Gpr55 |
A |
C |
1: 85,868,969 (GRCm39) |
I204S |
probably damaging |
Het |
| Hyal5 |
T |
A |
6: 24,876,724 (GRCm39) |
M199K |
probably damaging |
Het |
| Ighg2c |
T |
C |
12: 113,248,986 (GRCm39) |
|
probably benign |
Het |
| Itga4 |
A |
G |
2: 79,122,413 (GRCm39) |
D542G |
probably damaging |
Het |
| Itgb2 |
T |
G |
10: 77,395,530 (GRCm39) |
Y544D |
possibly damaging |
Het |
| Lamb2 |
A |
G |
9: 108,364,318 (GRCm39) |
N1086D |
possibly damaging |
Het |
| Lhx2 |
C |
T |
2: 38,258,849 (GRCm39) |
|
probably benign |
Het |
| Nlrp4c |
T |
G |
7: 6,095,582 (GRCm39) |
L820R |
probably damaging |
Het |
| Phf20l1 |
C |
T |
15: 66,500,840 (GRCm39) |
S578F |
probably damaging |
Het |
| Pramel23 |
A |
T |
4: 143,423,644 (GRCm39) |
Y382N |
probably damaging |
Het |
| Ptpn3 |
A |
T |
4: 57,222,019 (GRCm39) |
D557E |
probably damaging |
Het |
| Slc6a6 |
G |
A |
6: 91,712,160 (GRCm39) |
V230I |
probably benign |
Het |
| Stap2 |
T |
C |
17: 56,312,473 (GRCm39) |
H20R |
probably damaging |
Het |
| Sult1c2 |
T |
C |
17: 54,279,068 (GRCm39) |
T83A |
possibly damaging |
Het |
| Tspyl2 |
A |
T |
X: 151,122,103 (GRCm39) |
D501E |
probably damaging |
Het |
| Unc13b |
A |
G |
4: 43,091,270 (GRCm39) |
K32R |
probably null |
Het |
| Wnt3 |
G |
A |
11: 103,703,185 (GRCm39) |
A223T |
probably benign |
Het |
| Zfpm2 |
A |
T |
15: 40,966,517 (GRCm39) |
N869Y |
probably damaging |
Het |
| Zranb1 |
T |
C |
7: 132,575,146 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Or5p68 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01152:Or5p68
|
APN |
7 |
107,946,156 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02484:Or5p68
|
APN |
7 |
107,945,813 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02961:Or5p68
|
APN |
7 |
107,945,334 (GRCm39) |
missense |
probably benign |
0.08 |
|
IGL03379:Or5p68
|
APN |
7 |
107,946,196 (GRCm39) |
unclassified |
probably benign |
|
|
PIT4486001:Or5p68
|
UTSW |
7 |
107,945,529 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0281:Or5p68
|
UTSW |
7 |
107,946,121 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0285:Or5p68
|
UTSW |
7 |
107,945,706 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1222:Or5p68
|
UTSW |
7 |
107,945,313 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1912:Or5p68
|
UTSW |
7 |
107,946,014 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4178:Or5p68
|
UTSW |
7 |
107,945,765 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5239:Or5p68
|
UTSW |
7 |
107,945,853 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5421:Or5p68
|
UTSW |
7 |
107,946,182 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5452:Or5p68
|
UTSW |
7 |
107,945,312 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6991:Or5p68
|
UTSW |
7 |
107,945,295 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R7372:Or5p68
|
UTSW |
7 |
107,945,703 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7374:Or5p68
|
UTSW |
7 |
107,946,095 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7571:Or5p68
|
UTSW |
7 |
107,945,689 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8232:Or5p68
|
UTSW |
7 |
107,945,495 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8354:Or5p68
|
UTSW |
7 |
107,945,889 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8454:Or5p68
|
UTSW |
7 |
107,945,889 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8914:Or5p68
|
UTSW |
7 |
107,945,759 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9087:Or5p68
|
UTSW |
7 |
107,945,958 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9258:Or5p68
|
UTSW |
7 |
107,945,886 (GRCm39) |
missense |
probably benign |
0.21 |
|
R9608:Or5p68
|
UTSW |
7 |
107,945,513 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9751:Or5p68
|
UTSW |
7 |
107,945,645 (GRCm39) |
missense |
probably benign |
0.02 |
|
X0025:Or5p68
|
UTSW |
7 |
107,945,808 (GRCm39) |
missense |
probably benign |
0.01 |
|
| Posted On |
2015-04-16 |
Incidental Mutation