Incidental Mutation 'IGL02624:Or5p1'
| ID |
300983 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or5p1
|
| Ensembl Gene |
ENSMUSG00000094612 |
| Gene Name |
olfactory receptor family 5 subfamily P member 1 |
| Synonyms |
MOR204-11, GA_x6K02T2PBJ9-10646917-10647849, Olfr491 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.094)
|
| Stock # |
IGL02624
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
107916103-107917035 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 107916130 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Serine
at position 10
(T10S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150694
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053179]
[ENSMUST00000209545]
[ENSMUST00000214605]
|
| AlphaFold |
Q8VG06 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000053179
AA Change: T10S
PolyPhen 2
Score 0.379 (Sensitivity: 0.90; Specificity: 0.89)
|
| SMART Domains |
Protein: ENSMUSP00000061188
Gene: ENSMUSG00000094612
AA Change: T10S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
307 |
3.4e-50 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
5.4e-20 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000209545
AA Change: T10S
PolyPhen 2
Score 0.379 (Sensitivity: 0.90; Specificity: 0.89)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214605
AA Change: T10S
PolyPhen 2
Score 0.379 (Sensitivity: 0.90; Specificity: 0.89)
|
| 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: 33 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A930004D18Rik |
A |
G |
2: 18,032,004 (GRCm39) |
V38A |
unknown |
Het |
| Armc8 |
T |
C |
9: 99,409,122 (GRCm39) |
|
probably benign |
Het |
| Brk1 |
T |
G |
6: 113,581,805 (GRCm39) |
I22M |
possibly damaging |
Het |
| Cd3g |
A |
G |
9: 44,885,459 (GRCm39) |
|
probably null |
Het |
| Cep192 |
T |
C |
18: 68,013,866 (GRCm39) |
V2422A |
probably benign |
Het |
| Ces2g |
T |
C |
8: 105,691,380 (GRCm39) |
V172A |
probably damaging |
Het |
| Clcn2 |
G |
T |
16: 20,522,098 (GRCm39) |
S830R |
probably damaging |
Het |
| Cyp26b1 |
T |
C |
6: 84,561,321 (GRCm39) |
S114G |
probably benign |
Het |
| Dnali1 |
T |
C |
4: 124,952,791 (GRCm39) |
Q244R |
probably benign |
Het |
| Entpd1 |
A |
T |
19: 40,714,502 (GRCm39) |
K204* |
probably null |
Het |
| Gm5070 |
A |
G |
3: 95,318,219 (GRCm39) |
|
noncoding transcript |
Het |
| Gpsm2 |
G |
T |
3: 108,589,349 (GRCm39) |
D596E |
probably benign |
Het |
| Hectd1 |
C |
T |
12: 51,809,233 (GRCm39) |
A1743T |
possibly damaging |
Het |
| Kcnq5 |
T |
G |
1: 21,472,654 (GRCm39) |
L845F |
probably benign |
Het |
| Lmx1a |
G |
T |
1: 167,672,192 (GRCm39) |
|
probably benign |
Het |
| Lrp1 |
A |
T |
10: 127,408,291 (GRCm39) |
I1795N |
probably damaging |
Het |
| Lsp1 |
C |
T |
7: 142,044,288 (GRCm39) |
|
probably benign |
Het |
| Mcm6 |
C |
T |
1: 128,277,185 (GRCm39) |
A213T |
possibly damaging |
Het |
| Mylk |
G |
T |
16: 34,750,266 (GRCm39) |
V1202L |
probably benign |
Het |
| Myo5b |
T |
C |
18: 74,848,010 (GRCm39) |
Y1083H |
probably damaging |
Het |
| Ncoa5 |
T |
A |
2: 164,854,981 (GRCm39) |
D47V |
probably damaging |
Het |
| Npat |
C |
T |
9: 53,478,110 (GRCm39) |
T954I |
probably damaging |
Het |
| Or2b28 |
A |
G |
13: 21,531,682 (GRCm39) |
T195A |
probably benign |
Het |
| Pfkm |
T |
C |
15: 98,024,276 (GRCm39) |
I428T |
probably benign |
Het |
| Rai1 |
T |
C |
11: 60,079,569 (GRCm39) |
F1211S |
probably damaging |
Het |
| Reln |
T |
C |
5: 22,308,355 (GRCm39) |
E338G |
probably benign |
Het |
| Tbx18 |
T |
C |
9: 87,609,459 (GRCm39) |
Y192C |
probably damaging |
Het |
| Tex21 |
T |
A |
12: 76,261,398 (GRCm39) |
D250V |
probably damaging |
Het |
| Tpo |
A |
G |
12: 30,150,413 (GRCm39) |
V489A |
probably benign |
Het |
| Tspo |
T |
C |
15: 83,455,616 (GRCm39) |
M1T |
probably null |
Het |
| Wdr38 |
A |
T |
2: 38,888,424 (GRCm39) |
N7I |
probably damaging |
Het |
| Wnk2 |
C |
T |
13: 49,256,278 (GRCm39) |
G281D |
probably damaging |
Het |
| Zfhx2 |
T |
C |
14: 55,304,085 (GRCm39) |
T1300A |
probably benign |
Het |
|
| Other mutations in Or5p1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01672:Or5p1
|
APN |
7 |
107,916,725 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01731:Or5p1
|
APN |
7 |
107,916,682 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02227:Or5p1
|
APN |
7 |
107,916,408 (GRCm39) |
nonsense |
probably null |
|
|
IGL03164:Or5p1
|
APN |
7 |
107,916,901 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0143:Or5p1
|
UTSW |
7 |
107,916,202 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0217:Or5p1
|
UTSW |
7 |
107,916,505 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0295:Or5p1
|
UTSW |
7 |
107,916,892 (GRCm39) |
missense |
probably benign |
0.42 |
|
R2100:Or5p1
|
UTSW |
7 |
107,916,761 (GRCm39) |
missense |
probably benign |
0.04 |
|
R2379:Or5p1
|
UTSW |
7 |
107,916,499 (GRCm39) |
missense |
probably benign |
0.25 |
|
R4178:Or5p1
|
UTSW |
7 |
107,916,565 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4365:Or5p1
|
UTSW |
7 |
107,916,313 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4734:Or5p1
|
UTSW |
7 |
107,916,959 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4828:Or5p1
|
UTSW |
7 |
107,916,677 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6424:Or5p1
|
UTSW |
7 |
107,916,412 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6784:Or5p1
|
UTSW |
7 |
107,916,989 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7109:Or5p1
|
UTSW |
7 |
107,916,959 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7348:Or5p1
|
UTSW |
7 |
107,916,920 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R7590:Or5p1
|
UTSW |
7 |
107,916,386 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8124:Or5p1
|
UTSW |
7 |
107,916,984 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R8782:Or5p1
|
UTSW |
7 |
107,916,296 (GRCm39) |
missense |
probably damaging |
0.99 |
|
X0060:Or5p1
|
UTSW |
7 |
107,916,427 (GRCm39) |
missense |
probably benign |
0.06 |
|
| Posted On |
2015-04-16 |
Incidental Mutation