Incidental Mutation 'R8965:Or10ag53'
| ID |
682659 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or10ag53
|
| Ensembl Gene |
ENSMUSG00000070856 |
| Gene Name |
olfactory receptor family 10 subfamily AG member 53 |
| Synonyms |
GA_x6K02T2Q125-48736906-48737886, MOR273-4P, MOR273-4P, Olfr1530-ps1, MOR264-20, Olfr1115 |
| MMRRC Submission |
068799-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.055)
|
| Stock # |
R8965 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
87082184-87083285 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 87082901 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Phenylalanine
at position 207
(I207F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150996
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000081986]
[ENSMUST00000213513]
[ENSMUST00000214119]
[ENSMUST00000217196]
|
| AlphaFold |
Q7TR53 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000081986
AA Change: I207F
PolyPhen 2
Score 0.864 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000080647
Gene: ENSMUSG00000070856
AA Change: I207F
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
46 |
323 |
5e-54 |
PFAM |
|
Pfam:7tm_1
|
56 |
305 |
3e-23 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000213513
AA Change: I207F
PolyPhen 2
Score 0.864 (Sensitivity: 0.83; Specificity: 0.93)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000214119
AA Change: I207F
PolyPhen 2
Score 0.864 (Sensitivity: 0.83; Specificity: 0.93)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000217196
AA Change: I207F
PolyPhen 2
Score 0.864 (Sensitivity: 0.83; Specificity: 0.93)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.5%
- 20x: 98.5%
|
| 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: 43 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2210408I21Rik |
T |
A |
13: 77,760,723 (GRCm39) |
I1260K |
probably benign |
Het |
| Ace3 |
G |
T |
11: 105,896,175 (GRCm39) |
C707F |
probably benign |
Het |
| Ahi1 |
A |
G |
10: 20,839,761 (GRCm39) |
H224R |
probably benign |
Het |
| Atp1a2 |
T |
C |
1: 172,107,612 (GRCm39) |
D669G |
probably benign |
Het |
| Cdk5rap2 |
A |
C |
4: 70,185,042 (GRCm39) |
V1136G |
probably benign |
Het |
| Cntnap4 |
T |
A |
8: 113,479,646 (GRCm39) |
V277E |
probably damaging |
Het |
| Cyp2d12 |
T |
C |
15: 82,443,186 (GRCm39) |
L416P |
possibly damaging |
Het |
| Dnah17 |
T |
G |
11: 117,915,492 (GRCm39) |
T4376P |
probably damaging |
Het |
| E4f1 |
C |
T |
17: 24,664,504 (GRCm39) |
V429M |
probably benign |
Het |
| Epha8 |
G |
T |
4: 136,665,897 (GRCm39) |
L420M |
probably damaging |
Het |
| Erich6 |
A |
T |
3: 58,531,738 (GRCm39) |
D419E |
probably benign |
Het |
| Grid2 |
A |
G |
6: 64,296,990 (GRCm39) |
E451G |
probably damaging |
Het |
| Herpud1 |
T |
C |
8: 95,118,469 (GRCm39) |
Y181H |
probably damaging |
Het |
| Igkv2-109 |
A |
T |
6: 68,280,112 (GRCm39) |
Y111F |
probably damaging |
Het |
| Lztr1 |
T |
C |
16: 17,327,296 (GRCm39) |
|
probably null |
Het |
| Myh13 |
A |
T |
11: 67,255,432 (GRCm39) |
M1601L |
probably benign |
Het |
| Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
| Or2w2 |
T |
C |
13: 21,758,387 (GRCm39) |
T80A |
probably benign |
Het |
| Or5p52 |
T |
C |
7: 107,502,314 (GRCm39) |
L130P |
probably damaging |
Het |
| P2rx1 |
T |
C |
11: 72,900,051 (GRCm39) |
V156A |
probably benign |
Het |
| P3h2 |
T |
C |
16: 25,791,134 (GRCm39) |
N444S |
probably benign |
Het |
| Patz1 |
T |
C |
11: 3,257,815 (GRCm39) |
Y559H |
probably damaging |
Het |
| Pcna |
T |
C |
2: 132,094,769 (GRCm39) |
D63G |
possibly damaging |
Het |
| Pcnx2 |
G |
A |
8: 126,485,853 (GRCm39) |
A1915V |
probably benign |
Het |
| Peli1 |
T |
C |
11: 21,098,488 (GRCm39) |
Y408H |
probably damaging |
Het |
| Psma5 |
T |
A |
3: 108,172,510 (GRCm39) |
|
probably null |
Het |
| Ptpn11 |
G |
A |
5: 121,301,229 (GRCm39) |
T205M |
possibly damaging |
Het |
| Rapgef2 |
A |
G |
3: 78,999,851 (GRCm39) |
L453P |
probably damaging |
Het |
| Slc12a4 |
A |
G |
8: 106,671,982 (GRCm39) |
V910A |
possibly damaging |
Het |
| Spaca6 |
A |
G |
17: 18,058,718 (GRCm39) |
T306A |
probably damaging |
Het |
| Spata6 |
T |
A |
4: 111,680,009 (GRCm39) |
Y422* |
probably null |
Het |
| Svop |
A |
G |
5: 114,173,271 (GRCm39) |
Y367H |
probably benign |
Het |
| Trgv3 |
T |
A |
13: 19,427,180 (GRCm39) |
L21Q |
probably damaging |
Het |
| Trim38 |
T |
C |
13: 23,975,006 (GRCm39) |
L315S |
possibly damaging |
Het |
| Ttc12 |
A |
G |
9: 49,349,718 (GRCm39) |
V693A |
probably benign |
Het |
| Usp20 |
T |
A |
2: 30,901,797 (GRCm39) |
Y521N |
possibly damaging |
Het |
| Vcam1 |
T |
A |
3: 115,922,422 (GRCm39) |
K34* |
probably null |
Het |
| Vwa1 |
A |
T |
4: 155,857,440 (GRCm39) |
Y119* |
probably null |
Het |
| Vwa5b2 |
A |
G |
16: 20,415,076 (GRCm39) |
H366R |
possibly damaging |
Het |
| Wac |
C |
A |
18: 7,905,936 (GRCm39) |
Q168K |
probably benign |
Het |
| Wipf2 |
A |
G |
11: 98,783,497 (GRCm39) |
S308G |
probably benign |
Het |
| Zbtb25 |
A |
C |
12: 76,396,577 (GRCm39) |
I215S |
probably benign |
Het |
| Zfp677 |
T |
C |
17: 21,617,155 (GRCm39) |
S71P |
probably damaging |
Het |
|
| Other mutations in Or10ag53 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01101:Or10ag53
|
APN |
2 |
87,082,806 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01376:Or10ag53
|
APN |
2 |
87,083,217 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
IGL02167:Or10ag53
|
APN |
2 |
87,082,542 (GRCm39) |
missense |
probably benign |
0.18 |
|
IGL02224:Or10ag53
|
APN |
2 |
87,082,821 (GRCm39) |
missense |
probably benign |
0.42 |
|
IGL02388:Or10ag53
|
APN |
2 |
87,082,295 (GRCm39) |
missense |
probably benign |
|
|
IGL02596:Or10ag53
|
APN |
2 |
87,082,473 (GRCm39) |
missense |
probably damaging |
0.98 |
|
PIT4131001:Or10ag53
|
UTSW |
2 |
87,082,973 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0140:Or10ag53
|
UTSW |
2 |
87,082,969 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0468:Or10ag53
|
UTSW |
2 |
87,082,599 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1222:Or10ag53
|
UTSW |
2 |
87,082,766 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1418:Or10ag53
|
UTSW |
2 |
87,082,766 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1742:Or10ag53
|
UTSW |
2 |
87,083,122 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1822:Or10ag53
|
UTSW |
2 |
87,083,054 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R2332:Or10ag53
|
UTSW |
2 |
87,083,217 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R3123:Or10ag53
|
UTSW |
2 |
87,083,135 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R3407:Or10ag53
|
UTSW |
2 |
87,083,243 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4571:Or10ag53
|
UTSW |
2 |
87,082,802 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R4710:Or10ag53
|
UTSW |
2 |
87,082,384 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R4889:Or10ag53
|
UTSW |
2 |
87,082,991 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5031:Or10ag53
|
UTSW |
2 |
87,082,426 (GRCm39) |
missense |
probably benign |
|
|
R5288:Or10ag53
|
UTSW |
2 |
87,082,827 (GRCm39) |
missense |
probably benign |
0.06 |
|
R5385:Or10ag53
|
UTSW |
2 |
87,082,827 (GRCm39) |
missense |
probably benign |
0.06 |
|
R5386:Or10ag53
|
UTSW |
2 |
87,082,827 (GRCm39) |
missense |
probably benign |
0.06 |
|
R5669:Or10ag53
|
UTSW |
2 |
87,082,785 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6187:Or10ag53
|
UTSW |
2 |
87,083,042 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6226:Or10ag53
|
UTSW |
2 |
87,082,736 (GRCm39) |
missense |
probably benign |
0.27 |
|
R6598:Or10ag53
|
UTSW |
2 |
87,083,100 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8208:Or10ag53
|
UTSW |
2 |
87,083,007 (GRCm39) |
missense |
probably benign |
0.24 |
|
R8493:Or10ag53
|
UTSW |
2 |
87,083,215 (GRCm39) |
missense |
probably benign |
0.24 |
|
R8724:Or10ag53
|
UTSW |
2 |
87,082,704 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9015:Or10ag53
|
UTSW |
2 |
87,082,546 (GRCm39) |
nonsense |
probably null |
|
|
R9302:Or10ag53
|
UTSW |
2 |
87,082,906 (GRCm39) |
missense |
probably benign |
0.10 |
|
R9742:Or10ag53
|
UTSW |
2 |
87,082,376 (GRCm39) |
missense |
probably benign |
0.29 |
|
R9758:Or10ag53
|
UTSW |
2 |
87,082,439 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R9775:Or10ag53
|
UTSW |
2 |
87,082,568 (GRCm39) |
missense |
probably damaging |
0.96 |
|
| Predicted Primers |
PCR Primer
(F):5'- GTCATGAGTTCCAAGGTGTGTAC -3'
(R):5'- ACAGAGAGAAGTTTGTCTGTCTCC -3'
Sequencing Primer
(F):5'- ACCCAGTTAGTGGTTGGTTCC -3'
(R):5'- AGAGAAGTTTGTCTGTCTCCTCATAC -3'
|
| Posted On |
2021-10-11 |
Incidental Mutation