Incidental Mutation 'R6551:Or1o1'
| ID |
521652 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or1o1
|
| Ensembl Gene |
ENSMUSG00000063188 |
| Gene Name |
olfactory receptor family 1 subfamily O member 1 |
| Synonyms |
MOR156-3, GA_x6K02T2PSCP-1867165-1868094, Olfr107 |
| MMRRC Submission |
044676-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.051)
|
| Stock # |
R6551 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
17 |
| Chromosomal Location |
37716368-37717400 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 37716796 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Histidine
at position 119
(R119H)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148879
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077008]
[ENSMUST00000215894]
[ENSMUST00000215947]
[ENSMUST00000215974]
[ENSMUST00000216844]
|
| AlphaFold |
Q7TRK4 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000077008
AA Change: R119H
PolyPhen 2
Score 0.300 (Sensitivity: 0.90; Specificity: 0.89)
|
| SMART Domains |
Protein: ENSMUSP00000076267
Gene: ENSMUSG00000063188
AA Change: R119H
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
28 |
305 |
1.3e-54 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
32 |
302 |
1.3e-5 |
PFAM |
|
Pfam:7tm_1
|
38 |
287 |
3.7e-19 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000174238
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215894
AA Change: R119H
PolyPhen 2
Score 0.300 (Sensitivity: 0.90; Specificity: 0.89)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215947
AA Change: R119H
PolyPhen 2
Score 0.300 (Sensitivity: 0.90; Specificity: 0.89)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215974
AA Change: R119H
PolyPhen 2
Score 0.300 (Sensitivity: 0.90; Specificity: 0.89)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000216844
AA Change: R119H
PolyPhen 2
Score 0.300 (Sensitivity: 0.90; Specificity: 0.89)
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.3%
- 20x: 97.6%
|
| Validation Efficiency |
100% (41/41) |
| 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: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A130010J15Rik |
A |
T |
1: 192,856,831 (GRCm39) |
Q61L |
probably damaging |
Het |
| Acss2 |
T |
C |
2: 155,393,128 (GRCm39) |
S285P |
probably benign |
Het |
| Ager |
A |
G |
17: 34,818,442 (GRCm39) |
|
probably null |
Het |
| Alkbh7 |
T |
A |
17: 57,305,945 (GRCm39) |
Y115* |
probably null |
Het |
| Brwd1 |
T |
C |
16: 95,795,162 (GRCm39) |
D2184G |
possibly damaging |
Het |
| Chp1 |
T |
A |
2: 119,402,294 (GRCm39) |
H89Q |
possibly damaging |
Het |
| Clmp |
T |
C |
9: 40,682,573 (GRCm39) |
V119A |
probably benign |
Het |
| Cryge |
A |
T |
1: 65,087,796 (GRCm39) |
M171K |
probably benign |
Het |
| Cttnbp2nl |
A |
T |
3: 104,912,433 (GRCm39) |
S484T |
possibly damaging |
Het |
| Dsg3 |
C |
A |
18: 20,672,968 (GRCm39) |
P880T |
unknown |
Het |
| Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
| Espn |
T |
C |
4: 152,213,223 (GRCm39) |
|
|
Het |
| Fbxo31 |
A |
C |
8: 122,291,443 (GRCm39) |
|
probably benign |
Het |
| Grin2b |
A |
G |
6: 135,710,342 (GRCm39) |
V1068A |
probably damaging |
Het |
| Jak1 |
C |
A |
4: 101,051,040 (GRCm39) |
|
probably benign |
Het |
| Klra10 |
A |
T |
6: 130,252,718 (GRCm39) |
D185E |
probably benign |
Het |
| Lhx1 |
A |
C |
11: 84,412,739 (GRCm39) |
D60E |
probably benign |
Het |
| Lyar |
C |
A |
5: 38,390,616 (GRCm39) |
A326D |
probably damaging |
Het |
| Muc16 |
A |
C |
9: 18,473,858 (GRCm39) |
S1280A |
possibly damaging |
Het |
| Nol9 |
G |
A |
4: 152,136,325 (GRCm39) |
V466I |
possibly damaging |
Het |
| Or10d1 |
C |
A |
9: 39,483,856 (GRCm39) |
R233L |
probably benign |
Het |
| Or12e8 |
T |
C |
2: 87,677,005 (GRCm39) |
V130A |
possibly damaging |
Het |
| Or1e17 |
T |
C |
11: 73,831,129 (GRCm39) |
I19T |
probably benign |
Het |
| Or2w3b |
A |
T |
11: 58,623,583 (GRCm39) |
M136K |
probably damaging |
Het |
| Or2y10 |
G |
T |
11: 49,454,816 (GRCm39) |
V23L |
probably benign |
Het |
| Pik3c2a |
A |
T |
7: 116,016,731 (GRCm39) |
I342N |
probably damaging |
Het |
| Pnldc1 |
A |
G |
17: 13,124,456 (GRCm39) |
M133T |
probably damaging |
Het |
| Rab11fip1 |
G |
A |
8: 27,646,512 (GRCm39) |
S188L |
probably damaging |
Het |
| Rapgef2 |
A |
T |
3: 79,122,342 (GRCm39) |
|
probably null |
Het |
| Rnf103 |
G |
A |
6: 71,487,349 (GRCm39) |
C660Y |
probably damaging |
Het |
| Rph3al |
G |
A |
11: 75,797,372 (GRCm39) |
S108F |
possibly damaging |
Het |
| Srsf7 |
A |
C |
17: 80,511,648 (GRCm39) |
|
probably benign |
Het |
| Ssrp1 |
A |
G |
2: 84,871,450 (GRCm39) |
|
probably null |
Het |
| Tamm41 |
T |
C |
6: 114,989,142 (GRCm39) |
D284G |
possibly damaging |
Het |
| Tmem161b |
C |
A |
13: 84,370,537 (GRCm39) |
|
probably benign |
Het |
| Tmem39b |
A |
G |
4: 129,585,896 (GRCm39) |
V25A |
probably benign |
Het |
| Tmem88b |
G |
T |
4: 155,870,149 (GRCm39) |
|
probably benign |
Het |
| Unk |
T |
C |
11: 115,941,550 (GRCm39) |
W266R |
probably damaging |
Het |
| Usp8 |
T |
A |
2: 126,575,102 (GRCm39) |
|
probably benign |
Het |
| Zbtb48 |
T |
G |
4: 152,106,678 (GRCm39) |
Q142P |
probably benign |
Het |
| Zdhhc18 |
T |
C |
4: 133,340,960 (GRCm39) |
T267A |
probably benign |
Het |
| Zfp335 |
G |
A |
2: 164,751,285 (GRCm39) |
P94S |
probably benign |
Het |
|
| Other mutations in Or1o1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01323:Or1o1
|
APN |
17 |
37,717,031 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01614:Or1o1
|
APN |
17 |
37,716,529 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02390:Or1o1
|
APN |
17 |
37,716,986 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1051:Or1o1
|
UTSW |
17 |
37,717,341 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R4767:Or1o1
|
UTSW |
17 |
37,717,091 (GRCm39) |
nonsense |
probably null |
|
|
R4849:Or1o1
|
UTSW |
17 |
37,716,589 (GRCm39) |
missense |
probably benign |
0.16 |
|
R6182:Or1o1
|
UTSW |
17 |
37,716,883 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R6550:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
|
R6552:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
|
R6555:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
|
R6584:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
|
R6586:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
|
R6588:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
|
R6688:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
|
R6758:Or1o1
|
UTSW |
17 |
37,716,586 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7024:Or1o1
|
UTSW |
17 |
37,717,095 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7083:Or1o1
|
UTSW |
17 |
37,717,063 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8350:Or1o1
|
UTSW |
17 |
37,717,260 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GCTCTCACTAGTGGATCTTTGC -3'
(R):5'- ATCATCAGGCCCTCACTGAG -3'
Sequencing Primer
(F):5'- GGATCTTTGCTTCATCACCACAACAG -3'
(R):5'- CACTGAGGTGAGTGTCTGAGC -3'
|
| Posted On |
2018-06-06 |
Incidental Mutation