Incidental Mutation 'R9783:Or5d38'
| ID |
734151 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or5d38
|
| Ensembl Gene |
ENSMUSG00000101078 |
| Gene Name |
olfactory receptor family 5 subfamily D member 38 |
| Synonyms |
GA_x6K02T2Q125-49616865-49615915, MOR174-6, Olfr1166 |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.095)
|
| Stock # |
R9783 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
87953704-87955337 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 87954610 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Phenylalanine to Isoleucine
at position 240
(F240I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149099
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099833]
[ENSMUST00000217575]
|
| AlphaFold |
Q7TR27 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099833
AA Change: F240I
PolyPhen 2
Score 0.066 (Sensitivity: 0.94; Specificity: 0.84)
|
| SMART Domains |
Protein: ENSMUSP00000097421
Gene: ENSMUSG00000101078
AA Change: F240I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
33 |
310 |
6e-51 |
PFAM |
|
Pfam:7tm_1
|
43 |
292 |
3e-14 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000217575
AA Change: F240I
PolyPhen 2
Score 0.066 (Sensitivity: 0.94; Specificity: 0.84)
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.8%
- 10x: 99.4%
- 20x: 98.7%
|
| 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: 37 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Cdkn2aip |
A |
G |
8: 48,164,090 (GRCm39) |
V541A |
possibly damaging |
Het |
| Cep170b |
C |
A |
12: 112,711,118 (GRCm39) |
D1499E |
probably damaging |
Het |
| Cers2 |
T |
C |
3: 95,229,438 (GRCm39) |
S248P |
probably benign |
Het |
| Chd5 |
T |
A |
4: 152,458,865 (GRCm39) |
I1076N |
probably damaging |
Het |
| Col6a2 |
T |
C |
10: 76,440,720 (GRCm39) |
|
probably null |
Het |
| D6Ertd527e |
G |
A |
6: 87,088,602 (GRCm39) |
G255D |
unknown |
Het |
| Dennd5b |
T |
C |
6: 148,911,342 (GRCm39) |
T954A |
probably damaging |
Het |
| Dmc1 |
A |
G |
15: 79,484,296 (GRCm39) |
L65P |
probably damaging |
Het |
| Dock2 |
A |
G |
11: 34,208,128 (GRCm39) |
Y1307H |
possibly damaging |
Het |
| Gckr |
G |
A |
5: 31,466,399 (GRCm39) |
S458N |
probably benign |
Het |
| Gpx4 |
T |
C |
10: 79,890,851 (GRCm39) |
V181A |
possibly damaging |
Het |
| Hmcn1 |
C |
T |
1: 150,598,380 (GRCm39) |
E1641K |
probably benign |
Het |
| Htr7 |
A |
G |
19: 35,946,787 (GRCm39) |
I409T |
probably damaging |
Het |
| Ighv8-9 |
C |
T |
12: 115,431,994 (GRCm39) |
V106M |
probably benign |
Het |
| Kri1 |
T |
C |
9: 21,190,709 (GRCm39) |
E384G |
|
Het |
| Lyz3 |
T |
C |
10: 117,073,653 (GRCm39) |
N60S |
possibly damaging |
Het |
| Mfhas1 |
T |
C |
8: 36,057,934 (GRCm39) |
L803P |
probably damaging |
Het |
| Mfsd14b |
C |
A |
13: 65,221,414 (GRCm39) |
V293L |
probably benign |
Het |
| Noxa1 |
C |
A |
2: 24,985,053 (GRCm39) |
|
probably benign |
Het |
| Or1j16 |
A |
G |
2: 36,530,161 (GRCm39) |
T37A |
probably benign |
Het |
| Otof |
T |
C |
5: 30,536,576 (GRCm39) |
K1302E |
probably benign |
Het |
| Pdcl |
A |
G |
2: 37,242,174 (GRCm39) |
V192A |
probably benign |
Het |
| Plxdc2 |
C |
T |
2: 16,674,349 (GRCm39) |
Q310* |
probably null |
Het |
| Pola2 |
C |
T |
19: 5,990,904 (GRCm39) |
V597M |
probably damaging |
Het |
| Prkcd |
T |
A |
14: 30,321,444 (GRCm39) |
Y549F |
probably damaging |
Het |
| Rho |
T |
C |
6: 115,910,920 (GRCm39) |
M155T |
probably benign |
Het |
| Scap |
C |
T |
9: 110,202,132 (GRCm39) |
H167Y |
probably benign |
Het |
| Sfn |
T |
C |
4: 133,329,128 (GRCm39) |
|
probably benign |
Het |
| Shank1 |
G |
A |
7: 43,962,342 (GRCm39) |
S71N |
unknown |
Het |
| Slc13a2 |
T |
A |
11: 78,294,177 (GRCm39) |
T235S |
probably damaging |
Het |
| Slc40a1 |
A |
G |
1: 45,951,513 (GRCm39) |
S215P |
probably damaging |
Het |
| Spam1 |
G |
A |
6: 24,796,226 (GRCm39) |
R59H |
probably benign |
Het |
| Tmeff1 |
T |
C |
4: 48,662,005 (GRCm39) |
C347R |
probably damaging |
Het |
| Tmprss15 |
T |
C |
16: 78,887,890 (GRCm39) |
|
probably benign |
Het |
| Ugt2b37 |
G |
T |
5: 87,388,840 (GRCm39) |
L458M |
probably damaging |
Het |
| Unc13c |
T |
A |
9: 73,392,227 (GRCm39) |
I2042F |
probably benign |
Het |
| Zfp12 |
C |
A |
5: 143,230,513 (GRCm39) |
T312K |
probably damaging |
Het |
|
| Other mutations in Or5d38 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01109:Or5d38
|
APN |
2 |
87,955,023 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1037:Or5d38
|
UTSW |
2 |
87,954,573 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1452:Or5d38
|
UTSW |
2 |
87,954,655 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1842:Or5d38
|
UTSW |
2 |
87,954,471 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2005:Or5d38
|
UTSW |
2 |
87,954,891 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4106:Or5d38
|
UTSW |
2 |
87,954,817 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R4930:Or5d38
|
UTSW |
2 |
87,954,684 (GRCm39) |
missense |
probably benign |
0.08 |
|
R5473:Or5d38
|
UTSW |
2 |
87,954,981 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R5911:Or5d38
|
UTSW |
2 |
87,955,027 (GRCm39) |
missense |
probably benign |
|
|
R6596:Or5d38
|
UTSW |
2 |
87,954,543 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7842:Or5d38
|
UTSW |
2 |
87,955,330 (GRCm39) |
start gained |
probably benign |
|
|
R8902:Or5d38
|
UTSW |
2 |
87,954,778 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8943:Or5d38
|
UTSW |
2 |
87,954,718 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9120:Or5d38
|
UTSW |
2 |
87,955,123 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9240:Or5d38
|
UTSW |
2 |
87,955,231 (GRCm39) |
missense |
probably benign |
0.26 |
|
R9733:Or5d38
|
UTSW |
2 |
87,955,000 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- CAGTTTTGAGCTGATAAGTCTCCTG -3'
(R):5'- CTTTGGCTGTGAGTACTCCG -3'
Sequencing Primer
(F):5'- GTCCTTCACATCTTTATTTCTAAGGC -3'
(R):5'- GCTGTGAGTACTCCGCTGTC -3'
|
| Posted On |
2022-11-14 |
Incidental Mutation