Incidental Mutation 'R3853:Or8b1'
| ID |
276014 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or8b1
|
| Ensembl Gene |
ENSMUSG00000039962 |
| Gene Name |
olfactory receptor family 8 subfamily B member 1 |
| Synonyms |
Olfr906, GA_x6K02T2PVTD-32194085-32195020, MOR167-2 |
| MMRRC Submission |
040900-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.060)
|
| Stock # |
R3853 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
38399327-38400262 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 38400247 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Serine
at position 307
(R307S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151008
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000045493]
[ENSMUST00000214344]
|
| AlphaFold |
K7N5P3 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000045493
AA Change: R307S
PolyPhen 2
Score 0.179 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000039040
Gene: ENSMUSG00000039962
AA Change: R307S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
307 |
3.6e-50 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
2.1e-21 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214344
AA Change: R307S
PolyPhen 2
Score 0.179 (Sensitivity: 0.92; Specificity: 0.87)
|
| Coding Region Coverage |
- 1x: 99.6%
- 3x: 98.8%
- 10x: 97.2%
- 20x: 94.4%
|
| Validation Efficiency |
96% (47/49) |
| 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: 44 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2010315B03Rik |
T |
A |
9: 124,055,976 (GRCm39) |
H316L |
probably damaging |
Het |
| Cadps |
A |
G |
14: 12,509,090 (GRCm38) |
|
probably benign |
Het |
| Cluh |
A |
G |
11: 74,547,279 (GRCm39) |
D44G |
probably benign |
Het |
| Copb1 |
A |
G |
7: 113,822,551 (GRCm39) |
V726A |
probably damaging |
Het |
| Dsg4 |
T |
C |
18: 20,582,291 (GRCm39) |
V79A |
probably benign |
Het |
| Exo1 |
A |
T |
1: 175,720,554 (GRCm39) |
I291F |
probably benign |
Het |
| Eya4 |
C |
T |
10: 22,992,574 (GRCm39) |
A460T |
probably damaging |
Het |
| Gjd3 |
G |
T |
11: 102,690,952 (GRCm39) |
D350E |
probably benign |
Het |
| Hcar2 |
T |
C |
5: 124,002,475 (GRCm39) |
M343V |
probably benign |
Het |
| Ifna15 |
T |
C |
4: 88,476,046 (GRCm39) |
Y146C |
probably damaging |
Het |
| Lce3e |
C |
T |
3: 92,875,139 (GRCm39) |
Q32* |
probably null |
Het |
| Llgl1 |
T |
C |
11: 60,598,075 (GRCm39) |
L373P |
probably damaging |
Het |
| Mark2 |
A |
G |
19: 7,254,655 (GRCm39) |
C642R |
probably damaging |
Het |
| Mbd3l2 |
A |
G |
9: 18,356,092 (GRCm39) |
Q139R |
probably benign |
Het |
| Mki67 |
A |
C |
7: 135,297,859 (GRCm39) |
S2392A |
probably benign |
Het |
| Nynrin |
T |
A |
14: 56,101,562 (GRCm39) |
N410K |
probably benign |
Het |
| Or10g7 |
A |
T |
9: 39,905,450 (GRCm39) |
T115S |
probably damaging |
Het |
| Or4a71 |
A |
T |
2: 89,357,917 (GRCm39) |
M279K |
possibly damaging |
Het |
| Or5b112 |
A |
G |
19: 13,319,862 (GRCm39) |
T247A |
possibly damaging |
Het |
| Or7a38 |
T |
A |
10: 78,752,781 (GRCm39) |
Y36N |
probably damaging |
Het |
| Padi3 |
T |
C |
4: 140,518,580 (GRCm39) |
|
probably benign |
Het |
| Prkce |
A |
G |
17: 86,476,277 (GRCm39) |
D86G |
probably damaging |
Het |
| Pwwp3b |
C |
T |
X: 138,137,403 (GRCm39) |
|
probably null |
Het |
| Rad21 |
T |
G |
15: 51,835,712 (GRCm39) |
I234L |
probably benign |
Het |
| Scn4a |
A |
T |
11: 106,210,932 (GRCm39) |
M1695K |
possibly damaging |
Het |
| Sdccag8 |
T |
C |
1: 176,681,361 (GRCm39) |
S325P |
probably damaging |
Het |
| Sebox |
G |
A |
11: 78,394,975 (GRCm39) |
G106R |
probably benign |
Het |
| Serpinb9 |
A |
G |
13: 33,199,503 (GRCm39) |
E266G |
possibly damaging |
Het |
| Shoc1 |
T |
C |
4: 59,047,390 (GRCm39) |
N1410D |
possibly damaging |
Het |
| Snx14 |
T |
C |
9: 88,289,372 (GRCm39) |
|
probably benign |
Het |
| Tmc6 |
A |
T |
11: 117,663,884 (GRCm39) |
L474* |
probably null |
Het |
| Tmem132c |
T |
C |
5: 127,436,933 (GRCm39) |
Y141H |
probably benign |
Het |
| Trap1 |
G |
A |
16: 3,872,686 (GRCm39) |
R328C |
possibly damaging |
Het |
| Trim36 |
C |
A |
18: 46,305,439 (GRCm39) |
|
probably benign |
Het |
| Trmt2a |
A |
T |
16: 18,069,055 (GRCm39) |
Y299F |
possibly damaging |
Het |
| Trrap |
A |
G |
5: 144,728,975 (GRCm39) |
K630E |
probably damaging |
Het |
| Tsnaxip1 |
A |
T |
8: 106,567,333 (GRCm39) |
|
probably benign |
Het |
| Ttc6 |
G |
T |
12: 57,775,335 (GRCm39) |
C1677F |
possibly damaging |
Het |
| Ugt2a3 |
A |
T |
5: 87,485,018 (GRCm39) |
V2D |
|
Het |
| Usp9x |
A |
G |
X: 12,964,822 (GRCm39) |
D77G |
probably benign |
Het |
| Wfs1 |
C |
A |
5: 37,125,968 (GRCm39) |
V308L |
probably benign |
Het |
| Zan |
A |
C |
5: 137,472,326 (GRCm39) |
L140R |
probably damaging |
Het |
| Zc3h3 |
A |
T |
15: 75,709,346 (GRCm39) |
S508T |
probably benign |
Het |
| Zswim3 |
A |
G |
2: 164,662,777 (GRCm39) |
Y419C |
possibly damaging |
Het |
|
| Other mutations in Or8b1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL03127:Or8b1
|
APN |
9 |
38,399,882 (GRCm39) |
missense |
probably benign |
0.13 |
|
R0948:Or8b1
|
UTSW |
9 |
38,400,244 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1236:Or8b1
|
UTSW |
9 |
38,399,525 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1246:Or8b1
|
UTSW |
9 |
38,400,086 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1442:Or8b1
|
UTSW |
9 |
38,399,939 (GRCm39) |
missense |
probably benign |
0.10 |
|
R2016:Or8b1
|
UTSW |
9 |
38,399,309 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R2264:Or8b1
|
UTSW |
9 |
38,399,351 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R2268:Or8b1
|
UTSW |
9 |
38,399,504 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4066:Or8b1
|
UTSW |
9 |
38,399,778 (GRCm39) |
missense |
probably benign |
0.17 |
|
R4594:Or8b1
|
UTSW |
9 |
38,400,057 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5192:Or8b1
|
UTSW |
9 |
38,400,101 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R5436:Or8b1
|
UTSW |
9 |
38,399,835 (GRCm39) |
missense |
probably benign |
0.31 |
|
R5598:Or8b1
|
UTSW |
9 |
38,399,821 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R5694:Or8b1
|
UTSW |
9 |
38,399,532 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5914:Or8b1
|
UTSW |
9 |
38,399,657 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5959:Or8b1
|
UTSW |
9 |
38,400,207 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6318:Or8b1
|
UTSW |
9 |
38,399,673 (GRCm39) |
missense |
probably benign |
|
|
R6870:Or8b1
|
UTSW |
9 |
38,399,382 (GRCm39) |
missense |
probably benign |
0.19 |
|
R7482:Or8b1
|
UTSW |
9 |
38,399,747 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7571:Or8b1
|
UTSW |
9 |
38,399,952 (GRCm39) |
missense |
probably benign |
0.08 |
|
R7917:Or8b1
|
UTSW |
9 |
38,399,905 (GRCm39) |
nonsense |
probably null |
|
|
R8837:Or8b1
|
UTSW |
9 |
38,399,597 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9562:Or8b1
|
UTSW |
9 |
38,400,092 (GRCm39) |
missense |
possibly damaging |
0.45 |
|
R9628:Or8b1
|
UTSW |
9 |
38,399,871 (GRCm39) |
missense |
probably benign |
0.17 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGCAGTTCCCACATAATTGCTG -3'
(R):5'- GGTAGACATAGTCTCATTTGTGAGTTC -3'
Sequencing Primer
(F):5'- AGTTCCCACATAATTGCTGTTTCTC -3'
(R):5'- GCAAAATTTCATCTCAGCATTCG -3'
|
| Posted On |
2015-04-06 |
Incidental Mutation