Incidental Mutation 'R5342:Olfr857'
| ID |
422391 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Olfr857
|
| Ensembl Gene |
ENSMUSG00000094678 |
| Gene Name |
olfactory receptor 857 |
| Synonyms |
MOR146-8P, GA_x6K02T2PVTD-13452606-13453535 |
| MMRRC Submission |
042921-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.066)
|
| Stock # |
R5342 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
19709433-19714930 bp(+) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 19713037 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 70
(D70G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150889
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077023]
[ENSMUST00000212013]
[ENSMUST00000217450]
|
| AlphaFold |
A0A1L1SUS1 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000077023
AA Change: D70G
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000076281
Gene: ENSMUSG00000094678
AA Change: D70G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
2.5e-49 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
304 |
1.5e-5 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
9.4e-21 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000212013
AA Change: D70G
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000212753
AA Change: D35G
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000217450
AA Change: D70G
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.8%
- 10x: 97.6%
- 20x: 96.1%
|
| 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: 48 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adrb3 |
A |
C |
8: 27,226,781 (GRCm38) |
Y392* |
probably null |
Het |
| Arap1 |
G |
A |
7: 101,404,960 (GRCm38) |
E1330K |
probably benign |
Het |
| Atg2b |
G |
T |
12: 105,658,916 (GRCm38) |
D600E |
possibly damaging |
Het |
| Atp1b2 |
C |
T |
11: 69,602,828 (GRCm38) |
V142I |
probably damaging |
Het |
| AW551984 |
A |
T |
9: 39,594,551 (GRCm38) |
M450K |
probably damaging |
Het |
| BC067074 |
T |
C |
13: 113,366,269 (GRCm38) |
|
probably null |
Het |
| Bcar3 |
A |
G |
3: 122,426,649 (GRCm38) |
D65G |
probably damaging |
Het |
| Ccnt2 |
T |
C |
1: 127,791,733 (GRCm38) |
|
silent |
Het |
| Cdca7l |
A |
G |
12: 117,877,033 (GRCm38) |
Y430C |
probably damaging |
Het |
| Ces4a |
A |
G |
8: 105,146,143 (GRCm38) |
T343A |
probably benign |
Het |
| Clec2g |
C |
T |
6: 128,948,751 (GRCm38) |
A41V |
probably benign |
Het |
| Crybg3 |
A |
T |
16: 59,522,149 (GRCm38) |
Y2708N |
probably damaging |
Het |
| Dmxl1 |
A |
T |
18: 49,951,235 (GRCm38) |
E2758V |
probably damaging |
Het |
| Dusp27 |
T |
C |
1: 166,110,250 (GRCm38) |
E80G |
probably benign |
Het |
| Eci2 |
C |
T |
13: 34,978,724 (GRCm38) |
E283K |
probably benign |
Het |
| Edrf1 |
T |
A |
7: 133,651,910 (GRCm38) |
|
probably null |
Het |
| Eif3b |
T |
C |
5: 140,425,280 (GRCm38) |
L162P |
probably damaging |
Het |
| Ercc3 |
A |
G |
18: 32,245,595 (GRCm38) |
I210V |
probably benign |
Het |
| Exoc1 |
A |
G |
5: 76,567,014 (GRCm38) |
N739S |
probably damaging |
Het |
| Gm7334 |
A |
G |
17: 50,698,754 (GRCm38) |
K23E |
probably benign |
Het |
| Gm7356 |
T |
G |
17: 14,001,098 (GRCm38) |
D223A |
possibly damaging |
Het |
| Klhl26 |
A |
G |
8: 70,455,565 (GRCm38) |
L47P |
probably damaging |
Het |
| Klhl42 |
C |
T |
6: 147,092,286 (GRCm38) |
T252I |
possibly damaging |
Het |
| Morc1 |
G |
T |
16: 48,618,509 (GRCm38) |
G756W |
probably damaging |
Het |
| Mroh2b |
G |
T |
15: 4,914,133 (GRCm38) |
E384* |
probably null |
Het |
| Nol10 |
G |
A |
12: 17,369,620 (GRCm38) |
|
probably null |
Het |
| Nxpe5 |
T |
C |
5: 138,239,241 (GRCm38) |
L9P |
probably damaging |
Het |
| Olfr457 |
A |
G |
6: 42,471,902 (GRCm38) |
I92T |
probably damaging |
Het |
| Olfr617 |
C |
T |
7: 103,584,828 (GRCm38) |
R269C |
probably benign |
Het |
| Pak2 |
T |
C |
16: 32,044,488 (GRCm38) |
E94G |
probably damaging |
Het |
| Pcdha7 |
A |
G |
18: 36,974,671 (GRCm38) |
K250E |
possibly damaging |
Het |
| Pde8b |
T |
C |
13: 95,041,990 (GRCm38) |
T541A |
probably damaging |
Het |
| Peg3 |
A |
T |
7: 6,709,970 (GRCm38) |
I751N |
probably damaging |
Het |
| Prpsap2 |
T |
C |
11: 61,731,570 (GRCm38) |
D269G |
probably damaging |
Het |
| Raver2 |
C |
A |
4: 101,102,692 (GRCm38) |
T123K |
possibly damaging |
Het |
| Rpgrip1 |
G |
A |
14: 52,145,209 (GRCm38) |
D600N |
possibly damaging |
Het |
| Scn2b |
A |
G |
9: 45,125,518 (GRCm38) |
Y108C |
probably damaging |
Het |
| Sdr16c6 |
T |
C |
4: 4,069,923 (GRCm38) |
E139G |
probably damaging |
Het |
| Sgpp2 |
A |
G |
1: 78,360,188 (GRCm38) |
I68V |
probably benign |
Het |
| Sorbs2 |
T |
A |
8: 45,796,013 (GRCm38) |
I687N |
probably damaging |
Het |
| Sorcs3 |
G |
A |
19: 48,796,472 (GRCm38) |
|
probably null |
Het |
| Stk16 |
T |
A |
1: 75,212,965 (GRCm38) |
C174S |
probably benign |
Het |
| Ttll9 |
C |
A |
2: 152,991,652 (GRCm38) |
N198K |
possibly damaging |
Het |
| Unc13c |
A |
T |
9: 73,930,823 (GRCm38) |
D915E |
probably benign |
Het |
| Unc5b |
T |
A |
10: 60,778,267 (GRCm38) |
K268* |
probably null |
Het |
| Vim |
T |
A |
2: 13,580,013 (GRCm38) |
|
probably null |
Het |
| Xirp2 |
T |
A |
2: 67,513,461 (GRCm38) |
N2015K |
probably damaging |
Het |
| Zfp160 |
T |
G |
17: 21,020,733 (GRCm38) |
M21R |
possibly damaging |
Het |
|
| Other mutations in Olfr857 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01510:Olfr857
|
APN |
9 |
19,713,279 (GRCm38) |
missense |
probably benign |
0.00 |
|
IGL01919:Olfr857
|
APN |
9 |
19,713,342 (GRCm38) |
missense |
probably benign |
0.00 |
|
IGL02157:Olfr857
|
APN |
9 |
19,713,289 (GRCm38) |
missense |
probably benign |
0.07 |
|
IGL02550:Olfr857
|
APN |
9 |
19,713,047 (GRCm38) |
missense |
possibly damaging |
0.92 |
|
IGL03329:Olfr857
|
APN |
9 |
19,713,301 (GRCm38) |
missense |
probably benign |
0.16 |
|
IGL02799:Olfr857
|
UTSW |
9 |
19,713,018 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R0356:Olfr857
|
UTSW |
9 |
19,713,447 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0927:Olfr857
|
UTSW |
9 |
19,713,649 (GRCm38) |
missense |
probably benign |
0.39 |
|
R1161:Olfr857
|
UTSW |
9 |
19,713,180 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1848:Olfr857
|
UTSW |
9 |
19,713,090 (GRCm38) |
missense |
probably benign |
0.01 |
|
R5191:Olfr857
|
UTSW |
9 |
19,713,334 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R5216:Olfr857
|
UTSW |
9 |
19,713,289 (GRCm38) |
missense |
probably benign |
0.07 |
|
R5259:Olfr857
|
UTSW |
9 |
19,712,813 (GRCm38) |
splice site |
probably null |
|
|
R5506:Olfr857
|
UTSW |
9 |
19,713,274 (GRCm38) |
missense |
possibly damaging |
0.61 |
|
R5526:Olfr857
|
UTSW |
9 |
19,713,698 (GRCm38) |
nonsense |
probably null |
|
|
R5594:Olfr857
|
UTSW |
9 |
19,713,006 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5928:Olfr857
|
UTSW |
9 |
19,713,753 (GRCm38) |
missense |
probably benign |
0.02 |
|
R6569:Olfr857
|
UTSW |
9 |
19,713,342 (GRCm38) |
missense |
probably benign |
0.00 |
|
R6858:Olfr857
|
UTSW |
9 |
19,713,469 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R7077:Olfr857
|
UTSW |
9 |
19,713,132 (GRCm38) |
missense |
probably benign |
|
|
R7378:Olfr857
|
UTSW |
9 |
19,712,887 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7771:Olfr857
|
UTSW |
9 |
19,713,471 (GRCm38) |
missense |
probably benign |
|
|
R8038:Olfr857
|
UTSW |
9 |
19,713,680 (GRCm38) |
missense |
possibly damaging |
0.52 |
|
R8160:Olfr857
|
UTSW |
9 |
19,712,789 (GRCm38) |
intron |
probably benign |
|
|
R8223:Olfr857
|
UTSW |
9 |
19,713,409 (GRCm38) |
missense |
probably benign |
|
|
R8400:Olfr857
|
UTSW |
9 |
19,713,093 (GRCm38) |
missense |
probably benign |
0.45 |
|
R8780:Olfr857
|
UTSW |
9 |
19,713,357 (GRCm38) |
missense |
possibly damaging |
0.92 |
|
R8946:Olfr857
|
UTSW |
9 |
19,713,589 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R9164:Olfr857
|
UTSW |
9 |
19,713,658 (GRCm38) |
missense |
probably benign |
0.25 |
|
R9475:Olfr857
|
UTSW |
9 |
19,713,643 (GRCm38) |
missense |
probably benign |
0.01 |
|
| Predicted Primers |
PCR Primer
(F):5'- GGAATTCATTCTCCTTGGACTCTCAG -3'
(R):5'- ACATCTACAGAGGCAAGGGC -3'
Sequencing Primer
(F):5'- TCTCAGAGGACCCTGAACTG -3'
(R):5'- TAGAGGGTGACAAATAGCTACCCATC -3'
|
| Posted On |
2016-08-04 |
Incidental Mutation