Incidental Mutation 'R7688:Or52e8'
| ID |
593209 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or52e8
|
| Ensembl Gene |
ENSMUSG00000094531 |
| Gene Name |
olfactory receptor family 52 subfamily E member 8 |
| Synonyms |
MOR32-12, Olfr671, GA_x6K02T2PBJ9-7604826-7603885 |
| MMRRC Submission |
045752-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.071)
|
| Stock # |
R7688 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
7 |
| Chromosomal Location |
104621683-104625202 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 104624332 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Alanine to Serine
at position 291
(A291S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148008
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000078710]
[ENSMUST00000210963]
[ENSMUST00000217091]
|
| AlphaFold |
A0A1B0GSN5 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000078710
AA Change: A287S
PolyPhen 2
Score 0.471 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000077774
Gene: ENSMUSG00000094531
AA Change: A287S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
33 |
311 |
1.4e-117 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
37 |
308 |
3.7e-7 |
PFAM |
|
Pfam:7tm_1
|
43 |
293 |
1.5e-17 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000210963
AA Change: A291S
PolyPhen 2
Score 0.600 (Sensitivity: 0.87; Specificity: 0.91)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000217091
AA Change: A291S
PolyPhen 2
Score 0.600 (Sensitivity: 0.87; Specificity: 0.91)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.2%
|
| Validation Efficiency |
100% (47/47) |
| 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: 46 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Bag6 |
T |
C |
17: 35,365,868 (GRCm39) |
Y1102H |
probably damaging |
Het |
| Cldn24 |
G |
A |
8: 48,275,740 (GRCm39) |
C188Y |
probably damaging |
Het |
| Dennd4c |
T |
C |
4: 86,713,377 (GRCm39) |
W443R |
probably damaging |
Het |
| Dmxl1 |
T |
A |
18: 50,088,938 (GRCm39) |
C2806S |
probably benign |
Het |
| Epb41l2 |
T |
C |
10: 25,355,036 (GRCm39) |
Y449H |
probably damaging |
Het |
| Ets1 |
T |
A |
9: 32,607,720 (GRCm39) |
I14N |
probably benign |
Het |
| F11 |
A |
T |
8: 45,703,127 (GRCm39) |
F188I |
probably damaging |
Het |
| Fam13a |
C |
T |
6: 58,912,692 (GRCm39) |
V654I |
probably benign |
Het |
| Flt1 |
C |
T |
5: 147,613,135 (GRCm39) |
V369I |
probably benign |
Het |
| Focad |
T |
A |
4: 88,096,370 (GRCm39) |
Y251N |
probably damaging |
Het |
| Gm5150 |
A |
G |
3: 16,017,747 (GRCm39) |
S175P |
probably benign |
Het |
| Hnrnpul2 |
T |
A |
19: 8,797,994 (GRCm39) |
S117T |
probably benign |
Het |
| Kcnj5 |
A |
G |
9: 32,234,264 (GRCm39) |
V17A |
probably benign |
Het |
| Kctd1 |
T |
G |
18: 15,107,255 (GRCm39) |
T737P |
probably benign |
Het |
| Kif14 |
T |
C |
1: 136,422,392 (GRCm39) |
V894A |
probably damaging |
Het |
| Klhl12 |
A |
T |
1: 134,416,768 (GRCm39) |
T497S |
probably benign |
Het |
| Klhl6 |
C |
A |
16: 19,765,881 (GRCm39) |
V574L |
probably damaging |
Het |
| Lama1 |
A |
T |
17: 68,068,623 (GRCm39) |
D774V |
|
Het |
| Leng1 |
G |
A |
7: 3,665,809 (GRCm39) |
P176L |
probably benign |
Het |
| Lig1 |
T |
C |
7: 13,023,389 (GRCm39) |
L196P |
probably benign |
Het |
| Macrod1 |
C |
A |
19: 7,174,230 (GRCm39) |
Y245* |
probably null |
Het |
| Mcf2l |
T |
A |
8: 12,998,130 (GRCm39) |
I6N |
possibly damaging |
Het |
| Megf11 |
A |
G |
9: 64,599,146 (GRCm39) |
D687G |
possibly damaging |
Het |
| Muc4 |
A |
T |
16: 32,570,278 (GRCm39) |
H446L |
possibly damaging |
Het |
| Oasl2 |
A |
T |
5: 115,035,909 (GRCm39) |
I62F |
probably benign |
Het |
| Oog4 |
CAA |
CA |
4: 143,164,022 (GRCm39) |
|
probably null |
Het |
| Or14a257 |
A |
G |
7: 86,138,183 (GRCm39) |
V192A |
probably benign |
Het |
| Or4b12 |
A |
T |
2: 90,095,959 (GRCm39) |
F272I |
probably damaging |
Het |
| Pdcl2 |
T |
C |
5: 76,465,770 (GRCm39) |
N150S |
probably benign |
Het |
| Pfkfb3 |
A |
G |
2: 11,497,450 (GRCm39) |
Y54H |
probably damaging |
Het |
| Rab25 |
A |
T |
3: 88,452,270 (GRCm39) |
|
probably null |
Het |
| Slc22a18 |
G |
A |
7: 143,033,560 (GRCm39) |
G104S |
probably damaging |
Het |
| Slc44a5 |
T |
A |
3: 153,679,437 (GRCm39) |
|
probably null |
Het |
| Slc5a8 |
A |
G |
10: 88,757,561 (GRCm39) |
Y517C |
probably damaging |
Het |
| Spata18 |
A |
G |
5: 73,809,005 (GRCm39) |
N26S |
probably benign |
Het |
| Tas2r115 |
T |
A |
6: 132,714,643 (GRCm39) |
S103C |
probably damaging |
Het |
| Tigd2 |
T |
A |
6: 59,187,382 (GRCm39) |
M83K |
probably damaging |
Het |
| Tnxb |
T |
A |
17: 34,890,880 (GRCm39) |
C408S |
probably benign |
Het |
| Trbj2-3 |
T |
A |
6: 41,520,159 (GRCm39) |
S1R |
possibly damaging |
Het |
| Triobp |
T |
C |
15: 78,845,311 (GRCm39) |
|
probably null |
Het |
| Uaca |
A |
G |
9: 60,781,409 (GRCm39) |
Q1349R |
probably benign |
Het |
| Ube2j2 |
T |
A |
4: 156,040,885 (GRCm39) |
L171I |
probably damaging |
Het |
| Usp17ld |
C |
A |
7: 102,899,982 (GRCm39) |
G317W |
probably damaging |
Het |
| Vinac1 |
G |
A |
2: 128,880,964 (GRCm39) |
Q321* |
probably null |
Het |
| Vmn2r72 |
T |
A |
7: 85,404,098 (GRCm39) |
D31V |
probably benign |
Het |
| Zfp317 |
T |
G |
9: 19,559,251 (GRCm39) |
H488Q |
probably damaging |
Het |
|
| Other mutations in Or52e8 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01359:Or52e8
|
APN |
7 |
104,625,193 (GRCm39) |
splice site |
probably null |
|
|
IGL02154:Or52e8
|
APN |
7 |
104,625,188 (GRCm39) |
start codon destroyed |
probably null |
0.14 |
|
IGL02308:Or52e8
|
APN |
7 |
104,624,665 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
IGL02794:Or52e8
|
APN |
7 |
104,624,596 (GRCm39) |
missense |
probably benign |
|
|
R0919:Or52e8
|
UTSW |
7 |
104,624,519 (GRCm39) |
nonsense |
probably null |
|
|
R1819:Or52e8
|
UTSW |
7 |
104,624,605 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1972:Or52e8
|
UTSW |
7 |
104,625,106 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R2025:Or52e8
|
UTSW |
7 |
104,624,451 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4910:Or52e8
|
UTSW |
7 |
104,624,686 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R5442:Or52e8
|
UTSW |
7 |
104,624,435 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R5554:Or52e8
|
UTSW |
7 |
104,625,189 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
|
R5932:Or52e8
|
UTSW |
7 |
104,624,862 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6683:Or52e8
|
UTSW |
7 |
104,625,175 (GRCm39) |
missense |
probably benign |
|
|
R6962:Or52e8
|
UTSW |
7 |
104,624,580 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7000:Or52e8
|
UTSW |
7 |
104,624,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7059:Or52e8
|
UTSW |
7 |
104,625,224 (GRCm39) |
splice site |
probably null |
|
|
R7276:Or52e8
|
UTSW |
7 |
104,624,857 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R7425:Or52e8
|
UTSW |
7 |
104,624,268 (GRCm39) |
nonsense |
probably null |
|
|
R8043:Or52e8
|
UTSW |
7 |
104,625,080 (GRCm39) |
nonsense |
probably null |
|
|
R8074:Or52e8
|
UTSW |
7 |
104,624,934 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8432:Or52e8
|
UTSW |
7 |
104,625,199 (GRCm39) |
missense |
probably benign |
|
|
R8705:Or52e8
|
UTSW |
7 |
104,624,446 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8757:Or52e8
|
UTSW |
7 |
104,624,325 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8759:Or52e8
|
UTSW |
7 |
104,624,325 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9489:Or52e8
|
UTSW |
7 |
104,624,856 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9597:Or52e8
|
UTSW |
7 |
104,624,413 (GRCm39) |
missense |
probably benign |
0.19 |
|
| Predicted Primers |
PCR Primer
(F):5'- TTCCCAGTTTTCTATGGACTAGAC -3'
(R):5'- TTGTGCCAGCATCAAAGTCAAC -3'
Sequencing Primer
(F):5'- TTTCTATGGACTAGACACAAAACAAC -3'
(R):5'- CTATGTCAGGATCCTCTATGCAGTG -3'
|
| Posted On |
2019-11-12 |
Incidental Mutation