Incidental Mutation 'R5672:Or7e165'
| ID |
442679 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or7e165
|
| Ensembl Gene |
ENSMUSG00000058659 |
| Gene Name |
olfactory receptor family 7 subfamily E member 165 |
| Synonyms |
Olfr58, MOR146-7P, IG6, GA_x6K02T2PVTD-13523015-13523944, MOR146-3 |
| MMRRC Submission |
043174-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.055)
|
| Stock # |
R5672 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
19691579-19695360 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 19694507 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Asparagine
at position 26
(I26N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150309
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000079660]
[ENSMUST00000212363]
[ENSMUST00000215112]
|
| AlphaFold |
Q7TRF6 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000079660
AA Change: I26N
PolyPhen 2
Score 0.920 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000078603
Gene: ENSMUSG00000063842
AA Change: I26N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
1.3e-51 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
303 |
8.3e-8 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
4.5e-22 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000212363
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000215112
AA Change: I26N
PolyPhen 2
Score 0.920 (Sensitivity: 0.81; Specificity: 0.94)
|
| Meta Mutation Damage Score |
0.1795 |
| Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.8%
- 10x: 97.6%
- 20x: 96.0%
|
| 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: 40 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A4gnt |
A |
G |
9: 99,502,383 (GRCm39) |
N181S |
possibly damaging |
Het |
| Abcf3 |
A |
T |
16: 20,368,002 (GRCm39) |
Q74L |
probably benign |
Het |
| Ankrd13c |
T |
C |
3: 157,666,664 (GRCm39) |
|
probably null |
Het |
| Bub1 |
A |
G |
2: 127,646,800 (GRCm39) |
F827L |
possibly damaging |
Het |
| Cfap68 |
T |
C |
9: 50,675,227 (GRCm39) |
T67A |
probably benign |
Het |
| Cyp2c55 |
A |
G |
19: 39,023,990 (GRCm39) |
I355V |
probably benign |
Het |
| Dido1 |
A |
G |
2: 180,313,696 (GRCm39) |
S319P |
probably damaging |
Het |
| Efna5 |
A |
T |
17: 63,188,025 (GRCm39) |
V34D |
probably damaging |
Het |
| Fam131a |
G |
T |
16: 20,518,389 (GRCm39) |
E88D |
probably damaging |
Het |
| Fsip2 |
A |
T |
2: 82,817,838 (GRCm39) |
R4524* |
probably null |
Het |
| Gm6899 |
C |
T |
11: 26,543,484 (GRCm39) |
|
probably benign |
Het |
| Iqcg |
C |
T |
16: 32,839,878 (GRCm39) |
R356Q |
probably damaging |
Het |
| Itgae |
T |
A |
11: 73,036,377 (GRCm39) |
I1105N |
possibly damaging |
Het |
| Klb |
T |
C |
5: 65,537,292 (GRCm39) |
I874T |
possibly damaging |
Het |
| Klc3 |
T |
C |
7: 19,130,256 (GRCm39) |
Y307C |
probably damaging |
Het |
| Lrp1b |
T |
A |
2: 41,231,771 (GRCm39) |
H378L |
probably benign |
Het |
| Mxd4 |
G |
A |
5: 34,335,044 (GRCm39) |
R114C |
probably damaging |
Het |
| Nrdc |
A |
T |
4: 108,895,242 (GRCm39) |
R241* |
probably null |
Het |
| Ofcc1 |
G |
A |
13: 40,433,905 (GRCm39) |
H67Y |
probably damaging |
Het |
| Or10ak9 |
A |
G |
4: 118,726,379 (GRCm39) |
T134A |
possibly damaging |
Het |
| Or5p5 |
A |
G |
7: 107,413,844 (GRCm39) |
T18A |
probably damaging |
Het |
| Pard3b |
G |
T |
1: 62,049,625 (GRCm39) |
A128S |
probably benign |
Het |
| Plat |
T |
C |
8: 23,263,664 (GRCm39) |
Y188H |
probably benign |
Het |
| Pop1 |
A |
G |
15: 34,530,325 (GRCm39) |
K908E |
possibly damaging |
Het |
| Pten |
A |
G |
19: 32,735,866 (GRCm39) |
I8V |
probably benign |
Het |
| Pwwp2a |
C |
T |
11: 43,596,968 (GRCm39) |
A436V |
probably damaging |
Het |
| Rnf145 |
G |
A |
11: 44,422,120 (GRCm39) |
V68M |
possibly damaging |
Het |
| Sdk1 |
T |
C |
5: 142,173,900 (GRCm39) |
C2023R |
possibly damaging |
Het |
| Serpina1d |
A |
C |
12: 103,730,101 (GRCm39) |
D360E |
possibly damaging |
Het |
| Serpinb9b |
A |
G |
13: 33,223,582 (GRCm39) |
D258G |
probably benign |
Het |
| Smgc |
G |
A |
15: 91,726,108 (GRCm39) |
S18N |
possibly damaging |
Het |
| Snx27 |
A |
T |
3: 94,410,157 (GRCm39) |
|
probably null |
Het |
| Spem1 |
T |
G |
11: 69,712,263 (GRCm39) |
K134Q |
probably damaging |
Het |
| Srgap3 |
T |
A |
6: 112,752,522 (GRCm39) |
M321L |
probably benign |
Het |
| Tanc1 |
T |
C |
2: 59,602,697 (GRCm39) |
C163R |
possibly damaging |
Het |
| Ube2ql1 |
A |
T |
13: 69,887,446 (GRCm39) |
L5H |
unknown |
Het |
| Ubn2 |
T |
C |
6: 38,438,462 (GRCm39) |
I225T |
probably damaging |
Het |
| Vmn1r181 |
A |
C |
7: 23,683,741 (GRCm39) |
T69P |
probably damaging |
Het |
| Vmn2r110 |
A |
G |
17: 20,816,494 (GRCm39) |
F10L |
probably benign |
Het |
| Yeats2 |
T |
C |
16: 19,980,779 (GRCm39) |
M236T |
probably damaging |
Het |
|
| Other mutations in Or7e165 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01461:Or7e165
|
APN |
9 |
19,695,245 (GRCm39) |
splice site |
probably null |
|
|
IGL01815:Or7e165
|
APN |
9 |
19,695,311 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02408:Or7e165
|
APN |
9 |
19,694,711 (GRCm39) |
missense |
probably benign |
0.31 |
|
IGL02644:Or7e165
|
APN |
9 |
19,695,010 (GRCm39) |
missense |
probably benign |
0.30 |
|
IGL03243:Or7e165
|
APN |
9 |
19,694,564 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0603:Or7e165
|
UTSW |
9 |
19,695,235 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2363:Or7e165
|
UTSW |
9 |
19,694,892 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2570:Or7e165
|
UTSW |
9 |
19,695,305 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3890:Or7e165
|
UTSW |
9 |
19,695,011 (GRCm39) |
missense |
probably benign |
0.03 |
|
R3892:Or7e165
|
UTSW |
9 |
19,695,011 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4163:Or7e165
|
UTSW |
9 |
19,695,086 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R4610:Or7e165
|
UTSW |
9 |
19,694,442 (GRCm39) |
nonsense |
probably null |
|
|
R4691:Or7e165
|
UTSW |
9 |
19,694,678 (GRCm39) |
missense |
probably benign |
0.33 |
|
R4707:Or7e165
|
UTSW |
9 |
19,694,596 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4825:Or7e165
|
UTSW |
9 |
19,694,872 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R4950:Or7e165
|
UTSW |
9 |
19,695,027 (GRCm39) |
missense |
probably benign |
|
|
R5185:Or7e165
|
UTSW |
9 |
19,694,672 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5202:Or7e165
|
UTSW |
9 |
19,694,514 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R5439:Or7e165
|
UTSW |
9 |
19,695,161 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5669:Or7e165
|
UTSW |
9 |
19,695,053 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6038:Or7e165
|
UTSW |
9 |
19,694,858 (GRCm39) |
missense |
probably benign |
|
|
R6038:Or7e165
|
UTSW |
9 |
19,694,858 (GRCm39) |
missense |
probably benign |
|
|
R6212:Or7e165
|
UTSW |
9 |
19,694,585 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6415:Or7e165
|
UTSW |
9 |
19,695,044 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7385:Or7e165
|
UTSW |
9 |
19,694,507 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R7669:Or7e165
|
UTSW |
9 |
19,694,839 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
| Predicted Primers |
PCR Primer
(F):5'- GAACAGTTCTCATGTATGAATGGTGTC -3'
(R):5'- TGTGCATGCAAGTTTATCAGC -3'
Sequencing Primer
(F):5'- GTCTTGTGAATTGCTGGTTTACAAAC -3'
(R):5'- CATGCAAGTTTATCAGCATTTTGGG -3'
|
| Posted On |
2016-11-09 |
Incidental Mutation