Incidental Mutation 'R6652:Or4e5'
| ID |
528111 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or4e5
|
| Ensembl Gene |
ENSMUSG00000059887 |
| Gene Name |
olfactory receptor family 4 subfamily E member 5 |
| Synonyms |
MOR28, MOR244-1, GA_x6K02T2RJGY-491851-492792, Olfr1507 |
| MMRRC Submission |
044773-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.054)
|
| Stock # |
R6652 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
14 |
| Chromosomal Location |
52727392-52733152 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 52728250 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Glutamine
at position 57
(R57Q)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000146152
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000073571]
[ENSMUST00000205963]
[ENSMUST00000206062]
[ENSMUST00000206069]
[ENSMUST00000206931]
|
| AlphaFold |
Q0VEP0 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000073571
AA Change: R57Q
PolyPhen 2
Score 0.071 (Sensitivity: 0.94; Specificity: 0.84)
|
| SMART Domains |
Protein: ENSMUSP00000073260
Gene: ENSMUSG00000059887
AA Change: R57Q
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
34 |
308 |
1.1e-47 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
38 |
305 |
3.6e-9 |
PFAM |
|
Pfam:7tm_1
|
44 |
290 |
9.1e-22 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000205963
AA Change: R30Q
PolyPhen 2
Score 0.018 (Sensitivity: 0.95; Specificity: 0.80)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000206062
AA Change: R57Q
PolyPhen 2
Score 0.071 (Sensitivity: 0.94; Specificity: 0.84)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000206069
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000206931
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.1%
- 20x: 94.7%
|
| Validation Efficiency |
100% (42/42) |
| 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: 43 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca14 |
A |
G |
7: 119,846,164 (GRCm39) |
D605G |
probably damaging |
Het |
| Cfh |
A |
T |
1: 140,071,806 (GRCm39) |
I294N |
probably benign |
Het |
| Clk3 |
A |
G |
9: 57,669,078 (GRCm39) |
S49P |
probably damaging |
Het |
| Cmya5 |
A |
G |
13: 93,229,403 (GRCm39) |
V1895A |
probably benign |
Het |
| Cmya5 |
T |
C |
13: 93,229,547 (GRCm39) |
D1847G |
probably damaging |
Het |
| Cwf19l1 |
T |
C |
19: 44,103,138 (GRCm39) |
D359G |
probably benign |
Het |
| Dag1 |
A |
T |
9: 108,086,289 (GRCm39) |
M284K |
probably damaging |
Het |
| Ergic2 |
T |
C |
6: 148,091,079 (GRCm39) |
Y211C |
probably damaging |
Het |
| Espnl |
A |
C |
1: 91,272,421 (GRCm39) |
I594L |
probably benign |
Het |
| Fam193b |
A |
G |
13: 55,690,603 (GRCm39) |
S226P |
probably damaging |
Het |
| Fat2 |
T |
A |
11: 55,143,088 (GRCm39) |
I4254L |
probably benign |
Het |
| Fhdc1 |
T |
C |
3: 84,371,631 (GRCm39) |
Y108C |
probably damaging |
Het |
| Fut9 |
G |
C |
4: 25,620,619 (GRCm39) |
T65S |
probably benign |
Het |
| Gm9507 |
A |
T |
10: 77,647,493 (GRCm39) |
|
probably benign |
Het |
| Gpt2 |
G |
A |
8: 86,244,681 (GRCm39) |
E325K |
probably benign |
Het |
| Grap2 |
A |
T |
15: 80,532,723 (GRCm39) |
N297Y |
probably damaging |
Het |
| Igfn1 |
A |
G |
1: 135,891,609 (GRCm39) |
F2302S |
probably damaging |
Het |
| Ighv1-81 |
T |
A |
12: 115,884,051 (GRCm39) |
I67F |
probably damaging |
Het |
| Kidins220 |
T |
A |
12: 25,060,059 (GRCm39) |
|
probably null |
Het |
| Kti12 |
T |
A |
4: 108,705,730 (GRCm39) |
S215T |
probably benign |
Het |
| Mc1r |
G |
A |
8: 124,134,370 (GRCm39) |
G41D |
probably damaging |
Het |
| Mov10l1 |
A |
G |
15: 88,878,105 (GRCm39) |
Y129C |
probably damaging |
Het |
| Mthfsd |
A |
T |
8: 121,825,560 (GRCm39) |
L337Q |
probably damaging |
Het |
| Musk |
C |
T |
4: 58,368,977 (GRCm39) |
A629V |
probably damaging |
Het |
| Nadsyn1 |
A |
T |
7: 143,364,955 (GRCm39) |
M250K |
probably benign |
Het |
| Ncapd2 |
G |
A |
6: 125,163,233 (GRCm39) |
H92Y |
probably benign |
Het |
| Or6y1 |
G |
A |
1: 174,276,627 (GRCm39) |
C146Y |
probably damaging |
Het |
| Plec |
A |
T |
15: 76,063,974 (GRCm39) |
V2100E |
probably damaging |
Het |
| Prss37 |
C |
A |
6: 40,496,090 (GRCm39) |
|
probably benign |
Het |
| Sebox |
A |
T |
11: 78,394,631 (GRCm39) |
E32V |
probably damaging |
Het |
| Senp7 |
C |
A |
16: 55,944,257 (GRCm39) |
Q194K |
probably benign |
Het |
| Sfxn3 |
G |
A |
19: 45,038,354 (GRCm39) |
|
probably null |
Het |
| Spart |
G |
A |
3: 55,032,248 (GRCm39) |
E361K |
probably benign |
Het |
| Stn1 |
T |
C |
19: 47,496,017 (GRCm39) |
T334A |
probably benign |
Het |
| Stoml1 |
A |
G |
9: 58,164,017 (GRCm39) |
D112G |
probably damaging |
Het |
| Thap2 |
T |
A |
10: 115,212,441 (GRCm39) |
D28V |
probably damaging |
Het |
| Ubap2 |
A |
T |
4: 41,196,743 (GRCm39) |
N872K |
possibly damaging |
Het |
| Vezt |
A |
G |
10: 93,806,141 (GRCm39) |
F757L |
probably damaging |
Het |
| Vmn1r204 |
T |
C |
13: 22,740,573 (GRCm39) |
I68T |
probably damaging |
Het |
| Wnt10a |
A |
G |
1: 74,842,613 (GRCm39) |
|
probably null |
Het |
| Yipf7 |
A |
G |
5: 69,698,504 (GRCm39) |
M1T |
probably null |
Het |
| Zdhhc19 |
T |
C |
16: 32,316,047 (GRCm39) |
F48S |
probably damaging |
Het |
| Zfp317 |
C |
T |
9: 19,558,335 (GRCm39) |
T183I |
probably damaging |
Het |
|
| Other mutations in Or4e5 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01336:Or4e5
|
APN |
14 |
52,728,205 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01367:Or4e5
|
APN |
14 |
52,727,624 (GRCm39) |
missense |
probably benign |
0.42 |
|
IGL01664:Or4e5
|
APN |
14 |
52,728,002 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02890:Or4e5
|
APN |
14 |
52,728,368 (GRCm39) |
missense |
probably benign |
|
|
IGL03108:Or4e5
|
APN |
14 |
52,727,533 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL03184:Or4e5
|
APN |
14 |
52,728,380 (GRCm39) |
missense |
probably benign |
0.20 |
|
R0563:Or4e5
|
UTSW |
14 |
52,727,714 (GRCm39) |
nonsense |
probably null |
|
|
R1080:Or4e5
|
UTSW |
14 |
52,728,042 (GRCm39) |
nonsense |
probably null |
|
|
R1558:Or4e5
|
UTSW |
14 |
52,727,603 (GRCm39) |
missense |
probably benign |
0.26 |
|
R1653:Or4e5
|
UTSW |
14 |
52,728,229 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1714:Or4e5
|
UTSW |
14 |
52,727,871 (GRCm39) |
splice site |
probably null |
|
|
R1720:Or4e5
|
UTSW |
14 |
52,728,051 (GRCm39) |
nonsense |
probably null |
|
|
R3430:Or4e5
|
UTSW |
14 |
52,727,882 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R4995:Or4e5
|
UTSW |
14 |
52,727,988 (GRCm39) |
nonsense |
probably null |
|
|
R5954:Or4e5
|
UTSW |
14 |
52,727,624 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6183:Or4e5
|
UTSW |
14 |
52,728,188 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6518:Or4e5
|
UTSW |
14 |
52,728,077 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6651:Or4e5
|
UTSW |
14 |
52,728,250 (GRCm39) |
missense |
probably benign |
0.07 |
|
R6653:Or4e5
|
UTSW |
14 |
52,728,250 (GRCm39) |
missense |
probably benign |
0.07 |
|
R7385:Or4e5
|
UTSW |
14 |
52,727,638 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7524:Or4e5
|
UTSW |
14 |
52,727,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8902:Or4e5
|
UTSW |
14 |
52,728,010 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9165:Or4e5
|
UTSW |
14 |
52,727,830 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R9763:Or4e5
|
UTSW |
14 |
52,728,307 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0025:Or4e5
|
UTSW |
14 |
52,727,923 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- CCTCAAAGGTTTACAAATGGCCAC -3'
(R):5'- TGGAAAAGGCTGTCCTCATC -3'
Sequencing Primer
(F):5'- GGTTTACAAATGGCCACATAGCGATC -3'
(R):5'- TCATCAACCAAACTTCAGTGATGTC -3'
|
| Posted On |
2018-07-24 |
Incidental Mutation