Incidental Mutation 'IGL01596:Or4e1'
| ID |
91935 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or4e1
|
| Ensembl Gene |
ENSMUSG00000057564 |
| Gene Name |
olfactory receptor family 4 subfamily E member 1 |
| Synonyms |
GA_x6K02T2RJGY-520647-521579, MOR244-4, MOR244-2, Olfr1508, MOR10 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.060)
|
| Stock # |
IGL01596
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
14 |
| Chromosomal Location |
52700178-52704918 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 52700822 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Methionine
at position 215
(V215M)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000145649
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000205811]
[ENSMUST00000206520]
|
| AlphaFold |
Q9R0K4 |
| Predicted Effect |
|
| SMART Domains |
Protein: ENSMUSP00000107167
Gene: ENSMUSG00000057564
AA Change: V188M
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
34 |
308 |
3.9e-48 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
38 |
305 |
1.7e-7 |
PFAM |
|
Pfam:7tm_1
|
44 |
290 |
1.4e-22 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000205811
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000206520
AA Change: V215M
PolyPhen 2
Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)
|
| Coding Region Coverage |
|
| 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: 27 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adh7 |
T |
C |
3: 137,932,003 (GRCm39) |
S206P |
probably damaging |
Het |
| Arhgef10 |
G |
T |
8: 15,049,468 (GRCm39) |
E869* |
probably null |
Het |
| C87436 |
T |
A |
6: 86,423,201 (GRCm39) |
D258E |
probably damaging |
Het |
| Casp8ap2 |
A |
G |
4: 32,646,365 (GRCm39) |
K1813E |
probably damaging |
Het |
| Cd209b |
T |
A |
8: 3,968,744 (GRCm39) |
D304V |
probably damaging |
Het |
| Chmp2b |
T |
C |
16: 65,359,363 (GRCm39) |
D11G |
probably benign |
Het |
| Comp |
A |
G |
8: 70,831,285 (GRCm39) |
N384S |
probably damaging |
Het |
| Dbnl |
A |
G |
11: 5,748,279 (GRCm39) |
Y336C |
probably damaging |
Het |
| Faf2 |
G |
T |
13: 54,769,716 (GRCm39) |
Q21H |
probably null |
Het |
| Fam117b |
A |
T |
1: 59,992,130 (GRCm39) |
K260* |
probably null |
Het |
| Gramd1b |
A |
G |
9: 40,214,809 (GRCm39) |
L379P |
probably damaging |
Het |
| Iars1 |
A |
G |
13: 49,856,652 (GRCm39) |
N302D |
probably benign |
Het |
| Kcnh6 |
C |
T |
11: 105,917,572 (GRCm39) |
T702I |
probably benign |
Het |
| Kdelr2 |
A |
G |
5: 143,398,330 (GRCm39) |
Y59C |
probably damaging |
Het |
| Mgam |
T |
C |
6: 40,635,204 (GRCm39) |
Y300H |
probably damaging |
Het |
| Or3a1d |
T |
C |
11: 74,238,245 (GRCm39) |
E55G |
possibly damaging |
Het |
| Or4k40 |
A |
G |
2: 111,251,237 (GRCm39) |
S20P |
probably benign |
Het |
| Pcdh17 |
T |
C |
14: 84,685,632 (GRCm39) |
W700R |
probably damaging |
Het |
| Pigq |
T |
G |
17: 26,146,660 (GRCm39) |
H615P |
possibly damaging |
Het |
| Pkhd1l1 |
T |
A |
15: 44,392,806 (GRCm39) |
S1714T |
possibly damaging |
Het |
| Polr1b |
G |
T |
2: 128,952,046 (GRCm39) |
R358I |
probably benign |
Het |
| Tmprss11a |
C |
A |
5: 86,570,378 (GRCm39) |
V194F |
probably damaging |
Het |
| Trhr |
T |
C |
15: 44,092,708 (GRCm39) |
I315T |
probably damaging |
Het |
| Ttc38 |
G |
A |
15: 85,720,274 (GRCm39) |
V79M |
possibly damaging |
Het |
| Ubr4 |
T |
A |
4: 139,189,845 (GRCm39) |
|
probably benign |
Het |
| Vmn2r45 |
T |
C |
7: 8,486,272 (GRCm39) |
T339A |
probably damaging |
Het |
| Vps53 |
A |
G |
11: 75,953,863 (GRCm39) |
F501S |
probably damaging |
Het |
|
| Other mutations in Or4e1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02601:Or4e1
|
APN |
14 |
52,700,802 (GRCm39) |
nonsense |
probably null |
|
|
IGL02635:Or4e1
|
APN |
14 |
52,701,251 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0139:Or4e1
|
UTSW |
14 |
52,700,669 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0501:Or4e1
|
UTSW |
14 |
52,701,383 (GRCm39) |
start codon destroyed |
possibly damaging |
0.79 |
|
R0600:Or4e1
|
UTSW |
14 |
52,700,966 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0612:Or4e1
|
UTSW |
14 |
52,701,008 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1691:Or4e1
|
UTSW |
14 |
52,701,288 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4290:Or4e1
|
UTSW |
14 |
52,701,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4837:Or4e1
|
UTSW |
14 |
52,701,103 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4946:Or4e1
|
UTSW |
14 |
52,700,740 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5073:Or4e1
|
UTSW |
14 |
52,701,032 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5135:Or4e1
|
UTSW |
14 |
52,701,311 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5384:Or4e1
|
UTSW |
14 |
52,700,714 (GRCm39) |
missense |
probably benign |
0.41 |
|
R5663:Or4e1
|
UTSW |
14 |
52,701,052 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5861:Or4e1
|
UTSW |
14 |
52,700,953 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6244:Or4e1
|
UTSW |
14 |
52,701,352 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7040:Or4e1
|
UTSW |
14 |
52,700,932 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R7216:Or4e1
|
UTSW |
14 |
52,700,945 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7560:Or4e1
|
UTSW |
14 |
52,700,851 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8310:Or4e1
|
UTSW |
14 |
52,701,280 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8691:Or4e1
|
UTSW |
14 |
52,701,358 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R8942:Or4e1
|
UTSW |
14 |
52,700,692 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9185:Or4e1
|
UTSW |
14 |
52,700,984 (GRCm39) |
missense |
probably benign |
0.33 |
|
R9218:Or4e1
|
UTSW |
14 |
52,700,788 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9516:Or4e1
|
UTSW |
14 |
52,700,873 (GRCm39) |
missense |
probably benign |
0.02 |
|
| Posted On |
2013-12-09 |
Incidental Mutation