Incidental Mutation 'IGL02304:Or5w15'
| ID |
287494 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or5w15
|
| Ensembl Gene |
ENSMUSG00000075149 |
| Gene Name |
olfactory receptor family 5 subfamily W member 15 |
| Synonyms |
MOR177-8, Olfr1138, GA_x6K02T2Q125-49242149-49241214 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.103)
|
| Stock # |
IGL02304
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
87567731-87568666 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 87568330 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Methionine
at position 113
(V113M)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148941
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099848]
[ENSMUST00000214573]
|
| AlphaFold |
Q8VFQ9 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099848
AA Change: V113M
PolyPhen 2
Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)
|
| SMART Domains |
Protein: ENSMUSP00000097435
Gene: ENSMUSG00000075149
AA Change: V113M
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
2.3e-45 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
1.5e-18 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214573
AA Change: V113M
PolyPhen 2
Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)
|
| 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: 40 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930546C10Rik |
G |
T |
18: 69,083,122 (GRCm39) |
H31N |
unknown |
Het |
| Adamts8 |
A |
G |
9: 30,867,952 (GRCm39) |
N592S |
possibly damaging |
Het |
| Atp1a2 |
C |
A |
1: 172,116,920 (GRCm39) |
E232D |
probably benign |
Het |
| Cacnb3 |
A |
T |
15: 98,540,263 (GRCm39) |
D323V |
probably damaging |
Het |
| Cdh9 |
A |
T |
15: 16,848,687 (GRCm39) |
T456S |
probably benign |
Het |
| Cep162 |
A |
T |
9: 87,109,200 (GRCm39) |
|
probably benign |
Het |
| Clvs2 |
T |
C |
10: 33,404,443 (GRCm39) |
M258V |
probably benign |
Het |
| Col6a5 |
T |
C |
9: 105,805,613 (GRCm39) |
T1098A |
unknown |
Het |
| Foxs1 |
T |
C |
2: 152,774,270 (GRCm39) |
D261G |
probably benign |
Het |
| Gas2l2 |
T |
C |
11: 83,315,064 (GRCm39) |
|
probably benign |
Het |
| Gins4 |
A |
T |
8: 23,722,625 (GRCm39) |
M98K |
probably benign |
Het |
| Gm9637 |
A |
T |
14: 19,402,545 (GRCm38) |
|
noncoding transcript |
Het |
| Herc1 |
A |
G |
9: 66,383,696 (GRCm39) |
D3720G |
probably benign |
Het |
| Kcnh5 |
C |
T |
12: 75,023,471 (GRCm39) |
M532I |
probably benign |
Het |
| Kcnk18 |
T |
C |
19: 59,223,295 (GRCm39) |
Y147H |
probably damaging |
Het |
| Kif21a |
A |
T |
15: 90,849,738 (GRCm39) |
F55Y |
probably damaging |
Het |
| Krt15 |
T |
A |
11: 100,024,503 (GRCm39) |
I278F |
possibly damaging |
Het |
| L3mbtl4 |
T |
A |
17: 68,894,180 (GRCm39) |
Y395* |
probably null |
Het |
| Mcm3ap |
T |
A |
10: 76,320,572 (GRCm39) |
N843K |
possibly damaging |
Het |
| Mpdz |
T |
C |
4: 81,228,394 (GRCm39) |
K1337E |
possibly damaging |
Het |
| Mpdz |
G |
A |
4: 81,215,796 (GRCm39) |
|
probably benign |
Het |
| Ms4a6d |
T |
C |
19: 11,580,505 (GRCm39) |
|
probably benign |
Het |
| Myo7a |
G |
T |
7: 97,726,943 (GRCm39) |
R922S |
possibly damaging |
Het |
| Nek1 |
G |
T |
8: 61,465,201 (GRCm39) |
G97C |
probably damaging |
Het |
| Obscn |
A |
G |
11: 58,967,448 (GRCm39) |
Y2963H |
probably damaging |
Het |
| Or4k44 |
T |
C |
2: 111,367,746 (GRCm39) |
N296S |
probably benign |
Het |
| Or4k6 |
T |
C |
14: 50,476,217 (GRCm39) |
N42D |
probably damaging |
Het |
| Prmt3 |
G |
A |
7: 49,476,485 (GRCm39) |
V365I |
probably benign |
Het |
| Prrc2c |
T |
C |
1: 162,511,705 (GRCm39) |
T958A |
probably benign |
Het |
| Ptprb |
T |
C |
10: 116,167,164 (GRCm39) |
Y947H |
probably damaging |
Het |
| Pus10 |
C |
T |
11: 23,662,275 (GRCm39) |
S315L |
probably damaging |
Het |
| Rmi1 |
C |
A |
13: 58,557,290 (GRCm39) |
S513* |
probably null |
Het |
| Sec14l3 |
C |
T |
11: 4,024,768 (GRCm39) |
P239L |
probably damaging |
Het |
| Slc44a3 |
T |
C |
3: 121,320,723 (GRCm39) |
T93A |
possibly damaging |
Het |
| Srsf3-ps |
C |
T |
11: 98,516,364 (GRCm39) |
R3H |
probably benign |
Het |
| Stat1 |
G |
A |
1: 52,171,703 (GRCm39) |
A125T |
probably benign |
Het |
| Tigd2 |
C |
T |
6: 59,188,683 (GRCm39) |
Q517* |
probably null |
Het |
| Trav13d-3 |
C |
T |
14: 53,270,837 (GRCm39) |
Q100* |
probably null |
Het |
| Trim67 |
G |
A |
8: 125,552,691 (GRCm39) |
D598N |
probably damaging |
Het |
| Trio |
A |
G |
15: 27,735,522 (GRCm39) |
L2856P |
probably damaging |
Het |
|
| Other mutations in Or5w15 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02490:Or5w15
|
APN |
2 |
87,568,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02730:Or5w15
|
APN |
2 |
87,567,985 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03106:Or5w15
|
APN |
2 |
87,568,462 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL03113:Or5w15
|
APN |
2 |
87,568,506 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0450:Or5w15
|
UTSW |
2 |
87,567,825 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0469:Or5w15
|
UTSW |
2 |
87,567,825 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0510:Or5w15
|
UTSW |
2 |
87,567,825 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3696:Or5w15
|
UTSW |
2 |
87,568,360 (GRCm39) |
missense |
probably benign |
|
|
R3698:Or5w15
|
UTSW |
2 |
87,568,360 (GRCm39) |
missense |
probably benign |
|
|
R5149:Or5w15
|
UTSW |
2 |
87,567,749 (GRCm39) |
missense |
probably benign |
|
|
R5156:Or5w15
|
UTSW |
2 |
87,568,119 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6245:Or5w15
|
UTSW |
2 |
87,568,240 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R6701:Or5w15
|
UTSW |
2 |
87,567,753 (GRCm39) |
missense |
probably benign |
|
|
R7170:Or5w15
|
UTSW |
2 |
87,568,056 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7185:Or5w15
|
UTSW |
2 |
87,568,489 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7260:Or5w15
|
UTSW |
2 |
87,568,852 (GRCm39) |
splice site |
probably null |
|
|
R8065:Or5w15
|
UTSW |
2 |
87,568,147 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8067:Or5w15
|
UTSW |
2 |
87,568,147 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8671:Or5w15
|
UTSW |
2 |
87,567,990 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8953:Or5w15
|
UTSW |
2 |
87,568,371 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9254:Or5w15
|
UTSW |
2 |
87,568,372 (GRCm39) |
missense |
probably benign |
|
|
R9356:Or5w15
|
UTSW |
2 |
87,568,089 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9481:Or5w15
|
UTSW |
2 |
87,568,576 (GRCm39) |
missense |
probably benign |
0.44 |
|
R9544:Or5w15
|
UTSW |
2 |
87,568,644 (GRCm39) |
missense |
probably benign |
|
|
R9588:Or5w15
|
UTSW |
2 |
87,568,644 (GRCm39) |
missense |
probably benign |
|
|
R9646:Or5w15
|
UTSW |
2 |
87,568,512 (GRCm39) |
missense |
probably damaging |
0.97 |
|
| Posted On |
2015-04-16 |
Incidental Mutation