Incidental Mutation 'IGL02713:Or10a3'
| ID |
304635 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or10a3
|
| Ensembl Gene |
ENSMUSG00000046431 |
| Gene Name |
olfactory receptor family 10 subfamily A member 3 |
| Synonyms |
Olfr518, MOR268-5, GA_x6K02T2PBJ9-11211854-11210853 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.165)
|
| Stock # |
IGL02713
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
108479810-108480811 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 108480060 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Isoleucine
at position 251
(T251I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151883
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000059617]
[ENSMUST00000217803]
|
| AlphaFold |
Q8VEW1 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000059617
AA Change: T251I
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000050503
Gene: ENSMUSG00000046431
AA Change: T251I
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
11 |
22 |
N/A |
INTRINSIC |
|
Pfam:7tm_4
|
50 |
327 |
7.1e-60 |
PFAM |
|
Pfam:7tm_1
|
60 |
318 |
1.4e-23 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000217803
AA Change: T251I
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
| 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: 41 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acan |
A |
G |
7: 78,749,992 (GRCm39) |
T1588A |
possibly damaging |
Het |
| Apeh |
A |
T |
9: 107,962,871 (GRCm39) |
L700Q |
probably damaging |
Het |
| Arid1b |
T |
C |
17: 5,393,286 (GRCm39) |
I2272T |
probably damaging |
Het |
| Best3 |
T |
G |
10: 116,860,434 (GRCm39) |
F565V |
probably benign |
Het |
| Birc6 |
A |
G |
17: 74,886,319 (GRCm39) |
N521S |
probably benign |
Het |
| Cd209f |
T |
A |
8: 4,153,732 (GRCm39) |
R191S |
probably benign |
Het |
| Clec4e |
A |
T |
6: 123,263,263 (GRCm39) |
Y63* |
probably null |
Het |
| Cracdl |
C |
A |
1: 37,663,218 (GRCm39) |
K893N |
possibly damaging |
Het |
| Cyp26c1 |
C |
T |
19: 37,681,667 (GRCm39) |
T490M |
probably damaging |
Het |
| Cyp2b9 |
T |
A |
7: 25,872,945 (GRCm39) |
H29Q |
probably benign |
Het |
| Cyp2d10 |
A |
C |
15: 82,290,283 (GRCm39) |
|
probably benign |
Het |
| Dgat1 |
C |
A |
15: 76,387,734 (GRCm39) |
R291L |
probably damaging |
Het |
| Dyrk1a |
C |
A |
16: 94,486,204 (GRCm39) |
|
probably benign |
Het |
| Esp4 |
T |
C |
17: 40,913,297 (GRCm39) |
F55L |
probably benign |
Het |
| Fam227a |
G |
A |
15: 79,520,997 (GRCm39) |
|
probably benign |
Het |
| Ggt1 |
T |
C |
10: 75,410,178 (GRCm39) |
Y37H |
probably damaging |
Het |
| Grsf1 |
A |
T |
5: 88,820,589 (GRCm39) |
I64K |
probably damaging |
Het |
| Itga6 |
C |
T |
2: 71,647,057 (GRCm39) |
T89I |
possibly damaging |
Het |
| Jph2 |
T |
C |
2: 163,217,837 (GRCm39) |
T280A |
probably damaging |
Het |
| Lipm |
A |
G |
19: 34,078,570 (GRCm39) |
M1V |
probably null |
Het |
| Nbeal1 |
C |
T |
1: 60,274,396 (GRCm39) |
A513V |
possibly damaging |
Het |
| Or10a48 |
A |
T |
7: 108,424,801 (GRCm39) |
M135K |
probably damaging |
Het |
| Or10q1b |
A |
T |
19: 13,682,553 (GRCm39) |
I121F |
possibly damaging |
Het |
| Or13a28 |
A |
T |
7: 140,217,829 (GRCm39) |
I72F |
probably damaging |
Het |
| Or5ak25 |
T |
A |
2: 85,268,981 (GRCm39) |
I174F |
probably damaging |
Het |
| Or8b101 |
C |
T |
9: 38,020,623 (GRCm39) |
P214S |
probably damaging |
Het |
| Orc6 |
A |
G |
8: 86,034,215 (GRCm39) |
E146G |
probably benign |
Het |
| Patl2 |
A |
G |
2: 121,956,328 (GRCm39) |
S179P |
probably benign |
Het |
| Pdzd8 |
C |
A |
19: 59,333,890 (GRCm39) |
G44C |
probably damaging |
Het |
| Phox2b |
A |
G |
5: 67,253,938 (GRCm39) |
|
probably benign |
Het |
| Ppp4r3b |
T |
G |
11: 29,138,445 (GRCm39) |
H264Q |
probably damaging |
Het |
| Ptprk |
T |
C |
10: 28,468,807 (GRCm39) |
I1409T |
possibly damaging |
Het |
| Pum1 |
T |
A |
4: 130,493,323 (GRCm39) |
I842N |
probably damaging |
Het |
| Rnf123 |
G |
A |
9: 107,945,501 (GRCm39) |
R390* |
probably null |
Het |
| Sgca |
T |
A |
11: 94,862,131 (GRCm39) |
N174Y |
probably damaging |
Het |
| Slc7a14 |
A |
T |
3: 31,311,912 (GRCm39) |
L36Q |
probably damaging |
Het |
| Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
| Stard13 |
G |
A |
5: 150,965,651 (GRCm39) |
Q935* |
probably null |
Het |
| Suds3 |
C |
T |
5: 117,232,970 (GRCm39) |
|
probably null |
Het |
| Sv2b |
A |
T |
7: 74,773,911 (GRCm39) |
L520Q |
possibly damaging |
Het |
| Tmem26 |
T |
C |
10: 68,587,125 (GRCm39) |
F191S |
probably damaging |
Het |
|
| Other mutations in Or10a3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02995:Or10a3
|
APN |
7 |
108,480,198 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03162:Or10a3
|
APN |
7 |
108,480,811 (GRCm39) |
start codon destroyed |
probably null |
|
|
IGL03389:Or10a3
|
APN |
7 |
108,479,982 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0731:Or10a3
|
UTSW |
7 |
108,480,740 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1669:Or10a3
|
UTSW |
7 |
108,479,920 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2235:Or10a3
|
UTSW |
7 |
108,480,172 (GRCm39) |
missense |
probably benign |
0.09 |
|
R4740:Or10a3
|
UTSW |
7 |
108,480,689 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4902:Or10a3
|
UTSW |
7 |
108,480,624 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5343:Or10a3
|
UTSW |
7 |
108,480,205 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R6744:Or10a3
|
UTSW |
7 |
108,480,037 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7157:Or10a3
|
UTSW |
7 |
108,480,475 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7326:Or10a3
|
UTSW |
7 |
108,480,023 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7713:Or10a3
|
UTSW |
7 |
108,479,889 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7819:Or10a3
|
UTSW |
7 |
108,480,610 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7939:Or10a3
|
UTSW |
7 |
108,480,481 (GRCm39) |
missense |
probably benign |
0.05 |
|
R8057:Or10a3
|
UTSW |
7 |
108,480,571 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8096:Or10a3
|
UTSW |
7 |
108,480,248 (GRCm39) |
nonsense |
probably null |
|
|
R8472:Or10a3
|
UTSW |
7 |
108,479,973 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8766:Or10a3
|
UTSW |
7 |
108,480,453 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9283:Or10a3
|
UTSW |
7 |
108,480,289 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9570:Or10a3
|
UTSW |
7 |
108,480,504 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9763:Or10a3
|
UTSW |
7 |
108,480,874 (GRCm39) |
start gained |
probably benign |
|
|
X0066:Or10a3
|
UTSW |
7 |
108,480,679 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Posted On |
2015-04-16 |
Incidental Mutation