Incidental Mutation 'IGL01564:Or10g1'
| ID |
90932 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or10g1
|
| Ensembl Gene |
ENSMUSG00000063106 |
| Gene Name |
olfactory receptor family 10 subfamily G member 1 |
| Synonyms |
MOR223-6, GA_x6K02T2RJGY-583652-584608, Olfr1510 |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL01564
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
14 |
| Chromosomal Location |
52647346-52648384 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 52648299 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 10
(D10G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150294
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000079459]
[ENSMUST00000215928]
|
| AlphaFold |
E9PZZ6 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000079459
AA Change: D10G
PolyPhen 2
Score 0.041 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000078424
Gene: ENSMUSG00000063106
AA Change: D10G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
35 |
311 |
8.1e-50 |
PFAM |
|
Pfam:7tm_1
|
45 |
293 |
1.8e-20 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000206257
AA Change: D10G
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215928
AA Change: D10G
PolyPhen 2
Score 0.041 (Sensitivity: 0.94; Specificity: 0.83)
|
| 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: 34 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adat3 |
T |
A |
10: 80,442,693 (GRCm39) |
M177K |
probably damaging |
Het |
| Ankrd28 |
G |
T |
14: 31,477,724 (GRCm39) |
T48K |
probably damaging |
Het |
| Capn3 |
T |
C |
2: 120,311,189 (GRCm39) |
I112T |
probably damaging |
Het |
| Clec3a |
T |
A |
8: 115,152,282 (GRCm39) |
I96N |
probably damaging |
Het |
| Clic4 |
C |
T |
4: 134,944,504 (GRCm39) |
A224T |
probably damaging |
Het |
| Eif2b3 |
T |
C |
4: 116,885,739 (GRCm39) |
Y94H |
probably benign |
Het |
| Ep300 |
A |
T |
15: 81,516,665 (GRCm39) |
|
probably benign |
Het |
| Errfi1 |
C |
A |
4: 150,951,487 (GRCm39) |
T305N |
probably damaging |
Het |
| Fam131c |
T |
A |
4: 141,106,984 (GRCm39) |
|
probably null |
Het |
| Fbxo11 |
G |
A |
17: 88,310,324 (GRCm39) |
T494I |
probably benign |
Het |
| Homer2 |
T |
C |
7: 81,268,320 (GRCm39) |
|
probably null |
Het |
| Hpf1 |
C |
A |
8: 61,343,513 (GRCm39) |
|
probably benign |
Het |
| Hspa1b |
T |
C |
17: 35,176,525 (GRCm39) |
N487D |
probably benign |
Het |
| Ikbke |
C |
A |
1: 131,185,658 (GRCm39) |
A617S |
probably benign |
Het |
| Jade1 |
G |
T |
3: 41,551,084 (GRCm39) |
R174S |
possibly damaging |
Het |
| Lcmt1 |
T |
C |
7: 123,003,663 (GRCm39) |
F139S |
probably benign |
Het |
| Lipo2 |
T |
C |
19: 33,698,424 (GRCm39) |
T318A |
probably benign |
Het |
| Lrp1b |
C |
T |
2: 40,567,498 (GRCm39) |
|
probably benign |
Het |
| Lsm14a |
T |
C |
7: 34,088,780 (GRCm39) |
|
probably benign |
Het |
| Mpp2 |
T |
C |
11: 101,952,345 (GRCm39) |
D393G |
probably benign |
Het |
| Nfyb |
T |
C |
10: 82,588,260 (GRCm39) |
Y137C |
probably damaging |
Het |
| Or5d35 |
A |
T |
2: 87,855,648 (GRCm39) |
H194L |
probably benign |
Het |
| Or5p55 |
T |
C |
7: 107,567,198 (GRCm39) |
I198T |
probably benign |
Het |
| Scn3a |
A |
C |
2: 65,291,790 (GRCm39) |
I1652S |
probably damaging |
Het |
| Slc33a1 |
C |
T |
3: 63,850,768 (GRCm39) |
V519I |
probably benign |
Het |
| Strada |
G |
T |
11: 106,064,118 (GRCm39) |
N66K |
probably damaging |
Het |
| Thoc2l |
A |
T |
5: 104,668,529 (GRCm39) |
Y1017F |
probably benign |
Het |
| Tlr1 |
T |
A |
5: 65,083,189 (GRCm39) |
I463F |
probably damaging |
Het |
| Tnfrsf19 |
G |
T |
14: 61,212,058 (GRCm39) |
F197L |
possibly damaging |
Het |
| Tph1 |
T |
A |
7: 46,300,305 (GRCm39) |
|
probably benign |
Het |
| Ttn |
A |
T |
2: 76,646,922 (GRCm39) |
L3287H |
probably damaging |
Het |
| Vmn2r18 |
A |
T |
5: 151,508,633 (GRCm39) |
S164T |
possibly damaging |
Het |
| Zan |
C |
T |
5: 137,444,995 (GRCm39) |
V1755I |
unknown |
Het |
| Zmym4 |
T |
C |
4: 126,805,073 (GRCm39) |
I396V |
possibly damaging |
Het |
|
| Other mutations in Or10g1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02097:Or10g1
|
APN |
14 |
52,647,511 (GRCm39) |
missense |
probably benign |
|
|
R0282:Or10g1
|
UTSW |
14 |
52,647,720 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R1449:Or10g1
|
UTSW |
14 |
52,648,024 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2113:Or10g1
|
UTSW |
14 |
52,647,753 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2870:Or10g1
|
UTSW |
14 |
52,648,318 (GRCm39) |
missense |
probably benign |
|
|
R2870:Or10g1
|
UTSW |
14 |
52,648,318 (GRCm39) |
missense |
probably benign |
|
|
R2872:Or10g1
|
UTSW |
14 |
52,648,318 (GRCm39) |
missense |
probably benign |
|
|
R2872:Or10g1
|
UTSW |
14 |
52,648,318 (GRCm39) |
missense |
probably benign |
|
|
R2873:Or10g1
|
UTSW |
14 |
52,648,318 (GRCm39) |
missense |
probably benign |
|
|
R3409:Or10g1
|
UTSW |
14 |
52,647,818 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R3411:Or10g1
|
UTSW |
14 |
52,647,818 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R4480:Or10g1
|
UTSW |
14 |
52,647,765 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5292:Or10g1
|
UTSW |
14 |
52,647,902 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5297:Or10g1
|
UTSW |
14 |
52,647,675 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5441:Or10g1
|
UTSW |
14 |
52,647,414 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5749:Or10g1
|
UTSW |
14 |
52,647,961 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5872:Or10g1
|
UTSW |
14 |
52,648,225 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5941:Or10g1
|
UTSW |
14 |
52,647,525 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7209:Or10g1
|
UTSW |
14 |
52,647,550 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R7379:Or10g1
|
UTSW |
14 |
52,647,718 (GRCm39) |
missense |
probably benign |
0.08 |
|
R7463:Or10g1
|
UTSW |
14 |
52,648,168 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7692:Or10g1
|
UTSW |
14 |
52,647,945 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8894:Or10g1
|
UTSW |
14 |
52,647,465 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9286:Or10g1
|
UTSW |
14 |
52,648,075 (GRCm39) |
nonsense |
probably null |
|
|
R9394:Or10g1
|
UTSW |
14 |
52,647,570 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-12-09 |
Incidental Mutation