Incidental Mutation 'IGL02240:Or8b56'
| ID |
286025 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or8b56
|
| Ensembl Gene |
ENSMUSG00000044798 |
| Gene Name |
olfactory receptor family 8 subfamily B member 56 |
| Synonyms |
Olfr923, MOR164-2, GA_x6K02T2PVTD-32530445-32531380 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.057)
|
| Stock # |
IGL02240
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
38738911-38739978 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 38739602 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Aspartic acid
at position 205
(V205D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151652
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000051238]
[ENSMUST00000213619]
[ENSMUST00000219798]
|
| AlphaFold |
Q7TRB9 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000051238
AA Change: V199D
PolyPhen 2
Score 0.100 (Sensitivity: 0.93; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000062073
Gene: ENSMUSG00000044798
AA Change: V199D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
37 |
314 |
1.2e-46 |
PFAM |
|
Pfam:7tm_1
|
47 |
296 |
3.5e-23 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000213550
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213619
AA Change: V199D
PolyPhen 2
Score 0.100 (Sensitivity: 0.93; Specificity: 0.86)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000219798
AA Change: V205D
PolyPhen 2
Score 0.122 (Sensitivity: 0.93; Specificity: 0.86)
|
| 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: 22 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Cand2 |
A |
G |
6: 115,780,623 (GRCm39) |
E1169G |
probably damaging |
Het |
| Cdc34 |
A |
G |
10: 79,523,823 (GRCm39) |
D168G |
possibly damaging |
Het |
| Cwc27 |
A |
T |
13: 104,943,151 (GRCm39) |
F130L |
probably damaging |
Het |
| Dglucy |
T |
A |
12: 100,837,672 (GRCm39) |
M635K |
possibly damaging |
Het |
| Eral1 |
G |
A |
11: 77,968,687 (GRCm39) |
R149* |
probably null |
Het |
| Gad1-ps |
A |
G |
10: 99,280,820 (GRCm39) |
|
noncoding transcript |
Het |
| Glis3 |
A |
T |
19: 28,508,925 (GRCm39) |
L353Q |
probably damaging |
Het |
| Gsta2 |
T |
A |
9: 78,238,441 (GRCm39) |
I213F |
probably benign |
Het |
| Ist1 |
A |
T |
8: 110,408,836 (GRCm39) |
|
probably benign |
Het |
| Kif1b |
A |
G |
4: 149,330,871 (GRCm39) |
V549A |
probably damaging |
Het |
| Lrp2 |
C |
T |
2: 69,365,390 (GRCm39) |
R261H |
probably benign |
Het |
| Msh4 |
T |
C |
3: 153,579,311 (GRCm39) |
N512S |
probably damaging |
Het |
| Nlrp2 |
A |
T |
7: 5,330,822 (GRCm39) |
S525T |
probably damaging |
Het |
| Nlrp4a |
G |
T |
7: 26,148,703 (GRCm39) |
K103N |
possibly damaging |
Het |
| Pcdhb10 |
A |
T |
18: 37,545,455 (GRCm39) |
H177L |
possibly damaging |
Het |
| Plcb3 |
A |
T |
19: 6,935,448 (GRCm39) |
|
probably benign |
Het |
| Podxl |
A |
G |
6: 31,501,933 (GRCm39) |
L342P |
probably damaging |
Het |
| Psd4 |
T |
G |
2: 24,286,389 (GRCm39) |
S330A |
probably benign |
Het |
| Sucla2 |
A |
G |
14: 73,828,287 (GRCm39) |
D298G |
probably damaging |
Het |
| Tecr |
T |
C |
8: 84,300,045 (GRCm39) |
D107G |
probably damaging |
Het |
| Vamp4 |
T |
A |
1: 162,405,446 (GRCm39) |
N24K |
possibly damaging |
Het |
| Zfp91 |
A |
G |
19: 12,753,770 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Or8b56 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01485:Or8b56
|
APN |
9 |
38,739,895 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL01521:Or8b56
|
APN |
9 |
38,739,185 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01548:Or8b56
|
APN |
9 |
38,739,646 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02794:Or8b56
|
APN |
9 |
38,739,511 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0116:Or8b56
|
UTSW |
9 |
38,739,860 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0118:Or8b56
|
UTSW |
9 |
38,739,154 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R0189:Or8b56
|
UTSW |
9 |
38,739,111 (GRCm39) |
nonsense |
probably null |
|
|
R1381:Or8b56
|
UTSW |
9 |
38,739,634 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1512:Or8b56
|
UTSW |
9 |
38,739,660 (GRCm39) |
nonsense |
probably null |
|
|
R1702:Or8b56
|
UTSW |
9 |
38,739,839 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2357:Or8b56
|
UTSW |
9 |
38,739,634 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2863:Or8b56
|
UTSW |
9 |
38,739,835 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R2985:Or8b56
|
UTSW |
9 |
38,739,406 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5475:Or8b56
|
UTSW |
9 |
38,739,762 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R5682:Or8b56
|
UTSW |
9 |
38,739,424 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8243:Or8b56
|
UTSW |
9 |
38,739,803 (GRCm39) |
missense |
|
|
|
R8743:Or8b56
|
UTSW |
9 |
38,738,995 (GRCm39) |
missense |
probably benign |
0.08 |
|
R9182:Or8b56
|
UTSW |
9 |
38,739,172 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9563:Or8b56
|
UTSW |
9 |
38,739,014 (GRCm39) |
missense |
probably benign |
|
|
| Posted On |
2015-04-16 |
Incidental Mutation