Incidental Mutation 'IGL01586:Or8b8'
| ID |
91795 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or8b8
|
| Ensembl Gene |
ENSMUSG00000066748 |
| Gene Name |
olfactory receptor family 8 subfamily B member 8 |
| Synonyms |
GA_x6K02T2PVTD-31578734-31579666, Olfr145, K21, MOR161-6 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.121)
|
| Stock # |
IGL01586
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
37808020-37814815 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 37809272 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 191
(T191A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150284
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000086062]
[ENSMUST00000213688]
|
| AlphaFold |
Q60882 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000086062
AA Change: T191A
PolyPhen 2
Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
|
| SMART Domains |
Protein: ENSMUSP00000083229
Gene: ENSMUSG00000066748
AA Change: T191A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
30 |
307 |
4e-51 |
PFAM |
|
Pfam:7tm_1
|
40 |
289 |
1.4e-23 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000213688
AA Change: T191A
PolyPhen 2
Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
|
| 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: 35 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 9830107B12Rik |
A |
T |
17: 48,439,125 (GRCm39) |
Y144N |
unknown |
Het |
| Abca9 |
A |
C |
11: 110,045,243 (GRCm39) |
C363W |
probably damaging |
Het |
| Acmsd |
G |
A |
1: 127,687,447 (GRCm39) |
R243H |
probably damaging |
Het |
| Adam33 |
T |
C |
2: 130,895,970 (GRCm39) |
T490A |
probably damaging |
Het |
| Ank1 |
A |
G |
8: 23,610,928 (GRCm39) |
D1411G |
probably benign |
Het |
| Arhgap39 |
T |
C |
15: 76,614,638 (GRCm39) |
E842G |
probably benign |
Het |
| Asgr2 |
T |
C |
11: 69,996,193 (GRCm39) |
|
probably benign |
Het |
| Bbs9 |
T |
C |
9: 22,557,293 (GRCm39) |
V14A |
possibly damaging |
Het |
| Cer1 |
A |
G |
4: 82,803,080 (GRCm39) |
S81P |
probably damaging |
Het |
| Cln6 |
T |
A |
9: 62,751,900 (GRCm39) |
H41Q |
probably damaging |
Het |
| Dock1 |
A |
G |
7: 134,355,106 (GRCm39) |
D334G |
probably damaging |
Het |
| Dpy19l2 |
A |
G |
9: 24,578,271 (GRCm39) |
I261T |
probably benign |
Het |
| Fhod3 |
T |
G |
18: 25,223,804 (GRCm39) |
I1050S |
probably damaging |
Het |
| Gbgt1 |
T |
C |
2: 28,387,842 (GRCm39) |
V22A |
probably benign |
Het |
| Izumo3 |
A |
G |
4: 92,034,532 (GRCm39) |
|
probably null |
Het |
| Kif11 |
T |
C |
19: 37,372,681 (GRCm39) |
|
probably benign |
Het |
| Krt1c |
C |
A |
15: 101,719,825 (GRCm39) |
G615V |
unknown |
Het |
| Midn |
A |
G |
10: 79,992,477 (GRCm39) |
|
probably benign |
Het |
| Mier1 |
C |
T |
4: 103,012,769 (GRCm39) |
T342I |
probably damaging |
Het |
| Mycbp2 |
A |
T |
14: 103,378,305 (GRCm39) |
|
probably null |
Het |
| Nrp1 |
A |
T |
8: 129,158,513 (GRCm39) |
S267C |
possibly damaging |
Het |
| Pcdh20 |
A |
T |
14: 88,708,344 (GRCm39) |
M28K |
probably benign |
Het |
| Prmt5 |
G |
A |
14: 54,747,408 (GRCm39) |
|
probably benign |
Het |
| Psmg2 |
G |
A |
18: 67,786,293 (GRCm39) |
V218I |
probably benign |
Het |
| Rps6ka5 |
T |
C |
12: 100,537,173 (GRCm39) |
E519G |
probably damaging |
Het |
| Samm50 |
T |
A |
15: 84,080,039 (GRCm39) |
I39N |
probably benign |
Het |
| Shc2 |
A |
T |
10: 79,458,138 (GRCm39) |
M515K |
probably damaging |
Het |
| Sorbs2 |
T |
A |
8: 46,248,631 (GRCm39) |
F608L |
probably damaging |
Het |
| Sos2 |
T |
C |
12: 69,654,172 (GRCm39) |
K727E |
probably damaging |
Het |
| Sox13 |
A |
T |
1: 133,317,182 (GRCm39) |
H150Q |
possibly damaging |
Het |
| Tmem132e |
T |
C |
11: 82,325,495 (GRCm39) |
V165A |
probably damaging |
Het |
| Trmt11 |
T |
C |
10: 30,473,747 (GRCm39) |
T43A |
probably benign |
Het |
| Tyrp1 |
G |
T |
4: 80,763,135 (GRCm39) |
V341L |
probably benign |
Het |
| Ugt2b35 |
C |
A |
5: 87,159,250 (GRCm39) |
H481Q |
probably benign |
Het |
| Zzz3 |
T |
A |
3: 152,161,476 (GRCm39) |
I290N |
possibly damaging |
Het |
|
| Other mutations in Or8b8 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01362:Or8b8
|
APN |
9 |
37,809,359 (GRCm39) |
missense |
probably benign |
0.13 |
|
IGL02185:Or8b8
|
APN |
9 |
37,809,531 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02895:Or8b8
|
APN |
9 |
37,809,278 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02956:Or8b8
|
APN |
9 |
37,809,404 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0391:Or8b8
|
UTSW |
9 |
37,809,138 (GRCm39) |
missense |
probably benign |
0.31 |
|
R0513:Or8b8
|
UTSW |
9 |
37,809,351 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4600:Or8b8
|
UTSW |
9 |
37,809,622 (GRCm39) |
missense |
probably benign |
|
|
R4610:Or8b8
|
UTSW |
9 |
37,809,622 (GRCm39) |
missense |
probably benign |
|
|
R4611:Or8b8
|
UTSW |
9 |
37,809,622 (GRCm39) |
missense |
probably benign |
|
|
R4982:Or8b8
|
UTSW |
9 |
37,808,811 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5574:Or8b8
|
UTSW |
9 |
37,808,877 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5608:Or8b8
|
UTSW |
9 |
37,809,078 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5688:Or8b8
|
UTSW |
9 |
37,809,359 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5906:Or8b8
|
UTSW |
9 |
37,809,174 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6286:Or8b8
|
UTSW |
9 |
37,809,074 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7138:Or8b8
|
UTSW |
9 |
37,809,360 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7145:Or8b8
|
UTSW |
9 |
37,808,859 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7993:Or8b8
|
UTSW |
9 |
37,808,633 (GRCm39) |
intron |
probably benign |
|
|
R8046:Or8b8
|
UTSW |
9 |
37,808,685 (GRCm39) |
splice site |
probably benign |
|
|
R8185:Or8b8
|
UTSW |
9 |
37,809,531 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9276:Or8b8
|
UTSW |
9 |
37,809,415 (GRCm39) |
missense |
probably benign |
0.04 |
|
R9352:Or8b8
|
UTSW |
9 |
37,808,712 (GRCm39) |
missense |
probably benign |
0.00 |
|
X0012:Or8b8
|
UTSW |
9 |
37,809,624 (GRCm39) |
nonsense |
probably null |
|
|
| Posted On |
2013-12-09 |
Incidental Mutation