Incidental Mutation 'IGL02727:Or8b40'
| ID |
305243 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or8b40
|
| Ensembl Gene |
ENSMUSG00000096356 |
| Gene Name |
olfactory receptor family 8 subfamily B member 40 |
| Synonyms |
GA_x6K02T2PVTD-31795028-31795957, Olfr889, MOR162-2 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.085)
|
| Stock # |
IGL02727
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
38027094-38028023 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 38027808 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 239
(T239A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148913
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000072290]
[ENSMUST00000217286]
|
| AlphaFold |
L7N1Y6 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000072290
AA Change: T244A
PolyPhen 2
Score 0.980 (Sensitivity: 0.75; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000072137
Gene: ENSMUSG00000096356
AA Change: T244A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
36 |
311 |
4.4e-50 |
PFAM |
|
Pfam:7tm_1
|
46 |
293 |
1e-25 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000213042
AA Change: T239A
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000217286
AA Change: T239A
PolyPhen 2
Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)
|
| 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: 44 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700019A02Rik |
T |
C |
1: 53,226,724 (GRCm39) |
T13A |
probably benign |
Het |
| Aldh1l2 |
T |
A |
10: 83,342,469 (GRCm39) |
K447I |
probably damaging |
Het |
| Ankrd17 |
A |
G |
5: 90,392,151 (GRCm39) |
S1840P |
possibly damaging |
Het |
| Ash1l |
A |
G |
3: 88,930,344 (GRCm39) |
I1940M |
probably benign |
Het |
| Bfar |
T |
G |
16: 13,506,791 (GRCm39) |
|
probably null |
Het |
| Bicra |
G |
T |
7: 15,713,390 (GRCm39) |
H937Q |
possibly damaging |
Het |
| Brip1 |
A |
T |
11: 86,043,562 (GRCm39) |
M334K |
probably benign |
Het |
| Camsap2 |
T |
G |
1: 136,232,050 (GRCm39) |
M182L |
probably benign |
Het |
| Chd6 |
A |
T |
2: 160,811,383 (GRCm39) |
C1407S |
probably damaging |
Het |
| Cmya5 |
A |
G |
13: 93,234,753 (GRCm39) |
S112P |
possibly damaging |
Het |
| Csmd1 |
A |
T |
8: 16,281,341 (GRCm39) |
V728E |
probably damaging |
Het |
| Cyp2j6 |
T |
A |
4: 96,434,001 (GRCm39) |
Q103L |
probably benign |
Het |
| Ddias |
A |
T |
7: 92,515,830 (GRCm39) |
I21K |
probably damaging |
Het |
| Derl2 |
A |
C |
11: 70,904,036 (GRCm39) |
|
probably benign |
Het |
| Dgka |
A |
T |
10: 128,558,317 (GRCm39) |
|
probably benign |
Het |
| Dusp11 |
T |
C |
6: 85,938,474 (GRCm39) |
D15G |
probably damaging |
Het |
| Enpp2 |
T |
C |
15: 54,773,577 (GRCm39) |
D110G |
probably damaging |
Het |
| Fkbp11 |
A |
T |
15: 98,622,471 (GRCm39) |
V134E |
probably damaging |
Het |
| Gm3248 |
T |
C |
14: 5,945,036 (GRCm38) |
T49A |
probably damaging |
Het |
| Gm57858 |
T |
A |
3: 36,087,065 (GRCm39) |
R176S |
possibly damaging |
Het |
| Irag2 |
T |
C |
6: 145,120,344 (GRCm39) |
S520P |
possibly damaging |
Het |
| Luzp2 |
T |
C |
7: 54,821,939 (GRCm39) |
|
probably benign |
Het |
| Manea |
T |
A |
4: 26,328,126 (GRCm39) |
E305V |
probably damaging |
Het |
| Manea |
C |
A |
4: 26,328,127 (GRCm39) |
E305* |
probably null |
Het |
| Megf6 |
A |
G |
4: 154,337,606 (GRCm39) |
|
probably null |
Het |
| Mrpl3 |
G |
T |
9: 104,931,726 (GRCm39) |
D59Y |
probably damaging |
Het |
| Myh9 |
T |
C |
15: 77,675,942 (GRCm39) |
Y248C |
probably benign |
Het |
| Nbeal2 |
G |
A |
9: 110,468,353 (GRCm39) |
|
probably benign |
Het |
| Or10a5 |
G |
T |
7: 106,635,902 (GRCm39) |
C180F |
probably damaging |
Het |
| Or1f19 |
T |
A |
16: 3,411,190 (GRCm39) |
I310K |
probably benign |
Het |
| Or2y1c |
G |
T |
11: 49,361,893 (GRCm39) |
G305V |
probably benign |
Het |
| Pax8 |
C |
A |
2: 24,331,642 (GRCm39) |
C147F |
probably damaging |
Het |
| Phf12 |
T |
C |
11: 77,914,493 (GRCm39) |
V96A |
possibly damaging |
Het |
| Psg18 |
A |
T |
7: 18,079,875 (GRCm39) |
I442K |
probably damaging |
Het |
| Pygl |
T |
A |
12: 70,254,442 (GRCm39) |
|
probably null |
Het |
| Rassf2 |
C |
A |
2: 131,846,307 (GRCm39) |
R150L |
probably benign |
Het |
| Rdh7 |
A |
T |
10: 127,723,487 (GRCm39) |
W123R |
probably damaging |
Het |
| Saal1 |
T |
C |
7: 46,339,223 (GRCm39) |
|
probably null |
Het |
| Sall1 |
T |
C |
8: 89,757,383 (GRCm39) |
D907G |
probably damaging |
Het |
| Spag1 |
T |
A |
15: 36,234,964 (GRCm39) |
F876I |
probably damaging |
Het |
| Syncrip |
G |
A |
9: 88,361,932 (GRCm39) |
A61V |
probably damaging |
Het |
| Trbv3 |
A |
T |
6: 41,025,576 (GRCm39) |
K55N |
probably benign |
Het |
| Vmn1r178 |
A |
G |
7: 23,593,871 (GRCm39) |
|
probably null |
Het |
| Vmn2r84 |
T |
C |
10: 130,229,995 (GRCm39) |
D39G |
possibly damaging |
Het |
|
| Other mutations in Or8b40 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02201:Or8b40
|
APN |
9 |
38,027,893 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02604:Or8b40
|
APN |
9 |
38,027,148 (GRCm39) |
nonsense |
probably null |
|
|
R0364:Or8b40
|
UTSW |
9 |
38,027,325 (GRCm39) |
missense |
probably benign |
0.26 |
|
R0387:Or8b40
|
UTSW |
9 |
38,027,066 (GRCm39) |
splice site |
probably null |
|
|
R0409:Or8b40
|
UTSW |
9 |
38,027,547 (GRCm39) |
missense |
probably benign |
|
|
R0515:Or8b40
|
UTSW |
9 |
38,027,313 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0693:Or8b40
|
UTSW |
9 |
38,027,325 (GRCm39) |
missense |
probably benign |
0.26 |
|
R1554:Or8b40
|
UTSW |
9 |
38,027,230 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1972:Or8b40
|
UTSW |
9 |
38,027,863 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R1973:Or8b40
|
UTSW |
9 |
38,027,863 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R3815:Or8b40
|
UTSW |
9 |
38,027,922 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R3816:Or8b40
|
UTSW |
9 |
38,027,922 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R3817:Or8b40
|
UTSW |
9 |
38,027,922 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R3819:Or8b40
|
UTSW |
9 |
38,027,922 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R5532:Or8b40
|
UTSW |
9 |
38,027,923 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5775:Or8b40
|
UTSW |
9 |
38,027,423 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5931:Or8b40
|
UTSW |
9 |
38,027,670 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6458:Or8b40
|
UTSW |
9 |
38,027,350 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R6751:Or8b40
|
UTSW |
9 |
38,027,271 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7168:Or8b40
|
UTSW |
9 |
38,027,959 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7673:Or8b40
|
UTSW |
9 |
38,027,523 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7698:Or8b40
|
UTSW |
9 |
38,027,188 (GRCm39) |
nonsense |
probably null |
|
|
R8432:Or8b40
|
UTSW |
9 |
38,027,272 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9034:Or8b40
|
UTSW |
9 |
38,027,550 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R9236:Or8b40
|
UTSW |
9 |
38,027,496 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R9561:Or8b40
|
UTSW |
9 |
38,028,010 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Posted On |
2015-04-16 |
Incidental Mutation