Incidental Mutation 'IGL03384:Or10g9b'
| ID |
420809 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or10g9b
|
| Ensembl Gene |
ENSMUSG00000060254 |
| Gene Name |
olfactory receptor family 10 subfamily G member 9B |
| Synonyms |
MOR223-2, GA_x6K02T2PVTD-33705428-33704496, Olfr980 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.073)
|
| Stock # |
IGL03384
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
39917290-39918325 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 39917766 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 160
(T160A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150496
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000073932]
[ENSMUST00000215523]
[ENSMUST00000216463]
|
| AlphaFold |
Q8VH08 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000073932
AA Change: T160A
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000091386
Gene: ENSMUSG00000060254
AA Change: T160A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
304 |
1.4e-55 |
PFAM |
|
Pfam:7tm_1
|
39 |
287 |
5.4e-23 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215523
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000216463
AA Change: T160A
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| 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 |
|---|
| 4933427D14Rik |
A |
G |
11: 72,086,673 (GRCm39) |
I246T |
possibly damaging |
Het |
| Ablim2 |
C |
T |
5: 36,032,216 (GRCm39) |
R614C |
probably damaging |
Het |
| B4galt7 |
T |
C |
13: 55,757,102 (GRCm39) |
L265P |
probably damaging |
Het |
| Col4a4 |
C |
T |
1: 82,462,159 (GRCm39) |
C1072Y |
probably benign |
Het |
| Cxcr2 |
T |
C |
1: 74,197,950 (GRCm39) |
V148A |
probably damaging |
Het |
| Dnah14 |
G |
A |
1: 181,573,514 (GRCm39) |
V2942M |
probably benign |
Het |
| Fam124b |
T |
A |
1: 80,177,673 (GRCm39) |
H442L |
probably benign |
Het |
| Haus6 |
T |
C |
4: 86,501,762 (GRCm39) |
H703R |
probably benign |
Het |
| Ice1 |
T |
C |
13: 70,751,368 (GRCm39) |
T1573A |
probably benign |
Het |
| Iftap |
G |
T |
2: 101,415,608 (GRCm39) |
T115N |
probably benign |
Het |
| Ighv1-31 |
A |
G |
12: 114,793,093 (GRCm39) |
F48L |
probably benign |
Het |
| Iws1 |
C |
A |
18: 32,226,203 (GRCm39) |
A697D |
probably damaging |
Het |
| Jhy |
T |
A |
9: 40,872,228 (GRCm39) |
N94Y |
probably benign |
Het |
| Kank2 |
C |
T |
9: 21,685,874 (GRCm39) |
V667M |
possibly damaging |
Het |
| Mcam |
G |
A |
9: 44,051,809 (GRCm39) |
|
probably benign |
Het |
| Muc5ac |
A |
T |
7: 141,366,140 (GRCm39) |
I2099F |
possibly damaging |
Het |
| Myo7a |
T |
C |
7: 97,742,800 (GRCm39) |
I410V |
probably damaging |
Het |
| Nub1 |
A |
T |
5: 24,902,425 (GRCm39) |
|
probably benign |
Het |
| Nub1 |
A |
T |
5: 24,902,424 (GRCm39) |
|
probably null |
Het |
| Panx2 |
C |
T |
15: 88,952,322 (GRCm39) |
A271V |
possibly damaging |
Het |
| Papss1 |
T |
A |
3: 131,285,113 (GRCm39) |
H13Q |
probably damaging |
Het |
| Pkd1 |
A |
G |
17: 24,784,871 (GRCm39) |
T438A |
probably benign |
Het |
| Ppdpf |
T |
C |
2: 180,829,673 (GRCm39) |
S43P |
probably benign |
Het |
| Ptchd4 |
T |
A |
17: 42,813,481 (GRCm39) |
C461S |
probably damaging |
Het |
| Rapgef2 |
A |
G |
3: 78,990,853 (GRCm39) |
F985S |
probably damaging |
Het |
| Rbm25 |
T |
C |
12: 83,706,297 (GRCm39) |
I214T |
probably benign |
Het |
| Sgpp1 |
T |
C |
12: 75,762,880 (GRCm39) |
|
probably benign |
Het |
| Slc22a20 |
A |
T |
19: 6,030,402 (GRCm39) |
C343* |
probably null |
Het |
| Slc22a22 |
T |
C |
15: 57,117,612 (GRCm39) |
I310V |
probably benign |
Het |
| Slc6a13 |
T |
C |
6: 121,309,350 (GRCm39) |
F287S |
probably damaging |
Het |
| Usp30 |
A |
G |
5: 114,259,635 (GRCm39) |
D447G |
probably damaging |
Het |
| Vmn1r78 |
A |
T |
7: 11,887,136 (GRCm39) |
Y249F |
possibly damaging |
Het |
| Vmn2r106 |
T |
C |
17: 20,488,405 (GRCm39) |
T665A |
probably damaging |
Het |
| Vps37b |
A |
G |
5: 124,145,670 (GRCm39) |
|
probably null |
Het |
| Wfdc1 |
T |
A |
8: 120,413,016 (GRCm39) |
N198K |
probably benign |
Het |
|
| Other mutations in Or10g9b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02256:Or10g9b
|
APN |
9 |
39,917,349 (GRCm39) |
missense |
probably benign |
|
|
IGL02378:Or10g9b
|
APN |
9 |
39,917,769 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03402:Or10g9b
|
APN |
9 |
39,917,802 (GRCm39) |
missense |
probably benign |
0.31 |
|
BB010:Or10g9b
|
UTSW |
9 |
39,918,431 (GRCm39) |
start gained |
probably benign |
|
|
PIT4651001:Or10g9b
|
UTSW |
9 |
39,917,526 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0013:Or10g9b
|
UTSW |
9 |
39,917,651 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1146:Or10g9b
|
UTSW |
9 |
39,917,390 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1146:Or10g9b
|
UTSW |
9 |
39,917,390 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4541:Or10g9b
|
UTSW |
9 |
39,917,589 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4562:Or10g9b
|
UTSW |
9 |
39,917,577 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4731:Or10g9b
|
UTSW |
9 |
39,917,564 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4732:Or10g9b
|
UTSW |
9 |
39,917,564 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4733:Or10g9b
|
UTSW |
9 |
39,917,564 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4825:Or10g9b
|
UTSW |
9 |
39,918,038 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R5619:Or10g9b
|
UTSW |
9 |
39,918,039 (GRCm39) |
missense |
probably benign |
0.07 |
|
R5770:Or10g9b
|
UTSW |
9 |
39,917,634 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5791:Or10g9b
|
UTSW |
9 |
39,918,030 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6813:Or10g9b
|
UTSW |
9 |
39,917,753 (GRCm39) |
missense |
probably benign |
|
|
R6819:Or10g9b
|
UTSW |
9 |
39,917,844 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6970:Or10g9b
|
UTSW |
9 |
39,918,009 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7490:Or10g9b
|
UTSW |
9 |
39,917,720 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7511:Or10g9b
|
UTSW |
9 |
39,918,229 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R7933:Or10g9b
|
UTSW |
9 |
39,918,431 (GRCm39) |
start gained |
probably benign |
|
|
R8243:Or10g9b
|
UTSW |
9 |
39,917,484 (GRCm39) |
missense |
probably benign |
0.19 |
|
Z1088:Or10g9b
|
UTSW |
9 |
39,917,892 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Posted On |
2016-08-02 |
Incidental Mutation