Incidental Mutation 'IGL02061:Or4g7'
| ID |
185398 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or4g7
|
| Ensembl Gene |
ENSMUSG00000044039 |
| Gene Name |
olfactory receptor family 4 subfamily G member 7 |
| Synonyms |
Olfr1288, GA_x6K02T2Q125-72530279-72531217, MOR245-9 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.071)
|
| Stock # |
IGL02061
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
111309131-111310069 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 111309614 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Phenylalanine to Isoleucine
at position 162
(F162I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150331
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000104889]
[ENSMUST00000120021]
[ENSMUST00000207494]
[ENSMUST00000214816]
|
| AlphaFold |
Q7TQY0 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000104889
AA Change: F162I
PolyPhen 2
Score 0.942 (Sensitivity: 0.80; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000100485
Gene: ENSMUSG00000044039
AA Change: F162I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
304 |
1.3e-43 |
PFAM |
|
Pfam:7tm_1
|
41 |
287 |
2.5e-20 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000120021
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000207494
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000214816
AA Change: F162I
PolyPhen 2
Score 0.942 (Sensitivity: 0.80; Specificity: 0.94)
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000225425
|
| 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 |
|---|
| Arl15 |
T |
A |
13: 113,931,193 (GRCm39) |
D3E |
probably benign |
Het |
| Atp4a |
A |
G |
7: 30,414,454 (GRCm39) |
Y159C |
probably damaging |
Het |
| Card10 |
A |
G |
15: 78,662,415 (GRCm39) |
F861S |
probably damaging |
Het |
| Ccdc85c |
A |
G |
12: 108,188,002 (GRCm39) |
V279A |
probably damaging |
Het |
| Cndp1 |
G |
A |
18: 84,652,751 (GRCm39) |
R136W |
probably damaging |
Het |
| Eif2b3 |
A |
G |
4: 116,885,608 (GRCm39) |
E50G |
possibly damaging |
Het |
| Entrep3 |
C |
T |
3: 89,095,903 (GRCm39) |
R545* |
probably null |
Het |
| Eva1c |
C |
T |
16: 90,663,163 (GRCm39) |
Q67* |
probably null |
Het |
| Exoc1 |
A |
G |
5: 76,689,967 (GRCm39) |
E169G |
probably damaging |
Het |
| Fsd2 |
T |
A |
7: 81,190,172 (GRCm39) |
K537* |
probably null |
Het |
| Gbf1 |
T |
G |
19: 46,267,697 (GRCm39) |
S1236A |
possibly damaging |
Het |
| Gpt |
C |
A |
15: 76,583,617 (GRCm39) |
|
probably benign |
Het |
| Gsap |
A |
G |
5: 21,486,609 (GRCm39) |
|
probably benign |
Het |
| Hdac6 |
A |
C |
X: 7,809,878 (GRCm39) |
|
probably null |
Het |
| Ivns1abp |
T |
A |
1: 151,227,324 (GRCm39) |
L44Q |
probably damaging |
Het |
| Kcnt1 |
T |
A |
2: 25,790,494 (GRCm39) |
|
probably null |
Het |
| Kdm2b |
A |
G |
5: 123,021,404 (GRCm39) |
I58T |
probably damaging |
Het |
| Mrpl23 |
C |
T |
7: 142,094,319 (GRCm39) |
P76S |
probably benign |
Het |
| Nbea |
A |
G |
3: 55,625,308 (GRCm39) |
I2261T |
possibly damaging |
Het |
| Oasl1 |
G |
A |
5: 115,061,651 (GRCm39) |
V61M |
probably damaging |
Het |
| Pabpc2 |
A |
G |
18: 39,908,046 (GRCm39) |
Q437R |
probably benign |
Het |
| Ppp1r26 |
T |
A |
2: 28,340,639 (GRCm39) |
C90S |
possibly damaging |
Het |
| Ppp3ca |
A |
G |
3: 136,503,624 (GRCm39) |
T66A |
probably benign |
Het |
| Prss55 |
A |
G |
14: 64,313,192 (GRCm39) |
Y231H |
possibly damaging |
Het |
| Psmb10 |
T |
C |
8: 106,664,343 (GRCm39) |
T38A |
probably damaging |
Het |
| Rfx5 |
A |
G |
3: 94,865,792 (GRCm39) |
T364A |
probably benign |
Het |
| Scgb2b26 |
T |
C |
7: 33,642,610 (GRCm39) |
N107S |
probably benign |
Het |
| Seh1l |
A |
G |
18: 67,920,328 (GRCm39) |
|
probably benign |
Het |
| Skic3 |
T |
A |
13: 76,277,660 (GRCm39) |
|
probably null |
Het |
| Sod1 |
T |
A |
16: 90,022,126 (GRCm39) |
H111Q |
probably benign |
Het |
| Thbs2 |
A |
T |
17: 14,900,176 (GRCm39) |
D592E |
probably benign |
Het |
| Tmem67 |
G |
A |
4: 12,053,526 (GRCm39) |
A740V |
probably damaging |
Het |
| Tra2a |
A |
G |
6: 49,226,032 (GRCm39) |
V136A |
possibly damaging |
Het |
| Utp18 |
T |
C |
11: 93,772,967 (GRCm39) |
D158G |
probably benign |
Het |
| Zfp524 |
A |
G |
7: 5,020,871 (GRCm39) |
E133G |
probably damaging |
Het |
|
| Other mutations in Or4g7 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01800:Or4g7
|
APN |
2 |
111,309,209 (GRCm39) |
missense |
probably benign |
|
|
IGL02021:Or4g7
|
APN |
2 |
111,309,825 (GRCm39) |
missense |
probably benign |
0.03 |
|
R2016:Or4g7
|
UTSW |
2 |
111,309,532 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2017:Or4g7
|
UTSW |
2 |
111,309,532 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2848:Or4g7
|
UTSW |
2 |
111,309,699 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2849:Or4g7
|
UTSW |
2 |
111,309,699 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3421:Or4g7
|
UTSW |
2 |
111,309,297 (GRCm39) |
missense |
probably benign |
0.12 |
|
R4223:Or4g7
|
UTSW |
2 |
111,309,489 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4432:Or4g7
|
UTSW |
2 |
111,309,757 (GRCm39) |
nonsense |
probably null |
|
|
R4433:Or4g7
|
UTSW |
2 |
111,309,757 (GRCm39) |
nonsense |
probably null |
|
|
R4476:Or4g7
|
UTSW |
2 |
111,310,009 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R4631:Or4g7
|
UTSW |
2 |
111,309,908 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6029:Or4g7
|
UTSW |
2 |
111,309,310 (GRCm39) |
nonsense |
probably null |
|
|
R6036:Or4g7
|
UTSW |
2 |
111,309,333 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6036:Or4g7
|
UTSW |
2 |
111,309,333 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6084:Or4g7
|
UTSW |
2 |
111,309,734 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6329:Or4g7
|
UTSW |
2 |
111,309,573 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7307:Or4g7
|
UTSW |
2 |
111,309,105 (GRCm39) |
start gained |
probably benign |
|
|
R7516:Or4g7
|
UTSW |
2 |
111,309,282 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7577:Or4g7
|
UTSW |
2 |
111,309,477 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8108:Or4g7
|
UTSW |
2 |
111,309,579 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R8210:Or4g7
|
UTSW |
2 |
111,309,753 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R8465:Or4g7
|
UTSW |
2 |
111,309,425 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8717:Or4g7
|
UTSW |
2 |
111,309,992 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8730:Or4g7
|
UTSW |
2 |
111,309,934 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9360:Or4g7
|
UTSW |
2 |
111,309,684 (GRCm39) |
missense |
probably benign |
0.10 |
|
Z1177:Or4g7
|
UTSW |
2 |
111,309,552 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Or4g7
|
UTSW |
2 |
111,309,159 (GRCm39) |
missense |
probably benign |
0.06 |
|
| Posted On |
2014-05-07 |
Incidental Mutation