Incidental Mutation 'IGL03185:Or7g21'
| ID |
412418 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or7g21
|
| Ensembl Gene |
ENSMUSG00000059303 |
| Gene Name |
olfactory receptor family 7 subfamily G member 21 |
| Synonyms |
GA_x6K02T2PVTD-12857805-12858749, MOR152-3, Olfr836 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.150)
|
| Stock # |
IGL03185
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
19032253-19033207 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 19033034 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Glutamic Acid
at position 258
(V258E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150026
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000074986]
[ENSMUST00000212730]
[ENSMUST00000215981]
|
| AlphaFold |
Q8VFJ3 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000074986
AA Change: V261E
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000074514
Gene: ENSMUSG00000059303
AA Change: V261E
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
34 |
311 |
1.2e-50 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
38 |
210 |
9.6e-6 |
PFAM |
|
Pfam:7tm_1
|
44 |
293 |
2.4e-20 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000212730
AA Change: V258E
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000215981
AA Change: V258E
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| 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: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam15 |
T |
C |
3: 89,255,212 (GRCm39) |
D77G |
probably benign |
Het |
| Ank2 |
C |
A |
3: 126,749,519 (GRCm39) |
E503D |
probably damaging |
Het |
| Babam2 |
T |
C |
5: 31,859,376 (GRCm39) |
I27T |
possibly damaging |
Het |
| Ccdc150 |
A |
G |
1: 54,339,482 (GRCm39) |
E442G |
probably damaging |
Het |
| Ccdc92 |
A |
G |
5: 124,913,014 (GRCm39) |
Y172H |
probably damaging |
Het |
| Chl1 |
T |
A |
6: 103,642,824 (GRCm39) |
D187E |
probably damaging |
Het |
| Col6a4 |
A |
T |
9: 105,896,653 (GRCm39) |
F1721I |
probably damaging |
Het |
| Corin |
C |
T |
5: 72,490,124 (GRCm39) |
G542D |
probably damaging |
Het |
| Dennd1c |
C |
T |
17: 57,373,803 (GRCm39) |
D587N |
probably benign |
Het |
| Dnah10 |
A |
G |
5: 124,894,707 (GRCm39) |
Y3424C |
probably damaging |
Het |
| Echdc1 |
T |
A |
10: 29,207,836 (GRCm39) |
F127I |
possibly damaging |
Het |
| F13b |
T |
A |
1: 139,444,124 (GRCm39) |
V486E |
probably benign |
Het |
| Fkbp15 |
C |
T |
4: 62,250,423 (GRCm39) |
|
probably null |
Het |
| Glt8d2 |
T |
A |
10: 82,498,110 (GRCm39) |
I100F |
probably damaging |
Het |
| Gmip |
C |
T |
8: 70,262,433 (GRCm39) |
P10L |
probably benign |
Het |
| Grm7 |
T |
C |
6: 110,623,183 (GRCm39) |
S119P |
possibly damaging |
Het |
| Klf4 |
T |
C |
4: 55,530,911 (GRCm39) |
T58A |
possibly damaging |
Het |
| Mink1 |
T |
C |
11: 70,494,686 (GRCm39) |
I289T |
probably damaging |
Het |
| Mptx2 |
A |
T |
1: 173,102,356 (GRCm39) |
V111D |
possibly damaging |
Het |
| Muc5b |
A |
T |
7: 141,416,559 (GRCm39) |
E3168D |
possibly damaging |
Het |
| Mylk3 |
C |
A |
8: 86,053,833 (GRCm39) |
V695F |
probably damaging |
Het |
| Or11j4 |
C |
A |
14: 50,630,855 (GRCm39) |
T214K |
probably damaging |
Het |
| Pcare |
A |
T |
17: 72,056,332 (GRCm39) |
I1115K |
probably damaging |
Het |
| Pira13 |
A |
G |
7: 3,826,229 (GRCm39) |
Y255H |
probably damaging |
Het |
| Poglut2 |
G |
A |
1: 44,156,359 (GRCm39) |
S76L |
probably benign |
Het |
| Pprc1 |
C |
A |
19: 46,058,186 (GRCm39) |
|
probably benign |
Het |
| Prkaa2 |
C |
T |
4: 104,896,918 (GRCm39) |
|
probably null |
Het |
| Prss50 |
A |
G |
9: 110,687,279 (GRCm39) |
Y74C |
probably benign |
Het |
| Rnf145 |
T |
C |
11: 44,422,157 (GRCm39) |
L80P |
probably damaging |
Het |
| Serpinb3b |
T |
C |
1: 107,084,662 (GRCm39) |
I120V |
probably benign |
Het |
| Sgca |
T |
C |
11: 94,861,610 (GRCm39) |
M212V |
probably benign |
Het |
| Slc1a6 |
T |
A |
10: 78,637,741 (GRCm39) |
D422E |
probably damaging |
Het |
| Slc30a9 |
A |
G |
5: 67,490,406 (GRCm39) |
R226G |
probably benign |
Het |
| Slc5a11 |
A |
G |
7: 122,864,412 (GRCm39) |
D336G |
possibly damaging |
Het |
| Slfn8 |
T |
C |
11: 82,908,333 (GRCm39) |
H70R |
probably benign |
Het |
| Stoml2 |
T |
C |
4: 43,029,065 (GRCm39) |
N269S |
probably benign |
Het |
| Synrg |
A |
G |
11: 83,872,305 (GRCm39) |
E142G |
probably damaging |
Het |
| Thbs2 |
G |
A |
17: 14,901,672 (GRCm39) |
Q436* |
probably null |
Het |
| Tyk2 |
T |
C |
9: 21,020,680 (GRCm39) |
N917S |
probably damaging |
Het |
| Zfhx4 |
C |
A |
3: 5,468,974 (GRCm39) |
T3069K |
probably benign |
Het |
| Zfp446 |
G |
T |
7: 12,712,925 (GRCm39) |
V88F |
probably null |
Het |
| Zp3 |
A |
G |
5: 136,011,575 (GRCm39) |
N131S |
possibly damaging |
Het |
|
| Other mutations in Or7g21 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00907:Or7g21
|
APN |
9 |
19,032,528 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
IGL01316:Or7g21
|
APN |
9 |
19,032,718 (GRCm39) |
missense |
probably benign |
0.10 |
|
IGL01412:Or7g21
|
APN |
9 |
19,032,895 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01815:Or7g21
|
APN |
9 |
19,032,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02003:Or7g21
|
APN |
9 |
19,032,361 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL02313:Or7g21
|
APN |
9 |
19,032,671 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03186:Or7g21
|
APN |
9 |
19,033,200 (GRCm39) |
missense |
probably benign |
0.16 |
|
R1337:Or7g21
|
UTSW |
9 |
19,033,099 (GRCm39) |
missense |
probably benign |
|
|
R2267:Or7g21
|
UTSW |
9 |
19,032,737 (GRCm39) |
missense |
probably benign |
0.22 |
|
R3969:Or7g21
|
UTSW |
9 |
19,032,956 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4695:Or7g21
|
UTSW |
9 |
19,032,306 (GRCm39) |
missense |
probably null |
0.04 |
|
R4976:Or7g21
|
UTSW |
9 |
19,032,797 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5176:Or7g21
|
UTSW |
9 |
19,032,656 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5379:Or7g21
|
UTSW |
9 |
19,032,373 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5638:Or7g21
|
UTSW |
9 |
19,032,676 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6084:Or7g21
|
UTSW |
9 |
19,032,623 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6236:Or7g21
|
UTSW |
9 |
19,032,409 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R6329:Or7g21
|
UTSW |
9 |
19,032,253 (GRCm39) |
start codon destroyed |
probably benign |
0.08 |
|
R7151:Or7g21
|
UTSW |
9 |
19,033,037 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R7326:Or7g21
|
UTSW |
9 |
19,032,965 (GRCm39) |
missense |
probably benign |
0.42 |
|
R8460:Or7g21
|
UTSW |
9 |
19,032,988 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8767:Or7g21
|
UTSW |
9 |
19,032,922 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8978:Or7g21
|
UTSW |
9 |
19,032,582 (GRCm39) |
nonsense |
probably null |
|
|
R9099:Or7g21
|
UTSW |
9 |
19,032,890 (GRCm39) |
missense |
probably benign |
0.35 |
|
R9220:Or7g21
|
UTSW |
9 |
19,033,193 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R9236:Or7g21
|
UTSW |
9 |
19,033,206 (GRCm39) |
makesense |
probably null |
|
|
R9265:Or7g21
|
UTSW |
9 |
19,032,984 (GRCm39) |
nonsense |
probably null |
|
|
R9530:Or7g21
|
UTSW |
9 |
19,033,051 (GRCm39) |
missense |
probably benign |
0.24 |
|
R9612:Or7g21
|
UTSW |
9 |
19,032,760 (GRCm39) |
missense |
probably benign |
0.16 |
|
| Posted On |
2016-08-02 |
Incidental Mutation