Incidental Mutation 'IGL02155:Or5m11'
| ID |
282188 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or5m11
|
| Ensembl Gene |
ENSMUSG00000057207 |
| Gene Name |
olfactory receptor family 5 subfamily M member 11 |
| Synonyms |
Olfr1028, GA_x6K02T2Q125-47430129-47431103, MOR198-3P, MOR198-4, MOR198-3P, MOR198-6_p, Olfr1534-ps1 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.062)
|
| Stock # |
IGL02155
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
85781409-85782383 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 85782352 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Lysine
at position 315
(M315K)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000079522
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000080698]
|
| AlphaFold |
Q7TR89 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000080698
AA Change: M315K
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000079522
Gene: ENSMUSG00000057207
AA Change: M315K
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
3.1e-55 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
1.5e-24 |
PFAM |
|
| 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: 30 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aacs |
A |
G |
5: 125,583,350 (GRCm39) |
H302R |
probably null |
Het |
| Abi3bp |
A |
T |
16: 56,408,327 (GRCm39) |
H254L |
probably damaging |
Het |
| Adcy3 |
G |
A |
12: 4,262,142 (GRCm39) |
W1064* |
probably null |
Het |
| Arvcf |
C |
T |
16: 18,222,650 (GRCm39) |
P70S |
probably damaging |
Het |
| Ceacam3 |
A |
G |
7: 16,896,906 (GRCm39) |
D624G |
possibly damaging |
Het |
| Cntrl |
T |
A |
2: 35,050,250 (GRCm39) |
|
probably benign |
Het |
| Cyp2a5 |
T |
A |
7: 26,542,471 (GRCm39) |
F491Y |
probably benign |
Het |
| Disp2 |
C |
T |
2: 118,622,285 (GRCm39) |
R1006C |
probably damaging |
Het |
| Dnajc22 |
T |
C |
15: 98,998,886 (GRCm39) |
Y24H |
probably damaging |
Het |
| Fat2 |
A |
G |
11: 55,153,245 (GRCm39) |
F3656L |
probably benign |
Het |
| Fbxo31 |
A |
G |
8: 122,285,814 (GRCm39) |
F212S |
probably damaging |
Het |
| Fsip2 |
T |
C |
2: 82,828,696 (GRCm39) |
M6831T |
probably benign |
Het |
| Gpi1 |
G |
T |
7: 33,929,614 (GRCm39) |
Q9K |
possibly damaging |
Het |
| Hmcn1 |
T |
A |
1: 150,439,349 (GRCm39) |
S5495C |
probably damaging |
Het |
| Ift74 |
A |
G |
4: 94,567,488 (GRCm39) |
I394V |
probably benign |
Het |
| Kcnh5 |
G |
A |
12: 75,223,312 (GRCm39) |
|
probably benign |
Het |
| Lars2 |
A |
G |
9: 123,284,047 (GRCm39) |
D745G |
probably damaging |
Het |
| Mitd1 |
T |
A |
1: 37,924,356 (GRCm39) |
I65F |
probably benign |
Het |
| Mlxip |
T |
C |
5: 123,591,455 (GRCm39) |
M878T |
probably benign |
Het |
| Mrgpra4 |
T |
C |
7: 47,631,292 (GRCm39) |
Y103C |
probably damaging |
Het |
| Notch2 |
T |
C |
3: 98,045,806 (GRCm39) |
I1657T |
probably damaging |
Het |
| Orc1 |
T |
A |
4: 108,447,874 (GRCm39) |
D40E |
probably benign |
Het |
| Rnf40 |
T |
C |
7: 127,189,888 (GRCm39) |
|
probably benign |
Het |
| Ro60 |
C |
T |
1: 143,637,007 (GRCm39) |
|
probably null |
Het |
| Sema4d |
A |
G |
13: 51,857,303 (GRCm39) |
V643A |
probably benign |
Het |
| Taf7 |
A |
T |
18: 37,776,564 (GRCm39) |
M1K |
probably null |
Het |
| Tnfsf10 |
A |
T |
3: 27,389,380 (GRCm39) |
D147V |
possibly damaging |
Het |
| Usp45 |
T |
A |
4: 21,798,743 (GRCm39) |
|
probably null |
Het |
| Wdr62 |
T |
C |
7: 29,962,068 (GRCm39) |
D2G |
probably damaging |
Het |
| Zp2 |
T |
A |
7: 119,743,340 (GRCm39) |
I50F |
probably benign |
Het |
|
| Other mutations in Or5m11 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
R0386:Or5m11
|
UTSW |
2 |
85,782,217 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0483:Or5m11
|
UTSW |
2 |
85,781,587 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0539:Or5m11
|
UTSW |
2 |
85,782,353 (GRCm39) |
missense |
probably benign |
|
|
R5701:Or5m11
|
UTSW |
2 |
85,782,168 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R6459:Or5m11
|
UTSW |
2 |
85,781,862 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7124:Or5m11
|
UTSW |
2 |
85,781,817 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R7631:Or5m11
|
UTSW |
2 |
85,782,218 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7943:Or5m11
|
UTSW |
2 |
85,782,342 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8025:Or5m11
|
UTSW |
2 |
85,781,856 (GRCm39) |
missense |
probably benign |
|
|
R9221:Or5m11
|
UTSW |
2 |
85,782,185 (GRCm39) |
nonsense |
probably null |
|
|
R9312:Or5m11
|
UTSW |
2 |
85,781,509 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
Z1177:Or5m11
|
UTSW |
2 |
85,781,826 (GRCm39) |
missense |
not run |
|
|
| Posted On |
2015-04-16 |
Incidental Mutation