Incidental Mutation 'IGL01661:Or4c58'
| ID |
103169 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or4c58
|
| Ensembl Gene |
ENSMUSG00000075072 |
| Gene Name |
olfactory receptor family 4 subfamily C member 58 |
| Synonyms |
Olfr48, IC3, GA_x6K02T2Q125-51285881-51284976, MOR232-5 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.068)
|
| Stock # |
IGL01661
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
89674410-89675315 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 89674439 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Leucine
at position 293
(M293L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150505
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099762]
[ENSMUST00000111520]
[ENSMUST00000213833]
[ENSMUST00000214428]
[ENSMUST00000215613]
|
| AlphaFold |
Q8VGN4 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099762
AA Change: M293L
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000097350
Gene: ENSMUSG00000075072
AA Change: M293L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
26 |
299 |
1e-47 |
PFAM |
|
Pfam:7tm_1
|
36 |
282 |
8.5e-16 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000111520
|
| SMART Domains |
Protein: ENSMUSP00000107145
Gene: ENSMUSG00000075073
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
303 |
2.5e-47 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
33 |
300 |
1.1e-5 |
PFAM |
|
Pfam:7tm_1
|
39 |
285 |
1.3e-16 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213833
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214428
AA Change: M293L
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215613
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000216674
|
| 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: 21 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca2 |
T |
C |
2: 25,333,007 (GRCm39) |
F1569L |
probably benign |
Het |
| Acly |
A |
G |
11: 100,405,168 (GRCm39) |
|
probably benign |
Het |
| Adgre5 |
T |
A |
8: 84,454,564 (GRCm39) |
N313I |
probably damaging |
Het |
| Ccdc17 |
A |
G |
4: 116,455,063 (GRCm39) |
H206R |
probably benign |
Het |
| Cenpo |
C |
T |
12: 4,284,023 (GRCm39) |
|
probably null |
Het |
| Galnt5 |
G |
T |
2: 57,889,494 (GRCm39) |
A365S |
probably benign |
Het |
| Josd1 |
G |
A |
15: 79,561,328 (GRCm39) |
P160L |
probably damaging |
Het |
| Lamc1 |
C |
A |
1: 153,097,319 (GRCm39) |
R1575L |
possibly damaging |
Het |
| Mrpl32 |
C |
T |
13: 14,785,178 (GRCm39) |
V153I |
probably benign |
Het |
| Mtor |
A |
G |
4: 148,599,308 (GRCm39) |
K1452R |
possibly damaging |
Het |
| Nob1 |
T |
C |
8: 108,139,814 (GRCm39) |
Y315C |
probably damaging |
Het |
| Or8k28 |
T |
C |
2: 86,285,846 (GRCm39) |
I256M |
possibly damaging |
Het |
| Prex2 |
A |
G |
1: 11,278,838 (GRCm39) |
N1389S |
probably benign |
Het |
| Ptprd |
G |
A |
4: 75,872,320 (GRCm39) |
T1383M |
probably damaging |
Het |
| Ralbp1 |
A |
G |
17: 66,168,384 (GRCm39) |
L307P |
probably damaging |
Het |
| Sema4f |
A |
G |
6: 82,895,036 (GRCm39) |
|
probably benign |
Het |
| Slc2a3 |
A |
G |
6: 122,706,915 (GRCm39) |
V486A |
probably benign |
Het |
| Spock2 |
T |
A |
10: 59,959,692 (GRCm39) |
H140Q |
probably damaging |
Het |
| Tmc4 |
A |
G |
7: 3,669,926 (GRCm39) |
I610T |
probably damaging |
Het |
| Tnc |
T |
C |
4: 63,888,544 (GRCm39) |
|
probably benign |
Het |
| Ttll8 |
T |
C |
15: 88,820,202 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Or4c58 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02184:Or4c58
|
APN |
2 |
89,674,729 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02408:Or4c58
|
APN |
2 |
89,675,315 (GRCm39) |
start codon destroyed |
probably benign |
0.04 |
|
IGL02437:Or4c58
|
APN |
2 |
89,675,128 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02985:Or4c58
|
APN |
2 |
89,674,684 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
IGL03230:Or4c58
|
APN |
2 |
89,674,457 (GRCm39) |
missense |
probably benign |
|
|
IGL03393:Or4c58
|
APN |
2 |
89,674,913 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0482:Or4c58
|
UTSW |
2 |
89,674,513 (GRCm39) |
missense |
probably benign |
0.20 |
|
R0555:Or4c58
|
UTSW |
2 |
89,674,787 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1268:Or4c58
|
UTSW |
2 |
89,674,498 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1617:Or4c58
|
UTSW |
2 |
89,674,598 (GRCm39) |
missense |
probably benign |
0.03 |
|
R3552:Or4c58
|
UTSW |
2 |
89,674,687 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R4172:Or4c58
|
UTSW |
2 |
89,675,122 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4173:Or4c58
|
UTSW |
2 |
89,675,122 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4174:Or4c58
|
UTSW |
2 |
89,675,122 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5540:Or4c58
|
UTSW |
2 |
89,675,011 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5909:Or4c58
|
UTSW |
2 |
89,674,735 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R5941:Or4c58
|
UTSW |
2 |
89,674,859 (GRCm39) |
missense |
probably benign |
0.07 |
|
R7425:Or4c58
|
UTSW |
2 |
89,674,789 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7445:Or4c58
|
UTSW |
2 |
89,674,616 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7660:Or4c58
|
UTSW |
2 |
89,674,787 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7978:Or4c58
|
UTSW |
2 |
89,674,611 (GRCm39) |
nonsense |
probably null |
|
|
R7996:Or4c58
|
UTSW |
2 |
89,674,759 (GRCm39) |
missense |
probably benign |
0.28 |
|
R8026:Or4c58
|
UTSW |
2 |
89,675,273 (GRCm39) |
missense |
probably benign |
0.06 |
|
R9184:Or4c58
|
UTSW |
2 |
89,675,294 (GRCm39) |
missense |
probably benign |
0.06 |
|
R9420:Or4c58
|
UTSW |
2 |
89,674,715 (GRCm39) |
missense |
probably benign |
0.14 |
|
| Posted On |
2014-01-21 |
Incidental Mutation