Incidental Mutation 'IGL01955:Or5g23'
| ID |
181406 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or5g23
|
| Ensembl Gene |
ENSMUSG00000075215 |
| Gene Name |
olfactory receptor family 5 subfamily G member 23 |
| Synonyms |
MOR175-9, Olfr1000, GA_x6K02T2Q125-47087719-47086775 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.056)
|
| Stock # |
IGL01955
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
85438308-85439252 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 85439051 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Phenylalanine to Leucine
at position 68
(F68L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150731
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099921]
[ENSMUST00000213837]
[ENSMUST00000216571]
|
| AlphaFold |
Q7TR99 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099921
AA Change: F68L
PolyPhen 2
Score 0.122 (Sensitivity: 0.93; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000097505
Gene: ENSMUSG00000075215
AA Change: F68L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
1.1e-49 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
2.9e-17 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213837
AA Change: F68L
PolyPhen 2
Score 0.122 (Sensitivity: 0.93; Specificity: 0.86)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000216571
AA Change: F68L
PolyPhen 2
Score 0.122 (Sensitivity: 0.93; Specificity: 0.86)
|
| 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: 39 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930432E11Rik |
G |
T |
7: 29,273,420 (GRCm39) |
|
noncoding transcript |
Het |
| Abcc1 |
T |
A |
16: 14,228,659 (GRCm39) |
I302N |
probably damaging |
Het |
| Abhd16a |
A |
G |
17: 35,320,316 (GRCm39) |
S394G |
probably damaging |
Het |
| Adgrv1 |
T |
C |
13: 81,330,902 (GRCm39) |
Y71C |
probably damaging |
Het |
| Apol8 |
A |
G |
15: 77,633,899 (GRCm39) |
C226R |
probably benign |
Het |
| Bbs7 |
A |
G |
3: 36,664,471 (GRCm39) |
S45P |
probably benign |
Het |
| Cacna1b |
T |
C |
2: 24,529,149 (GRCm39) |
Y1575C |
probably damaging |
Het |
| Cckbr |
T |
A |
7: 105,084,169 (GRCm39) |
V301E |
probably damaging |
Het |
| Cwc27 |
A |
G |
13: 104,944,245 (GRCm39) |
Y79H |
probably damaging |
Het |
| Dchs1 |
T |
C |
7: 105,406,798 (GRCm39) |
T2236A |
probably benign |
Het |
| Ddx50 |
T |
C |
10: 62,482,962 (GRCm39) |
R36G |
probably benign |
Het |
| Extl3 |
T |
A |
14: 65,313,415 (GRCm39) |
Y589F |
probably benign |
Het |
| Gab2 |
T |
C |
7: 96,953,430 (GRCm39) |
V601A |
probably damaging |
Het |
| Hsd3b1 |
T |
A |
3: 98,760,463 (GRCm39) |
N176I |
probably benign |
Het |
| L3mbtl3 |
A |
T |
10: 26,194,336 (GRCm39) |
S420R |
unknown |
Het |
| Odad2 |
C |
T |
18: 7,127,291 (GRCm39) |
R974Q |
possibly damaging |
Het |
| Or2ak6 |
T |
C |
11: 58,592,955 (GRCm39) |
S143P |
probably damaging |
Het |
| Or52e2 |
T |
A |
7: 102,804,061 (GRCm39) |
K298* |
probably null |
Het |
| Polr2a |
T |
C |
11: 69,632,674 (GRCm39) |
D974G |
probably damaging |
Het |
| Ptges3l |
T |
C |
11: 101,314,644 (GRCm39) |
K13E |
possibly damaging |
Het |
| Ptprk |
A |
G |
10: 28,471,861 (GRCm39) |
|
probably benign |
Het |
| Rassf3 |
T |
C |
10: 121,253,027 (GRCm39) |
Y60C |
probably damaging |
Het |
| Rnf157 |
T |
C |
11: 116,250,722 (GRCm39) |
T160A |
probably damaging |
Het |
| Secisbp2l |
A |
G |
2: 125,585,732 (GRCm39) |
|
probably null |
Het |
| Setd2 |
A |
G |
9: 110,378,386 (GRCm39) |
T734A |
probably benign |
Het |
| Skint5 |
A |
G |
4: 113,480,933 (GRCm39) |
|
probably null |
Het |
| Slc38a9 |
A |
G |
13: 112,831,952 (GRCm39) |
|
probably benign |
Het |
| Snx17 |
T |
G |
5: 31,354,426 (GRCm39) |
|
probably benign |
Het |
| Tas2r113 |
A |
T |
6: 132,870,817 (GRCm39) |
M282L |
probably benign |
Het |
| Tbc1d31 |
A |
G |
15: 57,805,766 (GRCm39) |
N404D |
probably benign |
Het |
| Tmem63c |
A |
T |
12: 87,123,982 (GRCm39) |
I487F |
probably benign |
Het |
| Tpm3 |
A |
G |
3: 89,995,742 (GRCm39) |
M164V |
probably benign |
Het |
| Trafd1 |
G |
T |
5: 121,513,217 (GRCm39) |
N340K |
probably benign |
Het |
| Trpv4 |
T |
A |
5: 114,760,743 (GRCm39) |
K863* |
probably null |
Het |
| Ttn |
A |
T |
2: 76,627,696 (GRCm39) |
M13003K |
possibly damaging |
Het |
| Tulp1 |
G |
A |
17: 28,575,398 (GRCm39) |
T103M |
probably damaging |
Het |
| Unc5b |
T |
C |
10: 60,614,034 (GRCm39) |
T272A |
probably benign |
Het |
| Vmn1r82 |
A |
C |
7: 12,039,650 (GRCm39) |
|
probably null |
Het |
| Zc3h7b |
A |
G |
15: 81,676,205 (GRCm39) |
N704D |
probably benign |
Het |
|
| Other mutations in Or5g23 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01548:Or5g23
|
APN |
2 |
85,439,105 (GRCm39) |
missense |
probably benign |
|
|
IGL01872:Or5g23
|
APN |
2 |
85,438,673 (GRCm39) |
missense |
probably benign |
|
|
IGL02132:Or5g23
|
APN |
2 |
85,438,664 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02139:Or5g23
|
APN |
2 |
85,438,574 (GRCm39) |
nonsense |
probably null |
|
|
IGL02717:Or5g23
|
APN |
2 |
85,439,116 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02950:Or5g23
|
APN |
2 |
85,438,501 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1866:Or5g23
|
UTSW |
2 |
85,439,188 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1868:Or5g23
|
UTSW |
2 |
85,438,409 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1869:Or5g23
|
UTSW |
2 |
85,438,844 (GRCm39) |
missense |
probably benign |
0.23 |
|
R2256:Or5g23
|
UTSW |
2 |
85,438,807 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R2919:Or5g23
|
UTSW |
2 |
85,438,754 (GRCm39) |
missense |
probably benign |
0.06 |
|
R4736:Or5g23
|
UTSW |
2 |
85,438,327 (GRCm39) |
missense |
probably benign |
|
|
R5197:Or5g23
|
UTSW |
2 |
85,438,791 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5256:Or5g23
|
UTSW |
2 |
85,438,817 (GRCm39) |
missense |
probably benign |
|
|
R5367:Or5g23
|
UTSW |
2 |
85,438,718 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5389:Or5g23
|
UTSW |
2 |
85,438,627 (GRCm39) |
missense |
probably benign |
|
|
R6991:Or5g23
|
UTSW |
2 |
85,438,592 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R7017:Or5g23
|
UTSW |
2 |
85,438,673 (GRCm39) |
missense |
probably benign |
|
|
R7020:Or5g23
|
UTSW |
2 |
85,438,976 (GRCm39) |
missense |
probably benign |
0.11 |
|
R7352:Or5g23
|
UTSW |
2 |
85,439,128 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7392:Or5g23
|
UTSW |
2 |
85,438,832 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R7586:Or5g23
|
UTSW |
2 |
85,438,528 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7727:Or5g23
|
UTSW |
2 |
85,438,751 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R8053:Or5g23
|
UTSW |
2 |
85,439,234 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8108:Or5g23
|
UTSW |
2 |
85,439,093 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R9332:Or5g23
|
UTSW |
2 |
85,438,331 (GRCm39) |
nonsense |
probably null |
|
|
| Posted On |
2014-05-07 |
Incidental Mutation