Incidental Mutation 'IGL01549:Or13n4'
| ID |
90554 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or13n4
|
| Ensembl Gene |
ENSMUSG00000056863 |
| Gene Name |
olfactory receptor family 13 subfamily N member 4 |
| Synonyms |
GA_x6K02T2PBJ9-9202245-9201289, MOR260-4, Olfr702 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.055)
|
| Stock # |
IGL01549
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
106422696-106425950 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 106423236 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Valine
at position 166
(I166V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151862
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000075414]
[ENSMUST00000080899]
[ENSMUST00000166880]
[ENSMUST00000208864]
[ENSMUST00000208895]
[ENSMUST00000217739]
[ENSMUST00000219803]
|
| AlphaFold |
Q920Z2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000075414
|
| SMART Domains |
Protein: ENSMUSP00000074868
Gene: ENSMUSG00000036744
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
2.9e-46 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
2.3e-24 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000080899
AA Change: I166V
PolyPhen 2
Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)
|
| SMART Domains |
Protein: ENSMUSP00000079704
Gene: ENSMUSG00000056863
AA Change: I166V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
307 |
2.7e-53 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
300 |
2.9e-8 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
1.5e-26 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000166880
|
| SMART Domains |
Protein: ENSMUSP00000130958
Gene: ENSMUSG00000036744
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_1
|
41 |
290 |
5.8e-31 |
PFAM |
|
Pfam:7tm_4
|
139 |
283 |
1.8e-44 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000208864
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000208895
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000217739
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000219803
AA Change: I166V
PolyPhen 2
Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)
|
| 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: 27 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930503L19Rik |
C |
T |
18: 70,601,106 (GRCm39) |
V259I |
possibly damaging |
Het |
| Abhd4 |
C |
T |
14: 54,504,589 (GRCm39) |
T273I |
probably damaging |
Het |
| Adamtsl3 |
T |
C |
7: 82,261,656 (GRCm39) |
S1691P |
probably damaging |
Het |
| Anapc1 |
A |
G |
2: 128,495,090 (GRCm39) |
S901P |
probably benign |
Het |
| Ank3 |
C |
T |
10: 69,768,250 (GRCm39) |
S56F |
probably damaging |
Het |
| Ccdc74a |
A |
G |
16: 17,468,406 (GRCm39) |
S343G |
probably benign |
Het |
| Clec7a |
A |
T |
6: 129,449,640 (GRCm39) |
Y3* |
probably null |
Het |
| Il6 |
A |
G |
5: 30,224,469 (GRCm39) |
T170A |
probably benign |
Het |
| Itgax |
C |
A |
7: 127,730,378 (GRCm39) |
|
probably null |
Het |
| Lrrc17 |
A |
T |
5: 21,775,288 (GRCm39) |
R283S |
probably benign |
Het |
| Muc1 |
C |
T |
3: 89,139,117 (GRCm39) |
P533S |
probably damaging |
Het |
| Or10j5 |
T |
C |
1: 172,784,541 (GRCm39) |
Y60H |
probably damaging |
Het |
| Or4c121 |
C |
T |
2: 89,024,133 (GRCm39) |
V82I |
probably benign |
Het |
| Or4d10c |
T |
A |
19: 12,065,329 (GRCm39) |
I276F |
probably benign |
Het |
| Or8k37 |
A |
C |
2: 86,469,705 (GRCm39) |
S116A |
probably benign |
Het |
| Or8k37 |
T |
C |
2: 86,469,876 (GRCm39) |
M59V |
possibly damaging |
Het |
| Pcnt |
A |
C |
10: 76,203,320 (GRCm39) |
|
probably null |
Het |
| Pde4b |
A |
T |
4: 102,462,265 (GRCm39) |
D647V |
probably damaging |
Het |
| Phldb2 |
T |
C |
16: 45,594,681 (GRCm39) |
M875V |
probably benign |
Het |
| Prkar2b |
T |
C |
12: 32,111,071 (GRCm39) |
E4G |
possibly damaging |
Het |
| Rab2a |
C |
A |
4: 8,582,393 (GRCm39) |
S125Y |
probably benign |
Het |
| Samm50 |
A |
G |
15: 84,086,982 (GRCm39) |
I264V |
probably benign |
Het |
| Sgsh |
C |
T |
11: 119,241,755 (GRCm39) |
A90T |
probably damaging |
Het |
| Tap2 |
A |
G |
17: 34,433,303 (GRCm39) |
T489A |
probably benign |
Het |
| Wdr38 |
T |
G |
2: 38,890,730 (GRCm39) |
S201R |
probably damaging |
Het |
| Zfhx4 |
A |
G |
3: 5,464,522 (GRCm39) |
D1560G |
probably damaging |
Het |
| Zfp462 |
A |
G |
4: 55,013,181 (GRCm39) |
T568A |
probably damaging |
Het |
|
| Other mutations in Or13n4 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02120:Or13n4
|
APN |
7 |
106,422,905 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0025:Or13n4
|
UTSW |
7 |
106,422,963 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R1213:Or13n4
|
UTSW |
7 |
106,423,404 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R1830:Or13n4
|
UTSW |
7 |
106,423,317 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2216:Or13n4
|
UTSW |
7 |
106,423,205 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2571:Or13n4
|
UTSW |
7 |
106,422,933 (GRCm39) |
missense |
probably benign |
0.09 |
|
R2876:Or13n4
|
UTSW |
7 |
106,423,664 (GRCm39) |
missense |
probably benign |
0.07 |
|
R2920:Or13n4
|
UTSW |
7 |
106,423,571 (GRCm39) |
missense |
probably benign |
0.11 |
|
R4082:Or13n4
|
UTSW |
7 |
106,423,245 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R4130:Or13n4
|
UTSW |
7 |
106,422,792 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4750:Or13n4
|
UTSW |
7 |
106,423,514 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5007:Or13n4
|
UTSW |
7 |
106,423,364 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5117:Or13n4
|
UTSW |
7 |
106,422,869 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5908:Or13n4
|
UTSW |
7 |
106,423,404 (GRCm39) |
missense |
probably benign |
0.09 |
|
R6824:Or13n4
|
UTSW |
7 |
106,423,664 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7193:Or13n4
|
UTSW |
7 |
106,423,798 (GRCm39) |
start gained |
probably benign |
|
|
R7254:Or13n4
|
UTSW |
7 |
106,422,777 (GRCm39) |
makesense |
probably null |
|
|
R7827:Or13n4
|
UTSW |
7 |
106,422,932 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8309:Or13n4
|
UTSW |
7 |
106,423,620 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8410:Or13n4
|
UTSW |
7 |
106,423,745 (GRCm39) |
start gained |
probably benign |
|
|
R9353:Or13n4
|
UTSW |
7 |
106,423,062 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9386:Or13n4
|
UTSW |
7 |
106,423,707 (GRCm39) |
missense |
probably benign |
|
|
R9562:Or13n4
|
UTSW |
7 |
106,423,020 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-12-09 |
Incidental Mutation