Incidental Mutation 'R8208:Or5k3'
| ID |
636030 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or5k3
|
| Ensembl Gene |
ENSMUSG00000062608 |
| Gene Name |
olfactory receptor family 5 subfamily K member 3 |
| Synonyms |
MOR184-5, GA_x54KRFPKG5P-55369823-55370749, Olfr195 |
| MMRRC Submission |
067631-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.085)
|
| Stock # |
R8208 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
16 |
| Chromosomal Location |
58969215-58970141 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 58969382 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Histidine to Glutamine
at position 56
(H56Q)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000073737
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000075381]
|
| AlphaFold |
Q8VGQ6 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000075381
AA Change: H56Q
PolyPhen 2
Score 0.411 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000073737
Gene: ENSMUSG00000062608
AA Change: H56Q
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
4.1e-53 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
161 |
2.7e-8 |
PFAM |
|
Pfam:7tm_1
|
41 |
307 |
9.4e-17 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000208239
AA Change: H56Q
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
| Validation Efficiency |
98% (47/48) |
| 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: 46 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcg2 |
G |
A |
6: 58,642,227 (GRCm39) |
V172I |
possibly damaging |
Het |
| Agbl1 |
T |
A |
7: 76,369,916 (GRCm39) |
C924S |
unknown |
Het |
| Arhgap11a |
T |
C |
2: 113,673,284 (GRCm39) |
S100G |
probably benign |
Het |
| Chd9 |
T |
A |
8: 91,763,891 (GRCm39) |
|
probably null |
Het |
| Col1a2 |
T |
A |
6: 4,515,260 (GRCm39) |
|
probably null |
Het |
| Colec10 |
C |
G |
15: 54,325,696 (GRCm39) |
H175Q |
possibly damaging |
Het |
| Cyp46a1 |
A |
T |
12: 108,318,171 (GRCm39) |
|
probably null |
Het |
| Dennd4b |
T |
A |
3: 90,178,278 (GRCm39) |
I501N |
possibly damaging |
Het |
| Dnah2 |
A |
G |
11: 69,411,678 (GRCm39) |
F315L |
probably benign |
Het |
| Emilin1 |
A |
G |
5: 31,074,860 (GRCm39) |
E367G |
probably damaging |
Het |
| Flvcr2 |
GTAGTGTATA |
GTA |
12: 85,849,922 (GRCm39) |
|
probably null |
Het |
| Folh1 |
A |
T |
7: 86,375,125 (GRCm39) |
H620Q |
probably damaging |
Het |
| Galnt10 |
A |
T |
11: 57,536,398 (GRCm39) |
E5V |
possibly damaging |
Het |
| Gmcl1 |
A |
G |
6: 86,698,381 (GRCm39) |
V172A |
probably damaging |
Het |
| Greb1l |
T |
C |
18: 10,510,703 (GRCm39) |
L599P |
probably damaging |
Het |
| Hcn2 |
T |
A |
10: 79,566,778 (GRCm39) |
M485K |
possibly damaging |
Het |
| Hirip3 |
G |
T |
7: 126,463,595 (GRCm39) |
C494F |
probably damaging |
Het |
| Hsfy2 |
A |
G |
1: 56,676,310 (GRCm39) |
F76L |
probably benign |
Het |
| Lamc3 |
A |
G |
2: 31,777,426 (GRCm39) |
H24R |
possibly damaging |
Het |
| Laptm4b |
G |
A |
15: 34,277,591 (GRCm39) |
S174N |
probably damaging |
Het |
| Lgals8 |
A |
G |
13: 12,468,255 (GRCm39) |
Y125H |
probably damaging |
Het |
| Mapk14 |
A |
T |
17: 28,943,807 (GRCm39) |
Y132F |
probably damaging |
Het |
| Mxd4 |
A |
T |
5: 34,335,070 (GRCm39) |
I115N |
probably benign |
Het |
| Ndufaf1 |
T |
C |
2: 119,490,827 (GRCm39) |
T80A |
probably benign |
Het |
| Or10ag53 |
A |
G |
2: 87,083,007 (GRCm39) |
K242R |
probably benign |
Het |
| Or11h6 |
T |
C |
14: 50,880,088 (GRCm39) |
F117L |
probably benign |
Het |
| Or56a5 |
T |
A |
7: 104,792,625 (GRCm39) |
I298F |
probably damaging |
Het |
| Pcf11 |
G |
T |
7: 92,298,731 (GRCm39) |
N1268K |
probably damaging |
Het |
| Plcl2 |
T |
C |
17: 50,915,343 (GRCm39) |
V784A |
probably damaging |
Het |
| Ptp4a2 |
C |
T |
4: 129,736,485 (GRCm39) |
T40I |
probably benign |
Het |
| Rab2b |
C |
T |
14: 52,502,224 (GRCm39) |
A159T |
possibly damaging |
Het |
| Sec61a2 |
G |
T |
2: 5,881,809 (GRCm39) |
T207K |
probably benign |
Het |
| Serpina5 |
A |
G |
12: 104,071,532 (GRCm39) |
I380V |
probably benign |
Het |
| Slc26a2 |
C |
T |
18: 61,331,806 (GRCm39) |
V542M |
probably damaging |
Het |
| Snd1 |
C |
T |
6: 28,526,054 (GRCm39) |
P144L |
possibly damaging |
Het |
| Spop |
C |
T |
11: 95,382,650 (GRCm39) |
R370C |
probably damaging |
Het |
| Sptbn1 |
T |
C |
11: 30,074,972 (GRCm39) |
D1300G |
probably damaging |
Het |
| Sptbn5 |
T |
A |
2: 119,878,326 (GRCm39) |
K891* |
noncoding transcript |
Het |
| Tnrc6b |
G |
A |
15: 80,742,901 (GRCm39) |
E45K |
possibly damaging |
Het |
| Tpst1 |
A |
G |
5: 130,130,751 (GRCm39) |
I74V |
probably benign |
Het |
| Ttn |
T |
C |
2: 76,556,192 (GRCm39) |
H30271R |
probably damaging |
Het |
| Ush2a |
G |
T |
1: 188,606,990 (GRCm39) |
A3962S |
possibly damaging |
Het |
| Vmn1r200 |
G |
A |
13: 22,579,470 (GRCm39) |
R91H |
probably damaging |
Het |
| Vmn2r22 |
T |
A |
6: 123,614,444 (GRCm39) |
N382I |
probably damaging |
Het |
| Vmn2r53 |
A |
G |
7: 12,335,322 (GRCm39) |
S113P |
probably damaging |
Het |
| Zfp335 |
C |
A |
2: 164,735,536 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Or5k3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01937:Or5k3
|
APN |
16 |
58,969,827 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01945:Or5k3
|
APN |
16 |
58,969,827 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0071:Or5k3
|
UTSW |
16 |
58,969,578 (GRCm39) |
missense |
probably benign |
0.23 |
|
R0390:Or5k3
|
UTSW |
16 |
58,969,662 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0601:Or5k3
|
UTSW |
16 |
58,970,117 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1499:Or5k3
|
UTSW |
16 |
58,969,287 (GRCm39) |
missense |
probably benign |
|
|
R1612:Or5k3
|
UTSW |
16 |
58,969,987 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1785:Or5k3
|
UTSW |
16 |
58,969,660 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2082:Or5k3
|
UTSW |
16 |
58,969,248 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3605:Or5k3
|
UTSW |
16 |
58,969,846 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4168:Or5k3
|
UTSW |
16 |
58,969,363 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4839:Or5k3
|
UTSW |
16 |
58,969,393 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4989:Or5k3
|
UTSW |
16 |
58,969,981 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5285:Or5k3
|
UTSW |
16 |
58,969,633 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7107:Or5k3
|
UTSW |
16 |
58,969,279 (GRCm39) |
missense |
probably benign |
0.10 |
|
R7136:Or5k3
|
UTSW |
16 |
58,969,327 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7317:Or5k3
|
UTSW |
16 |
58,969,684 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R7601:Or5k3
|
UTSW |
16 |
58,969,597 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7729:Or5k3
|
UTSW |
16 |
58,969,570 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8004:Or5k3
|
UTSW |
16 |
58,969,351 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8282:Or5k3
|
UTSW |
16 |
58,969,529 (GRCm39) |
nonsense |
probably null |
|
|
R8954:Or5k3
|
UTSW |
16 |
58,969,319 (GRCm39) |
nonsense |
probably null |
|
|
R9137:Or5k3
|
UTSW |
16 |
58,969,635 (GRCm39) |
missense |
probably benign |
0.30 |
|
R9197:Or5k3
|
UTSW |
16 |
58,969,489 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9396:Or5k3
|
UTSW |
16 |
58,969,302 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9547:Or5k3
|
UTSW |
16 |
58,970,107 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
| Predicted Primers |
PCR Primer
(F):5'- CTTTGTGATTCCAGTGGCAAC -3'
(R):5'- TAGCGGTCATAGGCCATTGC -3'
Sequencing Primer
(F):5'- CAACAGAGAAGGTGAGATGGCTG -3'
(R):5'- CATAGGCCATTGCTGCCAGAAG -3'
|
| Posted On |
2020-07-13 |
Incidental Mutation