Incidental Mutation 'R6504:Or10d3'
| ID |
523624 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or10d3
|
| Ensembl Gene |
ENSMUSG00000050853 |
| Gene Name |
olfactory receptor family 10 subfamily D member 3 |
| Synonyms |
GA_x6K02T2PVTD-33247839-33246901, MOR224-9, Olfr958 |
| MMRRC Submission |
044636-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.153)
|
| Stock # |
R6504 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
9 |
| Chromosomal Location |
39461227-39462165 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 39461574 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Methionine
at position 198
(V198M)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149788
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000062545]
[ENSMUST00000215505]
[ENSMUST00000217227]
|
| AlphaFold |
Q8VEY3 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000062545
AA Change: V198M
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000049930
Gene: ENSMUSG00000050853
AA Change: V198M
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
306 |
1.1e-49 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
36 |
236 |
1.5e-6 |
PFAM |
|
Pfam:7tm_1
|
41 |
288 |
3.4e-21 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000215505
AA Change: V198M
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000217227
AA Change: V198M
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.3%
- 20x: 95.5%
|
| Validation Efficiency |
100% (35/35) |
| 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: 37 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700006A11Rik |
T |
C |
3: 124,213,569 (GRCm39) |
T31A |
probably benign |
Het |
| Adam12 |
A |
T |
7: 133,531,713 (GRCm39) |
H507Q |
probably damaging |
Het |
| Ampd1 |
A |
G |
3: 103,006,911 (GRCm39) |
D712G |
possibly damaging |
Het |
| Ap4m1 |
T |
A |
5: 138,176,358 (GRCm39) |
D351E |
probably benign |
Het |
| Celsr1 |
T |
C |
15: 85,863,121 (GRCm39) |
T1304A |
probably benign |
Het |
| Dhx36 |
G |
T |
3: 62,396,060 (GRCm39) |
A449E |
probably benign |
Het |
| Dmkn |
A |
T |
7: 30,475,854 (GRCm39) |
K2N |
possibly damaging |
Het |
| Dnah10 |
T |
C |
5: 124,839,846 (GRCm39) |
I1217T |
possibly damaging |
Het |
| Dph5 |
A |
G |
3: 115,720,452 (GRCm39) |
|
probably null |
Het |
| Dysf |
T |
C |
6: 83,985,907 (GRCm39) |
V4A |
probably benign |
Het |
| Elavl4 |
A |
T |
4: 110,112,579 (GRCm39) |
|
probably null |
Het |
| Ep400 |
T |
C |
5: 110,856,703 (GRCm39) |
|
probably benign |
Het |
| Fat2 |
A |
G |
11: 55,153,223 (GRCm39) |
I3663T |
probably benign |
Het |
| Gm7233 |
T |
A |
14: 43,037,394 (GRCm39) |
D15E |
probably benign |
Het |
| Grik2 |
A |
G |
10: 49,232,198 (GRCm39) |
V444A |
probably damaging |
Het |
| Hdac4 |
T |
A |
1: 91,896,177 (GRCm39) |
I698F |
possibly damaging |
Het |
| Kank1 |
T |
C |
19: 25,405,518 (GRCm39) |
S1179P |
probably damaging |
Het |
| Kif1b |
T |
C |
4: 149,277,053 (GRCm39) |
M1337V |
probably benign |
Het |
| Med13l |
T |
A |
5: 118,892,386 (GRCm39) |
D1936E |
probably benign |
Het |
| Ofcc1 |
A |
T |
13: 40,250,531 (GRCm39) |
L595Q |
probably damaging |
Het |
| Or5b110-ps1 |
A |
C |
19: 13,259,848 (GRCm39) |
H191Q |
possibly damaging |
Het |
| Orc1 |
A |
G |
4: 108,447,914 (GRCm39) |
I54V |
probably benign |
Het |
| Pom121l2 |
A |
G |
13: 22,167,631 (GRCm39) |
Q634R |
possibly damaging |
Het |
| Prrc2c |
A |
G |
1: 162,525,364 (GRCm39) |
V414A |
unknown |
Het |
| Ranbp3l |
T |
C |
15: 8,997,946 (GRCm39) |
F13L |
probably benign |
Het |
| Scaf11 |
T |
C |
15: 96,317,341 (GRCm39) |
|
probably null |
Het |
| Sh3d19 |
A |
G |
3: 85,992,643 (GRCm39) |
T224A |
probably benign |
Het |
| Shq1 |
T |
A |
6: 100,625,208 (GRCm39) |
Y217F |
probably benign |
Het |
| Slitrk1 |
A |
T |
14: 109,149,129 (GRCm39) |
H527Q |
probably benign |
Het |
| Smap2 |
GACTCTAC |
GAC |
4: 120,830,282 (GRCm39) |
|
probably benign |
Het |
| Stxbp1 |
T |
C |
2: 32,691,895 (GRCm39) |
I432M |
possibly damaging |
Het |
| Sulf2 |
A |
G |
2: 165,925,841 (GRCm39) |
Y439H |
probably benign |
Het |
| Thoc5 |
T |
A |
11: 4,874,815 (GRCm39) |
C535* |
probably null |
Het |
| Tlr3 |
T |
C |
8: 45,850,486 (GRCm39) |
I280V |
possibly damaging |
Het |
| Ush2a |
A |
G |
1: 188,643,444 (GRCm39) |
S4269G |
probably benign |
Het |
| Vmn1r214 |
A |
T |
13: 23,219,610 (GRCm39) |
*368L |
probably null |
Het |
| Wif1 |
C |
G |
10: 120,870,996 (GRCm39) |
Q92E |
probably damaging |
Het |
|
| Other mutations in Or10d3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
R0446:Or10d3
|
UTSW |
9 |
39,461,747 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0539:Or10d3
|
UTSW |
9 |
39,461,593 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1512:Or10d3
|
UTSW |
9 |
39,461,390 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1521:Or10d3
|
UTSW |
9 |
39,462,080 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R1652:Or10d3
|
UTSW |
9 |
39,461,591 (GRCm39) |
missense |
probably benign |
0.03 |
|
R2099:Or10d3
|
UTSW |
9 |
39,461,963 (GRCm39) |
missense |
probably benign |
0.17 |
|
R2252:Or10d3
|
UTSW |
9 |
39,461,273 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2911:Or10d3
|
UTSW |
9 |
39,462,117 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R3722:Or10d3
|
UTSW |
9 |
39,461,418 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5745:Or10d3
|
UTSW |
9 |
39,461,987 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6460:Or10d3
|
UTSW |
9 |
39,462,088 (GRCm39) |
frame shift |
probably null |
|
|
R7063:Or10d3
|
UTSW |
9 |
39,461,411 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R7162:Or10d3
|
UTSW |
9 |
39,461,525 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8674:Or10d3
|
UTSW |
9 |
39,461,675 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8748:Or10d3
|
UTSW |
9 |
39,461,712 (GRCm39) |
nonsense |
probably null |
|
|
R8748:Or10d3
|
UTSW |
9 |
39,461,711 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8822:Or10d3
|
UTSW |
9 |
39,461,812 (GRCm39) |
missense |
probably benign |
0.11 |
|
R9529:Or10d3
|
UTSW |
9 |
39,461,723 (GRCm39) |
missense |
probably benign |
0.28 |
|
R9631:Or10d3
|
UTSW |
9 |
39,461,508 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TATAGGTCCATAGGCACAGAGG -3'
(R):5'- GACCGCTTTGCTGCCATTTG -3'
Sequencing Primer
(F):5'- TCCATAGGCACAGAGGATAGC -3'
(R):5'- CGGTACTCGGTCATCATGAAC -3'
|
| Posted On |
2018-06-22 |
Incidental Mutation