Incidental Mutation 'R5824:Or2r3'
| ID |
450064 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or2r3
|
| Ensembl Gene |
ENSMUSG00000091983 |
| Gene Name |
olfactory receptor family 2 subfamily R member 3 |
| Synonyms |
GA_x6K02T2P3E9-5088893-5089834, Olfr457, MOR257-1 |
| MMRRC Submission |
043216-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.149)
|
| Stock # |
R5824 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
6 |
| Chromosomal Location |
42448169-42449110 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 42448906 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Leucine
at position 69
(V69L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000144914
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000170504]
[ENSMUST00000203396]
[ENSMUST00000204324]
|
| AlphaFold |
Q8VGP5 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000170504
AA Change: V69L
PolyPhen 2
Score 0.183 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000127348
Gene: ENSMUSG00000091983
AA Change: V69L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
6.4e-53 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
2e-24 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000203396
AA Change: V69L
PolyPhen 2
Score 0.183 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000145162
Gene: ENSMUSG00000091983
AA Change: V69L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
6.4e-53 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
2e-24 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000204324
AA Change: V69L
PolyPhen 2
Score 0.183 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000144914
Gene: ENSMUSG00000091983
AA Change: V69L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
125 |
2.4e-19 |
PFAM |
|
Pfam:7tm_1
|
41 |
125 |
3.1e-14 |
PFAM |
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.3%
- 20x: 95.2%
|
| 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: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Agtpbp1 |
A |
T |
13: 59,613,913 (GRCm39) |
H66Q |
probably damaging |
Het |
| Ap1g1 |
T |
A |
8: 110,565,544 (GRCm39) |
|
probably null |
Het |
| Ap4b1 |
A |
T |
3: 103,720,701 (GRCm39) |
I124F |
probably benign |
Het |
| Arhgap10 |
A |
T |
8: 78,085,181 (GRCm39) |
Y462* |
probably null |
Het |
| Btnl10 |
G |
T |
11: 58,814,266 (GRCm39) |
M315I |
probably benign |
Het |
| Cep295 |
A |
G |
9: 15,236,952 (GRCm39) |
V1994A |
possibly damaging |
Het |
| Cherp |
G |
A |
8: 73,216,102 (GRCm39) |
|
probably benign |
Het |
| Ckap5 |
G |
A |
2: 91,389,481 (GRCm39) |
A318T |
probably benign |
Het |
| Cma1 |
T |
C |
14: 56,179,182 (GRCm39) |
K238E |
possibly damaging |
Het |
| Cspg4b |
T |
A |
13: 113,505,154 (GRCm39) |
H2094Q |
probably damaging |
Het |
| Ctif |
T |
C |
18: 75,743,749 (GRCm39) |
D141G |
possibly damaging |
Het |
| Ctnna1 |
T |
C |
18: 35,312,939 (GRCm39) |
S264P |
probably benign |
Het |
| Dnah12 |
G |
T |
14: 26,492,475 (GRCm39) |
|
probably null |
Het |
| Dnah5 |
A |
G |
15: 28,313,967 (GRCm39) |
T1928A |
probably benign |
Het |
| Etfdh |
G |
A |
3: 79,517,252 (GRCm39) |
P379L |
probably damaging |
Het |
| Gfra3 |
T |
C |
18: 34,844,264 (GRCm39) |
N92S |
probably damaging |
Het |
| Gpr161 |
C |
A |
1: 165,138,560 (GRCm39) |
T382K |
possibly damaging |
Het |
| Gspt2 |
T |
C |
X: 93,680,071 (GRCm39) |
V70A |
possibly damaging |
Het |
| Hmcn1 |
A |
G |
1: 150,868,774 (GRCm39) |
V10A |
probably benign |
Het |
| Iqgap2 |
C |
T |
13: 95,811,880 (GRCm39) |
R707H |
probably damaging |
Het |
| Kpna1 |
A |
G |
16: 35,840,575 (GRCm39) |
D205G |
possibly damaging |
Het |
| Man2a2 |
T |
G |
7: 80,002,780 (GRCm39) |
D1067A |
probably benign |
Het |
| Map3k4 |
G |
A |
17: 12,448,526 (GRCm39) |
H1551Y |
probably damaging |
Het |
| Moxd1 |
A |
T |
10: 24,162,995 (GRCm39) |
I486F |
probably damaging |
Het |
| Notch3 |
G |
T |
17: 32,372,835 (GRCm39) |
R579S |
possibly damaging |
Het |
| Or6c65 |
T |
C |
10: 129,604,250 (GRCm39) |
V295A |
probably damaging |
Het |
| Or8b4 |
A |
G |
9: 37,830,861 (GRCm39) |
T308A |
probably benign |
Het |
| Pira13 |
T |
C |
7: 3,827,753 (GRCm39) |
T135A |
probably damaging |
Het |
| Recql4 |
C |
T |
15: 76,592,785 (GRCm39) |
C302Y |
probably damaging |
Het |
| Reg3b |
G |
A |
6: 78,349,104 (GRCm39) |
V77I |
possibly damaging |
Het |
| Terb1 |
T |
C |
8: 105,212,079 (GRCm39) |
T301A |
probably benign |
Het |
| Tmem260 |
G |
A |
14: 48,742,785 (GRCm39) |
C540Y |
probably damaging |
Het |
| Tmprss15 |
A |
T |
16: 78,831,201 (GRCm39) |
F385I |
probably damaging |
Het |
| Trbv12-2 |
G |
A |
6: 41,095,774 (GRCm39) |
|
probably benign |
Het |
| Upk3bl |
T |
A |
5: 136,089,133 (GRCm39) |
Y196* |
probably null |
Het |
| Vmn1r199 |
A |
T |
13: 22,567,748 (GRCm39) |
K304N |
probably benign |
Het |
|
| Other mutations in Or2r3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01417:Or2r3
|
APN |
6 |
42,449,046 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01915:Or2r3
|
APN |
6 |
42,448,223 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02006:Or2r3
|
APN |
6 |
42,449,025 (GRCm39) |
missense |
probably benign |
0.37 |
|
IGL02440:Or2r3
|
APN |
6 |
42,449,100 (GRCm39) |
missense |
probably benign |
|
|
R0024:Or2r3
|
UTSW |
6 |
42,448,194 (GRCm39) |
missense |
probably benign |
|
|
R0662:Or2r3
|
UTSW |
6 |
42,448,708 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R1599:Or2r3
|
UTSW |
6 |
42,448,176 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2087:Or2r3
|
UTSW |
6 |
42,448,985 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5002:Or2r3
|
UTSW |
6 |
42,448,906 (GRCm39) |
missense |
probably benign |
0.18 |
|
R5022:Or2r3
|
UTSW |
6 |
42,448,221 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R5288:Or2r3
|
UTSW |
6 |
42,448,186 (GRCm39) |
missense |
probably benign |
|
|
R5342:Or2r3
|
UTSW |
6 |
42,448,836 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5823:Or2r3
|
UTSW |
6 |
42,448,906 (GRCm39) |
missense |
probably benign |
0.18 |
|
R6378:Or2r3
|
UTSW |
6 |
42,448,687 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7384:Or2r3
|
UTSW |
6 |
42,448,257 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R7442:Or2r3
|
UTSW |
6 |
42,448,434 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7631:Or2r3
|
UTSW |
6 |
42,448,870 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7811:Or2r3
|
UTSW |
6 |
42,448,635 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7896:Or2r3
|
UTSW |
6 |
42,449,100 (GRCm39) |
missense |
probably benign |
0.22 |
|
R9244:Or2r3
|
UTSW |
6 |
42,448,537 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R9579:Or2r3
|
UTSW |
6 |
42,448,574 (GRCm39) |
nonsense |
probably null |
|
|
X0017:Or2r3
|
UTSW |
6 |
42,448,752 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GGATTACAGACAGCCACATAGC -3'
(R):5'- GTCCCAACTGCTCCATGAAG -3'
Sequencing Primer
(F):5'- CACATAGCGGTCATAGGCCATG -3'
(R):5'- CAACCTGGGTAAGTGAGTTTATCCTC -3'
|
| Posted On |
2016-12-20 |
Incidental Mutation