Incidental Mutation 'R2893:Or51ai2'
| ID |
260670 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or51ai2
|
| Ensembl Gene |
ENSMUSG00000073938 |
| Gene Name |
olfactory receptor family 51 subfamily AI member 2 |
| Synonyms |
GA_x6K02T2PBJ9-6671256-6672209, MOR2-1, Olfr632 |
| MMRRC Submission |
040481-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.055)
|
| Stock # |
R2893 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
7 |
| Chromosomal Location |
103586589-103587542 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 103587389 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Serine
at position 267
(R267S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149598
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000098189]
[ENSMUST00000214711]
|
| AlphaFold |
Q9EPN9 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000098189
AA Change: R267S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000095791
Gene: ENSMUSG00000073938
AA Change: R267S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
35 |
313 |
2.5e-109 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
39 |
232 |
7.5e-11 |
PFAM |
|
Pfam:7tm_1
|
45 |
296 |
1.4e-16 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000211625
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000214509
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000214711
AA Change: R267S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 97.1%
- 20x: 94.4%
|
| 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: 37 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A2ml1 |
C |
T |
6: 128,557,349 (GRCm39) |
A115T |
probably benign |
Het |
| Abl1 |
T |
G |
2: 31,687,624 (GRCm39) |
S521R |
probably benign |
Het |
| Acox3 |
A |
G |
5: 35,757,192 (GRCm39) |
I344V |
probably benign |
Het |
| Ank2 |
T |
C |
3: 127,041,892 (GRCm39) |
|
probably null |
Het |
| Atoh8 |
A |
T |
6: 72,211,856 (GRCm39) |
F98Y |
probably benign |
Het |
| Caskin2 |
C |
T |
11: 115,692,103 (GRCm39) |
G894E |
probably benign |
Het |
| Cdh15 |
G |
A |
8: 123,583,374 (GRCm39) |
R59H |
probably benign |
Het |
| Cdk5rap2 |
T |
C |
4: 70,208,110 (GRCm39) |
K779E |
probably benign |
Het |
| Csmd2 |
T |
A |
4: 128,432,786 (GRCm39) |
|
probably null |
Het |
| Cubn |
T |
C |
2: 13,362,950 (GRCm39) |
D1687G |
possibly damaging |
Het |
| F11 |
A |
G |
8: 45,701,675 (GRCm39) |
S353P |
probably damaging |
Het |
| Faap100 |
T |
C |
11: 120,265,451 (GRCm39) |
D475G |
probably damaging |
Het |
| Fhip2a |
C |
T |
19: 57,372,601 (GRCm39) |
P617L |
probably benign |
Het |
| Gm13090 |
T |
A |
4: 151,175,157 (GRCm39) |
L78* |
probably null |
Het |
| Ikbke |
G |
A |
1: 131,197,961 (GRCm39) |
P382S |
probably damaging |
Het |
| Il4i1 |
A |
G |
7: 44,487,414 (GRCm39) |
I130V |
probably damaging |
Het |
| Islr2 |
A |
T |
9: 58,105,149 (GRCm39) |
S704T |
probably damaging |
Het |
| Itga10 |
A |
G |
3: 96,562,416 (GRCm39) |
N733D |
probably benign |
Het |
| Itih2 |
C |
T |
2: 10,107,008 (GRCm39) |
G662D |
possibly damaging |
Het |
| Kansl1l |
T |
C |
1: 66,840,493 (GRCm39) |
Q269R |
probably damaging |
Het |
| Kcnj3 |
A |
T |
2: 55,337,027 (GRCm39) |
I298F |
probably damaging |
Het |
| Kdr |
A |
G |
5: 76,107,496 (GRCm39) |
F1016L |
probably damaging |
Het |
| Miga2 |
A |
T |
2: 30,268,306 (GRCm39) |
|
probably null |
Het |
| Per2 |
C |
A |
1: 91,373,325 (GRCm39) |
Q154H |
probably damaging |
Het |
| Pik3ap1 |
G |
A |
19: 41,364,500 (GRCm39) |
A73V |
probably benign |
Het |
| Plod3 |
G |
C |
5: 137,017,000 (GRCm39) |
A50P |
probably benign |
Het |
| Psma5-ps |
T |
C |
10: 85,149,848 (GRCm39) |
|
noncoding transcript |
Het |
| Rad18 |
G |
A |
6: 112,652,734 (GRCm39) |
Q288* |
probably null |
Het |
| Rapsn |
A |
T |
2: 90,867,169 (GRCm39) |
D157V |
probably damaging |
Het |
| Slc2a8 |
A |
T |
2: 32,864,966 (GRCm39) |
W394R |
probably damaging |
Het |
| Srcap |
T |
C |
7: 127,138,237 (GRCm39) |
S1136P |
probably damaging |
Het |
| Tenm4 |
T |
A |
7: 96,544,197 (GRCm39) |
V2108D |
probably damaging |
Het |
| Trappc10 |
C |
T |
10: 78,029,235 (GRCm39) |
V1101M |
probably benign |
Het |
| Ttbk2 |
C |
A |
2: 120,576,091 (GRCm39) |
|
probably null |
Het |
| Usp8 |
A |
T |
2: 126,600,075 (GRCm39) |
Q998L |
probably damaging |
Het |
| Vmn2r114 |
ATTT |
ATT |
17: 23,509,906 (GRCm39) |
|
probably null |
Het |
| Vmn2r80 |
T |
C |
10: 78,984,699 (GRCm39) |
F17S |
possibly damaging |
Het |
|
| Other mutations in Or51ai2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01331:Or51ai2
|
APN |
7 |
103,586,782 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
IGL01817:Or51ai2
|
APN |
7 |
103,587,030 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02303:Or51ai2
|
APN |
7 |
103,586,770 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
IGL03392:Or51ai2
|
APN |
7 |
103,587,232 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0092:Or51ai2
|
UTSW |
7 |
103,586,934 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0492:Or51ai2
|
UTSW |
7 |
103,586,971 (GRCm39) |
missense |
probably benign |
0.05 |
|
R0711:Or51ai2
|
UTSW |
7 |
103,587,024 (GRCm39) |
missense |
probably benign |
0.29 |
|
R3911:Or51ai2
|
UTSW |
7 |
103,586,616 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4825:Or51ai2
|
UTSW |
7 |
103,586,710 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6106:Or51ai2
|
UTSW |
7 |
103,587,400 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6254:Or51ai2
|
UTSW |
7 |
103,586,741 (GRCm39) |
missense |
probably benign |
0.07 |
|
R6383:Or51ai2
|
UTSW |
7 |
103,587,030 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6821:Or51ai2
|
UTSW |
7 |
103,586,793 (GRCm39) |
missense |
probably benign |
0.07 |
|
R6890:Or51ai2
|
UTSW |
7 |
103,587,066 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R7646:Or51ai2
|
UTSW |
7 |
103,587,504 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8041:Or51ai2
|
UTSW |
7 |
103,586,788 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8232:Or51ai2
|
UTSW |
7 |
103,586,980 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R8266:Or51ai2
|
UTSW |
7 |
103,586,746 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8326:Or51ai2
|
UTSW |
7 |
103,586,809 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8783:Or51ai2
|
UTSW |
7 |
103,586,751 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
Z1177:Or51ai2
|
UTSW |
7 |
103,586,965 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
| Predicted Primers |
PCR Primer
(F):5'- CCATGGGTTCAGATGTCCTC -3'
(R):5'- CACTTCTCTGCTGAAAGGACTC -3'
Sequencing Primer
(F):5'- ATGGGTTCAGATGTCCTCTTCATC -3'
(R):5'- TCTCTGCTGAAAGGACTCTGAAAAG -3'
|
| Posted On |
2015-01-23 |
Incidental Mutation