Incidental Mutation 'R0782:Or51af1'
| ID |
76685 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or51af1
|
| Ensembl Gene |
ENSMUSG00000046396 |
| Gene Name |
olfactory receptor family 51 subfamily AF member 1 |
| Synonyms |
GA_x6K02T2PBJ9-6207735-6206776, Olfr609, MOR9-1 |
| MMRRC Submission |
038962-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.082)
|
| Stock # |
R0782 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
7 |
| Chromosomal Location |
103141124-103142083 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 103141722 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Leucine
at position 121
(R121L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149804
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055787]
[ENSMUST00000216075]
[ENSMUST00000216360]
|
| AlphaFold |
E9Q4X7 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000055787
AA Change: R121L
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000051749
Gene: ENSMUSG00000046396
AA Change: R121L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
30 |
308 |
1.4e-119 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
34 |
169 |
2.2e-10 |
PFAM |
|
Pfam:7tm_1
|
40 |
291 |
3.6e-22 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000216075
AA Change: R121L
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000216360
AA Change: R121L
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
| Meta Mutation Damage Score |
0.4839 |
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.0%
- 20x: 93.3%
|
| Validation Efficiency |
100% (39/39) |
| 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 |
|---|
| Arhgap23 |
C |
T |
11: 97,391,380 (GRCm39) |
P1299L |
possibly damaging |
Het |
| B3glct |
C |
T |
5: 149,650,275 (GRCm39) |
T126M |
probably damaging |
Het |
| Baz1a |
A |
T |
12: 54,941,273 (GRCm39) |
D1492E |
probably damaging |
Het |
| Cdc14a |
A |
G |
3: 116,115,785 (GRCm39) |
I259T |
probably damaging |
Het |
| Cog7 |
C |
A |
7: 121,543,020 (GRCm39) |
A464S |
possibly damaging |
Het |
| Csf2rb2 |
C |
A |
15: 78,170,951 (GRCm39) |
K368N |
probably damaging |
Het |
| Cspp1 |
T |
A |
1: 10,200,199 (GRCm39) |
|
probably benign |
Het |
| Cyp2c37 |
A |
G |
19: 39,982,269 (GRCm39) |
H90R |
probably benign |
Het |
| Dcst1 |
A |
G |
3: 89,264,807 (GRCm39) |
F314L |
possibly damaging |
Het |
| Dhx36 |
A |
T |
3: 62,414,135 (GRCm39) |
|
probably benign |
Het |
| Efr3b |
G |
A |
12: 4,034,686 (GRCm39) |
|
probably benign |
Het |
| Faap100 |
A |
G |
11: 120,267,530 (GRCm39) |
|
probably null |
Het |
| Hmcn1 |
A |
G |
1: 150,629,416 (GRCm39) |
I947T |
possibly damaging |
Het |
| Ilkap |
C |
T |
1: 91,306,272 (GRCm39) |
R103H |
probably damaging |
Het |
| Impa1 |
A |
T |
3: 10,387,956 (GRCm39) |
|
probably benign |
Het |
| Kbtbd8 |
C |
T |
6: 95,099,213 (GRCm39) |
R164C |
probably damaging |
Het |
| Lactb2 |
T |
G |
1: 13,717,675 (GRCm39) |
N116T |
probably benign |
Het |
| Myh8 |
T |
A |
11: 67,180,580 (GRCm39) |
N605K |
probably benign |
Het |
| Mylk |
G |
C |
16: 34,699,845 (GRCm39) |
E403Q |
possibly damaging |
Het |
| Napa |
T |
C |
7: 15,849,192 (GRCm39) |
M244T |
probably benign |
Het |
| Nckap5 |
G |
A |
1: 125,909,278 (GRCm39) |
S1719F |
probably damaging |
Het |
| Nfe2l2 |
T |
C |
2: 75,507,177 (GRCm39) |
I308V |
probably benign |
Het |
| Ppfia2 |
C |
T |
10: 106,763,592 (GRCm39) |
S1195L |
probably benign |
Het |
| Rasa4 |
A |
G |
5: 136,133,386 (GRCm39) |
K615R |
possibly damaging |
Het |
| Rnf216 |
T |
C |
5: 143,054,647 (GRCm39) |
K634E |
possibly damaging |
Het |
| Samd3 |
A |
G |
10: 26,146,138 (GRCm39) |
T388A |
probably damaging |
Het |
| Serping1 |
G |
A |
2: 84,597,790 (GRCm39) |
P364S |
probably damaging |
Het |
| Slc39a10 |
T |
C |
1: 46,875,156 (GRCm39) |
S49G |
probably damaging |
Het |
| Smc2 |
C |
A |
4: 52,469,799 (GRCm39) |
T762K |
probably benign |
Het |
| Smpd1 |
T |
A |
7: 105,204,550 (GRCm39) |
V143E |
possibly damaging |
Het |
| Synj2bp |
A |
T |
12: 81,579,507 (GRCm39) |
L16Q |
probably damaging |
Het |
| Tcof1 |
G |
A |
18: 60,949,352 (GRCm39) |
R1188W |
probably damaging |
Het |
| Unc80 |
A |
G |
1: 66,661,740 (GRCm39) |
R1722G |
possibly damaging |
Het |
| Vamp5 |
T |
C |
6: 72,346,453 (GRCm39) |
S48G |
probably damaging |
Het |
| Vps13d |
G |
A |
4: 144,853,195 (GRCm39) |
|
probably benign |
Het |
| Zfp292 |
T |
C |
4: 34,839,382 (GRCm39) |
N161S |
possibly damaging |
Het |
| Zfp831 |
A |
G |
2: 174,488,423 (GRCm39) |
T1033A |
probably benign |
Het |
|
| Other mutations in Or51af1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02213:Or51af1
|
APN |
7 |
103,141,695 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL02309:Or51af1
|
APN |
7 |
103,141,206 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0988:Or51af1
|
UTSW |
7 |
103,141,954 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4013:Or51af1
|
UTSW |
7 |
103,141,840 (GRCm39) |
missense |
probably benign |
|
|
R4600:Or51af1
|
UTSW |
7 |
103,141,788 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4735:Or51af1
|
UTSW |
7 |
103,141,267 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R4941:Or51af1
|
UTSW |
7 |
103,141,458 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5204:Or51af1
|
UTSW |
7 |
103,141,747 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5281:Or51af1
|
UTSW |
7 |
103,141,180 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5941:Or51af1
|
UTSW |
7 |
103,141,927 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6319:Or51af1
|
UTSW |
7 |
103,141,932 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R6505:Or51af1
|
UTSW |
7 |
103,141,858 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7258:Or51af1
|
UTSW |
7 |
103,141,796 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8680:Or51af1
|
UTSW |
7 |
103,142,029 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8709:Or51af1
|
UTSW |
7 |
103,141,519 (GRCm39) |
missense |
probably benign |
|
|
R8994:Or51af1
|
UTSW |
7 |
103,141,800 (GRCm39) |
missense |
probably benign |
0.03 |
|
X0065:Or51af1
|
UTSW |
7 |
103,141,125 (GRCm39) |
makesense |
probably null |
|
|
Z1177:Or51af1
|
UTSW |
7 |
103,141,817 (GRCm39) |
missense |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- CGCTTCTGGCAGTAAGGTAGCTTC -3'
(R):5'- TGAGACAGTGTATCTCTGGCTCTCC -3'
Sequencing Primer
(F):5'- GCAGTAAGGTAGCTTCTTCAGC -3'
(R):5'- GTTGTAAAGTCAGAGCCCTCC -3'
|
| Posted On |
2013-10-16 |
Incidental Mutation