Incidental Mutation 'R4401:Or2a25'
| ID |
326628 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or2a25
|
| Ensembl Gene |
ENSMUSG00000045708 |
| Gene Name |
olfactory receptor family 2 subfamily A member 25 |
| Synonyms |
GA_x6K02T2P3E9-4647978-4647046, MOR261-1, Olfr447 |
| MMRRC Submission |
041132-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.226)
|
| Stock # |
R4401 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
6 |
| Chromosomal Location |
42888459-42889391 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
G to T
at 42889260 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Stop codon
at position 268
(E268*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149325
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055763]
[ENSMUST00000216408]
|
| AlphaFold |
Q8VGP6 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000055763
AA Change: E268*
|
| SMART Domains |
Protein: ENSMUSP00000052312
Gene: ENSMUSG00000045708
AA Change: E268*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
30 |
307 |
1.8e-60 |
PFAM |
|
Pfam:7tm_1
|
40 |
289 |
6.3e-27 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000216408
AA Change: E268*
|
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.1%
|
| 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: 32 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcb1a |
A |
G |
5: 8,752,390 (GRCm39) |
I454V |
possibly damaging |
Het |
| Acvr2a |
A |
G |
2: 48,789,714 (GRCm39) |
T486A |
probably benign |
Het |
| Ap3b1 |
C |
A |
13: 94,554,607 (GRCm39) |
L248I |
probably damaging |
Het |
| Atad2b |
T |
A |
12: 4,990,145 (GRCm39) |
C157S |
probably damaging |
Het |
| Cage1 |
T |
A |
13: 38,207,078 (GRCm39) |
I256F |
probably damaging |
Het |
| Cct2 |
A |
G |
10: 116,893,714 (GRCm39) |
I287T |
possibly damaging |
Het |
| Cntn4 |
A |
G |
6: 106,466,625 (GRCm39) |
T176A |
possibly damaging |
Het |
| Cracd |
G |
A |
5: 76,996,763 (GRCm39) |
V74I |
probably damaging |
Het |
| Cyp2c54 |
T |
C |
19: 40,060,615 (GRCm39) |
N122S |
probably benign |
Het |
| Cytip |
T |
C |
2: 58,023,947 (GRCm39) |
D291G |
probably benign |
Het |
| Eef1d |
C |
T |
15: 75,774,769 (GRCm39) |
V213I |
probably benign |
Het |
| Fnbp4 |
A |
G |
2: 90,577,102 (GRCm39) |
T145A |
possibly damaging |
Het |
| Fras1 |
C |
A |
5: 96,790,479 (GRCm39) |
T951K |
probably damaging |
Het |
| Gm11937 |
C |
T |
11: 99,500,901 (GRCm39) |
V39M |
probably damaging |
Het |
| Gm6712 |
C |
T |
17: 17,538,366 (GRCm39) |
|
noncoding transcript |
Het |
| Hira |
A |
G |
16: 18,744,470 (GRCm39) |
I352V |
probably damaging |
Het |
| Homer3 |
G |
A |
8: 70,742,793 (GRCm39) |
|
probably null |
Het |
| Lpcat2 |
T |
C |
8: 93,599,683 (GRCm39) |
V217A |
possibly damaging |
Het |
| Mroh2a |
G |
T |
1: 88,182,657 (GRCm39) |
R1195L |
possibly damaging |
Het |
| Or4k35 |
A |
G |
2: 111,100,178 (GRCm39) |
F178S |
probably damaging |
Het |
| Or51f5 |
C |
T |
7: 102,424,006 (GRCm39) |
R92* |
probably null |
Het |
| Pla2g1b |
T |
A |
5: 115,608,947 (GRCm39) |
Y47* |
probably null |
Het |
| Rfng |
A |
T |
11: 120,673,306 (GRCm39) |
V245E |
possibly damaging |
Het |
| Rpf2 |
A |
G |
10: 40,112,124 (GRCm39) |
V104A |
possibly damaging |
Het |
| Rps6kc1 |
G |
T |
1: 190,532,155 (GRCm39) |
H616N |
probably benign |
Het |
| Slc66a1 |
T |
C |
4: 139,033,854 (GRCm39) |
I22V |
probably benign |
Het |
| Slc9b2 |
T |
C |
3: 135,042,305 (GRCm39) |
V528A |
probably benign |
Het |
| Srgap1 |
T |
C |
10: 121,640,826 (GRCm39) |
|
probably null |
Het |
| Trrap |
A |
G |
5: 144,780,128 (GRCm39) |
T3240A |
possibly damaging |
Het |
| Vmn2r68 |
TCC |
TC |
7: 84,870,758 (GRCm39) |
|
probably null |
Het |
| Zfhx4 |
C |
A |
3: 5,468,405 (GRCm39) |
Y2854* |
probably null |
Het |
| Zfp986 |
C |
T |
4: 145,625,513 (GRCm39) |
R58C |
probably benign |
Het |
|
| Other mutations in Or2a25 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02302:Or2a25
|
APN |
6 |
42,889,272 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02604:Or2a25
|
APN |
6 |
42,888,992 (GRCm39) |
nonsense |
probably null |
|
|
IGL02894:Or2a25
|
APN |
6 |
42,888,451 (GRCm39) |
splice site |
probably benign |
|
|
R0122:Or2a25
|
UTSW |
6 |
42,888,889 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0172:Or2a25
|
UTSW |
6 |
42,888,913 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0371:Or2a25
|
UTSW |
6 |
42,888,872 (GRCm39) |
missense |
probably benign |
0.14 |
|
R1709:Or2a25
|
UTSW |
6 |
42,889,078 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R2431:Or2a25
|
UTSW |
6 |
42,888,946 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3809:Or2a25
|
UTSW |
6 |
42,889,271 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4032:Or2a25
|
UTSW |
6 |
42,888,559 (GRCm39) |
missense |
probably benign |
0.08 |
|
R4242:Or2a25
|
UTSW |
6 |
42,888,480 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R4369:Or2a25
|
UTSW |
6 |
42,889,211 (GRCm39) |
nonsense |
probably null |
|
|
R4565:Or2a25
|
UTSW |
6 |
42,888,472 (GRCm39) |
missense |
probably benign |
|
|
R5646:Or2a25
|
UTSW |
6 |
42,888,457 (GRCm39) |
splice site |
probably null |
|
|
R5968:Or2a25
|
UTSW |
6 |
42,888,480 (GRCm39) |
missense |
probably benign |
|
|
R6804:Or2a25
|
UTSW |
6 |
42,888,852 (GRCm39) |
missense |
probably benign |
|
|
R6925:Or2a25
|
UTSW |
6 |
42,888,791 (GRCm39) |
nonsense |
probably null |
|
|
R8170:Or2a25
|
UTSW |
6 |
42,889,125 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R8358:Or2a25
|
UTSW |
6 |
42,888,976 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R8765:Or2a25
|
UTSW |
6 |
42,889,102 (GRCm39) |
missense |
probably benign |
0.34 |
|
R9005:Or2a25
|
UTSW |
6 |
42,889,170 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9015:Or2a25
|
UTSW |
6 |
42,888,825 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R9308:Or2a25
|
UTSW |
6 |
42,888,931 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9520:Or2a25
|
UTSW |
6 |
42,889,051 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9743:Or2a25
|
UTSW |
6 |
42,888,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GTGCTTGTCGGACCATTTTC -3'
(R):5'- GATGAACAAGTTACATGTCCTGGTC -3'
Sequencing Primer
(F):5'- GTCGGACCATTTTCTTCAATTGTAG -3'
(R):5'- AGTGTCCTCTTCAGAGCA -3'
|
| Posted On |
2015-07-07 |
Incidental Mutation