Incidental Mutation 'R6405:Or2g25'
| ID |
516275 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or2g25
|
| Ensembl Gene |
ENSMUSG00000095286 |
| Gene Name |
olfactory receptor family 2 subfamily G member 25 |
| Synonyms |
MOR256-33, GA_x6K02T2PSCP-2119438-2118485, Olfr117 |
| MMRRC Submission |
044550-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.064)
|
| Stock # |
R6405 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
17 |
| Chromosomal Location |
37970269-37971222 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 37971014 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 70
(I70T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150204
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000073636]
[ENSMUST00000213638]
[ENSMUST00000215414]
|
| AlphaFold |
L7N1Z1 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000073636
AA Change: I70T
PolyPhen 2
Score 0.580 (Sensitivity: 0.88; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000073320
Gene: ENSMUSG00000095286
AA Change: I70T
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
307 |
2.7e-44 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
34 |
222 |
2e-5 |
PFAM |
|
Pfam:7tm_1
|
40 |
289 |
2.9e-23 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000213638
AA Change: I70T
PolyPhen 2
Score 0.580 (Sensitivity: 0.88; Specificity: 0.91)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000215414
AA Change: I70T
PolyPhen 2
Score 0.580 (Sensitivity: 0.88; Specificity: 0.91)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.4%
- 20x: 98.2%
|
| 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: 40 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930562C15Rik |
T |
C |
16: 4,669,742 (GRCm39) |
V769A |
probably damaging |
Het |
| Abca4 |
A |
G |
3: 121,967,311 (GRCm39) |
|
probably null |
Het |
| Ahnak2 |
A |
T |
12: 112,739,771 (GRCm39) |
S628T |
probably damaging |
Het |
| Ano8 |
T |
C |
8: 71,935,674 (GRCm39) |
T315A |
probably damaging |
Het |
| Arhgap32 |
T |
A |
9: 32,159,784 (GRCm39) |
V267E |
probably benign |
Het |
| Asnsd1 |
A |
T |
1: 53,387,154 (GRCm39) |
S158T |
probably damaging |
Het |
| Asxl2 |
T |
A |
12: 3,543,758 (GRCm39) |
V309E |
probably damaging |
Het |
| Bhlhe40 |
TG |
TGG |
6: 108,641,818 (GRCm39) |
254 |
probably null |
Het |
| Ccdc110 |
T |
A |
8: 46,394,734 (GRCm39) |
Y208* |
probably null |
Het |
| Cfap157 |
G |
T |
2: 32,671,408 (GRCm39) |
Q133K |
probably damaging |
Het |
| Cfap53 |
A |
G |
18: 74,492,677 (GRCm39) |
E467G |
probably damaging |
Het |
| Csmd3 |
T |
C |
15: 47,683,767 (GRCm39) |
I1688M |
probably damaging |
Het |
| Cyp3a11 |
A |
T |
5: 145,799,230 (GRCm39) |
L319Q |
probably damaging |
Het |
| Dchs2 |
A |
G |
3: 83,261,570 (GRCm39) |
I2613V |
probably benign |
Het |
| Dhx35 |
T |
A |
2: 158,636,839 (GRCm39) |
W11R |
probably damaging |
Het |
| Dscam |
C |
T |
16: 96,479,625 (GRCm39) |
G1174D |
probably damaging |
Het |
| Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
| Fsip2 |
A |
G |
2: 82,820,430 (GRCm39) |
T5388A |
possibly damaging |
Het |
| Gm10549 |
C |
A |
18: 33,597,358 (GRCm39) |
|
probably benign |
Het |
| Greb1l |
T |
A |
18: 10,501,076 (GRCm39) |
I402K |
probably benign |
Het |
| Hectd3 |
A |
T |
4: 116,857,821 (GRCm39) |
M585L |
probably benign |
Het |
| Inpp5k |
T |
C |
11: 75,524,004 (GRCm39) |
|
probably null |
Het |
| Lalba |
T |
G |
15: 98,378,632 (GRCm39) |
|
probably null |
Het |
| Lgals9 |
C |
A |
11: 78,862,211 (GRCm39) |
V125L |
probably benign |
Het |
| Ncbp2 |
CGTCTGGATG |
CG |
16: 31,775,161 (GRCm39) |
|
probably null |
Het |
| Peg10 |
C |
CTCG |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
| Rab4b |
T |
A |
7: 26,872,379 (GRCm39) |
D94V |
probably damaging |
Het |
| Rhpn2 |
A |
G |
7: 35,071,864 (GRCm39) |
E243G |
probably benign |
Het |
| Rp1 |
T |
C |
1: 4,415,994 (GRCm39) |
D1706G |
probably damaging |
Het |
| Slc29a3 |
A |
T |
10: 60,551,805 (GRCm39) |
I413N |
probably damaging |
Het |
| Slc7a9 |
T |
C |
7: 35,154,064 (GRCm39) |
L229P |
probably damaging |
Het |
| Tenm2 |
T |
C |
11: 36,755,686 (GRCm39) |
H104R |
probably benign |
Het |
| Tmem87a |
A |
G |
2: 120,210,231 (GRCm39) |
Y241H |
probably damaging |
Het |
| Trpv5 |
G |
T |
6: 41,651,602 (GRCm39) |
T192K |
probably damaging |
Het |
| Unc79 |
T |
C |
12: 103,134,595 (GRCm39) |
V2189A |
probably damaging |
Het |
| Vmn2r106 |
A |
C |
17: 20,499,361 (GRCm39) |
S183R |
probably benign |
Het |
| Vmn2r112 |
G |
T |
17: 22,837,216 (GRCm39) |
C559F |
probably damaging |
Het |
| Wdhd1 |
T |
C |
14: 47,481,324 (GRCm39) |
D1031G |
possibly damaging |
Het |
| Wnt5b |
T |
C |
6: 119,410,457 (GRCm39) |
S328G |
probably benign |
Het |
| Zcchc7 |
T |
C |
4: 44,926,032 (GRCm39) |
Y344H |
probably damaging |
Het |
|
| Other mutations in Or2g25 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01862:Or2g25
|
APN |
17 |
37,970,368 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01949:Or2g25
|
APN |
17 |
37,970,357 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02085:Or2g25
|
APN |
17 |
37,970,579 (GRCm39) |
missense |
probably benign |
0.11 |
|
IGL02481:Or2g25
|
APN |
17 |
37,970,363 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02483:Or2g25
|
APN |
17 |
37,970,363 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03274:Or2g25
|
APN |
17 |
37,970,646 (GRCm39) |
missense |
probably benign |
0.35 |
|
R0234:Or2g25
|
UTSW |
17 |
37,970,997 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0234:Or2g25
|
UTSW |
17 |
37,970,997 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1522:Or2g25
|
UTSW |
17 |
37,970,661 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1712:Or2g25
|
UTSW |
17 |
37,970,799 (GRCm39) |
missense |
probably benign |
0.42 |
|
R1750:Or2g25
|
UTSW |
17 |
37,970,564 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1865:Or2g25
|
UTSW |
17 |
37,970,754 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R2371:Or2g25
|
UTSW |
17 |
37,971,044 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2382:Or2g25
|
UTSW |
17 |
37,970,822 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3798:Or2g25
|
UTSW |
17 |
37,970,997 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4831:Or2g25
|
UTSW |
17 |
37,970,969 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5087:Or2g25
|
UTSW |
17 |
37,970,612 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5365:Or2g25
|
UTSW |
17 |
37,970,586 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5812:Or2g25
|
UTSW |
17 |
37,970,630 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5822:Or2g25
|
UTSW |
17 |
37,971,122 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6945:Or2g25
|
UTSW |
17 |
37,970,405 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7121:Or2g25
|
UTSW |
17 |
37,970,699 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7312:Or2g25
|
UTSW |
17 |
37,970,403 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R7502:Or2g25
|
UTSW |
17 |
37,971,122 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8116:Or2g25
|
UTSW |
17 |
37,970,631 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8425:Or2g25
|
UTSW |
17 |
37,970,975 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8960:Or2g25
|
UTSW |
17 |
37,970,760 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9168:Or2g25
|
UTSW |
17 |
37,971,047 (GRCm39) |
missense |
probably damaging |
1.00 |
|
RF017:Or2g25
|
UTSW |
17 |
37,970,672 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CTCCTGCAAGAGATTGGCAG -3'
(R):5'- ATCCTGGTGGGCTTCTCTGATC -3'
Sequencing Primer
(F):5'- CCGTGGGTGCATAACTGTAGC -3'
(R):5'- TCTCTGATCAGCCACAACTTGAG -3'
|
| Posted On |
2018-05-04 |
Incidental Mutation