Incidental Mutation 'R5649:Or14a258'
| ID |
441321 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or14a258
|
| Ensembl Gene |
ENSMUSG00000062426 |
| Gene Name |
olfactory receptor family 14 subfamily A member 258 |
| Synonyms |
GA_x6K02T2NHDJ-9721756-9722757, MOR219-3P, Olfr304 |
| MMRRC Submission |
043170-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.093)
|
| Stock # |
R5649 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
7 |
| Chromosomal Location |
86034865-86035866 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 86035521 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Valine
at position 116
(M116V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000076449
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077210]
|
| AlphaFold |
Q7TS03 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000077210
AA Change: M116V
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000076449
Gene: ENSMUSG00000062426
AA Change: M116V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
306 |
8.9e-38 |
PFAM |
|
Pfam:7tm_1
|
39 |
288 |
1.1e-21 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.8%
- 10x: 97.5%
- 20x: 96.0%
|
| 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 |
|---|
| Abca12 |
T |
C |
1: 71,330,501 (GRCm39) |
T1385A |
probably damaging |
Het |
| Apc2 |
T |
A |
10: 80,149,972 (GRCm39) |
D1646E |
probably damaging |
Het |
| Aspm |
G |
A |
1: 139,407,407 (GRCm39) |
R2098H |
probably benign |
Het |
| Atl3 |
C |
A |
19: 7,509,592 (GRCm39) |
T435N |
possibly damaging |
Het |
| Cdh22 |
G |
T |
2: 164,958,200 (GRCm39) |
T589K |
probably damaging |
Het |
| Cnot3 |
T |
C |
7: 3,661,082 (GRCm39) |
L561S |
probably benign |
Het |
| Col5a1 |
A |
G |
2: 27,841,468 (GRCm39) |
D363G |
unknown |
Het |
| Cyp24a1 |
T |
C |
2: 170,338,229 (GRCm39) |
D105G |
possibly damaging |
Het |
| Dennd4a |
C |
A |
9: 64,758,491 (GRCm39) |
|
probably null |
Het |
| Dnah8 |
A |
G |
17: 31,019,561 (GRCm39) |
K3878R |
probably benign |
Het |
| Dock4 |
T |
C |
12: 40,894,539 (GRCm39) |
S1900P |
probably benign |
Het |
| Fancg |
A |
G |
4: 43,008,736 (GRCm39) |
L167P |
probably damaging |
Het |
| Ighd2-8 |
A |
G |
12: 113,414,487 (GRCm39) |
S1P |
possibly damaging |
Het |
| Kif28 |
A |
G |
1: 179,525,336 (GRCm39) |
|
probably null |
Het |
| Mrpl55 |
T |
A |
11: 59,095,397 (GRCm39) |
C20* |
probably null |
Het |
| Myo5a |
A |
G |
9: 75,079,001 (GRCm39) |
K920E |
possibly damaging |
Het |
| Naa35 |
G |
A |
13: 59,770,680 (GRCm39) |
|
probably benign |
Het |
| Olfm3 |
A |
G |
3: 114,890,573 (GRCm39) |
R76G |
probably damaging |
Het |
| Or2ag1 |
T |
C |
7: 106,313,373 (GRCm39) |
R172G |
possibly damaging |
Het |
| Pcdha12 |
A |
T |
18: 37,155,468 (GRCm39) |
D729V |
probably benign |
Het |
| Phf11c |
T |
C |
14: 59,622,981 (GRCm39) |
|
probably null |
Het |
| Phf20 |
T |
A |
2: 156,093,688 (GRCm39) |
|
probably null |
Het |
| Plbd1 |
T |
A |
6: 136,593,987 (GRCm39) |
Y376F |
probably benign |
Het |
| Poglut1 |
A |
G |
16: 38,352,173 (GRCm39) |
V257A |
probably damaging |
Het |
| Reln |
A |
G |
5: 22,106,623 (GRCm39) |
I3249T |
probably benign |
Het |
| Rgsl1 |
G |
A |
1: 153,701,639 (GRCm39) |
P272S |
possibly damaging |
Het |
| Slc15a2 |
A |
T |
16: 36,592,472 (GRCm39) |
Y197* |
probably null |
Het |
| Slc45a2 |
C |
T |
15: 11,012,693 (GRCm39) |
T232I |
probably benign |
Het |
| Ssc5d |
T |
A |
7: 4,929,517 (GRCm39) |
|
probably null |
Het |
| Thbs2 |
T |
C |
17: 14,910,215 (GRCm39) |
Y128C |
probably damaging |
Het |
| Them4 |
A |
T |
3: 94,238,851 (GRCm39) |
L219F |
possibly damaging |
Het |
| Tmem30b |
G |
T |
12: 73,592,940 (GRCm39) |
N58K |
probably benign |
Het |
| Trappc2b |
T |
C |
11: 51,576,799 (GRCm39) |
E33G |
probably benign |
Het |
| Ttc29 |
G |
A |
8: 78,972,942 (GRCm39) |
E131K |
possibly damaging |
Het |
| Vmn1r29 |
C |
G |
6: 58,284,676 (GRCm39) |
S132C |
probably benign |
Het |
| Vmn1r53 |
G |
A |
6: 90,200,742 (GRCm39) |
A194V |
probably benign |
Het |
| Wdr86 |
A |
T |
5: 24,923,085 (GRCm39) |
H202Q |
probably benign |
Het |
| Xirp2 |
A |
G |
2: 67,347,239 (GRCm39) |
D3160G |
probably benign |
Het |
| Xkr5 |
T |
C |
8: 18,983,982 (GRCm39) |
D520G |
probably benign |
Het |
| Zfp607b |
T |
G |
7: 27,403,406 (GRCm39) |
C621G |
probably damaging |
Het |
|
| Other mutations in Or14a258 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01391:Or14a258
|
APN |
7 |
86,035,208 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL02152:Or14a258
|
APN |
7 |
86,035,251 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02540:Or14a258
|
APN |
7 |
86,035,386 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL03108:Or14a258
|
APN |
7 |
86,034,929 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL03374:Or14a258
|
APN |
7 |
86,035,574 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0040:Or14a258
|
UTSW |
7 |
86,035,715 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0130:Or14a258
|
UTSW |
7 |
86,035,514 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0194:Or14a258
|
UTSW |
7 |
86,035,582 (GRCm39) |
nonsense |
probably null |
|
|
R0267:Or14a258
|
UTSW |
7 |
86,035,475 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R1026:Or14a258
|
UTSW |
7 |
86,035,467 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1865:Or14a258
|
UTSW |
7 |
86,035,769 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2090:Or14a258
|
UTSW |
7 |
86,035,289 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3607:Or14a258
|
UTSW |
7 |
86,034,903 (GRCm39) |
missense |
probably benign |
|
|
R3861:Or14a258
|
UTSW |
7 |
86,035,331 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R3909:Or14a258
|
UTSW |
7 |
86,035,182 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4113:Or14a258
|
UTSW |
7 |
86,035,733 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R5268:Or14a258
|
UTSW |
7 |
86,034,867 (GRCm39) |
makesense |
probably null |
|
|
R6343:Or14a258
|
UTSW |
7 |
86,035,059 (GRCm39) |
nonsense |
probably null |
|
|
R7716:Or14a258
|
UTSW |
7 |
86,035,262 (GRCm39) |
missense |
probably benign |
0.22 |
|
R8118:Or14a258
|
UTSW |
7 |
86,034,976 (GRCm39) |
nonsense |
probably null |
|
|
R9047:Or14a258
|
UTSW |
7 |
86,035,248 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9503:Or14a258
|
UTSW |
7 |
86,035,228 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9528:Or14a258
|
UTSW |
7 |
86,035,059 (GRCm39) |
nonsense |
probably null |
|
|
X0054:Or14a258
|
UTSW |
7 |
86,034,938 (GRCm39) |
missense |
probably benign |
0.00 |
|
X0063:Or14a258
|
UTSW |
7 |
86,035,700 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1186:Or14a258
|
UTSW |
7 |
86,035,487 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCCTTAGTAACGAGGGAACATCAC -3'
(R):5'- CACGGTCATCACTCTGGATC -3'
Sequencing Primer
(F):5'- CAGAAAAACTGTGGGATCACC -3'
(R):5'- GGTCATCACTCTGGATCTGAAAC -3'
|
| Posted On |
2016-11-08 |
Incidental Mutation