Incidental Mutation 'R3150:Or7e169'
| ID |
271633 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or7e169
|
| Ensembl Gene |
ENSMUSG00000066905 |
| Gene Name |
olfactory receptor family 7 subfamily E member 169 |
| Synonyms |
GA_x6K02T2PVTD-13586614-13585661, Olfr860, MOR146-2 |
| MMRRC Submission |
040602-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.057)
|
| Stock # |
R3150 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
19756919-19761043 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 19757510 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 135
(I135T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148658
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000086482]
[ENSMUST00000211924]
[ENSMUST00000212353]
|
| AlphaFold |
Q8VFF7 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000086482
AA Change: I135T
PolyPhen 2
Score 0.622 (Sensitivity: 0.87; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000130735
Gene: ENSMUSG00000066905
AA Change: I135T
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
3.5e-56 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
305 |
1.1e-8 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
9.3e-23 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000211924
AA Change: I135T
PolyPhen 2
Score 0.795 (Sensitivity: 0.85; Specificity: 0.93)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000212353
AA Change: I135T
PolyPhen 2
Score 0.622 (Sensitivity: 0.87; Specificity: 0.91)
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000212525
AA Change: I135T
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000212838
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.1%
|
| 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: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Akna |
A |
T |
4: 63,313,590 (GRCm39) |
S178T |
possibly damaging |
Het |
| Cabin1 |
A |
G |
10: 75,492,745 (GRCm39) |
L1850P |
probably damaging |
Het |
| Ccdc178 |
G |
T |
18: 22,200,709 (GRCm39) |
A416E |
possibly damaging |
Het |
| Ces1g |
C |
T |
8: 94,052,444 (GRCm39) |
V282I |
probably benign |
Het |
| Col4a3 |
T |
G |
1: 82,634,858 (GRCm39) |
|
probably null |
Het |
| Crat |
C |
T |
2: 30,303,871 (GRCm39) |
|
probably null |
Het |
| Csf2ra |
C |
A |
19: 61,215,758 (GRCm39) |
A16S |
possibly damaging |
Het |
| Cspg4b |
A |
T |
13: 113,488,294 (GRCm39) |
Q105H |
probably damaging |
Het |
| Cyp4f18 |
T |
C |
8: 72,747,044 (GRCm39) |
D317G |
possibly damaging |
Het |
| Ddb1 |
T |
A |
19: 10,590,346 (GRCm39) |
M291K |
probably benign |
Het |
| Fcgbpl1 |
C |
A |
7: 27,853,620 (GRCm39) |
T1528N |
probably benign |
Het |
| Gfod2 |
C |
T |
8: 106,443,853 (GRCm39) |
G230D |
probably benign |
Het |
| Git2 |
A |
G |
5: 114,868,410 (GRCm39) |
S257P |
probably damaging |
Het |
| Gm5592 |
A |
G |
7: 40,937,804 (GRCm39) |
E362G |
probably benign |
Het |
| Gpatch2l |
A |
G |
12: 86,291,089 (GRCm39) |
T91A |
possibly damaging |
Het |
| Hjurp |
A |
G |
1: 88,194,283 (GRCm39) |
|
probably benign |
Het |
| Hnrnph1 |
T |
A |
11: 50,276,619 (GRCm39) |
V439E |
probably benign |
Het |
| Itgad |
C |
A |
7: 127,790,153 (GRCm39) |
H651N |
possibly damaging |
Het |
| Map3k20 |
C |
T |
2: 72,202,336 (GRCm39) |
T189M |
probably damaging |
Het |
| Mapk11 |
T |
C |
15: 89,029,653 (GRCm39) |
|
probably null |
Het |
| Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
| Nmral1 |
G |
A |
16: 4,534,333 (GRCm39) |
T36I |
probably damaging |
Het |
| Or4c1 |
C |
T |
2: 89,133,562 (GRCm39) |
V125M |
possibly damaging |
Het |
| Or5b119 |
A |
G |
19: 13,456,824 (GRCm39) |
V246A |
probably damaging |
Het |
| Padi6 |
A |
G |
4: 140,462,700 (GRCm39) |
L307P |
probably damaging |
Het |
| Pkd1 |
G |
T |
17: 24,798,765 (GRCm39) |
R2691L |
probably benign |
Het |
| Ppp2r2a |
G |
A |
14: 67,261,214 (GRCm39) |
R169W |
probably damaging |
Het |
| Prdm1 |
A |
T |
10: 44,334,488 (GRCm39) |
|
probably null |
Het |
| Robo1 |
C |
T |
16: 72,767,157 (GRCm39) |
P443L |
possibly damaging |
Het |
| Rtn4 |
CGAGGAGGAGGAGGAGGA |
CGAGGAGGAGGAGGA |
11: 29,643,308 (GRCm39) |
|
probably benign |
Het |
| Shprh |
A |
G |
10: 11,045,774 (GRCm39) |
H865R |
probably damaging |
Het |
| Spats1 |
A |
T |
17: 45,775,480 (GRCm39) |
S15T |
probably damaging |
Het |
| Srgap2 |
T |
C |
1: 131,220,327 (GRCm39) |
T216A |
probably benign |
Het |
| Sry |
ACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
ACTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
Y: 2,662,944 (GRCm39) |
|
probably benign |
Het |
| Tie1 |
G |
A |
4: 118,333,022 (GRCm39) |
A902V |
probably damaging |
Het |
| Usp22 |
T |
C |
11: 61,051,407 (GRCm39) |
Q312R |
probably damaging |
Het |
| Vmn2r32 |
T |
C |
7: 7,475,554 (GRCm39) |
Y443C |
probably benign |
Het |
| Vps13d |
A |
C |
4: 144,813,360 (GRCm39) |
D3274E |
probably damaging |
Het |
| Wdr62 |
A |
T |
7: 29,971,095 (GRCm39) |
N167K |
possibly damaging |
Het |
| Xpo5 |
A |
G |
17: 46,553,173 (GRCm39) |
|
probably null |
Het |
| Zswim7 |
A |
T |
11: 62,164,611 (GRCm39) |
I43N |
possibly damaging |
Het |
| Zswim9 |
T |
C |
7: 13,011,196 (GRCm39) |
T51A |
possibly damaging |
Het |
|
| Other mutations in Or7e169 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00942:Or7e169
|
APN |
9 |
19,757,555 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02216:Or7e169
|
APN |
9 |
19,757,861 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02269:Or7e169
|
APN |
9 |
19,757,024 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
IGL02964:Or7e169
|
APN |
9 |
19,757,550 (GRCm39) |
nonsense |
probably null |
|
|
R0042:Or7e169
|
UTSW |
9 |
19,757,075 (GRCm39) |
missense |
probably benign |
|
|
R1505:Or7e169
|
UTSW |
9 |
19,757,084 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1941:Or7e169
|
UTSW |
9 |
19,757,246 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2030:Or7e169
|
UTSW |
9 |
19,757,709 (GRCm39) |
missense |
probably benign |
0.30 |
|
R4597:Or7e169
|
UTSW |
9 |
19,756,987 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5004:Or7e169
|
UTSW |
9 |
19,757,398 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5006:Or7e169
|
UTSW |
9 |
19,757,567 (GRCm39) |
missense |
probably benign |
0.33 |
|
R5350:Or7e169
|
UTSW |
9 |
19,757,912 (GRCm39) |
start codon destroyed |
probably null |
0.97 |
|
R6163:Or7e169
|
UTSW |
9 |
19,757,024 (GRCm39) |
missense |
probably benign |
0.45 |
|
R6368:Or7e169
|
UTSW |
9 |
19,757,705 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7206:Or7e169
|
UTSW |
9 |
19,757,856 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7315:Or7e169
|
UTSW |
9 |
19,757,131 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8195:Or7e169
|
UTSW |
9 |
19,757,780 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8537:Or7e169
|
UTSW |
9 |
19,757,848 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8546:Or7e169
|
UTSW |
9 |
19,757,685 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8803:Or7e169
|
UTSW |
9 |
19,757,462 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9049:Or7e169
|
UTSW |
9 |
19,757,045 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9164:Or7e169
|
UTSW |
9 |
19,757,504 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R9254:Or7e169
|
UTSW |
9 |
19,757,212 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R9379:Or7e169
|
UTSW |
9 |
19,757,212 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R9513:Or7e169
|
UTSW |
9 |
19,757,816 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R9515:Or7e169
|
UTSW |
9 |
19,757,816 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
| Predicted Primers |
PCR Primer
(F):5'- GAGGAATCCAACAATGATACTGAC -3'
(R):5'- TCTGACATGGGCTTCAGCAG -3'
Sequencing Primer
(F):5'- CTATTTATAGAGGTGTCAGAACAGGC -3'
(R):5'- TTCAGCAGCACCACCATC -3'
|
| Posted On |
2015-03-25 |
Incidental Mutation