Incidental Mutation 'R3421:Or1e1'
| ID |
267053 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or1e1
|
| Ensembl Gene |
ENSMUSG00000062128 |
| Gene Name |
olfactory receptor family 1 subfamily E member 1 |
| Synonyms |
MTPCR06, MOR135-11, Olfr20, Olfr21, MTPCR55, GA_x6K02T2P1NL-3514066-3515010 |
| MMRRC Submission |
040639-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.124)
|
| Stock # |
R3421 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
73241685-73245525 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 73245460 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Aspartic acid
at position 294
(N294D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000114110
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000108465]
[ENSMUST00000117445]
[ENSMUST00000120137]
|
| AlphaFold |
Q7TRX9 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000108465
AA Change: N294D
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000104105
Gene: ENSMUSG00000062128
AA Change: N294D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
7.9e-60 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
305 |
7.8e-8 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
1e-23 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000117445
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000120137
AA Change: N294D
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000114110
Gene: ENSMUSG00000062128
AA Change: N294D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
2.3e-61 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
305 |
1.5e-6 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
2.2e-26 |
PFAM |
|
| Meta Mutation Damage Score |
0.4186 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.0%
|
| Validation Efficiency |
100% (46/46) |
| 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 |
|---|
| Acacb |
T |
A |
5: 114,350,697 (GRCm39) |
|
probably null |
Het |
| Agbl3 |
A |
G |
6: 34,770,900 (GRCm39) |
T132A |
probably benign |
Het |
| Amn1 |
A |
T |
6: 149,070,950 (GRCm39) |
L196* |
probably null |
Het |
| Ap3b2 |
C |
T |
7: 81,123,598 (GRCm39) |
|
probably benign |
Het |
| Atp7b |
C |
T |
8: 22,518,686 (GRCm39) |
D51N |
probably damaging |
Het |
| Brip1 |
A |
T |
11: 86,043,495 (GRCm39) |
Y356* |
probably null |
Het |
| Ccdc40 |
C |
T |
11: 119,125,605 (GRCm39) |
P348L |
probably benign |
Het |
| Chrdl2 |
G |
A |
7: 99,673,075 (GRCm39) |
C9Y |
probably damaging |
Het |
| Chst4 |
T |
C |
8: 110,757,038 (GRCm39) |
D192G |
probably damaging |
Het |
| Col9a2 |
C |
G |
4: 120,911,455 (GRCm39) |
R599G |
probably damaging |
Het |
| D930048N14Rik |
T |
C |
11: 51,545,785 (GRCm39) |
*226R |
probably null |
Het |
| Dmgdh |
T |
C |
13: 93,847,869 (GRCm39) |
V522A |
probably benign |
Het |
| Dtx2 |
T |
A |
5: 136,041,332 (GRCm39) |
Y246N |
probably damaging |
Het |
| Gtf2ird1 |
T |
A |
5: 134,417,354 (GRCm39) |
M518L |
probably benign |
Het |
| Hoxc6 |
T |
A |
15: 102,919,327 (GRCm39) |
W188R |
probably damaging |
Het |
| Igfn1 |
C |
T |
1: 135,904,655 (GRCm39) |
|
probably null |
Het |
| Kcnip1 |
A |
G |
11: 33,595,594 (GRCm39) |
V43A |
probably damaging |
Het |
| Kif4-ps |
A |
T |
12: 101,113,230 (GRCm39) |
E453V |
probably damaging |
Het |
| Kifap3 |
T |
A |
1: 163,621,595 (GRCm39) |
I81N |
probably damaging |
Het |
| Mgat4d |
T |
C |
8: 84,084,772 (GRCm39) |
S172P |
probably damaging |
Het |
| Mr1 |
T |
C |
1: 155,013,337 (GRCm39) |
Y80C |
probably damaging |
Het |
| Nuak2 |
A |
G |
1: 132,259,818 (GRCm39) |
D532G |
probably benign |
Het |
| Odad2 |
T |
C |
18: 7,223,523 (GRCm39) |
|
probably benign |
Het |
| Or4c123 |
C |
G |
2: 89,126,897 (GRCm39) |
S239T |
probably benign |
Het |
| Or4g7 |
A |
G |
2: 111,309,297 (GRCm39) |
H56R |
probably benign |
Het |
| Or4k15b |
T |
C |
14: 50,271,997 (GRCm39) |
T288A |
possibly damaging |
Het |
| Or8d1 |
A |
G |
9: 38,766,621 (GRCm39) |
K88E |
possibly damaging |
Het |
| Pik3cg |
A |
T |
12: 32,254,738 (GRCm39) |
F416L |
probably damaging |
Het |
| Prex1 |
A |
G |
2: 166,459,774 (GRCm39) |
V124A |
probably damaging |
Het |
| Psmb2 |
T |
C |
4: 126,571,630 (GRCm39) |
M28T |
probably damaging |
Het |
| Ric1 |
T |
C |
19: 29,544,990 (GRCm39) |
I230T |
probably damaging |
Het |
| Saysd1 |
T |
A |
14: 20,132,994 (GRCm39) |
K54N |
probably benign |
Het |
| Slc25a17 |
C |
T |
15: 81,244,901 (GRCm39) |
V11I |
probably benign |
Het |
| Slc5a4a |
T |
C |
10: 76,012,407 (GRCm39) |
V359A |
probably benign |
Het |
| Slc7a3 |
T |
A |
X: 100,124,481 (GRCm39) |
|
probably benign |
Het |
| Slco1a5 |
A |
T |
6: 142,213,964 (GRCm39) |
D52E |
possibly damaging |
Het |
| Soat2 |
T |
C |
15: 102,065,244 (GRCm39) |
|
probably benign |
Het |
| Tafa1 |
C |
A |
6: 96,626,099 (GRCm39) |
D112E |
probably damaging |
Het |
| Telo2 |
C |
T |
17: 25,329,726 (GRCm39) |
R262Q |
probably damaging |
Het |
| Zdhhc14 |
T |
A |
17: 5,803,366 (GRCm39) |
*490R |
probably null |
Het |
| Zfp217 |
A |
G |
2: 169,961,937 (GRCm39) |
F130S |
possibly damaging |
Het |
| Zfp712 |
C |
T |
13: 67,200,456 (GRCm39) |
V10M |
probably damaging |
Het |
|
| Other mutations in Or1e1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00589:Or1e1
|
APN |
11 |
73,244,869 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02163:Or1e1
|
APN |
11 |
73,245,320 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0598:Or1e1
|
UTSW |
11 |
73,244,729 (GRCm39) |
missense |
probably benign |
|
|
R1348:Or1e1
|
UTSW |
11 |
73,244,682 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2006:Or1e1
|
UTSW |
11 |
73,245,518 (GRCm39) |
missense |
probably benign |
|
|
R2085:Or1e1
|
UTSW |
11 |
73,245,247 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2263:Or1e1
|
UTSW |
11 |
73,245,131 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R3422:Or1e1
|
UTSW |
11 |
73,245,460 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4229:Or1e1
|
UTSW |
11 |
73,245,058 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4749:Or1e1
|
UTSW |
11 |
73,245,322 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5410:Or1e1
|
UTSW |
11 |
73,244,632 (GRCm39) |
missense |
probably benign |
0.11 |
|
R6035:Or1e1
|
UTSW |
11 |
73,244,582 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
R6035:Or1e1
|
UTSW |
11 |
73,244,582 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
R6499:Or1e1
|
UTSW |
11 |
73,245,011 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7840:Or1e1
|
UTSW |
11 |
73,244,585 (GRCm39) |
missense |
probably benign |
|
|
R7959:Or1e1
|
UTSW |
11 |
73,244,744 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8186:Or1e1
|
UTSW |
11 |
73,245,247 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9072:Or1e1
|
UTSW |
11 |
73,244,797 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9135:Or1e1
|
UTSW |
11 |
73,245,316 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9225:Or1e1
|
UTSW |
11 |
73,244,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CGTAAAGCCTTCTCCACCTGTG -3'
(R):5'- GCAAATCATGAGAAGCCATTCTTAACC -3'
Sequencing Primer
(F):5'- TGGGTCCCACCTGTCTGTG -3'
(R):5'- CCAAATAGACATTCCTACTTCTGC -3'
|
| Posted On |
2015-02-18 |
Incidental Mutation