Incidental Mutation 'R2336:Or2r11'
| ID |
246548 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or2r11
|
| Ensembl Gene |
ENSMUSG00000068574 |
| Gene Name |
olfactory receptor family 2 subfamily R member 11 |
| Synonyms |
Olfr458, GA_x6K02T2P3E9-5100053-5100994, MOR257-4 |
| MMRRC Submission |
040323-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.075)
|
| Stock # |
R2336 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
6 |
| Chromosomal Location |
42437010-42437951 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 42437663 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Arginine
at position 97
(C97R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149459
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000090156]
[ENSMUST00000216650]
|
| AlphaFold |
Q8VF80 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000090156
AA Change: C97R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000087617
Gene: ENSMUSG00000068574
AA Change: C97R
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
8.6e-52 |
PFAM |
|
Pfam:7tm_1
|
41 |
310 |
3.7e-25 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000216650
AA Change: C97R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Meta Mutation Damage Score |
0.6467 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.7%
- 10x: 97.4%
- 20x: 95.2%
|
| Validation Efficiency |
100% (38/38) |
| 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: 35 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A430110L20Rik |
T |
A |
1: 181,055,206 (GRCm39) |
|
noncoding transcript |
Het |
| Arhgap21 |
G |
A |
2: 20,884,862 (GRCm39) |
R772C |
probably damaging |
Het |
| Arid2 |
A |
G |
15: 96,260,430 (GRCm39) |
E393G |
probably damaging |
Het |
| Atrn |
C |
T |
2: 130,799,874 (GRCm39) |
T417I |
probably damaging |
Het |
| Baiap3 |
T |
C |
17: 25,469,378 (GRCm39) |
K173R |
probably damaging |
Het |
| Bdp1 |
A |
T |
13: 100,189,510 (GRCm39) |
N1497K |
probably damaging |
Het |
| Ceacam5 |
T |
C |
7: 17,481,300 (GRCm39) |
V349A |
probably benign |
Het |
| Chrnd |
T |
C |
1: 87,122,615 (GRCm39) |
F132S |
probably damaging |
Het |
| Ddx42 |
A |
G |
11: 106,121,976 (GRCm39) |
M164V |
possibly damaging |
Het |
| Dtwd2 |
A |
G |
18: 49,833,320 (GRCm39) |
|
probably benign |
Het |
| Eprs1 |
T |
A |
1: 185,143,571 (GRCm39) |
|
probably benign |
Het |
| Fut8 |
A |
G |
12: 77,459,730 (GRCm39) |
|
probably benign |
Het |
| Gabrr3 |
C |
T |
16: 59,250,313 (GRCm39) |
T104M |
probably damaging |
Het |
| Gcat |
G |
A |
15: 78,915,180 (GRCm39) |
R16H |
probably benign |
Het |
| Gnb2 |
A |
T |
5: 137,527,460 (GRCm39) |
W125R |
probably damaging |
Het |
| Grik4 |
C |
T |
9: 42,477,651 (GRCm39) |
D512N |
probably damaging |
Het |
| Hnf4g |
T |
C |
3: 3,706,284 (GRCm39) |
F60L |
probably benign |
Het |
| Lrp6 |
A |
G |
6: 134,484,546 (GRCm39) |
I359T |
probably damaging |
Het |
| Lrrfip2 |
A |
G |
9: 111,051,283 (GRCm39) |
D325G |
probably damaging |
Het |
| Mttp |
A |
T |
3: 137,821,856 (GRCm39) |
I222K |
possibly damaging |
Het |
| Myom1 |
A |
T |
17: 71,330,189 (GRCm39) |
H107L |
possibly damaging |
Het |
| Obi1 |
G |
A |
14: 104,716,318 (GRCm39) |
P685L |
probably damaging |
Het |
| Or10al4 |
A |
T |
17: 38,037,689 (GRCm39) |
Y258F |
probably benign |
Het |
| Ppfia3 |
T |
C |
7: 45,006,121 (GRCm39) |
|
probably null |
Het |
| Prokr2 |
A |
T |
2: 132,223,359 (GRCm39) |
M61K |
probably damaging |
Het |
| Ptk2 |
A |
G |
15: 73,137,965 (GRCm39) |
C502R |
probably damaging |
Het |
| Rbm25 |
T |
A |
12: 83,698,192 (GRCm39) |
W172R |
probably damaging |
Het |
| Rdh16f1 |
A |
G |
10: 127,624,624 (GRCm39) |
K154R |
probably benign |
Het |
| Rnf213 |
G |
A |
11: 119,305,430 (GRCm39) |
E554K |
probably benign |
Het |
| St3gal6 |
A |
T |
16: 58,314,067 (GRCm39) |
I22K |
probably damaging |
Het |
| Tut7 |
G |
T |
13: 59,946,868 (GRCm39) |
P585Q |
probably damaging |
Het |
| Usp43 |
G |
A |
11: 67,782,258 (GRCm39) |
R387* |
probably null |
Het |
| Vmn2r106 |
T |
C |
17: 20,488,470 (GRCm39) |
N643S |
probably benign |
Het |
| Zdbf2 |
G |
T |
1: 63,342,623 (GRCm39) |
R334L |
probably benign |
Het |
| Zfp868 |
G |
T |
8: 70,066,558 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Or2r11 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00915:Or2r11
|
APN |
6 |
42,437,884 (GRCm39) |
missense |
probably benign |
|
|
IGL00983:Or2r11
|
APN |
6 |
42,437,029 (GRCm39) |
missense |
probably benign |
|
|
IGL01655:Or2r11
|
APN |
6 |
42,437,474 (GRCm39) |
missense |
probably benign |
0.41 |
|
IGL02017:Or2r11
|
APN |
6 |
42,437,758 (GRCm39) |
missense |
probably benign |
0.40 |
|
IGL02420:Or2r11
|
APN |
6 |
42,437,110 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL03145:Or2r11
|
APN |
6 |
42,437,434 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL03171:Or2r11
|
APN |
6 |
42,437,464 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL03333:Or2r11
|
APN |
6 |
42,437,773 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1768:Or2r11
|
UTSW |
6 |
42,437,611 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1908:Or2r11
|
UTSW |
6 |
42,437,360 (GRCm39) |
missense |
probably benign |
0.15 |
|
R2198:Or2r11
|
UTSW |
6 |
42,437,950 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
R2512:Or2r11
|
UTSW |
6 |
42,437,207 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3433:Or2r11
|
UTSW |
6 |
42,437,888 (GRCm39) |
missense |
probably benign |
|
|
R5338:Or2r11
|
UTSW |
6 |
42,437,908 (GRCm39) |
missense |
probably benign |
0.11 |
|
R5341:Or2r11
|
UTSW |
6 |
42,437,098 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5498:Or2r11
|
UTSW |
6 |
42,437,228 (GRCm39) |
missense |
probably benign |
0.11 |
|
R6558:Or2r11
|
UTSW |
6 |
42,437,711 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6594:Or2r11
|
UTSW |
6 |
42,437,309 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7107:Or2r11
|
UTSW |
6 |
42,437,488 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R7853:Or2r11
|
UTSW |
6 |
42,437,573 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8050:Or2r11
|
UTSW |
6 |
42,437,764 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8684:Or2r11
|
UTSW |
6 |
42,437,827 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9777:Or2r11
|
UTSW |
6 |
42,437,029 (GRCm39) |
missense |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- GCCACATGGTTGAGCACATTG -3'
(R):5'- GTAACCTACCTGCTGACTCTGC -3'
Sequencing Primer
(F):5'- ACATTGTGCCCACAGGTG -3'
(R):5'- CTGACTCTGCTGGGCAATG -3'
|
| Posted On |
2014-10-30 |
Incidental Mutation