Incidental Mutation 'R5711:Or1e22'
| ID |
452228 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or1e22
|
| Ensembl Gene |
ENSMUSG00000072708 |
| Gene Name |
olfactory receptor family 1 subfamily E member 22 |
| Synonyms |
Olfr381, GA_x6K02T2P1NL-3646409-3645474, MOR135-4 |
| MMRRC Submission |
043185-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.092)
|
| Stock # |
R5711 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
73376713-73377648 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 73377008 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 214
(I214T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149355
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000078358]
[ENSMUST00000119863]
[ENSMUST00000214623]
[ENSMUST00000215358]
|
| AlphaFold |
Q5SSP0 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000078358
AA Change: I214T
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000077467
Gene: ENSMUSG00000072708
AA Change: I214T
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_1
|
41 |
290 |
1.3e-35 |
PFAM |
|
Pfam:7tm_4
|
139 |
283 |
5.3e-42 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000119863
AA Change: I214T
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000113846
Gene: ENSMUSG00000072708
AA Change: I214T
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
4.2e-57 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
2e-27 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000206673
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000214623
AA Change: I214T
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000215358
AA Change: I214T
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.4%
|
| 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 |
|---|
| Ak6 |
A |
T |
13: 100,790,722 (GRCm39) |
T18S |
probably damaging |
Het |
| Aqp7 |
G |
A |
4: 41,035,510 (GRCm39) |
T115I |
probably benign |
Het |
| Arhgap19 |
A |
G |
19: 41,773,227 (GRCm39) |
V275A |
possibly damaging |
Het |
| Cebpz |
T |
A |
17: 79,242,040 (GRCm39) |
Q538L |
probably damaging |
Het |
| Chgb |
A |
T |
2: 132,634,618 (GRCm39) |
I187F |
probably benign |
Het |
| Cldn1 |
C |
A |
16: 26,190,167 (GRCm39) |
L70F |
probably damaging |
Het |
| Crybg2 |
A |
T |
4: 133,809,938 (GRCm39) |
D1230V |
probably damaging |
Het |
| Csmd1 |
C |
T |
8: 16,003,703 (GRCm39) |
C2617Y |
probably damaging |
Het |
| D7Ertd443e |
T |
A |
7: 133,951,110 (GRCm39) |
N188Y |
probably benign |
Het |
| Ddx51 |
A |
G |
5: 110,802,790 (GRCm39) |
I214M |
probably benign |
Het |
| Dlg5 |
A |
G |
14: 24,200,716 (GRCm39) |
V1328A |
probably damaging |
Het |
| Dnah2 |
C |
T |
11: 69,326,216 (GRCm39) |
C3639Y |
probably damaging |
Het |
| Dync1i2 |
C |
T |
2: 71,081,326 (GRCm39) |
T511I |
probably benign |
Het |
| Fam220a |
A |
T |
5: 143,549,212 (GRCm39) |
E208V |
probably damaging |
Het |
| Gm4846 |
T |
C |
1: 166,311,594 (GRCm39) |
S422G |
probably benign |
Het |
| Grin2c |
C |
T |
11: 115,141,115 (GRCm39) |
R1001Q |
probably benign |
Het |
| H2-T3 |
T |
C |
17: 36,498,301 (GRCm39) |
E248G |
probably damaging |
Het |
| Idi2 |
T |
C |
13: 9,008,518 (GRCm39) |
V92A |
probably benign |
Het |
| Iqcd |
C |
T |
5: 120,740,571 (GRCm39) |
Q301* |
probably null |
Het |
| Klhl26 |
T |
C |
8: 70,904,974 (GRCm39) |
D278G |
probably damaging |
Het |
| Mok |
G |
T |
12: 110,774,503 (GRCm39) |
T228K |
probably damaging |
Het |
| Otogl |
G |
A |
10: 107,612,978 (GRCm39) |
|
silent |
Het |
| Pabpc1 |
T |
C |
15: 36,606,074 (GRCm39) |
I101V |
probably benign |
Het |
| Ppargc1a |
G |
T |
5: 51,631,562 (GRCm39) |
Q356K |
probably damaging |
Het |
| Ptprt |
T |
A |
2: 161,652,524 (GRCm39) |
D608V |
probably damaging |
Het |
| Rxfp1 |
C |
T |
3: 79,586,054 (GRCm39) |
C96Y |
probably damaging |
Het |
| Scn11a |
A |
C |
9: 119,618,990 (GRCm39) |
V784G |
probably damaging |
Het |
| Septin4 |
T |
C |
11: 87,458,723 (GRCm39) |
S366P |
probably benign |
Het |
| Slc12a8 |
A |
G |
16: 33,410,679 (GRCm39) |
Y226C |
probably damaging |
Het |
| Slc25a33 |
A |
G |
4: 149,846,914 (GRCm39) |
V49A |
possibly damaging |
Het |
| Slc25a45 |
T |
C |
19: 5,934,451 (GRCm39) |
S140P |
probably benign |
Het |
| Slc35e2 |
C |
T |
4: 155,694,483 (GRCm39) |
P10L |
probably benign |
Het |
| Spty2d1 |
G |
T |
7: 46,647,845 (GRCm39) |
N361K |
possibly damaging |
Het |
| Stk4 |
G |
A |
2: 163,941,674 (GRCm39) |
A297T |
probably benign |
Het |
| Thsd7b |
T |
A |
1: 129,688,139 (GRCm39) |
N683K |
probably damaging |
Het |
| Tln2 |
T |
C |
9: 67,299,829 (GRCm39) |
E141G |
probably benign |
Het |
| Tmem125 |
A |
T |
4: 118,399,216 (GRCm39) |
C72S |
probably damaging |
Het |
| Ttn |
G |
T |
2: 76,572,437 (GRCm39) |
T26152K |
probably damaging |
Het |
| Uhrf1 |
G |
A |
17: 56,627,259 (GRCm39) |
G643D |
possibly damaging |
Het |
| Vmn2r50 |
C |
T |
7: 9,774,299 (GRCm39) |
M532I |
possibly damaging |
Het |
|
| Other mutations in Or1e22 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00156:Or1e22
|
APN |
11 |
73,377,398 (GRCm39) |
missense |
probably benign |
0.22 |
|
IGL02867:Or1e22
|
APN |
11 |
73,376,817 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03202:Or1e22
|
APN |
11 |
73,377,351 (GRCm39) |
nonsense |
probably null |
|
|
R0207:Or1e22
|
UTSW |
11 |
73,377,401 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0539:Or1e22
|
UTSW |
11 |
73,376,889 (GRCm39) |
missense |
probably benign |
0.22 |
|
R1469:Or1e22
|
UTSW |
11 |
73,377,149 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R1469:Or1e22
|
UTSW |
11 |
73,377,149 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R1835:Or1e22
|
UTSW |
11 |
73,377,200 (GRCm39) |
missense |
probably benign |
0.08 |
|
R2095:Or1e22
|
UTSW |
11 |
73,377,420 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3612:Or1e22
|
UTSW |
11 |
73,376,766 (GRCm39) |
missense |
probably benign |
0.23 |
|
R3983:Or1e22
|
UTSW |
11 |
73,376,961 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R4959:Or1e22
|
UTSW |
11 |
73,376,893 (GRCm39) |
nonsense |
probably null |
|
|
R4983:Or1e22
|
UTSW |
11 |
73,377,623 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5297:Or1e22
|
UTSW |
11 |
73,377,215 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5447:Or1e22
|
UTSW |
11 |
73,377,002 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5569:Or1e22
|
UTSW |
11 |
73,377,518 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5580:Or1e22
|
UTSW |
11 |
73,377,036 (GRCm39) |
missense |
probably benign |
|
|
R5810:Or1e22
|
UTSW |
11 |
73,376,921 (GRCm39) |
nonsense |
probably null |
|
|
R6974:Or1e22
|
UTSW |
11 |
73,377,299 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7383:Or1e22
|
UTSW |
11 |
73,376,715 (GRCm39) |
makesense |
probably null |
|
|
R7661:Or1e22
|
UTSW |
11 |
73,377,426 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7748:Or1e22
|
UTSW |
11 |
73,376,994 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7913:Or1e22
|
UTSW |
11 |
73,377,224 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9400:Or1e22
|
UTSW |
11 |
73,376,807 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9666:Or1e22
|
UTSW |
11 |
73,376,885 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Z1177:Or1e22
|
UTSW |
11 |
73,376,979 (GRCm39) |
missense |
probably benign |
0.36 |
|
| Predicted Primers |
PCR Primer
(F):5'- TTCAGCATGGGAGTCACCAC -3'
(R):5'- ATGCTGTATTCCATGTTGCAC -3'
Sequencing Primer
(F):5'- GAGTCACCACTGTGTACATCATGG -3'
(R):5'- GCACACTCTACTCTTGGCTAGATTG -3'
|
| Posted On |
2017-01-03 |
Incidental Mutation