Incidental Mutation 'R4033:Or51e1'
| ID |
313583 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or51e1
|
| Ensembl Gene |
ENSMUSG00000070423 |
| Gene Name |
olfactory receptor family 51 subfamily E member 1 |
| Synonyms |
GA_x6K02T2PBJ9-5425951-5426904, MOR18-1, Olfr558 |
| MMRRC Submission |
040961-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.074)
|
| Stock # |
R4033 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
7 |
| Chromosomal Location |
102351530-102361261 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 102358697 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Isoleucine
at position 77
(T77I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000091674
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000084817]
[ENSMUST00000094124]
[ENSMUST00000216312]
|
| AlphaFold |
Q8VGZ7 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000084817
|
| SMART Domains |
Protein: ENSMUSP00000081877
Gene: ENSMUSG00000066273
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
37 |
317 |
2.1e-117 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
41 |
211 |
7.5e-11 |
PFAM |
|
Pfam:7tm_1
|
47 |
299 |
2.4e-19 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000094124
AA Change: T77I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000091674
Gene: ENSMUSG00000070423
AA Change: T77I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
33 |
311 |
6.2e-117 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
37 |
308 |
2.4e-7 |
PFAM |
|
Pfam:7tm_1
|
43 |
293 |
2.4e-19 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000210002
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000216312
|
| Meta Mutation Damage Score |
0.1744 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.2%
|
| Validation Efficiency |
100% (47/47) |
| 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: 44 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam34l |
C |
G |
8: 44,079,710 (GRCm39) |
M171I |
probably benign |
Het |
| Als2 |
G |
T |
1: 59,235,400 (GRCm39) |
S761R |
probably benign |
Het |
| Ankrd63 |
C |
A |
2: 118,533,412 (GRCm39) |
|
probably benign |
Het |
| Brf1 |
G |
A |
12: 112,943,352 (GRCm39) |
T166M |
probably damaging |
Het |
| Car9 |
T |
C |
4: 43,508,624 (GRCm39) |
V131A |
possibly damaging |
Het |
| Cerk |
T |
G |
15: 86,039,228 (GRCm39) |
H221P |
possibly damaging |
Het |
| Cfap69 |
A |
T |
5: 5,654,389 (GRCm39) |
I458N |
possibly damaging |
Het |
| Chil4 |
T |
C |
3: 106,121,765 (GRCm39) |
Y28C |
probably damaging |
Het |
| Cracd |
A |
G |
5: 77,006,312 (GRCm39) |
N891S |
unknown |
Het |
| Dmxl1 |
A |
G |
18: 49,984,498 (GRCm39) |
T165A |
possibly damaging |
Het |
| Erich6b |
A |
T |
14: 75,896,207 (GRCm39) |
N31I |
probably benign |
Het |
| Fgf17 |
G |
T |
14: 70,878,966 (GRCm39) |
|
probably benign |
Het |
| Fhit |
A |
T |
14: 10,751,671 (GRCm38) |
|
probably benign |
Het |
| Fnip1 |
A |
T |
11: 54,393,297 (GRCm39) |
I578L |
probably benign |
Het |
| Gm17641 |
C |
T |
3: 68,777,146 (GRCm39) |
R36W |
probably damaging |
Het |
| Gprin2 |
A |
T |
14: 33,916,635 (GRCm39) |
D378E |
probably benign |
Het |
| Grhl3 |
T |
A |
4: 135,300,735 (GRCm39) |
M1L |
probably benign |
Het |
| Hsp90aa1 |
T |
A |
12: 110,662,114 (GRCm39) |
M1L |
possibly damaging |
Het |
| Hsp90aa1 |
C |
A |
12: 110,662,115 (GRCm39) |
|
probably null |
Het |
| Ifih1 |
G |
A |
2: 62,465,534 (GRCm39) |
S212L |
probably benign |
Het |
| Iqck |
T |
C |
7: 118,540,827 (GRCm39) |
I242T |
probably damaging |
Het |
| Kalrn |
C |
T |
16: 33,810,180 (GRCm39) |
D2525N |
possibly damaging |
Het |
| Lsm14b |
A |
G |
2: 179,673,309 (GRCm39) |
K195E |
probably benign |
Het |
| Mical1 |
G |
A |
10: 41,357,172 (GRCm39) |
V326I |
probably benign |
Het |
| Mtnr1b |
A |
T |
9: 15,774,830 (GRCm39) |
N76K |
probably damaging |
Het |
| Nalcn |
T |
C |
14: 123,837,401 (GRCm39) |
|
probably benign |
Het |
| Nop14 |
T |
C |
5: 34,807,861 (GRCm39) |
D367G |
probably benign |
Het |
| Nrxn3 |
T |
C |
12: 89,499,771 (GRCm39) |
C721R |
probably damaging |
Het |
| Prr27 |
G |
T |
5: 87,991,164 (GRCm39) |
E259* |
probably null |
Het |
| Psmg3 |
G |
A |
5: 139,812,086 (GRCm39) |
P5S |
probably damaging |
Het |
| Pxdn |
A |
G |
12: 30,053,224 (GRCm39) |
T1134A |
probably benign |
Het |
| Rbm28 |
T |
C |
6: 29,159,668 (GRCm39) |
N120S |
probably damaging |
Het |
| Reg3b |
A |
T |
6: 78,350,192 (GRCm39) |
K157N |
possibly damaging |
Het |
| Rlf |
T |
G |
4: 121,004,540 (GRCm39) |
Q1480P |
probably damaging |
Het |
| Slc16a12 |
A |
T |
19: 34,652,567 (GRCm39) |
L193Q |
probably damaging |
Het |
| Smo |
G |
A |
6: 29,759,917 (GRCm39) |
R672H |
probably damaging |
Het |
| Smyd4 |
A |
G |
11: 75,240,580 (GRCm39) |
D25G |
probably benign |
Het |
| Sorbs2 |
C |
G |
8: 46,228,632 (GRCm39) |
D264E |
probably damaging |
Het |
| Tctn3 |
G |
T |
19: 40,585,767 (GRCm39) |
Q593K |
probably benign |
Het |
| Tdrd9 |
A |
T |
12: 111,958,973 (GRCm39) |
I136L |
possibly damaging |
Het |
| Tshz3 |
G |
A |
7: 36,470,009 (GRCm39) |
S666N |
possibly damaging |
Het |
| Ubn1 |
C |
T |
16: 4,882,475 (GRCm39) |
T69M |
probably damaging |
Het |
| Unk |
A |
T |
11: 115,944,353 (GRCm39) |
H368L |
probably benign |
Het |
| Zan |
A |
T |
5: 137,436,122 (GRCm39) |
L2051* |
probably null |
Het |
|
| Other mutations in Or51e1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01670:Or51e1
|
APN |
7 |
102,358,772 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01925:Or51e1
|
APN |
7 |
102,359,410 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02172:Or51e1
|
APN |
7 |
102,359,051 (GRCm39) |
missense |
probably benign |
|
|
R0197:Or51e1
|
UTSW |
7 |
102,359,202 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0883:Or51e1
|
UTSW |
7 |
102,359,202 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1870:Or51e1
|
UTSW |
7 |
102,358,961 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R2894:Or51e1
|
UTSW |
7 |
102,358,882 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4695:Or51e1
|
UTSW |
7 |
102,358,764 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4738:Or51e1
|
UTSW |
7 |
102,359,378 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4739:Or51e1
|
UTSW |
7 |
102,359,378 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4740:Or51e1
|
UTSW |
7 |
102,359,378 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4901:Or51e1
|
UTSW |
7 |
102,359,405 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5187:Or51e1
|
UTSW |
7 |
102,358,868 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5385:Or51e1
|
UTSW |
7 |
102,358,553 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5529:Or51e1
|
UTSW |
7 |
102,358,900 (GRCm39) |
nonsense |
probably null |
|
|
R6666:Or51e1
|
UTSW |
7 |
102,359,135 (GRCm39) |
splice site |
probably null |
|
|
R7318:Or51e1
|
UTSW |
7 |
102,359,226 (GRCm39) |
nonsense |
probably null |
|
|
R7453:Or51e1
|
UTSW |
7 |
102,358,724 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7546:Or51e1
|
UTSW |
7 |
102,358,996 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7643:Or51e1
|
UTSW |
7 |
102,358,745 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8387:Or51e1
|
UTSW |
7 |
102,359,402 (GRCm39) |
missense |
probably benign |
|
|
R8984:Or51e1
|
UTSW |
7 |
102,359,219 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R9154:Or51e1
|
UTSW |
7 |
102,358,541 (GRCm39) |
missense |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- CAATGAATCCAGTGCCACATATTTC -3'
(R):5'- AGGCAATGTCAGCACAGTGG -3'
Sequencing Primer
(F):5'- CATCTTAATAGGCCTTCCAGGATTGG -3'
(R):5'- ATGTCAGCACAGTGGCATGC -3'
|
| Posted On |
2015-04-30 |
Incidental Mutation