Incidental Mutation 'IGL02876:Or1e1f'
| ID |
406212 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or1e1f
|
| Ensembl Gene |
ENSMUSG00000057050 |
| Gene Name |
olfactory receptor family 1 subfamily E member 1F |
| Synonyms |
Olfr397, GA_x6K02T2P1NL-4121434-4122381, MOR135-28 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.093)
|
| Stock # |
IGL02876
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
73855436-73856383 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 73855539 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Phenylalanine
at position 35
(Y35F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150172
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000121280]
[ENSMUST00000213134]
[ENSMUST00000216291]
|
| AlphaFold |
Q8VEZ6 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000121280
AA Change: Y35F
PolyPhen 2
Score 0.946 (Sensitivity: 0.80; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000113870
Gene: ENSMUSG00000057050
AA Change: Y35F
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srsx
|
35 |
305 |
1.3e-6 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
4.3e-35 |
PFAM |
|
Pfam:7tm_4
|
139 |
283 |
1.2e-44 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000213134
AA Change: Y35F
PolyPhen 2
Score 0.946 (Sensitivity: 0.80; Specificity: 0.95)
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000215020
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000216291
AA Change: Y35F
PolyPhen 2
Score 0.946 (Sensitivity: 0.80; Specificity: 0.95)
|
| Coding Region Coverage |
|
| 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 |
|---|
| Aadacl4fm2 |
A |
G |
4: 144,282,343 (GRCm39) |
Y150H |
probably damaging |
Het |
| Abcb5 |
A |
G |
12: 118,883,576 (GRCm39) |
V564A |
probably damaging |
Het |
| Adamts15 |
A |
T |
9: 30,815,818 (GRCm39) |
N679K |
probably damaging |
Het |
| Angpt1 |
T |
G |
15: 42,290,373 (GRCm39) |
D497A |
possibly damaging |
Het |
| Asap2 |
A |
G |
12: 21,308,164 (GRCm39) |
K849R |
probably benign |
Het |
| Aspm |
T |
C |
1: 139,401,391 (GRCm39) |
V1137A |
probably damaging |
Het |
| Atp12a |
A |
G |
14: 56,610,746 (GRCm39) |
I297V |
probably benign |
Het |
| Atp2a2 |
A |
G |
5: 122,604,071 (GRCm39) |
V454A |
probably benign |
Het |
| Carmil1 |
T |
A |
13: 24,338,651 (GRCm39) |
|
probably benign |
Het |
| Csmd2 |
A |
T |
4: 128,215,128 (GRCm39) |
K517* |
probably null |
Het |
| Csmd3 |
A |
T |
15: 47,469,492 (GRCm39) |
|
probably benign |
Het |
| Cyp2d11 |
T |
A |
15: 82,273,697 (GRCm39) |
Q427L |
possibly damaging |
Het |
| Eml5 |
C |
T |
12: 98,825,100 (GRCm39) |
V706M |
probably damaging |
Het |
| Entpd8 |
A |
C |
2: 24,975,072 (GRCm39) |
S428R |
probably benign |
Het |
| Gm10283 |
T |
C |
8: 60,954,253 (GRCm39) |
|
probably benign |
Het |
| Gpatch3 |
T |
A |
4: 133,307,995 (GRCm39) |
V363E |
probably damaging |
Het |
| Hoxb5 |
T |
A |
11: 96,194,594 (GRCm39) |
M52K |
probably damaging |
Het |
| Ift52 |
T |
C |
2: 162,878,627 (GRCm39) |
V307A |
probably benign |
Het |
| Igkv1-115 |
T |
C |
6: 68,138,424 (GRCm39) |
|
noncoding transcript |
Het |
| Kdm5a |
T |
C |
6: 120,367,605 (GRCm39) |
|
probably benign |
Het |
| Lama1 |
T |
A |
17: 68,057,687 (GRCm39) |
|
probably null |
Het |
| Lrp6 |
G |
A |
6: 134,433,077 (GRCm39) |
P1418L |
probably benign |
Het |
| Mill2 |
T |
C |
7: 18,590,432 (GRCm39) |
F156L |
probably damaging |
Het |
| Mnat1 |
A |
G |
12: 73,217,378 (GRCm39) |
R85G |
probably damaging |
Het |
| Myrip |
A |
T |
9: 120,261,740 (GRCm39) |
D451V |
probably damaging |
Het |
| Pdzph1 |
C |
A |
17: 59,281,064 (GRCm39) |
S406I |
probably benign |
Het |
| Ptprb |
A |
G |
10: 116,184,116 (GRCm39) |
|
probably benign |
Het |
| Rxfp4 |
T |
A |
3: 88,559,742 (GRCm39) |
R236S |
possibly damaging |
Het |
| Ryr2 |
T |
C |
13: 11,722,679 (GRCm39) |
M2604V |
probably benign |
Het |
| Setd1a |
G |
A |
7: 127,377,673 (GRCm39) |
|
probably benign |
Het |
| Spata33 |
A |
T |
8: 123,948,719 (GRCm39) |
H88L |
probably damaging |
Het |
| Spcs3 |
A |
T |
8: 54,979,486 (GRCm39) |
N98K |
probably damaging |
Het |
| Srgap3 |
A |
G |
6: 112,748,414 (GRCm39) |
S413P |
probably damaging |
Het |
| Stap2 |
T |
C |
17: 56,306,961 (GRCm39) |
R239G |
probably benign |
Het |
| Surf6 |
A |
G |
2: 26,782,638 (GRCm39) |
Y230H |
probably damaging |
Het |
| Tasp1 |
C |
T |
2: 139,676,283 (GRCm39) |
V382M |
probably benign |
Het |
| Tnc |
G |
T |
4: 63,933,338 (GRCm39) |
A642E |
possibly damaging |
Het |
| Vmn1r202 |
G |
A |
13: 22,685,640 (GRCm39) |
T259I |
probably benign |
Het |
| Vmn2r110 |
T |
A |
17: 20,794,558 (GRCm39) |
T704S |
probably damaging |
Het |
| Vtcn1 |
A |
T |
3: 100,791,145 (GRCm39) |
D61V |
probably damaging |
Het |
| Zc3h12d |
G |
A |
10: 7,738,364 (GRCm39) |
M223I |
probably damaging |
Het |
| Zfp592 |
T |
A |
7: 80,687,875 (GRCm39) |
S934T |
probably benign |
Het |
|
| Other mutations in Or1e1f |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01797:Or1e1f
|
APN |
11 |
73,855,644 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01839:Or1e1f
|
APN |
11 |
73,855,437 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
IGL02247:Or1e1f
|
APN |
11 |
73,855,688 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL03051:Or1e1f
|
APN |
11 |
73,855,860 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL03123:Or1e1f
|
APN |
11 |
73,855,812 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03401:Or1e1f
|
APN |
11 |
73,856,388 (GRCm39) |
utr 3 prime |
probably benign |
|
|
3-1:Or1e1f
|
UTSW |
11 |
73,855,803 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R0496:Or1e1f
|
UTSW |
11 |
73,855,706 (GRCm39) |
missense |
probably benign |
0.42 |
|
R0811:Or1e1f
|
UTSW |
11 |
73,856,246 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0812:Or1e1f
|
UTSW |
11 |
73,856,246 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1503:Or1e1f
|
UTSW |
11 |
73,855,394 (GRCm39) |
utr 5 prime |
probably null |
|
|
R2067:Or1e1f
|
UTSW |
11 |
73,855,740 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2111:Or1e1f
|
UTSW |
11 |
73,855,740 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4912:Or1e1f
|
UTSW |
11 |
73,856,166 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5240:Or1e1f
|
UTSW |
11 |
73,855,632 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5656:Or1e1f
|
UTSW |
11 |
73,855,536 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5801:Or1e1f
|
UTSW |
11 |
73,855,772 (GRCm39) |
missense |
probably benign |
0.39 |
|
R6329:Or1e1f
|
UTSW |
11 |
73,855,568 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R6720:Or1e1f
|
UTSW |
11 |
73,856,291 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7149:Or1e1f
|
UTSW |
11 |
73,856,257 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7283:Or1e1f
|
UTSW |
11 |
73,855,634 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8194:Or1e1f
|
UTSW |
11 |
73,856,240 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8466:Or1e1f
|
UTSW |
11 |
73,855,913 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8472:Or1e1f
|
UTSW |
11 |
73,856,223 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R8882:Or1e1f
|
UTSW |
11 |
73,855,940 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9256:Or1e1f
|
UTSW |
11 |
73,856,135 (GRCm39) |
missense |
probably benign |
0.18 |
|
Z1176:Or1e1f
|
UTSW |
11 |
73,856,123 (GRCm39) |
frame shift |
probably null |
|
|
Z1177:Or1e1f
|
UTSW |
11 |
73,855,586 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2016-08-02 |
Incidental Mutation