Incidental Mutation 'IGL01614:Or1o1'
ID |
92312 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Or1o1
|
Ensembl Gene |
ENSMUSG00000063188 |
Gene Name |
olfactory receptor family 1 subfamily O member 1 |
Synonyms |
MOR156-3, GA_x6K02T2PSCP-1867165-1868094, Olfr107 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.051)
|
Stock # |
IGL01614
|
Quality Score |
|
Status
|
|
Chromosome |
17 |
Chromosomal Location |
37716368-37717400 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 37716529 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Tyrosine
at position 30
(C30Y)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000148879
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077008]
[ENSMUST00000215894]
[ENSMUST00000215947]
[ENSMUST00000215974]
[ENSMUST00000216844]
|
AlphaFold |
Q7TRK4 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000077008
AA Change: C30Y
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
SMART Domains |
Protein: ENSMUSP00000076267 Gene: ENSMUSG00000063188 AA Change: C30Y
Domain | Start | End | E-Value | Type |
Pfam:7tm_4
|
28 |
305 |
1.3e-54 |
PFAM |
Pfam:7TM_GPCR_Srsx
|
32 |
302 |
1.3e-5 |
PFAM |
Pfam:7tm_1
|
38 |
287 |
3.7e-19 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000174238
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000215894
AA Change: C30Y
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000215947
AA Change: C30Y
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000215974
AA Change: C30Y
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000216844
AA Change: C30Y
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
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: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrf5 |
T |
A |
17: 43,735,362 (GRCm39) |
S143T |
possibly damaging |
Het |
Arhgap32 |
G |
T |
9: 32,171,801 (GRCm39) |
S1527I |
probably damaging |
Het |
Atp8a2 |
A |
G |
14: 60,282,437 (GRCm39) |
V128A |
probably damaging |
Het |
Bpi |
T |
C |
2: 158,113,866 (GRCm39) |
F255L |
probably damaging |
Het |
Clptm1 |
A |
T |
7: 19,371,625 (GRCm39) |
D269E |
probably benign |
Het |
Cyria |
T |
C |
12: 12,411,574 (GRCm39) |
|
probably null |
Het |
E2f7 |
T |
C |
10: 110,595,839 (GRCm39) |
V63A |
probably damaging |
Het |
Eif4e1b |
T |
A |
13: 54,934,729 (GRCm39) |
I184N |
probably damaging |
Het |
Gal3st1 |
T |
A |
11: 3,948,996 (GRCm39) |
L401Q |
probably damaging |
Het |
Gm7808 |
G |
A |
9: 19,839,442 (GRCm39) |
|
probably benign |
Het |
Hdac5 |
G |
A |
11: 102,090,854 (GRCm39) |
T741I |
probably benign |
Het |
Ipo5 |
A |
G |
14: 121,172,507 (GRCm39) |
T522A |
probably benign |
Het |
Lama5 |
A |
C |
2: 179,822,657 (GRCm39) |
F2832V |
probably damaging |
Het |
Ltk |
A |
C |
2: 119,583,968 (GRCm39) |
L230R |
probably damaging |
Het |
Mettl14 |
A |
T |
3: 123,167,609 (GRCm39) |
|
probably benign |
Het |
Myom1 |
T |
C |
17: 71,433,173 (GRCm39) |
F1507L |
possibly damaging |
Het |
Nsd3 |
T |
A |
8: 26,156,095 (GRCm39) |
I554K |
possibly damaging |
Het |
Or1j12 |
T |
G |
2: 36,342,636 (GRCm39) |
I13S |
probably benign |
Het |
Or51a43 |
C |
T |
7: 103,717,576 (GRCm39) |
V221I |
probably benign |
Het |
Or8u9 |
A |
T |
2: 86,001,741 (GRCm39) |
I140N |
possibly damaging |
Het |
Prr14 |
T |
A |
7: 127,074,305 (GRCm39) |
L279H |
probably damaging |
Het |
Rbm25 |
G |
T |
12: 83,706,341 (GRCm39) |
D229Y |
probably damaging |
Het |
Sdk2 |
T |
C |
11: 113,684,684 (GRCm39) |
K1926E |
probably damaging |
Het |
Slc25a23 |
C |
T |
17: 57,352,579 (GRCm39) |
R435Q |
probably null |
Het |
Srebf2 |
A |
G |
15: 82,063,054 (GRCm39) |
N457S |
probably benign |
Het |
Stac2 |
T |
C |
11: 97,943,774 (GRCm39) |
D12G |
probably benign |
Het |
Tal1 |
A |
C |
4: 114,920,325 (GRCm39) |
|
probably null |
Het |
Usp25 |
G |
A |
16: 76,874,005 (GRCm39) |
R527Q |
probably damaging |
Het |
|
Other mutations in Or1o1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01323:Or1o1
|
APN |
17 |
37,717,031 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02390:Or1o1
|
APN |
17 |
37,716,986 (GRCm39) |
missense |
probably benign |
0.04 |
R1051:Or1o1
|
UTSW |
17 |
37,717,341 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4767:Or1o1
|
UTSW |
17 |
37,717,091 (GRCm39) |
nonsense |
probably null |
|
R4849:Or1o1
|
UTSW |
17 |
37,716,589 (GRCm39) |
missense |
probably benign |
0.16 |
R6182:Or1o1
|
UTSW |
17 |
37,716,883 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6550:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
R6551:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
R6552:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
R6555:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
R6584:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
R6586:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
R6588:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
R6688:Or1o1
|
UTSW |
17 |
37,716,796 (GRCm39) |
missense |
probably benign |
0.30 |
R6758:Or1o1
|
UTSW |
17 |
37,716,586 (GRCm39) |
missense |
probably damaging |
0.97 |
R7024:Or1o1
|
UTSW |
17 |
37,717,095 (GRCm39) |
missense |
probably benign |
0.04 |
R7083:Or1o1
|
UTSW |
17 |
37,717,063 (GRCm39) |
missense |
probably benign |
0.00 |
R8350:Or1o1
|
UTSW |
17 |
37,717,260 (GRCm39) |
missense |
probably benign |
0.00 |
|
Posted On |
2013-12-09 |