Incidental Mutation 'IGL01919:Or1l8'
| ID |
180055 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or1l8
|
| Ensembl Gene |
ENSMUSG00000075380 |
| Gene Name |
olfactory receptor family 1 subfamily L member 8 |
| Synonyms |
Olfr355, MOR138-2, GA_x6K02T2NLDC-33622642-33621710 |
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.422)
|
| Stock # |
IGL01919
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
36817192-36818124 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
G to A
at 36817824 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamine to Stop codon
at position 101
(Q101*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151206
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000100147]
[ENSMUST00000213574]
|
| AlphaFold |
Q8VFP6 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000100147
AA Change: Q101*
|
| SMART Domains |
Protein: ENSMUSP00000097725
Gene: ENSMUSG00000075380
AA Change: Q101*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
32 |
308 |
2.9e-55 |
PFAM |
|
Pfam:7tm_1
|
42 |
290 |
2.2e-26 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000213574
AA Change: Q101*
|
| 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: 35 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2700062C07Rik |
A |
G |
18: 24,608,580 (GRCm39) |
|
probably null |
Het |
| Alms1 |
T |
C |
6: 85,604,986 (GRCm39) |
F2212S |
possibly damaging |
Het |
| Anpep |
T |
C |
7: 79,475,098 (GRCm39) |
I155V |
possibly damaging |
Het |
| Aoc1 |
G |
A |
6: 48,885,223 (GRCm39) |
V653M |
probably damaging |
Het |
| Arl8b |
T |
C |
6: 108,798,518 (GRCm39) |
|
probably benign |
Het |
| Bax |
A |
C |
7: 45,115,552 (GRCm39) |
|
probably null |
Het |
| Cpne7 |
G |
A |
8: 123,852,382 (GRCm39) |
E195K |
probably damaging |
Het |
| Csmd3 |
A |
G |
15: 47,539,168 (GRCm39) |
I2330T |
possibly damaging |
Het |
| Dnajc16 |
A |
G |
4: 141,501,940 (GRCm39) |
S297P |
probably benign |
Het |
| Farp2 |
A |
G |
1: 93,504,155 (GRCm39) |
K311E |
probably damaging |
Het |
| Fhad1 |
A |
G |
4: 141,691,906 (GRCm39) |
L410P |
probably damaging |
Het |
| Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
| Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
| Gm12185 |
T |
C |
11: 48,798,886 (GRCm39) |
T536A |
possibly damaging |
Het |
| Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
| Hydin |
C |
T |
8: 111,245,806 (GRCm39) |
T2173I |
possibly damaging |
Het |
| Kpnb1 |
A |
G |
11: 97,055,556 (GRCm39) |
V783A |
probably benign |
Het |
| Krt1 |
A |
G |
15: 101,754,811 (GRCm39) |
V509A |
unknown |
Het |
| Lrwd1 |
A |
T |
5: 136,164,729 (GRCm39) |
L26* |
probably null |
Het |
| Mal2 |
T |
A |
15: 54,451,728 (GRCm39) |
W50R |
probably damaging |
Het |
| Map3k21 |
A |
T |
8: 126,668,871 (GRCm39) |
E819V |
probably damaging |
Het |
| Mrgprx3-ps |
T |
C |
7: 46,959,959 (GRCm39) |
T11A |
probably benign |
Het |
| Mroh2b |
T |
C |
15: 4,953,170 (GRCm39) |
F635L |
probably benign |
Het |
| Mylip |
G |
A |
13: 45,562,178 (GRCm39) |
E327K |
probably damaging |
Het |
| Nfix |
T |
C |
8: 85,453,103 (GRCm39) |
D308G |
probably damaging |
Het |
| Or7e166 |
G |
A |
9: 19,624,638 (GRCm39) |
V172I |
probably benign |
Het |
| Psma6 |
A |
G |
12: 55,454,254 (GRCm39) |
E26G |
probably damaging |
Het |
| Rgs16 |
T |
A |
1: 153,617,804 (GRCm39) |
S105T |
probably damaging |
Het |
| Slc25a23 |
T |
A |
17: 57,354,291 (GRCm39) |
N372Y |
possibly damaging |
Het |
| Slc35e2 |
A |
G |
4: 155,697,187 (GRCm39) |
M234V |
probably benign |
Het |
| Tbc1d8 |
A |
G |
1: 39,431,334 (GRCm39) |
V346A |
probably damaging |
Het |
| Tgfb1i1 |
C |
T |
7: 127,847,654 (GRCm39) |
|
probably benign |
Het |
| Triml2 |
A |
C |
8: 43,643,349 (GRCm39) |
T177P |
probably damaging |
Het |
| Uba6 |
T |
C |
5: 86,267,245 (GRCm39) |
T959A |
probably benign |
Het |
| Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
|
| Other mutations in Or1l8 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02523:Or1l8
|
APN |
2 |
36,817,967 (GRCm39) |
missense |
probably damaging |
0.99 |
|
BB002:Or1l8
|
UTSW |
2 |
36,817,371 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
BB012:Or1l8
|
UTSW |
2 |
36,817,371 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
IGL03050:Or1l8
|
UTSW |
2 |
36,817,820 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0458:Or1l8
|
UTSW |
2 |
36,817,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1019:Or1l8
|
UTSW |
2 |
36,817,764 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1115:Or1l8
|
UTSW |
2 |
36,817,514 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R1460:Or1l8
|
UTSW |
2 |
36,817,820 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1663:Or1l8
|
UTSW |
2 |
36,817,346 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1902:Or1l8
|
UTSW |
2 |
36,817,197 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2964:Or1l8
|
UTSW |
2 |
36,817,419 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4751:Or1l8
|
UTSW |
2 |
36,817,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4884:Or1l8
|
UTSW |
2 |
36,818,024 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R4935:Or1l8
|
UTSW |
2 |
36,817,713 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6114:Or1l8
|
UTSW |
2 |
36,817,701 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6184:Or1l8
|
UTSW |
2 |
36,817,404 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6476:Or1l8
|
UTSW |
2 |
36,817,595 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R7167:Or1l8
|
UTSW |
2 |
36,817,533 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7323:Or1l8
|
UTSW |
2 |
36,817,986 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7539:Or1l8
|
UTSW |
2 |
36,817,221 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7925:Or1l8
|
UTSW |
2 |
36,817,371 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R8284:Or1l8
|
UTSW |
2 |
36,818,018 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9786:Or1l8
|
UTSW |
2 |
36,817,416 (GRCm39) |
nonsense |
probably null |
|
|
X0025:Or1l8
|
UTSW |
2 |
36,817,962 (GRCm39) |
missense |
probably benign |
0.33 |
|
| Posted On |
2014-05-07 |
Incidental Mutation