Incidental Mutation 'R1356:Or8g18'
| ID |
156326 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or8g18
|
| Ensembl Gene |
ENSMUSG00000096109 |
| Gene Name |
olfactory receptor family 8 subfamily G member 18 |
| Synonyms |
MOR171-41P, Olfr1537-ps1, Olfr144, GA_x6K02T2PVTD-32935684-32934749, MOR171-32P, K4, MOR171-32P, Olfr1537 |
| MMRRC Submission |
039421-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.102)
|
| Stock # |
R1356 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
9 |
| Chromosomal Location |
39148783-39149727 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to C
at 39149547 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Proline to Alanine
at position 58
(P58A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149992
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000073248]
[ENSMUST00000213472]
|
| AlphaFold |
P34983 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000073248
AA Change: P61A
PolyPhen 2
Score 0.277 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000072979
Gene: ENSMUSG00000096109
AA Change: P61A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
34 |
311 |
2.4e-51 |
PFAM |
|
Pfam:7tm_1
|
44 |
293 |
1.1e-20 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213472
AA Change: P58A
PolyPhen 2
Score 0.391 (Sensitivity: 0.90; Specificity: 0.89)
|
| Meta Mutation Damage Score |
0.0728 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.2%
- 20x: 92.7%
|
| Validation Efficiency |
100% (34/34) |
| 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: 31 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca12 |
A |
G |
1: 71,342,112 (GRCm39) |
|
probably benign |
Het |
| Adam18 |
A |
G |
8: 25,158,611 (GRCm39) |
|
probably benign |
Het |
| Cd274 |
C |
A |
19: 29,350,970 (GRCm39) |
T22K |
possibly damaging |
Het |
| Cfap45 |
G |
A |
1: 172,355,430 (GRCm39) |
R26Q |
possibly damaging |
Het |
| Dvl3 |
AGCGGCGGCGGCGG |
AGCGGCGGCGG |
16: 20,343,055 (GRCm39) |
|
probably benign |
Het |
| E2f8 |
A |
G |
7: 48,530,018 (GRCm39) |
|
probably benign |
Het |
| Ercc4 |
A |
G |
16: 12,943,146 (GRCm39) |
H255R |
probably damaging |
Het |
| Fam227b |
C |
T |
2: 125,960,928 (GRCm39) |
D234N |
probably damaging |
Het |
| Foxp1 |
A |
T |
6: 98,993,637 (GRCm39) |
|
probably benign |
Het |
| Fsip2 |
T |
A |
2: 82,820,089 (GRCm39) |
V5274D |
probably benign |
Het |
| Gm21718 |
A |
G |
14: 51,554,104 (GRCm39) |
|
noncoding transcript |
Het |
| Gpr85 |
G |
A |
6: 13,836,146 (GRCm39) |
P253S |
probably benign |
Het |
| Grm7 |
A |
T |
6: 111,335,985 (GRCm39) |
I799F |
probably damaging |
Het |
| Inpp1 |
A |
G |
1: 52,836,215 (GRCm39) |
F84L |
possibly damaging |
Het |
| Kprp |
T |
A |
3: 92,732,909 (GRCm39) |
E47V |
probably damaging |
Het |
| Krt9 |
CTGC |
CTGCNNNNNNNNNNNNNNNNNNNNNTGC |
11: 100,079,640 (GRCm39) |
|
probably benign |
Het |
| Lama3 |
G |
A |
18: 12,633,634 (GRCm39) |
|
probably benign |
Het |
| Lurap1l |
C |
G |
4: 80,829,767 (GRCm39) |
A59G |
probably benign |
Het |
| Macc1 |
A |
T |
12: 119,410,290 (GRCm39) |
T353S |
probably benign |
Het |
| Mctp2 |
A |
G |
7: 71,814,471 (GRCm39) |
|
probably benign |
Het |
| Mdn1 |
T |
C |
4: 32,700,334 (GRCm39) |
|
probably benign |
Het |
| Mpeg1 |
T |
A |
19: 12,438,689 (GRCm39) |
V49D |
probably damaging |
Het |
| Nos2 |
C |
T |
11: 78,843,629 (GRCm39) |
P859S |
probably benign |
Het |
| Parn |
A |
T |
16: 13,468,538 (GRCm39) |
Y214* |
probably null |
Het |
| Pibf1 |
A |
G |
14: 99,374,632 (GRCm39) |
E357G |
possibly damaging |
Het |
| Prex2 |
C |
T |
1: 11,150,316 (GRCm39) |
Q163* |
probably null |
Het |
| Prune2 |
T |
A |
19: 17,189,681 (GRCm39) |
S294T |
probably benign |
Het |
| Slc46a1 |
A |
G |
11: 78,361,550 (GRCm39) |
N399D |
probably benign |
Het |
| Sstr2 |
T |
C |
11: 113,515,720 (GRCm39) |
F213S |
probably damaging |
Het |
| Tnxb |
A |
G |
17: 34,914,446 (GRCm39) |
E1967G |
possibly damaging |
Het |
| Vmn2r59 |
A |
G |
7: 41,661,218 (GRCm39) |
*866Q |
probably null |
Het |
|
| Other mutations in Or8g18 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00981:Or8g18
|
APN |
9 |
39,148,901 (GRCm39) |
missense |
probably benign |
0.25 |
|
IGL01691:Or8g18
|
APN |
9 |
39,149,315 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02606:Or8g18
|
APN |
9 |
39,149,490 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02656:Or8g18
|
APN |
9 |
39,149,456 (GRCm39) |
missense |
probably benign |
0.13 |
|
R0133:Or8g18
|
UTSW |
9 |
39,149,307 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0548:Or8g18
|
UTSW |
9 |
39,149,667 (GRCm39) |
missense |
probably benign |
0.13 |
|
R0558:Or8g18
|
UTSW |
9 |
39,149,496 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0616:Or8g18
|
UTSW |
9 |
39,148,946 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0626:Or8g18
|
UTSW |
9 |
39,149,162 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R0826:Or8g18
|
UTSW |
9 |
39,149,725 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
|
R0839:Or8g18
|
UTSW |
9 |
39,149,146 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R1074:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1224:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1226:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1252:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1256:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1355:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1416:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1499:Or8g18
|
UTSW |
9 |
39,149,547 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1658:Or8g18
|
UTSW |
9 |
39,149,255 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1815:Or8g18
|
UTSW |
9 |
39,149,286 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2198:Or8g18
|
UTSW |
9 |
39,149,048 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R4178:Or8g18
|
UTSW |
9 |
39,149,375 (GRCm39) |
nonsense |
probably null |
|
|
R5112:Or8g18
|
UTSW |
9 |
39,149,717 (GRCm39) |
start codon destroyed |
probably null |
0.94 |
|
R6251:Or8g18
|
UTSW |
9 |
39,149,514 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6850:Or8g18
|
UTSW |
9 |
39,149,271 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7032:Or8g18
|
UTSW |
9 |
39,148,983 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R7573:Or8g18
|
UTSW |
9 |
39,148,977 (GRCm39) |
missense |
probably benign |
0.42 |
|
R7715:Or8g18
|
UTSW |
9 |
39,149,174 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7722:Or8g18
|
UTSW |
9 |
39,148,885 (GRCm39) |
nonsense |
probably null |
|
|
R7729:Or8g18
|
UTSW |
9 |
39,149,546 (GRCm39) |
missense |
probably benign |
0.28 |
|
R8710:Or8g18
|
UTSW |
9 |
39,149,306 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9513:Or8g18
|
UTSW |
9 |
39,149,625 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9515:Or8g18
|
UTSW |
9 |
39,149,625 (GRCm39) |
missense |
probably benign |
0.05 |
|
| Predicted Primers |
PCR Primer
(F):5'- AACTTGCCCTCCCTGGAGTGAATG -3'
(R):5'- GGAAACCACTGCACAGTGACTGAG -3'
Sequencing Primer
(F):5'- ACATATCGGTCATAGGCCATTGC -3'
(R):5'- ACAGTGACTGAGTTCTTCTTAGC -3'
|
| Posted On |
2014-02-11 |
Incidental Mutation