Incidental Mutation 'R1658:Or8g18'
| ID |
186536 |
| 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 |
039694-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.102)
|
| Stock # |
R1658 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
39148783-39149727 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 39149255 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Tyrosine
at position 155
(C155Y)
|
| 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: C158Y
PolyPhen 2
Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
|
| SMART Domains |
Protein: ENSMUSP00000072979
Gene: ENSMUSG00000096109
AA Change: C158Y
| 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: C155Y
PolyPhen 2
Score 0.033 (Sensitivity: 0.95; Specificity: 0.82)
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.4%
- 20x: 92.8%
|
| 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: 54 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgrd1 |
T |
G |
5: 129,255,164 (GRCm39) |
S604A |
probably benign |
Het |
| Apbb1 |
G |
A |
7: 105,223,291 (GRCm39) |
P107S |
probably damaging |
Het |
| Baz2a |
T |
A |
10: 127,960,252 (GRCm39) |
M1489K |
probably benign |
Het |
| Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
| Cdca2 |
A |
G |
14: 67,915,148 (GRCm39) |
S704P |
possibly damaging |
Het |
| Cemip2 |
T |
C |
19: 21,779,243 (GRCm39) |
V351A |
probably damaging |
Het |
| Chfr |
T |
C |
5: 110,301,035 (GRCm39) |
I312T |
probably damaging |
Het |
| Csmd1 |
A |
G |
8: 16,131,739 (GRCm39) |
V1662A |
possibly damaging |
Het |
| Dgkd |
T |
A |
1: 87,853,990 (GRCm39) |
L611Q |
probably damaging |
Het |
| Dicer1 |
A |
G |
12: 104,666,673 (GRCm39) |
V1376A |
probably benign |
Het |
| Elp2 |
C |
T |
18: 24,750,470 (GRCm39) |
T269M |
probably benign |
Het |
| Ephb6 |
T |
A |
6: 41,591,179 (GRCm39) |
V112E |
probably damaging |
Het |
| Fbxo11 |
A |
T |
17: 88,320,086 (GRCm39) |
Y209N |
probably benign |
Het |
| Frem1 |
C |
T |
4: 82,920,045 (GRCm39) |
R437Q |
probably damaging |
Het |
| G6pc2 |
A |
T |
2: 69,057,413 (GRCm39) |
K353M |
probably damaging |
Het |
| Gabbr1 |
A |
G |
17: 37,358,399 (GRCm39) |
T46A |
probably damaging |
Het |
| Gbp9 |
T |
A |
5: 105,242,334 (GRCm39) |
Q135L |
probably damaging |
Het |
| Gstp1 |
A |
T |
19: 4,087,375 (GRCm39) |
M20K |
probably damaging |
Het |
| Heatr6 |
A |
G |
11: 83,649,193 (GRCm39) |
R183G |
probably damaging |
Het |
| Ints11 |
A |
G |
4: 155,972,185 (GRCm39) |
K397E |
probably damaging |
Het |
| Intu |
A |
G |
3: 40,647,211 (GRCm39) |
T695A |
probably benign |
Het |
| Kif21b |
T |
C |
1: 136,099,023 (GRCm39) |
V1437A |
probably damaging |
Het |
| Klhl24 |
T |
A |
16: 19,925,842 (GRCm39) |
Y123* |
probably null |
Het |
| Lipm |
C |
T |
19: 34,093,847 (GRCm39) |
L255F |
probably benign |
Het |
| Max |
A |
T |
12: 76,985,355 (GRCm39) |
M121K |
probably benign |
Het |
| Mga |
A |
T |
2: 119,772,170 (GRCm39) |
I1677L |
possibly damaging |
Het |
| Msantd1 |
T |
A |
5: 35,078,906 (GRCm39) |
L147Q |
probably benign |
Het |
| Msantd1 |
C |
A |
5: 35,078,905 (GRCm39) |
L147M |
probably damaging |
Het |
| Mylk4 |
T |
C |
13: 32,896,772 (GRCm39) |
D363G |
possibly damaging |
Het |
| Naaa |
T |
C |
5: 92,420,300 (GRCm39) |
|
probably null |
Het |
| Ninl |
A |
G |
2: 150,806,079 (GRCm39) |
Y381H |
probably damaging |
Het |
| Nwd2 |
A |
G |
5: 63,964,589 (GRCm39) |
N1391S |
probably damaging |
Het |
| Or6k8-ps1 |
G |
A |
1: 173,979,789 (GRCm39) |
A236T |
probably damaging |
Het |
| Phip |
A |
G |
9: 82,753,551 (GRCm39) |
V1731A |
probably benign |
Het |
| Plxnb1 |
T |
A |
9: 108,931,939 (GRCm39) |
C488* |
probably null |
Het |
| Rgs7 |
T |
C |
1: 174,907,120 (GRCm39) |
I374V |
probably benign |
Het |
| Rin2 |
A |
T |
2: 145,718,376 (GRCm39) |
M574L |
probably benign |
Het |
| Rps18 |
A |
T |
17: 34,171,392 (GRCm39) |
D92E |
probably benign |
Het |
| Scrn1 |
T |
A |
6: 54,497,791 (GRCm39) |
I267L |
probably benign |
Het |
| Stard9 |
T |
C |
2: 120,532,023 (GRCm39) |
V67A |
probably benign |
Het |
| Syne1 |
T |
G |
10: 5,317,616 (GRCm39) |
M493L |
probably benign |
Het |
| Tbc1d2 |
G |
A |
4: 46,614,207 (GRCm39) |
R625C |
probably damaging |
Het |
| Tcerg1l |
A |
G |
7: 137,995,909 (GRCm39) |
S200P |
probably damaging |
Het |
| Tet3 |
A |
T |
6: 83,346,039 (GRCm39) |
V1331E |
probably benign |
Het |
| Ticrr |
A |
T |
7: 79,345,297 (GRCm39) |
I1721F |
possibly damaging |
Het |
| Tjp2 |
T |
C |
19: 24,090,311 (GRCm39) |
D577G |
probably damaging |
Het |
| Tmem38b |
A |
G |
4: 53,840,713 (GRCm39) |
M43V |
probably benign |
Het |
| Trabd |
T |
A |
15: 88,970,069 (GRCm39) |
|
probably null |
Het |
| Trpv5 |
C |
A |
6: 41,651,216 (GRCm39) |
D277Y |
probably damaging |
Het |
| Tubb1 |
A |
C |
2: 174,298,416 (GRCm39) |
D67A |
probably damaging |
Het |
| Ubxn7 |
A |
G |
16: 32,200,054 (GRCm39) |
|
probably null |
Het |
| Ugp2 |
G |
A |
11: 21,283,774 (GRCm39) |
P98S |
probably benign |
Het |
| Vmn2r66 |
G |
T |
7: 84,656,955 (GRCm39) |
P150Q |
probably benign |
Het |
| Zbtb11 |
A |
T |
16: 55,794,588 (GRCm39) |
H55L |
possibly damaging |
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 |
|
R1356: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 |
|
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'- CTCTGAATGCATGGCTCAGCTCTAC -3'
Sequencing Primer
(F):5'- TAATAATGGTCAGCACTGGGAC -3'
(R):5'- ATGGCTCAGCTCTACTTCTTC -3'
|
| Posted On |
2014-05-09 |
Incidental Mutation