Incidental Mutation 'R3086:Or6c88'
ID |
265641 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Or6c88
|
Ensembl Gene |
ENSMUSG00000044293 |
Gene Name |
olfactory receptor family 6 subfamily C member 88 |
Synonyms |
MOR114-11, Olfr794, GA_x6K02T2PULF-11248702-11249664 |
MMRRC Submission |
040575-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.062)
|
Stock # |
R3086 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
10 |
Chromosomal Location |
129406526-129407488 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 129407276 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glycine to Serine
at position 251
(G251S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000145301
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000059957]
[ENSMUST00000204820]
|
AlphaFold |
Q8VF26 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000059957
AA Change: G251S
PolyPhen 2
Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000049790 Gene: ENSMUSG00000044293 AA Change: G251S
Domain | Start | End | E-Value | Type |
Pfam:7tm_4
|
29 |
306 |
2.8e-49 |
PFAM |
Pfam:7tm_1
|
39 |
288 |
2e-22 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000204820
AA Change: G251S
PolyPhen 2
Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000145301 Gene: ENSMUSG00000044293 AA Change: G251S
Domain | Start | End | E-Value | Type |
Pfam:7tm_4
|
29 |
306 |
2.8e-49 |
PFAM |
Pfam:7tm_1
|
39 |
288 |
2e-22 |
PFAM |
|
Meta Mutation Damage Score |
0.6467 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.2%
- 20x: 94.8%
|
Validation Efficiency |
100% (42/42) |
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: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310039H08Rik |
T |
C |
17: 47,083,881 (GRCm39) |
L48P |
probably damaging |
Het |
Adgra3 |
A |
T |
5: 50,170,733 (GRCm39) |
|
probably null |
Het |
Alms1 |
A |
G |
6: 85,655,122 (GRCm39) |
R3223G |
probably benign |
Het |
Bltp1 |
A |
G |
3: 37,065,852 (GRCm39) |
D3483G |
possibly damaging |
Het |
Cabyr |
T |
C |
18: 12,884,023 (GRCm39) |
V170A |
probably damaging |
Het |
Ces2b |
A |
T |
8: 105,559,401 (GRCm39) |
D89V |
possibly damaging |
Het |
Dhrs2 |
G |
T |
14: 55,477,301 (GRCm39) |
V179L |
probably benign |
Het |
Dlg5 |
T |
C |
14: 24,216,258 (GRCm39) |
T595A |
probably damaging |
Het |
Dock10 |
T |
C |
1: 80,510,074 (GRCm39) |
N1585D |
possibly damaging |
Het |
Dock4 |
T |
C |
12: 40,781,862 (GRCm39) |
I689T |
probably benign |
Het |
Fgfr4 |
G |
T |
13: 55,315,205 (GRCm39) |
|
probably benign |
Het |
Frk |
G |
A |
10: 34,483,950 (GRCm39) |
G437D |
probably damaging |
Het |
Frzb |
T |
G |
2: 80,248,858 (GRCm39) |
I199L |
possibly damaging |
Het |
Gsg1l |
C |
T |
7: 125,490,852 (GRCm39) |
R284H |
probably benign |
Het |
Helq |
A |
G |
5: 100,921,858 (GRCm39) |
L782S |
probably benign |
Het |
Kif20b |
T |
C |
19: 34,907,115 (GRCm39) |
F128S |
probably damaging |
Het |
Kifc2 |
T |
C |
15: 76,551,452 (GRCm39) |
F725L |
probably benign |
Het |
Lekr1 |
A |
G |
3: 65,634,581 (GRCm39) |
|
noncoding transcript |
Het |
Macf1 |
T |
A |
4: 123,328,901 (GRCm39) |
M2490L |
probably benign |
Het |
Megf8 |
T |
A |
7: 25,048,444 (GRCm39) |
Y1706N |
probably damaging |
Het |
N4bp2 |
A |
G |
5: 65,948,396 (GRCm39) |
Y342C |
probably damaging |
Het |
Nf1 |
T |
C |
11: 79,437,812 (GRCm39) |
C2057R |
probably damaging |
Het |
Or4f60 |
C |
A |
2: 111,902,320 (GRCm39) |
G203* |
probably null |
Het |
Or4k36 |
A |
G |
2: 111,146,461 (GRCm39) |
I212M |
probably benign |
Het |
Orc4 |
G |
A |
2: 48,827,501 (GRCm39) |
P31S |
probably benign |
Het |
Pcdha1 |
G |
C |
18: 37,064,001 (GRCm39) |
E222Q |
possibly damaging |
Het |
Prune2 |
A |
T |
19: 17,098,777 (GRCm39) |
D1427V |
possibly damaging |
Het |
Rnps1 |
C |
T |
17: 24,631,393 (GRCm39) |
|
probably benign |
Het |
Rsph4a |
G |
C |
10: 33,785,198 (GRCm39) |
V370L |
probably damaging |
Het |
Sema5b |
T |
A |
16: 35,443,093 (GRCm39) |
S33T |
probably benign |
Het |
Stk-ps2 |
A |
C |
1: 46,068,236 (GRCm39) |
|
noncoding transcript |
Het |
Tep1 |
A |
T |
14: 51,064,511 (GRCm39) |
|
probably null |
Het |
Tet1 |
T |
C |
10: 62,715,400 (GRCm39) |
K132E |
probably benign |
Het |
Tiam2 |
A |
G |
17: 3,471,857 (GRCm39) |
K500E |
probably damaging |
Het |
Tmem131l |
G |
T |
3: 83,839,046 (GRCm39) |
R635S |
probably benign |
Het |
Tmem68 |
T |
C |
4: 3,569,594 (GRCm39) |
E32G |
possibly damaging |
Het |
Vmn2r101 |
T |
A |
17: 19,809,077 (GRCm39) |
|
probably null |
Het |
Zfp780b |
A |
G |
7: 27,663,055 (GRCm39) |
I500T |
probably damaging |
Het |
Zfyve26 |
G |
T |
12: 79,312,457 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Or6c88 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01867:Or6c88
|
APN |
10 |
129,406,696 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02157:Or6c88
|
APN |
10 |
129,407,019 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02804:Or6c88
|
APN |
10 |
129,407,306 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL02833:Or6c88
|
APN |
10 |
129,406,619 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02930:Or6c88
|
APN |
10 |
129,407,184 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03038:Or6c88
|
APN |
10 |
129,406,790 (GRCm39) |
missense |
probably benign |
0.07 |
G4846:Or6c88
|
UTSW |
10 |
129,407,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R1539:Or6c88
|
UTSW |
10 |
129,406,640 (GRCm39) |
missense |
probably damaging |
0.99 |
R1737:Or6c88
|
UTSW |
10 |
129,406,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R1845:Or6c88
|
UTSW |
10 |
129,407,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R2198:Or6c88
|
UTSW |
10 |
129,406,915 (GRCm39) |
nonsense |
probably null |
|
R4960:Or6c88
|
UTSW |
10 |
129,406,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R5938:Or6c88
|
UTSW |
10 |
129,407,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:Or6c88
|
UTSW |
10 |
129,406,571 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6598:Or6c88
|
UTSW |
10 |
129,407,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R7034:Or6c88
|
UTSW |
10 |
129,406,941 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7066:Or6c88
|
UTSW |
10 |
129,407,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R7226:Or6c88
|
UTSW |
10 |
129,406,584 (GRCm39) |
missense |
probably benign |
0.01 |
R7324:Or6c88
|
UTSW |
10 |
129,406,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R7408:Or6c88
|
UTSW |
10 |
129,406,493 (GRCm39) |
start gained |
probably benign |
|
R7779:Or6c88
|
UTSW |
10 |
129,407,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R8733:Or6c88
|
UTSW |
10 |
129,406,579 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8891:Or6c88
|
UTSW |
10 |
129,407,046 (GRCm39) |
missense |
probably damaging |
0.99 |
R8931:Or6c88
|
UTSW |
10 |
129,406,550 (GRCm39) |
missense |
probably benign |
0.09 |
R9310:Or6c88
|
UTSW |
10 |
129,406,687 (GRCm39) |
missense |
probably benign |
0.00 |
R9681:Or6c88
|
UTSW |
10 |
129,406,664 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Or6c88
|
UTSW |
10 |
129,407,105 (GRCm39) |
nonsense |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- AGCAGACTGTCATTGTTTGTGC -3'
(R):5'- GGCTGAAATAGTTAAAACCTCCAG -3'
Sequencing Primer
(F):5'- GTGCAGTGCTGACTTTCATC -3'
(R):5'- CCAACATGTTCTTATTGGTGTAAGAG -3'
|
Posted On |
2015-02-05 |