Incidental Mutation 'R9533:Or6c69'
| ID |
719571 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or6c69
|
| Ensembl Gene |
ENSMUSG00000063715 |
| Gene Name |
olfactory receptor family 6 subfamily C member 69 |
| Synonyms |
MOR113-1, Olfr816, GA_x6K02T2PULF-11590830-11589892 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.082)
|
| Stock # |
R9533 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
10 |
| Chromosomal Location |
129747207-129748145 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 129747404 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Phenylalanine
at position 248
(I248F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149515
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000071605]
[ENSMUST00000213438]
|
| AlphaFold |
Q8VFU2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000071605
AA Change: I248F
PolyPhen 2
Score 0.196 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000071534
Gene: ENSMUSG00000063715
AA Change: I248F
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
306 |
6.9e-50 |
PFAM |
|
Pfam:7tm_1
|
39 |
288 |
1.2e-24 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213438
AA Change: I248F
PolyPhen 2
Score 0.196 (Sensitivity: 0.92; Specificity: 0.87)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
| Validation Efficiency |
100% (40/40) |
| 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: 40 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca6 |
C |
T |
11: 110,102,582 (GRCm39) |
V881I |
probably benign |
Het |
| Acot1 |
C |
T |
12: 84,063,988 (GRCm39) |
S57F |
|
Het |
| Actr3 |
T |
C |
1: 125,339,048 (GRCm39) |
I97V |
probably benign |
Het |
| C4b |
A |
T |
17: 34,956,698 (GRCm39) |
C633* |
probably null |
Het |
| Cdh19 |
T |
A |
1: 110,817,589 (GRCm39) |
T718S |
probably damaging |
Het |
| Coasy |
T |
A |
11: 100,975,852 (GRCm39) |
S355T |
probably benign |
Het |
| Coch |
A |
G |
12: 51,650,132 (GRCm39) |
I374V |
possibly damaging |
Het |
| Dhrs7l |
C |
T |
12: 72,675,050 (GRCm39) |
|
probably benign |
Het |
| Dip2b |
T |
A |
15: 100,073,178 (GRCm39) |
M760K |
probably benign |
Het |
| Evi5 |
A |
G |
5: 107,957,566 (GRCm39) |
Y428H |
probably damaging |
Het |
| Fst |
G |
A |
13: 114,592,397 (GRCm39) |
R107* |
probably null |
Het |
| Gba1 |
A |
G |
3: 89,114,756 (GRCm39) |
T387A |
probably benign |
Het |
| Gid8 |
A |
T |
2: 180,358,713 (GRCm39) |
Q126L |
probably damaging |
Het |
| Iqgap1 |
A |
G |
7: 80,383,929 (GRCm39) |
V1045A |
possibly damaging |
Het |
| Kif23 |
G |
A |
9: 61,832,924 (GRCm39) |
S535L |
probably benign |
Het |
| Krt79 |
G |
A |
15: 101,848,417 (GRCm39) |
A78V |
possibly damaging |
Het |
| Lama2 |
A |
G |
10: 26,862,871 (GRCm39) |
F2964S |
probably damaging |
Het |
| Lamp3 |
T |
C |
16: 19,519,808 (GRCm39) |
D125G |
probably benign |
Het |
| Lrrc15 |
C |
T |
16: 30,092,637 (GRCm39) |
G234D |
possibly damaging |
Het |
| Myo7b |
A |
G |
18: 32,108,297 (GRCm39) |
V1188A |
probably benign |
Het |
| Nbeal2 |
T |
C |
9: 110,473,729 (GRCm39) |
T37A |
probably benign |
Het |
| Nlrp1b |
T |
C |
11: 71,109,095 (GRCm39) |
I135M |
probably benign |
Het |
| Or2a51 |
A |
G |
6: 43,178,991 (GRCm39) |
R138G |
probably benign |
Het |
| P3h2 |
T |
C |
16: 25,789,725 (GRCm39) |
Y514C |
probably damaging |
Het |
| Pcdha5 |
A |
G |
18: 37,093,986 (GRCm39) |
N165S |
probably damaging |
Het |
| Phf10 |
G |
C |
17: 15,175,366 (GRCm39) |
H157D |
probably damaging |
Het |
| Ppip5k2 |
C |
T |
1: 97,661,792 (GRCm39) |
R708H |
probably benign |
Het |
| Prr12 |
A |
G |
7: 44,698,692 (GRCm39) |
S408P |
unknown |
Het |
| Rab3a |
A |
T |
8: 71,209,804 (GRCm39) |
Y123F |
probably damaging |
Het |
| Rbak |
A |
T |
5: 143,160,172 (GRCm39) |
S294T |
probably damaging |
Het |
| Sarm1 |
T |
C |
11: 78,373,996 (GRCm39) |
D677G |
probably damaging |
Het |
| Scly |
A |
T |
1: 91,228,413 (GRCm39) |
|
probably benign |
Het |
| Slc26a6 |
T |
C |
9: 108,735,481 (GRCm39) |
V385A |
probably damaging |
Het |
| Slc66a2 |
T |
C |
18: 80,327,034 (GRCm39) |
V209A |
unknown |
Het |
| Srp72 |
T |
C |
5: 77,128,274 (GRCm39) |
V165A |
probably benign |
Het |
| Tars3 |
A |
C |
7: 65,333,808 (GRCm39) |
|
probably null |
Het |
| Tspan1 |
T |
A |
4: 116,020,211 (GRCm39) |
M233L |
probably benign |
Het |
| Zfp574 |
G |
A |
7: 24,780,379 (GRCm39) |
G467D |
probably damaging |
Het |
| Zfp85 |
A |
G |
13: 67,897,722 (GRCm39) |
S117P |
probably benign |
Het |
| Zfp932 |
C |
G |
5: 110,157,787 (GRCm39) |
P495R |
probably damaging |
Het |
|
| Other mutations in Or6c69 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01448:Or6c69
|
APN |
10 |
129,748,114 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL01650:Or6c69
|
APN |
10 |
129,747,550 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01766:Or6c69
|
APN |
10 |
129,747,649 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02738:Or6c69
|
APN |
10 |
129,747,200 (GRCm39) |
utr 3 prime |
probably benign |
|
|
IGL02824:Or6c69
|
APN |
10 |
129,747,565 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0401:Or6c69
|
UTSW |
10 |
129,747,785 (GRCm39) |
missense |
probably benign |
0.18 |
|
R0688:Or6c69
|
UTSW |
10 |
129,747,752 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1589:Or6c69
|
UTSW |
10 |
129,747,550 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1744:Or6c69
|
UTSW |
10 |
129,747,262 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2049:Or6c69
|
UTSW |
10 |
129,748,036 (GRCm39) |
missense |
probably benign |
0.30 |
|
R3763:Or6c69
|
UTSW |
10 |
129,747,314 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3952:Or6c69
|
UTSW |
10 |
129,747,505 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3971:Or6c69
|
UTSW |
10 |
129,747,742 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4557:Or6c69
|
UTSW |
10 |
129,747,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5538:Or6c69
|
UTSW |
10 |
129,747,871 (GRCm39) |
missense |
probably benign |
0.13 |
|
R6127:Or6c69
|
UTSW |
10 |
129,747,284 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6227:Or6c69
|
UTSW |
10 |
129,747,536 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6394:Or6c69
|
UTSW |
10 |
129,747,789 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6707:Or6c69
|
UTSW |
10 |
129,747,608 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7257:Or6c69
|
UTSW |
10 |
129,748,156 (GRCm39) |
start gained |
probably benign |
|
|
R7258:Or6c69
|
UTSW |
10 |
129,748,156 (GRCm39) |
start gained |
probably benign |
|
|
R7260:Or6c69
|
UTSW |
10 |
129,748,156 (GRCm39) |
start gained |
probably benign |
|
|
R7409:Or6c69
|
UTSW |
10 |
129,748,120 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R7539:Or6c69
|
UTSW |
10 |
129,747,932 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7782:Or6c69
|
UTSW |
10 |
129,747,392 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7984:Or6c69
|
UTSW |
10 |
129,747,941 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8879:Or6c69
|
UTSW |
10 |
129,747,731 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9717:Or6c69
|
UTSW |
10 |
129,748,048 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0019:Or6c69
|
UTSW |
10 |
129,747,964 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1191:Or6c69
|
UTSW |
10 |
129,747,826 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
| Predicted Primers |
|
| Posted On |
2022-07-18 |
Incidental Mutation