Incidental Mutation 'R3107:Or8b51'
| ID |
263623 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or8b51
|
| Ensembl Gene |
ENSMUSG00000094701 |
| Gene Name |
olfactory receptor family 8 subfamily B member 51 |
| Synonyms |
Olfr916, MOR168-1, GA_x6K02T2PVTD-32360710-32359778 |
| MMRRC Submission |
040581-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.344)
|
| Stock # |
R3107 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
38568754-38569686 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 38569307 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Tyrosine
at position 127
(C127Y)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149578
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000081196]
[ENSMUST00000213714]
[ENSMUST00000214093]
[ENSMUST00000215291]
|
| AlphaFold |
Q8VG53 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000081196
AA Change: C127Y
PolyPhen 2
Score 0.482 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000079959
Gene: ENSMUSG00000094701
AA Change: C127Y
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
1.3e-45 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
1.3e-22 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000213714
AA Change: C127Y
PolyPhen 2
Score 0.482 (Sensitivity: 0.89; Specificity: 0.90)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000214093
AA Change: C127Y
PolyPhen 2
Score 0.482 (Sensitivity: 0.89; Specificity: 0.90)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215291
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000217596
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.1%
- 20x: 94.3%
|
| 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: 37 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgrf4 |
A |
T |
17: 42,977,758 (GRCm39) |
Y528* |
probably null |
Het |
| Ankrd26 |
A |
T |
6: 118,533,204 (GRCm39) |
F198L |
probably benign |
Het |
| Arnt2 |
A |
G |
7: 83,911,652 (GRCm39) |
S607P |
possibly damaging |
Het |
| Brd10 |
A |
T |
19: 29,700,847 (GRCm39) |
L814H |
probably damaging |
Het |
| Ccdc17 |
T |
C |
4: 116,455,464 (GRCm39) |
V269A |
probably benign |
Het |
| Cers1 |
T |
A |
8: 70,775,286 (GRCm39) |
H233Q |
probably benign |
Het |
| Cfap54 |
T |
C |
10: 92,830,545 (GRCm39) |
N1197S |
probably benign |
Het |
| Cfb |
A |
G |
17: 35,080,800 (GRCm39) |
Y66H |
possibly damaging |
Het |
| Clspn |
A |
G |
4: 126,485,452 (GRCm39) |
D1247G |
probably benign |
Het |
| Cnnm1 |
T |
C |
19: 43,430,000 (GRCm39) |
C373R |
probably damaging |
Het |
| Col19a1 |
T |
C |
1: 24,377,017 (GRCm39) |
T443A |
possibly damaging |
Het |
| Cubn |
T |
C |
2: 13,367,158 (GRCm39) |
S1571G |
possibly damaging |
Het |
| Ddt |
C |
T |
10: 75,608,597 (GRCm39) |
E42K |
probably benign |
Het |
| Dmrt2 |
C |
A |
19: 25,655,055 (GRCm39) |
T218N |
probably benign |
Het |
| Dnah7b |
G |
A |
1: 46,392,033 (GRCm39) |
G3798E |
probably benign |
Het |
| Espl1 |
A |
G |
15: 102,221,424 (GRCm39) |
I944V |
probably damaging |
Het |
| Fam114a2 |
C |
A |
11: 57,390,561 (GRCm39) |
K317N |
probably benign |
Het |
| Fyn |
G |
C |
10: 39,427,451 (GRCm39) |
D445H |
probably damaging |
Het |
| Gprasp1 |
A |
T |
X: 134,700,508 (GRCm39) |
M234L |
probably benign |
Het |
| Ibtk |
T |
C |
9: 85,592,467 (GRCm39) |
Y997C |
probably damaging |
Het |
| Il12rb2 |
A |
G |
6: 67,337,782 (GRCm39) |
V33A |
probably damaging |
Het |
| Ints6 |
T |
C |
14: 62,998,041 (GRCm39) |
T23A |
possibly damaging |
Het |
| Itk |
C |
A |
11: 46,218,291 (GRCm39) |
G624V |
probably benign |
Het |
| Lama2 |
C |
T |
10: 26,877,231 (GRCm39) |
E2652K |
probably benign |
Het |
| Mab21l3 |
T |
A |
3: 101,734,112 (GRCm39) |
I109F |
probably damaging |
Het |
| Mov10 |
T |
C |
3: 104,707,040 (GRCm39) |
E653G |
probably damaging |
Het |
| Plg |
T |
C |
17: 12,603,316 (GRCm39) |
V74A |
probably benign |
Het |
| Ptprn2 |
A |
G |
12: 116,839,800 (GRCm39) |
D441G |
probably benign |
Het |
| Rbmxl2 |
G |
A |
7: 106,809,624 (GRCm39) |
G303E |
probably damaging |
Het |
| Satb1 |
A |
T |
17: 52,089,810 (GRCm39) |
Y346N |
possibly damaging |
Het |
| Serpina1a |
A |
T |
12: 103,820,100 (GRCm39) |
I382N |
probably damaging |
Het |
| Slc6a2 |
C |
A |
8: 93,687,906 (GRCm39) |
Q11K |
probably benign |
Het |
| Slc6a20a |
A |
C |
9: 123,470,773 (GRCm39) |
|
probably null |
Het |
| Sorcs1 |
T |
C |
19: 50,199,088 (GRCm39) |
E825G |
possibly damaging |
Het |
| Sval1 |
C |
G |
6: 41,932,876 (GRCm39) |
P145A |
probably damaging |
Het |
| Trhde |
C |
T |
10: 114,427,971 (GRCm39) |
E442K |
probably damaging |
Het |
| Vmn2r61 |
A |
T |
7: 41,916,491 (GRCm39) |
D368V |
possibly damaging |
Het |
|
| Other mutations in Or8b51 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01965:Or8b51
|
APN |
9 |
38,568,918 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02313:Or8b51
|
APN |
9 |
38,569,362 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL03221:Or8b51
|
APN |
9 |
38,569,661 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0479:Or8b51
|
UTSW |
9 |
38,569,478 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1507:Or8b51
|
UTSW |
9 |
38,569,310 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1521:Or8b51
|
UTSW |
9 |
38,569,014 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1860:Or8b51
|
UTSW |
9 |
38,569,661 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3964:Or8b51
|
UTSW |
9 |
38,569,023 (GRCm39) |
missense |
probably benign |
0.42 |
|
R3965:Or8b51
|
UTSW |
9 |
38,569,023 (GRCm39) |
missense |
probably benign |
0.42 |
|
R4419:Or8b51
|
UTSW |
9 |
38,569,365 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5249:Or8b51
|
UTSW |
9 |
38,569,374 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R5481:Or8b51
|
UTSW |
9 |
38,568,916 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6299:Or8b51
|
UTSW |
9 |
38,569,073 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6555:Or8b51
|
UTSW |
9 |
38,569,585 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6702:Or8b51
|
UTSW |
9 |
38,569,073 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6703:Or8b51
|
UTSW |
9 |
38,569,073 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6851:Or8b51
|
UTSW |
9 |
38,569,481 (GRCm39) |
missense |
probably benign |
0.31 |
|
R6895:Or8b51
|
UTSW |
9 |
38,569,385 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8688:Or8b51
|
UTSW |
9 |
38,569,047 (GRCm39) |
missense |
probably benign |
0.24 |
|
R8985:Or8b51
|
UTSW |
9 |
38,569,621 (GRCm39) |
nonsense |
probably null |
|
|
R9259:Or8b51
|
UTSW |
9 |
38,569,642 (GRCm39) |
splice site |
probably benign |
|
|
R9292:Or8b51
|
UTSW |
9 |
38,569,071 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9634:Or8b51
|
UTSW |
9 |
38,568,869 (GRCm39) |
missense |
probably benign |
0.06 |
|
R9641:Or8b51
|
UTSW |
9 |
38,568,915 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9772:Or8b51
|
UTSW |
9 |
38,568,964 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- AGCTTTGGACCTGCCTTCAG -3'
(R):5'- ACCTAGTCACTGCATTGGGG -3'
Sequencing Primer
(F):5'- CTTTGGACCTGCCTTCAGAAGAATG -3'
(R):5'- CTAGTCACTGCATTGGGGAATTTATC -3'
|
| Posted On |
2015-02-05 |
Incidental Mutation