Incidental Mutation 'R4190:Or5p64'
ID |
319914 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Or5p64
|
Ensembl Gene |
ENSMUSG00000096465 |
Gene Name |
olfactory receptor family 5 subfamily P member 64 |
Synonyms |
Olfr488, MOR204-15, GA_x6K02T2PBJ9-10586187-10585243 |
MMRRC Submission |
041021-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.258)
|
Stock # |
R4190 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
7 |
Chromosomal Location |
107854399-107855343 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 107855330 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glycine
at position 5
(D5G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000149427
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000072968]
[ENSMUST00000211345]
[ENSMUST00000211508]
[ENSMUST00000215173]
|
AlphaFold |
Q8VG02 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000072968
AA Change: D5G
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000072735 Gene: ENSMUSG00000096465 AA Change: D5G
Domain | Start | End | E-Value | Type |
Pfam:7tm_4
|
34 |
311 |
5.7e-53 |
PFAM |
Pfam:7tm_1
|
44 |
293 |
2.6e-22 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000211345
AA Change: D5G
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000211508
AA Change: D5G
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000215173
AA Change: D5G
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.2%
- 20x: 95.1%
|
Validation Efficiency |
96% (50/52) |
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: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot4 |
T |
C |
12: 84,089,948 (GRCm39) |
|
probably benign |
Het |
Adgre1 |
A |
G |
17: 57,709,811 (GRCm39) |
Y156C |
unknown |
Het |
Ankrd13b |
G |
A |
11: 77,367,201 (GRCm39) |
A21V |
probably damaging |
Het |
Atf7ip |
T |
C |
6: 136,564,499 (GRCm39) |
V914A |
probably damaging |
Het |
C230029F24Rik |
AGAAAG |
A |
1: 49,350,088 (GRCm39) |
|
noncoding transcript |
Het |
Calcr |
T |
A |
6: 3,717,106 (GRCm39) |
D118V |
possibly damaging |
Het |
Cdc42bpg |
T |
C |
19: 6,371,711 (GRCm39) |
V1330A |
probably damaging |
Het |
Cfap54 |
T |
C |
10: 92,720,885 (GRCm39) |
E2567G |
unknown |
Het |
Ctse |
T |
A |
1: 131,590,479 (GRCm39) |
V67D |
probably benign |
Het |
Ddx19b |
A |
T |
8: 111,737,980 (GRCm39) |
L256Q |
probably damaging |
Het |
Dipk1b |
T |
C |
2: 26,526,193 (GRCm39) |
Y376H |
probably damaging |
Het |
Fahd2a |
C |
T |
2: 127,280,486 (GRCm39) |
V156I |
probably benign |
Het |
Fam185a |
T |
A |
5: 21,630,122 (GRCm39) |
|
probably benign |
Het |
Fam234a |
A |
T |
17: 26,432,834 (GRCm39) |
L467Q |
probably damaging |
Het |
Gabra2 |
G |
A |
5: 71,165,341 (GRCm39) |
P210S |
probably benign |
Het |
Heatr3 |
T |
C |
8: 88,864,888 (GRCm39) |
|
probably benign |
Het |
Herc2 |
T |
C |
7: 55,772,196 (GRCm39) |
V1125A |
probably benign |
Het |
Itga11 |
T |
A |
9: 62,639,391 (GRCm39) |
C129S |
probably damaging |
Het |
Lama2 |
A |
G |
10: 27,142,660 (GRCm39) |
L606P |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,366,835 (GRCm39) |
F1077S |
possibly damaging |
Het |
Mtmr10 |
G |
T |
7: 63,963,934 (GRCm39) |
W223L |
probably benign |
Het |
Nlgn1 |
T |
A |
3: 25,488,062 (GRCm39) |
T758S |
probably benign |
Het |
Nr4a1 |
T |
C |
15: 101,171,993 (GRCm39) |
S556P |
probably damaging |
Het |
Or4c126 |
C |
A |
2: 89,823,918 (GRCm39) |
Y60* |
probably null |
Het |
Or6c201 |
T |
C |
10: 128,968,836 (GRCm39) |
N267S |
possibly damaging |
Het |
Or6c33 |
A |
T |
10: 129,853,847 (GRCm39) |
I206F |
probably damaging |
Het |
Pcdhgb8 |
G |
C |
18: 37,896,594 (GRCm39) |
D555H |
probably damaging |
Het |
Plscr5 |
T |
C |
9: 92,080,651 (GRCm39) |
S46P |
probably benign |
Het |
Ppp2r3d |
T |
C |
9: 124,424,123 (GRCm38) |
|
probably benign |
Het |
Prodh |
C |
T |
16: 17,891,504 (GRCm39) |
V480I |
probably benign |
Het |
Senp2 |
G |
T |
16: 21,865,417 (GRCm39) |
W580L |
probably damaging |
Het |
Sorcs3 |
T |
C |
19: 48,737,812 (GRCm39) |
V743A |
possibly damaging |
Het |
Sp110 |
C |
G |
1: 85,516,839 (GRCm39) |
E219D |
probably damaging |
Het |
Stab2 |
G |
T |
10: 86,714,808 (GRCm39) |
N119K |
probably damaging |
Het |
Telo2 |
T |
C |
17: 25,320,987 (GRCm39) |
T743A |
probably benign |
Het |
Trav6-1 |
A |
G |
14: 52,875,976 (GRCm39) |
N2S |
probably benign |
Het |
Trmt44 |
C |
A |
5: 35,732,314 (GRCm39) |
V26L |
possibly damaging |
Het |
Ttbk1 |
A |
T |
17: 46,790,173 (GRCm39) |
C91S |
probably damaging |
Het |
Vit |
A |
G |
17: 78,894,255 (GRCm39) |
H219R |
probably benign |
Het |
Vmn2r84 |
A |
T |
10: 130,227,163 (GRCm39) |
L225* |
probably null |
Het |
Vmn2r87 |
A |
G |
10: 130,308,556 (GRCm39) |
Y561H |
probably damaging |
Het |
Yars1 |
T |
A |
4: 129,093,820 (GRCm39) |
C60* |
probably null |
Het |
Zfp202 |
T |
C |
9: 40,122,633 (GRCm39) |
V465A |
probably benign |
Het |
|
Other mutations in Or5p64 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01575:Or5p64
|
APN |
7 |
107,854,742 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02510:Or5p64
|
APN |
7 |
107,855,348 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02943:Or5p64
|
APN |
7 |
107,854,623 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02962:Or5p64
|
APN |
7 |
107,854,910 (GRCm39) |
missense |
possibly damaging |
0.78 |
PIT4472001:Or5p64
|
UTSW |
7 |
107,855,310 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0980:Or5p64
|
UTSW |
7 |
107,855,229 (GRCm39) |
small deletion |
probably benign |
|
R0981:Or5p64
|
UTSW |
7 |
107,855,229 (GRCm39) |
small deletion |
probably benign |
|
R0981:Or5p64
|
UTSW |
7 |
107,855,228 (GRCm39) |
small deletion |
probably benign |
|
R1957:Or5p64
|
UTSW |
7 |
107,854,403 (GRCm39) |
nonsense |
probably null |
|
R3147:Or5p64
|
UTSW |
7 |
107,854,883 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4163:Or5p64
|
UTSW |
7 |
107,855,039 (GRCm39) |
missense |
probably benign |
0.06 |
R4911:Or5p64
|
UTSW |
7 |
107,855,244 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5274:Or5p64
|
UTSW |
7 |
107,854,842 (GRCm39) |
missense |
probably benign |
0.02 |
R5684:Or5p64
|
UTSW |
7 |
107,855,246 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6394:Or5p64
|
UTSW |
7 |
107,854,970 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6467:Or5p64
|
UTSW |
7 |
107,855,109 (GRCm39) |
missense |
probably damaging |
0.99 |
R7173:Or5p64
|
UTSW |
7 |
107,854,955 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7317:Or5p64
|
UTSW |
7 |
107,854,425 (GRCm39) |
missense |
probably benign |
0.00 |
R7348:Or5p64
|
UTSW |
7 |
107,855,330 (GRCm39) |
missense |
probably benign |
|
R7485:Or5p64
|
UTSW |
7 |
107,855,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R9358:Or5p64
|
UTSW |
7 |
107,854,799 (GRCm39) |
missense |
probably damaging |
0.99 |
R9715:Or5p64
|
UTSW |
7 |
107,855,198 (GRCm39) |
missense |
probably benign |
0.45 |
|
Predicted Primers |
PCR Primer
(F):5'- TCAACAGTAGCTAAGTGGCTG -3'
(R):5'- TGTGTCTGAAGAGAGCGACAC -3'
Sequencing Primer
(F):5'- AGTCACCAGGTAGATGCA -3'
(R):5'- GACAACATCCAGGAATTAGCTTTC -3'
|
Posted On |
2015-06-10 |