Incidental Mutation 'R7063:Or5p55'
| ID |
548393 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or5p55
|
| Ensembl Gene |
ENSMUSG00000095301 |
| Gene Name |
olfactory receptor family 5 subfamily P member 55 |
| Synonyms |
GA_x6K02T2PBJ9-10296787-10297719, Olfr476, MOR204-3 |
| MMRRC Submission |
045159-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.057)
|
| Stock # |
R7063 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
7 |
| Chromosomal Location |
107566606-107567538 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 107567411 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Alanine to Glutamic Acid
at position 269
(A269E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149760
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077249]
[ENSMUST00000217173]
|
| AlphaFold |
Q8VGI4 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000077249
AA Change: A269E
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000076485
Gene: ENSMUSG00000095301
AA Change: A269E
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
1.7e-51 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
4.1e-19 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000217173
AA Change: A269E
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
| Validation Efficiency |
100% (43/43) |
| 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: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Arhgap35 |
A |
G |
7: 16,299,038 (GRCm39) |
V9A |
probably benign |
Het |
| Btbd6 |
A |
G |
12: 112,941,132 (GRCm39) |
Y148C |
probably damaging |
Het |
| Casr |
T |
C |
16: 36,314,936 (GRCm39) |
I968V |
probably benign |
Het |
| Celf1 |
T |
C |
2: 90,843,189 (GRCm39) |
|
probably null |
Het |
| Chst2 |
G |
T |
9: 95,287,621 (GRCm39) |
R242S |
probably benign |
Het |
| Clca3a1 |
T |
A |
3: 144,460,967 (GRCm39) |
D228V |
probably damaging |
Het |
| Cwf19l2 |
A |
G |
9: 3,430,532 (GRCm39) |
Y288C |
probably benign |
Het |
| Cyp2r1 |
A |
G |
7: 114,152,184 (GRCm39) |
S49P |
probably damaging |
Het |
| Dnah5 |
A |
G |
15: 28,233,394 (GRCm39) |
E251G |
probably benign |
Het |
| Eepd1 |
A |
G |
9: 25,394,332 (GRCm39) |
R199G |
possibly damaging |
Het |
| Fat1 |
C |
T |
8: 45,493,812 (GRCm39) |
T3986I |
probably benign |
Het |
| Gbp4 |
G |
A |
5: 105,266,314 (GRCm39) |
R576C |
probably damaging |
Het |
| Glp1r |
A |
G |
17: 31,144,532 (GRCm39) |
Y235C |
probably damaging |
Het |
| Gm6408 |
T |
C |
5: 146,420,594 (GRCm39) |
I158T |
probably benign |
Het |
| Gpr89 |
C |
G |
3: 96,783,014 (GRCm39) |
R312P |
probably damaging |
Het |
| Idh2 |
A |
G |
7: 79,745,432 (GRCm39) |
V403A |
probably damaging |
Het |
| Lclat1 |
A |
G |
17: 73,546,986 (GRCm39) |
E301G |
possibly damaging |
Het |
| Lgmn |
A |
G |
12: 102,368,937 (GRCm39) |
Y181H |
probably damaging |
Het |
| Lgr5 |
T |
C |
10: 115,292,639 (GRCm39) |
Y417C |
probably damaging |
Het |
| Man1a |
G |
T |
10: 53,906,840 (GRCm39) |
N311K |
probably damaging |
Het |
| Nat10 |
G |
A |
2: 103,578,422 (GRCm39) |
L228F |
probably benign |
Het |
| Or10d3 |
T |
G |
9: 39,461,411 (GRCm39) |
Y252S |
possibly damaging |
Het |
| Or10v5 |
A |
G |
19: 11,805,548 (GRCm39) |
F281L |
probably damaging |
Het |
| Or5b12b |
A |
G |
19: 12,861,449 (GRCm39) |
D68G |
probably damaging |
Het |
| Pcmtd2 |
T |
A |
2: 181,496,776 (GRCm39) |
Y130* |
probably null |
Het |
| Potefam3f |
G |
A |
8: 20,479,013 (GRCm39) |
C7Y |
|
Het |
| Qrfprl |
A |
G |
6: 65,418,387 (GRCm39) |
|
probably benign |
Het |
| Rapgef5 |
A |
G |
12: 117,652,864 (GRCm39) |
D62G |
possibly damaging |
Het |
| Serpina3m |
A |
T |
12: 104,357,726 (GRCm39) |
I217L |
probably benign |
Het |
| Supt16 |
T |
C |
14: 52,409,505 (GRCm39) |
R802G |
possibly damaging |
Het |
| Sypl2 |
A |
T |
3: 108,124,971 (GRCm39) |
M130K |
probably benign |
Het |
| Tmtc2 |
A |
T |
10: 105,184,386 (GRCm39) |
L503Q |
probably damaging |
Het |
| Ubald2 |
A |
G |
11: 116,325,443 (GRCm39) |
Q60R |
probably benign |
Het |
| Vav1 |
C |
T |
17: 57,618,860 (GRCm39) |
Q673* |
probably null |
Het |
| Vgll2 |
T |
C |
10: 51,904,072 (GRCm39) |
S312P |
probably benign |
Het |
| Vmn1r191 |
C |
T |
13: 22,362,864 (GRCm39) |
A297T |
probably benign |
Het |
| Vmn1r7 |
T |
A |
6: 57,001,418 (GRCm39) |
I281F |
possibly damaging |
Het |
| Vmn2r108 |
T |
C |
17: 20,701,410 (GRCm39) |
Y30C |
probably damaging |
Het |
| Vmn2r16 |
A |
G |
5: 109,511,650 (GRCm39) |
N619S |
probably damaging |
Het |
| Vstm5 |
A |
G |
9: 15,150,549 (GRCm39) |
|
probably benign |
Het |
| Zfp7 |
A |
G |
15: 76,775,919 (GRCm39) |
I654V |
possibly damaging |
Het |
| Zmat2 |
A |
G |
18: 36,929,627 (GRCm39) |
N129S |
probably null |
Het |
|
| Other mutations in Or5p55 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01063:Or5p55
|
APN |
7 |
107,566,741 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01403:Or5p55
|
APN |
7 |
107,566,828 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
IGL01564:Or5p55
|
APN |
7 |
107,567,198 (GRCm39) |
missense |
probably benign |
0.11 |
|
IGL01615:Or5p55
|
APN |
7 |
107,567,144 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01777:Or5p55
|
APN |
7 |
107,566,709 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01999:Or5p55
|
APN |
7 |
107,566,675 (GRCm39) |
missense |
probably benign |
|
|
IGL02239:Or5p55
|
APN |
7 |
107,567,254 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0636:Or5p55
|
UTSW |
7 |
107,566,679 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1986:Or5p55
|
UTSW |
7 |
107,566,877 (GRCm39) |
missense |
probably benign |
|
|
R5109:Or5p55
|
UTSW |
7 |
107,567,104 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6363:Or5p55
|
UTSW |
7 |
107,566,957 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R6526:Or5p55
|
UTSW |
7 |
107,566,669 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6907:Or5p55
|
UTSW |
7 |
107,567,459 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7218:Or5p55
|
UTSW |
7 |
107,566,874 (GRCm39) |
missense |
probably benign |
|
|
R7240:Or5p55
|
UTSW |
7 |
107,567,395 (GRCm39) |
missense |
probably benign |
0.42 |
|
R7444:Or5p55
|
UTSW |
7 |
107,566,811 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7939:Or5p55
|
UTSW |
7 |
107,566,986 (GRCm39) |
nonsense |
probably null |
|
|
R8060:Or5p55
|
UTSW |
7 |
107,566,612 (GRCm39) |
missense |
probably benign |
|
|
R8953:Or5p55
|
UTSW |
7 |
107,567,251 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9159:Or5p55
|
UTSW |
7 |
107,567,524 (GRCm39) |
nonsense |
probably null |
|
|
R9438:Or5p55
|
UTSW |
7 |
107,567,000 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0025:Or5p55
|
UTSW |
7 |
107,567,395 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
| Predicted Primers |
PCR Primer
(F):5'- GACTTCCCTGCTGTGTTGAAAC -3'
(R):5'- TACTAGGTACTAACAGTGGTATGC -3'
Sequencing Primer
(F):5'- GCTGGATCCATCATTGTGATCACAG -3'
(R):5'- TAGGTACTAACAGTGGTATGCATACG -3'
|
| Posted On |
2019-05-13 |
Incidental Mutation