Incidental Mutation 'R9285:Or5p5'
| ID |
703860 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or5p5
|
| Ensembl Gene |
ENSMUSG00000066242 |
| Gene Name |
olfactory receptor family 5 subfamily P member 5 |
| Synonyms |
MOR204-33P, Olfr467, GA_x6K02T2PBJ9-10144091-10145011 |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.105)
|
| Stock # |
R9285 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
7 |
| Chromosomal Location |
107413793-107414713 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 107413821 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Isoleucine
at position 10
(T10I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000147125
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000084756]
[ENSMUST00000208563]
[ENSMUST00000214253]
|
| AlphaFold |
L7N455 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000084756
AA Change: T12I
PolyPhen 2
Score 0.134 (Sensitivity: 0.92; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000081811
Gene: ENSMUSG00000066242
AA Change: T12I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
33 |
308 |
5.3e-52 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
37 |
307 |
8.3e-7 |
PFAM |
|
Pfam:7tm_1
|
43 |
292 |
2.2e-23 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000208563
AA Change: T10I
PolyPhen 2
Score 0.958 (Sensitivity: 0.78; Specificity: 0.95)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000214253
AA Change: T10I
PolyPhen 2
Score 0.958 (Sensitivity: 0.78; Specificity: 0.95)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
100% (49/49) |
| 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: 46 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A2ml1 |
G |
T |
6: 128,526,756 (GRCm39) |
T1085K |
probably benign |
Het |
| Asxl3 |
A |
T |
18: 22,654,989 (GRCm39) |
I1000F |
probably damaging |
Het |
| Atp2c2 |
A |
G |
8: 120,465,141 (GRCm39) |
M308V |
probably benign |
Het |
| Chd3 |
G |
T |
11: 69,249,954 (GRCm39) |
R736S |
possibly damaging |
Het |
| Chst9 |
T |
A |
18: 15,586,017 (GRCm39) |
H182L |
probably damaging |
Het |
| Cnot1 |
A |
G |
8: 96,452,746 (GRCm39) |
F2112S |
probably damaging |
Het |
| Csmd1 |
A |
T |
8: 15,956,088 (GRCm39) |
L3373H |
probably damaging |
Het |
| Ctsll3 |
T |
A |
13: 60,946,402 (GRCm39) |
D303V |
probably benign |
Het |
| Cyp7b1 |
T |
A |
3: 18,151,564 (GRCm39) |
K216N |
probably damaging |
Het |
| Dock9 |
A |
C |
14: 121,833,012 (GRCm39) |
F1315V |
probably benign |
Het |
| Eme2 |
T |
C |
17: 25,108,132 (GRCm39) |
|
probably benign |
Het |
| Eml2 |
A |
G |
7: 18,925,568 (GRCm39) |
I222M |
probably damaging |
Het |
| Ggcx |
T |
A |
6: 72,395,402 (GRCm39) |
Y164* |
probably null |
Het |
| Gm20939 |
T |
C |
17: 95,184,188 (GRCm39) |
F279L |
probably damaging |
Het |
| Gm44511 |
T |
C |
6: 128,777,017 (GRCm39) |
|
probably benign |
Het |
| Gprin1 |
A |
G |
13: 54,886,523 (GRCm39) |
S584P |
probably damaging |
Het |
| Ighv2-2 |
A |
T |
12: 113,551,903 (GRCm39) |
Y112N |
probably damaging |
Het |
| Kansl3 |
T |
C |
1: 36,383,148 (GRCm39) |
|
probably benign |
Het |
| Kcnu1 |
T |
A |
8: 26,381,611 (GRCm39) |
I449K |
probably damaging |
Het |
| Lima1 |
T |
C |
15: 99,678,687 (GRCm39) |
R585G |
probably damaging |
Het |
| Lrrk2 |
T |
A |
15: 91,662,686 (GRCm39) |
V1905E |
probably damaging |
Het |
| Map3k6 |
T |
A |
4: 132,972,870 (GRCm39) |
V343E |
probably damaging |
Het |
| Mei1 |
T |
C |
15: 81,985,170 (GRCm39) |
F279S |
|
Het |
| Mgat3 |
A |
G |
15: 80,096,538 (GRCm39) |
D455G |
probably damaging |
Het |
| Mycbp2 |
T |
A |
14: 103,434,753 (GRCm39) |
Q2230L |
probably damaging |
Het |
| Myog |
T |
C |
1: 134,218,895 (GRCm39) |
F179S |
possibly damaging |
Het |
| Nlrc5 |
A |
C |
8: 95,199,604 (GRCm39) |
I72L |
probably damaging |
Het |
| Or2ag1 |
T |
C |
7: 106,472,715 (GRCm39) |
T246A |
probably benign |
Het |
| Or4k2 |
A |
C |
14: 50,424,122 (GRCm39) |
V185G |
probably benign |
Het |
| Or4s2b |
T |
A |
2: 88,508,680 (GRCm39) |
H153Q |
probably damaging |
Het |
| Or5k15 |
T |
A |
16: 58,710,569 (GRCm39) |
K5* |
probably null |
Het |
| Pcdh18 |
A |
G |
3: 49,707,786 (GRCm39) |
L895P |
probably damaging |
Het |
| Pibf1 |
C |
T |
14: 99,480,345 (GRCm39) |
T707M |
probably benign |
Het |
| Ptk2b |
A |
T |
14: 66,410,844 (GRCm39) |
Y418N |
possibly damaging |
Het |
| Ptx4 |
T |
G |
17: 25,343,930 (GRCm39) |
Y393* |
probably null |
Het |
| Sass6 |
C |
A |
3: 116,422,354 (GRCm39) |
|
probably benign |
Het |
| Sh2b1 |
TGGGGACCAGCTCAGCCACGGGGACCAGCTC |
TGGGGACCAGCTCAGCCACGGGGACCAGCTCAGCCACGGGGACCAGCTC |
7: 126,066,742 (GRCm39) |
|
probably benign |
Het |
| Spatc1l |
T |
C |
10: 76,398,264 (GRCm39) |
V22A |
probably damaging |
Het |
| Strc |
T |
C |
2: 121,195,279 (GRCm39) |
E1668G |
probably damaging |
Het |
| Sulf2 |
T |
A |
2: 165,935,435 (GRCm39) |
H226L |
probably damaging |
Het |
| Sun5 |
T |
C |
2: 153,709,426 (GRCm39) |
|
probably benign |
Het |
| Svep1 |
C |
T |
4: 58,084,809 (GRCm39) |
|
probably null |
Het |
| Tektl1 |
C |
A |
10: 78,588,234 (GRCm39) |
|
probably benign |
Het |
| Xylt2 |
A |
T |
11: 94,558,536 (GRCm39) |
I540N |
probably benign |
Het |
| Zfp804b |
T |
C |
5: 6,820,723 (GRCm39) |
N780S |
probably benign |
Het |
| Zfp983 |
T |
A |
17: 21,876,520 (GRCm39) |
M8K |
possibly damaging |
Het |
|
| Other mutations in Or5p5 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
R0110:Or5p5
|
UTSW |
7 |
107,413,895 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0450:Or5p5
|
UTSW |
7 |
107,413,895 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0707:Or5p5
|
UTSW |
7 |
107,414,331 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0918:Or5p5
|
UTSW |
7 |
107,414,418 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1416:Or5p5
|
UTSW |
7 |
107,414,469 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1988:Or5p5
|
UTSW |
7 |
107,413,907 (GRCm39) |
missense |
probably benign |
|
|
R1989:Or5p5
|
UTSW |
7 |
107,413,907 (GRCm39) |
missense |
probably benign |
|
|
R2219:Or5p5
|
UTSW |
7 |
107,414,429 (GRCm39) |
missense |
probably benign |
|
|
R2241:Or5p5
|
UTSW |
7 |
107,414,040 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R2866:Or5p5
|
UTSW |
7 |
107,414,126 (GRCm39) |
missense |
probably benign |
0.06 |
|
R4946:Or5p5
|
UTSW |
7 |
107,414,589 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R4972:Or5p5
|
UTSW |
7 |
107,413,953 (GRCm39) |
missense |
probably benign |
0.10 |
|
R5099:Or5p5
|
UTSW |
7 |
107,413,809 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5310:Or5p5
|
UTSW |
7 |
107,414,171 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5323:Or5p5
|
UTSW |
7 |
107,413,883 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R5531:Or5p5
|
UTSW |
7 |
107,414,451 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5672:Or5p5
|
UTSW |
7 |
107,413,844 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5758:Or5p5
|
UTSW |
7 |
107,414,022 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5891:Or5p5
|
UTSW |
7 |
107,414,387 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6016:Or5p5
|
UTSW |
7 |
107,414,219 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6399:Or5p5
|
UTSW |
7 |
107,413,961 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R6466:Or5p5
|
UTSW |
7 |
107,413,901 (GRCm39) |
missense |
probably benign |
|
|
R6894:Or5p5
|
UTSW |
7 |
107,414,271 (GRCm39) |
missense |
probably benign |
0.25 |
|
R7543:Or5p5
|
UTSW |
7 |
107,414,308 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8316:Or5p5
|
UTSW |
7 |
107,414,030 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
| Predicted Primers |
PCR Primer
(F):5'- CATGATGTAACTTGGTCTGGGAAG -3'
(R):5'- TGAGCTGGAGTACCCAATGTC -3'
Sequencing Primer
(F):5'- AACTTGGTCTGGGAAGGATTTG -3'
(R):5'- TGTCCACAAAGGCCAAGTG -3'
|
| Posted On |
2022-03-25 |
Incidental Mutation