Incidental Mutation 'R3120:Or5p70'
| ID |
263173 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or5p70
|
| Ensembl Gene |
ENSMUSG00000110253 |
| Gene Name |
olfactory receptor family 5 subfamily P member 70 |
| Synonyms |
MOR204-37, Olfr495, GA_x6K02T2PBJ9-10725148-10726140 |
| MMRRC Submission |
040593-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.168)
|
| Stock # |
R3120 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
7 |
| Chromosomal Location |
107994329-107995321 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 107994930 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 201
(I201T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150689
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000210990]
[ENSMUST00000215215]
|
| AlphaFold |
Q8VF12 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000071505
AA Change: I201T
PolyPhen 2
Score 0.667 (Sensitivity: 0.86; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000071440
Gene: ENSMUSG00000094104
AA Change: I201T
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
34 |
311 |
3.6e-51 |
PFAM |
|
Pfam:7tm_1
|
44 |
293 |
2.7e-20 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000210990
AA Change: I201T
PolyPhen 2
Score 0.667 (Sensitivity: 0.86; Specificity: 0.91)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000215215
AA Change: I201T
PolyPhen 2
Score 0.667 (Sensitivity: 0.86; Specificity: 0.91)
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.0%
|
| 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: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Bsx |
A |
G |
9: 40,788,908 (GRCm39) |
K155R |
possibly damaging |
Het |
| Ccdc39 |
T |
C |
3: 33,891,987 (GRCm39) |
K162E |
probably damaging |
Het |
| Crygs |
C |
T |
16: 22,624,301 (GRCm39) |
G102D |
possibly damaging |
Het |
| Dnah1 |
G |
A |
14: 30,988,779 (GRCm39) |
R3351* |
probably null |
Het |
| Eml1 |
A |
G |
12: 108,479,312 (GRCm39) |
R362G |
probably benign |
Het |
| Fam222b |
T |
C |
11: 78,044,742 (GRCm39) |
L101P |
probably damaging |
Het |
| Fars2 |
A |
G |
13: 36,430,400 (GRCm39) |
E276G |
probably damaging |
Het |
| Gatad1 |
G |
T |
5: 3,691,456 (GRCm39) |
Y33* |
probably null |
Het |
| Gclc |
A |
C |
9: 77,688,552 (GRCm39) |
E219A |
possibly damaging |
Het |
| Gm4846 |
A |
G |
1: 166,319,117 (GRCm39) |
V207A |
probably benign |
Het |
| H1f5 |
A |
T |
13: 21,964,215 (GRCm39) |
S170R |
probably benign |
Het |
| Hbq1a |
T |
C |
11: 32,250,472 (GRCm39) |
L87P |
probably damaging |
Het |
| Magea6 |
A |
T |
X: 153,707,291 (GRCm39) |
I255N |
probably benign |
Het |
| Mfsd12 |
T |
G |
10: 81,197,049 (GRCm39) |
V206G |
probably benign |
Het |
| Mis18bp1 |
T |
C |
12: 65,203,762 (GRCm39) |
|
probably null |
Het |
| Nf1 |
C |
A |
11: 79,455,725 (GRCm39) |
T550K |
probably damaging |
Het |
| Nlrp4f |
T |
C |
13: 65,342,530 (GRCm39) |
T372A |
probably benign |
Het |
| Pkdcc |
T |
C |
17: 83,527,466 (GRCm39) |
Y215H |
probably damaging |
Het |
| Plekha5 |
A |
G |
6: 140,537,367 (GRCm39) |
T253A |
probably benign |
Het |
| Polr2f |
T |
A |
15: 79,028,788 (GRCm39) |
|
probably null |
Het |
| Prph2 |
C |
T |
17: 47,234,298 (GRCm39) |
A289V |
possibly damaging |
Het |
| Ptdss2 |
C |
T |
7: 140,732,132 (GRCm39) |
H140Y |
probably damaging |
Het |
| Rlf |
T |
A |
4: 121,006,680 (GRCm39) |
I877L |
probably benign |
Het |
| Scgb2b2 |
T |
C |
7: 31,003,001 (GRCm39) |
L32S |
possibly damaging |
Het |
| Sfpq |
T |
A |
4: 126,915,926 (GRCm39) |
H239Q |
unknown |
Het |
| St6gal2 |
A |
T |
17: 55,789,111 (GRCm39) |
R48S |
probably benign |
Het |
| Sybu |
T |
C |
15: 44,536,355 (GRCm39) |
D657G |
possibly damaging |
Het |
| Syt15 |
A |
G |
14: 33,944,950 (GRCm39) |
I166V |
probably benign |
Het |
| Taar7f |
C |
A |
10: 23,925,478 (GRCm39) |
T24K |
probably benign |
Het |
| Tbcd |
T |
C |
11: 121,499,474 (GRCm39) |
S1093P |
probably damaging |
Het |
| Tfap2c |
G |
A |
2: 172,399,015 (GRCm39) |
V396M |
possibly damaging |
Het |
| Tnxb |
C |
T |
17: 34,911,329 (GRCm39) |
T1544I |
possibly damaging |
Het |
| Trim28 |
A |
G |
7: 12,762,341 (GRCm39) |
T322A |
probably damaging |
Het |
| Tubgcp3 |
G |
A |
8: 12,707,626 (GRCm39) |
A121V |
possibly damaging |
Het |
| Vmn2r14 |
A |
T |
5: 109,372,431 (GRCm39) |
W20R |
probably null |
Het |
| Zfp551 |
A |
G |
7: 12,149,943 (GRCm39) |
F489L |
possibly damaging |
Het |
|
| Other mutations in Or5p70 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01382:Or5p70
|
APN |
7 |
107,994,452 (GRCm39) |
missense |
probably benign |
0.31 |
|
IGL02430:Or5p70
|
APN |
7 |
107,994,929 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02511:Or5p70
|
APN |
7 |
107,995,265 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL02932:Or5p70
|
APN |
7 |
107,994,720 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL03222:Or5p70
|
APN |
7 |
107,994,393 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
FR4340:Or5p70
|
UTSW |
7 |
107,995,105 (GRCm39) |
missense |
probably benign |
|
|
FR4340:Or5p70
|
UTSW |
7 |
107,995,100 (GRCm39) |
missense |
probably benign |
|
|
FR4342:Or5p70
|
UTSW |
7 |
107,995,105 (GRCm39) |
missense |
probably benign |
|
|
FR4342:Or5p70
|
UTSW |
7 |
107,995,100 (GRCm39) |
missense |
probably benign |
|
|
R0141:Or5p70
|
UTSW |
7 |
107,994,575 (GRCm39) |
missense |
probably benign |
0.06 |
|
R0600:Or5p70
|
UTSW |
7 |
107,994,438 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0635:Or5p70
|
UTSW |
7 |
107,994,971 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0685:Or5p70
|
UTSW |
7 |
107,994,470 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R1220:Or5p70
|
UTSW |
7 |
107,994,539 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1398:Or5p70
|
UTSW |
7 |
107,994,708 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1501:Or5p70
|
UTSW |
7 |
107,995,289 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1990:Or5p70
|
UTSW |
7 |
107,995,041 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2091:Or5p70
|
UTSW |
7 |
107,995,068 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2473:Or5p70
|
UTSW |
7 |
107,994,711 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4771:Or5p70
|
UTSW |
7 |
107,995,229 (GRCm39) |
nonsense |
probably null |
|
|
R5240:Or5p70
|
UTSW |
7 |
107,994,909 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5510:Or5p70
|
UTSW |
7 |
107,994,332 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5703:Or5p70
|
UTSW |
7 |
107,994,707 (GRCm39) |
missense |
probably benign |
0.23 |
|
R6102:Or5p70
|
UTSW |
7 |
107,994,491 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6110:Or5p70
|
UTSW |
7 |
107,995,035 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6782:Or5p70
|
UTSW |
7 |
107,994,744 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7062:Or5p70
|
UTSW |
7 |
107,995,037 (GRCm39) |
nonsense |
probably null |
|
|
R7783:Or5p70
|
UTSW |
7 |
107,995,296 (GRCm39) |
missense |
probably benign |
0.15 |
|
R8386:Or5p70
|
UTSW |
7 |
107,994,555 (GRCm39) |
small deletion |
probably benign |
|
|
R9347:Or5p70
|
UTSW |
7 |
107,995,259 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9468:Or5p70
|
UTSW |
7 |
107,994,849 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R9554:Or5p70
|
UTSW |
7 |
107,994,365 (GRCm39) |
missense |
probably benign |
0.03 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATGTCCAGAGAAGCCTGTATCC -3'
(R):5'- CAGTGGAGTAGCTGGACTTG -3'
Sequencing Primer
(F):5'- TCCAGAGAAGCCTGTATCCAGTTG -3'
(R):5'- CTGGACTTGGGCATCACATAAATG -3'
|
| Posted On |
2015-02-05 |
Incidental Mutation