Incidental Mutation 'IGL03222:Or5p70'
| ID |
413671 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or5p70
|
| Ensembl Gene |
ENSMUSG00000110253 |
| Gene Name |
olfactory receptor family 5 subfamily P member 70 |
| Synonyms |
MOR204-37, Olfr495, GA_x6K02T2PBJ9-10725148-10726140 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.168)
|
| Stock # |
IGL03222
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
107994329-107995321 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 107994393 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Valine
at position 22
(D22V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150689
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000210990]
[ENSMUST00000215215]
|
| AlphaFold |
Q8VF12 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000210990
AA Change: D22V
PolyPhen 2
Score 0.769 (Sensitivity: 0.85; Specificity: 0.92)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000215215
AA Change: D22V
PolyPhen 2
Score 0.769 (Sensitivity: 0.85; Specificity: 0.92)
|
| Coding Region Coverage |
|
| 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: 22 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4921511C20Rik |
A |
G |
X: 126,303,093 (GRCm39) |
D344G |
probably benign |
Het |
| Aqr |
A |
T |
2: 113,951,737 (GRCm39) |
L877Q |
probably damaging |
Het |
| Ctr9 |
T |
C |
7: 110,642,257 (GRCm39) |
Y328H |
probably benign |
Het |
| Ebf2 |
A |
G |
14: 67,649,441 (GRCm39) |
|
probably null |
Het |
| Ebpl |
A |
G |
14: 61,579,682 (GRCm39) |
|
probably benign |
Het |
| Efcab5 |
A |
T |
11: 77,028,193 (GRCm39) |
D515E |
probably benign |
Het |
| Gon4l |
A |
G |
3: 88,802,950 (GRCm39) |
N1187S |
possibly damaging |
Het |
| Hmces |
A |
G |
6: 87,902,674 (GRCm39) |
R172G |
probably damaging |
Het |
| Ighv14-2 |
T |
C |
12: 113,958,114 (GRCm39) |
D109G |
possibly damaging |
Het |
| Kcnn1 |
C |
T |
8: 71,300,843 (GRCm39) |
R423H |
probably damaging |
Het |
| Muc13 |
T |
C |
16: 33,619,335 (GRCm39) |
S28P |
unknown |
Het |
| Or7e170 |
G |
T |
9: 19,795,495 (GRCm39) |
Y35* |
probably null |
Het |
| Polg |
T |
C |
7: 79,104,404 (GRCm39) |
T824A |
probably damaging |
Het |
| Rapgef2 |
A |
T |
3: 78,995,302 (GRCm39) |
V782D |
probably damaging |
Het |
| Rin2 |
T |
A |
2: 145,702,115 (GRCm39) |
C270* |
probably null |
Het |
| Sdk2 |
C |
A |
11: 113,729,257 (GRCm39) |
V1107L |
probably benign |
Het |
| Sema5a |
T |
A |
15: 32,628,304 (GRCm39) |
V539E |
probably benign |
Het |
| Tiam2 |
T |
C |
17: 3,488,983 (GRCm39) |
S764P |
probably damaging |
Het |
| Tnfrsf11a |
A |
G |
1: 105,749,215 (GRCm39) |
Y211C |
probably damaging |
Het |
| Ttn |
T |
C |
2: 76,586,083 (GRCm39) |
T21883A |
probably damaging |
Het |
| Xkr5 |
T |
C |
8: 18,987,315 (GRCm39) |
T117A |
probably damaging |
Het |
| Xkr9 |
T |
A |
1: 13,771,505 (GRCm39) |
Y340* |
probably null |
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 |
|
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 |
|
R3120:Or5p70
|
UTSW |
7 |
107,994,930 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
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 |
|
| Posted On |
2016-08-02 |
Incidental Mutation