Incidental Mutation 'R3609:Or5al1'
| ID |
269178 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or5al1
|
| Ensembl Gene |
ENSMUSG00000075202 |
| Gene Name |
olfactory receptor family 5 subfamily AL member 1 |
| Synonyms |
Olfr1042, MOR185-10, GA_x6K02T2Q125-47629317-47628376 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.062)
|
| Stock # |
R3609 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
85989689-85990785 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 85989976 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Isoleucine
at position 246
(T246I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151053
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099907]
[ENSMUST00000099908]
[ENSMUST00000213886]
[ENSMUST00000213949]
[ENSMUST00000215624]
[ENSMUST00000216028]
|
| AlphaFold |
Q7TR81 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099907
|
| SMART Domains |
Protein: ENSMUSP00000097491
Gene: ENSMUSG00000075201
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
307 |
6.9e-46 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
1.5e-16 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099908
AA Change: T246I
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000097492
Gene: ENSMUSG00000075202
AA Change: T246I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
307 |
1.2e-48 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
1.3e-14 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213886
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213949
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215624
AA Change: T246I
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000216028
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.0%
|
| 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: 20 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Bpifc |
A |
T |
10: 85,836,502 (GRCm39) |
M1K |
probably null |
Het |
| Cc2d2a |
A |
T |
5: 43,869,668 (GRCm39) |
E856D |
probably damaging |
Het |
| Ces1c |
A |
T |
8: 93,846,960 (GRCm39) |
I98N |
probably damaging |
Het |
| Clec4b1 |
T |
A |
6: 123,027,591 (GRCm39) |
L16Q |
probably damaging |
Het |
| Crygs |
C |
T |
16: 22,624,301 (GRCm39) |
G102D |
possibly damaging |
Het |
| Dop1b |
A |
G |
16: 93,536,220 (GRCm39) |
Y106C |
probably damaging |
Het |
| Irak3 |
G |
T |
10: 119,981,582 (GRCm39) |
T441K |
possibly damaging |
Het |
| Kif18a |
A |
C |
2: 109,168,941 (GRCm39) |
D833A |
probably benign |
Het |
| Lypd8l |
G |
A |
11: 58,503,384 (GRCm39) |
T48I |
possibly damaging |
Het |
| Morc2b |
A |
G |
17: 33,355,252 (GRCm39) |
V840A |
probably damaging |
Het |
| Or4a47 |
A |
G |
2: 89,665,420 (GRCm39) |
S290P |
probably damaging |
Het |
| Or5p57 |
A |
G |
7: 107,665,576 (GRCm39) |
F143S |
probably damaging |
Het |
| Or8k23 |
G |
C |
2: 86,185,826 (GRCm39) |
A300G |
probably damaging |
Het |
| Pgap6 |
G |
A |
17: 26,337,860 (GRCm39) |
V415I |
probably benign |
Het |
| Rest |
A |
C |
5: 77,430,647 (GRCm39) |
N1022T |
probably benign |
Het |
| Setx |
GTGGCT |
GT |
2: 29,044,073 (GRCm39) |
1814 |
probably null |
Het |
| Tsc2 |
A |
C |
17: 24,841,524 (GRCm39) |
I365S |
possibly damaging |
Het |
| Ttn |
C |
T |
2: 76,589,603 (GRCm39) |
R21217H |
probably damaging |
Het |
| Vim |
A |
T |
2: 13,583,437 (GRCm39) |
H253L |
possibly damaging |
Het |
| Vmn2r71 |
T |
A |
7: 85,268,870 (GRCm39) |
C358S |
probably damaging |
Het |
|
| Other mutations in Or5al1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01914:Or5al1
|
APN |
2 |
85,990,391 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL02071:Or5al1
|
APN |
2 |
85,990,219 (GRCm39) |
missense |
probably benign |
|
|
IGL02935:Or5al1
|
APN |
2 |
85,990,714 (GRCm39) |
unclassified |
probably benign |
|
|
IGL03152:Or5al1
|
APN |
2 |
85,990,030 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0089:Or5al1
|
UTSW |
2 |
85,989,918 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R1419:Or5al1
|
UTSW |
2 |
85,989,773 (GRCm39) |
makesense |
probably null |
|
|
R1699:Or5al1
|
UTSW |
2 |
85,990,280 (GRCm39) |
missense |
probably benign |
|
|
R1804:Or5al1
|
UTSW |
2 |
85,990,417 (GRCm39) |
missense |
probably benign |
0.38 |
|
R3162:Or5al1
|
UTSW |
2 |
85,990,439 (GRCm39) |
missense |
probably benign |
0.03 |
|
R3162:Or5al1
|
UTSW |
2 |
85,990,439 (GRCm39) |
missense |
probably benign |
0.03 |
|
R3953:Or5al1
|
UTSW |
2 |
85,990,282 (GRCm39) |
missense |
probably benign |
0.02 |
|
R3955:Or5al1
|
UTSW |
2 |
85,990,282 (GRCm39) |
missense |
probably benign |
0.02 |
|
R3956:Or5al1
|
UTSW |
2 |
85,990,282 (GRCm39) |
missense |
probably benign |
0.02 |
|
R3957:Or5al1
|
UTSW |
2 |
85,990,282 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4771:Or5al1
|
UTSW |
2 |
85,990,417 (GRCm39) |
missense |
probably benign |
0.38 |
|
R5685:Or5al1
|
UTSW |
2 |
85,990,139 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6241:Or5al1
|
UTSW |
2 |
85,990,380 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6324:Or5al1
|
UTSW |
2 |
85,989,800 (GRCm39) |
missense |
probably benign |
|
|
R6678:Or5al1
|
UTSW |
2 |
85,990,529 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6921:Or5al1
|
UTSW |
2 |
85,990,196 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7215:Or5al1
|
UTSW |
2 |
85,989,800 (GRCm39) |
missense |
probably benign |
|
|
R7386:Or5al1
|
UTSW |
2 |
85,989,874 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R8030:Or5al1
|
UTSW |
2 |
85,990,586 (GRCm39) |
missense |
probably benign |
|
|
R9694:Or5al1
|
UTSW |
2 |
85,990,681 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGTGCTGCGAATGTAGATGC -3'
(R):5'- GGCCTGTTCTGACACTCATG -3'
Sequencing Primer
(F):5'- GACACCTGATTATTTTATCCAGTGG -3'
(R):5'- CTCATGTCAAAGAGCTGATGTTGC -3'
|
| Posted On |
2015-02-19 |
Incidental Mutation