Incidental Mutation 'R6654:Or5aq6'
| ID |
526543 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or5aq6
|
| Ensembl Gene |
ENSMUSG00000075161 |
| Gene Name |
olfactory receptor family 5 subfamily AQ member 6 |
| Synonyms |
Olfr1109, GA_x6K02T2Q125-48586461-48585523, MOR172-5 |
| MMRRC Submission |
044775-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.067)
|
| Stock # |
R6654 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
86921539-86926352 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 86923394 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 116
(S116P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149282
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099863]
[ENSMUST00000214636]
[ENSMUST00000217066]
|
| AlphaFold |
A2AT96 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099863
AA Change: S116P
PolyPhen 2
Score 0.232 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000097449
Gene: ENSMUSG00000075161
AA Change: S116P
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
307 |
8.3e-52 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
6.1e-21 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214636
AA Change: S116P
PolyPhen 2
Score 0.232 (Sensitivity: 0.91; Specificity: 0.88)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000217066
AA Change: S116P
PolyPhen 2
Score 0.232 (Sensitivity: 0.91; Specificity: 0.88)
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.0%
- 20x: 94.0%
|
| Validation Efficiency |
97% (35/36) |
| 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: 35 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Akr1b1 |
C |
T |
6: 34,286,939 (GRCm39) |
V206M |
possibly damaging |
Het |
| Armc6 |
T |
C |
8: 70,684,025 (GRCm39) |
E9G |
probably damaging |
Het |
| Bhlhe40 |
TG |
TGG |
6: 108,641,818 (GRCm39) |
254 |
probably null |
Het |
| Ddc |
A |
T |
11: 11,830,452 (GRCm39) |
I64N |
probably damaging |
Het |
| Exd1 |
T |
A |
2: 119,355,198 (GRCm39) |
|
probably null |
Het |
| Gm4847 |
C |
A |
1: 166,457,956 (GRCm39) |
G466C |
probably damaging |
Het |
| Gm5431 |
T |
C |
11: 48,785,427 (GRCm39) |
D316G |
possibly damaging |
Het |
| Gsta4 |
T |
C |
9: 78,116,381 (GRCm39) |
F197L |
probably damaging |
Het |
| Irs2 |
A |
G |
8: 11,056,486 (GRCm39) |
Y649H |
probably damaging |
Het |
| Kif16b |
T |
C |
2: 142,543,197 (GRCm39) |
|
probably benign |
Het |
| Krtap12-1 |
T |
C |
10: 77,556,537 (GRCm39) |
|
probably benign |
Het |
| Ktn1 |
G |
A |
14: 47,927,457 (GRCm39) |
S537N |
probably damaging |
Het |
| Med12l |
G |
T |
3: 59,169,713 (GRCm39) |
G1626W |
probably damaging |
Het |
| Mfng |
T |
A |
15: 78,643,539 (GRCm39) |
T223S |
probably damaging |
Het |
| Msh3 |
T |
C |
13: 92,481,550 (GRCm39) |
T321A |
probably benign |
Het |
| Myo7b |
T |
C |
18: 32,123,322 (GRCm39) |
I672V |
possibly damaging |
Het |
| Nbas |
C |
T |
12: 13,533,875 (GRCm39) |
Q1837* |
probably null |
Het |
| Nlrc4 |
G |
A |
17: 74,752,523 (GRCm39) |
A620V |
possibly damaging |
Het |
| Nubpl |
T |
A |
12: 52,357,516 (GRCm39) |
V310E |
probably damaging |
Het |
| Or4p21 |
T |
G |
2: 88,277,016 (GRCm39) |
T89P |
possibly damaging |
Het |
| P2ry12 |
A |
G |
3: 59,125,441 (GRCm39) |
L78P |
probably damaging |
Het |
| Pira1 |
A |
T |
7: 3,738,928 (GRCm39) |
S560T |
probably benign |
Het |
| Pkd1l3 |
T |
G |
8: 110,350,915 (GRCm39) |
S587A |
probably benign |
Het |
| Potefam1 |
T |
A |
2: 111,002,229 (GRCm39) |
M154L |
unknown |
Het |
| Prkacb |
A |
G |
3: 146,456,298 (GRCm39) |
V145A |
possibly damaging |
Het |
| Rpgrip1l |
T |
C |
8: 91,946,833 (GRCm39) |
E1256G |
probably benign |
Het |
| Rsph4a |
A |
G |
10: 33,788,988 (GRCm39) |
Q611R |
probably benign |
Het |
| Sorl1 |
T |
C |
9: 41,891,941 (GRCm39) |
D1903G |
possibly damaging |
Het |
| Tmem39b |
A |
T |
4: 129,580,619 (GRCm39) |
V291D |
probably damaging |
Het |
| Unc79 |
A |
C |
12: 103,045,307 (GRCm39) |
K685Q |
probably damaging |
Het |
| Unc79 |
A |
T |
12: 103,045,308 (GRCm39) |
K685I |
probably damaging |
Het |
| Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
| Vmn2r112 |
G |
T |
17: 22,822,450 (GRCm39) |
S376I |
possibly damaging |
Het |
| Zfp850 |
A |
T |
7: 27,684,640 (GRCm39) |
C35* |
probably null |
Het |
| Zfp974 |
A |
G |
7: 27,625,828 (GRCm39) |
V14A |
probably damaging |
Het |
|
| Other mutations in Or5aq6 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01341:Or5aq6
|
APN |
2 |
86,923,643 (GRCm39) |
missense |
probably benign |
|
|
IGL01926:Or5aq6
|
APN |
2 |
86,923,318 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03195:Or5aq6
|
APN |
2 |
86,922,913 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0550:Or5aq6
|
UTSW |
2 |
86,923,473 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1334:Or5aq6
|
UTSW |
2 |
86,923,571 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1677:Or5aq6
|
UTSW |
2 |
86,923,081 (GRCm39) |
missense |
probably benign |
|
|
R1753:Or5aq6
|
UTSW |
2 |
86,923,571 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3933:Or5aq6
|
UTSW |
2 |
86,923,106 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4151:Or5aq6
|
UTSW |
2 |
86,923,514 (GRCm39) |
missense |
probably benign |
0.07 |
|
R4296:Or5aq6
|
UTSW |
2 |
86,922,974 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6657:Or5aq6
|
UTSW |
2 |
86,923,403 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7697:Or5aq6
|
UTSW |
2 |
86,923,162 (GRCm39) |
missense |
probably benign |
0.30 |
|
R8178:Or5aq6
|
UTSW |
2 |
86,923,220 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R8413:Or5aq6
|
UTSW |
2 |
86,923,502 (GRCm39) |
missense |
probably benign |
0.25 |
|
R8531:Or5aq6
|
UTSW |
2 |
86,923,670 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8681:Or5aq6
|
UTSW |
2 |
86,923,390 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R8682:Or5aq6
|
UTSW |
2 |
86,923,390 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R8771:Or5aq6
|
UTSW |
2 |
86,923,294 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9185:Or5aq6
|
UTSW |
2 |
86,923,200 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R9387:Or5aq6
|
UTSW |
2 |
86,923,390 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R9388:Or5aq6
|
UTSW |
2 |
86,923,390 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R9389:Or5aq6
|
UTSW |
2 |
86,923,390 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R9390:Or5aq6
|
UTSW |
2 |
86,923,390 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R9483:Or5aq6
|
UTSW |
2 |
86,923,390 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R9680:Or5aq6
|
UTSW |
2 |
86,923,390 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
Z1176:Or5aq6
|
UTSW |
2 |
86,923,568 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
| Predicted Primers |
PCR Primer
(F):5'- TTCACAACGTTGGGACCAC -3'
(R):5'- GGGTAACTGGGGAATGATCTTC -3'
Sequencing Primer
(F):5'- CGTTGGGACCACAGAAGTC -3'
(R):5'- GATCTGGTTGAATGCCCACC -3'
|
| Posted On |
2018-07-23 |
Incidental Mutation