Incidental Mutation 'R1201:Or7a39'
| ID |
101393 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or7a39
|
| Ensembl Gene |
ENSMUSG00000062873 |
| Gene Name |
olfactory receptor family 7 subfamily A member 39 |
| Synonyms |
GA_x6K02T2QGN0-2932609-2931677, Olfr1355, MOR139-6 |
| MMRRC Submission |
039271-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.072)
|
| Stock # |
R1201 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
10 |
| Chromosomal Location |
78711383-78715940 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 78715311 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Leucine
at position 102
(M102L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000077517
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000078414]
|
| AlphaFold |
Q7TQU9 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000078414
AA Change: M102L
PolyPhen 2
Score 0.115 (Sensitivity: 0.93; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000077517
Gene: ENSMUSG00000062873
AA Change: M102L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
32 |
309 |
3.1e-48 |
PFAM |
|
Pfam:7tm_1
|
42 |
291 |
1.1e-20 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.0%
- 10x: 95.2%
- 20x: 89.4%
|
| 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: 39 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4932414N04Rik |
A |
G |
2: 68,546,626 (GRCm39) |
T103A |
possibly damaging |
Het |
| Acly |
A |
G |
11: 100,384,761 (GRCm39) |
I674T |
probably damaging |
Het |
| Aco2 |
C |
T |
15: 81,779,394 (GRCm39) |
S33L |
probably damaging |
Het |
| Actc1 |
A |
G |
2: 113,879,994 (GRCm39) |
|
probably null |
Het |
| Amph |
G |
A |
13: 19,326,198 (GRCm39) |
V643M |
probably damaging |
Het |
| Arhgap40 |
A |
C |
2: 158,376,689 (GRCm39) |
D275A |
probably damaging |
Het |
| Bltp1 |
A |
G |
3: 37,002,524 (GRCm39) |
S1490G |
probably benign |
Het |
| Car11 |
A |
G |
7: 45,352,904 (GRCm39) |
D221G |
probably benign |
Het |
| Catsperg1 |
A |
T |
7: 28,891,095 (GRCm39) |
H596Q |
possibly damaging |
Het |
| Ccm2 |
T |
C |
11: 6,543,682 (GRCm39) |
V231A |
probably benign |
Het |
| Crh |
A |
G |
3: 19,748,090 (GRCm39) |
I184T |
probably damaging |
Het |
| Csgalnact2 |
A |
G |
6: 118,091,393 (GRCm39) |
S424P |
probably damaging |
Het |
| Dbf4 |
A |
C |
5: 8,447,498 (GRCm39) |
L571V |
possibly damaging |
Het |
| Fancm |
A |
G |
12: 65,153,542 (GRCm39) |
K66E |
possibly damaging |
Het |
| Hydin |
T |
C |
8: 111,296,487 (GRCm39) |
V3672A |
probably benign |
Het |
| Kcnh2 |
C |
T |
5: 24,527,670 (GRCm39) |
R894H |
probably damaging |
Het |
| Krt36 |
T |
C |
11: 99,994,883 (GRCm39) |
N230D |
probably benign |
Het |
| Nlrp4b |
G |
T |
7: 10,449,363 (GRCm39) |
R522L |
possibly damaging |
Het |
| Ntn1 |
T |
C |
11: 68,104,052 (GRCm39) |
D532G |
probably damaging |
Het |
| Numb |
A |
T |
12: 83,848,059 (GRCm39) |
V215D |
probably damaging |
Het |
| Or1x2 |
T |
A |
11: 50,917,937 (GRCm39) |
M36K |
probably damaging |
Het |
| Or4k15 |
T |
A |
14: 50,364,813 (GRCm39) |
W260R |
probably damaging |
Het |
| Or5k8 |
A |
G |
16: 58,644,226 (GRCm39) |
I282T |
probably damaging |
Het |
| Or6b2b |
T |
G |
1: 92,418,875 (GRCm39) |
I201L |
probably benign |
Het |
| Otulinl |
G |
A |
15: 27,658,259 (GRCm39) |
Q84* |
probably null |
Het |
| Pidd1 |
A |
G |
7: 141,020,187 (GRCm39) |
F580L |
probably benign |
Het |
| Plekhg4 |
A |
G |
8: 106,108,305 (GRCm39) |
D1116G |
probably damaging |
Het |
| Prss33 |
G |
T |
17: 24,054,084 (GRCm39) |
S74* |
probably null |
Het |
| Rab34 |
T |
A |
11: 78,081,222 (GRCm39) |
|
probably null |
Het |
| Rims2 |
A |
C |
15: 39,479,720 (GRCm39) |
T1251P |
possibly damaging |
Het |
| Skint5 |
A |
G |
4: 113,413,342 (GRCm39) |
S1152P |
unknown |
Het |
| Slc6a17 |
T |
A |
3: 107,400,388 (GRCm39) |
Q206L |
possibly damaging |
Het |
| Tmem59l |
C |
T |
8: 70,937,037 (GRCm39) |
W310* |
probably null |
Het |
| Tnrc6c |
T |
G |
11: 117,612,500 (GRCm39) |
N379K |
probably damaging |
Het |
| Vmn1r76 |
A |
C |
7: 11,664,252 (GRCm39) |
F286V |
probably benign |
Het |
| Xdh |
T |
C |
17: 74,225,413 (GRCm39) |
D463G |
probably benign |
Het |
| Zfp251 |
C |
T |
15: 76,738,436 (GRCm39) |
R219Q |
possibly damaging |
Het |
| Zfp263 |
T |
A |
16: 3,567,294 (GRCm39) |
H536Q |
probably damaging |
Het |
| Zfp607a |
T |
A |
7: 27,578,736 (GRCm39) |
F602Y |
probably damaging |
Het |
|
| Other mutations in Or7a39 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01571:Or7a39
|
APN |
10 |
78,715,671 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL01773:Or7a39
|
APN |
10 |
78,715,770 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL02707:Or7a39
|
APN |
10 |
78,715,759 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03233:Or7a39
|
APN |
10 |
78,715,406 (GRCm39) |
nonsense |
probably null |
|
|
R1067:Or7a39
|
UTSW |
10 |
78,715,517 (GRCm39) |
nonsense |
probably null |
|
|
R1956:Or7a39
|
UTSW |
10 |
78,715,267 (GRCm39) |
missense |
probably benign |
0.28 |
|
R1978:Or7a39
|
UTSW |
10 |
78,715,114 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2014:Or7a39
|
UTSW |
10 |
78,715,222 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R2015:Or7a39
|
UTSW |
10 |
78,715,222 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R2245:Or7a39
|
UTSW |
10 |
78,715,765 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3725:Or7a39
|
UTSW |
10 |
78,715,766 (GRCm39) |
nonsense |
probably null |
|
|
R4899:Or7a39
|
UTSW |
10 |
78,715,041 (GRCm39) |
missense |
probably benign |
0.32 |
|
R5696:Or7a39
|
UTSW |
10 |
78,715,919 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5982:Or7a39
|
UTSW |
10 |
78,715,787 (GRCm39) |
nonsense |
probably null |
|
|
R6448:Or7a39
|
UTSW |
10 |
78,715,516 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R7126:Or7a39
|
UTSW |
10 |
78,715,411 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7385:Or7a39
|
UTSW |
10 |
78,715,288 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7807:Or7a39
|
UTSW |
10 |
78,715,043 (GRCm39) |
missense |
probably benign |
|
|
R7886:Or7a39
|
UTSW |
10 |
78,715,657 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R8313:Or7a39
|
UTSW |
10 |
78,715,170 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8747:Or7a39
|
UTSW |
10 |
78,715,155 (GRCm39) |
missense |
probably benign |
0.14 |
|
R9507:Or7a39
|
UTSW |
10 |
78,715,597 (GRCm39) |
missense |
probably benign |
0.30 |
|
R9642:Or7a39
|
UTSW |
10 |
78,715,395 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Or7a39
|
UTSW |
10 |
78,715,393 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
Z1177:Or7a39
|
UTSW |
10 |
78,714,990 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TGACTGACTGATGGAATCAGGCAAC -3'
(R):5'- GCATGTAGGATGCTAACAACCCAGG -3'
Sequencing Primer
(F):5'- TCCATGTACCTGGTAACAGTG -3'
(R):5'- GGACAGCAGAACCATCAGC -3'
|
| Posted On |
2014-01-15 |
Incidental Mutation