Incidental Mutation 'R1201:Or6b2b'
| ID |
101342 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or6b2b
|
| Ensembl Gene |
ENSMUSG00000057464 |
| Gene Name |
olfactory receptor family 6 subfamily B member 2B |
| Synonyms |
MOR103-12, GA_x6K02T2R7CC-81266841-81267776, Olfr1415 |
| MMRRC Submission |
039271-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.101)
|
| Stock # |
R1201 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
1 |
| Chromosomal Location |
92418540-92419475 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to G
at 92418875 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Leucine
at position 201
(I201L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000145446
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000071521]
[ENSMUST00000204009]
[ENSMUST00000204766]
|
| AlphaFold |
Q7TQS4 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000071521
AA Change: I201L
PolyPhen 2
Score 0.039 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000084047
Gene: ENSMUSG00000057464
AA Change: I201L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
307 |
1.3e-53 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
1.2e-16 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000204009
AA Change: I201L
PolyPhen 2
Score 0.039 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000145446
Gene: ENSMUSG00000057464
AA Change: I201L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
307 |
1.3e-53 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
1.2e-16 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000204766
|
| SMART Domains |
Protein: ENSMUSP00000144986
Gene: ENSMUSG00000057464
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:CLECT
|
1 |
65 |
1e-7 |
BLAST |
|
| 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 |
| Or7a39 |
A |
T |
10: 78,715,311 (GRCm39) |
M102L |
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 Or6b2b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL03066:Or6b2b
|
APN |
1 |
92,419,305 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0538:Or6b2b
|
UTSW |
1 |
92,419,055 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R0924:Or6b2b
|
UTSW |
1 |
92,419,127 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0930:Or6b2b
|
UTSW |
1 |
92,419,127 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1025:Or6b2b
|
UTSW |
1 |
92,419,445 (GRCm39) |
missense |
probably benign |
0.19 |
|
R1413:Or6b2b
|
UTSW |
1 |
92,418,610 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1510:Or6b2b
|
UTSW |
1 |
92,419,339 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1846:Or6b2b
|
UTSW |
1 |
92,418,822 (GRCm39) |
nonsense |
probably null |
|
|
R1850:Or6b2b
|
UTSW |
1 |
92,419,124 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R1940:Or6b2b
|
UTSW |
1 |
92,419,457 (GRCm39) |
missense |
probably benign |
0.14 |
|
R2760:Or6b2b
|
UTSW |
1 |
92,418,802 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4066:Or6b2b
|
UTSW |
1 |
92,418,911 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4837:Or6b2b
|
UTSW |
1 |
92,418,697 (GRCm39) |
missense |
probably benign |
0.39 |
|
R5310:Or6b2b
|
UTSW |
1 |
92,418,758 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5503:Or6b2b
|
UTSW |
1 |
92,418,918 (GRCm39) |
missense |
probably benign |
0.07 |
|
R5748:Or6b2b
|
UTSW |
1 |
92,418,815 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5760:Or6b2b
|
UTSW |
1 |
92,418,922 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5853:Or6b2b
|
UTSW |
1 |
92,419,439 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5926:Or6b2b
|
UTSW |
1 |
92,419,288 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6199:Or6b2b
|
UTSW |
1 |
92,419,264 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R7585:Or6b2b
|
UTSW |
1 |
92,419,042 (GRCm39) |
missense |
probably benign |
0.10 |
|
R7627:Or6b2b
|
UTSW |
1 |
92,419,107 (GRCm39) |
nonsense |
probably null |
|
|
R7726:Or6b2b
|
UTSW |
1 |
92,419,029 (GRCm39) |
missense |
probably benign |
0.30 |
|
R8011:Or6b2b
|
UTSW |
1 |
92,418,997 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R8306:Or6b2b
|
UTSW |
1 |
92,419,247 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R9142:Or6b2b
|
UTSW |
1 |
92,419,411 (GRCm39) |
missense |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- GGTAACCAACACAGTGGGTCTCAG -3'
(R):5'- ATGTGTCCAGCTTGTGGCCTTC -3'
Sequencing Primer
(F):5'- ACTATCCTACTATAGAGTGTGACCC -3'
(R):5'- AGCTTGTGGCCTTCTCTTTTG -3'
|
| Posted On |
2014-01-15 |
Incidental Mutation