Incidental Mutation 'IGL03157:Or2b2b'
| ID |
411307 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or2b2b
|
| Ensembl Gene |
ENSMUSG00000108534 |
| Gene Name |
olfactory receptor family 2 subfamily B member 2B |
| Synonyms |
MOR256-10, MOR256-35, GA_x6K02T2QHY8-11561962-11562903, Olfr1360 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.116)
|
| Stock # |
IGL03157
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
13 |
| Chromosomal Location |
21858171-21859150 bp(-) (GRCm39) |
| Type of Mutation |
start codon destroyed |
| DNA Base Change (assembly) |
T to C
at 21859112 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Valine
at position 1
(M1V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149423
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000079135]
[ENSMUST00000205788]
[ENSMUST00000216083]
|
| AlphaFold |
K9J6X0 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000079135
AA Change: M1V
PolyPhen 2
Score 0.482 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000074361
Gene: ENSMUSG00000108534
AA Change: M1V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
3e-55 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
1.1e-30 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000205788
AA Change: M1V
PolyPhen 2
Score 0.482 (Sensitivity: 0.89; Specificity: 0.90)
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000216083
AA Change: M1V
PolyPhen 2
Score 0.482 (Sensitivity: 0.89; Specificity: 0.90)
|
| 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: 29 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcc9 |
G |
A |
6: 142,551,649 (GRCm39) |
|
probably benign |
Het |
| Adam30 |
A |
C |
3: 98,069,612 (GRCm39) |
K482Q |
possibly damaging |
Het |
| Aqp4 |
T |
C |
18: 15,533,037 (GRCm39) |
R19G |
probably benign |
Het |
| Arhgap32 |
C |
T |
9: 32,170,430 (GRCm39) |
P1070L |
probably damaging |
Het |
| Bcat2 |
T |
C |
7: 45,224,922 (GRCm39) |
I31T |
probably benign |
Het |
| Csmd2 |
T |
A |
4: 128,308,092 (GRCm39) |
C1283* |
probably null |
Het |
| Fasn |
A |
G |
11: 120,698,735 (GRCm39) |
I2487T |
probably benign |
Het |
| Gys1 |
A |
G |
7: 45,089,323 (GRCm39) |
|
probably benign |
Het |
| Helz |
A |
G |
11: 107,468,714 (GRCm39) |
D79G |
possibly damaging |
Het |
| Il16 |
T |
C |
7: 83,371,611 (GRCm39) |
D65G |
probably damaging |
Het |
| Iqgap1 |
C |
T |
7: 80,401,636 (GRCm39) |
E490K |
probably benign |
Het |
| Kcnv2 |
A |
G |
19: 27,301,366 (GRCm39) |
K406E |
probably damaging |
Het |
| Kif26b |
T |
A |
1: 178,743,930 (GRCm39) |
L1342H |
probably damaging |
Het |
| Nlrp3 |
A |
G |
11: 59,440,372 (GRCm39) |
K650E |
possibly damaging |
Het |
| Opn1sw |
T |
A |
6: 29,379,803 (GRCm39) |
N144Y |
possibly damaging |
Het |
| Or6z1 |
A |
G |
7: 6,504,892 (GRCm39) |
L111P |
probably damaging |
Het |
| Or8k30 |
T |
C |
2: 86,339,367 (GRCm39) |
L188P |
possibly damaging |
Het |
| Ovol1 |
T |
C |
19: 5,601,635 (GRCm39) |
H129R |
probably benign |
Het |
| Pigv |
T |
C |
4: 133,392,841 (GRCm39) |
S110G |
probably benign |
Het |
| Pole |
T |
A |
5: 110,441,619 (GRCm39) |
F253L |
probably benign |
Het |
| Samd3 |
T |
C |
10: 26,139,740 (GRCm39) |
Y291H |
probably benign |
Het |
| Slc4a4 |
T |
A |
5: 89,304,372 (GRCm39) |
I605N |
probably damaging |
Het |
| Sult1a1 |
T |
A |
7: 126,274,489 (GRCm39) |
Y58F |
probably damaging |
Het |
| Tfrc |
T |
A |
16: 32,439,223 (GRCm39) |
D362E |
probably benign |
Het |
| Thnsl2 |
T |
C |
6: 71,108,930 (GRCm39) |
T294A |
probably benign |
Het |
| Tnfsf10 |
G |
A |
3: 27,380,106 (GRCm39) |
G57R |
possibly damaging |
Het |
| Vps25 |
A |
T |
11: 101,147,723 (GRCm39) |
N73I |
probably benign |
Het |
| Wdfy1 |
G |
A |
1: 79,684,035 (GRCm39) |
H367Y |
probably damaging |
Het |
| Zfp568 |
T |
C |
7: 29,722,189 (GRCm39) |
L378P |
probably damaging |
Het |
|
| Other mutations in Or2b2b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01736:Or2b2b
|
APN |
13 |
21,858,787 (GRCm39) |
missense |
probably benign |
0.12 |
|
IGL02886:Or2b2b
|
APN |
13 |
21,859,122 (GRCm39) |
utr 5 prime |
probably benign |
|
|
R1540:Or2b2b
|
UTSW |
13 |
21,858,700 (GRCm39) |
missense |
probably benign |
0.11 |
|
R1756:Or2b2b
|
UTSW |
13 |
21,858,865 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1843:Or2b2b
|
UTSW |
13 |
21,858,842 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3793:Or2b2b
|
UTSW |
13 |
21,859,153 (GRCm39) |
splice site |
probably null |
|
|
R5707:Or2b2b
|
UTSW |
13 |
21,858,769 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7566:Or2b2b
|
UTSW |
13 |
21,858,737 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R8781:Or2b2b
|
UTSW |
13 |
21,859,013 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8849:Or2b2b
|
UTSW |
13 |
21,858,226 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R9070:Or2b2b
|
UTSW |
13 |
21,858,985 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9462:Or2b2b
|
UTSW |
13 |
21,859,015 (GRCm39) |
missense |
probably benign |
0.19 |
|
Z1177:Or2b2b
|
UTSW |
13 |
21,859,324 (GRCm39) |
start gained |
probably benign |
|
|
| Posted On |
2016-08-02 |
Incidental Mutation