Incidental Mutation 'IGL02283:Or2y1b'
| ID |
289901 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or2y1b
|
| Ensembl Gene |
ENSMUSG00000100923 |
| Gene Name |
olfactory receptor family 2 subfamily Y member 1B |
| Synonyms |
L45, MOR256-55, Olfr10, GA_x6K02T2QP88-6117098-6116163 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.084)
|
| Stock # |
IGL02283
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
49208375-49209310 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 49209162 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 263
(D263G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149724
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000187570]
[ENSMUST00000215671]
[ENSMUST00000217290]
|
| AlphaFold |
Q60883 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000187570
AA Change: D263G
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000139744
Gene: ENSMUSG00000100923
AA Change: D263G
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
23 |
34 |
N/A |
INTRINSIC |
|
Pfam:7TM_GPCR_Srsx
|
35 |
222 |
4.7e-7 |
PFAM |
|
Pfam:7tm_1
|
41 |
289 |
1.3e-33 |
PFAM |
|
Pfam:7tm_4
|
139 |
282 |
4.6e-43 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215671
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000217290
AA Change: D263G
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| 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: 26 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aldh1l2 |
T |
C |
10: 83,331,759 (GRCm39) |
Y682C |
probably benign |
Het |
| Ank1 |
G |
A |
8: 23,609,450 (GRCm39) |
|
probably null |
Het |
| Arhgap1 |
A |
G |
2: 91,501,121 (GRCm39) |
N399S |
probably damaging |
Het |
| Atp8a2 |
A |
T |
14: 60,254,248 (GRCm39) |
I511N |
possibly damaging |
Het |
| Birc6 |
T |
A |
17: 74,906,935 (GRCm39) |
C1428S |
probably benign |
Het |
| Col18a1 |
T |
C |
10: 76,948,943 (GRCm39) |
T190A |
possibly damaging |
Het |
| Cpd |
A |
T |
11: 76,731,251 (GRCm39) |
D318E |
probably benign |
Het |
| Dync2h1 |
A |
T |
9: 7,125,912 (GRCm39) |
V1898E |
probably damaging |
Het |
| Gon4l |
T |
C |
3: 88,802,671 (GRCm39) |
M1095T |
probably damaging |
Het |
| Gypa |
G |
A |
8: 81,220,721 (GRCm39) |
|
probably benign |
Het |
| Irf9 |
G |
A |
14: 55,845,196 (GRCm39) |
R352H |
probably damaging |
Het |
| Macf1 |
T |
C |
4: 123,365,168 (GRCm39) |
T1633A |
probably benign |
Het |
| Mars2 |
T |
C |
1: 55,277,933 (GRCm39) |
V512A |
probably damaging |
Het |
| Myo9a |
A |
G |
9: 59,778,956 (GRCm39) |
N1571D |
probably benign |
Het |
| Myrfl |
T |
C |
10: 116,613,265 (GRCm39) |
D846G |
probably benign |
Het |
| Or2ak6 |
A |
T |
11: 58,593,102 (GRCm39) |
T192S |
probably damaging |
Het |
| Or4d11 |
A |
G |
19: 12,013,219 (GRCm39) |
S296P |
possibly damaging |
Het |
| Or7a41 |
T |
C |
10: 78,871,379 (GRCm39) |
S250P |
probably damaging |
Het |
| Rprd2 |
A |
T |
3: 95,672,815 (GRCm39) |
S863T |
probably damaging |
Het |
| Sdf4 |
T |
A |
4: 156,093,293 (GRCm39) |
N208K |
probably benign |
Het |
| Sftpd |
A |
T |
14: 40,894,423 (GRCm39) |
V332D |
probably benign |
Het |
| Sh2b3 |
T |
C |
5: 121,956,718 (GRCm39) |
D321G |
probably benign |
Het |
| Slc45a2 |
T |
A |
15: 11,001,268 (GRCm39) |
N122K |
probably damaging |
Het |
| Slk |
T |
A |
19: 47,630,432 (GRCm39) |
F1170Y |
probably damaging |
Het |
| Spata7 |
A |
C |
12: 98,624,517 (GRCm39) |
T140P |
probably damaging |
Het |
| Vmn2r117 |
A |
G |
17: 23,694,356 (GRCm39) |
L497S |
probably damaging |
Het |
|
| Other mutations in Or2y1b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01349:Or2y1b
|
APN |
11 |
49,209,127 (GRCm39) |
nonsense |
probably null |
0.00 |
|
IGL03010:Or2y1b
|
APN |
11 |
49,208,973 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0575:Or2y1b
|
UTSW |
11 |
49,208,880 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1430:Or2y1b
|
UTSW |
11 |
49,208,928 (GRCm39) |
splice site |
probably null |
|
|
R1891:Or2y1b
|
UTSW |
11 |
49,208,684 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2509:Or2y1b
|
UTSW |
11 |
49,209,048 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R2511:Or2y1b
|
UTSW |
11 |
49,209,048 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4942:Or2y1b
|
UTSW |
11 |
49,208,375 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
|
R5080:Or2y1b
|
UTSW |
11 |
49,208,914 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5413:Or2y1b
|
UTSW |
11 |
49,209,240 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5843:Or2y1b
|
UTSW |
11 |
49,209,076 (GRCm39) |
missense |
probably benign |
0.34 |
|
R6354:Or2y1b
|
UTSW |
11 |
49,208,465 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6605:Or2y1b
|
UTSW |
11 |
49,208,541 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8005:Or2y1b
|
UTSW |
11 |
49,208,968 (GRCm39) |
missense |
probably benign |
0.12 |
|
R8284:Or2y1b
|
UTSW |
11 |
49,209,002 (GRCm39) |
missense |
probably benign |
|
|
R8902:Or2y1b
|
UTSW |
11 |
49,209,206 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9003:Or2y1b
|
UTSW |
11 |
49,209,155 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R9431:Or2y1b
|
UTSW |
11 |
49,208,459 (GRCm39) |
missense |
probably benign |
|
|
R9696:Or2y1b
|
UTSW |
11 |
49,208,390 (GRCm39) |
missense |
probably benign |
|
|
| Posted On |
2015-04-16 |
Incidental Mutation