Incidental Mutation 'IGL02739:Olfr33'
| ID |
305798 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Olfr33
|
| Ensembl Gene |
ENSMUSG00000066273 |
| Gene Name |
olfactory receptor 33 |
| Synonyms |
MTPCR33, GA_x6K02T2PBJ9-5431102-5430146, MOR11-2 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.164)
|
| Stock # |
IGL02739
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
102712151-102719070 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 102714314 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 33
(I33T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149588
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000084817]
[ENSMUST00000094124]
[ENSMUST00000216312]
|
| AlphaFold |
Q8VGX7 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000084817
AA Change: I33T
PolyPhen 2
Score 0.577 (Sensitivity: 0.88; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000081877
Gene: ENSMUSG00000066273
AA Change: I33T
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
37 |
317 |
2.1e-117 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
41 |
211 |
7.5e-11 |
PFAM |
|
Pfam:7tm_1
|
47 |
299 |
2.4e-19 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000094124
|
| SMART Domains |
Protein: ENSMUSP00000091674
Gene: ENSMUSG00000070423
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
33 |
311 |
6.2e-117 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
37 |
308 |
2.4e-7 |
PFAM |
|
Pfam:7tm_1
|
43 |
293 |
2.4e-19 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000210002
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000216312
AA Change: I33T
PolyPhen 2
Score 0.577 (Sensitivity: 0.88; Specificity: 0.91)
|
| 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: 40 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aasdh |
A |
T |
5: 76,878,517 (GRCm38) |
C887S |
possibly damaging |
Het |
| Adamdec1 |
C |
A |
14: 68,570,156 (GRCm38) |
E352* |
probably null |
Het |
| Bglap2 |
A |
T |
3: 88,378,012 (GRCm38) |
|
probably null |
Het |
| Bsn |
A |
T |
9: 108,112,546 (GRCm38) |
H2002Q |
probably benign |
Het |
| Chtop |
T |
A |
3: 90,502,250 (GRCm38) |
Q165L |
possibly damaging |
Het |
| Clcn1 |
A |
T |
6: 42,286,780 (GRCm38) |
|
probably null |
Het |
| Ctsr |
T |
C |
13: 61,161,844 (GRCm38) |
T184A |
probably benign |
Het |
| Defb36 |
T |
C |
2: 152,604,519 (GRCm38) |
L11P |
unknown |
Het |
| Dock8 |
A |
G |
19: 25,188,488 (GRCm38) |
E1912G |
probably damaging |
Het |
| Dpp3 |
A |
G |
19: 4,923,728 (GRCm38) |
Y106H |
probably damaging |
Het |
| Epas1 |
A |
G |
17: 86,805,282 (GRCm38) |
T103A |
probably damaging |
Het |
| Epcam |
A |
T |
17: 87,640,494 (GRCm38) |
T131S |
probably benign |
Het |
| Fam169a |
A |
G |
13: 97,094,055 (GRCm38) |
|
probably benign |
Het |
| Gh |
T |
A |
11: 106,301,733 (GRCm38) |
|
probably benign |
Het |
| Kif20a |
A |
T |
18: 34,628,943 (GRCm38) |
K399* |
probably null |
Het |
| Lrp1b |
A |
G |
2: 41,498,215 (GRCm38) |
I466T |
probably damaging |
Het |
| Nlk |
A |
G |
11: 78,574,851 (GRCm38) |
V409A |
probably benign |
Het |
| Nomo1 |
A |
G |
7: 46,044,307 (GRCm38) |
|
probably null |
Het |
| Nr2c1 |
T |
A |
10: 94,156,972 (GRCm38) |
M16K |
probably damaging |
Het |
| Nxph2 |
A |
T |
2: 23,399,900 (GRCm38) |
Q88L |
probably benign |
Het |
| Pkdrej |
T |
A |
15: 85,819,694 (GRCm38) |
R680S |
probably benign |
Het |
| Pkhd1l1 |
A |
T |
15: 44,540,950 (GRCm38) |
N2325I |
probably benign |
Het |
| Pnliprp2 |
T |
C |
19: 58,760,509 (GRCm38) |
|
probably null |
Het |
| Ppp1r42 |
T |
A |
1: 9,968,853 (GRCm38) |
K347N |
probably benign |
Het |
| Prtg |
T |
C |
9: 72,851,585 (GRCm38) |
V407A |
possibly damaging |
Het |
| Psmb8 |
C |
A |
17: 34,200,754 (GRCm38) |
S194* |
probably null |
Het |
| Rnf214 |
T |
C |
9: 45,869,474 (GRCm38) |
I406V |
probably benign |
Het |
| Rreb1 |
C |
T |
13: 37,893,821 (GRCm38) |
S3L |
probably damaging |
Het |
| Sdad1 |
C |
T |
5: 92,290,072 (GRCm38) |
A539T |
probably benign |
Het |
| Sema3a |
A |
G |
5: 13,451,161 (GRCm38) |
Y57C |
probably damaging |
Het |
| Susd5 |
A |
G |
9: 114,096,033 (GRCm38) |
E328G |
possibly damaging |
Het |
| Syngr3 |
T |
C |
17: 24,686,398 (GRCm38) |
T175A |
probably damaging |
Het |
| Tcf20 |
T |
A |
15: 82,856,080 (GRCm38) |
Q390L |
probably damaging |
Het |
| Tex15 |
A |
G |
8: 33,581,693 (GRCm38) |
T2423A |
possibly damaging |
Het |
| Tlr1 |
T |
C |
5: 64,927,126 (GRCm38) |
N36S |
probably benign |
Het |
| Uchl4 |
C |
T |
9: 64,235,537 (GRCm38) |
T100M |
probably damaging |
Het |
| Uhrf1 |
A |
G |
17: 56,305,129 (GRCm38) |
K11R |
probably benign |
Het |
| Vps13b |
T |
A |
15: 35,879,900 (GRCm38) |
D3040E |
probably damaging |
Het |
| Wdr62 |
A |
T |
7: 30,242,460 (GRCm38) |
Y640* |
probably null |
Het |
| Zkscan17 |
T |
G |
11: 59,503,526 (GRCm38) |
E83A |
probably damaging |
Het |
|
| Other mutations in Olfr33 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02064:Olfr33
|
APN |
7 |
102,713,601 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02349:Olfr33
|
APN |
7 |
102,714,126 (GRCm38) |
missense |
probably damaging |
0.99 |
|
IGL03110:Olfr33
|
APN |
7 |
102,713,883 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL03014:Olfr33
|
UTSW |
7 |
102,713,546 (GRCm38) |
missense |
probably null |
0.91 |
|
R0158:Olfr33
|
UTSW |
7 |
102,713,955 (GRCm38) |
missense |
probably benign |
0.03 |
|
R1455:Olfr33
|
UTSW |
7 |
102,713,998 (GRCm38) |
nonsense |
probably null |
|
|
R1996:Olfr33
|
UTSW |
7 |
102,713,792 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2032:Olfr33
|
UTSW |
7 |
102,713,876 (GRCm38) |
missense |
probably benign |
0.00 |
|
R2152:Olfr33
|
UTSW |
7 |
102,713,581 (GRCm38) |
missense |
probably benign |
0.01 |
|
R4852:Olfr33
|
UTSW |
7 |
102,713,543 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4965:Olfr33
|
UTSW |
7 |
102,713,495 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5264:Olfr33
|
UTSW |
7 |
102,714,351 (GRCm38) |
missense |
probably benign |
0.00 |
|
R5464:Olfr33
|
UTSW |
7 |
102,713,682 (GRCm38) |
missense |
probably benign |
|
|
R6680:Olfr33
|
UTSW |
7 |
102,714,315 (GRCm38) |
missense |
possibly damaging |
0.70 |
|
R7195:Olfr33
|
UTSW |
7 |
102,713,666 (GRCm38) |
missense |
possibly damaging |
0.74 |
|
R7373:Olfr33
|
UTSW |
7 |
102,714,099 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R7391:Olfr33
|
UTSW |
7 |
102,713,982 (GRCm38) |
missense |
probably benign |
0.02 |
|
R7872:Olfr33
|
UTSW |
7 |
102,714,182 (GRCm38) |
missense |
probably benign |
0.01 |
|
R7948:Olfr33
|
UTSW |
7 |
102,713,688 (GRCm38) |
missense |
probably benign |
0.00 |
|
R8097:Olfr33
|
UTSW |
7 |
102,713,990 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R8969:Olfr33
|
UTSW |
7 |
102,714,351 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9349:Olfr33
|
UTSW |
7 |
102,713,668 (GRCm38) |
nonsense |
probably null |
|
|
R9589:Olfr33
|
UTSW |
7 |
102,714,165 (GRCm38) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2015-04-16 |
Incidental Mutation