Incidental Mutation 'IGL01304:Or4b1b'
| ID |
73346 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or4b1b
|
| Ensembl Gene |
ENSMUSG00000075061 |
| Gene Name |
olfactory receptor family 4 subfamily B member 1B |
| Synonyms |
Olfr1272, GA_x6K02T2Q125-51636504-51635578, MOR227-3 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.117)
|
| Stock # |
IGL01304
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
90111991-90112917 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 90112425 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Proline to Serine
at position 165
(P165S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150745
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099750]
[ENSMUST00000117141]
|
| AlphaFold |
Q8VGN8 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000099750
AA Change: P165S
PolyPhen 2
Score 0.546 (Sensitivity: 0.88; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000097339
Gene: ENSMUSG00000075061
AA Change: P165S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
303 |
7.5e-52 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
33 |
300 |
1.5e-5 |
PFAM |
|
Pfam:7tm_1
|
39 |
285 |
1.8e-24 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000117141
AA Change: P165S
PolyPhen 2
Score 0.546 (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: 43 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Ablim1 |
A |
T |
19: 57,204,153 (GRCm39) |
D79E |
probably benign |
Het |
| Aplf |
A |
C |
6: 87,618,882 (GRCm39) |
S421A |
possibly damaging |
Het |
| Arnt |
T |
G |
3: 95,355,696 (GRCm39) |
D13E |
probably damaging |
Het |
| Asap1 |
T |
C |
15: 64,184,298 (GRCm39) |
E45G |
probably damaging |
Het |
| C2cd2l |
T |
C |
9: 44,230,884 (GRCm39) |
N101S |
probably damaging |
Het |
| Cby2 |
T |
A |
14: 75,830,085 (GRCm39) |
D36V |
possibly damaging |
Het |
| Chmp7 |
G |
A |
14: 69,956,062 (GRCm39) |
P402L |
probably benign |
Het |
| Cir1 |
A |
T |
2: 73,118,068 (GRCm39) |
|
probably null |
Het |
| Clock |
A |
G |
5: 76,414,202 (GRCm39) |
|
probably null |
Het |
| Col18a1 |
T |
G |
10: 76,911,975 (GRCm39) |
|
probably benign |
Het |
| Csf2ra |
G |
A |
19: 61,215,271 (GRCm39) |
H115Y |
possibly damaging |
Het |
| Cspg5 |
T |
A |
9: 110,085,236 (GRCm39) |
L469H |
probably damaging |
Het |
| Dapk2 |
T |
C |
9: 66,139,139 (GRCm39) |
|
probably benign |
Het |
| F13a1 |
T |
C |
13: 37,172,852 (GRCm39) |
D176G |
probably benign |
Het |
| Fbn2 |
T |
C |
18: 58,194,817 (GRCm39) |
E1448G |
probably damaging |
Het |
| Gtf2b |
C |
T |
3: 142,487,359 (GRCm39) |
S265L |
probably benign |
Het |
| Hmcn1 |
C |
T |
1: 150,498,675 (GRCm39) |
G4068D |
probably damaging |
Het |
| Krt81 |
G |
A |
15: 101,361,269 (GRCm39) |
H104Y |
probably benign |
Het |
| Ksr1 |
T |
C |
11: 78,918,468 (GRCm39) |
Q562R |
probably damaging |
Het |
| Lrif1 |
C |
T |
3: 106,639,049 (GRCm39) |
P20S |
probably damaging |
Het |
| Mamdc4 |
T |
C |
2: 25,453,588 (GRCm39) |
T1194A |
possibly damaging |
Het |
| Med18 |
C |
A |
4: 132,186,930 (GRCm39) |
A190S |
probably damaging |
Het |
| Mia2 |
G |
A |
12: 59,151,324 (GRCm39) |
E105K |
probably damaging |
Het |
| Mnt |
T |
A |
11: 74,733,011 (GRCm39) |
Y48N |
probably damaging |
Het |
| Mpp4 |
A |
C |
1: 59,188,678 (GRCm39) |
|
probably null |
Het |
| Popdc3 |
T |
G |
10: 45,194,005 (GRCm39) |
S269A |
probably benign |
Het |
| Ppp6r3 |
A |
T |
19: 3,517,261 (GRCm39) |
M662K |
probably damaging |
Het |
| Qser1 |
C |
A |
2: 104,617,976 (GRCm39) |
Q945H |
probably damaging |
Het |
| Rad52 |
A |
G |
6: 119,895,594 (GRCm39) |
E198G |
probably damaging |
Het |
| Ranbp17 |
A |
G |
11: 33,216,147 (GRCm39) |
V867A |
possibly damaging |
Het |
| Rdh16 |
G |
T |
10: 127,649,365 (GRCm39) |
A274S |
probably benign |
Het |
| Slco1a5 |
G |
T |
6: 142,187,876 (GRCm39) |
Q488K |
probably benign |
Het |
| Snai2 |
T |
C |
16: 14,524,635 (GRCm39) |
I47T |
probably benign |
Het |
| Snw1 |
T |
C |
12: 87,500,685 (GRCm39) |
D358G |
possibly damaging |
Het |
| Speg |
T |
C |
1: 75,404,841 (GRCm39) |
F2878L |
probably benign |
Het |
| Spg11 |
T |
C |
2: 121,902,771 (GRCm39) |
Y1386C |
probably damaging |
Het |
| Tgfb2 |
A |
C |
1: 186,357,670 (GRCm39) |
I435S |
probably damaging |
Het |
| Ttc9b |
G |
A |
7: 27,355,410 (GRCm39) |
D227N |
probably benign |
Het |
| Txndc2 |
T |
C |
17: 65,945,448 (GRCm39) |
E243G |
possibly damaging |
Het |
| Usp28 |
A |
G |
9: 48,938,119 (GRCm39) |
D563G |
probably damaging |
Het |
| Vmn1r77 |
T |
C |
7: 11,775,962 (GRCm39) |
V178A |
probably damaging |
Het |
| Zfp316 |
A |
G |
5: 143,240,181 (GRCm39) |
F613L |
probably benign |
Het |
| Zfp870 |
A |
T |
17: 33,101,980 (GRCm39) |
C450S |
possibly damaging |
Het |
|
| Other mutations in Or4b1b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01824:Or4b1b
|
APN |
2 |
90,112,263 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01951:Or4b1b
|
APN |
2 |
90,112,351 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02473:Or4b1b
|
APN |
2 |
90,112,040 (GRCm39) |
missense |
probably null |
1.00 |
|
IGL02494:Or4b1b
|
APN |
2 |
90,112,295 (GRCm39) |
missense |
probably benign |
0.35 |
|
IGL03410:Or4b1b
|
APN |
2 |
90,112,557 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0350:Or4b1b
|
UTSW |
2 |
90,112,926 (GRCm39) |
splice site |
probably null |
|
|
R0363:Or4b1b
|
UTSW |
2 |
90,112,200 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0401:Or4b1b
|
UTSW |
2 |
90,112,748 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0666:Or4b1b
|
UTSW |
2 |
90,112,212 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1860:Or4b1b
|
UTSW |
2 |
90,112,502 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1861:Or4b1b
|
UTSW |
2 |
90,112,502 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2374:Or4b1b
|
UTSW |
2 |
90,112,795 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R4256:Or4b1b
|
UTSW |
2 |
90,112,406 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4737:Or4b1b
|
UTSW |
2 |
90,112,725 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4827:Or4b1b
|
UTSW |
2 |
90,112,547 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5198:Or4b1b
|
UTSW |
2 |
90,126,737 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5589:Or4b1b
|
UTSW |
2 |
90,112,313 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6412:Or4b1b
|
UTSW |
2 |
90,112,202 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7130:Or4b1b
|
UTSW |
2 |
90,112,266 (GRCm39) |
missense |
probably benign |
|
|
R7317:Or4b1b
|
UTSW |
2 |
90,112,748 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7497:Or4b1b
|
UTSW |
2 |
90,112,098 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R7762:Or4b1b
|
UTSW |
2 |
90,126,975 (GRCm39) |
nonsense |
probably null |
|
|
R8271:Or4b1b
|
UTSW |
2 |
90,112,616 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R8347:Or4b1b
|
UTSW |
2 |
90,112,020 (GRCm39) |
missense |
probably benign |
0.22 |
|
R8703:Or4b1b
|
UTSW |
2 |
90,126,837 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8794:Or4b1b
|
UTSW |
2 |
90,112,150 (GRCm39) |
nonsense |
probably null |
|
|
R8824:Or4b1b
|
UTSW |
2 |
90,126,356 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8910:Or4b1b
|
UTSW |
2 |
90,126,848 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R8934:Or4b1b
|
UTSW |
2 |
90,112,356 (GRCm39) |
missense |
probably benign |
0.07 |
|
R9548:Or4b1b
|
UTSW |
2 |
90,111,991 (GRCm39) |
makesense |
probably null |
|
|
| Posted On |
2013-10-07 |
Incidental Mutation