Incidental Mutation 'IGL01447:Or56b1b'
| ID |
84451 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or56b1b
|
| Ensembl Gene |
ENSMUSG00000060105 |
| Gene Name |
olfactory receptor family 56 subfamily B member 1B |
| Synonyms |
MOR40-15, MOR40-7P, Olfr504, GA_x6K02T2PBJ9-10895499-10894543 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.060)
|
| Stock # |
IGL01447
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
108164044-108165000 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 108164216 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 262
(V262A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000075025
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000075595]
|
| AlphaFold |
Q7TRU7 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000075595
AA Change: V262A
PolyPhen 2
Score 0.753 (Sensitivity: 0.85; Specificity: 0.92)
|
| SMART Domains |
Protein: ENSMUSP00000075025
Gene: ENSMUSG00000060105
AA Change: V262A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
37 |
314 |
3.9e-70 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
40 |
311 |
5.1e-10 |
PFAM |
|
Pfam:7tm_1
|
47 |
296 |
3.1e-14 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000207199
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000207240
|
| 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 |
|---|
| Apbb1ip |
T |
G |
2: 22,743,194 (GRCm39) |
I342S |
probably damaging |
Het |
| Armh4 |
A |
T |
14: 50,005,923 (GRCm39) |
S591T |
probably damaging |
Het |
| Atp6v1e1 |
T |
C |
6: 120,772,654 (GRCm39) |
|
probably benign |
Het |
| Brwd1 |
A |
T |
16: 95,848,579 (GRCm39) |
C533* |
probably null |
Het |
| Cacna2d4 |
A |
G |
6: 119,219,865 (GRCm39) |
S212G |
probably damaging |
Het |
| Ccn5 |
A |
G |
2: 163,670,942 (GRCm39) |
R150G |
probably damaging |
Het |
| Cit |
T |
C |
5: 116,011,902 (GRCm39) |
|
probably benign |
Het |
| Clca3a1 |
C |
T |
3: 144,713,539 (GRCm39) |
M697I |
probably benign |
Het |
| Cmklr1 |
T |
C |
5: 113,752,282 (GRCm39) |
T240A |
probably benign |
Het |
| D630003M21Rik |
T |
C |
2: 158,059,276 (GRCm39) |
D208G |
probably benign |
Het |
| Egr3 |
C |
A |
14: 70,316,732 (GRCm39) |
P143Q |
probably damaging |
Het |
| Fbxw18 |
T |
A |
9: 109,530,675 (GRCm39) |
S41C |
probably damaging |
Het |
| Focad |
T |
A |
4: 88,244,465 (GRCm39) |
I815N |
unknown |
Het |
| Heatr5b |
T |
C |
17: 79,137,026 (GRCm39) |
T165A |
probably benign |
Het |
| Iqub |
G |
T |
6: 24,505,627 (GRCm39) |
L94I |
probably benign |
Het |
| Lrrc32 |
T |
C |
7: 98,147,583 (GRCm39) |
L121P |
probably damaging |
Het |
| Mansc1 |
G |
A |
6: 134,594,289 (GRCm39) |
L118F |
probably damaging |
Het |
| Mtor |
A |
G |
4: 148,615,214 (GRCm39) |
H1693R |
possibly damaging |
Het |
| Muc5b |
A |
G |
7: 141,416,831 (GRCm39) |
Q3259R |
probably benign |
Het |
| Nmnat2 |
A |
G |
1: 152,988,189 (GRCm39) |
S273G |
possibly damaging |
Het |
| Npr2 |
T |
C |
4: 43,640,554 (GRCm39) |
C336R |
possibly damaging |
Het |
| Or10al6 |
C |
T |
17: 38,083,122 (GRCm39) |
L193F |
probably damaging |
Het |
| Or1f19 |
A |
G |
16: 3,410,848 (GRCm39) |
N196S |
possibly damaging |
Het |
| Or1j11 |
A |
T |
2: 36,311,466 (GRCm39) |
I19F |
probably damaging |
Het |
| Or5aq1 |
A |
T |
2: 86,966,343 (GRCm39) |
Y107* |
probably null |
Het |
| Or5d36 |
T |
C |
2: 87,901,468 (GRCm39) |
N86S |
possibly damaging |
Het |
| Rad54l2 |
C |
T |
9: 106,579,971 (GRCm39) |
A967T |
probably damaging |
Het |
| Rspo1 |
T |
C |
4: 124,898,829 (GRCm39) |
V50A |
possibly damaging |
Het |
| Sar1b |
C |
T |
11: 51,682,274 (GRCm39) |
|
probably benign |
Het |
| Scamp1 |
C |
T |
13: 94,340,530 (GRCm39) |
A280T |
probably damaging |
Het |
| Spcs2 |
A |
G |
7: 99,488,911 (GRCm39) |
I251T |
probably benign |
Het |
| Sspo |
G |
T |
6: 48,441,600 (GRCm39) |
|
probably null |
Het |
| Tpm2 |
T |
A |
4: 43,518,251 (GRCm39) |
K251* |
probably null |
Het |
| Ttn |
A |
G |
2: 76,571,250 (GRCm39) |
S26548P |
probably damaging |
Het |
| Ugcg |
T |
G |
4: 59,213,865 (GRCm39) |
V149G |
possibly damaging |
Het |
| Unc79 |
T |
A |
12: 103,045,177 (GRCm39) |
N784K |
probably damaging |
Het |
| Vit |
A |
G |
17: 78,932,633 (GRCm39) |
D580G |
probably damaging |
Het |
| Vmn1r83 |
T |
C |
7: 12,055,424 (GRCm39) |
K211R |
probably benign |
Het |
| Zbtb3 |
A |
G |
19: 8,781,680 (GRCm39) |
Y431C |
probably damaging |
Het |
| Zfp608 |
T |
C |
18: 55,032,083 (GRCm39) |
D619G |
possibly damaging |
Het |
|
| Other mutations in Or56b1b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01358:Or56b1b
|
APN |
7 |
108,164,409 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01845:Or56b1b
|
APN |
7 |
108,164,343 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
IGL02110:Or56b1b
|
APN |
7 |
108,164,286 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03196:Or56b1b
|
APN |
7 |
108,164,061 (GRCm39) |
missense |
probably benign |
|
|
R0282:Or56b1b
|
UTSW |
7 |
108,164,684 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0359:Or56b1b
|
UTSW |
7 |
108,164,721 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0514:Or56b1b
|
UTSW |
7 |
108,164,879 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0727:Or56b1b
|
UTSW |
7 |
108,164,315 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0744:Or56b1b
|
UTSW |
7 |
108,164,205 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R0836:Or56b1b
|
UTSW |
7 |
108,164,205 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R0840:Or56b1b
|
UTSW |
7 |
108,164,823 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0883:Or56b1b
|
UTSW |
7 |
108,164,483 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1750:Or56b1b
|
UTSW |
7 |
108,164,564 (GRCm39) |
nonsense |
probably null |
|
|
R1827:Or56b1b
|
UTSW |
7 |
108,164,282 (GRCm39) |
missense |
probably benign |
0.35 |
|
R1933:Or56b1b
|
UTSW |
7 |
108,164,730 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R3004:Or56b1b
|
UTSW |
7 |
108,164,151 (GRCm39) |
missense |
probably benign |
0.42 |
|
R3766:Or56b1b
|
UTSW |
7 |
108,164,402 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5179:Or56b1b
|
UTSW |
7 |
108,164,433 (GRCm39) |
missense |
probably benign |
|
|
R5408:Or56b1b
|
UTSW |
7 |
108,164,376 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5493:Or56b1b
|
UTSW |
7 |
108,164,774 (GRCm39) |
missense |
probably benign |
0.24 |
|
R5569:Or56b1b
|
UTSW |
7 |
108,164,772 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6520:Or56b1b
|
UTSW |
7 |
108,164,046 (GRCm39) |
makesense |
probably null |
|
|
R6798:Or56b1b
|
UTSW |
7 |
108,164,967 (GRCm39) |
nonsense |
probably null |
|
|
R6803:Or56b1b
|
UTSW |
7 |
108,164,620 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7242:Or56b1b
|
UTSW |
7 |
108,164,919 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7559:Or56b1b
|
UTSW |
7 |
108,164,763 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7644:Or56b1b
|
UTSW |
7 |
108,164,649 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R8498:Or56b1b
|
UTSW |
7 |
108,164,833 (GRCm39) |
nonsense |
probably null |
|
|
R8970:Or56b1b
|
UTSW |
7 |
108,164,997 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9014:Or56b1b
|
UTSW |
7 |
108,164,882 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R9093:Or56b1b
|
UTSW |
7 |
108,164,454 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9103:Or56b1b
|
UTSW |
7 |
108,164,780 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9548:Or56b1b
|
UTSW |
7 |
108,164,334 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
| Posted On |
2013-11-11 |
Incidental Mutation