Incidental Mutation 'IGL02106:Or5b99'
| ID |
279976 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or5b99
|
| Ensembl Gene |
ENSMUSG00000046913 |
| Gene Name |
olfactory receptor family 5 subfamily B member 99 |
| Synonyms |
GA_x6K02T2RE5P-3328502-3329434, Olfr1451, MOR202-1 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.151)
|
| Stock # |
IGL02106
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
19 |
| Chromosomal Location |
12976352-12977284 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 12976929 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Isoleucine
at position 193
(S193I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000146874
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000063144]
[ENSMUST00000207997]
|
| AlphaFold |
Q8VFX5 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000063144
AA Change: S193I
PolyPhen 2
Score 0.800 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000049885
Gene: ENSMUSG00000046913
AA Change: S193I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
306 |
2e-51 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
33 |
303 |
2.2e-5 |
PFAM |
|
Pfam:7tm_1
|
39 |
289 |
6.9e-23 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000207997
AA Change: S193I
PolyPhen 2
Score 0.800 (Sensitivity: 0.84; Specificity: 0.93)
|
| 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: 44 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Bcl9l |
A |
G |
9: 44,420,496 (GRCm39) |
N1264D |
probably benign |
Het |
| Bmyc |
A |
G |
2: 25,597,082 (GRCm39) |
K49E |
probably damaging |
Het |
| Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
| Ceacam2 |
A |
G |
7: 25,230,166 (GRCm39) |
S147P |
probably benign |
Het |
| Cep152 |
G |
T |
2: 125,444,856 (GRCm39) |
|
probably null |
Het |
| Cnbd1 |
G |
T |
4: 18,894,993 (GRCm39) |
P250T |
possibly damaging |
Het |
| Col6a4 |
A |
G |
9: 105,940,304 (GRCm39) |
C1209R |
possibly damaging |
Het |
| Coro1c |
T |
C |
5: 113,990,334 (GRCm39) |
T116A |
probably benign |
Het |
| Ddx46 |
A |
G |
13: 55,825,416 (GRCm39) |
|
probably benign |
Het |
| Dnaaf5 |
T |
C |
5: 139,137,268 (GRCm39) |
I207T |
probably damaging |
Het |
| Erap1 |
A |
G |
13: 74,794,758 (GRCm39) |
D139G |
probably benign |
Het |
| Fbxw22 |
A |
T |
9: 109,231,087 (GRCm39) |
I121N |
possibly damaging |
Het |
| Fcmr |
T |
C |
1: 130,802,872 (GRCm39) |
S162P |
probably benign |
Het |
| Gadl1 |
A |
G |
9: 115,766,225 (GRCm39) |
|
probably benign |
Het |
| Gli2 |
T |
A |
1: 118,764,465 (GRCm39) |
S1229C |
probably benign |
Het |
| Gm10717 |
A |
T |
9: 3,026,287 (GRCm39) |
Y195F |
probably damaging |
Het |
| Gne |
T |
C |
4: 44,037,306 (GRCm39) |
N692D |
probably damaging |
Het |
| Knl1 |
A |
G |
2: 118,902,489 (GRCm39) |
T1397A |
possibly damaging |
Het |
| Lama3 |
C |
A |
18: 12,601,371 (GRCm39) |
A1016E |
probably damaging |
Het |
| Lhfpl2 |
A |
G |
13: 94,328,419 (GRCm39) |
D160G |
probably benign |
Het |
| Lmtk2 |
T |
A |
5: 144,112,769 (GRCm39) |
V1163E |
probably benign |
Het |
| Lrrtm2 |
G |
T |
18: 35,345,868 (GRCm39) |
S478* |
probably null |
Het |
| Nfatc2ip |
T |
C |
7: 125,989,736 (GRCm39) |
|
probably null |
Het |
| Nlrp12 |
A |
G |
7: 3,282,574 (GRCm39) |
I775T |
probably benign |
Het |
| Npr1 |
A |
G |
3: 90,372,165 (GRCm39) |
F216L |
probably benign |
Het |
| Or4m1 |
A |
T |
14: 50,557,617 (GRCm39) |
L225H |
probably damaging |
Het |
| Or5ac24 |
T |
A |
16: 59,165,387 (GRCm39) |
N226Y |
probably benign |
Het |
| Pkd1l1 |
C |
A |
11: 8,783,800 (GRCm39) |
G2052C |
probably damaging |
Het |
| Ppp1r16b |
A |
G |
2: 158,588,451 (GRCm39) |
N112S |
possibly damaging |
Het |
| Prr11 |
A |
G |
11: 86,994,141 (GRCm39) |
|
probably benign |
Het |
| Scap |
A |
G |
9: 110,210,724 (GRCm39) |
|
probably benign |
Het |
| Sirt1 |
C |
T |
10: 63,171,608 (GRCm39) |
R191Q |
probably damaging |
Het |
| Slc38a6 |
A |
C |
12: 73,397,320 (GRCm39) |
S321R |
possibly damaging |
Het |
| Sp140 |
T |
C |
1: 85,570,940 (GRCm39) |
V460A |
probably benign |
Het |
| Spdye4c |
A |
T |
2: 128,434,586 (GRCm39) |
K54N |
possibly damaging |
Het |
| Spta1 |
T |
A |
1: 174,030,860 (GRCm39) |
N947K |
probably benign |
Het |
| Srgap1 |
A |
G |
10: 121,621,598 (GRCm39) |
V965A |
possibly damaging |
Het |
| Tmem209 |
A |
C |
6: 30,508,659 (GRCm39) |
|
probably null |
Het |
| Trim37 |
A |
T |
11: 87,092,230 (GRCm39) |
K123* |
probably null |
Het |
| Trio |
T |
C |
15: 27,744,244 (GRCm39) |
T2563A |
possibly damaging |
Het |
| Utrn |
A |
T |
10: 12,289,717 (GRCm39) |
S734T |
possibly damaging |
Het |
| Vars2 |
A |
G |
17: 35,975,513 (GRCm39) |
|
probably benign |
Het |
| Xrn1 |
G |
A |
9: 95,859,858 (GRCm39) |
E417K |
probably benign |
Het |
| Yeats2 |
T |
A |
16: 20,011,970 (GRCm39) |
V515E |
possibly damaging |
Het |
|
| Other mutations in Or5b99 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00264:Or5b99
|
APN |
19 |
12,976,683 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01301:Or5b99
|
APN |
19 |
12,976,781 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01369:Or5b99
|
APN |
19 |
12,977,125 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
IGL02098:Or5b99
|
APN |
19 |
12,976,937 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02369:Or5b99
|
APN |
19 |
12,977,072 (GRCm39) |
missense |
probably damaging |
1.00 |
|
ANU18:Or5b99
|
UTSW |
19 |
12,976,781 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0316:Or5b99
|
UTSW |
19 |
12,976,766 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0926:Or5b99
|
UTSW |
19 |
12,976,554 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0988:Or5b99
|
UTSW |
19 |
12,977,151 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1268:Or5b99
|
UTSW |
19 |
12,976,625 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R1509:Or5b99
|
UTSW |
19 |
12,976,815 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R1991:Or5b99
|
UTSW |
19 |
12,976,866 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R2103:Or5b99
|
UTSW |
19 |
12,976,866 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R2132:Or5b99
|
UTSW |
19 |
12,976,402 (GRCm39) |
missense |
probably benign |
0.21 |
|
R2206:Or5b99
|
UTSW |
19 |
12,976,404 (GRCm39) |
missense |
probably benign |
0.06 |
|
R3687:Or5b99
|
UTSW |
19 |
12,976,466 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4077:Or5b99
|
UTSW |
19 |
12,977,235 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4803:Or5b99
|
UTSW |
19 |
12,976,533 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4948:Or5b99
|
UTSW |
19 |
12,977,195 (GRCm39) |
missense |
probably benign |
0.06 |
|
R4999:Or5b99
|
UTSW |
19 |
12,976,583 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6274:Or5b99
|
UTSW |
19 |
12,977,234 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6843:Or5b99
|
UTSW |
19 |
12,976,362 (GRCm39) |
missense |
probably benign |
0.09 |
|
R6928:Or5b99
|
UTSW |
19 |
12,977,202 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6941:Or5b99
|
UTSW |
19 |
12,976,861 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R7485:Or5b99
|
UTSW |
19 |
12,976,922 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7611:Or5b99
|
UTSW |
19 |
12,976,431 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7823:Or5b99
|
UTSW |
19 |
12,976,781 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8948:Or5b99
|
UTSW |
19 |
12,976,445 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8950:Or5b99
|
UTSW |
19 |
12,976,445 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8970:Or5b99
|
UTSW |
19 |
12,976,353 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
R9155:Or5b99
|
UTSW |
19 |
12,976,428 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9236:Or5b99
|
UTSW |
19 |
12,976,763 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9556:Or5b99
|
UTSW |
19 |
12,976,938 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9563:Or5b99
|
UTSW |
19 |
12,976,983 (GRCm39) |
missense |
probably damaging |
0.97 |
|
| Posted On |
2015-04-16 |
Incidental Mutation