Incidental Mutation 'IGL01418:Or5w19'
| ID |
80282 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or5w19
|
| Ensembl Gene |
ENSMUSG00000045225 |
| Gene Name |
olfactory receptor family 5 subfamily W member 19 |
| Synonyms |
Olfr1152, MOR177-12, GA_x6K02T2Q125-49372426-49373358 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.133)
|
| Stock # |
IGL01418
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
87698337-87699269 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 87698809 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 158
(V158A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151045
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000051058]
[ENSMUST00000213308]
|
| AlphaFold |
Q7TR34 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000051058
AA Change: V158A
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000054645
Gene: ENSMUSG00000045225
AA Change: V158A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
30 |
307 |
4e-46 |
PFAM |
|
Pfam:7tm_1
|
40 |
290 |
1e-13 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000121994
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213308
AA Change: V158A
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| 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 |
|---|
| Adam7 |
T |
A |
14: 68,762,655 (GRCm39) |
H190L |
probably benign |
Het |
| Apoo-ps |
T |
A |
13: 107,551,032 (GRCm39) |
|
noncoding transcript |
Het |
| Asic1 |
T |
A |
15: 99,569,998 (GRCm39) |
N106K |
probably damaging |
Het |
| Ceacam5 |
G |
A |
7: 17,479,524 (GRCm39) |
A214T |
probably damaging |
Het |
| Cfap221 |
T |
A |
1: 119,912,801 (GRCm39) |
H91L |
possibly damaging |
Het |
| Cnga4 |
A |
T |
7: 105,054,169 (GRCm39) |
M46L |
probably benign |
Het |
| Ctcfl |
T |
C |
2: 172,960,124 (GRCm39) |
E153G |
probably benign |
Het |
| Cubn |
C |
T |
2: 13,288,852 (GRCm39) |
V3374I |
probably benign |
Het |
| Cyb561a3 |
T |
A |
19: 10,562,610 (GRCm39) |
H83Q |
probably damaging |
Het |
| Dnah11 |
C |
T |
12: 117,951,217 (GRCm39) |
W1126* |
probably null |
Het |
| E130311K13Rik |
A |
C |
3: 63,827,683 (GRCm39) |
L141R |
possibly damaging |
Het |
| Ercc5 |
A |
G |
1: 44,206,440 (GRCm39) |
K451R |
probably benign |
Het |
| Fbxo34 |
T |
A |
14: 47,768,241 (GRCm39) |
C585S |
possibly damaging |
Het |
| Hoxc9 |
T |
A |
15: 102,892,432 (GRCm39) |
M215K |
probably damaging |
Het |
| Ifi214 |
T |
A |
1: 173,356,995 (GRCm39) |
N36I |
probably damaging |
Het |
| Il17ra |
A |
G |
6: 120,452,542 (GRCm39) |
N242D |
probably benign |
Het |
| Itpr1 |
T |
A |
6: 108,316,585 (GRCm39) |
|
probably null |
Het |
| Lactb |
T |
C |
9: 66,875,045 (GRCm39) |
D349G |
possibly damaging |
Het |
| Lrp2 |
C |
T |
2: 69,355,630 (GRCm39) |
V405I |
probably benign |
Het |
| Map1b |
A |
T |
13: 99,568,338 (GRCm39) |
I1461K |
unknown |
Het |
| Mdh2 |
T |
A |
5: 135,814,879 (GRCm39) |
I116N |
probably damaging |
Het |
| Nek5 |
A |
C |
8: 22,585,285 (GRCm39) |
I364S |
probably damaging |
Het |
| Nr2c1 |
A |
T |
10: 94,026,552 (GRCm39) |
M476L |
probably damaging |
Het |
| Or10j2 |
T |
A |
1: 173,098,275 (GRCm39) |
C178S |
probably damaging |
Het |
| Or1d2 |
T |
C |
11: 74,255,810 (GRCm39) |
V105A |
possibly damaging |
Het |
| Or4k42 |
T |
C |
2: 111,319,984 (GRCm39) |
E173G |
probably benign |
Het |
| Pcdhb8 |
A |
G |
18: 37,489,029 (GRCm39) |
N236D |
probably damaging |
Het |
| Phf10 |
C |
A |
17: 15,165,396 (GRCm39) |
V487L |
probably benign |
Het |
| Pramel22 |
A |
T |
4: 143,381,887 (GRCm39) |
F270I |
probably benign |
Het |
| Ptpn3 |
G |
A |
4: 57,270,156 (GRCm39) |
T2I |
probably damaging |
Het |
| Rbl1 |
T |
C |
2: 156,994,812 (GRCm39) |
|
probably null |
Het |
| Slc24a3 |
A |
G |
2: 145,482,169 (GRCm39) |
D609G |
probably damaging |
Het |
| Slc25a40 |
A |
C |
5: 8,503,298 (GRCm39) |
*338Y |
probably null |
Het |
| Slc5a8 |
G |
T |
10: 88,740,895 (GRCm39) |
C270F |
probably damaging |
Het |
| Slfn8 |
T |
C |
11: 82,895,462 (GRCm39) |
D448G |
probably damaging |
Het |
| Tmem87a |
T |
C |
2: 120,216,351 (GRCm39) |
T180A |
probably benign |
Het |
| Trim30c |
A |
G |
7: 104,031,541 (GRCm39) |
S425P |
possibly damaging |
Het |
| Ubap1 |
A |
T |
4: 41,387,333 (GRCm39) |
R414S |
probably benign |
Het |
| Vipas39 |
G |
A |
12: 87,296,171 (GRCm39) |
T274I |
probably benign |
Het |
| Zfp507 |
T |
A |
7: 35,493,237 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Or5w19 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01618:Or5w19
|
APN |
2 |
87,698,488 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL02326:Or5w19
|
APN |
2 |
87,699,019 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03162:Or5w19
|
APN |
2 |
87,698,484 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03189:Or5w19
|
APN |
2 |
87,698,559 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
I2288:Or5w19
|
UTSW |
2 |
87,698,479 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0761:Or5w19
|
UTSW |
2 |
87,698,880 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R1558:Or5w19
|
UTSW |
2 |
87,698,459 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1938:Or5w19
|
UTSW |
2 |
87,698,805 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3810:Or5w19
|
UTSW |
2 |
87,698,745 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3812:Or5w19
|
UTSW |
2 |
87,698,745 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4728:Or5w19
|
UTSW |
2 |
87,698,779 (GRCm39) |
missense |
probably benign |
0.13 |
|
R4928:Or5w19
|
UTSW |
2 |
87,698,574 (GRCm39) |
missense |
probably benign |
0.32 |
|
R5172:Or5w19
|
UTSW |
2 |
87,699,171 (GRCm39) |
missense |
probably benign |
0.20 |
|
R5174:Or5w19
|
UTSW |
2 |
87,698,755 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R6147:Or5w19
|
UTSW |
2 |
87,699,061 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6195:Or5w19
|
UTSW |
2 |
87,698,904 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R6233:Or5w19
|
UTSW |
2 |
87,698,904 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R6541:Or5w19
|
UTSW |
2 |
87,698,638 (GRCm39) |
missense |
probably benign |
0.11 |
|
R7507:Or5w19
|
UTSW |
2 |
87,698,713 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8068:Or5w19
|
UTSW |
2 |
87,698,995 (GRCm39) |
missense |
probably benign |
0.20 |
|
R8407:Or5w19
|
UTSW |
2 |
87,698,437 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9110:Or5w19
|
UTSW |
2 |
87,698,543 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9408:Or5w19
|
UTSW |
2 |
87,698,379 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9797:Or5w19
|
UTSW |
2 |
87,698,478 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
| Posted On |
2013-11-05 |
Incidental Mutation