Incidental Mutation 'IGL01388:Or5w11'
| ID |
79100 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or5w11
|
| Ensembl Gene |
ENSMUSG00000068819 |
| Gene Name |
olfactory receptor family 5 subfamily W member 11 |
| Synonyms |
GA_x6K02T2Q125-49133664-49134593, MOR177-4, Olfr1131 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.061)
|
| Stock # |
IGL01388
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
87458809-87459738 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 87458973 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Histidine to Glutamine
at position 55
(H55Q)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150754
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000090712]
[ENSMUST00000213302]
[ENSMUST00000216082]
[ENSMUST00000216756]
|
| AlphaFold |
Q7TR45 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000090712
AA Change: H55Q
PolyPhen 2
Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)
|
| SMART Domains |
Protein: ENSMUSP00000088214
Gene: ENSMUSG00000068819
AA Change: H55Q
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
30 |
307 |
5.2e-47 |
PFAM |
|
Pfam:7tm_1
|
40 |
289 |
1.7e-18 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213302
AA Change: H55Q
PolyPhen 2
Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000216082
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000216756
|
| 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: 33 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Arhgap28 |
T |
G |
17: 68,160,034 (GRCm39) |
|
probably benign |
Het |
| Ces2b |
A |
C |
8: 105,561,236 (GRCm39) |
|
probably benign |
Het |
| Col20a1 |
T |
A |
2: 180,645,264 (GRCm39) |
M924K |
probably benign |
Het |
| Commd4 |
G |
A |
9: 57,063,273 (GRCm39) |
|
probably benign |
Het |
| Ctnna3 |
A |
G |
10: 63,339,886 (GRCm39) |
E24G |
possibly damaging |
Het |
| Cyp2a22 |
C |
T |
7: 26,637,217 (GRCm39) |
R189H |
probably benign |
Het |
| Gapdhrt |
T |
C |
14: 11,281,836 (GRCm38) |
D33G |
probably damaging |
Het |
| Gm20426 |
T |
C |
6: 90,155,694 (GRCm39) |
|
probably benign |
Het |
| Gm6802 |
T |
G |
12: 19,540,546 (GRCm39) |
|
noncoding transcript |
Het |
| Igkv8-21 |
A |
G |
6: 70,292,153 (GRCm39) |
S30P |
probably benign |
Het |
| Lig4 |
A |
G |
8: 10,023,586 (GRCm39) |
Y65H |
probably damaging |
Het |
| Mpzl1 |
T |
C |
1: 165,433,336 (GRCm39) |
D105G |
probably benign |
Het |
| Myo10 |
A |
G |
15: 25,736,703 (GRCm39) |
I451V |
possibly damaging |
Het |
| Nos2 |
G |
T |
11: 78,848,278 (GRCm39) |
V1062L |
probably damaging |
Het |
| Oas2 |
A |
G |
5: 120,886,657 (GRCm39) |
S170P |
probably damaging |
Het |
| Or1j19 |
G |
T |
2: 36,677,367 (GRCm39) |
V277L |
probably benign |
Het |
| Or8b3b |
A |
T |
9: 38,584,379 (GRCm39) |
Y120* |
probably null |
Het |
| Or8g37 |
A |
G |
9: 39,731,298 (GRCm39) |
D121G |
probably damaging |
Het |
| Pcdh7 |
T |
C |
5: 57,877,546 (GRCm39) |
L367P |
probably damaging |
Het |
| Pde3a |
A |
G |
6: 141,405,464 (GRCm39) |
T439A |
probably damaging |
Het |
| Plekhm2 |
T |
C |
4: 141,369,312 (GRCm39) |
Y124C |
probably damaging |
Het |
| Ppp4r4 |
T |
A |
12: 103,543,108 (GRCm39) |
W155R |
probably damaging |
Het |
| Prl7c1 |
C |
A |
13: 27,960,198 (GRCm39) |
A115S |
probably damaging |
Het |
| Psg25 |
T |
C |
7: 18,263,590 (GRCm39) |
I78V |
possibly damaging |
Het |
| Ptpn9 |
T |
A |
9: 56,944,002 (GRCm39) |
V292E |
probably benign |
Het |
| Ptprs |
G |
A |
17: 56,728,261 (GRCm39) |
R908C |
probably damaging |
Het |
| Rps6ka1 |
C |
T |
4: 133,599,275 (GRCm39) |
V51I |
probably damaging |
Het |
| Scube1 |
T |
C |
15: 83,504,332 (GRCm39) |
I492V |
probably benign |
Het |
| Trappc2 |
G |
A |
X: 165,232,775 (GRCm39) |
|
probably benign |
Het |
| Ubr4 |
T |
C |
4: 139,187,554 (GRCm39) |
V739A |
possibly damaging |
Het |
| Unc79 |
T |
C |
12: 103,136,018 (GRCm39) |
|
probably benign |
Het |
| Vmn2r27 |
G |
A |
6: 124,200,791 (GRCm39) |
P389S |
possibly damaging |
Het |
| Wipi2 |
T |
A |
5: 142,646,798 (GRCm39) |
F212I |
possibly damaging |
Het |
|
| Other mutations in Or5w11 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02186:Or5w11
|
APN |
2 |
87,459,715 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0266:Or5w11
|
UTSW |
2 |
87,459,626 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R0849:Or5w11
|
UTSW |
2 |
87,459,626 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R1607:Or5w11
|
UTSW |
2 |
87,459,321 (GRCm39) |
missense |
probably benign |
0.14 |
|
R2077:Or5w11
|
UTSW |
2 |
87,459,173 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2105:Or5w11
|
UTSW |
2 |
87,459,283 (GRCm39) |
missense |
probably benign |
0.20 |
|
R2322:Or5w11
|
UTSW |
2 |
87,459,118 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R3434:Or5w11
|
UTSW |
2 |
87,459,418 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4357:Or5w11
|
UTSW |
2 |
87,458,810 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
R5139:Or5w11
|
UTSW |
2 |
87,459,000 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5333:Or5w11
|
UTSW |
2 |
87,459,458 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5719:Or5w11
|
UTSW |
2 |
87,459,475 (GRCm39) |
splice site |
probably null |
|
|
R6449:Or5w11
|
UTSW |
2 |
87,459,493 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R7640:Or5w11
|
UTSW |
2 |
87,459,436 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7941:Or5w11
|
UTSW |
2 |
87,459,248 (GRCm39) |
missense |
probably benign |
0.06 |
|
R8110:Or5w11
|
UTSW |
2 |
87,458,951 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R8393:Or5w11
|
UTSW |
2 |
87,459,197 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8877:Or5w11
|
UTSW |
2 |
87,459,212 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9250:Or5w11
|
UTSW |
2 |
87,459,278 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9290:Or5w11
|
UTSW |
2 |
87,459,209 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9313:Or5w11
|
UTSW |
2 |
87,459,076 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9666:Or5w11
|
UTSW |
2 |
87,459,152 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
X0027:Or5w11
|
UTSW |
2 |
87,459,647 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
Z1176:Or5w11
|
UTSW |
2 |
87,459,659 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-11-05 |
Incidental Mutation