Incidental Mutation 'IGL01773:Or11g25'
| ID |
153706 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or11g25
|
| Ensembl Gene |
ENSMUSG00000095765 |
| Gene Name |
olfactory receptor family 11 subfamily G member 25 |
| Synonyms |
MOR106-15, MOR106-10, Olfr741, GA_x6K02T2PMLR-6197851-6198786 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.106)
|
| Stock # |
IGL01773
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
14 |
| Chromosomal Location |
50710514-50723852 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 50723230 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Phenylalanine to Serine
at position 105
(F105S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151020
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000071932]
[ENSMUST00000205518]
[ENSMUST00000213903]
|
| AlphaFold |
L7N1Y5 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000071932
AA Change: F105S
PolyPhen 2
Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000071824
Gene: ENSMUSG00000095765
AA Change: F105S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
35 |
311 |
1.2e-55 |
PFAM |
|
Pfam:7tm_1
|
45 |
294 |
2.4e-20 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000205518
AA Change: F105S
PolyPhen 2
Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000213903
AA Change: F105S
PolyPhen 2
Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)
|
| 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: 30 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Cacna1s |
C |
A |
1: 136,046,491 (GRCm39) |
H1775Q |
probably benign |
Het |
| Calcrl |
A |
G |
2: 84,200,787 (GRCm39) |
Y86H |
probably benign |
Het |
| Ccdc63 |
T |
C |
5: 122,251,208 (GRCm39) |
K401E |
possibly damaging |
Het |
| Col9a1 |
A |
G |
1: 24,244,147 (GRCm39) |
T127A |
probably benign |
Het |
| Cpq |
T |
A |
15: 33,212,996 (GRCm39) |
F5Y |
probably benign |
Het |
| Cuzd1 |
T |
A |
7: 130,916,614 (GRCm39) |
M282L |
probably damaging |
Het |
| Ddx10 |
C |
A |
9: 53,115,430 (GRCm39) |
D635Y |
possibly damaging |
Het |
| Ect2l |
T |
C |
10: 18,037,252 (GRCm39) |
D382G |
probably damaging |
Het |
| Ganc |
T |
C |
2: 120,290,365 (GRCm39) |
S901P |
possibly damaging |
Het |
| Gpr179 |
G |
A |
11: 97,232,192 (GRCm39) |
R671C |
probably benign |
Het |
| Isl2 |
T |
C |
9: 55,451,504 (GRCm39) |
L219P |
probably damaging |
Het |
| Mfsd13a |
T |
C |
19: 46,357,733 (GRCm39) |
S296P |
possibly damaging |
Het |
| Mtmr7 |
A |
T |
8: 41,034,461 (GRCm39) |
L287Q |
probably damaging |
Het |
| Or52d13 |
T |
G |
7: 103,110,221 (GRCm39) |
M60L |
possibly damaging |
Het |
| Or7a39 |
A |
G |
10: 78,715,770 (GRCm39) |
T255A |
possibly damaging |
Het |
| Or8g28 |
A |
G |
9: 39,169,830 (GRCm39) |
I46T |
probably damaging |
Het |
| Pik3c3 |
T |
A |
18: 30,410,155 (GRCm39) |
F130I |
probably damaging |
Het |
| Rab3gap1 |
T |
A |
1: 127,845,958 (GRCm39) |
S277R |
possibly damaging |
Het |
| Rassf9 |
A |
G |
10: 102,381,494 (GRCm39) |
K290R |
probably benign |
Het |
| Rnaseh2a |
A |
T |
8: 85,691,767 (GRCm39) |
V136D |
probably damaging |
Het |
| Rnf39 |
C |
T |
17: 37,256,328 (GRCm39) |
S140L |
possibly damaging |
Het |
| Sbno2 |
A |
G |
10: 79,893,665 (GRCm39) |
V1212A |
probably damaging |
Het |
| Slc4a10 |
A |
T |
2: 62,021,101 (GRCm39) |
I50F |
probably damaging |
Het |
| Slfn5 |
A |
T |
11: 82,852,157 (GRCm39) |
E761V |
probably damaging |
Het |
| Sptlc1 |
A |
G |
13: 53,531,334 (GRCm39) |
Y18H |
probably damaging |
Het |
| Tfam |
A |
G |
10: 71,072,805 (GRCm39) |
M9T |
possibly damaging |
Het |
| Tmem186 |
A |
G |
16: 8,453,841 (GRCm39) |
L140P |
probably damaging |
Het |
| Try4 |
A |
T |
6: 41,281,960 (GRCm39) |
N182I |
probably damaging |
Het |
| Vmn1r209 |
C |
T |
13: 22,990,450 (GRCm39) |
C80Y |
probably damaging |
Het |
| Vmn2r104 |
A |
T |
17: 20,260,930 (GRCm39) |
S498T |
probably benign |
Het |
|
| Other mutations in Or11g25 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01796:Or11g25
|
APN |
14 |
50,722,998 (GRCm39) |
missense |
probably benign |
0.28 |
|
IGL01916:Or11g25
|
APN |
14 |
50,722,950 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02686:Or11g25
|
APN |
14 |
50,723,426 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02874:Or11g25
|
APN |
14 |
50,723,686 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
IGL02898:Or11g25
|
APN |
14 |
50,723,643 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4515001:Or11g25
|
UTSW |
14 |
50,723,536 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0085:Or11g25
|
UTSW |
14 |
50,723,791 (GRCm39) |
missense |
probably benign |
0.16 |
|
R1777:Or11g25
|
UTSW |
14 |
50,723,757 (GRCm39) |
missense |
probably benign |
0.08 |
|
R1850:Or11g25
|
UTSW |
14 |
50,723,055 (GRCm39) |
missense |
probably benign |
|
|
R2270:Or11g25
|
UTSW |
14 |
50,723,494 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2338:Or11g25
|
UTSW |
14 |
50,723,097 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R2971:Or11g25
|
UTSW |
14 |
50,723,065 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4594:Or11g25
|
UTSW |
14 |
50,723,619 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5383:Or11g25
|
UTSW |
14 |
50,723,509 (GRCm39) |
nonsense |
probably null |
|
|
R5708:Or11g25
|
UTSW |
14 |
50,723,452 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6038:Or11g25
|
UTSW |
14 |
50,723,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6038:Or11g25
|
UTSW |
14 |
50,723,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7116:Or11g25
|
UTSW |
14 |
50,723,025 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7702:Or11g25
|
UTSW |
14 |
50,723,751 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R8169:Or11g25
|
UTSW |
14 |
50,723,692 (GRCm39) |
missense |
probably benign |
0.13 |
|
R9040:Or11g25
|
UTSW |
14 |
50,722,995 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9139:Or11g25
|
UTSW |
14 |
50,723,707 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Posted On |
2014-02-04 |
Incidental Mutation