Incidental Mutation 'IGL02319:Or51l14'
| ID |
288167 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or51l14
|
| Ensembl Gene |
ENSMUSG00000073949 |
| Gene Name |
olfactory receptor family 51 subfamily L member 14 |
| Synonyms |
Olfr606, GA_x6K02T2PBJ9-6173009-6173968, MOR17-2 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.087)
|
| Stock # |
IGL02319
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
103100546-103101505 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 103101474 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Tyrosine
at position 310
(C310Y)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151177
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000098200]
[ENSMUST00000214347]
[ENSMUST00000214631]
[ENSMUST00000217250]
|
| AlphaFold |
Q8VGZ8 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000098200
AA Change: C310Y
PolyPhen 2
Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)
|
| SMART Domains |
Protein: ENSMUSP00000095802
Gene: ENSMUSG00000073949
AA Change: C310Y
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
12 |
N/A |
INTRINSIC |
|
Pfam:7tm_4
|
33 |
312 |
7.1e-116 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
37 |
307 |
9e-8 |
PFAM |
|
Pfam:7tm_1
|
43 |
294 |
7.4e-16 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214347
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214631
AA Change: C310Y
PolyPhen 2
Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000217250
AA Change: C310Y
PolyPhen 2
Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)
|
| 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: 31 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acss3 |
T |
C |
10: 106,784,611 (GRCm39) |
Y537C |
probably damaging |
Het |
| Ambra1 |
A |
G |
2: 91,717,265 (GRCm39) |
H854R |
probably damaging |
Het |
| Atf7ip |
A |
G |
6: 136,570,116 (GRCm39) |
N981S |
probably benign |
Het |
| Atp6v1d |
A |
G |
12: 78,908,230 (GRCm39) |
S2P |
probably damaging |
Het |
| Cd59a |
A |
T |
2: 103,944,373 (GRCm39) |
I74F |
possibly damaging |
Het |
| Chek2 |
T |
C |
5: 111,014,877 (GRCm39) |
Y449H |
possibly damaging |
Het |
| Ctif |
C |
T |
18: 75,654,944 (GRCm39) |
|
probably benign |
Het |
| Dnaaf3 |
T |
C |
7: 4,526,946 (GRCm39) |
E403G |
probably damaging |
Het |
| Dock1 |
T |
G |
7: 134,374,178 (GRCm39) |
V608G |
possibly damaging |
Het |
| Fcf1 |
T |
C |
12: 85,017,982 (GRCm39) |
|
probably null |
Het |
| Fgf17 |
T |
G |
14: 70,874,183 (GRCm39) |
Q202P |
possibly damaging |
Het |
| Hnrnpm |
A |
T |
17: 33,868,924 (GRCm39) |
L501Q |
probably damaging |
Het |
| Itgb4 |
G |
A |
11: 115,879,752 (GRCm39) |
V635I |
probably damaging |
Het |
| Klra6 |
A |
T |
6: 130,002,177 (GRCm39) |
S2R |
probably damaging |
Het |
| Krtap19-9b |
T |
A |
16: 88,729,002 (GRCm39) |
Y33F |
unknown |
Het |
| Lpcat4 |
G |
A |
2: 112,074,229 (GRCm39) |
V264M |
probably damaging |
Het |
| Lyzl6 |
T |
C |
11: 103,525,862 (GRCm39) |
Y86C |
probably damaging |
Het |
| Myo18b |
T |
C |
5: 112,939,005 (GRCm39) |
K1669E |
probably damaging |
Het |
| Nbea |
A |
G |
3: 55,893,159 (GRCm39) |
V1558A |
probably damaging |
Het |
| Or51a42 |
A |
G |
7: 103,708,140 (GRCm39) |
I223T |
probably damaging |
Het |
| Or5b105 |
A |
G |
19: 13,080,026 (GRCm39) |
I214T |
probably benign |
Het |
| Or8b47 |
T |
A |
9: 38,435,166 (GRCm39) |
I46N |
probably damaging |
Het |
| Pex11b |
T |
C |
3: 96,550,885 (GRCm39) |
|
probably benign |
Het |
| Rbm5 |
A |
T |
9: 107,621,064 (GRCm39) |
L689* |
probably null |
Het |
| Rd3 |
G |
T |
1: 191,715,452 (GRCm39) |
G76C |
probably null |
Het |
| Rgs16 |
A |
T |
1: 153,617,852 (GRCm39) |
I121F |
probably damaging |
Het |
| Tmem30a |
A |
T |
9: 79,681,485 (GRCm39) |
M264K |
probably damaging |
Het |
| Traf2 |
T |
C |
2: 25,426,695 (GRCm39) |
E127G |
probably damaging |
Het |
| Trmt11 |
A |
T |
10: 30,436,869 (GRCm39) |
D290E |
probably damaging |
Het |
| Wdr35 |
C |
A |
12: 9,077,480 (GRCm39) |
|
probably benign |
Het |
| Wnk2 |
A |
G |
13: 49,214,914 (GRCm39) |
S1211P |
possibly damaging |
Het |
|
| Other mutations in Or51l14 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01287:Or51l14
|
APN |
7 |
103,101,002 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01608:Or51l14
|
APN |
7 |
103,101,011 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02251:Or51l14
|
APN |
7 |
103,100,978 (GRCm39) |
nonsense |
probably null |
|
|
R0369:Or51l14
|
UTSW |
7 |
103,101,423 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0480:Or51l14
|
UTSW |
7 |
103,100,835 (GRCm39) |
missense |
probably benign |
0.07 |
|
R1759:Or51l14
|
UTSW |
7 |
103,101,356 (GRCm39) |
missense |
probably benign |
0.11 |
|
R1858:Or51l14
|
UTSW |
7 |
103,101,332 (GRCm39) |
missense |
probably benign |
0.16 |
|
R2156:Or51l14
|
UTSW |
7 |
103,101,371 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4226:Or51l14
|
UTSW |
7 |
103,100,784 (GRCm39) |
missense |
probably benign |
0.31 |
|
R4422:Or51l14
|
UTSW |
7 |
103,101,450 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5071:Or51l14
|
UTSW |
7 |
103,100,617 (GRCm39) |
missense |
probably benign |
|
|
R5074:Or51l14
|
UTSW |
7 |
103,100,617 (GRCm39) |
missense |
probably benign |
|
|
R5137:Or51l14
|
UTSW |
7 |
103,100,920 (GRCm39) |
nonsense |
probably null |
|
|
R5137:Or51l14
|
UTSW |
7 |
103,100,919 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8914:Or51l14
|
UTSW |
7 |
103,101,090 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9457:Or51l14
|
UTSW |
7 |
103,100,618 (GRCm39) |
missense |
probably benign |
0.00 |
|
X0018:Or51l14
|
UTSW |
7 |
103,101,005 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
| Posted On |
2015-04-16 |
Incidental Mutation