Incidental Mutation 'IGL02684:Or51v8'
| ID |
303492 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or51v8
|
| Ensembl Gene |
ENSMUSG00000045780 |
| Gene Name |
olfactory receptor family 51 subfamily V member 8 |
| Synonyms |
Olfr624, MOR4-2P, GA_x6K02T2PBJ9-6394126-6393197 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.115)
|
| Stock # |
IGL02684
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
103319310-103320236 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 103319591 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Valine
at position 216
(M216V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000049938
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000062144]
|
| AlphaFold |
F8VQI7 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000062144
AA Change: M216V
PolyPhen 2
Score 0.057 (Sensitivity: 0.94; Specificity: 0.84)
|
| SMART Domains |
Protein: ENSMUSP00000049938
Gene: ENSMUSG00000045780
AA Change: M216V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
27 |
306 |
3.3e-138 |
PFAM |
|
Pfam:7tm_1
|
37 |
288 |
1.8e-19 |
PFAM |
|
| 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: 32 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930596D02Rik |
A |
T |
14: 35,532,020 (GRCm39) |
L185* |
probably null |
Het |
| Aadacl4fm5 |
A |
G |
4: 144,504,755 (GRCm39) |
|
probably benign |
Het |
| Actrt3 |
A |
T |
3: 30,653,840 (GRCm39) |
D53E |
probably benign |
Het |
| Ankrd34b |
T |
C |
13: 92,575,016 (GRCm39) |
S83P |
probably damaging |
Het |
| Asap1 |
A |
G |
15: 63,966,018 (GRCm39) |
V1029A |
probably benign |
Het |
| Blk |
T |
C |
14: 63,617,143 (GRCm39) |
E288G |
probably benign |
Het |
| Cep192 |
T |
G |
18: 67,967,634 (GRCm39) |
V706G |
probably damaging |
Het |
| Chd2 |
T |
C |
7: 73,125,097 (GRCm39) |
K908E |
probably damaging |
Het |
| Dnm1l |
A |
T |
16: 16,139,521 (GRCm39) |
I391N |
possibly damaging |
Het |
| Fmn1 |
A |
G |
2: 113,355,622 (GRCm39) |
R688G |
unknown |
Het |
| Gdap2 |
A |
G |
3: 100,078,336 (GRCm39) |
D100G |
probably benign |
Het |
| Gm43638 |
T |
C |
5: 87,610,769 (GRCm39) |
I522V |
possibly damaging |
Het |
| Gsap |
A |
T |
5: 21,447,801 (GRCm39) |
|
probably null |
Het |
| Hoxd12 |
A |
G |
2: 74,505,905 (GRCm39) |
S159G |
probably benign |
Het |
| Ints7 |
A |
G |
1: 191,345,749 (GRCm39) |
|
probably null |
Het |
| Iqsec3 |
G |
A |
6: 121,389,900 (GRCm39) |
Q524* |
probably null |
Het |
| Klra10 |
T |
A |
6: 130,258,845 (GRCm39) |
H14L |
possibly damaging |
Het |
| Lratd1 |
T |
C |
12: 14,200,646 (GRCm39) |
D27G |
probably damaging |
Het |
| Mettl15 |
T |
C |
2: 108,961,925 (GRCm39) |
E228G |
probably damaging |
Het |
| Or9s18 |
G |
A |
13: 65,300,210 (GRCm39) |
M57I |
probably damaging |
Het |
| Pabpc1l |
A |
G |
2: 163,873,197 (GRCm39) |
N156D |
probably benign |
Het |
| Pkhd1l1 |
G |
T |
15: 44,379,605 (GRCm39) |
|
probably null |
Het |
| Pm20d1 |
T |
A |
1: 131,732,697 (GRCm39) |
N345K |
probably benign |
Het |
| Rasgrp1 |
A |
G |
2: 117,113,057 (GRCm39) |
V785A |
probably benign |
Het |
| Sos2 |
A |
G |
12: 69,643,440 (GRCm39) |
L980S |
probably damaging |
Het |
| Stam2 |
A |
T |
2: 52,609,947 (GRCm39) |
H56Q |
probably damaging |
Het |
| Trpm6 |
T |
A |
19: 18,779,571 (GRCm39) |
|
probably benign |
Het |
| Trpm7 |
A |
T |
2: 126,688,079 (GRCm39) |
D249E |
probably damaging |
Het |
| Vmn1r203 |
A |
T |
13: 22,708,539 (GRCm39) |
T107S |
possibly damaging |
Het |
| Vmn2r55 |
A |
G |
7: 12,404,887 (GRCm39) |
L172P |
probably damaging |
Het |
| Vrtn |
A |
G |
12: 84,696,923 (GRCm39) |
R558G |
probably benign |
Het |
| Zfp977 |
A |
T |
7: 42,232,439 (GRCm39) |
D7E |
probably damaging |
Het |
|
| Other mutations in Or51v8 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02419:Or51v8
|
APN |
7 |
103,319,682 (GRCm39) |
nonsense |
probably null |
|
|
IGL02536:Or51v8
|
APN |
7 |
103,320,164 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
FR4548:Or51v8
|
UTSW |
7 |
103,320,174 (GRCm39) |
nonsense |
probably null |
|
|
FR4548:Or51v8
|
UTSW |
7 |
103,320,167 (GRCm39) |
small insertion |
probably benign |
|
|
FR4976:Or51v8
|
UTSW |
7 |
103,320,173 (GRCm39) |
small insertion |
probably benign |
|
|
R0295:Or51v8
|
UTSW |
7 |
103,319,518 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0518:Or51v8
|
UTSW |
7 |
103,319,696 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R0521:Or51v8
|
UTSW |
7 |
103,319,696 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R1352:Or51v8
|
UTSW |
7 |
103,319,518 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1779:Or51v8
|
UTSW |
7 |
103,319,845 (GRCm39) |
missense |
probably benign |
0.15 |
|
R1878:Or51v8
|
UTSW |
7 |
103,319,389 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1965:Or51v8
|
UTSW |
7 |
103,320,103 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2162:Or51v8
|
UTSW |
7 |
103,320,079 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2316:Or51v8
|
UTSW |
7 |
103,319,674 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R3792:Or51v8
|
UTSW |
7 |
103,319,353 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3848:Or51v8
|
UTSW |
7 |
103,319,908 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4120:Or51v8
|
UTSW |
7 |
103,320,221 (GRCm39) |
missense |
probably benign |
|
|
R4183:Or51v8
|
UTSW |
7 |
103,320,178 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R4853:Or51v8
|
UTSW |
7 |
103,320,010 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6351:Or51v8
|
UTSW |
7 |
103,320,163 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7717:Or51v8
|
UTSW |
7 |
103,320,152 (GRCm39) |
missense |
probably benign |
|
|
R9091:Or51v8
|
UTSW |
7 |
103,320,124 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9270:Or51v8
|
UTSW |
7 |
103,320,124 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9273:Or51v8
|
UTSW |
7 |
103,319,633 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9378:Or51v8
|
UTSW |
7 |
103,319,389 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0026:Or51v8
|
UTSW |
7 |
103,319,602 (GRCm39) |
missense |
probably benign |
|
|
| Posted On |
2015-04-16 |
Incidental Mutation