Incidental Mutation 'IGL02930:Vmn1r8'
ID |
364043 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vmn1r8
|
Ensembl Gene |
ENSMUSG00000061208 |
Gene Name |
vomeronasal 1 receptor 8 |
Synonyms |
V1rc32 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.059)
|
Stock # |
IGL02930
|
Quality Score |
|
Status
|
|
Chromosome |
6 |
Chromosomal Location |
57012898-57014110 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 57013579 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Arginine
at position 210
(K210R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000154298
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000078186]
[ENSMUST00000227706]
[ENSMUST00000228690]
|
AlphaFold |
Q8R2C2 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000078186
AA Change: K210R
PolyPhen 2
Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)
|
SMART Domains |
Protein: ENSMUSP00000093561 Gene: ENSMUSG00000061208 AA Change: K210R
Domain | Start | End | E-Value | Type |
Pfam:V1R
|
28 |
293 |
1.2e-58 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000227706
AA Change: K210R
PolyPhen 2
Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000228690
AA Change: K210R
PolyPhen 2
Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,328,226 (GRCm39) |
N3433S |
possibly damaging |
Het |
Actl9 |
T |
C |
17: 33,653,073 (GRCm39) |
S378P |
probably damaging |
Het |
Aldh6a1 |
C |
A |
12: 84,480,756 (GRCm39) |
L426F |
possibly damaging |
Het |
Ankef1 |
T |
C |
2: 136,392,245 (GRCm39) |
I478T |
possibly damaging |
Het |
Cabs1 |
A |
G |
5: 88,127,745 (GRCm39) |
D132G |
probably damaging |
Het |
Ccdc39 |
T |
C |
3: 33,879,643 (GRCm39) |
E475G |
probably damaging |
Het |
Cmtm2b |
A |
C |
8: 105,056,402 (GRCm39) |
M104L |
probably benign |
Het |
Cops2 |
T |
C |
2: 125,674,109 (GRCm39) |
|
probably benign |
Het |
Dnajc4 |
C |
A |
19: 6,966,801 (GRCm39) |
V176F |
possibly damaging |
Het |
Eepd1 |
A |
G |
9: 25,394,536 (GRCm39) |
N267D |
probably damaging |
Het |
Elobl |
T |
G |
11: 88,856,012 (GRCm39) |
D17A |
possibly damaging |
Het |
Erich6 |
G |
A |
3: 58,529,775 (GRCm39) |
|
probably benign |
Het |
Flna |
G |
A |
X: 73,267,506 (GRCm39) |
R2548C |
probably damaging |
Het |
Gm6878 |
T |
G |
14: 67,548,439 (GRCm39) |
|
probably benign |
Het |
Gpc1 |
G |
T |
1: 92,785,021 (GRCm39) |
E355* |
probably null |
Het |
Islr |
C |
T |
9: 58,065,483 (GRCm39) |
|
probably benign |
Het |
Mex3a |
A |
T |
3: 88,443,532 (GRCm39) |
I203L |
probably benign |
Het |
Or5p58 |
A |
T |
7: 107,694,621 (GRCm39) |
I52N |
probably damaging |
Het |
Or6c88 |
T |
C |
10: 129,407,184 (GRCm39) |
I220T |
probably damaging |
Het |
Or8g24 |
G |
T |
9: 38,989,308 (GRCm39) |
H244Q |
probably damaging |
Het |
Prokr2 |
T |
C |
2: 132,215,394 (GRCm39) |
S195G |
probably benign |
Het |
Pyroxd1 |
A |
T |
6: 142,304,778 (GRCm39) |
D335V |
probably damaging |
Het |
Rps6kl1 |
T |
C |
12: 85,196,548 (GRCm39) |
T39A |
probably benign |
Het |
Rusc2 |
G |
A |
4: 43,416,376 (GRCm39) |
A561T |
probably damaging |
Het |
Sel1l3 |
A |
C |
5: 53,280,559 (GRCm39) |
V937G |
possibly damaging |
Het |
Sh3pxd2b |
A |
G |
11: 32,367,161 (GRCm39) |
T382A |
possibly damaging |
Het |
Tbx21 |
A |
G |
11: 96,990,865 (GRCm39) |
I271T |
probably damaging |
Het |
Timeless |
T |
C |
10: 128,083,060 (GRCm39) |
V632A |
probably benign |
Het |
Tle3 |
A |
G |
9: 61,301,981 (GRCm39) |
N67S |
possibly damaging |
Het |
Tln2 |
G |
A |
9: 67,300,944 (GRCm39) |
R95* |
probably null |
Het |
Trim24 |
A |
G |
6: 37,928,380 (GRCm39) |
|
probably benign |
Het |
Uggt1 |
A |
T |
1: 36,196,537 (GRCm39) |
D1253E |
probably benign |
Het |
|
Other mutations in Vmn1r8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01569:Vmn1r8
|
APN |
6 |
57,013,272 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL01820:Vmn1r8
|
APN |
6 |
57,013,653 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02416:Vmn1r8
|
APN |
6 |
57,013,605 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02496:Vmn1r8
|
APN |
6 |
57,013,556 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02954:Vmn1r8
|
APN |
6 |
57,013,315 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03235:Vmn1r8
|
APN |
6 |
57,013,746 (GRCm39) |
nonsense |
probably null |
|
IGL03353:Vmn1r8
|
APN |
6 |
57,013,776 (GRCm39) |
missense |
probably benign |
0.03 |
PIT4494001:Vmn1r8
|
UTSW |
6 |
57,013,712 (GRCm39) |
missense |
probably benign |
0.01 |
R0656:Vmn1r8
|
UTSW |
6 |
57,013,573 (GRCm39) |
missense |
probably benign |
0.35 |
R1328:Vmn1r8
|
UTSW |
6 |
57,013,278 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1846:Vmn1r8
|
UTSW |
6 |
57,013,413 (GRCm39) |
missense |
probably benign |
0.06 |
R2083:Vmn1r8
|
UTSW |
6 |
57,013,325 (GRCm39) |
missense |
probably benign |
0.21 |
R3683:Vmn1r8
|
UTSW |
6 |
57,013,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R4134:Vmn1r8
|
UTSW |
6 |
57,013,705 (GRCm39) |
missense |
probably benign |
|
R4754:Vmn1r8
|
UTSW |
6 |
57,012,952 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R4857:Vmn1r8
|
UTSW |
6 |
57,013,338 (GRCm39) |
missense |
probably benign |
0.00 |
R5787:Vmn1r8
|
UTSW |
6 |
57,013,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R6158:Vmn1r8
|
UTSW |
6 |
57,013,274 (GRCm39) |
missense |
probably benign |
0.00 |
R6711:Vmn1r8
|
UTSW |
6 |
57,013,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R6971:Vmn1r8
|
UTSW |
6 |
57,013,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R8066:Vmn1r8
|
UTSW |
6 |
57,013,419 (GRCm39) |
missense |
probably benign |
0.03 |
R8261:Vmn1r8
|
UTSW |
6 |
57,013,158 (GRCm39) |
missense |
probably benign |
0.00 |
R8526:Vmn1r8
|
UTSW |
6 |
57,013,362 (GRCm39) |
missense |
probably benign |
0.05 |
R8552:Vmn1r8
|
UTSW |
6 |
57,013,138 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8692:Vmn1r8
|
UTSW |
6 |
57,013,557 (GRCm39) |
missense |
probably benign |
0.01 |
R8712:Vmn1r8
|
UTSW |
6 |
57,013,665 (GRCm39) |
missense |
probably benign |
0.07 |
R9306:Vmn1r8
|
UTSW |
6 |
57,013,713 (GRCm39) |
missense |
probably benign |
0.12 |
|
Posted On |
2015-12-18 |