Incidental Mutation 'IGL01577:Vmn1r87'
ID |
91306 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vmn1r87
|
Ensembl Gene |
ENSMUSG00000070815 |
Gene Name |
vomeronasal 1 receptor 87 |
Synonyms |
V1rk1 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.050)
|
Stock # |
IGL01577
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
12865398-12866285 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 12865775 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Phenylalanine
at position 171
(V171F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000154184
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000094827]
[ENSMUST00000211249]
[ENSMUST00000227443]
[ENSMUST00000228800]
|
AlphaFold |
Q8R255 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000094827
AA Change: V171F
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
SMART Domains |
Protein: ENSMUSP00000092422 Gene: ENSMUSG00000070815 AA Change: V171F
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
1 |
285 |
1.2e-11 |
PFAM |
Pfam:V1R
|
14 |
280 |
1.8e-36 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000211249
AA Change: V171F
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000227443
AA Change: V171F
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000228800
AA Change: V171F
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr8 |
A |
G |
14: 29,709,232 (GRCm39) |
T279A |
probably benign |
Het |
Adamts9 |
T |
G |
6: 92,835,128 (GRCm39) |
|
probably benign |
Het |
Apba3 |
G |
A |
10: 81,108,053 (GRCm39) |
G403D |
probably damaging |
Het |
Atp13a4 |
C |
T |
16: 29,260,102 (GRCm39) |
V235I |
possibly damaging |
Het |
Brca2 |
T |
A |
5: 150,465,085 (GRCm39) |
C1616* |
probably null |
Het |
Ccdc7a |
T |
A |
8: 129,715,244 (GRCm39) |
E280V |
probably damaging |
Het |
Cdc42bpb |
A |
G |
12: 111,268,477 (GRCm39) |
I1241T |
possibly damaging |
Het |
Cplx4 |
G |
T |
18: 66,103,015 (GRCm39) |
A35E |
probably damaging |
Het |
Cyp2j8 |
T |
G |
4: 96,367,308 (GRCm39) |
D270A |
probably damaging |
Het |
Cyp7a1 |
T |
C |
4: 6,273,618 (GRCm39) |
D96G |
probably damaging |
Het |
Ddx11 |
G |
A |
17: 66,446,398 (GRCm39) |
R429H |
possibly damaging |
Het |
Depdc5 |
C |
A |
5: 33,113,241 (GRCm39) |
T419N |
possibly damaging |
Het |
Diaph3 |
A |
C |
14: 87,143,467 (GRCm39) |
I737R |
probably damaging |
Het |
Elf2 |
C |
T |
3: 51,163,773 (GRCm39) |
|
probably benign |
Het |
Epha6 |
T |
A |
16: 59,777,289 (GRCm39) |
I673L |
possibly damaging |
Het |
Ephx1 |
A |
G |
1: 180,829,545 (GRCm39) |
M1T |
probably null |
Het |
Fndc3a |
A |
T |
14: 72,827,298 (GRCm39) |
M84K |
probably damaging |
Het |
Gad2 |
T |
C |
2: 22,571,292 (GRCm39) |
|
probably benign |
Het |
Gba2 |
G |
A |
4: 43,573,753 (GRCm39) |
Q180* |
probably null |
Het |
Gga2 |
A |
G |
7: 121,589,006 (GRCm39) |
Y574H |
probably damaging |
Het |
Gm7168 |
A |
T |
17: 14,169,649 (GRCm39) |
R339W |
probably damaging |
Het |
Hdac10 |
T |
C |
15: 89,010,416 (GRCm39) |
E302G |
possibly damaging |
Het |
Ighv1-72 |
A |
G |
12: 115,721,893 (GRCm39) |
V21A |
possibly damaging |
Het |
Kif15 |
A |
G |
9: 122,825,399 (GRCm39) |
E774G |
probably benign |
Het |
Lig3 |
A |
G |
11: 82,674,303 (GRCm39) |
N43S |
probably benign |
Het |
Nmnat1 |
T |
A |
4: 149,554,135 (GRCm39) |
D135V |
possibly damaging |
Het |
Or1s2 |
A |
G |
19: 13,758,162 (GRCm39) |
Y62C |
probably damaging |
Het |
Or52n2 |
A |
G |
7: 104,542,730 (GRCm39) |
F35S |
probably benign |
Het |
Pak6 |
A |
C |
2: 118,524,129 (GRCm39) |
K428T |
probably benign |
Het |
Pou2f3 |
G |
A |
9: 43,058,178 (GRCm39) |
Q56* |
probably null |
Het |
Prep |
T |
C |
10: 44,948,144 (GRCm39) |
|
probably benign |
Het |
Psd4 |
C |
T |
2: 24,293,234 (GRCm39) |
P700S |
probably damaging |
Het |
Rad18 |
A |
T |
6: 112,642,302 (GRCm39) |
|
probably benign |
Het |
Rbbp5 |
A |
G |
1: 132,420,393 (GRCm39) |
K209E |
possibly damaging |
Het |
Smurf1 |
G |
A |
5: 144,829,998 (GRCm39) |
T335I |
probably damaging |
Het |
Tbcd |
G |
A |
11: 121,387,838 (GRCm39) |
R72Q |
probably damaging |
Het |
Tsga10 |
T |
C |
1: 37,874,538 (GRCm39) |
T116A |
possibly damaging |
Het |
Unc80 |
A |
G |
1: 66,569,127 (GRCm39) |
|
probably null |
Het |
Ythdc2 |
A |
T |
18: 44,991,349 (GRCm39) |
M786L |
probably benign |
Het |
Zmym6 |
C |
A |
4: 126,999,223 (GRCm39) |
T469K |
probably damaging |
Het |
|
Other mutations in Vmn1r87 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01400:Vmn1r87
|
APN |
7 |
12,866,230 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02972:Vmn1r87
|
APN |
7 |
12,866,256 (GRCm39) |
nonsense |
probably null |
|
IGL03246:Vmn1r87
|
APN |
7 |
12,866,288 (GRCm39) |
utr 5 prime |
probably benign |
|
PIT4142001:Vmn1r87
|
UTSW |
7 |
12,866,112 (GRCm39) |
missense |
probably benign |
0.00 |
R0153:Vmn1r87
|
UTSW |
7 |
12,866,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R0502:Vmn1r87
|
UTSW |
7 |
12,865,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R0658:Vmn1r87
|
UTSW |
7 |
12,865,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R1589:Vmn1r87
|
UTSW |
7 |
12,865,703 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1731:Vmn1r87
|
UTSW |
7 |
12,865,703 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2027:Vmn1r87
|
UTSW |
7 |
12,865,823 (GRCm39) |
missense |
probably damaging |
0.99 |
R2044:Vmn1r87
|
UTSW |
7 |
12,865,748 (GRCm39) |
missense |
probably benign |
0.02 |
R3124:Vmn1r87
|
UTSW |
7 |
12,865,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R4208:Vmn1r87
|
UTSW |
7 |
12,866,185 (GRCm39) |
missense |
probably benign |
0.37 |
R4731:Vmn1r87
|
UTSW |
7 |
12,866,254 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4732:Vmn1r87
|
UTSW |
7 |
12,866,254 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4733:Vmn1r87
|
UTSW |
7 |
12,866,254 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5079:Vmn1r87
|
UTSW |
7 |
12,866,253 (GRCm39) |
missense |
probably benign |
0.01 |
R5125:Vmn1r87
|
UTSW |
7 |
12,865,792 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5178:Vmn1r87
|
UTSW |
7 |
12,865,792 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6599:Vmn1r87
|
UTSW |
7 |
12,865,886 (GRCm39) |
nonsense |
probably null |
|
R7067:Vmn1r87
|
UTSW |
7 |
12,865,849 (GRCm39) |
missense |
probably benign |
0.02 |
R7560:Vmn1r87
|
UTSW |
7 |
12,865,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Vmn1r87
|
UTSW |
7 |
12,865,613 (GRCm39) |
missense |
probably benign |
0.01 |
R7910:Vmn1r87
|
UTSW |
7 |
12,865,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R8040:Vmn1r87
|
UTSW |
7 |
12,866,086 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8220:Vmn1r87
|
UTSW |
7 |
12,865,427 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9690:Vmn1r87
|
UTSW |
7 |
12,866,263 (GRCm39) |
missense |
probably benign |
0.01 |
X0028:Vmn1r87
|
UTSW |
7 |
12,865,910 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
Posted On |
2013-12-09 |