Incidental Mutation 'IGL03246:Vmn1r87'
| ID |
414421 |
| 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 # |
IGL03246
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
12865398-12866285 bp(-) (GRCm39) |
| Type of Mutation |
utr 5 prime |
| DNA Base Change (assembly) |
G to A
at 12866288 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| 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
|
| SMART Domains |
Protein: ENSMUSP00000092422
Gene: ENSMUSG00000070815
| 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
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000227443
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000228800
|
| 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 |
|---|
| 4921511C20Rik |
T |
A |
X: 126,303,238 (GRCm39) |
H392Q |
probably benign |
Het |
| Alox8 |
T |
A |
11: 69,076,841 (GRCm39) |
I547L |
probably damaging |
Het |
| Capn13 |
T |
C |
17: 73,689,855 (GRCm39) |
H52R |
probably benign |
Het |
| Cfap57 |
T |
A |
4: 118,433,842 (GRCm39) |
I979L |
probably benign |
Het |
| Ctdnep1 |
T |
C |
11: 69,875,156 (GRCm39) |
|
probably benign |
Het |
| Ercc5 |
C |
A |
1: 44,206,241 (GRCm39) |
P385T |
probably damaging |
Het |
| Fam98a |
C |
T |
17: 75,845,848 (GRCm39) |
M299I |
probably damaging |
Het |
| Flcn |
A |
T |
11: 59,684,936 (GRCm39) |
I505N |
possibly damaging |
Het |
| Fn1 |
G |
A |
1: 71,663,455 (GRCm39) |
T1011I |
possibly damaging |
Het |
| Klhl28 |
T |
C |
12: 65,004,060 (GRCm39) |
D151G |
probably benign |
Het |
| Klk13 |
T |
A |
7: 43,370,422 (GRCm39) |
N28K |
probably damaging |
Het |
| Macc1 |
T |
C |
12: 119,410,420 (GRCm39) |
V396A |
probably benign |
Het |
| Mageb11 |
C |
A |
X: 89,936,008 (GRCm39) |
H87Q |
probably benign |
Het |
| Magi2 |
T |
A |
5: 20,563,948 (GRCm39) |
I360K |
probably damaging |
Het |
| Myh7b |
T |
C |
2: 155,459,792 (GRCm39) |
I251T |
probably damaging |
Het |
| Naalad2 |
A |
T |
9: 18,296,395 (GRCm39) |
I85K |
possibly damaging |
Het |
| Or5ae1 |
T |
C |
7: 84,565,919 (GRCm39) |
C311R |
probably benign |
Het |
| Pbrm1 |
A |
T |
14: 30,832,506 (GRCm39) |
M1490L |
probably benign |
Het |
| Pclo |
C |
T |
5: 14,727,631 (GRCm39) |
|
probably benign |
Het |
| Pdcd6ip |
T |
C |
9: 113,507,485 (GRCm39) |
K357R |
possibly damaging |
Het |
| Pnpla6 |
C |
T |
8: 3,581,530 (GRCm39) |
T601I |
probably benign |
Het |
| Pof1b |
A |
T |
X: 111,557,817 (GRCm39) |
N366K |
probably benign |
Het |
| Prr9 |
A |
G |
3: 92,030,286 (GRCm39) |
|
probably benign |
Het |
| Ptprz1 |
G |
T |
6: 22,986,159 (GRCm39) |
A320S |
probably damaging |
Het |
| Ripor1 |
A |
G |
8: 106,342,490 (GRCm39) |
Y187C |
possibly damaging |
Het |
| Rnf13 |
A |
G |
3: 57,676,471 (GRCm39) |
E42G |
probably damaging |
Het |
| Sdf4 |
T |
C |
4: 156,085,154 (GRCm39) |
V163A |
probably benign |
Het |
| Smc2 |
C |
T |
4: 52,440,301 (GRCm39) |
Q16* |
probably null |
Het |
| Srsf3-ps |
T |
A |
11: 98,516,119 (GRCm39) |
R85* |
probably null |
Het |
| Tbck |
T |
A |
3: 132,480,331 (GRCm39) |
C737S |
probably benign |
Het |
| Tra2a |
A |
T |
6: 49,226,019 (GRCm39) |
Y140* |
probably null |
Het |
| Vcpip1 |
A |
C |
1: 9,816,182 (GRCm39) |
L734V |
probably benign |
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 |
|
IGL01577:Vmn1r87
|
APN |
7 |
12,865,775 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02972:Vmn1r87
|
APN |
7 |
12,866,256 (GRCm39) |
nonsense |
probably null |
|
|
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 |
2016-08-02 |
Incidental Mutation