Incidental Mutation 'IGL01551:Vmn1r177'
ID |
93256 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vmn1r177
|
Ensembl Gene |
ENSMUSG00000057513 |
Gene Name |
vomeronasal 1 receptor 177 |
Synonyms |
V1rd12 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.075)
|
Stock # |
IGL01551
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
23564945-23565874 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 23565688 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Valine
at position 63
(I63V)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000073621
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000073967]
|
AlphaFold |
E9PXM3 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000073967
AA Change: I63V
PolyPhen 2
Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)
|
SMART Domains |
Protein: ENSMUSP00000073621 Gene: ENSMUSG00000057513 AA Change: I63V
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
8 |
299 |
4.1e-13 |
PFAM |
Pfam:V1R
|
41 |
297 |
5.3e-14 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000207027
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
G |
A |
10: 78,924,147 (GRCm39) |
S103L |
possibly damaging |
Het |
Acvr2a |
G |
A |
2: 48,787,071 (GRCm39) |
A389T |
probably damaging |
Het |
Adamts9 |
A |
G |
6: 92,784,001 (GRCm39) |
S1037P |
probably damaging |
Het |
Adcyap1 |
A |
G |
17: 93,511,446 (GRCm39) |
Y140C |
probably damaging |
Het |
Ampd3 |
A |
G |
7: 110,404,183 (GRCm39) |
N569S |
probably damaging |
Het |
Bin1 |
G |
T |
18: 32,510,511 (GRCm39) |
V18L |
probably benign |
Het |
Ccdc158 |
A |
G |
5: 92,814,620 (GRCm39) |
Y69H |
probably damaging |
Het |
Ccdc70 |
A |
G |
8: 22,463,611 (GRCm39) |
R134G |
possibly damaging |
Het |
Cmtm2a |
A |
G |
8: 105,019,286 (GRCm39) |
V101A |
probably damaging |
Het |
Edar |
T |
C |
10: 58,441,860 (GRCm39) |
|
probably benign |
Het |
Gcc2 |
T |
C |
10: 58,134,691 (GRCm39) |
|
probably benign |
Het |
Gm10961 |
A |
G |
3: 107,540,281 (GRCm39) |
|
probably benign |
Het |
Hsd3b3 |
T |
C |
3: 98,649,216 (GRCm39) |
D369G |
probably benign |
Het |
Ifi202b |
T |
A |
1: 173,798,928 (GRCm39) |
K373N |
probably benign |
Het |
Khk |
C |
A |
5: 31,082,189 (GRCm39) |
H67N |
probably benign |
Het |
Kif7 |
T |
A |
7: 79,360,314 (GRCm39) |
|
probably null |
Het |
Mbd1 |
C |
T |
18: 74,402,614 (GRCm39) |
|
probably benign |
Het |
Mtor |
A |
G |
4: 148,556,494 (GRCm39) |
H968R |
probably damaging |
Het |
Nadk |
A |
G |
4: 155,673,157 (GRCm39) |
|
probably benign |
Het |
Or11g27 |
A |
G |
14: 50,771,618 (GRCm39) |
T250A |
probably benign |
Het |
Or2f1b |
A |
G |
6: 42,739,046 (GRCm39) |
D20G |
probably damaging |
Het |
Or5d40 |
A |
T |
2: 88,015,629 (GRCm39) |
H136L |
probably benign |
Het |
Otol1 |
T |
C |
3: 69,935,057 (GRCm39) |
F350L |
probably damaging |
Het |
Pramel22 |
T |
C |
4: 143,383,042 (GRCm39) |
N59S |
probably damaging |
Het |
Prkcg |
G |
A |
7: 3,352,342 (GRCm39) |
|
probably benign |
Het |
Rps6kc1 |
A |
T |
1: 190,505,837 (GRCm39) |
S1042T |
possibly damaging |
Het |
Rtn1 |
C |
T |
12: 72,263,709 (GRCm39) |
V741I |
possibly damaging |
Het |
Tor2a |
T |
A |
2: 32,650,595 (GRCm39) |
|
probably benign |
Het |
Vmn2r58 |
T |
A |
7: 41,514,703 (GRCm39) |
I89F |
probably damaging |
Het |
Xirp2 |
A |
G |
2: 67,343,849 (GRCm39) |
D2030G |
probably benign |
Het |
Zfp326 |
T |
C |
5: 106,036,451 (GRCm39) |
S121P |
probably damaging |
Het |
|
Other mutations in Vmn1r177 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01456:Vmn1r177
|
APN |
7 |
23,565,753 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL01504:Vmn1r177
|
APN |
7 |
23,565,835 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01535:Vmn1r177
|
APN |
7 |
23,565,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01647:Vmn1r177
|
APN |
7 |
23,565,600 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU74:Vmn1r177
|
UTSW |
7 |
23,565,645 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0396:Vmn1r177
|
UTSW |
7 |
23,565,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R0894:Vmn1r177
|
UTSW |
7 |
23,565,475 (GRCm39) |
missense |
probably benign |
0.09 |
R1446:Vmn1r177
|
UTSW |
7 |
23,565,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Vmn1r177
|
UTSW |
7 |
23,565,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R1893:Vmn1r177
|
UTSW |
7 |
23,565,573 (GRCm39) |
missense |
probably benign |
0.02 |
R1995:Vmn1r177
|
UTSW |
7 |
23,565,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Vmn1r177
|
UTSW |
7 |
23,565,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R3889:Vmn1r177
|
UTSW |
7 |
23,565,289 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4458:Vmn1r177
|
UTSW |
7 |
23,565,645 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4579:Vmn1r177
|
UTSW |
7 |
23,565,772 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5290:Vmn1r177
|
UTSW |
7 |
23,565,498 (GRCm39) |
missense |
probably damaging |
0.99 |
R6128:Vmn1r177
|
UTSW |
7 |
23,565,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R6128:Vmn1r177
|
UTSW |
7 |
23,565,267 (GRCm39) |
missense |
probably damaging |
0.99 |
R6730:Vmn1r177
|
UTSW |
7 |
23,565,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R6785:Vmn1r177
|
UTSW |
7 |
23,565,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R7100:Vmn1r177
|
UTSW |
7 |
23,565,535 (GRCm39) |
missense |
probably benign |
0.15 |
R7738:Vmn1r177
|
UTSW |
7 |
23,565,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R8191:Vmn1r177
|
UTSW |
7 |
23,565,736 (GRCm39) |
nonsense |
probably null |
|
R8980:Vmn1r177
|
UTSW |
7 |
23,565,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R9723:Vmn1r177
|
UTSW |
7 |
23,565,774 (GRCm39) |
missense |
probably damaging |
0.97 |
R9771:Vmn1r177
|
UTSW |
7 |
23,565,657 (GRCm39) |
missense |
probably damaging |
0.98 |
X0020:Vmn1r177
|
UTSW |
7 |
23,565,718 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Vmn1r177
|
UTSW |
7 |
23,565,360 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Posted On |
2013-12-09 |