Incidental Mutation 'IGL00487:Vmn1r180'
ID |
5310 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vmn1r180
|
Ensembl Gene |
ENSMUSG00000092473 |
Gene Name |
vomeronasal 1 receptor 180 |
Synonyms |
V1rd16, LOC232962 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.054)
|
Stock # |
IGL00487
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
23651812-23652781 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 23651948 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Histidine to Leucine
at position 37
(H37L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000134362
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000173816]
|
AlphaFold |
B9EK86 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000173816
AA Change: H37L
PolyPhen 2
Score 0.363 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000134362 Gene: ENSMUSG00000092473 AA Change: H37L
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
8 |
298 |
2.9e-15 |
PFAM |
Pfam:7tm_1
|
31 |
286 |
6.7e-9 |
PFAM |
Pfam:V1R
|
41 |
297 |
1.4e-17 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 15 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
T |
A |
11: 110,200,276 (GRCm39) |
|
probably null |
Het |
Cfap251 |
T |
G |
5: 123,412,240 (GRCm39) |
I84S |
probably damaging |
Het |
Dusp23 |
T |
C |
1: 172,459,199 (GRCm39) |
|
probably benign |
Het |
Invs |
C |
T |
4: 48,407,689 (GRCm39) |
Q555* |
probably null |
Het |
Mak16 |
T |
C |
8: 31,656,778 (GRCm39) |
N9D |
probably benign |
Het |
Mrps7 |
T |
C |
11: 115,495,684 (GRCm39) |
I74T |
possibly damaging |
Het |
Nlrp4a |
T |
G |
7: 26,149,410 (GRCm39) |
V339G |
possibly damaging |
Het |
Nucb1 |
A |
G |
7: 45,151,075 (GRCm39) |
L102P |
probably damaging |
Het |
Pdp2 |
T |
C |
8: 105,320,829 (GRCm39) |
M226T |
probably benign |
Het |
Pik3r2 |
T |
C |
8: 71,223,073 (GRCm39) |
D449G |
probably damaging |
Het |
Rnf157 |
G |
A |
11: 116,253,181 (GRCm39) |
P76S |
probably benign |
Het |
Senp6 |
C |
A |
9: 80,021,120 (GRCm39) |
Q267K |
probably damaging |
Het |
Slc9a2 |
A |
G |
1: 40,781,818 (GRCm39) |
E349G |
probably damaging |
Het |
Snx14 |
G |
T |
9: 88,284,243 (GRCm39) |
S475Y |
probably damaging |
Het |
Xrn1 |
A |
T |
9: 95,921,002 (GRCm39) |
H1371L |
probably benign |
Het |
|
Other mutations in Vmn1r180 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01309:Vmn1r180
|
APN |
7 |
23,652,424 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01793:Vmn1r180
|
APN |
7 |
23,652,668 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02653:Vmn1r180
|
APN |
7 |
23,652,500 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03277:Vmn1r180
|
APN |
7 |
23,652,710 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03352:Vmn1r180
|
APN |
7 |
23,652,077 (GRCm39) |
nonsense |
probably null |
|
R1298:Vmn1r180
|
UTSW |
7 |
23,652,572 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1701:Vmn1r180
|
UTSW |
7 |
23,652,395 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1702:Vmn1r180
|
UTSW |
7 |
23,652,394 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2122:Vmn1r180
|
UTSW |
7 |
23,652,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R4241:Vmn1r180
|
UTSW |
7 |
23,652,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R5683:Vmn1r180
|
UTSW |
7 |
23,652,635 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7241:Vmn1r180
|
UTSW |
7 |
23,651,891 (GRCm39) |
missense |
probably damaging |
0.96 |
R7522:Vmn1r180
|
UTSW |
7 |
23,652,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R8749:Vmn1r180
|
UTSW |
7 |
23,652,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R8991:Vmn1r180
|
UTSW |
7 |
23,652,076 (GRCm39) |
missense |
probably benign |
0.06 |
R9442:Vmn1r180
|
UTSW |
7 |
23,651,620 (GRCm39) |
start gained |
probably benign |
|
|
Posted On |
2012-04-20 |