Incidental Mutation 'IGL03208:Vmn1r67'
ID |
413202 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vmn1r67
|
Ensembl Gene |
ENSMUSG00000046716 |
Gene Name |
vomeronasal 1 receptor 67 |
Synonyms |
V1re10 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.079)
|
Stock # |
IGL03208
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
10180716-10181714 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 10181025 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Arginine
at position 96
(S96R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000060746
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055964]
[ENSMUST00000226237]
|
AlphaFold |
G5E8C1 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000055964
AA Change: S96R
PolyPhen 2
Score 0.941 (Sensitivity: 0.80; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000060746 Gene: ENSMUSG00000046716 AA Change: S96R
Domain | Start | End | E-Value | Type |
Pfam:V1R
|
34 |
292 |
4.3e-31 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000226237
AA Change: S35R
PolyPhen 2
Score 0.912 (Sensitivity: 0.81; Specificity: 0.94)
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 24 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aco1 |
T |
C |
4: 40,186,424 (GRCm39) |
V612A |
possibly damaging |
Het |
Cd72 |
T |
A |
4: 43,452,337 (GRCm39) |
T195S |
probably damaging |
Het |
Cluh |
C |
A |
11: 74,560,332 (GRCm39) |
|
probably null |
Het |
Cntn3 |
T |
C |
6: 102,164,060 (GRCm39) |
Y882C |
probably damaging |
Het |
Ctnnal1 |
T |
A |
4: 56,813,833 (GRCm39) |
K645N |
probably benign |
Het |
Entpd6 |
T |
A |
2: 150,610,838 (GRCm39) |
Y385N |
probably damaging |
Het |
Epha3 |
T |
C |
16: 63,431,452 (GRCm39) |
Y484C |
probably damaging |
Het |
Exo1 |
G |
A |
1: 175,723,811 (GRCm39) |
A386T |
probably benign |
Het |
Fam149b |
T |
C |
14: 20,401,370 (GRCm39) |
|
probably benign |
Het |
Fastkd2 |
G |
A |
1: 63,778,365 (GRCm39) |
E413K |
probably damaging |
Het |
Fbxl3 |
A |
T |
14: 103,320,376 (GRCm39) |
L405* |
probably null |
Het |
Gpr75 |
A |
T |
11: 30,842,699 (GRCm39) |
I535F |
probably damaging |
Het |
Irf2 |
A |
C |
8: 47,260,340 (GRCm39) |
I53L |
probably damaging |
Het |
Lca5l |
T |
C |
16: 95,980,046 (GRCm39) |
E28G |
probably damaging |
Het |
Mon2 |
A |
G |
10: 122,853,974 (GRCm39) |
|
probably benign |
Het |
Or10z1 |
A |
G |
1: 174,077,959 (GRCm39) |
F178S |
probably damaging |
Het |
Or52n4b |
T |
C |
7: 108,144,326 (GRCm39) |
V196A |
probably benign |
Het |
Plekhm1 |
T |
C |
11: 103,267,596 (GRCm39) |
K792E |
probably benign |
Het |
Ppp1r14c |
A |
T |
10: 3,373,531 (GRCm39) |
D114V |
probably damaging |
Het |
Rnf20 |
G |
T |
4: 49,645,706 (GRCm39) |
|
probably benign |
Het |
Srgap1 |
G |
A |
10: 121,628,171 (GRCm39) |
P934S |
possibly damaging |
Het |
Sult2b1 |
T |
C |
7: 45,383,053 (GRCm39) |
E243G |
probably damaging |
Het |
Tecta |
A |
G |
9: 42,248,396 (GRCm39) |
|
probably benign |
Het |
Tshr |
T |
C |
12: 91,500,716 (GRCm39) |
L147P |
probably damaging |
Het |
|
Other mutations in Vmn1r67 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01690:Vmn1r67
|
APN |
7 |
10,180,767 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02812:Vmn1r67
|
APN |
7 |
10,180,945 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03121:Vmn1r67
|
APN |
7 |
10,181,394 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4142001:Vmn1r67
|
UTSW |
7 |
10,180,877 (GRCm39) |
missense |
probably benign |
0.13 |
R0048:Vmn1r67
|
UTSW |
7 |
10,180,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R0549:Vmn1r67
|
UTSW |
7 |
10,181,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R1595:Vmn1r67
|
UTSW |
7 |
10,181,597 (GRCm39) |
missense |
probably benign |
0.18 |
R1608:Vmn1r67
|
UTSW |
7 |
10,180,907 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2284:Vmn1r67
|
UTSW |
7 |
10,181,600 (GRCm39) |
missense |
probably damaging |
0.97 |
R3614:Vmn1r67
|
UTSW |
7 |
10,181,356 (GRCm39) |
missense |
probably damaging |
0.98 |
R4399:Vmn1r67
|
UTSW |
7 |
10,181,476 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4542:Vmn1r67
|
UTSW |
7 |
10,181,357 (GRCm39) |
missense |
probably damaging |
0.99 |
R5216:Vmn1r67
|
UTSW |
7 |
10,181,090 (GRCm39) |
missense |
probably benign |
0.00 |
R5655:Vmn1r67
|
UTSW |
7 |
10,181,315 (GRCm39) |
missense |
probably benign |
0.43 |
R5837:Vmn1r67
|
UTSW |
7 |
10,180,949 (GRCm39) |
missense |
probably benign |
0.26 |
R6526:Vmn1r67
|
UTSW |
7 |
10,181,598 (GRCm39) |
missense |
probably benign |
0.05 |
R6735:Vmn1r67
|
UTSW |
7 |
10,181,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R6846:Vmn1r67
|
UTSW |
7 |
10,180,840 (GRCm39) |
missense |
probably benign |
0.04 |
R7086:Vmn1r67
|
UTSW |
7 |
10,181,044 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7227:Vmn1r67
|
UTSW |
7 |
10,181,475 (GRCm39) |
nonsense |
probably null |
|
R7594:Vmn1r67
|
UTSW |
7 |
10,181,342 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7608:Vmn1r67
|
UTSW |
7 |
10,181,290 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7797:Vmn1r67
|
UTSW |
7 |
10,180,903 (GRCm39) |
missense |
probably benign |
0.30 |
R8681:Vmn1r67
|
UTSW |
7 |
10,181,128 (GRCm39) |
missense |
probably benign |
0.30 |
|
Posted On |
2016-08-02 |