Incidental Mutation 'IGL03023:Vmn1r74'
ID |
408036 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vmn1r74
|
Ensembl Gene |
ENSMUSG00000047655 |
Gene Name |
vomeronasal 1 receptor 74 |
Synonyms |
V1rg5 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.062)
|
Stock # |
IGL03023
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
11580702-11581616 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 11581257 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Arginine
at position 186
(C186R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000154746
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000050416]
[ENSMUST00000228471]
|
AlphaFold |
Q8R290 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000050416
AA Change: C186R
PolyPhen 2
Score 0.458 (Sensitivity: 0.89; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000055148 Gene: ENSMUSG00000047655 AA Change: C186R
Domain | Start | End | E-Value | Type |
Pfam:7tm_1
|
22 |
290 |
1.3e-7 |
PFAM |
Pfam:V1R
|
34 |
296 |
1.2e-31 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000210930
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000228471
AA Change: C186R
PolyPhen 2
Score 0.458 (Sensitivity: 0.89; Specificity: 0.90)
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 23 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd18 |
A |
G |
3: 40,859,419 (GRCm39) |
D28G |
probably damaging |
Het |
Btaf1 |
C |
T |
19: 36,987,415 (GRCm39) |
R1746C |
possibly damaging |
Het |
Comp |
T |
C |
8: 70,831,260 (GRCm39) |
|
probably benign |
Het |
Cspg4b |
A |
G |
13: 113,488,275 (GRCm39) |
D99G |
probably benign |
Het |
Cyp2d9 |
A |
G |
15: 82,339,719 (GRCm39) |
T313A |
probably damaging |
Het |
Cyp3a59 |
T |
A |
5: 146,022,660 (GRCm39) |
D55E |
probably benign |
Het |
Dysf |
A |
G |
6: 84,169,989 (GRCm39) |
Y1790C |
probably damaging |
Het |
Fmo3 |
A |
C |
1: 162,786,034 (GRCm39) |
F319V |
probably benign |
Het |
Frem2 |
A |
T |
3: 53,563,049 (GRCm39) |
V486D |
probably benign |
Het |
Gucy2c |
A |
T |
6: 136,679,794 (GRCm39) |
|
probably null |
Het |
Hdac7 |
A |
T |
15: 97,695,838 (GRCm39) |
Y674N |
probably damaging |
Het |
Inpp5a |
G |
A |
7: 139,105,702 (GRCm39) |
|
probably null |
Het |
Jup |
T |
C |
11: 100,271,518 (GRCm39) |
|
probably benign |
Het |
Krt84 |
T |
C |
15: 101,436,880 (GRCm39) |
T385A |
possibly damaging |
Het |
Nbeal1 |
T |
C |
1: 60,292,572 (GRCm39) |
Y1075H |
probably damaging |
Het |
Nphp4 |
A |
G |
4: 152,608,692 (GRCm39) |
|
probably null |
Het |
Or10ak11 |
A |
T |
4: 118,687,449 (GRCm39) |
F63I |
probably damaging |
Het |
Or12d17 |
A |
G |
17: 37,777,885 (GRCm39) |
T263A |
probably benign |
Het |
Or4p7 |
G |
A |
2: 88,221,687 (GRCm39) |
C32Y |
probably damaging |
Het |
Psmc4 |
T |
A |
7: 27,742,285 (GRCm39) |
I264L |
possibly damaging |
Het |
Rwdd4a |
T |
C |
8: 47,995,803 (GRCm39) |
V61A |
probably benign |
Het |
Setx |
A |
G |
2: 29,035,914 (GRCm39) |
T800A |
probably benign |
Het |
Vsig2 |
A |
G |
9: 37,453,708 (GRCm39) |
Y136C |
probably damaging |
Het |
|
Other mutations in Vmn1r74 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01608:Vmn1r74
|
APN |
7 |
11,581,560 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01673:Vmn1r74
|
APN |
7 |
11,581,317 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03409:Vmn1r74
|
APN |
7 |
11,581,240 (GRCm39) |
missense |
probably damaging |
0.99 |
R0393:Vmn1r74
|
UTSW |
7 |
11,581,242 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1488:Vmn1r74
|
UTSW |
7 |
11,581,510 (GRCm39) |
missense |
probably benign |
0.02 |
R1707:Vmn1r74
|
UTSW |
7 |
11,581,504 (GRCm39) |
missense |
probably damaging |
0.98 |
R1998:Vmn1r74
|
UTSW |
7 |
11,581,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R1999:Vmn1r74
|
UTSW |
7 |
11,581,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R2139:Vmn1r74
|
UTSW |
7 |
11,581,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R4027:Vmn1r74
|
UTSW |
7 |
11,580,898 (GRCm39) |
missense |
probably damaging |
0.98 |
R4576:Vmn1r74
|
UTSW |
7 |
11,580,696 (GRCm39) |
splice site |
probably null |
|
R4619:Vmn1r74
|
UTSW |
7 |
11,581,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R4619:Vmn1r74
|
UTSW |
7 |
11,581,398 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5371:Vmn1r74
|
UTSW |
7 |
11,580,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R5606:Vmn1r74
|
UTSW |
7 |
11,580,822 (GRCm39) |
missense |
probably benign |
0.01 |
R6464:Vmn1r74
|
UTSW |
7 |
11,581,131 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6901:Vmn1r74
|
UTSW |
7 |
11,581,368 (GRCm39) |
missense |
probably benign |
0.00 |
R6920:Vmn1r74
|
UTSW |
7 |
11,581,575 (GRCm39) |
missense |
probably benign |
0.01 |
R7223:Vmn1r74
|
UTSW |
7 |
11,580,894 (GRCm39) |
nonsense |
probably null |
|
R7231:Vmn1r74
|
UTSW |
7 |
11,580,888 (GRCm39) |
missense |
probably benign |
0.34 |
R7418:Vmn1r74
|
UTSW |
7 |
11,581,081 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8135:Vmn1r74
|
UTSW |
7 |
11,581,530 (GRCm39) |
missense |
probably benign |
0.36 |
R8692:Vmn1r74
|
UTSW |
7 |
11,580,972 (GRCm39) |
missense |
probably benign |
0.03 |
R8748:Vmn1r74
|
UTSW |
7 |
11,580,903 (GRCm39) |
missense |
probably benign |
0.10 |
R9004:Vmn1r74
|
UTSW |
7 |
11,580,840 (GRCm39) |
missense |
probably benign |
0.00 |
R9258:Vmn1r74
|
UTSW |
7 |
11,580,999 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9564:Vmn1r74
|
UTSW |
7 |
11,581,534 (GRCm39) |
missense |
probably damaging |
1.00 |
RF049:Vmn1r74
|
UTSW |
7 |
11,581,067 (GRCm39) |
frame shift |
probably null |
|
RF063:Vmn1r74
|
UTSW |
7 |
11,581,067 (GRCm39) |
frame shift |
probably null |
|
Z1176:Vmn1r74
|
UTSW |
7 |
11,580,936 (GRCm39) |
missense |
probably benign |
|
|
Posted On |
2016-08-02 |