Incidental Mutation 'IGL01131:Vmn1r212'
| ID |
52597 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Vmn1r212
|
| Ensembl Gene |
ENSMUSG00000071490 |
| Gene Name |
vomeronasal 1 receptor 212 |
| Synonyms |
V1rh18 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.065)
|
| Stock # |
IGL01131
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
13 |
| Chromosomal Location |
23067212-23068375 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 23067329 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Aspartic acid
at position 335
(N335D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000093655
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000095960]
|
| AlphaFold |
Q8R268 |
| Predicted Effect |
unknown
Transcript: ENSMUST00000095960
AA Change: N335D
|
| SMART Domains |
Protein: ENSMUSP00000093655
Gene: ENSMUSG00000071490
AA Change: N335D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:TAS2R
|
2 |
292 |
1.2e-7 |
PFAM |
|
Pfam:V1R
|
34 |
297 |
5.4e-36 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000158990
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000226672
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000226881
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 29 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1110038F14Rik |
G |
A |
15: 76,834,475 (GRCm39) |
V124I |
probably damaging |
Het |
| Adgrf5 |
G |
T |
17: 43,733,400 (GRCm39) |
D75Y |
possibly damaging |
Het |
| Cfap20 |
T |
C |
8: 96,151,287 (GRCm39) |
D18G |
probably damaging |
Het |
| Cpne3 |
T |
C |
4: 19,543,318 (GRCm39) |
D160G |
probably damaging |
Het |
| Ercc3 |
A |
G |
18: 32,402,942 (GRCm39) |
*784W |
probably null |
Het |
| Fam53b |
T |
C |
7: 132,317,511 (GRCm39) |
E377G |
probably damaging |
Het |
| Far2 |
T |
C |
6: 148,052,096 (GRCm39) |
V125A |
possibly damaging |
Het |
| Fasn |
T |
C |
11: 120,705,445 (GRCm39) |
E1192G |
probably benign |
Het |
| Irf5 |
A |
G |
6: 29,536,102 (GRCm39) |
E372G |
probably damaging |
Het |
| Kif2c |
C |
T |
4: 117,029,562 (GRCm39) |
V140M |
probably damaging |
Het |
| Klre1 |
T |
C |
6: 129,561,133 (GRCm39) |
F165L |
possibly damaging |
Het |
| Kmt2a |
C |
T |
9: 44,732,467 (GRCm39) |
|
probably benign |
Het |
| Lrp2 |
C |
T |
2: 69,329,583 (GRCm39) |
C1728Y |
probably damaging |
Het |
| Muc4 |
C |
A |
16: 32,753,901 (GRCm38) |
T1259N |
possibly damaging |
Het |
| Nlrp9b |
A |
G |
7: 19,757,462 (GRCm39) |
D233G |
probably damaging |
Het |
| Nuf2 |
T |
C |
1: 169,349,933 (GRCm39) |
|
probably benign |
Het |
| Nynrin |
A |
G |
14: 56,110,142 (GRCm39) |
K1750E |
probably damaging |
Het |
| Or5b109 |
A |
G |
19: 13,212,103 (GRCm39) |
D163G |
probably benign |
Het |
| Parp4 |
C |
A |
14: 56,823,217 (GRCm39) |
|
probably benign |
Het |
| Rbms1 |
T |
C |
2: 60,589,180 (GRCm39) |
M287V |
probably benign |
Het |
| Rhox3c |
G |
A |
X: 36,651,982 (GRCm39) |
R71K |
probably damaging |
Het |
| Rufy1 |
A |
G |
11: 50,282,850 (GRCm39) |
L638P |
probably damaging |
Het |
| Slc15a3 |
G |
A |
19: 10,834,986 (GRCm39) |
|
probably benign |
Het |
| Slc26a9 |
T |
C |
1: 131,683,280 (GRCm39) |
|
probably null |
Het |
| Slc6a13 |
A |
G |
6: 121,298,600 (GRCm39) |
Y150C |
probably damaging |
Het |
| Slitrk6 |
A |
T |
14: 110,989,008 (GRCm39) |
L233Q |
probably damaging |
Het |
| Ugt3a1 |
T |
A |
15: 9,365,248 (GRCm39) |
I287N |
probably damaging |
Het |
| Unc13c |
T |
C |
9: 73,471,335 (GRCm39) |
N1778S |
probably benign |
Het |
| Wdfy1 |
C |
T |
1: 79,691,589 (GRCm39) |
V273I |
probably benign |
Het |
|
| Other mutations in Vmn1r212 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01678:Vmn1r212
|
APN |
13 |
23,068,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0798:Vmn1r212
|
UTSW |
13 |
23,067,868 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1237:Vmn1r212
|
UTSW |
13 |
23,067,638 (GRCm39) |
nonsense |
probably null |
|
|
R1331:Vmn1r212
|
UTSW |
13 |
23,067,562 (GRCm39) |
missense |
probably benign |
0.33 |
|
R2064:Vmn1r212
|
UTSW |
13 |
23,068,285 (GRCm39) |
missense |
probably benign |
0.28 |
|
R2356:Vmn1r212
|
UTSW |
13 |
23,068,120 (GRCm39) |
nonsense |
probably null |
|
|
R2846:Vmn1r212
|
UTSW |
13 |
23,068,262 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3896:Vmn1r212
|
UTSW |
13 |
23,068,067 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3937:Vmn1r212
|
UTSW |
13 |
23,067,358 (GRCm39) |
missense |
unknown |
|
|
R4722:Vmn1r212
|
UTSW |
13 |
23,068,078 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5233:Vmn1r212
|
UTSW |
13 |
23,067,304 (GRCm39) |
missense |
unknown |
|
|
R6043:Vmn1r212
|
UTSW |
13 |
23,068,258 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7199:Vmn1r212
|
UTSW |
13 |
23,067,731 (GRCm39) |
missense |
probably benign |
0.12 |
|
R7413:Vmn1r212
|
UTSW |
13 |
23,067,718 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7840:Vmn1r212
|
UTSW |
13 |
23,067,323 (GRCm39) |
missense |
unknown |
|
|
R8054:Vmn1r212
|
UTSW |
13 |
23,067,935 (GRCm39) |
missense |
probably benign |
0.25 |
|
R8844:Vmn1r212
|
UTSW |
13 |
23,067,526 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8929:Vmn1r212
|
UTSW |
13 |
23,067,494 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R9538:Vmn1r212
|
UTSW |
13 |
23,067,451 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9612:Vmn1r212
|
UTSW |
13 |
23,067,443 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
Z1088:Vmn1r212
|
UTSW |
13 |
23,067,932 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-06-21 |
Incidental Mutation