Incidental Mutation 'IGL02082:Vmn1r113'
ID |
283391 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vmn1r113
|
Ensembl Gene |
ENSMUSG00000091638 |
Gene Name |
vomeronasal 1 receptor 113 |
Synonyms |
Gm5748 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.060)
|
Stock # |
IGL02082
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
20521210-20522133 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 20521672 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Histidine to Tyrosine
at position 155
(H155Y)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000133307
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000168794]
[ENSMUST00000173723]
|
AlphaFold |
G3UWI8 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000168794
AA Change: H155Y
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000126041 Gene: ENSMUSG00000091638 AA Change: H155Y
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
8 |
288 |
4.2e-8 |
PFAM |
Pfam:V1R
|
41 |
288 |
2.8e-8 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000173723
AA Change: H155Y
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000133307 Gene: ENSMUSG00000091638 AA Change: H155Y
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
8 |
298 |
4e-16 |
PFAM |
Pfam:7tm_1
|
31 |
290 |
9.3e-7 |
PFAM |
Pfam:V1R
|
41 |
298 |
5e-17 |
PFAM |
|
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 |
Atp9b |
A |
C |
18: 80,935,145 (GRCm39) |
|
probably benign |
Het |
Brinp3 |
T |
C |
1: 146,627,600 (GRCm39) |
C278R |
probably damaging |
Het |
Cfap54 |
T |
C |
10: 92,917,320 (GRCm39) |
S47G |
unknown |
Het |
Clec16a |
T |
C |
16: 10,432,432 (GRCm39) |
L484P |
probably damaging |
Het |
Cnksr1 |
C |
A |
4: 133,963,363 (GRCm39) |
G71C |
probably damaging |
Het |
Dnah12 |
A |
T |
14: 26,428,317 (GRCm39) |
N246I |
possibly damaging |
Het |
Fbh1 |
T |
C |
2: 11,768,938 (GRCm39) |
D285G |
probably benign |
Het |
Focad |
C |
T |
4: 88,148,815 (GRCm39) |
Q511* |
probably null |
Het |
Gpr63 |
A |
G |
4: 25,008,564 (GRCm39) |
|
probably benign |
Het |
Iah1 |
C |
A |
12: 21,367,405 (GRCm39) |
S37* |
probably null |
Het |
Inpp4a |
T |
A |
1: 37,405,708 (GRCm39) |
|
probably benign |
Het |
Mcm2 |
A |
T |
6: 88,865,218 (GRCm39) |
Y486* |
probably null |
Het |
Mtmr10 |
A |
G |
7: 63,983,238 (GRCm39) |
|
probably benign |
Het |
Nbea |
A |
G |
3: 55,875,588 (GRCm39) |
L1694S |
possibly damaging |
Het |
Pafah1b1 |
A |
G |
11: 74,590,159 (GRCm39) |
S4P |
probably benign |
Het |
Rnase10 |
A |
T |
14: 51,246,856 (GRCm39) |
E41V |
probably damaging |
Het |
Slc17a6 |
G |
T |
7: 51,318,777 (GRCm39) |
R473L |
probably benign |
Het |
Spata31g1 |
A |
G |
4: 42,970,198 (GRCm39) |
T2A |
probably benign |
Het |
Tbc1d9b |
A |
G |
11: 50,054,709 (GRCm39) |
D951G |
probably benign |
Het |
Tk1 |
C |
A |
11: 117,716,553 (GRCm39) |
|
probably null |
Het |
Trim46 |
C |
A |
3: 89,146,307 (GRCm39) |
A395S |
probably benign |
Het |
Vmn1r222 |
A |
G |
13: 23,416,499 (GRCm39) |
M238T |
probably damaging |
Het |
Vmn2r72 |
A |
T |
7: 85,387,374 (GRCm39) |
V730E |
probably benign |
Het |
|
Other mutations in Vmn1r113 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01908:Vmn1r113
|
APN |
7 |
20,521,943 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02148:Vmn1r113
|
APN |
7 |
20,521,747 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03169:Vmn1r113
|
APN |
7 |
20,522,012 (GRCm39) |
missense |
probably benign |
0.11 |
R0593:Vmn1r113
|
UTSW |
7 |
20,521,388 (GRCm39) |
missense |
probably damaging |
0.99 |
R0669:Vmn1r113
|
UTSW |
7 |
20,521,345 (GRCm39) |
missense |
probably benign |
0.00 |
R1212:Vmn1r113
|
UTSW |
7 |
20,521,356 (GRCm39) |
missense |
probably benign |
0.19 |
R1693:Vmn1r113
|
UTSW |
7 |
20,521,532 (GRCm39) |
missense |
probably damaging |
0.98 |
R2228:Vmn1r113
|
UTSW |
7 |
20,521,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R3945:Vmn1r113
|
UTSW |
7 |
20,521,637 (GRCm39) |
missense |
probably benign |
0.00 |
R4209:Vmn1r113
|
UTSW |
7 |
20,521,535 (GRCm39) |
missense |
probably benign |
0.44 |
R5038:Vmn1r113
|
UTSW |
7 |
20,521,419 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6306:Vmn1r113
|
UTSW |
7 |
20,521,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R6623:Vmn1r113
|
UTSW |
7 |
20,521,991 (GRCm39) |
missense |
probably benign |
0.01 |
R6675:Vmn1r113
|
UTSW |
7 |
20,521,903 (GRCm39) |
missense |
probably benign |
0.02 |
R6677:Vmn1r113
|
UTSW |
7 |
20,521,903 (GRCm39) |
missense |
probably benign |
0.02 |
R6678:Vmn1r113
|
UTSW |
7 |
20,521,903 (GRCm39) |
missense |
probably benign |
0.02 |
R6968:Vmn1r113
|
UTSW |
7 |
20,521,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R7054:Vmn1r113
|
UTSW |
7 |
20,521,427 (GRCm39) |
missense |
probably benign |
0.14 |
R7256:Vmn1r113
|
UTSW |
7 |
20,521,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R8926:Vmn1r113
|
UTSW |
7 |
20,521,874 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9131:Vmn1r113
|
UTSW |
7 |
20,521,342 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2015-04-16 |