Incidental Mutation 'IGL01797:Vmn2r121'
| ID |
155406 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Vmn2r121
|
| Ensembl Gene |
ENSMUSG00000072049 |
| Gene Name |
vomeronasal 2, receptor 121 |
| Synonyms |
EG625699 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.076)
|
| Stock # |
IGL01797
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
X |
| Chromosomal Location |
123037036-123045607 bp(-) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
G to A
at 123041048 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000092067
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000094491]
|
| AlphaFold |
A2BE32 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000094491
|
| SMART Domains |
Protein: ENSMUSP00000092067
Gene: ENSMUSG00000072049
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
|
Pfam:ANF_receptor
|
75 |
448 |
3.2e-26 |
PFAM |
|
Pfam:NCD3G
|
506 |
560 |
2.1e-19 |
PFAM |
|
Pfam:7tm_3
|
593 |
828 |
3.8e-56 |
PFAM |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 31 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca16 |
T |
C |
7: 120,113,760 (GRCm39) |
V877A |
probably benign |
Het |
| Clcn2 |
T |
C |
16: 20,531,511 (GRCm39) |
I178V |
probably damaging |
Het |
| Cnbp |
A |
G |
6: 87,822,542 (GRCm39) |
|
probably benign |
Het |
| Coq8a |
A |
T |
1: 179,997,284 (GRCm39) |
|
probably null |
Het |
| Dctn2 |
A |
G |
10: 127,113,182 (GRCm39) |
D244G |
possibly damaging |
Het |
| Dync1h1 |
T |
A |
12: 110,618,630 (GRCm39) |
|
probably null |
Het |
| Efcab15 |
T |
C |
11: 103,089,794 (GRCm39) |
Y381C |
probably damaging |
Het |
| Faiml |
T |
C |
9: 99,116,442 (GRCm39) |
K83E |
probably damaging |
Het |
| Fdx1 |
A |
T |
9: 51,854,925 (GRCm39) |
C159* |
probably null |
Het |
| Fgd3 |
A |
T |
13: 49,443,065 (GRCm39) |
V169E |
probably damaging |
Het |
| Ice1 |
G |
T |
13: 70,772,065 (GRCm39) |
T51K |
probably damaging |
Het |
| Iqca1 |
A |
C |
1: 90,072,541 (GRCm39) |
|
probably null |
Het |
| Jup |
C |
A |
11: 100,272,498 (GRCm39) |
|
probably benign |
Het |
| Krt84 |
A |
G |
15: 101,436,915 (GRCm39) |
V373A |
possibly damaging |
Het |
| Ndst4 |
T |
A |
3: 125,476,802 (GRCm39) |
M9K |
probably damaging |
Het |
| Nomo1 |
T |
C |
7: 45,706,086 (GRCm39) |
V480A |
probably damaging |
Het |
| Nsun5 |
A |
G |
5: 135,404,225 (GRCm39) |
H344R |
probably damaging |
Het |
| Or13a21 |
A |
G |
7: 139,998,931 (GRCm39) |
Y252H |
probably damaging |
Het |
| Or1e1f |
A |
T |
11: 73,855,644 (GRCm39) |
D70V |
probably damaging |
Het |
| Pjvk |
T |
C |
2: 76,487,883 (GRCm39) |
|
probably benign |
Het |
| Prkaa1 |
G |
A |
15: 5,198,187 (GRCm39) |
D159N |
probably damaging |
Het |
| Sap130 |
T |
A |
18: 31,831,721 (GRCm39) |
I736N |
probably damaging |
Het |
| Tlcd1 |
A |
G |
11: 78,071,160 (GRCm39) |
|
probably null |
Het |
| Tpp1 |
T |
C |
7: 105,398,459 (GRCm39) |
I286V |
probably benign |
Het |
| Ttll5 |
T |
A |
12: 86,003,371 (GRCm39) |
I1069K |
possibly damaging |
Het |
| Ttn |
T |
G |
2: 76,540,257 (GRCm39) |
E34243A |
possibly damaging |
Het |
| Uqcr10 |
A |
C |
11: 4,654,179 (GRCm39) |
I43S |
possibly damaging |
Het |
| Ush2a |
T |
A |
1: 187,995,706 (GRCm39) |
M159K |
probably damaging |
Het |
| Vmn2r30 |
T |
A |
7: 7,337,195 (GRCm39) |
D147V |
probably benign |
Het |
| Xntrpc |
T |
C |
7: 101,739,753 (GRCm39) |
I559T |
possibly damaging |
Het |
| Zfp268 |
T |
A |
4: 145,347,241 (GRCm39) |
N48K |
probably damaging |
Het |
|
| Other mutations in Vmn2r121 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00990:Vmn2r121
|
APN |
X |
123,037,480 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL00990:Vmn2r121
|
APN |
X |
123,037,499 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL00990:Vmn2r121
|
APN |
X |
123,043,413 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01125:Vmn2r121
|
APN |
X |
123,042,504 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01450:Vmn2r121
|
APN |
X |
123,040,888 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
IGL01619:Vmn2r121
|
APN |
X |
123,041,997 (GRCm39) |
missense |
probably benign |
|
|
IGL02227:Vmn2r121
|
APN |
X |
123,042,378 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02971:Vmn2r121
|
APN |
X |
123,037,591 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03058:Vmn2r121
|
APN |
X |
123,042,618 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03142:Vmn2r121
|
APN |
X |
123,042,635 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL03183:Vmn2r121
|
APN |
X |
123,042,023 (GRCm39) |
missense |
probably benign |
0.03 |
|
E0370:Vmn2r121
|
UTSW |
X |
123,037,617 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0196:Vmn2r121
|
UTSW |
X |
123,041,879 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1381:Vmn2r121
|
UTSW |
X |
123,037,837 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1399:Vmn2r121
|
UTSW |
X |
123,039,545 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R1423:Vmn2r121
|
UTSW |
X |
123,039,602 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R1687:Vmn2r121
|
UTSW |
X |
123,042,488 (GRCm39) |
missense |
probably benign |
0.39 |
|
R2121:Vmn2r121
|
UTSW |
X |
123,043,439 (GRCm39) |
splice site |
probably null |
|
|
R2124:Vmn2r121
|
UTSW |
X |
123,043,439 (GRCm39) |
splice site |
probably null |
|
|
R3151:Vmn2r121
|
UTSW |
X |
123,040,849 (GRCm39) |
missense |
probably benign |
0.20 |
|
R4460:Vmn2r121
|
UTSW |
X |
123,038,281 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4735:Vmn2r121
|
UTSW |
X |
123,038,335 (GRCm39) |
missense |
probably benign |
|
|
R5332:Vmn2r121
|
UTSW |
X |
123,043,272 (GRCm39) |
missense |
probably benign |
|
|
R6102:Vmn2r121
|
UTSW |
X |
123,043,272 (GRCm39) |
missense |
probably benign |
|
|
X0023:Vmn2r121
|
UTSW |
X |
123,045,354 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
| Posted On |
2014-02-04 |
Incidental Mutation