Incidental Mutation 'IGL01632:Vmn1r210'
| ID |
93483 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Vmn1r210
|
| Ensembl Gene |
ENSMUSG00000061296 |
| Gene Name |
vomeronasal 1 receptor 210 |
| Synonyms |
V1rh10 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.059)
|
| Stock # |
IGL01632
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
13 |
| Chromosomal Location |
23011364-23012284 bp(-) (GRCm39) |
| Type of Mutation |
makesense |
| DNA Base Change (assembly) |
A to T
at 23011366 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Stop codon to Arginine
at position 307
(*307R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000153776
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000072044]
[ENSMUST00000226180]
[ENSMUST00000226294]
|
| AlphaFold |
Q8R274 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000072044
AA Change: *307R
|
| SMART Domains |
Protein: ENSMUSP00000071925
Gene: ENSMUSG00000061296
AA Change: *307R
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:V1R
|
34 |
297 |
8.6e-38 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000226180
AA Change: *307R
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000226294
AA Change: *307R
|
| 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 |
|---|
| Adgra2 |
G |
A |
8: 27,608,761 (GRCm39) |
A540T |
possibly damaging |
Het |
| Alms1 |
T |
A |
6: 85,604,928 (GRCm39) |
C1724S |
probably benign |
Het |
| Anapc10 |
T |
C |
8: 80,439,795 (GRCm39) |
M1T |
probably null |
Het |
| Antxrl |
A |
G |
14: 33,789,904 (GRCm39) |
N332S |
probably damaging |
Het |
| Cdkl3 |
A |
G |
11: 51,895,899 (GRCm39) |
R49G |
probably damaging |
Het |
| Chodl |
A |
G |
16: 78,741,452 (GRCm39) |
|
probably benign |
Het |
| Clca3a1 |
G |
T |
3: 144,733,202 (GRCm39) |
A102D |
probably damaging |
Het |
| Clip1 |
T |
C |
5: 123,755,559 (GRCm39) |
E1029G |
probably damaging |
Het |
| Cpeb2 |
T |
A |
5: 43,394,765 (GRCm39) |
I581N |
probably benign |
Het |
| Dmxl1 |
T |
C |
18: 49,996,092 (GRCm39) |
V406A |
probably damaging |
Het |
| Dnah17 |
C |
T |
11: 117,924,707 (GRCm39) |
R3960Q |
probably damaging |
Het |
| Fstl5 |
A |
G |
3: 76,615,135 (GRCm39) |
D732G |
probably benign |
Het |
| Fyb2 |
G |
T |
4: 104,853,008 (GRCm39) |
V499L |
probably benign |
Het |
| Gm43191 |
A |
T |
3: 116,445,116 (GRCm39) |
H39Q |
probably damaging |
Het |
| Hspg2 |
A |
G |
4: 137,242,084 (GRCm39) |
K606R |
probably damaging |
Het |
| Klk1b27 |
C |
T |
7: 43,706,097 (GRCm39) |
|
probably benign |
Het |
| Mdga2 |
T |
C |
12: 66,676,672 (GRCm39) |
|
probably benign |
Het |
| Mup14 |
A |
T |
4: 61,259,383 (GRCm39) |
F56L |
probably benign |
Het |
| Myh15 |
A |
G |
16: 48,881,874 (GRCm39) |
K39E |
probably benign |
Het |
| Or1j10 |
A |
T |
2: 36,267,576 (GRCm39) |
N263Y |
probably benign |
Het |
| Or5m12 |
A |
G |
2: 85,734,714 (GRCm39) |
I228T |
probably benign |
Het |
| Ppp1r3a |
T |
A |
6: 14,754,810 (GRCm39) |
I146F |
probably damaging |
Het |
| Ryr2 |
A |
G |
13: 11,609,854 (GRCm39) |
I759T |
probably damaging |
Het |
| Sfmbt1 |
T |
C |
14: 30,539,669 (GRCm39) |
I819T |
probably damaging |
Het |
| Siglec1 |
A |
G |
2: 130,925,740 (GRCm39) |
V322A |
probably benign |
Het |
| Spata3 |
T |
C |
1: 85,950,030 (GRCm39) |
V87A |
possibly damaging |
Het |
| Tacstd2 |
A |
G |
6: 67,511,783 (GRCm39) |
V303A |
possibly damaging |
Het |
| Taok3 |
T |
A |
5: 117,403,993 (GRCm39) |
F723I |
possibly damaging |
Het |
| Tektl1 |
T |
C |
10: 78,584,536 (GRCm39) |
S329G |
probably benign |
Het |
| Vmn2r70 |
T |
C |
7: 85,215,280 (GRCm39) |
I85V |
probably benign |
Het |
| Zfp384 |
T |
C |
6: 125,001,724 (GRCm39) |
I123T |
probably damaging |
Het |
|
| Other mutations in Vmn1r210 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00938:Vmn1r210
|
APN |
13 |
23,011,538 (GRCm39) |
nonsense |
probably null |
|
|
IGL01541:Vmn1r210
|
APN |
13 |
23,011,778 (GRCm39) |
missense |
probably benign |
|
|
IGL01610:Vmn1r210
|
APN |
13 |
23,011,977 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03268:Vmn1r210
|
APN |
13 |
23,011,405 (GRCm39) |
missense |
probably benign |
0.40 |
|
IGL03340:Vmn1r210
|
APN |
13 |
23,011,644 (GRCm39) |
missense |
probably benign |
0.23 |
|
R0227:Vmn1r210
|
UTSW |
13 |
23,011,561 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0629:Vmn1r210
|
UTSW |
13 |
23,012,044 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3792:Vmn1r210
|
UTSW |
13 |
23,011,573 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4125:Vmn1r210
|
UTSW |
13 |
23,011,779 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4132:Vmn1r210
|
UTSW |
13 |
23,011,819 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4773:Vmn1r210
|
UTSW |
13 |
23,011,374 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5653:Vmn1r210
|
UTSW |
13 |
23,011,378 (GRCm39) |
nonsense |
probably null |
|
|
R6128:Vmn1r210
|
UTSW |
13 |
23,012,277 (GRCm39) |
nonsense |
probably null |
|
|
R6452:Vmn1r210
|
UTSW |
13 |
23,011,840 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6501:Vmn1r210
|
UTSW |
13 |
23,011,705 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R6864:Vmn1r210
|
UTSW |
13 |
23,011,713 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7623:Vmn1r210
|
UTSW |
13 |
23,011,405 (GRCm39) |
missense |
probably benign |
0.40 |
|
R7991:Vmn1r210
|
UTSW |
13 |
23,011,684 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9244:Vmn1r210
|
UTSW |
13 |
23,012,089 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9439:Vmn1r210
|
UTSW |
13 |
23,011,397 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R9538:Vmn1r210
|
UTSW |
13 |
23,011,837 (GRCm39) |
nonsense |
probably null |
|
|
R9732:Vmn1r210
|
UTSW |
13 |
23,011,379 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R9794:Vmn1r210
|
UTSW |
13 |
23,011,432 (GRCm39) |
missense |
probably damaging |
0.97 |
|
| Posted On |
2013-12-09 |
Incidental Mutation