Incidental Mutation 'IGL03004:Vmn1r230'
| ID |
407492 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Vmn1r230
|
| Ensembl Gene |
ENSMUSG00000045417 |
| Gene Name |
vomeronasal 1 receptor 230 |
| Synonyms |
V1re8 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.054)
|
| Stock # |
IGL03004
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
17 |
| Chromosomal Location |
21066813-21067763 bp(+) (GRCm39) |
| Type of Mutation |
unclassified |
| DNA Base Change (assembly) |
T to C
at 21067772 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000061330
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053974]
|
| AlphaFold |
Q8R2A2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000053974
|
| SMART Domains |
Protein: ENSMUSP00000061330
Gene: ENSMUSG00000045417
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:TAS2R
|
20 |
315 |
2.4e-12 |
PFAM |
|
Pfam:V1R
|
50 |
312 |
7.9e-30 |
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 |
|---|
| Atrx |
A |
T |
X: 104,876,115 (GRCm39) |
C78* |
probably null |
Het |
| Birc6 |
T |
A |
17: 74,919,180 (GRCm39) |
N1999K |
probably benign |
Het |
| Bltp1 |
T |
A |
3: 37,019,826 (GRCm39) |
|
probably benign |
Het |
| Cdc42bpg |
G |
A |
19: 6,361,413 (GRCm39) |
R313Q |
probably benign |
Het |
| Clip3 |
A |
G |
7: 29,991,789 (GRCm39) |
Y55C |
probably damaging |
Het |
| Ddit4l |
A |
G |
3: 137,331,966 (GRCm39) |
N111D |
probably benign |
Het |
| Eprs1 |
T |
G |
1: 185,114,030 (GRCm39) |
M326R |
probably damaging |
Het |
| F8 |
C |
T |
X: 74,255,658 (GRCm39) |
G2045D |
probably damaging |
Het |
| Fstl5 |
A |
G |
3: 76,555,738 (GRCm39) |
|
probably benign |
Het |
| Gm10577 |
T |
C |
4: 100,877,526 (GRCm39) |
|
probably benign |
Het |
| Heatr6 |
T |
C |
11: 83,648,205 (GRCm39) |
S133P |
probably benign |
Het |
| Itpr3 |
T |
G |
17: 27,316,952 (GRCm39) |
F736V |
possibly damaging |
Het |
| Klf8 |
T |
C |
X: 152,165,716 (GRCm39) |
L95P |
probably damaging |
Het |
| Lrrc40 |
G |
A |
3: 157,747,302 (GRCm39) |
|
probably benign |
Het |
| Map3k12 |
A |
G |
15: 102,412,631 (GRCm39) |
V247A |
possibly damaging |
Het |
| Obscn |
A |
G |
11: 58,919,413 (GRCm39) |
Y6211H |
probably damaging |
Het |
| Or1j19 |
A |
G |
2: 36,677,194 (GRCm39) |
Y219C |
probably damaging |
Het |
| Pip4k2b |
A |
G |
11: 97,615,300 (GRCm39) |
Y187H |
probably damaging |
Het |
| Rabggta |
A |
G |
14: 55,956,687 (GRCm39) |
|
probably benign |
Het |
| Ranbp3 |
T |
A |
17: 57,014,207 (GRCm39) |
V246E |
probably damaging |
Het |
| Rtf1 |
C |
A |
2: 119,531,754 (GRCm39) |
|
probably benign |
Het |
| Sema3b |
G |
A |
9: 107,480,114 (GRCm39) |
P208L |
possibly damaging |
Het |
| Smpd1 |
A |
G |
7: 105,205,881 (GRCm39) |
D416G |
possibly damaging |
Het |
| Spam1 |
T |
C |
6: 24,796,913 (GRCm39) |
V288A |
probably damaging |
Het |
| Stac |
A |
C |
9: 111,431,608 (GRCm39) |
S248A |
probably benign |
Het |
| Tmem178b |
C |
A |
6: 40,222,515 (GRCm39) |
R77S |
probably damaging |
Het |
| Vegfd |
T |
C |
X: 163,185,104 (GRCm39) |
L352P |
probably benign |
Het |
| Vmn1r176 |
A |
T |
7: 23,534,702 (GRCm39) |
N150K |
probably damaging |
Het |
| Vsig10 |
A |
G |
5: 117,463,140 (GRCm39) |
Y122C |
probably damaging |
Het |
| Xpo5 |
T |
A |
17: 46,518,766 (GRCm39) |
V121E |
probably damaging |
Het |
| Zrsr2 |
T |
C |
X: 162,722,397 (GRCm39) |
Q285R |
probably benign |
Het |
|
| Other mutations in Vmn1r230 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02590:Vmn1r230
|
APN |
17 |
21,067,172 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0306:Vmn1r230
|
UTSW |
17 |
21,066,895 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R0318:Vmn1r230
|
UTSW |
17 |
21,067,078 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R2076:Vmn1r230
|
UTSW |
17 |
21,067,144 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2151:Vmn1r230
|
UTSW |
17 |
21,067,063 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2153:Vmn1r230
|
UTSW |
17 |
21,067,063 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2154:Vmn1r230
|
UTSW |
17 |
21,067,063 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2192:Vmn1r230
|
UTSW |
17 |
21,067,355 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2215:Vmn1r230
|
UTSW |
17 |
21,067,684 (GRCm39) |
missense |
probably benign |
0.25 |
|
R2309:Vmn1r230
|
UTSW |
17 |
21,067,492 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4493:Vmn1r230
|
UTSW |
17 |
21,066,863 (GRCm39) |
missense |
probably benign |
|
|
R4683:Vmn1r230
|
UTSW |
17 |
21,067,515 (GRCm39) |
missense |
probably benign |
0.07 |
|
R4804:Vmn1r230
|
UTSW |
17 |
21,067,345 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4949:Vmn1r230
|
UTSW |
17 |
21,067,625 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5138:Vmn1r230
|
UTSW |
17 |
21,067,230 (GRCm39) |
nonsense |
probably null |
|
|
R6248:Vmn1r230
|
UTSW |
17 |
21,067,036 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R7329:Vmn1r230
|
UTSW |
17 |
21,066,952 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7468:Vmn1r230
|
UTSW |
17 |
21,067,146 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7716:Vmn1r230
|
UTSW |
17 |
21,067,144 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R7817:Vmn1r230
|
UTSW |
17 |
21,066,823 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7832:Vmn1r230
|
UTSW |
17 |
21,066,933 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7977:Vmn1r230
|
UTSW |
17 |
21,067,159 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7986:Vmn1r230
|
UTSW |
17 |
21,067,119 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7987:Vmn1r230
|
UTSW |
17 |
21,067,159 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7993:Vmn1r230
|
UTSW |
17 |
21,067,312 (GRCm39) |
missense |
probably benign |
0.10 |
|
R8439:Vmn1r230
|
UTSW |
17 |
21,066,870 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8971:Vmn1r230
|
UTSW |
17 |
21,067,321 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R9576:Vmn1r230
|
UTSW |
17 |
21,067,163 (GRCm39) |
nonsense |
probably null |
|
|
R9578:Vmn1r230
|
UTSW |
17 |
21,067,163 (GRCm39) |
nonsense |
probably null |
|
|
R9687:Vmn1r230
|
UTSW |
17 |
21,067,604 (GRCm39) |
nonsense |
probably null |
|
|
U24488:Vmn1r230
|
UTSW |
17 |
21,067,014 (GRCm39) |
missense |
probably benign |
0.01 |
|
Z1176:Vmn1r230
|
UTSW |
17 |
21,067,214 (GRCm39) |
nonsense |
probably null |
|
|
| Posted On |
2016-08-02 |
Incidental Mutation