Incidental Mutation 'R0021:V1rd19'
ID |
64761 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
V1rd19
|
Ensembl Gene |
ENSMUSG00000092456 |
Gene Name |
vomeronasal 1 receptor, D19 |
Synonyms |
|
MMRRC Submission |
038316-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.061)
|
Stock # |
R0021 (G1)
|
Quality Score |
86 |
Status
|
Validated
|
Chromosome |
7 |
Chromosomal Location |
23702536-23703453 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 23703029 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Valine
at position 165
(D165V)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000133284
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000173571]
|
AlphaFold |
Q3KNP5 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000173571
AA Change: D165V
PolyPhen 2
Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000133284 Gene: ENSMUSG00000092456 AA Change: D165V
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
8 |
296 |
1e-9 |
PFAM |
Pfam:V1R
|
42 |
295 |
5.9e-13 |
PFAM |
|
Meta Mutation Damage Score |
0.6467 |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.8%
- 10x: 97.6%
- 20x: 95.8%
|
Validation Efficiency |
97% (60/62) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310016G11Rik |
A |
G |
7: 44,326,620 (GRCm39) |
|
noncoding transcript |
Het |
Abcc5 |
T |
A |
16: 20,197,411 (GRCm39) |
K647* |
probably null |
Het |
Aplp1 |
A |
G |
7: 30,135,241 (GRCm39) |
|
probably benign |
Het |
Arhgef25 |
A |
G |
10: 127,025,423 (GRCm39) |
I43T |
probably benign |
Het |
Brinp3 |
T |
G |
1: 146,777,189 (GRCm39) |
S545R |
probably benign |
Het |
Btnl1 |
A |
G |
17: 34,598,468 (GRCm39) |
E28G |
probably benign |
Het |
C5ar2 |
A |
G |
7: 15,971,601 (GRCm39) |
F109L |
probably benign |
Het |
D630045J12Rik |
G |
A |
6: 38,160,902 (GRCm39) |
Q1081* |
probably null |
Het |
Dhx36 |
T |
C |
3: 62,385,016 (GRCm39) |
I699V |
possibly damaging |
Het |
Dnah9 |
A |
G |
11: 65,860,805 (GRCm39) |
I2855T |
probably benign |
Het |
Dock8 |
T |
C |
19: 25,140,411 (GRCm39) |
I1317T |
probably benign |
Het |
Galnt11 |
A |
T |
5: 25,453,855 (GRCm39) |
D27V |
probably damaging |
Het |
Gm5134 |
T |
A |
10: 75,829,718 (GRCm39) |
C335S |
probably damaging |
Het |
Hdhd2 |
A |
T |
18: 77,058,311 (GRCm39) |
K227N |
probably damaging |
Het |
Impg1 |
A |
T |
9: 80,317,479 (GRCm39) |
L36Q |
probably damaging |
Het |
Krtcap3 |
A |
G |
5: 31,410,303 (GRCm39) |
H227R |
probably benign |
Het |
Lrrc7 |
A |
G |
3: 157,866,298 (GRCm39) |
Y1148H |
probably damaging |
Het |
Map2k4 |
A |
G |
11: 65,603,110 (GRCm39) |
I174T |
probably damaging |
Het |
Mef2c |
C |
A |
13: 83,804,359 (GRCm39) |
L282M |
probably damaging |
Het |
Nkapd1 |
A |
C |
9: 50,521,725 (GRCm39) |
D65E |
probably damaging |
Het |
Nqo2 |
T |
C |
13: 34,165,490 (GRCm39) |
I129T |
probably benign |
Het |
Pdgfrb |
T |
A |
18: 61,197,998 (GRCm39) |
|
probably benign |
Het |
Phf7 |
C |
T |
14: 30,960,443 (GRCm39) |
|
probably benign |
Het |
Plac8 |
T |
A |
5: 100,704,434 (GRCm39) |
T88S |
probably benign |
Het |
Pou2f1 |
G |
A |
1: 165,703,587 (GRCm39) |
T654M |
probably damaging |
Het |
Ptprk |
T |
A |
10: 28,468,891 (GRCm39) |
V1425E |
probably damaging |
Het |
Saal1 |
A |
T |
7: 46,342,316 (GRCm39) |
S376T |
probably damaging |
Het |
Scart2 |
G |
A |
7: 139,876,310 (GRCm39) |
R594H |
probably benign |
Het |
Serpini1 |
T |
C |
3: 75,526,620 (GRCm39) |
Y291H |
probably damaging |
Het |
Siah2 |
T |
C |
3: 58,583,713 (GRCm39) |
H191R |
probably benign |
Het |
Spaca6 |
T |
A |
17: 18,058,498 (GRCm39) |
Y39* |
probably null |
Het |
Tbc1d10a |
T |
C |
11: 4,163,680 (GRCm39) |
C277R |
probably damaging |
Het |
Trim45 |
A |
T |
3: 100,832,736 (GRCm39) |
D323V |
probably damaging |
Het |
Trim55 |
A |
C |
3: 19,698,866 (GRCm39) |
M32L |
probably benign |
Het |
Unc5b |
T |
C |
10: 60,614,698 (GRCm39) |
T200A |
probably benign |
Het |
Uqcc4 |
A |
G |
17: 25,403,957 (GRCm39) |
E99G |
possibly damaging |
Het |
|
Other mutations in V1rd19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02631:V1rd19
|
APN |
7 |
23,702,825 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02898:V1rd19
|
APN |
7 |
23,702,854 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03231:V1rd19
|
APN |
7 |
23,703,328 (GRCm39) |
missense |
probably benign |
0.00 |
R0184:V1rd19
|
UTSW |
7 |
23,702,632 (GRCm39) |
missense |
probably benign |
0.06 |
R0391:V1rd19
|
UTSW |
7 |
23,703,010 (GRCm39) |
missense |
probably damaging |
0.98 |
R1520:V1rd19
|
UTSW |
7 |
23,702,623 (GRCm39) |
missense |
probably damaging |
0.99 |
R1635:V1rd19
|
UTSW |
7 |
23,702,812 (GRCm39) |
missense |
probably benign |
0.30 |
R1861:V1rd19
|
UTSW |
7 |
23,703,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R1889:V1rd19
|
UTSW |
7 |
23,702,632 (GRCm39) |
missense |
probably benign |
0.06 |
R2008:V1rd19
|
UTSW |
7 |
23,702,726 (GRCm39) |
nonsense |
probably null |
|
R2059:V1rd19
|
UTSW |
7 |
23,703,259 (GRCm39) |
missense |
probably benign |
0.01 |
R2098:V1rd19
|
UTSW |
7 |
23,703,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R3001:V1rd19
|
UTSW |
7 |
23,703,310 (GRCm39) |
missense |
probably benign |
0.00 |
R3002:V1rd19
|
UTSW |
7 |
23,703,310 (GRCm39) |
missense |
probably benign |
0.00 |
R4271:V1rd19
|
UTSW |
7 |
23,702,839 (GRCm39) |
missense |
probably benign |
0.36 |
R5130:V1rd19
|
UTSW |
7 |
23,702,537 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R5169:V1rd19
|
UTSW |
7 |
23,703,209 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5297:V1rd19
|
UTSW |
7 |
23,702,714 (GRCm39) |
missense |
probably damaging |
0.99 |
R5924:V1rd19
|
UTSW |
7 |
23,703,374 (GRCm39) |
missense |
probably benign |
|
R6181:V1rd19
|
UTSW |
7 |
23,702,640 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6540:V1rd19
|
UTSW |
7 |
23,703,056 (GRCm39) |
nonsense |
probably null |
|
R7331:V1rd19
|
UTSW |
7 |
23,703,308 (GRCm39) |
missense |
probably damaging |
0.97 |
R7332:V1rd19
|
UTSW |
7 |
23,702,743 (GRCm39) |
missense |
probably benign |
0.09 |
R8338:V1rd19
|
UTSW |
7 |
23,702,674 (GRCm39) |
nonsense |
probably null |
|
R8398:V1rd19
|
UTSW |
7 |
23,703,374 (GRCm39) |
nonsense |
probably null |
|
R8881:V1rd19
|
UTSW |
7 |
23,703,081 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9536:V1rd19
|
UTSW |
7 |
23,703,253 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:V1rd19
|
UTSW |
7 |
23,702,761 (GRCm39) |
missense |
probably benign |
0.08 |
|
Predicted Primers |
PCR Primer
(F):5'- GGTTCTAAACAGAGGCCCAGACAAG -3'
(R):5'- CCAGCATCAGGATAGTATGGGTTGC -3'
Sequencing Primer
(F):5'- GCCCAGACAAGTGATTTTAAGAC -3'
(R):5'- CCTGATTGAGAGTGAATATGTACTGC -3'
|
Posted On |
2013-08-06 |