Incidental Mutation 'R1124:Vmn1r204'
ID |
95994 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Vmn1r204
|
Ensembl Gene |
ENSMUSG00000094637 |
Gene Name |
vomeronasal 1 receptor 204 |
Synonyms |
Gm11301 |
MMRRC Submission |
039197-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.074)
|
Stock # |
R1124 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
13 |
Chromosomal Location |
22740371-22741279 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 22741209 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Phenylalanine
at position 280
(Y280F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000154519
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000091728]
[ENSMUST00000228195]
|
AlphaFold |
I7HIK1 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000091728
AA Change: Y280F
PolyPhen 2
Score 0.764 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000089321 Gene: ENSMUSG00000094637 AA Change: Y280F
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
3 |
293 |
8.4e-8 |
PFAM |
Pfam:V1R
|
35 |
297 |
1.2e-40 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000228195
AA Change: Y280F
PolyPhen 2
Score 0.764 (Sensitivity: 0.85; Specificity: 0.92)
|
Coding Region Coverage |
- 1x: 98.8%
- 3x: 97.8%
- 10x: 94.7%
- 20x: 86.6%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
C |
T |
14: 32,384,039 (GRCm39) |
R642Q |
possibly damaging |
Het |
Aadacl2fm3 |
A |
G |
3: 59,772,639 (GRCm39) |
T48A |
probably benign |
Het |
Aadacl4fm1 |
A |
G |
4: 144,255,194 (GRCm39) |
T205A |
probably benign |
Het |
Aadacl4fm4 |
T |
C |
4: 144,396,845 (GRCm39) |
S296G |
probably benign |
Het |
Anxa10 |
C |
T |
8: 62,514,038 (GRCm39) |
|
probably null |
Het |
Bcl11a |
A |
T |
11: 24,113,928 (GRCm39) |
M424L |
probably damaging |
Het |
Bhlhe41 |
A |
G |
6: 145,809,456 (GRCm39) |
S119P |
probably damaging |
Het |
C2cd3 |
A |
G |
7: 100,071,888 (GRCm39) |
D1033G |
probably benign |
Het |
Ccdc174 |
T |
C |
6: 91,876,561 (GRCm39) |
V466A |
probably benign |
Het |
Dnaaf11 |
T |
A |
15: 66,310,264 (GRCm39) |
T335S |
possibly damaging |
Het |
Drd2 |
T |
C |
9: 49,306,940 (GRCm39) |
Y9H |
probably damaging |
Het |
Fbxw14 |
T |
A |
9: 109,105,236 (GRCm39) |
I310F |
possibly damaging |
Het |
Grm3 |
C |
T |
5: 9,620,297 (GRCm39) |
V316I |
probably benign |
Het |
Gys2 |
A |
G |
6: 142,391,739 (GRCm39) |
Y508H |
probably damaging |
Het |
Lrp1b |
T |
A |
2: 40,765,063 (GRCm39) |
D2921V |
probably damaging |
Het |
Macrod2 |
A |
G |
2: 140,294,547 (GRCm39) |
K71R |
probably damaging |
Het |
Myh7 |
A |
T |
14: 55,211,327 (GRCm39) |
V1614E |
possibly damaging |
Het |
Nckap1 |
C |
T |
2: 80,348,286 (GRCm39) |
S889N |
probably benign |
Het |
Or8k23 |
T |
A |
2: 86,186,239 (GRCm39) |
K162N |
probably damaging |
Het |
Pirb |
T |
A |
7: 3,722,731 (GRCm39) |
N87I |
probably benign |
Het |
Pmfbp1 |
A |
G |
8: 110,257,115 (GRCm39) |
|
probably null |
Het |
Rasa4 |
A |
G |
5: 136,134,510 (GRCm39) |
N627S |
probably benign |
Het |
Spata31d1b |
A |
C |
13: 59,864,468 (GRCm39) |
M539L |
probably benign |
Het |
Tbc1d23 |
A |
T |
16: 57,034,525 (GRCm39) |
|
probably null |
Het |
Tnfrsf1b |
A |
T |
4: 144,950,926 (GRCm39) |
L229Q |
probably benign |
Het |
Trip12 |
A |
T |
1: 84,714,758 (GRCm39) |
V443E |
probably damaging |
Het |
Ush2a |
G |
T |
1: 188,485,733 (GRCm39) |
V2948L |
probably damaging |
Het |
Vmn2r115 |
ATCTTCT |
ATCT |
17: 23,578,962 (GRCm39) |
|
probably benign |
Het |
Vmn2r93 |
G |
T |
17: 18,518,710 (GRCm39) |
K56N |
probably benign |
Het |
Xrn1 |
A |
G |
9: 95,885,918 (GRCm39) |
I880V |
probably benign |
Het |
Zfp106 |
C |
T |
2: 120,365,195 (GRCm39) |
G404E |
probably benign |
Het |
|
Other mutations in Vmn1r204 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00819:Vmn1r204
|
APN |
13 |
22,741,117 (GRCm39) |
nonsense |
probably null |
|
IGL01349:Vmn1r204
|
APN |
13 |
22,740,504 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02653:Vmn1r204
|
APN |
13 |
22,740,800 (GRCm39) |
missense |
probably benign |
0.34 |
R0029:Vmn1r204
|
UTSW |
13 |
22,740,588 (GRCm39) |
missense |
probably benign |
0.12 |
R0078:Vmn1r204
|
UTSW |
13 |
22,740,379 (GRCm39) |
missense |
probably benign |
0.01 |
R0562:Vmn1r204
|
UTSW |
13 |
22,740,848 (GRCm39) |
missense |
probably benign |
0.00 |
R1521:Vmn1r204
|
UTSW |
13 |
22,741,248 (GRCm39) |
missense |
probably benign |
0.30 |
R1544:Vmn1r204
|
UTSW |
13 |
22,740,465 (GRCm39) |
missense |
probably benign |
0.13 |
R2238:Vmn1r204
|
UTSW |
13 |
22,740,993 (GRCm39) |
missense |
probably benign |
0.01 |
R2418:Vmn1r204
|
UTSW |
13 |
22,740,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R2419:Vmn1r204
|
UTSW |
13 |
22,740,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R3944:Vmn1r204
|
UTSW |
13 |
22,741,014 (GRCm39) |
missense |
probably benign |
0.02 |
R4675:Vmn1r204
|
UTSW |
13 |
22,740,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R4782:Vmn1r204
|
UTSW |
13 |
22,740,867 (GRCm39) |
missense |
probably benign |
0.03 |
R4985:Vmn1r204
|
UTSW |
13 |
22,741,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R5219:Vmn1r204
|
UTSW |
13 |
22,741,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R5268:Vmn1r204
|
UTSW |
13 |
22,740,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R6652:Vmn1r204
|
UTSW |
13 |
22,740,573 (GRCm39) |
missense |
probably damaging |
0.99 |
R6943:Vmn1r204
|
UTSW |
13 |
22,740,474 (GRCm39) |
missense |
probably benign |
0.00 |
R7264:Vmn1r204
|
UTSW |
13 |
22,741,167 (GRCm39) |
missense |
probably benign |
0.23 |
R7299:Vmn1r204
|
UTSW |
13 |
22,740,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R7301:Vmn1r204
|
UTSW |
13 |
22,740,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R7593:Vmn1r204
|
UTSW |
13 |
22,740,754 (GRCm39) |
nonsense |
probably null |
|
R7872:Vmn1r204
|
UTSW |
13 |
22,740,404 (GRCm39) |
missense |
probably benign |
0.00 |
R8495:Vmn1r204
|
UTSW |
13 |
22,740,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R9110:Vmn1r204
|
UTSW |
13 |
22,740,564 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
Predicted Primers |
PCR Primer
(F):5'- TGCCAGGCCAGAAATCAGAGCTAC -3'
(R):5'- ATCCCTGCTTCCAGTTGAGAACCC -3'
Sequencing Primer
(F):5'- CCAGAAATCAGAGCTACACAGAGAG -3'
(R):5'- accaaacaaaaacaaaacaaaagaag -3'
|
Posted On |
2014-01-05 |