Incidental Mutation 'R4634:Vmn1r231'
ID |
349421 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Vmn1r231
|
Ensembl Gene |
ENSMUSG00000050933 |
Gene Name |
vomeronasal 1 receptor 231 |
Synonyms |
V1re7 |
MMRRC Submission |
042009-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.052)
|
Stock # |
R4634 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
17 |
Chromosomal Location |
21109978-21110913 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 21110660 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Alanine
at position 85
(V85A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000056228
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000061278]
|
AlphaFold |
Q8R2A3 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000061278
AA Change: V85A
PolyPhen 2
Score 0.461 (Sensitivity: 0.89; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000056228 Gene: ENSMUSG00000050933 AA Change: V85A
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
6 |
294 |
1.6e-13 |
PFAM |
Pfam:V1R
|
36 |
297 |
1.6e-27 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000232004
|
Meta Mutation Damage Score |
0.1795 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.1%
- 20x: 94.7%
|
Validation Efficiency |
98% (40/41) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb1 |
A |
G |
15: 74,456,278 (GRCm39) |
|
probably benign |
Het |
Atm |
T |
C |
9: 53,443,033 (GRCm39) |
T77A |
probably benign |
Het |
Brd8 |
T |
C |
18: 34,741,537 (GRCm39) |
M311V |
possibly damaging |
Het |
Cand2 |
T |
A |
6: 115,774,948 (GRCm39) |
I1052N |
probably damaging |
Het |
Ccdc121 |
G |
A |
5: 31,645,435 (GRCm39) |
R396Q |
probably benign |
Het |
Ceacam16 |
T |
A |
7: 19,592,531 (GRCm39) |
M126L |
probably benign |
Het |
Chd3 |
TGCTGCCGCTGCCGC |
TGCTGCCGCTGCCGCTGCCGC |
11: 69,253,013 (GRCm39) |
|
probably benign |
Het |
Cln8 |
C |
T |
8: 14,944,842 (GRCm39) |
T52I |
probably damaging |
Het |
Cops2 |
C |
A |
2: 125,682,400 (GRCm39) |
D194Y |
probably damaging |
Het |
Csf1 |
C |
T |
3: 107,656,483 (GRCm39) |
V71M |
probably damaging |
Het |
Dip2b |
T |
C |
15: 100,058,372 (GRCm39) |
F183S |
probably damaging |
Het |
Ears2 |
T |
A |
7: 121,643,832 (GRCm39) |
K375N |
probably benign |
Het |
Fbn1 |
C |
A |
2: 125,185,981 (GRCm39) |
G1596C |
probably damaging |
Het |
Fscn2 |
A |
T |
11: 120,258,546 (GRCm39) |
D390V |
possibly damaging |
Het |
Gm42669 |
A |
T |
5: 107,656,079 (GRCm39) |
I781F |
possibly damaging |
Het |
Gprin1 |
G |
T |
13: 54,885,871 (GRCm39) |
P801Q |
probably damaging |
Het |
Hira |
C |
A |
16: 18,765,150 (GRCm39) |
S609R |
probably damaging |
Het |
Htt |
G |
T |
5: 35,033,292 (GRCm39) |
K1853N |
probably benign |
Het |
Kif2c |
T |
C |
4: 117,035,437 (GRCm39) |
I4V |
probably benign |
Het |
Marveld2 |
A |
G |
13: 100,748,447 (GRCm39) |
Y211H |
probably damaging |
Het |
Myd88 |
G |
A |
9: 119,167,175 (GRCm39) |
|
probably null |
Het |
Nup153 |
A |
T |
13: 46,840,706 (GRCm39) |
N967K |
possibly damaging |
Het |
Or4a76 |
A |
C |
2: 89,460,516 (GRCm39) |
I242S |
possibly damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Rabepk |
A |
G |
2: 34,670,752 (GRCm39) |
M228T |
probably damaging |
Het |
Rcn3 |
T |
A |
7: 44,738,092 (GRCm39) |
D92V |
probably damaging |
Het |
Sec1 |
T |
A |
7: 45,328,297 (GRCm39) |
Y250F |
probably damaging |
Het |
Slc39a4 |
T |
C |
15: 76,498,693 (GRCm39) |
T334A |
probably benign |
Het |
Trip11 |
G |
T |
12: 101,803,875 (GRCm39) |
T1669K |
probably damaging |
Het |
Ttbk2 |
A |
G |
2: 120,570,673 (GRCm39) |
L1091P |
probably damaging |
Het |
Zfp280b |
T |
C |
10: 75,874,663 (GRCm39) |
C181R |
probably benign |
Het |
|
Other mutations in Vmn1r231 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00233:Vmn1r231
|
APN |
17 |
21,110,828 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02124:Vmn1r231
|
APN |
17 |
21,110,568 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02151:Vmn1r231
|
APN |
17 |
21,109,997 (GRCm39) |
missense |
probably benign |
0.06 |
R0066:Vmn1r231
|
UTSW |
17 |
21,109,998 (GRCm39) |
missense |
probably benign |
0.27 |
R0066:Vmn1r231
|
UTSW |
17 |
21,109,998 (GRCm39) |
missense |
probably benign |
0.27 |
R0396:Vmn1r231
|
UTSW |
17 |
21,110,661 (GRCm39) |
missense |
probably damaging |
0.98 |
R0427:Vmn1r231
|
UTSW |
17 |
21,110,490 (GRCm39) |
missense |
probably benign |
0.05 |
R0470:Vmn1r231
|
UTSW |
17 |
21,110,265 (GRCm39) |
nonsense |
probably null |
|
R0848:Vmn1r231
|
UTSW |
17 |
21,110,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R1692:Vmn1r231
|
UTSW |
17 |
21,110,871 (GRCm39) |
missense |
probably benign |
0.02 |
R1987:Vmn1r231
|
UTSW |
17 |
21,110,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R1988:Vmn1r231
|
UTSW |
17 |
21,110,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R2105:Vmn1r231
|
UTSW |
17 |
21,110,380 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4440:Vmn1r231
|
UTSW |
17 |
21,110,718 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4646:Vmn1r231
|
UTSW |
17 |
21,110,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R4678:Vmn1r231
|
UTSW |
17 |
21,110,489 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4696:Vmn1r231
|
UTSW |
17 |
21,110,901 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4938:Vmn1r231
|
UTSW |
17 |
21,110,613 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5544:Vmn1r231
|
UTSW |
17 |
21,110,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R5942:Vmn1r231
|
UTSW |
17 |
21,110,417 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6053:Vmn1r231
|
UTSW |
17 |
21,110,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R6692:Vmn1r231
|
UTSW |
17 |
21,110,745 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6712:Vmn1r231
|
UTSW |
17 |
21,109,992 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7131:Vmn1r231
|
UTSW |
17 |
21,110,140 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7854:Vmn1r231
|
UTSW |
17 |
21,110,894 (GRCm39) |
missense |
probably damaging |
0.98 |
R7918:Vmn1r231
|
UTSW |
17 |
21,110,236 (GRCm39) |
nonsense |
probably null |
|
R8187:Vmn1r231
|
UTSW |
17 |
21,110,893 (GRCm39) |
missense |
probably benign |
0.10 |
R8238:Vmn1r231
|
UTSW |
17 |
21,110,640 (GRCm39) |
missense |
probably benign |
0.08 |
R8313:Vmn1r231
|
UTSW |
17 |
21,110,289 (GRCm39) |
missense |
probably benign |
0.02 |
R8525:Vmn1r231
|
UTSW |
17 |
21,110,001 (GRCm39) |
missense |
probably benign |
0.06 |
R9276:Vmn1r231
|
UTSW |
17 |
21,110,560 (GRCm39) |
missense |
probably benign |
0.00 |
RF010:Vmn1r231
|
UTSW |
17 |
21,110,255 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Predicted Primers |
PCR Primer
(F):5'- GGGCCTGTAAATTCATCATGACC -3'
(R):5'- TCATCCTTCAATGTTCAGTGGG -3'
Sequencing Primer
(F):5'- GCCTGTAAATTCATCATGACCTAAAC -3'
(R):5'- CCTTCAATGTTCAGTGGGAATTC -3'
|
Posted On |
2015-10-08 |