Incidental Mutation 'R4362:Vmn2r32'
ID |
324947 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Vmn2r32
|
Ensembl Gene |
ENSMUSG00000096743 |
Gene Name |
vomeronasal 2, receptor 32 |
Synonyms |
V2r5 |
MMRRC Submission |
041671-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.206)
|
Stock # |
R4362 (G1)
|
Quality Score |
101 |
Status
|
Not validated
|
Chromosome |
7 |
Chromosomal Location |
7466968-7482972 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
A to T
at 7482857 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Leucine to Stop codon
at position 39
(L39*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000092462
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000094866]
|
AlphaFold |
K7N686 |
Predicted Effect |
probably null
Transcript: ENSMUST00000094866
AA Change: L39*
|
SMART Domains |
Protein: ENSMUSP00000092462 Gene: ENSMUSG00000096743 AA Change: L39*
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
Pfam:ANF_receptor
|
73 |
470 |
3.6e-33 |
PFAM |
Pfam:NCD3G
|
512 |
565 |
8.1e-21 |
PFAM |
Pfam:7tm_3
|
598 |
833 |
9.5e-55 |
PFAM |
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.2%
- 20x: 94.8%
|
Validation Efficiency |
100% (39/39) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
C |
T |
7: 28,947,687 (GRCm39) |
|
probably benign |
Het |
Abcc6 |
A |
G |
7: 45,648,256 (GRCm39) |
|
probably benign |
Het |
Adamts13 |
G |
A |
2: 26,894,794 (GRCm39) |
C1034Y |
probably damaging |
Het |
Atp2b4 |
G |
T |
1: 133,667,669 (GRCm39) |
P125Q |
possibly damaging |
Het |
Atp8b1 |
C |
T |
18: 64,697,608 (GRCm39) |
R412H |
probably damaging |
Het |
Bicc1 |
ATGTG |
ATG |
10: 70,779,204 (GRCm39) |
|
probably null |
Het |
Cap1 |
G |
A |
4: 122,756,780 (GRCm39) |
P302S |
probably benign |
Het |
Chodl |
G |
T |
16: 78,741,546 (GRCm39) |
|
probably null |
Het |
Cplane1 |
T |
A |
15: 8,300,229 (GRCm39) |
S3179T |
unknown |
Het |
Cplx2 |
A |
T |
13: 54,526,630 (GRCm39) |
T13S |
probably benign |
Het |
Dennd5a |
G |
A |
7: 109,495,550 (GRCm39) |
R1194W |
probably damaging |
Het |
Dsc2 |
T |
A |
18: 20,183,214 (GRCm39) |
D68V |
probably damaging |
Het |
Dus4l |
A |
C |
12: 31,698,827 (GRCm39) |
I59R |
probably damaging |
Het |
Edc3 |
C |
T |
9: 57,620,829 (GRCm39) |
P50L |
probably damaging |
Het |
Ext1 |
G |
A |
15: 52,970,987 (GRCm39) |
|
probably benign |
Het |
Fam219a |
C |
T |
4: 41,518,844 (GRCm39) |
|
probably benign |
Het |
Fbxl3 |
A |
T |
14: 103,329,749 (GRCm39) |
D106E |
probably damaging |
Het |
Garem1 |
T |
C |
18: 21,369,172 (GRCm39) |
N50D |
possibly damaging |
Het |
Gins1 |
G |
A |
2: 150,751,682 (GRCm39) |
R15H |
probably damaging |
Het |
Glrx2 |
A |
G |
1: 143,617,418 (GRCm39) |
K44R |
possibly damaging |
Het |
Icam1 |
A |
G |
9: 20,937,608 (GRCm39) |
D215G |
possibly damaging |
Het |
Nedd9 |
A |
T |
13: 41,471,429 (GRCm39) |
I184N |
probably damaging |
Het |
Or10a2 |
T |
C |
7: 106,673,799 (GRCm39) |
S255P |
probably damaging |
Het |
Or1e21 |
T |
C |
11: 73,344,391 (GRCm39) |
M216V |
probably benign |
Het |
Otulinl |
C |
T |
15: 27,664,429 (GRCm39) |
|
probably null |
Het |
Rhot2 |
A |
G |
17: 26,061,065 (GRCm39) |
C147R |
probably damaging |
Het |
Saxo4 |
T |
C |
19: 10,452,385 (GRCm39) |
Y375C |
probably damaging |
Het |
Setd4 |
T |
C |
16: 93,380,574 (GRCm39) |
|
probably null |
Het |
Slc6a4 |
A |
G |
11: 76,907,904 (GRCm39) |
N356S |
probably damaging |
Het |
Tas2r136 |
C |
A |
6: 132,754,972 (GRCm39) |
V52L |
probably damaging |
Het |
Tmem168 |
A |
C |
6: 13,595,072 (GRCm39) |
I381S |
probably benign |
Het |
Tnfrsf11b |
T |
A |
15: 54,119,555 (GRCm39) |
T140S |
possibly damaging |
Het |
Ttpa |
G |
T |
4: 20,023,827 (GRCm39) |
E130* |
probably null |
Het |
Ubr5 |
A |
G |
15: 38,078,647 (GRCm39) |
V8A |
probably damaging |
Het |
Vmn2r18 |
C |
T |
5: 151,496,368 (GRCm39) |
C450Y |
probably damaging |
Het |
|
Other mutations in Vmn2r32 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02140:Vmn2r32
|
APN |
7 |
7,479,696 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02333:Vmn2r32
|
APN |
7 |
7,467,143 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02406:Vmn2r32
|
APN |
7 |
7,479,709 (GRCm39) |
missense |
probably benign |
|
IGL02428:Vmn2r32
|
APN |
7 |
7,477,283 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02484:Vmn2r32
|
APN |
7 |
7,467,116 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03277:Vmn2r32
|
APN |
7 |
7,477,251 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03366:Vmn2r32
|
APN |
7 |
7,467,029 (GRCm39) |
missense |
probably damaging |
0.99 |
R1055:Vmn2r32
|
UTSW |
7 |
7,477,326 (GRCm39) |
nonsense |
probably null |
|
R1695:Vmn2r32
|
UTSW |
7 |
7,466,991 (GRCm39) |
missense |
probably benign |
0.01 |
R2172:Vmn2r32
|
UTSW |
7 |
7,477,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R2262:Vmn2r32
|
UTSW |
7 |
7,477,618 (GRCm39) |
missense |
probably benign |
|
R3150:Vmn2r32
|
UTSW |
7 |
7,475,554 (GRCm39) |
missense |
probably benign |
|
R4432:Vmn2r32
|
UTSW |
7 |
7,482,918 (GRCm39) |
missense |
probably damaging |
0.98 |
R4851:Vmn2r32
|
UTSW |
7 |
7,482,953 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4949:Vmn2r32
|
UTSW |
7 |
7,467,083 (GRCm39) |
missense |
probably benign |
0.22 |
R5990:Vmn2r32
|
UTSW |
7 |
7,482,809 (GRCm39) |
missense |
probably damaging |
0.97 |
R6083:Vmn2r32
|
UTSW |
7 |
7,467,209 (GRCm39) |
missense |
probably benign |
0.15 |
R6084:Vmn2r32
|
UTSW |
7 |
7,467,209 (GRCm39) |
missense |
probably benign |
0.15 |
R6116:Vmn2r32
|
UTSW |
7 |
7,467,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R6263:Vmn2r32
|
UTSW |
7 |
7,479,691 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6889:Vmn2r32
|
UTSW |
7 |
7,475,573 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7286:Vmn2r32
|
UTSW |
7 |
7,482,807 (GRCm39) |
missense |
probably benign |
0.21 |
R7390:Vmn2r32
|
UTSW |
7 |
7,482,851 (GRCm39) |
missense |
probably benign |
0.00 |
R7412:Vmn2r32
|
UTSW |
7 |
7,477,212 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7508:Vmn2r32
|
UTSW |
7 |
7,470,373 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8812:Vmn2r32
|
UTSW |
7 |
7,477,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R8968:Vmn2r32
|
UTSW |
7 |
7,477,204 (GRCm39) |
missense |
probably benign |
0.00 |
R9331:Vmn2r32
|
UTSW |
7 |
7,467,402 (GRCm39) |
nonsense |
probably null |
|
R9358:Vmn2r32
|
UTSW |
7 |
7,477,197 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Vmn2r32
|
UTSW |
7 |
7,477,160 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Predicted Primers |
PCR Primer
(F):5'- AAGGTTGTTTCTCAGAGTTCAGAC -3'
(R):5'- AGCTGGTAGAAATCTGATGTGC -3'
Sequencing Primer
(F):5'- TTCTCAGAGTTCAGACTTAGCACCAG -3'
(R):5'- GTGCTGATATGCATGGCACTTCAC -3'
|
Posted On |
2015-07-06 |