Incidental Mutation 'IGL02333:Vmn2r32'
ID |
288775 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vmn2r32
|
Ensembl Gene |
ENSMUSG00000096743 |
Gene Name |
vomeronasal 2, receptor 32 |
Synonyms |
V2r5 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.206)
|
Stock # |
IGL02333
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
7466968-7482972 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 7467143 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Tyrosine
at position 795
(F795Y)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000092462
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000094866]
|
AlphaFold |
K7N686 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000094866
AA Change: F795Y
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000092462 Gene: ENSMUSG00000096743 AA Change: F795Y
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 |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 25 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ace |
G |
A |
11: 105,862,273 (GRCm39) |
V276I |
probably benign |
Het |
Acss2 |
T |
A |
2: 155,397,804 (GRCm39) |
W289R |
probably damaging |
Het |
Alpk2 |
A |
G |
18: 65,482,551 (GRCm39) |
S19P |
probably damaging |
Het |
Ano3 |
T |
C |
2: 110,527,544 (GRCm39) |
|
probably benign |
Het |
Atxn1 |
G |
A |
13: 45,720,680 (GRCm39) |
S405F |
probably damaging |
Het |
Atxn2 |
A |
G |
5: 121,919,450 (GRCm39) |
Y386C |
probably damaging |
Het |
Bach2 |
T |
A |
4: 32,575,334 (GRCm39) |
L643* |
probably null |
Het |
Ccl22 |
T |
A |
8: 95,476,507 (GRCm39) |
L91Q |
probably damaging |
Het |
Cdc40 |
A |
G |
10: 40,743,855 (GRCm39) |
Y81H |
probably benign |
Het |
Col5a3 |
C |
A |
9: 20,710,602 (GRCm39) |
R549M |
unknown |
Het |
Eif3e |
A |
T |
15: 43,129,533 (GRCm39) |
N198K |
probably benign |
Het |
Emp2 |
A |
G |
16: 10,102,375 (GRCm39) |
Y146H |
probably damaging |
Het |
Impg1 |
G |
A |
9: 80,322,808 (GRCm39) |
L66F |
possibly damaging |
Het |
Itsn1 |
A |
G |
16: 91,617,564 (GRCm39) |
|
probably benign |
Het |
Khdrbs3 |
T |
C |
15: 68,921,243 (GRCm39) |
Y187H |
probably damaging |
Het |
Klhdc7a |
T |
A |
4: 139,694,467 (GRCm39) |
H160L |
probably benign |
Het |
Klhl2 |
G |
A |
8: 65,212,784 (GRCm39) |
R252W |
probably damaging |
Het |
Krba1 |
C |
T |
6: 48,390,021 (GRCm39) |
T595I |
probably damaging |
Het |
Myo9b |
G |
T |
8: 71,811,637 (GRCm39) |
D1887Y |
possibly damaging |
Het |
Olfm4 |
C |
T |
14: 80,259,210 (GRCm39) |
T453I |
probably damaging |
Het |
Sin3a |
A |
G |
9: 57,014,843 (GRCm39) |
N688S |
possibly damaging |
Het |
Slc47a1 |
A |
G |
11: 61,260,950 (GRCm39) |
V150A |
probably damaging |
Het |
Sptbn4 |
A |
G |
7: 27,063,724 (GRCm39) |
L2234P |
probably damaging |
Het |
Trpm4 |
C |
T |
7: 44,971,539 (GRCm39) |
V166M |
possibly damaging |
Het |
Usp54 |
A |
T |
14: 20,639,463 (GRCm39) |
F156L |
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 |
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 |
|
R4362:Vmn2r32
|
UTSW |
7 |
7,482,857 (GRCm39) |
nonsense |
probably null |
|
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 |
|
Posted On |
2015-04-16 |