Incidental Mutation 'IGL03244:Vmn1r32'
ID |
414329 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vmn1r32
|
Ensembl Gene |
ENSMUSG00000062905 |
Gene Name |
vomeronasal 1 receptor 32 |
Synonyms |
V1rc15 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.056)
|
Stock # |
IGL03244
|
Quality Score |
|
Status
|
|
Chromosome |
6 |
Chromosomal Location |
66529167-66536692 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 66530489 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Leucine to Phenylalanine
at position 96
(L96F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000153723
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000079584]
[ENSMUST00000227014]
|
AlphaFold |
Q8R2D9 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000079584
AA Change: L96F
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000078536 Gene: ENSMUSG00000062905 AA Change: L96F
Domain | Start | End | E-Value | Type |
Pfam:V1R
|
28 |
293 |
9.7e-56 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000227014
AA Change: L96F
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ank2 |
C |
A |
3: 126,749,519 (GRCm39) |
E503D |
probably damaging |
Het |
Aoc1 |
T |
C |
6: 48,882,756 (GRCm39) |
Y233H |
possibly damaging |
Het |
Apaf1 |
A |
T |
10: 90,885,211 (GRCm39) |
|
probably benign |
Het |
Asah2 |
T |
C |
19: 31,964,342 (GRCm39) |
Y696C |
probably damaging |
Het |
Atp8b3 |
A |
T |
10: 80,370,292 (GRCm39) |
D112E |
probably damaging |
Het |
B3gat3 |
T |
C |
19: 8,903,215 (GRCm39) |
Y191H |
probably damaging |
Het |
Capns2 |
T |
C |
8: 93,628,738 (GRCm39) |
I209T |
probably damaging |
Het |
Ccnl2 |
T |
C |
4: 155,905,479 (GRCm39) |
I303T |
probably benign |
Het |
Cdk5rap2 |
A |
T |
4: 70,199,672 (GRCm39) |
S817R |
probably benign |
Het |
Cep57 |
A |
T |
9: 13,729,683 (GRCm39) |
L36* |
probably null |
Het |
Cers4 |
T |
A |
8: 4,566,878 (GRCm39) |
V60E |
probably damaging |
Het |
Ces2e |
T |
C |
8: 105,655,451 (GRCm39) |
Y125H |
probably benign |
Het |
Cyp4f18 |
T |
C |
8: 72,742,489 (GRCm39) |
E497G |
probably benign |
Het |
Ddx24 |
A |
T |
12: 103,383,864 (GRCm39) |
M575K |
possibly damaging |
Het |
Dmxl2 |
A |
T |
9: 54,323,655 (GRCm39) |
V1243E |
probably damaging |
Het |
Elf2 |
A |
T |
3: 51,165,193 (GRCm39) |
Y270* |
probably null |
Het |
Ep400 |
A |
G |
5: 110,875,429 (GRCm39) |
L844S |
unknown |
Het |
F13a1 |
A |
T |
13: 37,172,870 (GRCm39) |
I170N |
possibly damaging |
Het |
Gm16506 |
T |
A |
14: 43,961,603 (GRCm39) |
|
probably benign |
Het |
Grm4 |
A |
G |
17: 27,653,797 (GRCm39) |
F463L |
probably damaging |
Het |
H2-M10.2 |
A |
T |
17: 36,596,463 (GRCm39) |
N127K |
probably benign |
Het |
Lrrc49 |
T |
C |
9: 60,495,140 (GRCm39) |
Y691C |
probably damaging |
Het |
Mbip |
A |
C |
12: 56,384,547 (GRCm39) |
|
probably null |
Het |
Or9k2 |
T |
A |
10: 129,998,269 (GRCm39) |
K309* |
probably null |
Het |
Plod1 |
C |
T |
4: 148,007,580 (GRCm39) |
|
probably null |
Het |
Primpol |
A |
G |
8: 47,039,475 (GRCm39) |
W382R |
probably damaging |
Het |
Rufy2 |
A |
G |
10: 62,840,483 (GRCm39) |
E418G |
probably benign |
Het |
Samm50 |
T |
C |
15: 84,098,341 (GRCm39) |
V460A |
probably benign |
Het |
Senp2 |
T |
C |
16: 21,859,329 (GRCm39) |
V460A |
probably damaging |
Het |
Simc1 |
A |
G |
13: 54,698,442 (GRCm39) |
H453R |
probably benign |
Het |
Slc22a22 |
A |
G |
15: 57,112,948 (GRCm39) |
|
probably benign |
Het |
Spag1 |
A |
T |
15: 36,234,529 (GRCm39) |
D763V |
probably benign |
Het |
Thsd7a |
T |
A |
6: 12,504,167 (GRCm39) |
|
probably benign |
Het |
Tppp |
G |
T |
13: 74,169,535 (GRCm39) |
V92F |
possibly damaging |
Het |
Vmn2r53 |
C |
A |
7: 12,340,435 (GRCm39) |
A13S |
probably damaging |
Het |
Vmn2r75 |
G |
A |
7: 85,820,933 (GRCm39) |
|
probably benign |
Het |
Zfp750 |
C |
A |
11: 121,404,513 (GRCm39) |
G121* |
probably null |
Het |
|
Other mutations in Vmn1r32 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01449:Vmn1r32
|
APN |
6 |
66,529,916 (GRCm39) |
missense |
probably benign |
|
IGL02399:Vmn1r32
|
APN |
6 |
66,529,913 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02964:Vmn1r32
|
APN |
6 |
66,529,922 (GRCm39) |
missense |
probably benign |
0.37 |
IGL03161:Vmn1r32
|
APN |
6 |
66,530,204 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL03248:Vmn1r32
|
APN |
6 |
66,529,897 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0668:Vmn1r32
|
UTSW |
6 |
66,530,644 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0732:Vmn1r32
|
UTSW |
6 |
66,530,690 (GRCm39) |
missense |
probably benign |
0.01 |
R1205:Vmn1r32
|
UTSW |
6 |
66,530,539 (GRCm39) |
missense |
probably benign |
0.01 |
R1638:Vmn1r32
|
UTSW |
6 |
66,529,939 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1732:Vmn1r32
|
UTSW |
6 |
66,530,285 (GRCm39) |
missense |
probably benign |
0.19 |
R2049:Vmn1r32
|
UTSW |
6 |
66,530,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R2127:Vmn1r32
|
UTSW |
6 |
66,530,533 (GRCm39) |
missense |
probably benign |
0.09 |
R3773:Vmn1r32
|
UTSW |
6 |
66,530,351 (GRCm39) |
missense |
probably benign |
0.01 |
R3834:Vmn1r32
|
UTSW |
6 |
66,530,647 (GRCm39) |
missense |
probably benign |
0.02 |
R3980:Vmn1r32
|
UTSW |
6 |
66,530,698 (GRCm39) |
missense |
probably damaging |
0.98 |
R4737:Vmn1r32
|
UTSW |
6 |
66,530,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R5569:Vmn1r32
|
UTSW |
6 |
66,530,156 (GRCm39) |
missense |
probably damaging |
0.98 |
R6382:Vmn1r32
|
UTSW |
6 |
66,530,345 (GRCm39) |
missense |
probably benign |
0.07 |
R6894:Vmn1r32
|
UTSW |
6 |
66,530,345 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7394:Vmn1r32
|
UTSW |
6 |
66,530,173 (GRCm39) |
missense |
probably benign |
0.06 |
R7980:Vmn1r32
|
UTSW |
6 |
66,530,305 (GRCm39) |
nonsense |
probably null |
|
R8833:Vmn1r32
|
UTSW |
6 |
66,530,623 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8867:Vmn1r32
|
UTSW |
6 |
66,530,651 (GRCm39) |
missense |
probably damaging |
0.98 |
R8975:Vmn1r32
|
UTSW |
6 |
66,530,189 (GRCm39) |
missense |
probably benign |
0.03 |
R9131:Vmn1r32
|
UTSW |
6 |
66,530,020 (GRCm39) |
missense |
probably benign |
0.30 |
R9135:Vmn1r32
|
UTSW |
6 |
66,530,120 (GRCm39) |
nonsense |
probably null |
|
R9429:Vmn1r32
|
UTSW |
6 |
66,530,237 (GRCm39) |
missense |
probably benign |
0.03 |
|
Posted On |
2016-08-02 |