Incidental Mutation 'IGL01890:Vmn1r194'
ID |
179221 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vmn1r194
|
Ensembl Gene |
ENSMUSG00000069297 |
Gene Name |
vomeronasal 1 receptor 194 |
Synonyms |
Gm11294 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.074)
|
Stock # |
IGL01890
|
Quality Score |
|
Status
|
|
Chromosome |
13 |
Chromosomal Location |
22428385-22429275 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 22428776 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Phenylalanine
at position 131
(Y131F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000089331
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000091737]
|
AlphaFold |
J3JS27 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000091737
AA Change: Y131F
PolyPhen 2
Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)
|
SMART Domains |
Protein: ENSMUSP00000089331 Gene: ENSMUSG00000069297 AA Change: Y131F
Domain | Start | End | E-Value | Type |
Pfam:V1R
|
35 |
296 |
3.4e-37 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 22 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn1 |
A |
T |
12: 80,231,642 (GRCm39) |
V265E |
probably damaging |
Het |
Anks1b |
A |
G |
10: 90,480,389 (GRCm39) |
I865V |
probably benign |
Het |
Car5a |
G |
A |
8: 122,650,349 (GRCm39) |
A182V |
probably benign |
Het |
Ccdc47 |
A |
G |
11: 106,096,277 (GRCm39) |
V249A |
probably damaging |
Het |
Cyb561d2 |
A |
G |
9: 107,418,722 (GRCm39) |
V34A |
probably damaging |
Het |
Dmbt1 |
A |
G |
7: 130,676,149 (GRCm39) |
|
probably benign |
Het |
Entpd6 |
G |
A |
2: 150,612,612 (GRCm39) |
D445N |
possibly damaging |
Het |
Fastkd2 |
A |
G |
1: 63,771,320 (GRCm39) |
I225M |
probably benign |
Het |
Flcn |
A |
G |
11: 59,685,996 (GRCm39) |
V424A |
probably benign |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gpn3 |
A |
G |
5: 122,519,328 (GRCm39) |
M176V |
probably benign |
Het |
Igkv12-38 |
C |
T |
6: 69,920,389 (GRCm39) |
C43Y |
probably damaging |
Het |
Oas1h |
A |
G |
5: 121,000,852 (GRCm39) |
|
probably null |
Het |
Rexo1 |
A |
T |
10: 80,378,845 (GRCm39) |
Y1064N |
possibly damaging |
Het |
Skint1 |
G |
A |
4: 111,867,878 (GRCm39) |
G2R |
probably damaging |
Het |
Slc4a9 |
G |
A |
18: 36,662,760 (GRCm39) |
A172T |
possibly damaging |
Het |
Synpo2 |
A |
G |
3: 122,906,146 (GRCm39) |
S727P |
probably damaging |
Het |
Tmem131 |
A |
T |
1: 36,862,237 (GRCm39) |
|
probably benign |
Het |
Trpm3 |
G |
T |
19: 22,689,083 (GRCm39) |
R4L |
probably damaging |
Het |
Upf1 |
A |
T |
8: 70,786,880 (GRCm39) |
V879E |
possibly damaging |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r95 |
T |
A |
17: 18,671,737 (GRCm39) |
N491K |
probably damaging |
Het |
|
Other mutations in Vmn1r194 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02140:Vmn1r194
|
APN |
13 |
22,428,706 (GRCm39) |
missense |
probably benign |
0.08 |
R0066:Vmn1r194
|
UTSW |
13 |
22,428,641 (GRCm39) |
missense |
probably benign |
0.33 |
R0066:Vmn1r194
|
UTSW |
13 |
22,428,641 (GRCm39) |
missense |
probably benign |
0.33 |
R0109:Vmn1r194
|
UTSW |
13 |
22,429,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R0109:Vmn1r194
|
UTSW |
13 |
22,429,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R1276:Vmn1r194
|
UTSW |
13 |
22,429,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R1426:Vmn1r194
|
UTSW |
13 |
22,429,236 (GRCm39) |
missense |
probably damaging |
0.99 |
R1620:Vmn1r194
|
UTSW |
13 |
22,429,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R4593:Vmn1r194
|
UTSW |
13 |
22,428,461 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4844:Vmn1r194
|
UTSW |
13 |
22,429,223 (GRCm39) |
missense |
probably benign |
0.02 |
R5011:Vmn1r194
|
UTSW |
13 |
22,429,058 (GRCm39) |
missense |
probably benign |
0.00 |
R5110:Vmn1r194
|
UTSW |
13 |
22,429,170 (GRCm39) |
missense |
probably benign |
0.07 |
R5588:Vmn1r194
|
UTSW |
13 |
22,428,512 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5810:Vmn1r194
|
UTSW |
13 |
22,428,597 (GRCm39) |
nonsense |
probably null |
|
R6648:Vmn1r194
|
UTSW |
13 |
22,428,694 (GRCm39) |
missense |
probably benign |
0.11 |
R7660:Vmn1r194
|
UTSW |
13 |
22,428,767 (GRCm39) |
missense |
not run |
|
R7663:Vmn1r194
|
UTSW |
13 |
22,428,911 (GRCm39) |
missense |
not run |
|
R7879:Vmn1r194
|
UTSW |
13 |
22,428,772 (GRCm39) |
missense |
probably benign |
0.06 |
R8344:Vmn1r194
|
UTSW |
13 |
22,429,247 (GRCm39) |
missense |
probably benign |
0.01 |
R8830:Vmn1r194
|
UTSW |
13 |
22,429,006 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9245:Vmn1r194
|
UTSW |
13 |
22,428,731 (GRCm39) |
missense |
probably benign |
0.44 |
R9291:Vmn1r194
|
UTSW |
13 |
22,428,875 (GRCm39) |
missense |
probably benign |
0.20 |
R9624:Vmn1r194
|
UTSW |
13 |
22,428,671 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Vmn1r194
|
UTSW |
13 |
22,428,596 (GRCm39) |
missense |
probably benign |
0.08 |
|
Posted On |
2014-05-07 |