Incidental Mutation 'IGL01673:Vmn1r74'
ID |
103554 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vmn1r74
|
Ensembl Gene |
ENSMUSG00000047655 |
Gene Name |
vomeronasal 1 receptor 74 |
Synonyms |
V1rg5 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.062)
|
Stock # |
IGL01673
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
11580702-11581616 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 11581317 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Phenylalanine
at position 206
(I206F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000154746
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000050416]
[ENSMUST00000228471]
|
AlphaFold |
Q8R290 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000050416
AA Change: I206F
PolyPhen 2
Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000055148 Gene: ENSMUSG00000047655 AA Change: I206F
Domain | Start | End | E-Value | Type |
Pfam:7tm_1
|
22 |
290 |
1.3e-7 |
PFAM |
Pfam:V1R
|
34 |
296 |
1.2e-31 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000210930
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000228471
AA Change: I206F
PolyPhen 2
Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 21 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Cpz |
A |
T |
5: 35,669,891 (GRCm39) |
V262E |
probably benign |
Het |
Cyp4f14 |
A |
G |
17: 33,130,125 (GRCm39) |
|
probably null |
Het |
Ddx46 |
G |
T |
13: 55,800,861 (GRCm39) |
V339F |
probably damaging |
Het |
Gpn1 |
T |
G |
5: 31,652,179 (GRCm39) |
C21W |
probably damaging |
Het |
Gpr63 |
A |
T |
4: 25,008,014 (GRCm39) |
Q246L |
probably benign |
Het |
Hsp90b1 |
T |
A |
10: 86,529,296 (GRCm39) |
M658L |
probably damaging |
Het |
Immp2l |
T |
C |
12: 41,118,320 (GRCm39) |
S4P |
probably benign |
Het |
Krtap9-5 |
A |
T |
11: 99,840,377 (GRCm39) |
*359C |
probably null |
Het |
Lgals7 |
A |
G |
7: 28,565,621 (GRCm39) |
|
probably benign |
Het |
Mak |
G |
T |
13: 41,201,699 (GRCm39) |
|
probably null |
Het |
Mrps18c |
A |
G |
5: 100,946,672 (GRCm39) |
R13G |
possibly damaging |
Het |
Myo7a |
A |
G |
7: 97,703,915 (GRCm39) |
V1946A |
probably benign |
Het |
Nfyc |
T |
C |
4: 120,636,307 (GRCm39) |
|
probably benign |
Het |
Nkx2-4 |
C |
T |
2: 146,925,834 (GRCm39) |
V343M |
possibly damaging |
Het |
Or5be3 |
T |
C |
2: 86,863,731 (GRCm39) |
Y278C |
probably damaging |
Het |
Or8d2 |
T |
C |
9: 38,760,316 (GRCm39) |
V302A |
probably benign |
Het |
Rapgef4 |
G |
T |
2: 72,071,781 (GRCm39) |
S743I |
probably damaging |
Het |
Tcf7 |
A |
G |
11: 52,147,823 (GRCm39) |
C210R |
probably damaging |
Het |
Ubqln3 |
T |
A |
7: 103,791,605 (GRCm39) |
I162F |
probably benign |
Het |
Vmn1r216 |
A |
G |
13: 23,283,641 (GRCm39) |
Q108R |
probably damaging |
Het |
Wdr64 |
T |
C |
1: 175,627,922 (GRCm39) |
I872T |
possibly damaging |
Het |
|
Other mutations in Vmn1r74 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01608:Vmn1r74
|
APN |
7 |
11,581,560 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03023:Vmn1r74
|
APN |
7 |
11,581,257 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL03409:Vmn1r74
|
APN |
7 |
11,581,240 (GRCm39) |
missense |
probably damaging |
0.99 |
R0393:Vmn1r74
|
UTSW |
7 |
11,581,242 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1488:Vmn1r74
|
UTSW |
7 |
11,581,510 (GRCm39) |
missense |
probably benign |
0.02 |
R1707:Vmn1r74
|
UTSW |
7 |
11,581,504 (GRCm39) |
missense |
probably damaging |
0.98 |
R1998:Vmn1r74
|
UTSW |
7 |
11,581,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R1999:Vmn1r74
|
UTSW |
7 |
11,581,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R2139:Vmn1r74
|
UTSW |
7 |
11,581,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R4027:Vmn1r74
|
UTSW |
7 |
11,580,898 (GRCm39) |
missense |
probably damaging |
0.98 |
R4576:Vmn1r74
|
UTSW |
7 |
11,580,696 (GRCm39) |
splice site |
probably null |
|
R4619:Vmn1r74
|
UTSW |
7 |
11,581,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R4619:Vmn1r74
|
UTSW |
7 |
11,581,398 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5371:Vmn1r74
|
UTSW |
7 |
11,580,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R5606:Vmn1r74
|
UTSW |
7 |
11,580,822 (GRCm39) |
missense |
probably benign |
0.01 |
R6464:Vmn1r74
|
UTSW |
7 |
11,581,131 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6901:Vmn1r74
|
UTSW |
7 |
11,581,368 (GRCm39) |
missense |
probably benign |
0.00 |
R6920:Vmn1r74
|
UTSW |
7 |
11,581,575 (GRCm39) |
missense |
probably benign |
0.01 |
R7223:Vmn1r74
|
UTSW |
7 |
11,580,894 (GRCm39) |
nonsense |
probably null |
|
R7231:Vmn1r74
|
UTSW |
7 |
11,580,888 (GRCm39) |
missense |
probably benign |
0.34 |
R7418:Vmn1r74
|
UTSW |
7 |
11,581,081 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8135:Vmn1r74
|
UTSW |
7 |
11,581,530 (GRCm39) |
missense |
probably benign |
0.36 |
R8692:Vmn1r74
|
UTSW |
7 |
11,580,972 (GRCm39) |
missense |
probably benign |
0.03 |
R8748:Vmn1r74
|
UTSW |
7 |
11,580,903 (GRCm39) |
missense |
probably benign |
0.10 |
R9004:Vmn1r74
|
UTSW |
7 |
11,580,840 (GRCm39) |
missense |
probably benign |
0.00 |
R9258:Vmn1r74
|
UTSW |
7 |
11,580,999 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9564:Vmn1r74
|
UTSW |
7 |
11,581,534 (GRCm39) |
missense |
probably damaging |
1.00 |
RF049:Vmn1r74
|
UTSW |
7 |
11,581,067 (GRCm39) |
frame shift |
probably null |
|
RF063:Vmn1r74
|
UTSW |
7 |
11,581,067 (GRCm39) |
frame shift |
probably null |
|
Z1176:Vmn1r74
|
UTSW |
7 |
11,580,936 (GRCm39) |
missense |
probably benign |
|
|
Posted On |
2014-01-21 |