Incidental Mutation 'IGL03080:Vmn2r44'
ID |
417842 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vmn2r44
|
Ensembl Gene |
ENSMUSG00000094098 |
Gene Name |
vomeronasal 2, receptor 44 |
Synonyms |
EG434113 |
Accession Numbers |
|
Essential gene? |
Not available
|
Stock # |
IGL03080
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
8370459-8386237 bp(-) (GRCm39) |
Type of Mutation |
utr 5 prime |
DNA Base Change (assembly) |
C to A
at 8386244 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000132467
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000166499]
|
AlphaFold |
L7N2E1 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000166499
|
SMART Domains |
Protein: ENSMUSP00000132467 Gene: ENSMUSG00000094098
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
Pfam:ANF_receptor
|
73 |
469 |
2.5e-34 |
PFAM |
Pfam:NCD3G
|
512 |
565 |
3.8e-20 |
PFAM |
Pfam:7tm_3
|
598 |
833 |
5.7e-55 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abce1 |
T |
C |
8: 80,429,630 (GRCm39) |
|
probably null |
Het |
Adgrf3 |
T |
C |
5: 30,401,827 (GRCm39) |
M734V |
probably benign |
Het |
Aqp8 |
T |
G |
7: 123,065,802 (GRCm39) |
|
probably benign |
Het |
Ces1d |
C |
A |
8: 93,896,346 (GRCm39) |
|
probably null |
Het |
Cntn4 |
A |
G |
6: 106,632,500 (GRCm39) |
D508G |
probably damaging |
Het |
Cyp11b1 |
A |
T |
15: 74,711,285 (GRCm39) |
|
probably null |
Het |
Dnah8 |
A |
G |
17: 30,937,980 (GRCm39) |
D1619G |
probably benign |
Het |
Eif1ad17 |
A |
T |
12: 87,978,615 (GRCm39) |
|
probably benign |
Het |
Ephb4 |
T |
A |
5: 137,352,345 (GRCm39) |
|
probably benign |
Het |
Ffar3 |
A |
T |
7: 30,554,747 (GRCm39) |
V191E |
probably damaging |
Het |
Galnt1 |
T |
A |
18: 24,402,574 (GRCm39) |
D310E |
probably damaging |
Het |
Igf2r |
T |
C |
17: 12,945,563 (GRCm39) |
Y342C |
probably benign |
Het |
Jade1 |
T |
A |
3: 41,554,510 (GRCm39) |
C251* |
probably null |
Het |
Jhy |
T |
C |
9: 40,855,653 (GRCm39) |
E278G |
probably damaging |
Het |
Kif24 |
A |
C |
4: 41,394,417 (GRCm39) |
S819A |
probably benign |
Het |
Lrp8 |
T |
C |
4: 107,712,996 (GRCm39) |
L344P |
probably damaging |
Het |
Lrrc27 |
A |
G |
7: 138,810,153 (GRCm39) |
T375A |
probably benign |
Het |
Mbd3 |
C |
T |
10: 80,229,085 (GRCm39) |
R204Q |
probably damaging |
Het |
Nab2 |
T |
C |
10: 127,500,663 (GRCm39) |
N143S |
possibly damaging |
Het |
Nkiras2 |
T |
C |
11: 100,515,105 (GRCm39) |
|
probably null |
Het |
Or7e174 |
A |
T |
9: 20,012,705 (GRCm39) |
I217F |
probably damaging |
Het |
Palm |
C |
A |
10: 79,654,951 (GRCm39) |
H74Q |
probably damaging |
Het |
Pros1 |
T |
A |
16: 62,738,506 (GRCm39) |
N408K |
probably damaging |
Het |
Psg23 |
T |
A |
7: 18,340,910 (GRCm39) |
Y448F |
probably damaging |
Het |
Ranbp2 |
C |
A |
10: 58,312,613 (GRCm39) |
P1111Q |
probably benign |
Het |
Rims2 |
A |
G |
15: 39,399,299 (GRCm39) |
S1115G |
probably damaging |
Het |
Scn7a |
T |
C |
2: 66,528,160 (GRCm39) |
T777A |
probably benign |
Het |
Spata31h1 |
T |
C |
10: 82,119,816 (GRCm39) |
D428G |
probably damaging |
Het |
Stard3nl |
A |
T |
13: 19,554,648 (GRCm39) |
|
probably null |
Het |
Sult1d1 |
T |
C |
5: 87,704,847 (GRCm39) |
D214G |
probably benign |
Het |
Tmprss12 |
T |
C |
15: 100,190,529 (GRCm39) |
W300R |
probably damaging |
Het |
Tmprss2 |
T |
C |
16: 97,398,044 (GRCm39) |
Y44C |
probably damaging |
Het |
Ttk |
A |
G |
9: 83,725,136 (GRCm39) |
N154D |
probably damaging |
Het |
Tut4 |
T |
A |
4: 108,363,021 (GRCm39) |
S444R |
probably damaging |
Het |
Tyw1 |
T |
C |
5: 130,295,896 (GRCm39) |
Y108H |
probably damaging |
Het |
Zfand1 |
A |
G |
3: 10,405,797 (GRCm39) |
*269Q |
probably null |
Het |
Zfp142 |
A |
T |
1: 74,610,368 (GRCm39) |
D1039E |
probably benign |
Het |
Zkscan5 |
G |
T |
5: 145,155,460 (GRCm39) |
S377I |
probably damaging |
Het |
|
Other mutations in Vmn2r44 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01650:Vmn2r44
|
APN |
7 |
8,383,103 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01723:Vmn2r44
|
APN |
7 |
8,380,915 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01767:Vmn2r44
|
APN |
7 |
8,383,237 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02161:Vmn2r44
|
APN |
7 |
8,380,814 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02299:Vmn2r44
|
APN |
7 |
8,380,815 (GRCm39) |
missense |
probably benign |
|
IGL02418:Vmn2r44
|
APN |
7 |
8,380,864 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02829:Vmn2r44
|
APN |
7 |
8,380,879 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02851:Vmn2r44
|
APN |
7 |
8,386,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Vmn2r44
|
UTSW |
7 |
8,380,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R1789:Vmn2r44
|
UTSW |
7 |
8,383,122 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1932:Vmn2r44
|
UTSW |
7 |
8,370,981 (GRCm39) |
missense |
probably benign |
0.04 |
R2354:Vmn2r44
|
UTSW |
7 |
8,373,639 (GRCm39) |
missense |
probably damaging |
0.99 |
R4009:Vmn2r44
|
UTSW |
7 |
8,380,987 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4130:Vmn2r44
|
UTSW |
7 |
8,370,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R4790:Vmn2r44
|
UTSW |
7 |
8,370,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R4854:Vmn2r44
|
UTSW |
7 |
8,383,300 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4887:Vmn2r44
|
UTSW |
7 |
8,380,985 (GRCm39) |
missense |
probably benign |
0.19 |
R4888:Vmn2r44
|
UTSW |
7 |
8,380,985 (GRCm39) |
missense |
probably benign |
0.19 |
R5484:Vmn2r44
|
UTSW |
7 |
8,383,123 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6110:Vmn2r44
|
UTSW |
7 |
8,381,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R6357:Vmn2r44
|
UTSW |
7 |
8,373,657 (GRCm39) |
missense |
probably benign |
0.01 |
R6526:Vmn2r44
|
UTSW |
7 |
8,381,098 (GRCm39) |
missense |
probably benign |
0.01 |
R7083:Vmn2r44
|
UTSW |
7 |
8,381,369 (GRCm39) |
missense |
probably benign |
0.44 |
R7087:Vmn2r44
|
UTSW |
7 |
8,381,366 (GRCm39) |
missense |
probably benign |
0.02 |
R7115:Vmn2r44
|
UTSW |
7 |
8,370,527 (GRCm39) |
nonsense |
probably null |
|
R7125:Vmn2r44
|
UTSW |
7 |
8,370,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R7258:Vmn2r44
|
UTSW |
7 |
8,380,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R7359:Vmn2r44
|
UTSW |
7 |
8,370,538 (GRCm39) |
missense |
probably benign |
0.30 |
R7494:Vmn2r44
|
UTSW |
7 |
8,386,122 (GRCm39) |
nonsense |
probably null |
|
R7766:Vmn2r44
|
UTSW |
7 |
8,371,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R7777:Vmn2r44
|
UTSW |
7 |
8,381,314 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8184:Vmn2r44
|
UTSW |
7 |
8,371,227 (GRCm39) |
nonsense |
probably null |
|
R8674:Vmn2r44
|
UTSW |
7 |
8,380,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R8752:Vmn2r44
|
UTSW |
7 |
8,370,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R8897:Vmn2r44
|
UTSW |
7 |
8,381,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R8915:Vmn2r44
|
UTSW |
7 |
8,370,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R8928:Vmn2r44
|
UTSW |
7 |
8,381,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R9163:Vmn2r44
|
UTSW |
7 |
8,371,091 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Vmn2r44
|
UTSW |
7 |
8,370,976 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Posted On |
2016-08-02 |